Venue R5 Basic Service Manual - SM - DOC2782487 - 2
Venue R5 Basic Service Manual - SM - DOC2782487 - 2
2024
GEHC_FRNT_CVR.FM
Technical Publication
Venue™ R5
Service Manual
Direction Number: 5945168-100
Operating Documentation
Table of Contents
Chapter 1: Introduction
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14
Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 15
Venue™ Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17
Patient Data Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17
Table of Contents 1
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Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 32
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 32
Chapter 2: Site Preparation
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 1
Purpose of Chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Console Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 2
Unit Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Cooling Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Lighting Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Time and Manpower Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Venue™ Power Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Inrush Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Site Circuit Breaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Site Power Outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Mains Power Plug . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3
Power Stability Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
EMI Prevention/Abatement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Operation and storage temperatures for probe . . . . . . . . . . . . . . . . . . . . 2 - 5
Time and Manpower Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7
Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Required Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 8
Desirable features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 8
Suggested Minimal Floor Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
Recommended Floor Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 10
Networking Pre-Installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 11
Stand-alone Unit (without Network Connection) . . . . . . . . . . . . . . . . . . 2 - 11
Unit Connected to Hospital’s Network . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 11
Purpose of the DICOM Network Function . . . . . . . . . . . . . . . . . . . . . . . 2 - 11
DICOM Option Pre-Installation Requirements . . . . . . . . . . . . . . . . . . . . 2 - 11
Setup Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2
Average Setup Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Setup Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
System Acclimation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Power on/Boot up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
Power Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
Complete Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Venue™ Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
EZ Config - Setup Wizard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Accessing System Configuration Settings . . . . . . . . . . . . . . . . . . . . . . . 3 - 27
Enter Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29
Adjust Date and Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30
Select Language for User Interface and Online Manuals . . . . . . . . . . . 3 - 32
Select Units of Measure and Controls Sound . . . . . . . . . . . . . . . . . . . . 3 - 33
Service Screen Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 34
Open Service Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 34
Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Approved Internal Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Approved External Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
External Peripherals for Connection to USB . . . . . . . . . . . . . . . . . . . . . 3 - 35
Software Options Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Software Option Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
To Install a Software Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Remote Check and Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35
Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36
Physical Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36
Stand-alone Venue™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36
Wireless Connection from Venue™ to DICOM Server . . . . . . . . . . . . . . . . . . 3 - 36
Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 37
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 37
Select TCP/IP Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 38
Finding the system network MAC (Physical) addresses . . . . . . . . . . . . . . . . . . 3 - 39
Set up Wireless connection (For broadcasting SSID networks) . . . . . . . . . . . . 3 - 40
Setting Up Non-Broadcasting (Hidden) Wireless Network Connection . . . . . . 3 - 41
Network Proxy/DNS/WINS configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45
Proxy setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45
DNS/WINS setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 46
Setup QView . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48
QView Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48
Changing the AE Title and/or Port Number (Port No.) . . . . . . . . . . . . . . . . . . . 3 - 49
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 49
DICOM Server IP Address on the Venue™ . . . . . . . . . . . . . . . . . . . . . 3 - 50
Verify the Network Connection to a Device . . . . . . . . . . . . . . . . . . . . . . 3 - 52
Verify the Connection to a Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 52
Table of Contents 4
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Options Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
Software Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
USB Flash Card Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
Wireless Network Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
Wireless Probe 1st time Registration Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
General Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power ON/Boot-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Table of Contents 5
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Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Connecting AC (Mains) Power to the Venue™ Ultrasound Unit . . . . . . . 4 - 4
Switch ON the AC Power to Venue™ . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Power Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
Logging On to the Venue™ as “ADM” . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
Select Config via the Cockpit (Monitor) . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
The Login dialog . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
Data Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
Deleting Patient Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
Cockpit (Monitor) Position Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
To Adjust the Cockpit (Monitor) Position . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
Moving and Transporting the Venue™ Ultrasound Scanner . . . . . . . . . . . . . . 4 - 10
The Casters (Wheels) Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
To Prepare the Venue™ to be Moved . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11
To Ensure Safety while Moving the Venue™ . . . . . . . . . . . . . . . . . . . . 4 - 12
Transporting the Venue™ by Vehicle . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12
At the New Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12
Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Performance Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Test Phantoms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
2D Mode (B Mode) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Adjust the 2D Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14
M Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14
M-Mode Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Using M-Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Optimizing M-Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Using Color Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
PW/CW Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
PW and CW Doppler Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
Using PW/CW Doppler Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17
Optimizing PW/CW Doppler Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17
Probe/Connectors Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18
Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Using Cineloop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Audio Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21
Table of Contents 6
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Printer Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21
Windows Print Test Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21
ECG Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23
Mechanical Functions Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Monitor Articulated Arm Movement Check . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Swivel and Full Lock Casters Function Check . . . . . . . . . . . . . . . . . . . . 4 - 26
Electrical Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27
Ground Continuity Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27
Chapter 5: Components and Function (Theory)
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 1
Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
System Configuration and Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
Electronics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 4
Connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 5
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Stand-alone Venue™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Direct Connection from Venue™ to a Review Workstation . . . . . . . . . . . . . . . . 5 - 5
Venue™ and a DICOM Server in a Network . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
InSite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 6
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
InSite ExC Icon . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
Initiating a Request For Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7
RFS History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8
InSite Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9
InSite Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
Exiting InSite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
External Input/Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 19
Cooling System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 30
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 30
Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Internal Peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Black & White Digital Graphic Printer . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
ECG Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
External Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Wi-Fi Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
Bar-code reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31
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Chapter 6: Service Adjustments
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 1
Purpose of Chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Network Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18
Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 20
Agent Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 22
Probe Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 25
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Background . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 25
Using the Probe Check Tool: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 26
Pass result . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 27
Failed result . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 28
e-Delivery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 29
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29
Accessing GE HealthCare portal and downloading SW . . . . . . . . . . . . . . . . . . 7 - 29
Burning Disk-on-Key Media with SW Downloaded from GE HealthCare Portal 7 - 34
Obtain SW update directly through RSVP . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 37
Verify WIFI and RSVP connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 37
Download and install the new SW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 38
To Rollback and install the previous (backed-up) SW . . . . . . . . . . . . . . 7 - 46
To upload SW from USB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 47
Noise Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 51
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 51
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 51
Overview of Types of Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 51
Noise Picked Up from the Air . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 51
Noise Received via the External Cables . . . . . . . . . . . . . . . . . . . . . . . . 7 - 51
Intermittent Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 52
Self-generated Noise Generated inside the Ultrasound system) . . . . . . 7 - 52
Heat Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 52
Hardware Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 52
Software Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 52
Different Power Outlet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 52
Different System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 53
Different Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 53
Disconnect External Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 53
Audio Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 54
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 54
Audio Troubleshooting Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 54
No Auxiliary Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 61
ViewPoint Reporting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 69
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 69
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 69
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 69
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 70
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 5
Preparation for Cover Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 5
Lower Front eTower Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 6
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6
Lower Front eTower Cover Removal Procedure . . . . . . . . . . . . . . . . . . . 8 - 6
Lower Front eTower Cover Installation Procedure . . . . . . . . . . . . . . . . . 8 - 6
Left Side eTower Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7
Left Side eTower Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 7
Left Side eTower Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . 8 - 8
Right Side eTower Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 9
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 9
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 9
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 9
Right Side eTower Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . 8 - 9
Right Side eTower Cover Installation Procedure . . . . . . . . . . . . . . . . . . . 8 - 9
Mid Thermal Baffle Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 10
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 10
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 10
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 10
Mid Thermal Baffle Cover Removal Procedure . . . . . . . . . . . . . . . . . . . 8 - 10
Mid Thermal Baffle Cover Installation Procedure . . . . . . . . . . . . . . . . . 8 - 10
Upper eTower Front Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . 8 - 11
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 11
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 11
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 11
Upper eTower Front Cover Removal Procedure . . . . . . . . . . . . . . . . . . 8 - 11
Upper eTower Front Cover Installation Procedure . . . . . . . . . . . . . . . . 8 - 12
Printer Insert Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
Printer Insert Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13
Printer Insert Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 14
MPB Door Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
MPB Door Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15
MPB Door Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 16
RS Probe Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
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Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
RS Probe Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
RS Probe Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17
Riser Thermal Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
Riser Thermal Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . 8 - 18
Riser Thermal Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 18
Riser Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 19
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 19
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 19
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 19
Riser Cover Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 19
Riser Cover Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 21
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Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 64
T-PSB Module Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 64
T-PSB Module Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 65
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Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 80
Halo Handle Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 80
Halo Handle Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 82
Articulated Arm Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83
Arm Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83
Arm Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 86
Venue Locking Release Handle Replacement Procedure . . . . . . . . . . . . . . . . 8 - 88
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 88
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 88
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 88
Handle Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 88
Handle Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 90
Riser Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 91
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 91
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 91
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 91
Riser Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 91
Riser Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 93
Casters Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
Casters Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
Casters Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 95
T-CFE Plastic Cable Guide Replacement Procedure . . . . . . . . . . . . . . . . . . . . 8 - 97
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 97
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 97
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 97
Plastic Cable Guide for CFE Removal Procedure . . . . . . . . . . . . . . . . . 8 - 97
Plastic Cable Guide for CFE Installation Procedure . . . . . . . . . . . . . . . 8 - 99
MPB Blower (Fan) Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 100
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 100
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 100
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 100
MPB Blower (Fan) Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 100
MPB Fan Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 102
IPP Module Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104
IPP Module Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104
IPP Module Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 107
Table of Contents 16
P R E L I M I N A R Y
Table of Contents 17
P R E L I M I N A R Y
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 144
MPB to BIB Control Cable Removal Procedure . . . . . . . . . . . . . . . . . . 8 - 144
MPB to BIB Control Cable Installation Procedure . . . . . . . . . . . . . . . . 8 - 146
Printer USB Cable Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 147
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 147
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 147
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 147
Printer USB Cable Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 147
Printer USB Cable Installation Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 148
BEP Cables Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 149
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 149
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 149
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 149
BEP Cables Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 149
BEP Cables Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 152
MPB TO T-FEPS - FRU Cable Replacement Procedure . . . . . . . . . . . . . . . . 8 - 157
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 157
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 157
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 157
MPB TO T-FEPS Cable Removal Procedure . . . . . . . . . . . . . . . . . . . 8 - 157
MPB TO T-FEPS Cable Installation Procedure . . . . . . . . . . . . . . . . . . 8 - 158
MPB To Peripherals Harness - FRU Cable Replacement Procedure . . . . . . 8 - 160
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 160
Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 160
Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 160
MPB To Peripherals Harness - FRU Cable Removal Procedure . . . . . 8 - 160
MPB To Peripherals Harness - FRU Cable Installation Procedure . . . 8 - 163
Table of Contents 18
P R E L I M I N A R Y
List of Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Why Do Maintenance? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3
Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3
Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3
Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3
Tools Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
Tools Required for Servicing the Venue™ . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
System Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Peripheral/Option Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8
Mains Cable Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
General Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
Table of Contents 20
P R E L I M I N A R Y
Table of Contents 21
P R E L I M I N A R Y 6/2/24
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Important Precautions
TRANSLATION POLICY
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DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write “Damage In
Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by
a GE HealthCare representative or hospital receiving agent. Whether noted or concealed, damage
MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after
receipt, and the contents and containers held for inspection by the carrier. A transportation company
will not pay a claim for damage if an inspection is not requested within this 14 day period.
The purchaser of GE HealthCare equipment shall only utilize qualified personnel (i.e., GE HealthCare’s
field engineers, personnel of third-party service companies with equivalent training, or licensed
electricians) to perform electrical servicing on the equipment.
Service Documentation,
GE Medical Systems
Ultrasound & Primary Care Diagnostics LLC
3200 N Grandview Blvd
Wauwatosa, WI 53188
USA
GE HealthCare employees should use TrackWise to report service documentation issues. These issues
will then be in the internal problem reporting tool and communicated to the writer.
WARNING Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety
glasses, and kneeling pad, to reduce the risk of injury.
For a complete review of all safety requirements, see the Chapter 1 Safety Considerations section in
the Service Manual.
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LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE HealthCare.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
COPYRIGHTS
©by General Electric Company Inc. All Rights Reserved.
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Revision History
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P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
Chapter 1
Introduction
Section 1-1
Overview
1-1-1 Purpose of Chapter 1
This chapter describes important issues related to safely servicing the Venue™ ultrasound scanner.
The service provider must read and understand all the information presented here before installing or
servicing a unit.
Section 1-2
Service Manual Overview
This manual provides setup and service information for the Venue™ ultrasound scanner. The ten
chapters it contains are outlined in Table 1-1 below.
In the beginning of the manual, before Chapter 1, you will find the language policy for GE HealthCare
service documentation, legal information, a revision overview and the Table of Contents (TOC).
In the beginning of the manual, before chapter 1, you will find the language policy for GE HealthCare
service documentation, legal information, a revision overview and the Table of Contents (TOC).
General Procedures and Contains functional checks that must be performed as part of the
Chapter 4
Functional Checks setup, or as required during servicing and periodic maintenance.
NOTE: The illustrations provided in this service manual are for illustration purposes only and are subject to
change without notice.
GP
PSI Group Cat No. Description
PSI Code Code
Venue™ R5 H45235VN Venue™ R5 ultrasound scanner UVENUO 25719A
Venue™ R5 ultrasound scanner
Venue™ R5 Wuxi H45235VNW UVENUP 25720B
WXB
The system provides image generation in 2D, Color Doppler, M-Mode, Color M-Mode and PW.
The fully digital architecture of the Venue™ system allows optimal usage of all scanning modes and
probe types throughout the full spectrum of operating frequencies.
Signal flows from the Probe Connector Panel to the Front End, and then over to the Back End Processor
and finally to the cockpit and peripherals.
All necessary software is loaded from the hard drive on power up.
Section 1-3
Important Conventions
1-3-1 Conventions Used in this Manual
1-3-1-2 Icons
Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
• DANGER
• WARNING
• CAUTION
When a hazard is present that can cause property damage, but has absolutely no personal injury risk,
a NOTICE is used.
CAUTION CAUTION IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL OR CAN CAUSE
MINOR PERSONAL INJURY OR PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
EQUIPMENT DAMAGE POSSIBLE.
NOTE: Notes are used to provide important information about an item or a procedure.
NOTE: Be sure to read the notes; the information contained in a note can often save you time or effort.
Refer to the User Manual for a complete list of icons used on the Ultrasound System; not all icons may
be listed in the table below.
Other hazard icons make you aware of specific procedures that should be followed.
Be sure to read the notes; the information contained in a note can often save you time or effort.
NOTE: The Venue™ system has no unintended or motorized moving parts that could cause pinching; all
moving parts are mechanically operated by the user.
Pay attention to move such parts carefully (e.g. articulated arm).
Section 1-4
Safety Considerations
1-4-1 Introduction
The following safety precautions must be observed during all phases of operation, service and repair of
this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this
manual violates safety standards of design, manufacture, and intended use of the equipment.
NOTE: Local laws may restrict this device for sale or use by or on the order of a physician.
WARNING BECAUSE OF THE LIMITED ACCESS TO CABINETS AND EQUIPMENT IN THE FIELD,
PLACING PEOPLE IN AWKWARD POSITIONS, GE HealthCare HAS LIMITED THE
LIFTING WEIGHT FOR ONE PERSON IN THE FIELD TO 16 KG (35 LBS). ANYTHING
OVER 16 KG (35 LBS) REQUIRES 2 PEOPLE.
WARNING USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY
SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJURY.
WARNING RISK OF ELECTRICAL SHOCK, ULTRASOUND SYSTEM MUST BE TURNED OFF AND
DISCONNECTED FROM POWER SOURCE. CORD MUST BE CONTROLLED AT ALL
TIMES.
WAIT FOR AT LEAST 30 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE
NO TEST POINTS TO VERIFY ISOLATION. THE LIGHT ON THE OP PANEL ON/OFF
BUTTON WILL TURN OFF.
ULTRASOUND SYSTEM COMPONENTS MAY BE ENERGIZED. ALWAYS REFER TO THE
ULTRASOUND SYSTEM'S SERVICE MANUAL FOR LOTO WARNINGS AND CAUTIONS.
CAPACITORS ON ULTRASOUND SYSTEMS WITH THE SHEARWAVE OPTION CAN
TAKE UP TO 5 MINUTES TO DISCHARGE.
WARNING USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY
SHOES, SAFETY GLASSES, AND KNEELING PADS, TO REDUCE THE RISK OF INJURY.
WARNING WEAR ALL PPE INCLUDING GLOVES AS INDICATED IN THE CHEMICAL MSDS.
CAUTION USE PROTECTIVE GLASSES DURING DRILLING, FILING AND DURING ALL OTHER WORK
WHERE EYES NEED PROTECTION.
CAUTION USE SAFETY SHOES WHEN DOING WORK WHERE THERE IS ANY CHANCE OF FOOT
DAMAGE.
WARNING PRIOR TO ELEVATING SCANNER, VERIFY THAT THE MONITOR IS LOCKED IN ITS
LOWEST POSITION. VERIFY THAT THE FRONT BRAKE IS LOCKED AND THE
SCANNER IS UNABLE TO SWIVEL. VERIFY THAT THE REAR BRAKES ARE IN THE
LOCKED POSITION.
DANGER WHENEVER THE UNIT IS TO BE MOVED ALONG ANY INCLINE, USE EXTREME
CAUTION. MAKE SURE THAT THE VENUE™ SCANNER AND ALL PERIPHERALS ARE
SECURELY MOUNTED IN PLACE BEFORE ATTEMPTING TO MOVE IT.
DANGER ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN
EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND
PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR
DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN
SERIOUS INJURY AND EQUIPMENT DAMAGE.
DANGER NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT
MAY BE DAMAGED.
CAUTION ULTRASOUND SYSTEM WEIGHTS CAN BE SIGNIFICANT, PLUS THE WEIGHT OF INSTALLED
PERIPHERALS, WHEN READY FOR USE. CARE MUST BE USED WHEN MOVING IT OR
REPLACING ITS PARTS.
FAILURE TO FOLLOW THE PRECAUTIONS LISTED BELOW COULD RESULT IN INJURY,
UNCONTROLLED MOTION AND COSTLY DAMAGE.
• USE THE HANDLE TO MOVE THE ULTRASOUND SYSTEM.
• BE SURE THE PATHWAY IS CLEAR. LIMIT MOVEMENT TO A SLOW
CAREFUL WALK.
• DO NOT LET THE ULTRASOUND SYSTEM STRIKE WALLS OR DOOR
FRAME.
• USE TWO PEOPLE WHEN MOVING ON INCLINES OR LIFTING MORE THAN
16 KG (35 LBS).
WARNING THE SYSTEM SHOULD ONLY BE MOVED WITH THE COCKPIT IN ITS CENTERED AND
LOCKED POSITION (IF EXISTS).
CAUTION TO AVOID INJURY WHEN YOU MOVE THE COCKPIT AND THE ARM, DO NOT PUT YOUR FINGER,
HAND, OR OBJECT ON THE JOINT OF THE COCKPIT OR THE ARM.
CAUTION ENSURE THAT NO-ONE TOUCHES THE CONSOLE ARM/FROGLEG WHEN MOVING THE
OPERATOR PANEL.
CAUTION KEEP THE HEAT VENTING HOLES ON THE MONITOR UNOBSTRUCTED TO AVOID
OVERHEATING OF THE MONITOR.
CAUTION DO NOT TRANSPORT THE VENUE™ SYSTEM IN A VEHICLE WITHOUT LOCKING THE
-
CASTERS (WHEELS)
NOTICE SPECIAL CARE SHOULD BE TAKEN WHEN TRANSPORTING THE ULTRASOUND SYSTEM IN A
-
VEHICLE:
• BEFORE TRANSPORTING, PLACE THE ULTRASOUND SYSTEM IN ITS
SPECIAL STORAGE CASE.
• ENSURE THAT THE ULTRASOUND SYSTEM IS FIRMLY SECURED WHILE
INSIDE THE VEHICLE.
• SECURE ULTRASOUND SYSTEM WITH STRAPS OR AS DIRECTED
OTHERWISE TO PREVENT MOTION DURING TRANSPORT.
• PREVENT VIBRATION DAMAGE BY DRIVING CAUTIOUSLY. AVOID
UNPAVED ROADS, EXCESSIVE SPEEDS, AND ERRATIC STOPS OR
STARTS.
jh
WARNING EQUIPMENT DAMAGE COULD RESULT IF SPECIAL CARE IS NOT TAKEN WHEN
TRANSPORTING THE VENUE™ SYSTEM IN A VEHICLE.
ALWAYS:
• Eject any media from the media storage devices USB Flash Drive or other.
• Ensure that the cockpit is in locked position.
• Ensure that the Venue™ system is well prepared and packed in its original packaging before
transporting. Special care must be taken to correctly position the packing material, using all
screws and brackets.
For further information, refer to Chapter 3 -System Setup.
• Place the probes in their carrying case.
• Secure the system in an full down position and lock the wheels (brake).
• Ensure that the Venue™ system is firmly secured while inside the vehicle.
• Secure the system with straps or as directed otherwise to prevent motion during transport.
• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds,
and erratic stops or starts.
CAUTION BE CAREFUL NOT TO PINCH ANY OF THE CABLES.
To ensure proper grounding, connect this equipment to a receptacle marked "HOSPITAL ONLY" OR
"HOSPITAL GRADE".
The power outlet used for this equipment should not be shared with other types of equipment. Both the
system power cable and the power connector must meet international electrical standards.
1-4-4-1 Probes
All the probes for the Venue™ ultrasound unit are designed and manufactured to provide trouble-free,
reliable service. To ensure this, correct handling of probes is important and the following points should
be noted:
• Do not drop a probe or strike it against a hard surface, as this may damage the transducer elements,
acoustic lens, or housing.
