GE HEALTHCARE

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Chapter 1
Introduction

Section 1-1
Overview
1-1-1 Purpose of this chapter
This chapter describes important issues related to safely servicing LOGIQ E9. The service provider
must read and understand all the information presented here before installing or servicing a unit.

Chapter 1 Introduction 1-1

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-2
Service manual overview
Attention

This manual contains necessary and sufficient information for the Field Service Engineer or Biotech
Engineer to maintain and service the system safely. Advanced equipment training may be provided by
factory trained Field Service trainers for the agreed-upon time period.

This service manual provides installation and service information for the LOGIQ E9 ultrasound scanning
unit. It is divided in 10 chapters as shown below, in Table 1-1 "Contents in this service manual" on page
1-3.

Indications for Use

The LOGIQ E9 is intended for use by a qualified physician for ultrasound evaluation. Specific clinical
applications and exam types include:

• Fetal/Obstetrics
• Abdominal (includes renal, GYN/Pelvic)
• Pediatric
• Small Organ (breast, testes, thyroid)
• Neonatal Cephalic
• Adult Cephalic
• Cardiac (adult and pediatric)
• Peripheral Vascular
• Musculo-skeletal Conventional and Superficial
• Urology (including prostate)
• Transrectal
• Transvaginal
• Transesophageal
• Intraoperative (abdominal, thoracic, vascular and neurosurgical)

Contraindication

The LOGIQ E9 ultrasound system is not intended for ophthalmic use or any use causing the acoustic
beam to pass through the eye.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-1 Contents in this service manual

The service manual is divided into ten chapters.

In the beginning of the manual, before chapter 1, you will find the language policy for GE Healthcare’s
service documentation, legal information, a revision overview, and the Table of Contents (TOC).

An Index has been included after chapter 10.

Table 1-1 Contents in this service manual

CHAPTER
NUMBER CHAPTER TITLE DESCRIPTION
1 Introduction Contains a content summary and warnings.

2 Site preparations Contains pre-setup requirements for the LOGIQ E9.

3 System Setup Contains setup procedure with procedure checklist.

4 Functional Checks Contains functional checks that must be performed as part of the
installation, or as required during servicing and periodic
maintenance.

5 Components and Functions (Theory) Contains block diagrams and functional explanations of the
electronics.

6 Service Adjustments Contains instructions on how to make any available adjustments to

the LOGIQ E9.

7 Diagnostics/Troubleshooting Provides procedures for running diagnostic or related routines for the
LOGIQ E9.

8 Replacement procedures Provides disassembly procedures and reassembly procedures for all
changeable FRUs, available option installation instructions, and
upgrade installation instructions.

9 Renewal Parts Contains a complete list of replacement parts for the LOGIQ E9.

10 Care & Maintenance Provides periodic maintenance procedures for LOGIQ E9.

N/A Index A quick way to the topic you’re looking for.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-2 Typical users of the “Basic” Service Manual

• Service Personnel (setup, maintenance, etc.)
• Hospital’s Service Personnel
• Architectural Planners/Installation Planners (some parts of Chapter 2 - Site preparations)

1-2-3 LOGIQ E9 models covered by this manual

Table 1-2 LOGIQ E9 Software Configurations and Hardware/Software Compatibility -

Upgrade Options

CONSOLE
MODEL
NUMBER DESCRIPTION SOFTWARE VERSION
Phase I BT2010 BT2011 BT2013
1.0.3 1.0.4 1.0.5 1.0.6 2.0.3 2.0.4 2.0.5 3.1.0 3.1.1 3.1.2 4 Rev. x.x
5205000 LOGIQ E9, 100-240 VAC Y Y Y Y U U U U U U U
5205000-2 LOGIQ E9, 220-240 VAC Y Y Y Y U U U U U U U
5205000-3 LOGIQ E9, 100-240 VAC N N N N Y Y Y U U U U
5205000-4 LOGIQ E9, 220-240 VAC N N N N Y Y Y U U U U
5205000-5 LOGIQ E9, 100-240 VAC N N N N N N N N Y Y U
5205000-6 LOGIQ E9, 220-240 VAC N N N N N N N N Y Y U
5205000-7 LOGIQ E9, 100-240 VAC N N N N N N N N N N Y