• Do not use a cracked or damaged probe. In this event, call your field service representative
immediately to obtain a replacement.
• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the
electrical safety of the probe.
• To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled,
or to be caught in the system’s wheels.
Follow these guidelines before connecting a probe to the scanner:
• Inspect the probe prior to each use for damage or degradation to the:
- housing
- cable strain relief
- lens
- seal
- connector pins
- locking mechanism
• Do not use a damaged or defective probe.
• Never immerse the probe connector or adapter into any liquid.
NOTE: For detailed information on handling endocavity probes, refer to the appropriate supplementary
instructions for each probe. In addition, refer to the Venue™ User Manual for detailed probe handling
instructions.
1-4-4-2 Peripherals
1-4-4-2-1 Safety and Environmental Guidelines
WARNING Do not attempt to use different peripherals & accessories (brand and model connected
via USB ports) other than approved and provided by GE HealthCare! The Ultrasound
system is extremely sensitive and complex medical system. Any unauthorized
peripherals may cause failure or damage!
WARNING Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate
AC outlets, are in violation of patient safety standards. Suitable electrical isolation of
such external AC outlets, or the provision of extra protective earth for the device, is
required in order to meet UL60601-1 and IEC60601-1-1 standards for electrical leakage.
• Patient Vicinity UL 60601-1
Sub clause 2.12.20DV - D2 Addition
An area in which patients are normally cared for, the patient vicinity is the space with surfaces likely
to be in contact with the patient or attendant who can touch the patient. This encloses a space within
the room of 1.83 m (6 ft.) beyond the perimeter of the bed (examination table, dental chair,
treatment booth, and the like) in its intended location, and extending vertically 2.29 m (7.5 ft.) above
the floor.
• Patient Environment IEC 60601-1-1
Sub clause 2.204
Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out.
It is very difficult to attach unique dimensions to the PATIENT ENVIRONMENT. In practice a
distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal
distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient
Environment. The patient environment/vicinity is depicted as a dashed line in this procedure - see
the example in Figure 1-1.
The lithium ion batteries provide power for scanning, safely shutting down the system or placing it in
Standby mode, when an AC power source is interrupted or the AC power cable is disconnected from the
wall outlet. Lithium ion batteries last longer than conventional batteries and do not require replacement as
often. In Working mode, you can expect 4 hours of battery life with fully-charged batteries.
Used batteries should not be placed with common household waste products. Contact local authorities
for the location of a chemical waste collection program nearest you.
NOTE: Regulations vary for different countries. Dispose of a used battery in accordance with local regulations.
CAUTION USE ONLY BATTERIES APPROVED BY GE HealthCare AS SUITABLE FOR USE WITH THE
VENUE™ ULTRASOUND SCANNER
CAUTION TO PREVENT THE BATTERY BURSTING, IGNITING, OR FUMES FROM THE BATTERY CAUSING
EQUIPMENT DAMAGE, ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:
Section 1-5
Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.
WARNING IF THE COVERS ARE REMOVED FROM AN OPERATING VENUE™ SYSTEM, SOME
METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD
IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.
Section 1-6
Lockout/Tagout (LOTO) Requirements
Follow Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all
times during the service process.
7. Verify isolation.
3. Unplug the Ultrasound system from the wall outlet, then from the Ultrasound System.
4. Maintain exclusive control of the Ultrasound system power cable.
5. Wait at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
6. Remove/disconnect the battery if present.
Section 1-7
Product Labels and Icons
The Venue™ ultrasound scanner comes equipped with product labels and icons. These represent
pertinent information regarding the operation of the unit.
Note: All labels presented in this section are subject to change and should be used for reference only.
A system Rating Label (examples shown in Figure 1-3 and Figure 1-4, below) is located at the rear of
the system. This indicates the ultrasound unit’s basic power compliance. In addition, a General Label
(Figure 1-7, below) provides details regarding regulatory compliance - as well as warnings and cautions.
When Upgrading the software to R5, an electronic label will be displayed under the About tab in the
Config screen.
If, the system was upgraded to R4 previously, an additional electronic label will be displayed in the
config screen:
If, the system was upgraded from R1 to R2 previously, an additional electronic label will be displayed
in the config screen:
If, the system was upgraded from R1/R2 to R3 previously, an additional electronic label will be displayed
in the config screen:
Table 1-3 Label Icons and Symbols - Description and Location (Continued)
Rating Plate
Model number
Probes
Rating Plate
Serial number
Probes
Rating Plate
The Month and Year of manufacture
Probes
Rating Plate
Manufacturer’s name and address Probes
Rear panel
Table 1-3 Label Icons and Symbols - Description and Location (Continued)
“Protective Earth” indicates the protective earth Inside of AC adapter with system
(grounding) terminal Console
Table 1-3 Label Icons and Symbols - Description and Location (Continued)
GE HealthCare Logo
Type CF Defib-Proof Applied Part (heart in the box with on ECG module, near ECG
paddle) symbol is in accordance with IEC 60878-02-06. patient cable connector
Table 1-3 Label Icons and Symbols - Description and Location (Continued)
Type/Class
Used to indicate the degree of safety or protection. Rear Panel.
Label
Type CF Defib-Proof Applied Part (heart in the box with on ECG module, near ECG patient
paddle) cable connector
Section 1-8
Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GE HealthCare policy states that body fluids must be properly removed from any part or equipment prior
to shipment. GE HealthCare employees, as well as customers, are responsible for ensuring that parts/
equipment have been properly decontaminated prior to shipment. Under no circumstance should a part
or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils
or an ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the
people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that “items that were saturated and/or
dripping with human blood that are now caked with dried blood; or which were used or intended
for use in patient care” are “regulated medical waste” for transportation purposes and must be
transported as a hazardous material.
NOTE: The USER/SERVICE staff should dispose of all the waste properly, per federal, state, and local waste
disposal regulations
The Venue™ ultrasound scanner is not meant to be used for long-term storage of patient data or
images. The user is responsible for the data on the Venue™ and a regular backup is highly
recommended.
If the Venue™ is sent for repair, ensure that any patient information is backed up and erased from the
Venue™ before shipping. It is always possible during system failure and repair to lose patient data. GE
HealthCare is not responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to GE HealthCare employees for service
purposes, GE HealthCare will ascertain agreement from the customer. Patient information shall only be
transferred by approved service processes, tools and devices restricting access, protecting or
encrypting data where required, and providing traceability in the form of paper or electronic documents
at each stage of the procedure while maintaining compliance with cross-border restrictions of patient
information transfers.
Section 1-9
Electromagnetic compatibility (EMC)
1-9-1 What is EMC?
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due to interference from its environment
or when the device produces unacceptable levels of emission to its environment. This interference is
often referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated
through space or conducted over interconnecting power of signal cables. In addition to electromagnetic
energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic
discharge and disturbances in the electrical power supply.
1-9-2 Compliance
The Venue™ ultrasound scanner conforms to all applicable conducted and radiated emission limits and
to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power
line transient requirements.
NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh and clamps are in good
condition and installed tightly without skew or stress. Proper installation following all comments noted
in this service manual is required in order to achieve full EMC performance.
WARNING IF THE COVERS ARE REMOVED FROM AN OPERATING Venue™ , SOME METAL
SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF
TOUCHED, EVEN WHILE IN SHUTDOWN MODE.
Section 1-10
Customer Assistance
1-10-1 Contact Information
If this equipment does not operate as indicated in this Service Manual or in the Venue™ User Manual,
or if you require additional assistance, please contact the local distributor or appropriate support
resource, as listed below.
USA USCAN
GE HealthCare Service: On-site 1-800-437-1171
Ultrasound Service Engineering Service Parts 1-800-558-2040
3200 N Grandview Blvd OLC 1-800-321-7937 or 1-262-524-5300
Wauwatosa, WI 53188 Application Support 1-800-682-5327 or 1-262-524-5698
1-800-321-7937
Canada OLC - USCAN
1-800-668-0732
LATAM
Latin America Service +1-262-524-5300
Application Support +1-262-524-5698
EMEA
GE Healthcare GmbH Hotline: +49 (0)211 7374-4789
Peter-Müller-Straße 24-26 +33 (0)1 3083-1300
40468 Düsseldorf Fax +49 (0)211 7374-4685
Germany
India
Wipro GE Healthcare Pvt. Ltd. Phone +(91) 1-800-425-8025
4, Kadugodi Industrial Area +(91) 1-800-425-7255
Bangalore - 560 067 +(91) 1-800-102-7750
India
Chapter 2
Site Preparations
Section 2-1
Overview
2-1-1 Purpose of Chapter 2
This chapter provides the information required to plan and prepare for the setup of a Venue™
ultrasound unit. Included are descriptions of the electrical and facility requirements that must be met by
the purchaser. A worksheet is provided at the end of this chapter (see Figure 2-3) to help ensure that
all the required network information is available, prior to setup.
Section 2-2
Console Requirements
2-2-1 Unit Environmental Requirements
Table 2-2 Environmental Requirements
Relative Humidity
Requirement Temperature (non-condensing) Air Pressure
NOTE: The Venue™ system may be operated at an altitude of up to 3000 meters (9842 ft).
CAUTION IF THE SYSTEM HAS BEEN IN STORAGE OR HAS BEEN TRANSPORTED, PLEASE SEE THE
ACCLIMATION REQUIREMENTS BEFORE POWERING ON AND/OR USING THE SYSTEM.
Refer to the Setup Warnings section
NOTE: After a long period of storage, or after transportation of the system with the monitor in the folded-down
position (transportation mode), it is highly recommended to place the monitor in the upright position -
and to leave it in this position for a period of longer than 1 hour before use. This will enable it to properly
adjust to the environmental conditions.
NOTE: Each person in the room places an additional 300 BTU/hr demand on the environmental cooling.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size Ground wire from the distribution panel to the Ultrasound outlet.
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size Ground wire from the distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within the facility, the Ground from the
main facility's incoming power source to the Ultrasound unit is only a conduit.
100 V 4.5 A
240 V 2.3 A
CAUTION Power outage may occur. The Ultrasound System requires a dedicated single branch circuit. To avoid
circuit overload and possible loss of critical care equipment, make sure you do not have any other
equipment operating on the same circuit.
It is recommended that the branch circuit breaker for the Ultrasound system be readily accessible.
GE HealthCare dealer. When necessary, the installation engineer will supply the appropriate power
plug to meet the applicable local regulations.
• Voltage drop-out
Max 10 msec
• Power Transients
The Venue™ is fully compliant with the following standard:
EN/IEC 60601-1-2 sections 36.202.1j, 7a(2).
NOTE: Possible EMI sources should be identified before the unit is installed, and should not be on the same
line as the ultrasound system. A dedicated line should be used for the ultrasound system.
Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Some of
these sources include:
• medical lasers
• scanners
• cauterizing guns
• computers
• monitors
• fans
• gel warmers
• microwave ovens
• light dimmers
• mobile phones
• in-house wireless phones (DECT phones)
• wireless computer keyboard and mouse
• air conditioning system
• High Frequency (HF) surgery equipment
• general AC/DC adapters
The presence of a broadcast station or broadcast van may also cause interference.
• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI sources.
Be aware of Radio
• Special shielding may be required to eliminate interference problems
Frequency sources
caused by high frequency, high powered radio or video broadcast signals.
Ground the Ultrasound Poor grounding is the most likely reason an Ultrasound system will have
system noisy images. Check grounding of the power cord and power outlet.
Replace all screws, Radio • After you finish repairing or updating the Ultrasound system, replace all covers and
Frequency gaskets, covers, tighten all screws.
cores • Any cable with an external connection requires a magnet wrap at each end.
• Install all covers. Loose or missing covers or Radio Frequency gaskets allow radio
frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on a Radio Frequency gasket are broken,
Replace broken Radio
replace the gasket. Do not turn on the Ultrasound system until any loose metallic part is
Frequency gaskets
removed.
Do not place labels where Where applicable, never place a label where Radio Frequency gaskets meet the
Radio Frequency gaskets Ultrasound system. Otherwise, the gap created will permit Radio Frequency leakage.
touch metal Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding.
Use GE HealthCare specified
Also, cable length, material, and routing are all important; do not change from what is
harnesses and peripherals
specified.
Where applicable, do not allow cables to lie across the top of the Card Rack or hang out
Properly route peripheral
of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral
cables
bays. Attach the monitor cables to the frame.
Section 2-3
Facility Needs
2-3-1 Purchaser Responsibilities
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay,
confusion, and waste of manpower can be avoided by completing pre-installation work before delivery.
Note: All electrical installations that are preliminary to the positioning of the equipment at the site
prepared for the equipment must be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, calibrations, and testing must also be
performed by qualified personnel. The products involved (and the accompanying electrical
installations) are highly sophisticated and special engineering competence is required. All
electrical work on these products must comply with the requirements of applicable electrical
codes. The purchaser of GE HealthCare equipment must only utilize qualified personnel to
perform electrical servicing on the equipment.
The desire to use a non–listed or customer provided product or to place an approved product further
from the Ultrasound system than the interface kit allows, presents challenges to the installation team.
To avoid delays during installation, such variances should be made known to the individuals or group
performing the installation at the earliest possible date (preferably prior to the purchase).
The ultrasound suite must be clean prior to delivery of the Ultrasound system. Carpet is not
recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic
interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact
Ultrasound system reliability.
To avoid delays during setup, the individual or team who will perform the setup should be notified at the
earliest possible date (preferably prior to setup), of the existence of any of the following variances:
NOTE: GE HealthCare requires a dedicated power and ground for the proper operation of its Ultrasound
equipment. This dedicated power shall originate at the last distribution panel before the Ultrasound
system.
The Ultrasound system will function on voltages from 100-240 Volts and 50 or 60 Hz. However, if using
220 volt power in North America, then a center tapped power source is required.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Scale:
Each square equals one square foot (app. 31 x 31 cm)
3. Counter Top, Sink with hot and cold water and 10. External Peripherals
Supplies Storage
6. Examination Table – 1930 x 610 mm (76 x 24 13. 457 mm (18 inches) distance of Ultrasound
inches) system from wall or objects
Scale:
Each square equals one square foot (app. 31 x 31 cm)
5. Counter Top and Sink with hot and cold water 14. Footswitch
6. Overhead Lights Dimmer - Dual Level Lighting 15. Storage for Linens and Equipment
(bright and dim)
• Details: DICOM network details for the Venue™ unit, including the host
name, local port, IP address, AE title and network subnet mask.
• Routing Information: IP addresses for the default gateway and other routers in use at
the site.
• DICOM Application Information:Details of the DICOM devices in use at the site, including the
DICOM host name, AE title and IP addresses.
Section 2-4
Connectivity Installation Worksheet
Dept: Room:
Type: REV:
Venue™ SN:
CONTACT INFORMATION
Name Title Phone E-Mail Address
TCP/IP Settings
Scanner IP Settings
Name - AE Title:
IP Address:
Subnet Mask:
Default Gateway:
Venue™
Host Name Local Port IP Address . . .
ROUTER1 . . . . . .
ROUTER2 . . . . . .
ROUTER3 . . . . . .
Store 1 . . .
Store 2 . . .
Store 3 . . .
Store 4 . . .
Store 5 . . .
Store 6 . . .
Work list . . .
Storage
. . .
Commit
MPPS . . .
Action Yes No
Notify setup team of the existence of any variances from the basic setup.
Make sure system and probes have been subject to acclimation period.
EMI precautions have been taken and all possible sources of interference have been
removed.
If a network is used, IP address has been set for the system and a dedicated network
outlet is available.
Chapter 3
System Setup
Section 3-1
Overview
3-1-1 Purpose of Chapter 3
This chapter provides instructions for setting up the Venue™ ultrasound unit. Before beginning the
setup process, an appropriate site must be prepared, as described in Section 2-3 - Facility Needs. Once
the site has b3-1een prepared, setup can proceed as described in this chapter.
Included in this chapter are guidelines for transporting the unit to a new site, as well as procedures that
describe how to receive and unpack the equipment, and (if necessary) how to file a damage or loss
claim. Instructions for checking and testing the unit, probes, and external peripherals for electrical safety
are also provided.
NOTE: A Venue™ is ready for use only if the tests and checks described in Chapter 3 -System Setup
(this chapter) and Chapter 4 -General Procedures and Functional Checks of this Service
Manual meet the expected results.
Section 3-2
Setup Reminders
3-2-1 Average Setup Time
The Venue™ setup and functional checkout will take approximately one hour; Venue™ consoles with
optional equipment may take slightly longer.
Once the site has been prepared, the average installation time required is shown in Table 3-6 below.
Table 3-6 Average Setup Time
Average
Description Setup Time Comments
Setting up the scanner 10 minutes Time may vary, according to the required configuration
DICOM Option 10 minutes Time may vary, according to the required configuration
(connectivity)
NOTE: For information on shipping carton labels, refer to Figure 3-5 and Figure 3-6.
CAUTION If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance
to acclimate to its operating environment.
Following transport, the Venue™ system may be very cold, or hot. Allow time for the system to
acclimate before being switched ON. Acclimation requires 1 hour for each 2.5oC increment, when the
temperature of the system is below 10oC or above 40oC.
CAUTION Turning the system ON after arrival at the site - without allowing time for acclimation - may
cause system damage!
6
Hrs 20 18 16 14 12 10 8 4 2 0 0 0 2 4 6 8
DANGER WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DO NOT TOUCH
THE UNIT!
CAUTION DO NOT WEAR THE ESD WRIST STRAP WHEN YOU WORK ON LIVE CIRCUITS WHERE MORE
THAN 30 V PEAK IS PRESENT.
CAUTION DO NOT OPERATE THE UNIT UNLESS ALL BOARD COVERS AND FRAME PANELS ARE
SECURELY IN PLACE, TO ENSURE OPTIMAL SYSTEM PERFORMANCE AND COOLING.
(WHEN COVERS ARE REMOVED, EMI MAY BE PRESENT).
NOTE: The Venue™ User Manual should be fully read and understood before operating the unit. Keep
the manual near the unit for reference.
Section 3-3
Receiving and Unpacking the Equipment
3-3-1 Warnings for Receiving and Unpacking the Equipment
CAUTION Two people are needed to unpack the Ultrasound system because of its weight. Attempts to
move the Ultrasound system considerable distances or on an incline by one person could result
in injury or damage or both.
Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted
CAUTION Remember to use relevant personal protecting equipment (PPE) during packing and unpacking.
Check with your local EHS representative.
3-3-2 Overview
CAUTION Please read this section fully before unpacking the Venue™ ultrasound unit.
The Venue™ ultrasound unit, together with the peripherals, probes, cables, and accessories, are
shipped from the factory in a single shipping carton or wooden crate mounted on a raised wooden base
- see Figure 3-5.
NOTE: When using utility a knife to cut the nylon wrap take extra care not to scratch the system or any
peripheral.
Probes
box #1
TV_TR tray
Additional
accessories
box
Small basket
Probes box #2
Probes boxes #3 and #4
5.) Remove the wooden ramps and then remove the nylon wrap from the system.
Nylon wrap
Wooden ramps
6.) Unlock the four butterfly locks and remove the two wooden brackets.
Wooden brackets
Butterfly locks
8.) Press down on the front locking brake to unlock the wheel. Repeat for the back wheel.
9.) Carefully roll the scanner forwards down the unloading ramp to remove it completely from the
shipping carton.
________________________________________________________________________________________________________________
3.3.5.1 Introduction
Overview
This document provides installation instruction for Vscan Air HW support kit.
Philips screwdriver
HW Prerequisites
APU backend
BT adaptor
dongle
________________________________________________________________________________________________________________
USB
connectors
of Venue BE
to WIFI and
BT cable
Including
scotches for
WIFI and BT
MPB to BEP
cable (Spilt
for charger)
________________________________________________________________________________________________________________
Wireless
probe
charger
Tower label
cockpit
cables cover
________________________________________________________________________________________________________________
Printer door
cover
Wireless
Probes SL /
CL
(purchased
separately)
________________________________________________________________________________________________________________
Step 3: Replace system mains power cable (MPB to BE) by split cable, see 3.3.5.4.3
Step 4: Add cable for charger WIFI and BT (Bluetooth), see 3.3.5.4.4
Step 5: Return all system parts and close the system, see 3.3.5.4.5
3. Disconnect system cable at the back side of the system, and remove the cable cover from the cart pole cable
rail by pinching
________________________________________________________________________________________________________________
1. Remove accessories, basket, covers, batteries, PSU, MPB, inner cable door, see 3.3.5.4.3.1
2. Disconnect and remove current Power Cable (MPB to BE PWR), see 3.3.5.4.3.2
3. Install the new split Power (MPB to BE PWR) Cable, see 3.3.5.4.3.3
________________________________________________________________________________________________________________
3.3.5.4.3.1 Remove accessories, covers, batteries, PSU, MPB, inner cable door
1. Remove all system accessories
2. Remove basket: Pull the basket upwards and remove it as shown below
3. RS Probe Cover: Grip the RS Probe Cover on the recess on its bottom and gently pull it towards you to
disconnect it from the holding magnets. Then slide the cover down to remove it
Remove RS
Probe Cover
4. Remove Lower Front eTower Cover: Grip the recess at the center of the cover, and pull the lower front
eTower cover out towards you
________________________________________________________________________________________________________________
5. Remove MPB Front Metal Door: Release four captive screws and remove the MPB Front Metal Door
6. Remove Left & Right Side eTower Covers: Grip the rubber holder and pull the cover toward you to remove it
from the system. Repeat for both sides.