LOGIQ E9 Software Configurations and Hardware/Software Compatibility - Upgrade Options

LOGIQ E9 Software Configurations and Hardware/Software

Compatibility - Upgrade Options
Y Original
U Upgrade available
N Not supported

Front End Processor - see: 9-12-2 "Front End Boards Compatible Configurations" on page 9-48.

Back End Processor - see: 9-13-1 "Back End Boards Compatible Configurations" on page 9-59.

NOTE: When not otherwise specified, the contents of this manual applies to all LOGIQ E9 models.

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GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-4 Product description

Chapter 1 Introduction 1-5

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-4-1 Overview of the LOGIQ E9 ultrasound scanner

The LOGIQ E9 ultrasound unit is a high performance digital ultrasound imaging system with total data
management.

The system provides image generation in B-Mode, Color Doppler, Power Doppler, M-Mode,
Color M-Mode, PW and 4D, Tissue Velocity imaging, Volume-Guided Ultrasound and Contrast
applications. The fully digital architecture of the LOGIQ E9 unit 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 monitor and peripherals.

System configuration is stored on the hard drive in the Back End Processor.

All necessary software is loaded from the hard drive on power up.

1-2-4-2 Purpose of the operator manual(s)

The operator manuals should be fully read and understood before operating the LOGIQ E9.

The online versions of the operator manuals are available via the Help function on LOGIQ E9’s operator
panel.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-3
Important conventions
1-3-1 Conventions used in book

1-3-1-1 Model designations

This manual covers the LOGIQ E9 scanners listed in 1-2-3 "LOGIQ E9 models covered by this manual"
on page 1-4.

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.

1-3-1-3 Safety precaution messages

Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identified by a flag word that precedes the precautionary
message. Known or potential hazards to personnel are labeled in one of three ways:

• DANGER
• WARNING
• CAUTION
When a hazard is present that can cause property damage, but has absolutely no personal injury risk,
a NOTICE is used.

DANGER DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL

CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE
IGNORED.
WARNING WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE
SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE
IGNORED.

CAUTION CAUTION IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL OR CAN CAUSE
MINOR PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
EQUIPMENT DAMAGE POSSIBLE.

NOTICE Notice is used when a hazard is present that can cause property damage but has absolutely no
personal injury risk.

Notice Example: Disk drive may crash.

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.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-2 Standard hazard icons

Important information will always be preceded by the exclamation point contained within a triangle,
as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be
used to make you aware of specific types of hazards that could possibly cause harm. Even if a symbol
isn’t used in this manual, it may be included for your reference.

Table 1-3 Standard hazard icons

DANGER WARNING CAUTION

BIOLOGICAL ELECTRICAL MOVING

ACOUSTIC OUTPUT EXPLOSION SMOKE / FIRE

LASER HEAT PINCH

LASER
LIGHT
or

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-2 Standard hazard icons (cont’d)

Table 1-4 Standard hazard icons (cont’d)

RADIATION “ “
“ “

Other icons make you aware of specific procedures that should be followed.

Table 1-5 Standard Icons that indicate that a special procedure is to be used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG
&
LOCKOUT

Signed Date

OR

HAND PROTECTION FOOT PROTECTION “

“

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-3 Product icons

The following table describes the purpose and location of safety labels and other important information
provided on the equipment.

Table 1-6 Product icons 1 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Identification and Rating Plate

Manufacturer’s name and address Rear panel

Identification and Rating Plate

Date of manufacture Rating Plate

Serial Number Rating Plate

Catalog Number Rating Plate

Type/Class Label Used to indicate the degree of safety or

protection.