________________________________________________________________________________________________________________
7. Remove the MPB (batteries) door cover: open 4 captive screws (two on each side). Then grip the MPB door
cover at the bottom and pull toward you to remove it
8. Open FE (Front End) door assembly: Open the two fastening latches on the left side of the FE door assembly
and loosen the captive screw. Then, carefully open the door
Open FE door
________________________________________________________________________________________________________________
9. Remove the batteries: Release the two captive screws securing each battery pack. Then pull out the top and
bottom battery packs
10. Remove PSU: Release the captive screw at the bottom of the PSU and pull the PSU out gently
________________________________________________________________________________________________________________
b. Release two captive screws at the bottom center and top center of the MPB
________________________________________________________________________________________________________________
J-Connectors map
2. Slide cable upwards to release it from the two plastic cable clips
________________________________________________________________________________________________________________
4. Carefully raise the arm to its up position and remove the arm base cover.
________________________________________________________________________________________________________________
5. Remove the side cover on the side of the thin cables: Using Allen key/Philips screwdriver, remove the side
screw of the arm side cover.
Open thin
cable side
7. Remove existing cockpit cables cover door located at top of chassis, by opening the thumb-screw and sliding
the plate outwards
________________________________________________________________________________________________________________
2. Insert the split cable through the (removed) cockpit cables cover door
________________________________________________________________________________________________________________
3. Install the new cockpit cables cover door (with extra hole for the split cable), and fasten the thumb-screw
________________________________________________________________________________________________________________
5. Route the cable through the replaced cockpit cables cover door and cover the cable with rubber grommet.
________________________________________________________________________________________________________________
Remove base
plastic cover
Open Allen
screw and
remove left side
cover
________________________________________________________________________________________________________________
c. Route the charger cable through the exposed hole and the side, and direct it towadrs the right side
of the system
Route charger
cable through
hole and
through left side
NOTE: ensure there is enough cable length to position the charger cable edge in its dedicated position, as
shown in the following figure:
________________________________________________________________________________________________________________
d. Return the side plastic cover and secure with the Allen screwdriver, and place the plastic cover on
top.
________________________________________________________________________________________________________________
7. Connect the probe charger on the left side of the system (see 3.3.5.4.6 for details)
________________________________________________________________________________________________________________
1. Prepare for cable installation (remove front cover, place label, replace printer door cover) see 3.3.5.4.4.1
2. Remove the cover off the tower label, and position the tower label:
________________________________________________________________________________________________________________
3. Apply one side of the scotches for WIFI and BT on the tower as illustrated below;
NOTE: The other side of each scotch will be applied on the relevant elements to be connected, see 3.3.5.4.4.2
________________________________________________________________________________________________________________
4. Remove printer door by unscrewing captive screw, and replace it by the new printer door cover
Replace
printer door
cover
________________________________________________________________________________________________________________
Towards
Sticker: attach BackEnd
to tower
NOTE: If ECG/printer are installed in your configuration, route their cables through the new cover and cover
with rubber grommets on these cables too.
3. Route the new BT/WIFI cable previously inserted through the printer door cover, through the tower front
towards the BE (Back End) module, and connect it to the dedicated (yellow) connector
Yellow
connector for
BT/WIFI cable
NOTE: Reaching the connector may be easier by removing the BE unit. If needed – remove the BE module;
Insert the cable to the yellow connector, and then return the BE module to the cart.
________________________________________________________________________________________________________________
4. Attach the cable WIFI and BT connectors to the tower, according to the label previously attached to chassis;
then attach the cable edges (connectors) to the scotches
Connect Netgear
WIFI dongle to
Attach WIFI extension cable
connector WIFI connector
3.3.5.4.5 Step 5: Return all system parts and Close the system
Return all the system parts:
3. Close the covers: MPB door, Side eTower Covers, front eTower Cover, RS Probe Cover, accessories (removed
in 3.3.5.4.3.1)
4. Close front cover and return the basket (removed in 3.3.5.4.4.1, 3.3.5.4.3.1)
________________________________________________________________________________________________________________
2. Position the charger cable female-side sticker on the system’s back-side, at the height as shown
________________________________________________________________________________________________________________
3. Connect the charger cable male-side to the female, and twist to lock, as shown
Section 3-4
Preparing for Setup
3-4-1 Verifying Customer Order
Compare items received by the customer to that which is listed on the delivery order. Report any items
that are missing, back ordered, or damaged.
If the Venue™ has been damaged, please refer to DAMAGE IN TRANSPORTATION on page xiv in the
beginning of this manual.
A Damage Inspection Checklist for the Venue™ ultrasound scanner is provided in Table 3-9 below.
Table 3-9 Damage Inspection Checklist - Venue™ Systems
Check all probes for wear and tear on the lens, cable, and connector. Look for bent
or damaged pins on the connector and in the connector socket on the unit. Verify
2 Probes
that the EMI fingers around the probe connector socket housing are intact. Check
the probe locking mechanism and probe switch.
Clean the Cockpit (monitor) by gently wiping with a dry, soft, lint-free non-abrasive
3 Cockpit (Monitor)
folded cloth. Inspect the screen surface for scratches and raster burn.
4 Fans Turn on the system and verify that the system’s cooling fans are operating.
Check the rear panel connectors for bent pins, loose connections and loose or
5 Rear Panel missing hardware. Screw all the cable connectors tightly to the connector sockets
on the panel. Verify that the labeling is in good condition.
6 Covers Check that there are no dents or scratches and that no internal parts are exposed.
Check and clean the peripherals in accordance with the manufacturer’s directions.
7 Peripherals To prevent EMI or system overheating, dress the peripheral cables inside the
peripheral cover.
Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or
8 Power Cord
any deterioration. Verify continuity.
9 Casters Visually check the casters for damages and for proper movement.
Check that the swivel and full lock castors can roll and swivel, and can be placed
Swivel and Full in the locked position by pressing the foot brake (lower lever) down on each.
10
Lock Castors Ensure that the wheels are locked, unable to swivel left or right, and that there is
no movement forwards or backwards.
3 3
4 5
15
14
13
1
12
11
6 10
9
4 5
8
# Item # Item
1 Cockpit (monitor) - rear 9 System Label - General Label International
Rear handle: used to pull/push the scanner and place it in
2 10 On/Off Switch Cover
the desired position.
Interface Panel:
3 Probe locking levers 11 Provides ports for LAN, Insulated USB and Dual USB (see
Figure 3-16).
Caster:
4 12 Probe Connectors - for 4 RS probes
(1x back) with free movement and no locking.
Swivel and full lock caster:
5 13 Articulated Arm
(1x back)
6 Power inlet connector 14 Probe holders
Gel Cup Holder: Provides convenient storage for US Gel
7 System Base 15
bottle.
8 System Label - Rating Plate
Figure 3-16 shows a view of the Venue™ ultrasound unit rear panel showing external peripheral/
accessory connectors.
1 2
See EMI Limitations on page 2 - 4 for more information about EMI protection.
Section 3-5
Completing the Setup
3-5-1 Purpose of this Section
This section describes how to complete the setup of the Venue™.
131 48 72.5 cm
Table 3-11 Mass of Venue™ with Cockpit (monitor), without Probes and Peripherals
Venue™ 63 139
The voltage setting for the Venue™ is found on a label near the Mains Power Circuit Breaker on the
rear of the Venue™ .
Frequency 50-60 Hz
CAUTION Do not allow the probe head to hang freely. Excessive impact
to the probe will result in irreparable damage.
There are 4 probe connectors on the rear panel of the system, numbered 1 through 4. Each connector
is comprised of a probe-socket (6) and a locking latch (5).
1) Hold the probe connector vertically with the cable pointing upward.
2.) Prior to inserting the probe, ensure that the connector locking handle is positioned to the left.
3) Align the connector with the probe port and carefully push into place.
4) Push the connector locking handle to the right to secure the probe connector.
5) Carefully position the probe cord so it is free to move and is not resting on the floor.
To connect a probe to one of the lower socket 4
1) Hold the probe connector vertically with the cable pointing downward.
2.) Prior to inserting the probe, ensure that the connector locking handle is positioned to the right
3) Align the connector with the probe port and carefully push into place.
4) Push the connector locking handle to the left to secure the probe connector.
5) Carefully position the probe cord so it is free to move and is not resting on the floor.
1) Move the connector locking lever to the left to unlock the connector (For lower socket 4, move the
connector locking lever to the right)
2) Carefully remove the connector from the port.
3) Ensure that the probe head is clean before placing the probe in its storage case.
For cleaning instructions, see the User Manual.
Section 3-6
Configuration
3-6-1 Purpose of this Section
This section describes how to configure the Venue™ .
1.) After the system reboots, the Venue™ setup wizard welcome screen appears:
2.) Select the interface language and tap OK to proceed.
Note: The initialization duration might take up to 15 minutes, due to automatic firmware updates.
5.) On the Local tab, enter the required details and tap Save. Then, proceed to the next tab.
6.) On the Network tab, define the required settings and tap Save.Then, proceed to the next tab.
7.) On the Thermal Printer tab, configure the printer and tap Save. Then, proceed to the next tab. If
the printer is already configured, skip this step and proceed to the next one .
8.) On the InSite tab, define the required settings and tap Submit Changes.
Make sure you fill the CRM No. Field as appears in the CRM system.
If there is a proxy, check the checkbox and fill in the proxy IP and port.
9.) On the Connectivity tab, enable the required settings in the Connectivity items list, by moving the
On/Off sliders to On. Then, select each Connectivity item to define its properties. Tap Apply and
then Save.Then, proceed to the next tab.
10.)On the OptionKey tab, enter the key string to enable the purchased options and tap Save. Then,
proceed to the next tab.
11.)On the Reports tab, view the defined settings and tap Save As to save the report. Save the report
on USB flash memory.Then, proceed to the next tab.
12.)On the About tab, view all settings defined on each tab, and click Save to save the entire set of
defined settings. Then click Exit, to exit the Setup Wizard.
NOTE: To reinitialize the EZ Config wizard, access the Service tab under the System Configuration menu (refer
to Open Service Screen on page 3 - 34).
2) Log on as ADM.
1 2
3
4 5
1 2
3 4
Table 3-15 Select Language for User Interface and Online Manuals
5. See Table 3-16 on page 3-33 See Table 3-16 on page 3-33
6. See Table 3-16 on page 3-33 See Table 3-16 on page 3-33
3-6-3-1-1 SW Recovery
In cases of abnormal system behavior, as a part of troubleshooting process, it is recommended to
reload the system software. To reload the software without affecting patient data, tap the SW Recovery
button on the Service screen and follow the displayed instructions (SW installation media is not required
for this process).
NOTE: There may be more than one Software Option Key in use, depending on the installed options.
1) Log on as adm.
2) Select Admin (lower part of window).
3) Select the System Admin tab.
4) Select New to open the New Key dialog where you type the SW Option Key.
Section 3-7
Connectivity Overview
3-7-1 Physical Connection
There are several possible connection methods, as outlined below.
Section 3-8
Connectivity Setup
NOTE: If connected to a stand-alone network (Peer-to-Peer network with a Venue™ scanner, and an optional
network printer), you should use default delivery settings.
3-8-1 Introduction
To be able to use the network functions when connected to a hospital network, the Venue™ must have
a proper network address.
• Before you can set up the Venue™ , you need to collect some information.
• The Worksheet (see sample Connectivity Installation Worksheet on page 2 - 12) can be used for
gathering this information.
• Typical source for this information is the network administrator.
1. Log on as adm.
2. Tap: Settings >> Config >> Connectivity >> TCP/IP.
The resulting screen gives you an overview of many of the network settings for Venue™ .
1 2
5 6 7 8
9 10 11
• Wired connection - connecting the system to the network using a RJ45 network cable.
• Wireless connection - this is an optional feature, providing wireless network interface to the hospital
network.
Each network interface has a unique physical address that is somtimes required by the network
administrator to allow connection to the hospital network.
3.) If the network key is correct, the status will change to Connected.
6.) Select Manually connect to a wireless network and click or tap Next.
NOTE: If you select the Connect even if the network is not broadcasting check box, Windows 10 searches
for the hidden network every time it is not connected to a network, even if the hidden network is not in
your area. This may put your privacy at risk because skilled professionals can intercept this search for
the hidden network.
10.)Windows 10 notifies you that it has successfully added the wireless network. Click or tap Close to
3.) Tap the up arrow located on the left side of the address bar
Qview can be associated with a different network than the PACs, Qpath Image Storage or Worklist and
require a proxy, DNS (domain name system) or WINS (windows Internet name service) configuration
to provide a clear route between Qview and Qpath. refer to 3-8-6 -Network Proxy/DNS/WINS
configuration.
3-8-8-1 Overview
In this case the Venue™ is configured to work with DICOM servers in a network environment. Images
are first saved on the local image buffer on the Venue™ . At the end of the examination the images are
sent to the DICOM server via a DICOM spooler and to the local database, depending on dataflows.
This scenario requires that the Venue™ is configured to be connected to DICOM servers as described
below.
To connect to the DICOM server, the following information has to be entered in the Venue™ :
If Caption Care feature is available, you may configure the Dicom Web option.
Note: The Dicom Web option is not available for Generic Dicom Web. The Dicom Web feature is
available only with Caption Guidance option key.
2) Select Check (2) to start the verification process of the connection to the device.
The verification process takes some time to run.
A sign is displayed next to the Check button, indicating if the passed or failed .
NOTE: If the Check button fails immediately, the AE Title is probably wrong. If the Check button fails after a
long time (corresponding to the timeout), the IP address or Port Number is probably wrong.
1) In the Dataflow menu, slide the DICOM Storage 1 On/Off slider to On.
2) Tap to select DICOM storage and to display the DICOM Storage properties screen.
3) If Direct Store is enabled, the image will go to the DICOM server immediately after it is acquired.
You will need to verify that the DICOM server is capable of keeping the connection open for the
time it takes to complete an examination.
NOTE: This option is available for only when Caption Care is available, and will not be enabled for
generic Dicom Web.
NOTE: The Dicom Web and patient QR code features are available only with Caption Guidance option
key
1) In the Dataflow menu, slide the DICOM Web On/Off slider to On.
2) Tap to select DICOM Web and to display the DICOM Web properties screen.
3-8-8-7 DICOM SR
DICOM Structured Reporting (SR) is a standardized format for medical results. Venue™ supports the
specialized form for Echo Ultrasound (“TID 5200 Echocardiography Procedure Report”) and Vascular
Ultrasound (“TID 5100 Vascular Ultrasound Procedure Report”) for M&A results.
With the DICOM SR support, M&A for an exam can be sent at the end of the exam or when exported
from local archive. The destination can be either a server on the network (Storage SCP) or a removable
media (DICOM Media) depending on the DICOM dataflow selected.
“TID 5200 Echocardiography Procedure Report” is sent if the exam contains M&A from category
Cardiac or Pediatric (Heart). “TID 5100 Vascular Ultrasound Procedure Report” is sent if the exam
contains M&A from category Vascular or Abdominal. If the exam contains M&A from both Cardiac/
Pediatric (Heart) and Vascular/Abdominal categories, two SR documents are sent.
“TID 5200 Echocardiography Procedure Report” and “TID 5100 Vascular Ultrasound Procedure
Report” do not support all M&A results from Venue™ . They are limited to the following:
• No unassigned measurement.
Refer to the Venue™ Reference manual for a complete list of supported parameters.
• The following modes: 2D, M-mode, Color Flow, PW Doppler, CW Doppler, 3D and TDI.
• Not Modified Simpson method or Bullet methods.
Refer to the Venue™ Reference manual for a complete list of supported methods.
• Basic derivations (Average, Last, Min and Max), no references between the derived measurements
and the ones they were made from.
• Wall Motion Scoring: individual segment scores only according to 16-segment model, no graded
Chapter 3 - System Setup 3-55
P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
NOTE: The patient QR code feature is available only with Caption Guidance option key.
The barcode reader option allows scanning patient ID from a printed barcode label; scanning needle
type barcode; scanning user QR code.
To set the barcode reader option and allow accessing patient data via patient QR code, do the
following:
1) Enable the Barcode reader option: In the connectivity --> Dataflow menu, slide the Barcode Reader
On/Off slider to On.
1) Add user/password
2) Set Share permissions
3) Set Security permissions
NOTE: The User on the remote share must have all rights/permissions for the shared folder.
It is possible to set a secondary user if required by the remote share. For instructions, see: Configurable
Remote Path User on page 3 - 58.
NOTE: The default User / Password is always used as primary log in credential. No attempt is made to use the
secondary if log in succeeds using the primary.
NOTE: The default User / Password is always used as primary log in credential. No attempt is made to use the
secondary user if log in succeeds using the primary.
NOTE: The configurable (secondary) user and password is used for all remote paths configurable throughout
the system as secondary log in credential.
NOTE: The User on the remote share must have all rights/permissions for the shared folder.
1) Log on as ADM.
2) Select Connectivity > Tcpip.
NOTE: The field “User” can either be on the form “username”, or “domain\username”.
3-8-11-1 Overview
The Query/Retrieve function makes it possible to search for and retrieve DICOM data from a DICOM
server for further analysis on the Venue™ .
5) Select the IP-address down-arrow to choose the DICOM Query/Retrieve server from the pull down
menu. In some cases, the server to use is the same as used for DICOM Storage.
6) Enter the correct AE Title and Port Number for the DICOM Query/Retrieve server in the respective
fields in the DICOM QR Properties screen.
2) Select the correct tag from the Select Tag pull-down menu.
3) If needed, type in the value.
Follow the steps below to do a first check (TCP-IP Ping) of the connection:
3) If the network connection to the server is OK, it will be illustrated by a green symbol .
NOTE: This check uses both Ping and DICOM Ping. Ping is used to verify the TCP/IP connection to the server.
DICOM Ping is used to verify that the DICOM application is answering.
3-8-12-1 Background
This encryption allows the modality user to encrypt the communication between the modality and the
DICOM destination. Services which support this encryption are:
• Modality Worklist
• PACS storage
• Query Retrieve
During configuration of any of the above-mentioned services - it is possible to select the Enable
Encryption checkbox.
After the checkbox was selected, a button with Enable Encryption becomes available.
Once clicking the button, you will get a dialog to choose a certificate from the local certificate store.
You can also decide whether he would like to verify the server certificate. (Check the other side
certificate).
In case the encryption environment was configured not to use certificates, it's possible to omit the
certificate selection and only select the Enable Encryption checkbox.
4.) Make sure the Production server is selected. If applicable, check the enable proxy check box and
fill in the proxy details (contact the local IT team for support).
Section 3-9
Options Setup
3-9-1 Software Options
Most of the options for Venue™ are activated by installing a password (alphanumeric text string).
NOTE: It is possible to connect the Wireless Network adapter both when the system is powered ON, and after
it is powered OFF.
All software drivers for the Wireless Network are pre-installed for the designated Wireless Network
adaptor only.
NOTICE IMPORTANT During Stand-by mode, it is NOT recommended to introduce or remove USB
devices; this may cause the system to lock-up during the boot-up procedure.
Section 3-10
Registration and Pairing (First-time Activation) of Wireless Probe
When a new wireless probe is presented to the system, a short setup procedure is required, to pair the
device with the system (i.e. “handshake”. where the BT recognizes the VA device); then identify and
register the specific device as GE user (i.e. find the device appears in GE Avory database, and relate it
to the specific user-account - either existing or new.) (This phase requires external internet); and then
open the device for on-going usage. After performing this first time pairing and activation, the probe can
be used with all GE systems.
1) Purchase Vscan Air CL or SL wireless probes and license key, see 3-9-1
2) Install the wireless-probe connection-aid device (Bluetooth for initial pairing, and WIFI for on-
going communication with the probe): HAM Box (for venue fit, venue go systems) or split power
cable and adjustments for wireless probes (for venue systems) (for details refer to your relevant
installation instructions document)
3.) Verify external Internet connection: Ensure the system is connected to external Internet, to allow
probe registration to GE Backoffice.
4) Turn ON the probe, see 3-10-3
5) Perform first time probe connection and activation (3-10-4). The system will guide you through
the following steps:
1.) Pairing: The system identifies the probe via BT and performs pairing, see 3-10-4-1
2.) Registration: The system identifies the probe is not registered, and requests that you register
the probe to GE HealthCare server, by entering an email address of either an existing GE user
accounts, or create a new one, see 3-10-4-2
3.) Registration complete: The system identifies the user, registers the probe as GE HealthCare
medical device and its relevant features, and opens it for on-going usage. see 3-10-4-1
Note: After registering via the access key and pairing, the system will indicate and allow selecting
the wireless probe, and setting it as default.
6) You may now: Connect and Use the activated (and paired) probe, see 3-10-5
2) Click Connect to initiate first time Bluetooth connection between the Wireless Probe and the venue
system (i.e. pairing; Handshake)
4) Follow the instructions to activate the software on the new registered probe:
1.) Press the button on the probe for 2 seconds, until blue lights appear. Then click Next
2.) Wait while the label indicates the probe is being initialized
3.) When the label indicates Connecting, press the button on the probe shortly (also
indicated by screen animation)
4.) Wait until the screen indicates the probe was found
2.) Click on the Register button. The following pop-up screen appears:
2) Click on Scan
3.) Follow the on-screen instructions, indicating if the probe is found, connected, charging, etc.
NOTICE IMPORTANT During Stand-by mode, it is NOT recommended to introduce or remove USB
devices; this may cause the system to lock-up during the boot-up procedure.
Section 3-11
Paperwork After Setup
NOTE: During and after setup, the documentation (i.e. storage media with documentation, User Manuals,
Installation Manuals, etc.) for the Venue™ and the peripherals must be kept as part of the original
Ultrasound system documentation. This ensures that all relevant safety and user information is
available during the operation and service of the complete Ultrasound system.
Section 3-12
Disk Encryption
3-12-1 Introduction
The user may format a USB memory device or a USB HD device and then use BitLocker s/w to encrypt the
device.
NOTE: BitLocker is a full disk encryption feature included with Windows 7 and later. It is designed to protect
data by providing encryption for entire volumes.
Disk encryption can be enabled for patient data stored on the system. By default, disk encryption is disabled.
When enabling disk encryption, you are prompted to choose an encryption password, as well as a storage
location for the recovery key.
NOTE: Should the system power down during disk encryption, or otherwise cease to function, a prompt
appears when restarting the system to continue disk encryption
When starting up the system, the encrypted disk must be unlocked for the users to access images, local
archive, and other patient information. The disk can be unlocked in one of the following ways:
WARNING! This step is mandatory for US customers, and is highly recommended for all Venue family
customers.
• Insert a USB device for encryption-password storage to any available USB port.
3. Select the Admin category and Disk encryption tab. The following tab appears:
4. Select Encryption ON radio button. A dialog appears, explaining that the procedure will take time, and is
recommended to be executed during night. Press Yes to continue procedure.
Select encryption
ON radio button
7. Enter the desired password and retype it in the password confirmation field. Ensure your password
complies with the password length policy: longer than 7 digits
9. In order to maintain the password, please save it to the USB drive. You may:
b. The system indicates the key, as illustrated below. Click Hide key to hide this information:
Show/hide
toggle button
Note: if you choose the Change Key, the system warns the user that the current key backups will no longer be
used to unlock patient data:
10. The user may change the recovery key and use another USB device. To do so: Click Change Key. The
system prompts that all previous backups will no longer be valid:
11. Press yes. Then select the USB drive on which you wish to save the data, from the roll-down menu:
• Connecting the USB that contains the Encryption key to the system.
Note: you may turn OFF the disk encryption at any time.
Chapter 4
General Procedures and Functional Checks
Section 4-1
Overview
4-1-1 Purpose of Chapter 4
This chapter includes the General Procedures, and the Functional Checks.
General Procedures is a collection of commonly-used procedures that are available by cross references
from other parts of this manual.
Functional Checks is a collection of procedures for quickly checking major functions of the Venue™
scanner and diagnostic instructions using the built-in service software. These checks can be a great
asset in determining whether the Venue™ is working as it should.
Section 4-2
General Procedures
4-2-1 Overview
Some procedures are used more often than others. The intention of this section is to keep the most used
procedures in one place.
4-2-2-1 Warnings
DANGER ENSURE THAT THE POWER CORD AND PLUG ARE INTACT AND THAT
THE POWER PLUG IS THE PROPER HOSPITAL-GRADE TYPE
(WHERE REQUIRED).
CAUTION USE ONLY POWER SUPPLY CORDS, CABLES AND PLUGS PROVIDED BY OR DESIGNATED BY GE
HealthCare.
NOTE: When turning on a system from standby mode, it takes a few seconds before it responds. Do not push
the On/off button again during this period. A second push will initiate a full shutdown.Do not cycle the
Power ON/OFF switch ON-OFF-ON in less than five (5) seconds.
When turning OFF the Power ON/OFF switch, the Ultrasound system should de-energize completely
before turning the switch ON
NOTE: Before performing Power ON or system reboot, disconnect any USB mass storage device from the
system (unless a Software Installation procedure is required and the appropriate software installation
storage device is connected).
Figure 4-1 Power ON/OFF Switch and Power (AC IN) Socket - Rear Panel
5.) Connect the AC Power Cable female plug to the Power Inlet (AC IN) at the rear of the unit - see
Figure 4-1.
6.) Screw the plastic cable clamp (into the hole provided in the support column - centrally located at
the rear of the system.
7.) Connect the other end of the AC Power Cable (male plug) to a hospital-grade mains power outlet
with the proper rated voltage.
NOTE: The System should be connected to mains few hours to fully charge the batteries before battery
operation.
NOTE: The LED on the Input Power Panel (IPP) is illuminated green, indicating that the system in connected
to mains. The AC power indicator on the cockpit (monitor) is illuminated green.
On/Off Button
a.) The unit’s ventilation fans start on full speed, but slow down after the application is loaded.
b.) The Back-End Processor and the rest of the scanner starts with the sequence listed in the next
steps:
1.) Back-End Processor is turned ON and starts to load the software.
2.) The Start Screen is displayed on the monitor.
3.) A start-up progress bar indicating the time used for software loading, is displayed.
4.) The software initiates and sets up the Front-End electronics and the rest of the scanner.
5.) As soon as the software has been loaded, either a 2D screen is displayed on the screen,
indicating that a probe has been connected, or a No Mode screen is displayed, indicating
that no probe has been connected.
CAUTION Before performing any service activities related to electronic boards and/or accessible metal
parts, make sure to disconnect any power source from the system:
- Switch off the circuit breaker located at the back side of the system.
- Disconnect the power cable from the wall outlet and from the system.
- Remove Internal battery packs.
After pressing the On/Off button on the cockpit, the SYSTEM - EXIT dialog window will be displayed.
• Exit
(Only available when logged in as GE HealthCare Service with Service Dongle)
Select this button when you want to exit to the Windows Desktop.
NOTE: If you need to restart Venue™ when logged on to the Windows Desktop, ensure that you do a complete
power down (Shut Down). This is required to power up the Front End Processor.
• Shutdown
Use this button to shut down the system. The entire system will shut down.
If the Shutdown button is greyed out or the system cannot be shutdown normally:
Set the power switch, located on the rear lower part of the system, to the OFF position.
Wait for 10 seconds and re-set the power switch to the ON position.
Figure 4-4 Power ON/OFF Switch and Power (AC IN) Socket - Rear Panel
• Cancel
Use this button to exit from the System-Exit menu and return to the previous operation.
The physical On/Off button functionality can be disabled in the Config screen.
In order to disable/enable the functionality of the On/Off physical button, open Settings -> Config ->
Imaging -> Global Settings and check or uncheck the Disable physical power button box.
To switch off the system tap Settings -> Off. This action will trigger the display of the System Exit
window.
1) Select Settings.
This will bring up the Operator Login dialog where you can log on to Venue™ .
• If you log on as USR, you will have a restricted access to the setup menus.
Example: To select a printer.
As default, no password has been set for USR. Just type the name USR and select Login.
• If you log on as ADM, you will have access to all setup menus and service adjustments on the
Venue™ system.
Example: Adjust network and connectivity settings.
NOTE: It is possible for the administrator (ADM) to establish new users and set unique passwords for each
user, including a new password for ADM. If the login as ADM fails, contact the responsible person in the
hospital to get access.
The Emergency button stores data for the duration of the current examination only.
WARNING Before you dispose of the hard drive, make sure you remove ALL
PATIENT DATA from the hard drive, given that the hard drive is still
functional. In some countries, you may be required to delete all software
from the disk before returning the hard drive to the parts warehouse.
Follow your local policies.
WARNING All patient information (images, reports and data base) must be backed
up before deleting it from the internal hard drive.
NOTE: Before adjusting the cockpit (monitor) position, lock the front swivel and full lock caster located
on the system front left side (user right side).
To tilt the cockpit (monitor), use the lever handle and adjust the cockpit (monitor) to the desired angle.
CAUTION Unlock the brakes on the front and back wheels when preparing to
transport the unit.
Lock the brakes on the front and back wheels, if parking the system on an
incline. Avoid ramp steeper than 10 degrees.
Related information:
6) Use two or more persons to move the unit over long distances or on inclines.
Related information:
Related information:
Section 4-3
Functional Checks
4-3-1 Overview
The functional checks for Venue™ are described in this section.
Functional checks are used to verify that the Venue™ operates as intended.
4-3-3-1 Introduction
The 2D Mode is the system’s default mode.
4-3-3-2 Preparations
1) Connect one of the probes.
2) Turn ON the Venue™ .
The 2D Mode window is displayed (default mode).
• Swipe to page 2 on the Touch panel and press either Soft or Sharp Auto Tissue setting.
- Soft: optimizes the radial and lateral uniformity and brightness of the tissue continuously in
real-time.
The mention “Soft” is displayed on the upper right corner of the image area
- Sharp: further enhances the image display by optimizing the gray scale curve.
The mention “Sharp” is displayed on the upper right corner of the image area
The Auto Tissue setting (Soft or Sharp) can be turned on/off by pressing Auto on the Control panel.
The last used setting is then applied.
The Auto Tissue settings are only available in live scanning and cannot be turned off when the
image is stored.
• If available, press Virtual Apex (probe dependent) to improve near field imaging, allowing
increased visibility up to the width of the full probe aperture close to the surface.
• Use the Gain and TGC controls to optimize the overall image.
Gain increases or decreases the amount of echo information displayed. TGC compensates for
depth-related attenuation in the image.
• Conventional M-Mode (MM): displays a distance/time plot of a cursor line in the axial plane of
the 2D-image.
• Anatomical M-Mode (AMM): displays a distance/time plot from a cursor line, which is
independent from the axial plane. AMM is available in greyscale, color, TVI, Tissue Tracking,
Strain rate and Strain modes.
Chapter 4 - General Procedures and Functional Checks 4-14
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DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
• Curved Anatomical M-Mode (CAMM): displays a distance/time plot from a free-drawn cursor
line. CAMM is available in greyscale, color, TVI, Tissue Tracking, Strain rate and Strain modes.
Conventional M-Mode can be combined with Color Mode.
4-3-4-2 Preparations
1) Connect one of the probes, to any of the probe connectors.
2) Turn ON the scanner.
The 2D Mode window is displayed (default mode).
NOTE: Anatomical M-Mode can also be used with previously acquired digitally stored 2D images. More than
one heart cycle should be stored if performing M-Mode in post processing.
NOTE: The time motion curve can be edited by following the curve back to the desired point and redraw.
NOTE: To edit the time motion curve, select a point, move it to a new position and press Select.
4-3-4-5-1 Color 2D
1) From an optimized 2D image, press Color.
2) Position the ROI frame over the area to be examined.
3) Press Select. The instruction Size should be highlighted.
4) Adjust the dimension of the ROI.
4-3-5-1 Introduction
PW and CW Doppler modes are used to measure velocity (most often in blood).
Doppler mode can be done with a special pencil probe or with an ordinary probe. By using an ordinary
probe, you can first bring up a 2D picture for navigation purpose and then add PW/CW Doppler.
4-3-5-3-1 Alternative 1
1) Press PW or CW. A scanning screen is displayed with a Doppler cursor on the 2D mode image and
a Doppler spectrum in the lower part of the screen.
2) Position the Doppler cursor line and in PW the sample volume location over the area of interest.
3) In PW, adjust the Sample Volume.
NOTE: Sample Volume adjustment may affect the Scale, Frame rate and LV rej. settings.
• Adjust the Active mode gain to set the gain in the spectral Doppler area.
• Adjust Low velocity reject to reduce unwanted low velocity blood flow and tissue movement.
• In PW mode, adjust Sample volume to low setting for better resolution, or higher setting to more
easily locate the disturbed flows. Adjustment of the Sample volume may affect the PRF (Nyquist
limit) settings.
• Adjust the Compress setting to balance the effect of stronger and weaker echoes and obtain the
desired intensity display.
• Adjust Frequency to optimize flow display. Higher setting will improve resolution and the lower
setting will increase the depth penetration.
• Adjust Frame rate to a higher setting to improve motion detection, or to a lower setting to improve
resolution.
NOTE: Frequency and Frame rate settings may affect the Low Velocity Reject.
• Adjust Power to obtain an acceptable image using the lowest setting possible. This is particularly
important in CW mode, as the energy duty cycle is 100% (constant).
NOTE: The Doppler Power setting affects only Doppler operating modes.
Adjust the following settings to further optimize the display of the image.
• Use the Horizontal sweep to optimize the sweep speed.
• To view signal detail, adjust Scale to enlarge the vertical spectral Doppler trace. Velocity range
directly controls the pulse repetition frequency, which is responsible for the setting of the Nyquist
limit (the ability to detect maximum velocity without aliasing).
• Use Invert to reverse the vertical component of the spectral Doppler area of the display.
• Use Quick angle and Angle correction to steer the ultrasound beam to the blood flow to be
measured (Not typically required during cardiac studies).
• Adjust LPRF (PW Doppler mode only) to toggle between high and low Pulse Repetition Frequency
(PRF). When the Doppler PRF is raised beyond a certain limit, more than one Doppler gate is
displayed on the screen.
• Press Auto on the Control panel to activate Automatic Spectrum Optimization (ASO). ASO is used
to automatically adjust baseline and scale of the PW/CW spectrum to optimize the spectral display.
It will avoid the display of a folded spectrum and stretch the spectrum vertically as large as possible.
ASO optimization is not continuous but performed instantaneously each time Auto is pressed.
Press Probe on the Operator Panel. A list of the connected probes will pop
1
up on the screen.
Select the desired probe. An application menu for the desired
2
probe is listed on the screen.
• Browse to the desired application. The selected application starts.
• Press Select to launch the application.
3
• To change application without changing the current
probe, press Appl. on the Operator Panel.
6 Check the probe in each active connector slot. It will display pictorial data each time.
Related information:
4-3-7-1 Introduction
A cineloop is a sequence of images recorded over a certain time frame. When frozen, the System
automatically displays the cineloop boundary markers on either side of the last detected heart cycle
4-3-7-2 Preparation
1) Connect one of the probes to the scanner.
2) Turn ON the scanner. The 2D Mode window is displayed (default mode).
NOTE: Cineloop storage can be configured to store heart cycles with additional time before and after the
R-wave and to display a preview before storage.
4-3-8-1 Introduction
• The system default settings is to play audible feedback while pressing any action key (i.e. storing
an image, changing mode, typing text etc.). This functionality can be disabled in the Config screen
under system settings tab.
1) On the Venue™ application main screen, tap: Settings > Config > Connectivity > Additional
Outputs.
2) In the Printer Setup section, verify that the selected printer is Sony UP-D711MD.
5) In the Sony UP-D711MD Properties window, tap Print Test Page (this will send a print to the
printer bypassing all of the Scanner software).
6) The message A test page has been sent to your printer appears.
NOTE: For the Sony small-format printers, you will see an incomplete Test Page printed out. This is normal.
In order to check the functionality of the ECG device, the ECG leads need to be connected to person
body or to an ECG simulator.
Push down on the upper grey lever to unlock the brake Ensure that the wheels move freely in all directions.
1 and swivel on the casters. Push and pull the unit right, Check the wheels for wear and tear, and replace if
left, backwards and forwards. necessary.
Ground prong
Chapter 5
Venue™Components and Function (Theory)
Section 5-1
Overview
5-1-1 Purpose of Chapter 5
This chapter explains Venue™ system concepts, component arrangement, and sub-system functions.
It also describes the power distribution system, the cabling system and probes.
Section 5-2
General Information
5-2-1 Introduction
The Venue™ system is a compact ultrasound scanner that can be used with both phased array and
linear array ultrasound probes.
Weighing less than 70 kg (154.3 lb), the Venue™ ultrasound scanner is extremely versatile and -
depending upon the installed software - can be used for various imaging modes. These include:
Cockpit (monitor)
eTower
(Front End and Back End)
Base
NOTE: For a detailed description of Venue™ system operating modes, refer to the Venue™ User Manual.
Signal flow from the Probe Connector Panel, to the Front End (FE) Electronics, and to the Back End
Unit, are finally displayed on the cockpit (monitor).
At power up, all necessary software is loaded from the hard disk.
5-2-1-2 Electronics
The Venue™ system internal electronics are divided into three:
• Front End Unit - see page 5 - 20
• Back End Processor - see page 5 - 24
• System Power Distribution - see page 5 - 27
Venue™ system internal electronics comprise an eTower that contains both the Front End Unit and the
Back End Unit. The Interconnecting signals between the two sections are routed internally via PCIe
cable. All the interconnections to the cockpit (monitor) and peripherals (data signals) are via the Back
End. All power signals are via the Main Power Board (MPB).
The design of the Venue™ ultrasound scanner comprises three main sections (illustrated in Figure 5-2):
Note:
Section 5-3
Options
• For a list of the available options, see Optional Peripherals .
• For descriptions of the options, see the User Manual.
• For Installation instructions, see: Options Setup .
• For configuration, see: Options Setup .
Section 5-4
Connectivity
5-4-1 Purpose of this Section
This section describes communication and connection options between the Venue™ ultrasound
scanner and other devices in the Hospital Information System.
• Connection via a Local Area Network (LAN) - set up for this special use only
• Connection via the hospital network (Local Area Network - LAN or Wide Area Network - WAN)
The database on the review station is used as the master and images are stored directly to the review
station’s storage.
In this configuration the ultrasound scanner is just an intermediate acquisition unit which after
completion of a study, will not contain any patient information, measurements or images. The
acquisition can be done online or offline.
Images are first saved on the local image buffer on the Venue™.
At the end of the examination the images are sent to the DICOM server via a DICOM spooler.
This scenario requires that Venue™ is configured to be connected to the DICOM server.
Section 5-5
InSite
5-5-1 Introduction
InSite ExC is your direct link with a GE HealthCare Online Service Engineer or Applications Support
Engineer, or a Request for Service via the InSite ExC link at the bottom of the display screen.
Menu Choices:
• Service Desktop
Opens the Common Service Desktop on the Venue™.
• Request For Service
Generates a request for service (RFS). Allows the customer to generate a Service or Apps request.
• Connect to GE HealthCare
Increase polling rate. Click this icon to increase the contact Poll Rate from 15 minutes to 15
seconds. The increased polling rate continues for 15 minutes.
5.) The Request will be sent to the back office and a request number will be displayed.
Virtual Console Observation (VCO). Allows Technical Support to control Venue™ functionality
remotely.
Disruptive. Allows GE HealthCare’s Technical Support person to connect to your system via VCO, to
run diagnostics directly on your Venue™ system, and to collect system logs. When the system is in
Disruptive Mode, the icons are red. There are two disruptive states. If you see a telephone with a clock,
then the system is in Disruptive, Not Connected Mode. If you see a telephone with GE HealthCare, then
the system is in Disruptive, Connected Mode.
Non-Disruptive. Allows GE HealthCare’s Technical support person to look around on your system, but
cannot perform any service-related functions, depending on whether InSite has connected or not
connected. There are two Non-Disruptive states. If you see a black and white icon, InSite ExC is
activated, but not open for Technical Support access. If you see a yellow icon, InSite ExC is activated
and the Technical Support person can look around on your system, but cannot perform any service-
related functions.
NOTE: When Disruptive mode has been activated or a diagnostic has been run, the system will notify the user
that a reboot is required to allow scanning.
Section 5-6
My GE HealthCare Utilization reporting (APM)
5-6-1 Introduction
My GE HealthCare utilization reporting allows customers to receive machine data and asset
performance of their Ultrasound fleet. The Venue family software allows connection to GE back office
servers at no additional cost, however the customer must purchase My GE HealthCare app to utilize
the tools capabilities.
5-6-3-1 Introduction
This section describes Imaging Insights and My GE Healthcare reporting.
Data is sent to the imaging insights server in DICOM format. The data is being sent so often (not limited
to actual images) with dummy data in various DICOM tags.
NOTE: Imagining Insights server is setup like any other DICOM destination.
NOTE: Interval can be set to any value. Remember this value is just for the time period between exams
(data is regularly sent to imaging insights with images)
Check box to
enable
MyGEHealthcare
Section 5-7
Cockpit (Monitor) Module
5-7-1 General
The cockpit (monitor) supports the following operating systems: Windows 10.IoT 64 bit.
Probe Holder
The system On/Off button has two colors for power status indication:
• A bare finger
• A Latex gloved hand
• A Latex gloved hand with ultrasound gel.
The system Sleep Mode button has one color for sleep status indication:
When the scanner is connected, the AC Power LED indicator turns green.
System is Off
¤ AC main power switch is on and power
cord is connected
System is Off
¤ AC main power switch is off or power cord
is disconnected
• LCD Panel
• LCD Controller
• Multi-Touch Surface
• Multi-Touch Controller
• Glass Layer
• Active on touch
• Activate on release
• Drag-and-drop
• Double-click
• Right-click
User interaction with the Touch Panel is by way of touching (tapping) the screen with one finger, or
swiping (sliding multiple fingers across the surface of the screen). The touch panel display is sensitive
to finger and latex gloved hand. In addition to facilitating quick selection of the applicable controls, these
actions enable smooth scrolling, browsing and scaling of the display, as required.
To facilitate comfortable positioning for the operator, the height of the Main Display can be adjusted as
required. For optimal viewing, the screen angle is adjustable; tilting may be between +0o and -50o
At the tilt of 45o, the tilt mechanism is automatically locked and the cockpit can be tilted by additional 5o
only. To release the tilt clocking mechanism, pull down the tilt and locking handle, located at the front
of the Venue™system, under the cockpit.
In order to optimize the display settings, a light-sensing device (ambient light sensors) located on the
Cockpit (monitor) front is used for measuring the ambient light. This data is processed by the main CPU
which adapts the display setting, accordingly.
Item Value
Size 19 inch wide
Item Value
Contrast Ratio Min 600
The AD module is a graphic Active Matrix Liquid Crystal Display (AMLCD) located on the top right
corner of the cockpit (monitor).
When the system is on standby or running, there is a battery readout screen on the upper right corner
of the display. The battery status display indicates the operational time remaining in hours and minutes.
It also shows a progress bar indicating the relative amount of remaining charge, and a background color
which depends on the remaining scanning time.