United States only Rear panel

Prescription Requirement label

Authorized European Representative

Rear panel
address

Equipment Type BF (man in the box

symbol) IEC 878-02-03 indicates B Probe connectors including Doppler
Type equipment having a floating probe connector
applied part.

Equipment Type BF Applied Part (man

in the box with paddle) symbol is in Probe
accordance with IEC 60417-5334.

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Table 1-6 Product icons (Continued) 2 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Equipment Type CF (heart in the box

symbol) IEC 878-02-05 indicates Probe connectors and ECG connector.
equipment having a floating applied part On newer systems also on the rear of
having a degree of protection suitable the system.
for direct cardiac contact.

DEFIBRILLATOR-PROOF TYPE CF At the ECG connector on front of

EQUIPMENT. system.

Laboratory logo or labels denoting

Device Listing/Certification Labels conformance with industry safety Rear of console
standards such as UL or IEC.

This precaution is intended to prevent

injury that may result if one person
attempt to move the unit considerable Rear cover label
distances or on an incline due to the
weight of the unit.

DO NOT push the system. Use the

handle to push/pull the system, e.g., DO Rear of LCD Monitor
NOT use the LCD. Failure to do so may Rear of On-Board V Nav Stand
cause serious injury or system damage.

Follow Instructions for Use.

“ATTENTION” - Consult accompanying Rear Cover,
documents is intended to alert the user
Rear of LCD Monitor,
to refer to the operator manual or other Miscellaneous Probe Labels
instructions when complete information
cannot be provided on the label.

Follow Instructions for Use.

“ATTENTION” - Consult accompanying
documents is intended to alert the user Rear of particular Main Power Supply
to refer to the operator manual or other
instructions when complete information
cannot be provided on the label.

The system is not designed for use with

“DANGER - Risk of explosion used in...” Rear cover console
flammable anesthetic gases.

The system is not designed for use with

Rear of console
flammable anesthetic gases.

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Table 1-6 Product icons (Continued) 3 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

C-UL Mark Parts

Indicates that the product has been Rear of LCD Monitor (inside)
tested and approved in UL Laboratories, Footswitch
based on UL and CSA standards,
through mutual approval activities.

This unit carries the CE mark.

The LOGIQ E9 unit complies with
regulatory requirements of the
European Directive 93/ 42/EEC
concerning medical devices. Rear of console
It also complies with emission limits for
a Group 1, Class B Medical Device as
stated in EN 60601-1-2
(IEC 60601-1-2).

“CAUTION” The equilateral triangle is

usually used in combination with other Various
symbols to advise or warn the user.

“ATTENTION - Consult
accompanying documents”
is intended to alert the user to refer to Various,
the operator manual or other Rear Cover,
instructions when complete information
Probe Label
cannot be provided on the label.

General Warning

“Warning - Dangerous Voltage”

(the lightning flash with arrowhead in Various
equilateral triangle) is used to indicate
electric shock hazards.

“Mains OFF” Rear of system adjacent to

Indicates the power off position of the
MAINS Switch
mains power switch.

“PINCH POINT”
Indicates moving parts that may cause Various
injury (such as LCD arm or XYZ Mech)

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Table 1-6 Product icons (Continued) 4 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

“Mains ON”
Indicates the Power ON position of the
mains power switch.
“ON” Indicates the power on position of
the power switch.
CAUTION Rear of console
THE ON/OFF BUTTON ON
THE OPERATOR PANEL
DOES NOT ISOLATE MAINS
SUPPLY

ON/OFF button
CAUTION
SYSTEM SHUTDOWN USING
THE ON/OFF BUTTON DOES
or NOT DISCONNECT LOGIQ E9
Operating Panel
FROM MAINS VOLTAGE.
For disconnecting LOGIQ E9 from
mains voltage after system shutdown,
please set the circuit breaker close to
the mains inlet to OFF as described in
4-2-4 "Power shut down" on page 4-7.