• If the AC power cable is plugged-in, the AC mains power indicator is lit green and the battery is
being charged, until reaching full charge.
The background color of the battery status display changes according to the remaining operational time
as follows:
When using battery and less than 2 minutes of operational time remains, the system will initiate the End
Exam” phase, if required, to archive the current exam, and then the system will turn off.
5-7-3 Speaker
The Venue™ cockpit (monitor) includes one speaker (with self-contained amplifier) for delivering
Doppler Audio signals to the user.
Section 5-8
External Input/Output
The Venue™ ultrasound scanner has a connection panel (located at the rear of the eTower) that can
host the connections illustrated below.
Figure 5-12 shows a view of the Venue™ ultrasound unit interface panel showing external peripheral/
accessory connectors.
1 2
NOTE: Non insulated I/O can be populated either by certified medical devices or a self powered device
(powered by the system, not by external AC). All other devices should be connected to the system by
means of additional insulation.
Section 5-9
Front End Unit
5-9-1 General Information
The Venue™ Front End Unit is designed to support the cSound SW beam-forming architecture for 128
channels.
The Front End Unit, located in the door of the Electronic Cage, comprises the following modules:
Figure 5-13
WARNING WHEN OPENING AND CLOSING THE ELECTRONIC CAGE ASSEMBLY, TAKE CARE
NOT TO DAMAGE THE CABLES CONNECTED TO THE BEP.
• PCI-e channel for Setup and communication between the BEP and the DSP located on the T-
CFE Module via the PCI Bridge.
• PCI-e channel for Acquired Data Transfer between T-CFE and BEP.
• Control Signals between the BEP and T-CFE for power management and Status Monitoring.
• Power Cable connected between the MPB to the Front End Power Supply (T-FEPS).
The Front End Modules are connected via the following Interfaces:
• The 128 Transmit and Receive System channels are routed to the PSB via the T-CFE Module.
• The PSB is connected to the T-CFE via 3 connectors
The Interface between the T-CFE and the PSB modules consists of the following:
Ultrasound echoes returned from a body structure are received by the probes and routed via the
PSB Board to the T-CFE2 board which amplify the signals. Then the signals are A/D converted. The
digitized signal is transferred via the PCIe 8x Bus to the Back End Processor for software beamforming
and further signal processing.
The Back End Processor receives input commands from the User Interface (Operator Panel), handles
the communication with the rest of the system, and delivers signals (digital video) to the LCD screen
and the Touch Screen. It also provides output to an optional, internal printer. The communication to the
network (Ethernet) is also handled by the Back End Processor.
The main purpose of the T-PSB is to select the active probe and transfer the probe data to the T-CFE
Board. The PSB provides a mechanical and electrical interface for 4 RS probes.
• No connector is selected.
• High voltage supplies to all probes are disconnected.
Section 5-10
Back End Processor
5-10-1 Introduction
The Back End Processor (BEP), which supports the operation of the Venue™ ultrasound unit and is the
main controller for the system, comprises the following modules:
For information on cables connected to the BEP Module, see Figure 8-35
• PCI-e channels
• Control and Status signals between the BEP and the Front End.
BEP Interface Panel- this panel allows external connections of multiple interfaces by extension cables
that connects the internal ports to the IP panel.
• The BEP Interface Panel is located on the rear side of the Venue™ ultrasound scanner, and
contains the following connectors:
• HDMI port - supports connection of external monitor
• 2 USB 3.0 ports - support for external USB devices such as Bar-code reader etc.
• RJ45 - Ethernet port: supports wired network connection.
The Back End Board (BIB) module, responsible for the scanner Interfaces, comprises three main
Interfaces:
Section 5-11
System Power Distribution
5-11-1 Introduction
The Venue™ system power distribution consists of the following modules:
• An Isolated AC/DC Power supply to all System modules (18v/400W) called the PSU Unit.
• Optional Battery Packs that supplies Power to the system when AC power line is not present or in
the event of AC power failure (12-16.8V).
• Input filter unit, IPP, before PSU, for filtering AC line noises.
5-11-2 AC Distribution
The PSU module converts the AC power line (100-240V AC) to 18V DC @ 400 W. this module is the
main power supply for the Venue™ ultrasound scanner:
The battery module consists of 3 batteries bound together by plastic brackets. All battery packs are
electrically isolated.
Venue™ ultrasound scanner is supplied with two battery packs installed in the battery bay as standard.
Each battery pack includes three lithium ion batteries bounded in plastic enclosure.
The Venue™ has built-in charger functionality and switches automatically from battery operation to AC
operation and vice versa.
When shutting down the system, leave the main power cable connected to keep the battery fully charged.
NOTE: Before removing or inserting the Battery, perform system shut-down and disconnect the AC power
cable from the Venue™ ultrasound scanner.
NOTE: The lithium ion technology used in the system's battery is significantly less hazardous to the
environment than the lithium metal technology used in some other batteries.
- Do not disassemble or alter it. Charge the batteries only when the ambient temperature is
between 0 °C and 40 °C (32 °F and 104 °F) and discharge the batteries between -20 °C and
50 °C (-4 °F and 122 °F).
- Do not short-circuit the battery by directly connecting the battery terminals with metal objects.
- Do not heat the battery or incinerate.
- Do not expose the battery to temperature over 60 °C (140 °F). Keep it away from fire and
other heat sources.
- Do not charge the battery near a heat source, e.g. fire or heaters.
- Do not leave the battery in direct sunlight.
- Do not pierce the battery with a sharp object, hit it, or step on it.
- Do not use a damaged battery. Do not solder a battery.
- Do not connect the battery to an electrical outlet.
- Do not immerse the battery in water or allow it to get wet.
- Do not put the battery into a microwave oven or pressurized container. If the battery leaks or
emits an odor, remove it from all possible flammable sources.
- If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal
during use, recharging or storage, immediately remove it and stop using it.
- If you have any questions about the battery, consult GE HealthCare or your local
representative.
Short term (less than one month): 0 °C (32 °F) to 50 °C (122 °F)
Long term (more than three months): -20 °C (-4 °F) to 20 °C (68 °F).
Section 5-12
Cooling System
5-12-1 General Information
The Venue™ system has 3 fans for system cooling:
The cooling requirement for the Venue™ ultrasound scanner with monitor and on board peripherals, is
up to 2000 BTU/h. This figure does not include cooling needed for lights, people, or other equipment in
the room.
NOTE: Each person in the room places an additional 300 BTU/h demand on the cooling system.
Section 5-13
Peripherals
5-13-1 Internal Peripheral
CAUTION USE ONLY APPROVED, DEFIBRILLATION-PROOF ECG PATIENT CABLES, SEE Table 9-4-11.
The Wi-Fi adapter is connected at the back side of the cockpit (monitor) via a L shape USB adapter.
The bar code reader is connected to the Venue system via a USB port located on the rear.
Chapter 6
Service Adjustments
Section 6-1
Overview
6-1-1 Purpose of Chapter 6
This chapter explains that there are no service adjustments required on a Venue™ .
Section 6-2
Power Supply Adjustments
There are no adjustments on the power supply.
If a voltage is outside the specified range, it means that something is wrong, either with the power supply
itself or with one (or more) of the units connected to that specific power outlet.
Section 6-3
Cockpit (Monitor) Adjustments
There are no adjustments required on the Cockpit (monitor).
Section 6-4
Articulated Arm Movement Adjustments
6-4-1 Arm Movement Adjustment - General Instructions
1.) The cockpit adjustment movement resistance may be increased/decreased in the following axes
(red arrow shows location of the controlling screw per axis):
2.) Remove the cockpit rear cover if exists: disconnect four screws using appropriate Phillips
screwdriver.
3.) Using 8mm Allen key and 19mm open wrench release/tighten the Allen screw.
2.) Tighten or release the 4mm Allen screw to adjust the required arm movement resistance
NOTE: Ensure there is no arm autonomic movement.
Chapter 7
Diagnostics/Troubleshooting
Section 7-1
Overview
7-1-1 Purpose of Chapter 7
This chapter describes how to setup and run the tools and software that help maintain image quality
and system operation. Very basic host, system and board level diagnostics are run whenever power is
applied. Some Service Tools may be run at the application level.
Section 7-2
Service Safety Considerations
Section 7-3
Gathering Troubleshooting Data
7-3-1 Purpose of this Section
Trouble images and system data (logs) can be acquired at the device or through remote diagnostics
(InSite). These data can be used to perform service at the device, or can be sent back to the
manufacturer for analysis.
NOTE: You MUST select one of the available devices as the destination device if it is to be different than the
default Export directory on the hard drive.
The screen capture is a bitmap which eliminates the possibility of artifacts from compression.
Section 7-4
Disruptive mode is required to run diagnostics, clean presets, and reset the patient database, and turn
on Virtual Console Observation (VCO).
• When Disruptive mode is On, all service functionality on the Service desktop is allowed but user
operation of the system may be limited.
• When Disruptive mode is Off, some service functionality on the Service desktop is not available
and user operation of the system is normal.
• The ability to enable Disruptive mode depends on the logged in user access level:
• Local user - a user locally logged into the machine will not be able to set the Disruptive
mode. Local user can only allow a Disruptive mode request from a remote user through
the Service desktop. The local user must have Authorize Remote Service Access to allow
Disruptive mode. If the local user does not have this right, the remote user’s request will
be automatically denied.
• Remote user - a user remotely accessing the system will not be able to automatically
switch on the Disruptive mode. The local user has to grant remote access.
• The local user will be notified through a dialog box and asked to allow Disruptive mode.
7-4-3 Licenses
With Service Basic Access (Class A), these are the available options:
• HOME
• Utilities
• Change Password
• Delete Files
• Gather Logs
• Network Capture
• Thirty Party Licenses
• Options
• Agent Configuration
Note: The information on System Information is available to all service class licenses.
This table shows all the elements available on System Information with descriptions.
Table 7-2 System Information
Element DESCRIPTION
Note: The information on Software Status is available to all service class licenses.
The following table lists all the elements available on Software Status section.
Table 7-3 Software Status
Element DESCRIPTION
System Date Current date in the format: <day>, <month> <year>.
System Time Local time based on the last time the system desktop was refreshed in
the format <hh:mm:ss>.
Application Installation Date Date the application software was installed.
Base Image Installation Date Date the base image software was installed. The base image software
includes the operating system and other supporting software.
Base Image Version Version number of the base image software.
Note: The information on Connected Probes is available to all service class licenses.
The following table lists all the elements available on Connected Probes section:
Table 7-4 Connected Probes
Element DESCRIPTION
1.) Tap Utility on the top bar and select Gather Logs
2.) Select one of the following:
• 1 Day Logs
• 1 Week Logs
• All Logs
Chapter 7 - Diagnostics/Troubleshooting 7-12
P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
3.) Click Gather Logs. In the resulting dialog box, record the location of the log files and click OK.
• When the gather log operation is complete, click the notification icon in the banner to view
the location of the log files.
Note: The Delete Files utility is available to all service class licenses.
The following table lists all the elements available on Delete Files section:
Table 7-5 Delete Files
Element DESCRIPTION
Delete Files Displays the files that are available for deletion.
To delete files:
1.) From the Top menu bar, Tap: Utilities >> Delete Files.
2.) Under Delete Files, select the available folders and files that you want to delete.
3.) Click Delete.
4.) In the resulting dialog box, click Delete and then click OK.
Note: The Change Password utility is available to all service class licenses.
To access Change Password, From the Top Menu bar, tap Utilities >> Change Password.
The following table lists all the elements available on Change Password screen:
Table 7-6 Change Password
Element DESCRIPTION
1.) From the Top Menu bar, tap Utilities >> Change Password.
2.) Under User Type, select the user.
Note: Before changing the GEService password, make sure that the system is connected to the
network and the agent is configured. The GEService password is used to perform portions of
remote service. If the password is changed and the system information is not updated, it may
slow down remote service. Both file transfer and SSH depend on the GEService password.
3.) In New Password and Confirm Password, enter the new password.
Note: The Change Password utility is available to all service class licenses.
To access Third Party Software Licenses From the Top Menu bar, tap Utilities >> Third Party
Software Licenses.
To access Network Capture, From the Top Menu bar, tap Utilities >> Network Capture.
The following table lists all the elements available on Network Capture screen:
Element DESCRIPTION
Network Capture Parameters
Maximum Size Allowed size of the generated log file. Valid value
are:
• 256MB
• 512MB
• 1024MB
Devices DICOM-configured devices for which you want to
capture information. If no additional devices are
configured, only All will be available.
Start Network Capture Select to start the process. This causes the network capture to start, enables
the Stop button, and updates the Network Capture Status pane and chang-
es the Status to Running.
Stop Network Capture Select to stop the process.
Network Capture Status
1.) From the Top Menu bar, tap Utilities >> Network Capture.
2.) From Network Capture, do the following:
• Under Maximum Size, select the allowed size of the generated log file.
• Under Devices, select the DICOM-configured device for which you want to capture
information. If no additional devices are configured, only All will be available.
3.) Select Start Network Capture to start the process. This causes the network capture to start,
enables the Stop button, and updates the Network Capture Status panel and changes the
Status to Running.
4.) Click the Stop button to end data collection. Stopping is a two-step process:
- Stops the data collection and immediately closes the XXX.etl file.
- Collects additional diagnostic data that may help diagnose network issues. When the file is
closed, you see “There is no trace session currently in progress”. When the remaining data is
collected and the XXX.cab file is closed, you are notified in the banner.
7-4-4-10 Options
Use Options to:
• Add (or delete) a valid option key, add a duplicate option key, not add an invalid option key, and ask
for confirmation before deleting an option key.
• View software option key details. Key details are a list of options that are enabled by a particular key.
Under Available Keys, highlight the option string, select Details and then view the options on the left
side of the screen. Press Show All to view all of the activated options.
To access Options, From the Top Menu bar, tap Utilities >> Options.
The following table lists all the elements available on Options screen:
Table 7-9 Options
Element DESCRIPTION
Software Options
Option Software options on the system
Hardware Number Number for the hardware. The hardware number is the hash of the serial
number that is used to generate the option key.
Serial Number Serial number of the system
Software Option Keys
Note: The Agent Configuration utility is available to all service class licenses.
The following table lists all the elements available on Agent Configuration screen:
Table 7-10 Agent Configuration
Element DESCRIPTION
Agent Configuration
Contact Details Phone number for the person at the customer site a GE HealthCare remote
service engineer would contact. The phone number is entered during instal-
lation and reviewed at every service call to make sure the information is cor-
rect.
Agent Status Status for the agent. Valid values are:
• Running
• Not Running
Agent Registered Registered status of the agent. Valid values are:
• Yes - The agent is registered in the back office.
• No - The agent is not registered in the back office.
• Not Available - The agent is not configured or running.
Agent Quarantine Quarantine status of the agent. Valid values are:
• Yes - The agent has more than one device registered with the same CRM
Number in the back office. This scanner cannot send data back to GE
HealthCare or be remotely accessed.
• No - The agent has one device registered with the listed CRM Number in
the back office.
• Not Available - The agent is not configured or running.
Agent CRM Verified CRM verified status of the agent. Valid values are:
• Yes - The agent is verified in the back office.
• No - The agent is not verified in the back office.
• Not Available - The agent is not configured or running.
Agent Model Number GE HealthCare part number for the system. The same number as listed on
the rating plate.
Serial Number Serial number of the agent (read-only). If the agent is not registered with a
serial number, this field is populated with the serial number of the system.
The serial number of the agent is tied to the serial number of the system.
CRM No Customer Relationship Management (CRM) number. System identifier as-
signed to the customer unit by the service region. CRM is pre-populated by
adding system to the CRM number. The CRM number of the system is ed-
itable.
Display Name Displayed name of the agent.
Advanced Configuration
Proxy Configuration
Enable Proxy Enables the proxy server.
Proxy Server When Enable Proxy is selected, name of the proxy server IP.
Proxy Port When Enable Proxy is selected, number of the proxy server port.
Credentials
Enable Proxy Enables the proxy credentials.
Credentials
Username When Enable Proxy Credentials is selected, name of the user.
Password When Enable Proxy Credentials is selected, password for the user.
Section 7-5
Probe Check
7-5-1 Background
The Probe check is based on transmitting and receiving an ultrasound signal through the probe
elements to be able to diagnose if there are defective probe elements
Probe check tool can run automatically at first probe connection or manually through the probe selector
button.
Note: Before running the tool, verify that the probe to be tested is thoroughly clean from any dirt/gel
etc.
1.) Connect the probe to any RS probe connector on the back side of the system.:
2.) Select a probe from the probe selection menu and click on ’Probe Check’ button.
Note: It is possible to keep scanning with a fail result on a specific probe at the users discretion.
Section 7-6
e-Delivery
7-6-1 Purpose of this Section
In this section you will find e-Delivery procedures and hints.
7-6-2 Introduction
e-Delievery is available for customers who purchased the eDelivery HCAT.
Having this capability allows the users to receive notification emails upon the release of new SW
available for their Venue family ultrasound system and to download it from the GE HealthCare portal.
Before you start downloading your SW, make sure you have your entitlement credentials.
3.) You will get a mail from eDelivery admin system with your username and initial password for login.
You will be required to change your password when login with this password.
7.) Select the Image USB tool and the MD5Summer files.Select the relevant SW version (the SW
image filename contains the SW mediaPN):
8.) 2 ways are available to download the files. You may need to install an adds-on if you are using this
tool first time
9.) Once the SW image file download process ends, run the MD5Summer utility(MD5Summer.exe),
click OK if this window is shown:
10.)Browse to the folder to which you have downloaded the SW image file (.bin) and select “Create
sums”
11.)Select the .bin file and click on Add
13.)Verify that the calculated MD5 is identical to the value displayed in Flexera portal.
Requirement Description
NOTICE The minimum required size of the disk-on-key to be used must be 32GB.
1.) Browse to the downloaded file location and run the ImageUSB.exe file.
2.) If the Windows User Account Control dialog box appears, click Yes to allow the program to make
changes to your computer.
3.) The ImageUSB by PassMark Software main window appears.
5.) In the Step 2 section, select the Write image to USB drive check box.
6.) In the Step 3 section, click Browse and select the image-file (in BIN format) downloaded from the
GE HealthCare Portal.
7.) In the Step 4 section, click Write to start the burning process.
8.) Click Yes in the dialog boxes that appear to continue the burning process.
9.) View the burning progress in the Overall progress status bar.
10.)If the software burning process is successfully completed, the Imaging Completed message
appears. Click OK to close the notification window.
11.)If the burning process fails, a notification window appears. Click OK to close the window.
2) Select the new SW package from the presented list, and click on Download
3) In the warning message that appears, check the box and select Download
5.) The system will backup the current SW before installing the new one, as follows
6) Select the destination folder for the backup and click Begin Backup
7) Wait until the backup in progress bar is replaced by the backup is complete message.
Note: You may stop the backup process by clicking Stop Backup
8) When the Backup complete dialogue appears, check the box and click Install
Figure 7-58 Select the package to be reverted to, and click Rollback
3) Select the source of the package from the roll-down screen, check the box and click on Import
5) When the import process ends, you may now select and install the imported package, see 7-6-5-2
4.)
Section 7-7
Noise Troubleshooting
7-7-1 Purpose of this Section
In this section you will find Noise troubleshooting procedures and hints.
7-7-2 Introduction
Before you start troubleshooting the noise, you should read the following subsections:
• EMI Limitations
• EMI Prevention/Abatement
• Accessing GE HealthCare portal and downloading SW - see below
When talking to the customer, try to gather as much information as possible about the conditions when
the noise appear:
If picked up by a probe cable, the noise will be coherent -“penlight noise” pointing down in the picture -
due to the fact that the noise is received on all channels.
If the Venue™ has been used for scanning for some time before the noise appears, it may be due to either
heat problems or some software related issues. By doing a restart you may learn some more about the
cause.
Connect an external USB keyboard and click Ctrl+Alt+R to restart the back end processor without
power-cycling the unit.
• If the noise is present after the restart, the cause is most likely due to heat problems.
• If the noise is gone after the restart, it may be due to either the setup/adjustments or a software
failure.
Possible causes for heat problems:
NOTE: GE requires a dedicated power and ground for the proper operation of its Ultrasound equipment. This
dedicated power shall originate at the last distribution panel before the Ultrasound system.
The Venue™ will function on voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt
power in North America, then a center tapped power source is required.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Section 7-8
Audio Troubleshooting
7-8-1 Purpose of this Section
In this section you will find Audio troubleshooting procedures and hints, to be used if there is no Doppler
or system sound.
3.) Enter CW mode and select volume menu (right side) – increase the volume
Section 7-9
Probes not Recognized Troubleshooting
7-9-1 Purpose of this Section
If the system does not recognize any of the connected probes. perform the following procedure.
Section 7-10
System does not turn on Troubleshooting
7-10-1 Purpose of this Section
This section manages the most common scenarios where the system does not startup.
7-10-2 Cockpit ON/OFF Button turns orange -->BEP BIOS Jumper Setup
Symptom: The system does not turn ON (cockpit on/off button turns green for a few seconds and then
turns orange).
1.) Reset BIOS by changing the jumper position as shown in the picture: move from the 2 outer pins to
the 2 inner pins
7-10-3 BEP Fan does not Spin (ON/OFF button is Orange)-->MPB to BIB Connection
Symptom: T-CFE and T-FEPS LEDs turn On and then off; BEP fan does not spin,
The On/Off button on the cockpit turns green for a second and then turns orange)
1.) Inspect the BIB (blue) cable, if damaged - replace the BIB board.
2.) Reset the BIB (blue) cable on the T-CFE2 side (disconnect and re-connect).
3.) Inspect and re-connect MPB to T-FEPS power cable. Replace if damaged.
Section 7-11
MPB Diagnostics Failure Troubleshooting
7-11-1 Purpose of this Section
MPB diagnostics test fails if remaining scan time is less than 20 minutes. To identify if there is a real
failure of the MPB, perform the following procedure.
NOTE:
Section 7-12
RFID Badge Scanning Setup
7-12-1 Introduction
Personal IDs and associated passwords can be preset on the Venue, or the lock screen may be
configured to be the default start up screen.
If the User Auto Logon preset is blank, you are prompted to login by entering Operator and password.
You can also log in using a physical RFID element (i.e., Badge). When the RFID option is enabled, the
lock screen displays an indication to tap a badge to log in.
Note: Emergency logon allows you to store an exam but not save it into the Archive.
4.) To log in with a badge (Tap in), touch the RFID scanner with the badge/chip.
Note: If there is an issue logging in with an RFID, enter your Operator and Password to login.
5.) If the system screen locked during an active exam due to inactivity, and the logged in user taps in
or enters Operator and password, the screen unlocks.
Note: While in the lock screen, the system also allows for changing the system operator. When a
different user logs in (with a badge or by entering Operator and password), the system
prompts whether to end the current exam or continue. Tap End the current exam.
A "Grace Period” (amount of time during which the multifactor authentication is valid) may be added to
the multifactor login.
During the grace period, next time the user does not have to use the multifactor login and may use the
tap in tap out method.
er Venue requires a multifactor login or a multifactor login with grace period is determined via the
authentication server and is not part of the system configuration.
NOTE: Emergency mode is available in all scenarios where the screen is locked.
7-12-3 Logoff
To logoff, tap Patient on the top left of the screen and then tap Logout at the bottom of the patient
screen. When the RFID option is enabled, tap out by touching the RFID scanner with your badge a
second time. Venue prompts you if you wish to log-out.
NOTE: A second tap from a different user (When a user is already logged in) is ignored.
7-12-4 Configuration
NOTE: In order to enable RFID badge login there is a need to establish connectivity between the LDAP
server and Ultrasound system.
Before starting the setup process, please prepare the certificate. The certificate is provided by the
Imprivata team / Hospital IT.
14.)On the pop dialog window fill in the user credentials (UserName and password) and press ok.
15.)A 'Test connection' window will open, verify the connection = Success and click on 'close' button.
16.)Select a group for domain users in the following format: CN=Users, DC=ge, DC=local, DC=com
2) Choose which department shall have the Group access (For example: Operators)
Figure 7-78 RFID Badge Certificate Installation: Scan certificate from DiskOnKey
5.) Verify the certificate has Installed status = 'Yes' (as shown in picture below) and close the Window.
Section 7-13
ViewPoint Reporting
NOTE: Supported from R4.1 SW Only.
7-13-1 Introduction
Personal IDs and associated passwords can be preset on the Venue, or the lock screen may be
configured to be the default start up screen.
ViewPoint Reporting is an exam report package option for your Venue system that allows you to fill out
an exam specific report form directly on the system during the exam.
Fill in the report form by using the touch screen on the convenient user interface and toggling between
the report and exam screen at any time during the exam.
NOTE: Availability of the ViewPoint Reporting option is region dependent. This option may not be
available in your region.
7-13-2 Overview
The ViewPoint Reporting package requires a continuous connection to a ViewPoint 6 workstation. For
every new exam, a new report form is sent from the ViewPoint workstation to Venue. The user may
select and fill up multiple form-types.
Upon ending the exam, the filled report forms will all be communicated back to the ViewPoint 6
workstation. A final report may be produced, stored, or sent further to the institute's EMR system from
the ViewPoint 6 workstation.
NOTE: In the ViewPoint 6 workstation you may edit or add to the exam report's data. may be edited
further.
7-13-3 Configuration
NOTE: In order to establish connectivity between ViewPoint server and Ultrasound system there is a
need to load two certificates on to the system.
NOTE: Check the Jump to Report on EndExam box to configure ViewPoint to automatically jump back
to the report upon tapping End Exam.
7-13-4 Troubleshooting
For Venue to connect VP, Venue tries to resolve the host name, in a domain controlled environment
there is no issue and Venue does it successfully.
For security reasons most ports in Venue are blocked including ports that allows other protocols for
resolving the host name
In case there is an environment that Venue cannot connect because Host name cannot be resolved the
bellow will fix it:
1.) Step 1: Click the Windows button and type Notepad in the search bar.
2.) Step 2: Right click on Notepad and then Run as Administrator.
3.) Step 3: You'll be asked, "Do you want to allow this app to make changes to your device?". Choose
Yes.
4.) Step 4: In Notepad, choose File then Open.
5.) Step 5: Navigate to C:\Windows\System32\drivers\etc\hosts or click the address bar at the top and
paste in the path and choose Enter. If you don't readily see the host file in the /etc directory then
select All files from the File name: drop-down list, then click on the hosts file.
6.) Step 6: Add the appropriate IP and hostname at the end of your hosts' file, select Save, and then
close the file.
7.) Step 7: Finally, you will want to flush your DNS cache for your computer to recognize changes to
the file. Click the Windows button and search command prompt.
8.) Step 8: Type the following command in the terminal and press Enter
ipconfig /flushdns
Section 7-14
Venue HDMI connection troubleshooting
NOTE: This troubleshooting workflow is not applicable for LDM (Large Display Monitor), which is not
supported for Venue family products.
7-14-1 Troubleshooting
The following procedure describes Venue HDMI connection troubleshooting.
Section 7-15
Wireless Probe Indications and Management
7-15-1 Introduction
Vscan Air CL and SL wireless probes include indications for battery charge status, WIFI connection,
and thermal indication, displayed on the system screen. For guidelines and suggested work practice,
refer to the vendor’s documentation.
NOTE: For detailed information and for any support and liability issues related to Vscan Air CL and SL
wireless probes and related accessories, including charger, refer to the manufacturer manual
and customer support (3rd party policy).
NOTE: Wireless probe is supported for APU Back End only (will not work on CPU Back End).
The following figures provide illustrations for major on-screen indications regarding probe battery
charge status and WIFI connection:
• Probe battery and WIFI connection indications, when the wireless probe is connected but not
selected .
• Probe charging indication: when the probe is placed on the charger, it may not be selected, as
• When the wireless probe is in shutting down process, the screen indicates it as follows .
The wireless probe includes LED indications showing connecting, charging, and more. The following
figure s are for illustration only, showing the major indications. For more details, refer to the wireless
probe manual, see https://fccid.io/YOM-VSCANAIR/User-Manual/Product-Manual-5040759.
• Probe is being charged: Yellow light on both LEDs indicates probe is charging. Green light on both
LEDs indicates the Vscan Air CL is fully charged:
Chapter 8
Replacement Procedures
Section 8-1
Overview
8-1-1 Purpose of Chapter 8
This chapter provides replacement procedures for Venue™system parts, as outlined below.
NOTE: The illustrations provided in this chapter are for illustration purposes only and are subject to change
without notice.
CAUTION Before performing any service activities related to electronic boards and/or accessible metal
parts, make sure to disconnect any power source from the system:
- Switch off the circuit breaker located at the back side of the system.
- Disconnect the power cable from the wall outlet and from the system.
- Remove Internal battery packs.
Section 8-2
Accessories - Replacement Procedures
8-2-1 Basic Storage Basket/Large Storage Basket Replacement Procedure
8-2-1-1 Tools
None
8-2-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
8-2-2-1 Tools
None
8-2-2-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
by pushing it upwards.
Section 8-3
Covers - Replacement Procedures
8-3-1 Overview of Covers
18
14
16
15 8
3
9 6
4 2
5
7 1
12 4 11
13
17
10
2 Cover: Mid Thermal Baffle - CRU 11 Cover: Left Side Base- FRU
4 Cover: Right Side eTower - CRU 13 Cover: Right Base Bottom - FRU
5 Cover: Left Side eTower - CRU 14 Mechanical - RISER with Friction Adj. hole FRU
8 Halo Handle with Locking - FRU 17 Cover: Left Base Bottom - FRU
8-3-1-1 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
DANGER DO NOT WEAR THE ESD WRIST BAND STRAP WHEN REMOVING
PARTS FROM THE POWER SUPPLY UNIT. BEFORE REMOVING ANY
PART OF THE POWER UNIT, TURN THE POWER OFF AND
DISCONNECT THE POWER CORD.
CAUTION BEFORE REMOVING CIRCUIT BOARDS, TURN THE POWER OFF AND WEAR THE ESD WRIST
BAND STRAP.
CAUTION Before performing any service activities related to electronic boards and/or accessible metal
parts, make sure to disconnect any power source from the system:
- Switch off the circuit breaker located at the back side of the system.
- Disconnect the power cable from the wall outlet and from the system.
- Remove Internal battery packs.
8-3-2-1 Tools
None
8-3-2-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
8-3-3-1 Tools
None
8-3-3-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
3) Grip the rubber holder and pull the cover toward you to remove it from the system.
1 2 3
Grip here...
eTower pin
8-3-4-1 Tools
None
8-3-4-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2) The right side eTower cover removal procedure is identical to the left side eTower cover removal
procedure.:.
8-3-5-1 Tools
None
8-3-5-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
8-3-6-1 Tools
Appropriate Phillips screwdriver
8-3-6-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower cover, Right Side eTower
Cover and Left Side eTower Cover:.
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
.. ..
Printer Frame Cover
Printer Insert Cover
8-3-7-1 Tools
Appropriate Phillips screwdriver
8-3-7-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
3.) Release the two Phillips screws and remove the Printer Insert Cover.
8-3-8-1 Tools
Appropriate Phillips screwdriver
8-3-8-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2) Remove the following covers: Lower Front eTower cover, RS probe cover, Right Side eTower
Cover and the Left Side eTower Cover:.
• Lower Front eTower Cover Removal Procedure
• RS Probe Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
3.) Loosen the four captive screws (two on each side), grip the MPB Door Cover at the bottom and pull
toward you to remove it.
8-3-9-1 Tools
None
8-3-9-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
8-3-10-1 Tools
Appropriate Phillips screwdriver
8-3-10-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
Make sure the system is standing securely on a level surface, with the wheels in the locked position.
8-3-11-1 Tools
Appropriate Phillips screwdriver
8-3-11-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown
Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, RS Probe Cover. Right Side and Left Side
eTower covers, Upper Front eTower, and Riser Thermal Cover.
• Lower Front eTower Cover Removal Procedure
• RS Probe Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Upper eTower Front Cover Removal Procedure
• Riser Thermal Cover Removal Procedure
5.) Loosen and remove four screws securing the riser cover to the riser (access screws from
underneath).
2.) Install four rubber cable guides (two short guides on the back side and two long guides in the front
side) on the riser cover. Use a flat screwdriver to gently affix the rubber guide in place, if required
Short rubber guide
3.) Install new riser cover on riser and secure the four securing screws
6.) Refit the following covers: Lower Front eTower, Right Side and Left Side eTower covers, Front Base
Cover and Riser Thermal Cover
• Lower Front eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Upper eTower Front Cover Removal Procedure
• Riser Thermal Cover Installation Procedure
• RS Probe Cover Installation Procedure
7.) Install all accessories.
Section 8-4
System Modules- Replacement Procedures
8-4-1 Base Module Replacement Procedure
8-4-1-1 Tools
LOCTITE® 243™
8-4-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
3.) Remove the following covers: Lower Front eTower, RS Probe cover, Right Side and Left Side
eTower covers, and Front Base Cover
• Lower Front eTower Cover Removal Procedure
• RS Probe Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Front Base Cover Removal Procedure
4.) Position the system on its side to gain access to the system base.
5.) Unscrew the four base mounting screws.
3.) Apply LOCTITE® 243™ on the Base Module mounting screws and tighten them.
4.) Refit the following covers: Right Side and Left Side eTower covers., Lower Front eTowe and Front
Base Cover
• Front Base Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
8-4-2-1 Tools
Appropriate Phillips screwdriver
8-4-2-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
3.) Open the two fastening latches on the left side of the FE door assembly and loosen the captive
screw. Then, carefully open the door.
8-4-3-1 Tools
Appropriate Phillips screwdriver
8-4-3-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, and Mid Thermal Baffle Cover.
5.) Leave the door open by approximately 30 degrees, to make enough space for the FE door to be
removed.
6.) Slightly lift and slide the door upwards until completely removed.
7.) Remove the eight holding screws to separate the front end metal door from the scanner door cover
3.) Secure the FE Module to the FE Door with four screws (previously removed).
4.) Mount the FE Door assembly on the scanner.
5.) Reconnect the following cables:
• PCIe cable
• MPB TO T-FEPS Cable and secure it to the T-CFE2 module and to the T-FEPS module with
cable clips.
• Fan cable
6.) Close the FE door and close the two fastening latches on the left side of the Front End door
assembly.
7.) Tighten the captive screw.
8.) Refit the following covers: Mid Thermal Baffle Cover, Lower Front eTower, left side eTower, right
side eTower and RS Probe Cover.
CAUTION: The SSD contains patient information data. when replacing the SSD, Leave the faulty part
at the customer site.
8-4-4-1 Tools
Phillips screwdriver
8-4-4-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower.
Captive Screw
8-4-5-1 Tools
Appropriate Phillips screwdriver
Flat-head screwdriver
8-4-5-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove four Phillips screws securing the cockpit (monitor) to the arm.
3.) Remove the cockpit rear cables cover, if exists (see below).
Figure 8-23 Cockpit (Monitor) Securing Screws and Cockpit Rear Cover Removal
CAUTION Raise the Articulated Arm to its up position to prevent the unintentional injury to personnel from
the stored mechanical energy.
6.) Hold the cockpit (monitor) on its top, insert a screwdriver into the dedicated hole and press to
release the securing spring. The click is sounded, indicating the securing spring is released.
Spring locked
Spring released
8-4-6-1 Tools
Appropriate Phillips screwdriver.
8-4-6-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower cover, Right Side eTower
Cover and the Left Side eTower Cover:.
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
5.) Release the captive screw at the bottom of the PSU and pull the PSU out gently.
5.) Refit the following covers: Lower Front eTower cover, Right Side eTower Cover, Left Side eTower
Cover, and RS Probe Cover.
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
8-4-7-1 Tools
Appropriate Phillips screwdriver.
8-4-7-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower cover, Right Side eTower
Cover, Left Side eTower Cover and MPB Door Cover:.
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• MPB Door Cover Removal Procedure
3.) Release the two captive screws securing each battery pack.
4.) Pull out the top and bottom battery packs.
Battery Pack
8-4-8-1 Tools
Appropriate Phillips screwdriver.
8-4-8-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: Lower Front eTower cover, Left Side eTower cover, and Right Side
eTower cover.
5.) Open the two fastening latches on the left side of the FE door assembly and loosen the captive
screw. Then, carefully open the door.
9.) Disconnect the BIB blue cable from the CFE plastic cable guide.Disconnect the MPB to BIB cable.
5.) Reconnect the BIB blue cable to the CFE plastic cable guide.
6.) Reconnect the MPB to BE power cable.
7) Install the SSD module.
8) Close the FE door and close the two fastening latches on the left side of the Front End door
assembly.
9.) Tighten the captive screw.
10) Install the MPB Front Metal Door.
11.)Refit the following covers: left side eTower, right side eTower, and RS Probe Cover.
8-4-9-1 Tools
Appropriate Phillips screwdriver.
8-4-9-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove BIOS battery gently from the connector while holding the connector.
5) Install BE Module
8-4-10-1 Tools
• Appropriate Phillips screwdriver
8-4-10-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Front Metal Door Removal Procedure
4.) Remove omega bracket: release 5 screws connecting the omega bracket:
• Display port
Note: If the MiTx to BIB cable is preventing easy removal of the BEP PCB, disconnect the MiTx to BIB
cable connector latch (see yellow circle in the above figure).
5.) Reconnect omega bracket: attach 5 screws connecting the omega bracket
8.) Refit the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
• Upper eTower Front Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
9.) Install all accessories.
8-4-11-1 Tools
• Appropriate Phillips screwdriver.
FRU Part # Refer to Table 9-19.
8-4-11-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe cover, Lower Front eTower cover, Right Side eTower
cover, Left Side eTower cover and MPB Door Cover.
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• MPB Door Cover Removal Procedure
5.) Release the captive screw at the top center of the MPB.
6.) Release the captive screw at the bottom center of the MPB.
5.) Refit the following covers: MPB Door Cover, Lower Front eTower cover, Right Side and Left Side
eTower covers, and RS Probe cover
• MPB Door Cover Installation Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
9.) If PM_FW is not up to date (the Comment section states “expected version is 3.xx"):perform
software reload
8-4-12-1 Tools
Appropriate Phillips screwdriver.
8-4-12-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
4.) Loosen the 4 retaining screws and remove the T-CFE2 Fan box.
5.) Loosen the 2 retaining screws and remove the T-FEPS module..
7.) Separate the T-CFE board From the T-PSB board, by pulling the CFE Release Arm handle
upwards.
4.) Refit the following covers: Lower Front eTower, Left side eTower, Right Side eTower, and RS Probe
Cover.
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
5.) Install all accessories.
8-4-13-1 Tools
Appropriate Phillips screwdriver.
8-4-13-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
4.) Open and remove the full Front End assembly and place it on your laps in order not to damage the
probe locker levers.:
6.) Remove the PCIe plastic cable guide and attach it to the new T-PSB module.
5.) Refit the following covers: Lower Front eTower, Left side eTower, Right Side eTower, and RS Probe
Cover::
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
Section 8-5
Electronic Boards- Replacement Procedures
8-5-1 BIB Board Replacement Procedure
8-5-1-1 Tools
Appropriate Phillips Screwdriver.
8-5-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
5.) Disconnect BIB TO BE SPLIT CABLE connector that connects the BIB board to the BE module.
Figure 8-55 Removing BIB Board - Disconnecting BIB TO BE SPLIT CABLE Connector
6.) Disconnect the PCIe cable connector that connects the BIB board to the BE module.
5.) Close the FE door and close the two fastening latches on the left side of the Front End door
assembly.
6.) Tighten the captive screw.
7.) Refit the following covers: Lower Front eTower, Left side eTower, Right Side eTower, and RS Probe
cover:
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
8.) Install all accessories.
8-5-2-1 Tools
Appropriate Phillips screwdriver.
8-5-2-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
4.) Unscrew the two lever holding screws and remove the CFE Release Arm (Lever) from the PSB
Board.
6.) Refit the following covers: Lower Front eTower, Left side eTower, and Right Side eTower.::
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Removal Procedure
7.) Install all accessories.
8-5-3-1 Tools
Appropriate Phillips screwdriver.
8-5-3-3 Preparation
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower.
3.) Open the two fastening latches on the left side of the FE door assembly and carefully open the door.
6.) Using both hands, carefully pull the T-FEPS towards you and remove it from the T-CFE2.
8-5-4-1 Tools
Appropriate Phillips screwdriver.
8-5-4-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, and Right
Side eTower.
3.) Open the two fastening latches on the left side of the FE door assembly and loosen the captive
screw. Then, carefully open the door.
4.) Disconnect the MPB TO T-FEPS Cable.
5.) Disconnect the fan cable.
6.) Loosen the 4 screws and carefully remove the T-CFE2 Fan box.
Section 8-6
Mechanical Parts- Replacement Procedures
8-6-1 MPB Front Metal Door Replacement Procedure
8-6-1-1 Tools
Appropriate Phillips screwdriver.
8-6-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
3.) Release four captive screws and remove the MPB Front Metal Door.
8-6-2-1 Tools
Appropriate Phillips screwdriver.
8-6-2-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe cover, Lower Front eTower, Side Covers, MPB Power Door
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Door Cover Removal Procedure
4.) Unscrew the two mounting screws that hold the Guide L/R.
4.) Refit the following covers: MPB Door Cover, Left and Right Side eTower Covers, Lower Front
eTower Cover, and RS Probe cover
• MPB Door Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
5.) Install all accessories.
8-6-3-1 Tools
LOCTITE® 243™
8-6-3-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
6.) Remove the Halo Handle mounting screws: four (x4) front screws and four (x4) side screws (two
from each side).
8-6-4-1 Tools
Allen key 2.5 mm.
8-6-4-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower cover, Left Side eTower cover,
Right Side eTower cover and Riser Thermal Cover.
6.) If the cables are routed through the arm axis, refer to MPB TO Cockpit Cable Removal Procedure
and to BE to Cockpit Cable Removal Procedure
7.) Using Allen key screwdriver, remove the two securing screws of the arm side cover.
8.) Slide the arm side cover upwards and remove it.
9.) Perform steps 4-5 for the other arm side cover.
10.)Pull out the cockpit (monitor) cables routed inside the riser.
12.)Using Forged Steel Ring Pliers, remove the C-clip and then the Teflon ring.
Teflon ring
C-clip
8-6-5-1 Tools
• Appropriate Phillips screwdriver
FRU Part # Refer to Table 9-14.
8-6-5-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
4.) Remove 4 screws from the lower end of arm assembly and remove the lower black cover
6.) Remove 2 screws from spring metal brace part to release springs
7.) Slide out (on rail) black plastic screen locking release handle
8-6-6-1 Tools
• Allen key 2.5 mm.
• LOCTITE® 243™
• Forged Steel Ring Pliers
FRU Part # Refer to Table 9-14.