“Protective Earth”
Indicates the protective earth Used several places inside the system.
(grounding) terminal.

“Equipotential”
Indicates the terminal to be used for
connecting equipotential conductors Rear of console
when interconnecting (grounding) with
other equipment as described in
IEC60601-1.

Rear Panel, Rating Plate, Circuit

Alternating Current symbol is in breaker label of console and Front
accordance with IEC 60878-01-14.
Panel (if applicable).

This symbol indicates that waste

electrical and electronic equipment
must not be disposed of as unsorted
municipal waste and must be collected Rear of console
separately. Please contact an Rear of LCD Monitor (inside)
authorized representative of the
manufacturer for information concerning
the decommissioning of your
equipment.

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Table 1-6 Product icons (Continued) 5 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

This product consists of devices that

may contain mercury, which must be
recycled or disposed of in accordance Rear Panel
or with local, state, or country laws. (Within Rear of LCD Monitor (inside)
this system, the backlight lamps in the
monitor display, contain mercury.)

ETL Listing Mark Monogram Rear Panel

GOST Symbol. Russia Regulatory Rear Panel

Country Clearance.

ISO 7010 - P007 V Nav Transmitter

Volume Navigation Pacemaker Warning

Indicates the presence of hazardous

substance(s) above the maximum
concentration value. Maximum
concentration values for electronic
information products, as set by the
People’s Republic of China Electronic
Industry Standard SJ/T11364-2006,
include the hazardous substances of
lead, mercury, hexavalent chromium, Probe
cadmium, polybrominated biphenyl
(PBB), and polybrominated diphenyl
ether (PBDE). “10” indicates the number
of years during which the hazardous
substance(s) will not leak or mutate so
that the use of this product will not result
in any severe environmental pollution,
bodily injury, or damage to any assets.

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Table 1-6 Product icons (Continued) 6 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Indicates the presence of hazardous

substance(s) above the maximum
concentration value. Maximum
concentration values for electronic
information products, as set by the
People’s Republic of China Electronic
Industry Standard SJ/T11364-2006,
include the hazardous substances of
lead, mercury, hexavalent chromium, China Rating Plate
cadmium, polybrominated biphenyl
(PBB), and polybrominated diphenyl
ether (PBDE). “20” indicates the number
of years during which the hazardous
substance(s) will not leak or mutate so
that the use of this product will not result
in any severe environmental pollution,
bodily injury, or damage to any assets.

How to lower LCD prior to transport Rear of the LCD monitor.

How to lock Operator Panel prior to Rear of the LCD monitor.

transport

DO NOT place a finger, hand or any

object on the joint of the monitor or
monitor arm to avoid injury when moving
the monitor and monitor arm.

Non-ionizing Electromagnetic Radiation Rear Panel

Label

Chapter 1 Introduction 1 - 15
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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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.

1-4-2 Human safety

• Operating personnel must not remove the system covers.
• Servicing should be performed by authorized personnel only.
Only personnel who have participated in a LOGIQ E9 Training Seminar are authorized to service the
equipment.

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN

THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

WARNING IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ E9, SOME METAL
SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF
TOUCHED, EVEN WHILE IN SHUTDOWN MODE.

WARNING BECAUSE OF THE LIMITED ACCESS TO CABINETS AND EQUIPMENT IN THE FIELD,
PLACING PEOPLE IN AWKWARD POSITIONS, GE 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 EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT
CONSTITUTES A DEFINITE SAFETY HAZARD.

WARNING Do Not Substitute Parts or Modify Equipment

Because of the danger of introducing additional hazards, do not install substitute
parts or perform any unauthorized modification of the equipment.

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1-4-2 Human safety (cont’d)

WARNING When the top console is in its locked position, the gas shock is compressed and
stores mechanical energy. During normal operation the top console, the weight of
the monitor and the mechanical force of the gas shock are in balance. Take care if/
when you activate this gas shock. Personal injury can occur after the panel is
removed and the shock pressure is released. Take care when you repair the
elevation assembly.

WARNING Ensure that the system is turned off and unplugged.

Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation.
The Amber light on the Op Panel On/Off button will turn off.
Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be
energized even if the power is turned off when the cord is still plugged into the AC Outlet

WARNING Risk of electrical shock, system must be turned off and disconnected from power
source. Cord must be controlled at all times. Wait for at least 20 seconds for capacitors to
discharge as there are no test points to verify isolation. The Amber light on the Op Panel On/Off
button will turn off.
Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be
energized even if the power is turned off when the cord is still plugged into the AC Outlet

WARNING Use extreme caution as long as THE LOGIQ E9 is un-stable, not resting on all four
Casters.

WARNING Tilting the console requires two people in order to avoid injury to service personnel
and damage to the equipment.

WARNING Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety
glasses, and kneeling pad, to reduce the risk of injury.

WARNING Beware of possible sharp edges on all mechanical parts. If sharp edges are
encountered, the appropriate PPE should be used to reduce the risk of injury.

WARNING Wear all PPE including gloves as indicated in the chemical MSDS.

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1-4-3 Mechanical safety

WARNING While the software install procedure is designed to preserve data, you should save any
patient data, images, system setups to a DVD or hardcopy before doing a software
upgrade.

WARNING PRIOR TO ELEVATING THE SCANNER, VERIFY THAT THE KEYBOARD 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.

WARNING WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE
EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.

WARNING 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.

WARNING REMEMBER: If the front caster swivel lock is engaged for transportation, pressing the
release pedal once disengages the swivel lock. You must depress the release pedal a
second time to engage the brake.

WARNING The system should NOT be moved with the Operator I/O Panel extended. Move the
Operator I/O Panel to its centered and locked position. Lower the Operator I/O Panel as
much as possible before moving the system.

CAUTION BEFORE YOU MOVE OR TRANSPORT THE SYSTEM, MAKE SURE TO LOCK THE LCD
MONITOR ARM FIRMLY AND FLIP DOWN THE MONITOR TO PREVENT DAMAGE TO THE
SYSTEM.

CAUTION Always lock the Top/Upper Console in its parking (locked) position before moving the scanner
around.

CAUTION TO AVOID INJURY WHEN YOU MOVE THE LCD MONITOR AND THE MONITOR ARM, DO NOT
PUT YOUR FINGER, HAND, OR OBJECT ON THE JOINT OF THE MONITOR OR THE MONITOR
ARM.

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1-4-3 Mechanical safety (cont’d)

CAUTION LOGIQ E9 WEIGHS 135 KG (298 LB), R3.X AND EARLIER, 140 KG (309 LB), R4.X AND
LATER, OR MORE, DEPENDING ON 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. ALWAYS:
- BE SURE THE PATHWAY IS CLEAR.
- USE SLOW, CAREFUL MOTIONS.
- USE TWO PEOPLE WHEN MOVING ON INCLINES OR LIFTING MORE THAN
16 KG (35 LBS).

CAUTION TO AVOID INJURY OR DAMAGE TO THE MONITOR, MAKE SURE THERE IS NOTHING WITHIN
RANGE OF THE LCD BEFORE MOVING THE MONITOR AND MONITOR ARM. THIS INCLUDES
PEOPLE AS WELL AS THINGS.

CAUTION Ensure that nobody touches the console arm/frogleg when moving the Operator Panel.

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.

CAUTION Use Protective Gloves when drilling and cutting.

NOTICE Be careful not to pinch any of the cables.

NOTE: Special care should be taken when transporting the unit in a vehicle, see 4-2-14-4 "Transporting
the unit by vehicle" on page 4-18.

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1-4-4 Electrical safety

1-4-4-1 Safe practices

Follow these guidelines to minimize shock hazards whenever you are using the scanner:

• The equipment chassis must be connected to an electrical ground.