8-6-6-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
3.) Remove the following covers: RS Probe cover, Lower Front eTower cover, Left Side eTower cover,
Right Side eTower cover, Riser Thermal Cover and Upper Front eTower Cover.
5.) Loosen and remove four screws securing the riser cover to the riser.
4.) Remove the masking tape holding the pressure pin; ensure the pin is not dropped
5.) Install the riser cover and secure with four screws.
6.) Install scanner arm.
7.) Refit the following covers: Lower Front eTower cover, Left Side eTower cover, Right Side eTower
cover, Riser Thermal Cover, Upper Front eTower Cover and RS Probe cover.
NOTE: Make sure to install each type in its correct location.See Figure 8-81.
8-6-7-1 Tools
• Allen key 6mm
• LOCTITE® 243™
FRU Part # Refer to Table 9-16.
8-6-7-3 Preparations
Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
Make sure the system is standing securely on a level surface, with the wheels in the locked position.
Note: When installing the swivel lock wheel, lock the swivel before installing it to determine the
installation direction.
2) Push the wheel shaft all the way up into the socket, then gently lower the chassis to the ground.
3.) Apply LOCTITE® 243™ on the Allen screw.
4.) Return and fasten the Allen screw, making sure the screw is tightened sufficiently to secure the
wheel on the chassis. Do not over-tighten the screw!
NOTE: When installing wheels, make sure you install the correct type of the wheel. The wheels position is
crossover.
8-6-8-1 Tools
Appropriate Phillips screwdriver
8-6-8-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe cover, Lower Front eTower, Left side eTower, Right Side
eTower, Riser Thermal Cover
• Gently pull down the Plastic Cable Guide for CFE and disconnect the cable connector:
6.) Loosen and remove the two screws securing the cable guide to CFE board and remove it.
8-6-9-1 Tools
Appropriate Phillips screwdriver
8-6-9-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
4.) Disconnect MPB to BIB Control Cable from the fan cable connector.
MPB to BIB
Control Cable
5.) Loosen the elastic spring slings that hold the fan and carefully remove the MPB fan.
Elastic
spring sling
3.) Reconnect the MPB to BIB Control Cable to the fan cable connector.
5.) Install the following covers: Lower Front eTower, Left side eTower, Right Side eTower and RS
Probe cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
6.) Install all accessories.
8-6-10-1 Tools
Appropriate open-end wrench
Multimeter
Nose pliers
8-6-10-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe cover, Lower Front eTower, Left side eTower, Right Side
eTower, and MPB Front Metal Door
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Front Metal Door Removal Procedure
3.) Remove the MPB Power Door.
7.) Remove the three screws that hold the IPP metal frame.
8.) Using the nose pliers (or flat head screwdriver) squeeze the white plastic connector holders and
push them out to remove the power connector.
Connector holder
Connector holder
Ground cable
8.) Refit the following covers: MPB Front Metal Door, Left side eTower, Right Side eTower, Lower Front
eTower, and RS Probe cover.
• MPB Front Metal Door Installation Procedure
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
9.) Install all accessories.
Section 8-7
Cables - Replacement Procedures
8-7-1 MPB Rear USB Cable Replacement Procedure
8-7-1-1 Tools
Appropriate Phillips screwdriver.
8-7-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
4.) Remove the battery packs to gain access to the MPB module.
6.) Unscrew the two mounting screws and remove the MPB module.
7.) Place the MPB module on a flat surface and disconnect the MPB Rear USB Cable connector to the
MPB J12 Connector.
Figure 8-91 Disconnecting MPB Rear USB Cable - To MPB J12 Connector
8.) Using Phillips screwdriver, disconnect the two screws that hold the cable connector to the rear
panel and remove the cable.
Figure 8-92 Disconnecting MPB Rear USB Cable - To Rear Panel Connector
7.) Refit the following covers: Lower Front eTower, left side eTower, Right side eTower and RS Probe
cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
8.) Install all accessories.
8-7-2-1 Tools
• Appropriate Phillips screwdriver
• Flat-head screwdriver
8-7-2-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, Right Side eTower, and Riser
Thermal covers,,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Door Cover Removal Procedure
• Riser Thermal Cover Removal Procedure
4.) For systems with rear cockpit cable cover installed, perform the following steps:
a.) Disconnect the Wi-Fi adapter.
b.) Release the four Phillips screws and remove the rear cable cover.
Figure 8-94 MPB TO COCKPIT Cable and Cockpit Ground Cables Removal
6.) Gently pull out the MPB to Cockpit cable from the axis tilt.
7.) Release the MPB to Cockpit cable from the arm:
a.) Carefully raise the arm to its up position
b.) Remove the arm base cover
c.) Using Phillips screwdriver, remove the two securing screws of the arm side cover.
d.) Slide the right-side arm side cover upwards and remove it.
8.) Cut the tie wraps securing the MPB TO COCKPIT cable to the arm right side, and release the cable
from the arm.
9.) Route the cable and its connector downwards through the arm hole.
10.)Release plastic clips that hold the cable using a flat screwdriver:
• Three clips in the Front End
• Two clips between the connectors and the MPB receptacle side.
11.)Disconnect J1 and J2 connectors by sliding the connectors upwards from the MPB receptacle side.
12.)Gently slide the MPB TO COCKPIT cable upwards, ensuring not to pull and cause damage to the
other cables.
13.)) Open cable cover door:
- Open the captive screw of the cable cover door using a Phillips screwdriver.
- Slide the cable cover door towards you, to free the cable
- Slide the cable connectors upwards and gently route them- one after the other - through the
door, with the rubber grommet.
2.) Route the MPB to Cockpit cable through the articulated arm, so that the length of the exposed cable
toward the cockpit is minimum 44 cm. Do not use tie wraps to secure cable in place.
44 cm
3.) Remove the lower and then the upper cockpit covers.
4.) Apply moderate force and route the MPB to Cockpit cable through the tilt axis, keeping the routed
cable on the most left, and the connector facing to the right. Make sure it is routed above the tilt
release cable wire.
Connector facing
to the right
Figure 8-105 Routing the MPB to Cockpit Cable through Tilt Axis
5.) Reattach ferrite to the MPB to Cockpit cable, approximately 3 cm below the cable connector.
3 cm
6.) Connect the MPB to Cockpit cable to the cockpit, and fasten the flat screws.
Figure 8-108 Routing the MPB to Cockpit Cable under the Pin
9.) Refit the cockpit upper and then the lower covers.
10.)Route the MPB to Cockpit cable through the cable cover door and the arm hole.
14.)Gently slide the MPB TO COCKPIT cable through the MPB receptacle side, towards the front.
15.)Reconnect J1 and J2 connectors ensuring the connectors' arrow is pointing upwards.
22.)Refit the following covers: Riser Thermal, Left Side eTower, Right Side eTower, Lower Front
eTower, and RS Probe cover.
• Riser Thermal Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
23.)Install the rear cockpit cable cover if exists.
24.)Connect the Wi-Fi dongle if exists.
• Wi-Fi Adapter Installation Procedure (For Systems with No Existing Wi-Fi Adapter)
8-7-3-1 Tools
• Appropriate Phillips screwdriver
• Flat screwdriver
• 2.5 mm Allen key.
FRU Part # Refer to Table 9-23.
8-7-3-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe, Lower Front eTower, Left side eTower, Right Side eTower,
Riser Thermal, and MPB Door cover,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Riser Thermal Cover Removal Procedure
• MPB Front Metal Door Removal Procedure
3.) Disconnect the BE TO COCKPIT CABLE from the monitor:
• Disconnect the cable connector (use flat-head screwdriver)
• Release Ground cable (use Phillips screwdriver).
Figure 8-115 Cockpit (Monitor) Cable and Cockpit Ground Cables Removal
Chapter 8 - Replacement Procedures 8-123
P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
4.) For systems with rear cockpit cable cover installed, perform the following steps:
a.) Disconnect the Wi-Fi adapter.
b.) Release the four Phillips screws and remove the rear cable cover.
c.) Gently pull out the BE to Cockpit cable from the axis tilt.
5.) Release the BE to Cockpit cable from the arm:
a.) Carefully raise the arm to its up position.
b.) Remove the arm base cover.
c.) Using Allen key, remove the two securing screws of the arm side cover.
d.) Slide the left-side arm side cover upwards and remove it.
6.) Cut the tie wraps securing the BE to cockpit cable to the arm left side, and release the cable from
the arm.
7.) Route the cable and its connector downwards through the arm hole.
8.) Release the plastic clips that hold the cable using a flat screwdriver:
• Three in the front end
• One between the connectors and the MPB receptacle side.
9.) Disconnect the Cockpit to BEP split cable connected to BE module (green USB connector and black
display port connector).
35 cm
2.) Remove the lower and then the upper cockpit covers.
3.) Route the BE to Cockpit cable trough cockpit tilt axis. For easier routing, make sure the cable is
aligned to the left.
7.) Route the BE TO COCKPIT cable through the cable cover door and the arm hole.
9.) Gently slide the BE TO COCKPIT cable through the MPB receptacle side, towards the front.
10.)Reconnect the Cockpit to BEP split cable connected to BE module (green and black). Ensure the
cables are connected to the correct locations (see cable diagram below).
• Wi-Fi Adapter Installation Procedure (For Systems with No Existing Wi-Fi Adapter)
8-7-4-1 Tools
• Appropriate Phillips screwdriver
• Flat screwdriver.
FRU Part # Refer to Table 9-23.
8-7-4-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
a.) On each side of each connector, use a flat screwdriver to push one of the plastic flaps towards
the hole, and then push the other flap through the hole to release the connector.
b.) From the front side, release both cable edges, by pulling the rubber towards you.
8-7-5-1 Tools
Appropriate Phillips screwdriver
Flat screwdriver.
8-7-5-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe cover, Lower Front eTower, Side Covers, MPB Power Door
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Door Cover Removal Procedure
4.) Disconnect the two lower cable connectors J4, J5 by sliding them upwards (see J-connectors map
that follows).
5.) Release the cable from the two plastic cable clips.
5.) Refit the following covers: MPB Door Cover, Left and Right Side eTower Covers, Lower Front
eTower Cover, and RS Probe cover
• MPB Door Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
8-7-6-1 Tools
Flat screwdriver.
8-7-6-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
3.) Remove the battery packs to gain access to the MPB module.
4.) Unscrew the two mounting screws and remove the MPB module.
5.) Place the MPB module on a flat surface and disconnect the following cable connectors:
• Disconnect the ON/OFF Switch cable connector from the MPB J10 connector.
• Disconnect the ON/OFF Switch cable connector with the ON/OFF switch from the MPB module
by pressing the securing clips on both sides of the connector.
Securing clips
Figure 8-142 ON/OFF Switch Cable with ON/OFF Switch - Connection to MPB Module
5.) Refit the following covers: Lower Front eTower, left side eTower, Right side eTower and RS Probe
cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
8-7-7-1 Tools
Appropriate Phillips screwdriver.
8-7-7-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower.
4.) Disconnect one side of the PCIe cable from the BIB board and the other side from the BE module.
5.) Remove the PCIe cable.
3.) Refit the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
4.) Install all accessories.
8-7-8-1 Tools
Appropriate Phillips screwdriver.
8-7-8-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower.
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
6.) Disconnect MPB to BIB Control Cable from the fan cable connector.
MPB to BIB
Control Cable -
Fan Connector
Figure 8-146 Releasing MPB to BIB Control Cable from Plastic Clips
8.) Slide up and disconnect the other side of the MPB to BIB Control Cable from the J6 connector.
J6 Connector
6.) Install the following covers: Lower Front eTower, Left side eTower, Right Side eTower and RS
Probe cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
7.) Install all accessories.
8-7-9-1 Tools
Appropriate Phillips screwdriver
8-7-9-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
4.) Loosen the Phillips screw and remove the Peripheral Cable Cover.
5.) Disconnect the printer cable (yellow USB connector) from the Back End assembly.
NOTE: Make sure the Peripheral Cable Cover is properly aligned and affixed.
5.) Refit the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
• Upper eTower Front Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
6.) Install all accessories.
8-7-10-1 Tools
• Appropriate Phillips screwdriver
• Flat-head screwdriver
• Socket Wrench
8-7-10-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Remove the following covers: Lower Front eTower, Left side eTower, and Right Side eTower,
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• MPB Front Metal Door Removal Procedure
4.) Remove omega bracket: release 5 screws connecting the omega bracket:
• Display port
Note: If the MiTx to BIB cable is preventing easy removal of the PCB, disconnect the MiTx to BIB
cable connector latch (see yellow circle in the above figure).
• MiTx to BIB cable: release one connector on the BIB and pull upwards two connectors on the
BEP PCB
2.) Route the cables on the BEP bottom bracket as shown below
3.) Reconnect the PCB using four screws in the PCB corners using Phillips screwdriver
• Display port
7.) Reconnect omega bracket: attach 5 screws connecting the omega bracket
10.)Refit the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
• Upper eTower Front Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
8-7-11-1 Tools
• Appropriate Phillips screwdriver
• Flat-head screwdriver
8-7-11-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
4.) Disconnect the two lower cable connectors by sliding them upwards
5.) The cable is released.
6.) Install the following covers: Lower Front eTower, Left side eTower, Right Side eTower and RS
Probe cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
8-7-12-1 Tools
• Appropriate Phillips screwdriver
• Flat-head screwdriver
8-7-12-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Release the cable from the plastic cable clips using a screwdriver
3.) Release the cable from the upper plastic cable clips
• Disconnect the printer cable (yellow USB connector) from the Back End assembly.
6.) Install the following covers: Lower Front eTower, Left side eTower, Right Side eTower and RS
Probe cover.
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
7.) Install all accessories.
Section 8-8
Peripherals Replacement/Installation Procedures
8-8-1 Printer Replacement/Installation Procedure
8-8-1-1 Tools
Appropriate Phillips screwdriver
8-8-1-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
NOTE: Perform these steps only for Venue™ systems with printer already installed on them. For
systems with no previously installed printer, skip this section and proceed to section Printer
Installation Procedure (For Systems with No Existing Printer)
2.) Remove the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
2.) Install the Printer Frame Cover and secure with two Phillips screws.
..
Printer Frame Cover
Phillips screws
..
Metal bracket
5.) Unclip the white plastic cable holder and release the two printer cables: Printer Power Cable and
Printer USB Cable
..
Unclip cable holder
6.) Attach bracket to the Printer and tighten the four Phillips screws (the bracket and the screws are
supplied with the printer kit).
..
7.) Insert the Printer Power Cable and Printer USB cable through the dedicated opening.
..
8.) Connect the Printer USB Cable and Printer Power Cables to the Printer.
..
9.) Attach the Printer to the eTower and secure with two bottom screws.
10.)Attach the metal cable cover and secure the Phillips screw.
..
12.)Refit the following covers: RS Probe Cover, Lower Front eTower, Left side eTower, Right Side
eTower, Upper eTower Front Cover.
• Upper eTower Front Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Right Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
13.)Install all accessories.
8-8-2-1 Tools
Appropriate Phillips screwdriver
8-8-2-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
NOTE: Perform these steps only for Venue™ systems with Wi-Fi adapter already installed on them.
For systems with no previously installed Wi-Fi adapter skip this section and proceed to section
Wi-Fi Adapter Installation Procedure (For Systems with No Existing Wi-Fi Adapter)
1.) On the back of the cockpit, release four screws and remove the transparent Wi-Fi dongle cover.
2.) Disconnect the Wi-Fi dongle.
8-8-2-5 Wi-Fi Adapter Installation Procedure (For Systems with No Existing Wi-Fi Adapter)
1.) Attach the L-shape USB adapter to the Wi-Fi dongle.
NOTE: Perform this step only for Venue™ systems with no previously installed Wi-Fi adapter. For
systems with existing Wi-Fi adapter, skip this step and proceed to Step 2.
2.) Connect the L-shape USB adapter to the back of the Cockpit.
3.) Attach the transparent Wi-Fi dongle cover and secure with four screws.
2.) Wait for a few minutes for the system to accept the Barcode.
3.) Restart the system
Note: The barcode device is detected by the system as a COM Port under windows device manager:.
8-8-3-1 Tools
Appropriate Phillips screwdriver
8-8-3-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2.) Replace the printer insert cover with the one provided in the ECG installation kit.
3.) Attach ECG Bracket to printer bracket with 2 screws and 2 washers (verify correct orientation).
4.) Using two Thumb screws, install the bracket on the eTower.
5.) Connect the ECG USB cable to the USB 2.0 port on the BEP above the Green connector.
6.) Route the ECG USB cable through the dedicated opening in the eTower.
8.) Fold the excessive cable and use the cable clips to hold it.
9.) Attach the metal bracket to close the cable opening.
10.)Route the USB cable as shown below and connect the ECG USB cable to the ECG.
11.)Mount the ECG module and tighten the screw to fix the ECG module in place.
12.)Install the following covers: MPB Front Metal Door, Upper Front eTower, Lower Front eTower with
cutout for ECG.
8-8-4-1 Tools
Appropriate Phillips screwdriver
8-8-4-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
3.) Unscrew the two thumbscrews holding the printer bracket and remove the printer with the bracket.
5.) Attach the ECG bracket to the printer bracket with 2 screws and 2 washers (verify correct
orientation).
7.) Connect ECG USB cable to the USB 2.0 port on the BEP on top of the green connector.
8.) Route the USB cable through the dedicated opening in the eTower and affix it along with the printer
USB cable.
10.)Connect the USB cable and power cable to the printer and the USB cable to the ECG module.
11.).Using two Thumb screws, install the bracket on the eTower.
13.)Fold the excessive cable and use the cable clips to hold it.
14.)Install the following covers: MPB Front Metal Door, Upper Front eTower, Lower Front eTower with
cutout for ECG.
• MPB Front Metal Door Installation Procedure
• Lower Front eTower Cover Installation Procedure
• Upper eTower Front Cover Installation Procedure
8-8-5-1 Tools
Appropriate Phillips screwdriver
8-8-5-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
8-8-6-1 Tools
N/A
8-8-6-3 Preparations
1.) Lock all cart casters.
8-8-7-1 Tools
N/A
8-8-7-3 Preparations
1.) Shut down the Venue™ ultrasound unit, as described in Power Shutdown.
2.) Make sure the On/Off power switch is set to Off.
3.) Make sure the system is standing securely on a level surface, with the wheels in the locked position.
2) Remove the following covers: RS Probe Cover, Lower Front eTower cover, Right Side eTower
Cover and Left Side eTower Cover:.
• RS Probe Cover Removal Procedure
• Lower Front eTower Cover Removal Procedure
• Right Side eTower Cover Removal Procedure
• Left Side eTower Cover Removal Procedure
4.) Disconnect the WIFI and BT dongles from the cable and then disconnect the stickers connecting
Figure 8-207 Disconnect BT/WIFI dongles and release the cable from the tower
5.) Pull the cable out through the printer door cover.
NOTE: Reaching the connector may be easier by removing the BE unit. If needed - remove the BE
module; Remove the cable from the yellow connector, and then return the BE module to the cart
6.) Refit the following covers: Lower Front eTower cover, Right Side eTower Cover and the Left Side
eTower Cover and RS Probe Cover.
• Right Side eTower Cover Installation Procedure
• Left Side eTower Cover Installation Procedure
• Lower Front eTower Cover Installation Procedure
• RS Probe Cover Installation Procedure
7.) Install all accessories.
Section 8-9
Operating System and Application Software Loading Procedures
8-9-1 Software Update Procedure
NOTE: Images in this procedure are for reference only. There may be differences or variations, in accordance
with different software versions.
4.) Select Update Venue SW to install software without affecting user data.
7.) Click Reboot Venue Scanner. Wait until the INFORMATION dialog box appears:
8.) Disconnect the SW installation media and tap OK in the message box.
Chapter 8 - Replacement Procedures 8-190
P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
9.) In the Confirmation dialog box that appears, tap Yes to continue the reboot.:
1.) On your PC, insert the Disk-on-Key media into any available USB port.
2.) Browse to the folder that contains the files downloaded from GE HealthCare portal.
3.) Run the RevertFlashDisk.cmd command.
NOTE: If the Windows Protected Your PC window pops up, click More Info and then click Run Anyway.
4.) Wait until the formatting is complete. The process may take about 3 minutes.
NOTE: Images in this procedure are for reference only. There may be differences or variations, in accordance
with different software versions.
NOTICE IMPORTANT Before starting the upgrade procedure, make sure you received a new Activation String
in the upgrade kit.
4.) Connect USB memstick to any available USB port in the system.
5.) From the side menu, select Admin and then Backup.
3.) Select the Select All checkbox to select all patients for backup.
5.) In the Copy window, select USB Storage and click OK.
NOTICE IMPORTANT Make sure the selected option is USB Storage and not DICOM USB.
The selected data is copied. The backup process is indicated on the progress bar that appears.
NOTICE IMPORTANT Venue R2/R3 user presets are not compatible with R5 software. The backed up presets
can only be used if reverting back to previous software version. Do not try to import these presets to R5
software.
8.) Disconnect the SW installation media and tap OK in the message box.
9.) In the Confirmation dialog box that appears, tap Yes to continue the reboot.:
NOTE: Due to FPGAs programming as part of the initialization process, it might take up to 15 minutes before
the Local tab is displayed.
Note: In case of firmware update errors, the following messages may appear :
18.)Verify that an e-label is displayed in Config screen under the About tab as shown below:
Note: For every upgrade performed a new eLabel shall appear under the Config about tab
19.)Scan the UDI label that is attached to the installation media. Refer to Figure 8-238 as reference
only. always use the actual label.
Figure 8-238 Example of UDI label attached to Software installation media Label
The complete installation procedure can be performed using the Touch Screen only. An on-screen
(virtual) keyboard is available whenever text input is required. I
WARNING DO NOT ATTEMPT TO INSTALL SOFTWARE THAT WAS NOT DESIGNATED FOR YOUR
VENUE™ UNIT. ATTEMPTING TO INSTALL UN-APPROVED SOFTWARE WILL CAUSE
IRREVERSIBLE DAMAGE TO HARDWARE AND SOFTWARE!
NOTICE IMPORTANT Since neither the System Serial Number or the Computer Name can be changed after the
software installation procedure is completed, it is important to make sure that when prompted, the
correct information is inserted during the installation procedure.
When installing the Windows operating system software, after replacement of the SSD module, it is
necessary to format the hard disk.
Be aware that this will perform a full format of the Hard Disk and all patient data will be lost.
Normally, the Venue™ system is supplied with the software already installed. In some cases, it is
necessary to re-install the software.
NOTE: After performing a software installation, all logs are deleted. It is recommended that these
should be recorded should they be needed in the future.
NOTICE IMPORTANT Before performing any Venue™ software installation procedure, it is mandatory to
backup the Archive.
If you are upgrading the system software from a previous version, it is necessary to contact your local
OTR department to receive an appropriate software password. Make sure you specify the system serial
number located on the Venue™ unit.
NOTE: Make sure that the required Software Option keys are available prior to commencing the installation
process. Do not use the Software Option keys from a previous system version.
CAUTION THIS PROCESS FORMATS THE HARD DRIVE (WHEN SELECTION OF THIS OPTION IS
APPLICABLE) - MAKE SURE TO SAVE ALL THE REQUIRED PRESETS, SETTINGS AND
PATIENT DATA!
WARNING REMOVE ALL EXTERNAL DEVICES SUCH AS PRINTERS AND USB CONNECTIONS
BEFORE STARTING THE UPGRADE PROCEDURE.
At the site, perform the following steps before you start the upgrade procedure:
1.) Perform Disk Management for all database records and select the "Copy" option
(for instructions, refer to the Venue™ User Manual on your Document Media).
NOTE: It is recommended that Disk Management be executed using the "move" option to a network
repository.
Chapter 8 - Replacement Procedures 8-204
P R E L I M I N A R Y
DIRECTION DOC2782487, REVISION 2 VENUE™ SERVICE MANUAL
2.) Perform a full back-up for Patient Archive and System Configuration
(for instructions, refer to the Venue™ User Manual on your Document Media).
3.) Write down the following settings as it will be necessary to restore them at the end of the process:
- TCP/IP address
- Network printer (if present)
- Wireless network settings (if present)
- InSite ExC settings
4.) When done, continue to Table 8-13.
NOTE: A minimum of 1 hour is required to install both the Windows operating system and the Venue™
application software. This excludes preparation time, backup etc. and performing functional checks
following the installation procedures.
Throughout the installation processes, the Venue™ system will be unavailable for scanning.
Section Section 8-9 on page 8-189 provides step-by-step instructions for installation of Windows
operating system software and Venue™ ultrasound scanner software application.
It is necessary to perform the recommended Functionality Checks after completion of the installation
procedures
4.) For new installation (after SSD replacement), tap Format SSD and Install.
If patient information is stored on the SSD, perform one of the following:
Select Update Venue SW to install software without affecting user data.
7.) Select Exit and Reboot. Wait until the INFORMATION dialog box appears:
8.) Disconnect the SW installation media and tap OK in the message box.
9.) In the Confirmation dialog box that appears, tap Yes to continue the reboot.:
The software recovery procedure allows the user to reload the operating system and the application
(Drive C:\ partition) without affecting any user information or PHI data.
This procedure can be initiated from the configuration screen under the Service tab.
1.) Boot the system into the application screen and open the Config menu.
2.) Open the Service tab.
4.) A pop up window will be displayed, notifying the user about the next steps..
8.) The system will reboot automatically and the Venue SW reload window will be displayed.
9.) Select Reload Venue SW. The software reload process will start.
10.)Once the process is complete, The Venue SW reload window will be displayed again.
11.)Select Reboot Venue Scanner.
12.)The system will reboot.
Section 8-10
Functional Checks to be Performed after Replacement Procedures
8-10-1 General Overview
Table 8-13 below lists the Functional Checks to be performed after each Replacement Procedure.
For easy reference, these are grouped in accordance with the various categories of Venue™
replacement parts.
Cables MPB Rear USB Cable Replacement • Perform 7-2-1 -System Diagnostics
Procedure • Select Full System Diagnostics without JIG.
Chapter 9
Renewal Parts
Section 9-1
Overview
9-1-1 Purpose of Chapter 9
NOTE: This chapter gives you an overview of replacement parts for the Venue™ ultrasound scanner. In the
detailed Parts lists, illustrations are accompanied by FRU names, corresponding Part Numbers and a
compatibility matrix.
This Repl Proc icon indicates refer to the instructions in Chapter 8 - Replacement Procedures.
NOTE: The illustrations provided in this chapter are for illustration purposes only and are subject to change
without notice.
Section 9-2
List of Abbreviations
• Assy - Assembly
• T-BEP - Back End Processor
• T-CFE Control Front End
• CRU Customer-replaceable Unit
• Ctrl - Control
• T-FEPS Front End Power Supply
• LCD - Liquid Crystal Display
• Int - Internal
• I/O - Input/Output
• T-PSB Probe Selection Board
• TS - Touch Screen
Section 9-3
Main Assemblies and Sub Assemblies
eTower
Covers
Back End
Accessories
Optional Peripherals
Section 9-4
Renewal Parts Lists and Diagrams
9-4-1 Mechanical Hardware Parts
102
101
103
105
107 108
106
109
115
9-4-2 Covers
206 207
208
209
211 213
210
215
219 218
212
217
216
214
305 307
306
308 309
310
311
312
401
9-4-5 eTower
505
503 Module: T-FEPS Front End Power Supply - FRU S5721459P S5721459 RP
S5730757-
504 Venue T-CFE2 - FRU S5730757-2P S5730759 RP
2
S5730759-
505 Venue T-CFE2 FAN BOX - FRU S5730759-2P S5730757 RP
2
602
605
604
Can Be Not
Can Replace Repl
Item Part Name Part Number Replaced Compatible
Part # Proc
by Part # With
512GB SSD MODULE FRU Venue S5728760-4 S5728760-3
601 S5851010 RP
Venue 1TB SSD - FRU S5851010-1
To be obtained
606 BIOS Battery (CR 2032)- FRU
locally
709
9-4-6 Probes
Can Be Not
Can Replace
Part Name Part Number Picture Replaced by Compatible
Part #
Part # With
Probe: 8C - RS 5499508
Can Be Not
Can Replace
Part Name Part Number Picture Replaced by Compatible
Part #
Part # With
Probe: C1 - 5 - RS 5499608
Probe:ML6-15-RS 5499610
Probe:L10-22-RS 5459953
Probe:L4-20t-RS 5843289
Probe:L12n - RS 5505771
Can Be Not
Can Replace
Part Name Part Number Picture Replaced by Compatible
Part #
Part # With
5770783
NOTE: Wireless
Probe: C2-9-RS probe is supported
for APU Back End
only (will not work
on CPU Back End)
9-4-7 Software
901
9-4-9 Accessories
1201
1202 1203
1204
1205
1206
1207
1208
1209
1210
not
supported
Zebra USB Bar code Reader - CRU for software
1208 S5932297
Note: supported from R4.1 software and higher. versions
lower
than R4.1
Chapter 10
Care and Maintenance
Section 10-1
Overview
10-1-1 Care and Maintenance Inspections
It has been determined by engineering that your Venue™ System does not have any high wear
components that fail with use, therefore no Care and Maintenance inspections are mandatory.
However, some customers’ Quality Assurance Programs may require additional tasks and or
inspections at a different frequency than listed in this manual.
Read this chapter completely and familiarize yourself with the procedures before performing a task.
Section 10-2
Warnings
DANGER THERE ARE SEVERAL PLACES INSIDE THE CAGE, THE BATTERY,
THE AC DISTRIBUTION BOX, AND THE DISTRIBUTION INTERFACE
BOARD (DIB) THAT COULD BE DANGEROUS. BE SURE TO
DISCONNECT THE SYSTEM POWER PLUG AND TO TURN OFF THE
POWER ON/OFF SWITCH BEFORE YOU REMOVE ANY PARTS.
PROCEED WITH CAUTION WHENEVER POWER IS ON AND COVERS
ARE REMOVED.
CAUTION PRACTICE GOOD ESD PREVENTION. WEAR AN ANTI-STATIC STRAP WHEN HANDLING
ELECTRONIC PARTS AND WHEN DISCONNECTING/CONNECTING CABLES.
CAUTION DO NOT OPERATE THIS ULTRASOUND SYSTEM UNLESS ALL BOARD COVERS AND FRAME
PANELS ARE SECURELY IN PLACE. SYSTEM PERFORMANCE AND COOLING REQUIRE THIS.
Section 10-3
Why Do Maintenance?
10-3-1 Keeping Records
It is good business practice that ultrasound facilities maintain records of all corrective maintenance and
periodic maintenance on Ultrasound systems where it is applicable. The Ultrasound Equipment Quality
Check form provides the customer with documentation that the Ultrasound system is maintained on a
periodic basis.
A copy of the Ultrasound Equipment Quality Check form should be kept in the same room as the
Venue™ ultrasound scanner, or nearby.
Routine Quality Control testing of the system must be conducted regularly. The same tests are
performed during each period so that changes can be monitored over time and effective corrective
action can be taken.
Testing results, corrective action, and the effects of corrective action, must be documented and
maintained on site.
Your GE HealthCare Service Representative can help you with establishing, performing and
maintaining records for a Quality Assurance program. Contact GE HealthCare for coverage and/or price
for service.
The Customer Care & Maintenance Task Schedule (provided in Table 10-2 on page 10-4) specifies how
often the Venue™ ultrasound scanner should be serviced, and outlines items requiring special
attention.
NOTE: It is the customer’s responsibility to ensure the Care and Maintenance procedures are performed on the
Venue™ ultrasound scanner as scheduled in order to retain the high levels of safety, dependability, and
system performance.
Your GE HealthCare Service Representative has an in-depth knowledge of your Venue™ ultrasound
scanning system and can best provide competent, efficient service. Contact GE HealthCare for
coverage information and/or price for service.
The service procedures and recommended intervals shown in the Customer Care & Maintenance Task
Schedule assumes that you use your Venue™ scanner for an average patient load (10-12 patients per
day) and that you do not use it as a primary mobile Ultrasound system which is transported between
diagnostic facilities.
NOTE: If conditions exist which exceed typical usage and patient load, it is strongly recommended to increase
the care and maintenance frequencies.
Please refer to the Customer Care Schedule in the service manual for the Ultrasound System unit for
the correct maintenance care schedule.
Per
Facility’s
Service at Indicated Time Daily Weekly Monthly QA Program Notes
Section 10-4
Tools Required
10-4-1 Tools Required for Servicing the Venue™
The following tools (TORX bits or drivers) are needed to service the ultrasound scanner. .
2. Bit # TX-15 M3
5. Bit # TX-30 M6
Socket Set
7.
(must include 7mm socket)
Section 10-5
System Maintenance
10-5-1 Preliminary Checks
The preliminary checks take approximately 15 minutes to perform. Refer to the Venue™ User Manual
whenever necessary.
2. Paperwork Fill in the top of the EQC inspection form. Record all probes and Ultrasound system options.
• Turn the Ultrasound system power ON and verify that all fans and peripherals turn On.
• Watch the displays during power up to verify that no warning or error messages are
3. Power-up displayed.
• Where applicable, confirm that the battery is charged. If no AC Input present, use the
internal battery.
4. Probes Verify that the Ultrasound system properly recognizes all probes.
6. Review Error Logs Where applicable, Error Logs can be reviewed via system diagnostics.
The functional checks take approximately 60 minutes to perform. Refer to the Venue™ User Manual
whenever necessary.
Verify the basic operation of all optional modes such as Contrast. Check the basic
6 Applicable Software Options
Ultrasound system controls that affect each option’s operation.
2 B/W Printer Verify hardcopy output of the B/W video page printer. Clean heads and covers if necessary.
3 DICOM Verify that DICOM is functioning properly. Send an image to a DICOM device.
Inspect the cable weekly for cuts and abrasions, to verify it is intact
Ensure the cable paths are away from foot traffic (i.e.: cable is not positioned in the passage
2 Inspect nor underneath system casters).
Verify the cable along a wall if possible, to avoid stepping on the cable, that will lead to the
squishing and wear of the cable.
Verify that the LINE, NEUTRAL and GROUND wires are properly attached to the terminals,
3 Verify
and that no strands may cause a short circuit.
2 Scratches & Dents Inspect the exterior for dents, scratches or cracks.
Where applicable, verify all covers are secured in place and are properly aligned with other covers.
3 Covers
Replace any covers that are damaged.
• Where applicable, check all wheels and casters for wear and verify operation of foot brake, to stop
6 Wheels and Brakes the Ultrasound system from moving, and release mechanism.
• Where applicable, check all wheel locks and wheel swiveling for proper operation.
Check all internal cable harnesses and connectors for wear and secure connector seating. Pay
11 Cables and Connectors
special attention to probe strain or bend reliefs.
Check to ensure that all EMI shielding, internal covers, air flow panels and screws are in place.
12 Shielding and Covers
Missing covers and hardware could cause EMI/RFI problems while scanning.
13 Probe Holders Where applicable, inspect the Probe Holders for cracks or damage.
Where applicable, check that the battery is not damaged, does not leak, does not emit an odor, and
15 Battery is not deformed or discolored. Observe all warnings and cautions for battery handling, recharging,
storing, and/or disposal.
10-5-4 Cleaning
• Use only cleaning materials and solutions as recommended in the procedures described in the
Venue™ User Manual.
• Do not use any solutions or products not listed in the Venue™ User Manual.
• Never use thinner, benzene, ethanol or methanol alcohol, abrasive cleaners, or other strong
solvents. Only use isopropyl alcohol, when instructed to do so.
• Do not spray any liquid directly onto the Venue™ covers.
• Do not allow any liquid to drip or seep into the system.
• DO NOT scratch or press on the panel with any sharp objects, such as pencils or pens, as this may
result in damage to the panel.
• Make sure not to spill or spray any liquid on the controls, into the Venue™ cabinet, or in the probe
connection receptacle.
• Prior to cleaning, turn OFF power to the Venue™ and disconnect the mains cable.
The screen turns black, allowing you to use a soft cloth with glass cleaning solution to clean the
panel.
2.) Using your finger swipe the arrows >>> from left to right to return to normal operation.
CAUTION TO HELP PROTECT YOURSELF FROM BLOOD-BORNE DISEASES WHEN CLEANING AND
HANDLING PROBES, WEAR APPROVED, NON-ALLERGIC DISPOSABLE GLOVES. THESE ARE
MADE OF NITRILE DERIVED FROM VEGETABLE STARCH TO PREVENT ALLERGIC LATEX
REACTIONS.
WARNING DISINFECT A DEFECTIVE PROBE BEFORE YOU RETURN IT. BE SURE TO TAG THE
PROBE AS BEING DISINFECTED.
NOTE: GE HealthCare does not substantiate the effectiveness of recommended disinfectant products.
Questions regarding efficacy, instructions for use, and proper handling should be directed to the
disinfectant manufacturer. GE HealthCare publishes a list of material-compatible disinfectants (see
below and also refer to the GE HealthCare website at http://www3.gehealthcare.com/en/Products/
Categories/Ultrasound/Ultrasound Probes. DO NOT use non-GE HealthCare-approved disinfectants or
products that have not been evaluated by GE HealthCare for material compatibility. Damages linked to
the use of disapproved chemicals are not covered under product warranty or service contract.).
Thoroughly check the Ultrasound system probe connectors and remove dust from inside the
2 Probes
connector sockets if necessary. Visually check for bent, damaged or missing pins.
3 Probes Verify that the Ultrasound system properly recognizes all probes.
• Do not use a cracked or damaged probe. Any evidence of wear indicates the probe must not be
used. Call your field service representative immediately for a replacement.
• Perform a visual check of the probe pins and system sockets before plugging in a probe
• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the
electrical safety of the probe.
• To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled
with, or to be caught in the wheels of the system.
• Protect the probe when moving the unit.
• Use a soft cloth and warm, soapy water to clean the probe.
Note: For detailed information on handling Endocavity probes, refer to the appropriate supplementary
instructions for each probe.
NOTE: The most recent, up-to-date information on probes and probe care is available at:
http://www.gehealthcare.com/usen/ultrasound/products/probe_care.html
WARNING ANY EVIDENCE OF WEAR ON A PROBE INDICATES THAT IT MUST NOT BE USED.
IMPROPER HANDLING MAY EASILY DAMAGE ULTRASOUND PROBES.
SEE THE Venue™ USER MANUAL AND ALSO REFER TO THE PROBE
MANUFACTURER’S HANDLING INSTRUCTIONS, FOR MORE DETAILS.
Always perform a visual check of the probe pins and system sockets before plugging in a probe.
When handling probes, always observe the precautions listed in Probe Handling .
The Interoperative probes often have special usage considerations; always refer to the individual probe
manufacturers’ handling instructions/user manual.
NOTE: For details on general probe cleaning, refer to the information provided in the Venue™ User Manual.
NOTE: For specific probe cleaning instructions, refer to the individual probe Users Manual (or care card
supplied with the probe).
CAUTION TO HELP PROTECT YOURSELF FROM BLOOD-BORNE DISEASES WHEN CLEANING AND
HANDLING PROBES, WEAR APPROVED, NON-ALLERGIC DISPOSABLE GLOVES.
CAUTION TO HELP PROTECT YOURSELF FROM BLOOD-BORNE DISEASES WHEN CLEANING AND
HANDLING PROBES, WEAR APPROVED, NON-ALLERGIC DISPOSABLE GLOVES.
Equipment being returned must be properly clean and free of blood and other potentially infectious
contaminants.
GE HealthCare policy states that body fluids must be properly removed from any part or equipment prior
to shipment. GE HealthCare employees, as well as customers, are responsible for ensuring that parts/
equipment have been properly decontaminated prior to shipment. Under no circumstances should a
part or equipment be shipped before being visibly clean and properly disinfected.
The purpose of the regulation is to protect employees in the transportation industry, as well as the
persons who will receive and/or open the package.
NOTE: The US Department of Transportation (DOT) has ruled that “items that were saturated and/or dripping
with human blood that are now caked with dried blood; or which were used or intended for use in patient
care” are “regulated medical waste” for transportation purposes and must be transported as a
hazardous material.
Section 10-6
Electrical Safety Tests
10-6-1 Overview
The following topics and measurements are covered in this subsection:
• Uninterrupted Power Supply (UPS)
• Safety Test Overview
• Outlet Test - Wiring Arrangement - USA and Canada
• Grounding Continuity
CAUTION Please observe that some Uninterruptible Power Supplies (UPS) may not be medical
devices! If the UPS is not a medical device, it has to be located outside of the patient
environment (according to IEC 60601-1 / UL 60601-1).
DANGER TO AVOID ELECTRICAL SHOCK, THE ULTRASOUND SYSTEM UNDER TEST MUST NOT
BE CONNECTED TO OTHER ELECTRICAL EQUIPMENT. REMOVE ALL
INTERCONNECTING CABLES AND WIRES. THE ULTRASOUND SYSTEM UNDER TEST
MUST NOT BE CONTACTED BY USERS OR PATIENTS WHILE PERFORMING THESE
TESTS.
These tests may refer to specific safety analyzer equipment as an example. Always refer to the safety
analyzer’s user manual that will be used to perform the tests.
Prior to initiating any electrical test, the Ultrasound system must be visually inspected. Perform the
following visual checks:
• Check for missing or loose enclosure covers that could allow access to internal live parts.
• Examine the mains cord, mains plug and appliance inlet for damaged insulation and adequacy of
strain relief and cable clamps.
• Locate and examine all associated transducers. Inspect the cables and strain relief at each end.
Inspect the transducer enclosure and lens for cracks, holes and similar defects.
WARNING Users must ensure that safety inspections are performed whenever damage is suspected
and on a regular basis in accordance with local authorities and facility procedures.
DO NOT use the Venue™ or individual probes which fail any portion of the safety test.
WARNING To minimize risk of electric shock, only trained persons are allowed to perform the electrical
safety inspections and tests.
CAUTION Compare all safety-test results with safety-test results of previously performed safety tests
(e.g. last year etc). In case of unexplainable abrupt changes of safety-test results consult
experienced authorized service personnel or GE HealthCare for further analysis.
CAUTION To avoid electrical shock, the Ultrasound system under test MUST NOT be connected to
other electrical equipment.
Remove all interconnecting cables and wires. The Ultrasound system under test must not be
contacted by users or patients while performing these tests.
NOTE: No outlet tester can detect the condition where the Neutral (grounded supply) conductor and the
Grounding (protective earth) conductor are reversed. If later tests indicate high leakage currents, this
should be suspected as a possible cause and the outlet wiring should be visually inspected.
Measure the resistance from the third pin of the attachment plug to the exposed metal parts of the case.
The ground wire resistance should be less than 0.2 ohms. Reference the procedure in the IEC60601-1.
1. GROUND PIN
2. OHMMETER
3. Venue™
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• REAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT
GE Medical Systems
Ultrasound & Primary Care Diagnostics LLC
3200 N Grandview Blvd
Wauwatosa, WI 53188
USA
www.gehealthcare.com