• The unit is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety ground. A separate power outlet with a 20 amp circuit breaker for 120
VAC for 120V area, 7.5 amp circuit breaker for 220-240 VAC for 220/240V area or 15 amp circuit
breaker for 100 VAC for Japan.
• 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.

WARNING Connecting a LOGIQ E9 scanner to the wrong voltage level will most likely destroy it.

1-4-4-2 Probes
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.
• The system has more than one type of probe port. Use the appropriate probe port designed for the
probe you are connecting.

Section 1-5
Label locations
Refer to the current revision of the LOGIQ E9 Basic User Manual, 5180374-100, Chapter 2.

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Section 1-6
Dangerous procedure warnings
Warnings, such as the example below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN

THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

WARNING IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ E9, SOME METAL
SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF
TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

WARNING EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION
OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A
DEFINITE SAFETY HAZARD.

WARNING DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT.

BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT
INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION
OF THE EQUIPMENT.

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Section 1-7
Lockout/Tagout (LOTO) requirements
Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring
you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout:

1.) Plan and prepare for shutdown.

2.) Shutdown the equipment.
3.) Isolate the equipment.
4.) Apply Lockout/Tagout Devices.
5.) Disconnect the Extended Power Shutdown battery at J3 when working in the BEP.
6.) Control all stored and residual energy.
7.) Verify isolation.
All potentially hazardous stored or residual energy is relieved.

NOTICE Energy Control and Power Lockout for LOGIQ E9

When servicing parts of the system where there is exposure to voltage greater than 30 Volts:
1. Turn off the scanner.
2. Unplug the system.
3. Maintain control of the system power plug.
TAG

LOCKOUT
& 4. Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation.
Signed Date
The Amber light on the Op Panel On/Off button will turn off.
5. Disconnect the eps battery at j3 WHEN WORKING IN THE BEP.
Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be
energized even if the power is turned off when the cord is still plugged into the AC Outlet.

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.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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 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
LOGIQ E9 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.

Applicable standards are: 47CFR Part 18, IEC60601–1–2:2001.

NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are
in good condition, 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.

1-9-3 Electrostatic discharge (ESD) prevention

WARNING DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE
NECESSARY ESD PRECAUTIONS:
1. ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD
CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE RIGHT OF
THE POWER CONNECTOR).
2. FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE
EQUIPMENT.

WARNING Risk of electrical shock, system must be turned off. Avoid all contact with electrical
contacts, conductors and components. Always use non-conductive handles designed
for the removal and replacement of ESD sensitive parts. All parts that have the potential
for storing energy must be discharged or isolated before making contact.

Chapter 1 Introduction 1 - 23
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Section 1-10
Customer assistance
1-10-1 Contact information
If this equipment does not work as indicated in this service manual or in the user manual, or if you
require additional assistance, please contact the local distributor or appropriate support resource, as
listed below.

Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer
Care team:

1.) System ID serial number.

2.) Software version.
3.) Date and time of occurrence.
4.) Sequence of events leading to issue.
5.) Is the issue repeatable?
6.) Imaging mode, probe, preset/application.
7.) Media brand, speed, capacity, type.
8.) Save secondary image capture, cine loop, 4D multi-volume loop.

NOTE: Restart the application before resuming clinical scanning.

Table 1-7 Phone numbers for Customer Assistance

LOCATION PHONE NUMBER

USA Service: On-site 1-800-437-1171

GE Healthcare - GE Medical Systems
Ultrasound & Primary Care Diagnostics, LLC Service Parts 1-800-558-2040
9900 Innovation Drive
Wauwatosa, WI 53226 Application Support 1-800-682-5327 or 1-262-524-5698

Canada 1-800-668-0732

Service 1-262-524-5300
Latin America
Application Support 1-262-524-5698

Europe
Phone: +33 (0) 130-831-300 (General Imaging and Cardiac)
GE Ultraschall Deutschland Gmbh & Co. KG
+49 (0) 212-2802-652
Beethovenstrasse 239
Postfach 11 05 60, D-42655 Solingen
Fax: +49 (0) 2122-8024-31
Germany

Asia (Singapore)
GE Ultrasound Asia
Tel: +65 6291-8528
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Fax: +65 6291-7006
Central Placa
Singapore 168730

Phone: 81-426-48-2940
Japan Support Center
Fax: 81-426-48-2905

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1-10-2 System manufacturer

Table 1-8 System manufacturer

MANUFACTURER FAX NUMBER

GE Healthcare - GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC

9900 Innovation Drive
414-721-3865
Wauwatosa, WI 53226
USA

Table 1-9 Authorized Representative

AUTHORIZED REPRESENTATIVE TELEPHONE / FAX NUMBER

The location of the CE marking is shown in the Safety chapter of this manual.

+49 761 45 43 -0 /
+49 761 45 43 -233

Authorized EU Representative European registered place of business:

GE Medical Systems Information Technologies GmbH(GEMS IT GmbH)
Munzinger Strasse 3, D-79111 Freiburg, GERMANY

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Chapter 2
Site preparations

Section 2-1
Overview
2-1-1 Purpose of this chapter
This chapter provides the information required to plan and prepare for the setup of a LOGIQ E9.
Included are descriptions of the facility and electrical needs to be met by the purchaser of the LOGIQ E9.

Chapter 2 Site preparations 2-1

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 2-2
General console requirements
2-2-1 Console environmental requirements

2-2-1-1 If the LOGIQ E9 is very cold or hot

When unpacking the device, allow the temperature of the device to stabilize before powering up. The
following table describes guidelines for reaching operational temperatures from storage or transport
temperatures. See: Table 2-1’

Table 2-1 LOGIQ E9 Acclimate Time

oC 60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
o 140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40
F
Hrs 8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20

2-2-1-2 Environmental specifications

Table 2-2 Environmental Specifications for LOGIQ E9 Scanners

Operational Storage Transport (< 16 hrs.)

10º - 35º C -10º - 50º C -10º - 50º C
Temperature
(50º - 96º F) (-14º - 122º F) (-14º - 122º F)
30% - 80% 30% - 80% 30% - 80%
Humidity
non-condensing non-condensing non-condensing
Pressure 70 - 106 kPa 70 - 106 kPa 70 - 106 kPa

Heat Dissipation 4712 Btu/hour “ “

2-2-1-3 Cooling
The cooling requirement for the LOGIQ E9 scanner with LCD and onboard peripherals, is up to 4712
Btu/hr. This figure does not include cooling needed for lights, people, or other equipment in the room.
Each person in the room places an additional 300 Btu/hr demand on the cooling system.

2-2-1-4 Lighting
Bright light is needed for LOGIQ E9 installation, updates and repairs. However, operator and patient
comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting
system (dim/bright) is recommended. Keep in mind that lighting controls and dimmers can be a source
of EMI which could degrade image quality. These controls should be selected to minimize possible
interference.

2-2 Section 2-2 - General console requirements

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-2 Electrical requirements

2-2-2-1 General requirements

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 LOGIQ E9.

The LOGIQ E9 will function on Voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt
power, 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 LOGIQ E9 outlet.

Sites with a mains power system without a defined Neutral:

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 LOGIQ E9 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.

2-2-2-2 Electrical requirements for LOGIQ E9

In the table below, the electrical specifications for LOGIQ E9 include LCD and on board peripherals.

Table 2-3 Electrical specifications for the LOGIQ E9

POWER
PART NUMBER DESCRIPTION VOLTAGE TOLERANCES CONSUMPTION FREQUENCY
5205000-x LOGIQ E9, 100-240 VAC 100-240 VAC +/-10% 1100 W 50/60 Hz

The current drain varies, depending on the mains voltage.

• At 230 VAC, the current may be up to 7.5 A.

• At 100 VAC, the current may be up to 12 A.

2-2-2-3 Inrush current

During power on, an inrush circuit prevents the current from increasing above the stated values.

Table 2-4 Inrush current at different mains voltages

VOLTAGE 50 Hz 60 Hz
90 VAC 13 A 12 A
110 VAC 9A 11 A

220 VAC 5.5 A 6A

264 VAC 6A 5A

Chapter 2 Site preparations 2-3

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-2-4 Site circuit breaker

CAUTION POWER OUTAGE MAY OCCUR.

THE LOGIQ E9 SCANNER 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 LOGIQ E9 be readily accessible.

2-2-2-5 Site power outlets

A dedicated AC power outlet must be within reach of the LOGIQ E9 without extension cords. Other
outlets adequate for the external peripherals, medical and test equipment needed to support this
LOGIQ E9 must also be present within 1 m (3.2 ft.) of the LOGIQ E9. Electrical installation must meet
all current local, state, and national electrical codes.

2-2-2-6 LOGIQ E9 power plug

If the LOGIQ E9 arrives without a power plug, or with the wrong plug, you must contact your GE dealer
or the installation engineer must supply what is locally required.

2-2-2-7 Power stability requirements

Voltage drop-out

Max 10 ms.

Power transients (all applications)

Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including
line frequency, synchronous, asynchronous, or aperiodic transients.

2-4 Section 2-2 - General console requirements

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-3 EMI limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transients in the air or wiring. Ultrasound machines also generate EMI. The LOGIQ
E9 complies with limits as stated on the EMC label. However there is no guarantee that interference will
not occur in a particular installation.

Possible EMI sources should be identified before the LOGIQ E9 is installed.

Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. These
sources include:

• medical lasers,
• scanners,
• cauterizing guns,
• computers,
• monitors,
• fans,
• gel warmers,
• microwave ovens,
• light dimmers
• portable phones.
The presence of a broadcast station or broadcast van may also cause interference.

See: Table 2-5 on page 2-5 for EMI Prevention tips.

Table 2-5 EMI prevention/abatement

EMI RULE DETAILS

Keep the LOGIQ E9 at least 5 meters or 15 feet away from other EMI sources. Special
Be aware of RF sources shielding may be required to eliminate interference problems caused by high frequency, high
powered radio or video broadcast signals.

Ground the LOGIQ E9 Poor grounding is the most likely reason a LOGIQ E9 will have noisy images. Check grounding
of the power cord and power outlet.

After you finish repairing or updating the LOGIQ E9, replace all covers and tighten all screws.
Replace all screws, RF Any cable with an external connection requires a magnet wrap at each end. Install the Card
gaskets, covers, cores Rack cover over the Card Rack. Loose or missing covers or RF gaskets allow radio
frequencies to interfere with the ultrasound signals.

Replace broken RF If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket. Do
gaskets not turn on the LOGIQ E9 until any loose metallic part is removed.

Do not place labels where Never place a label where RF gaskets meet the LOGIQ E9. Otherwise, the gap created will
RF gaskets touch metal permit RF leakage. Or, if a label has been found in such a position, move the label.

Use GE specified The interconnect cables are grounded and require ferrite beads and other shielding. Also,
harnesses and peripherals cable length, material, and routing are all important; do not change from what is specified.

Take care with cellular

phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.

Properly dress peripheral Do not allow cables to lie across the top of the Card Rack or hang out of the peripheral bays.
Loop the excess length for peripheral cables inside the peripheral bays. Attach the LCD cables
cables
to the frame.

Chapter 2 Site preparations 2-5

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-4 Probes environmental requirements

Table 2-6 Environmental Requirements - Probes

Standard Probes 4D Probes

Operation: 10o to 40o C (50 to 104 ºF) 18o to 40o C (64.4 to 104 ºF)

-10° to 60° C (14 to 140 ºF)

Storage:
-10° to 60° C (14 to 140 ºF) -10o to 50 o C (14 to 122 ºF)

Temperatures in degrees Celsius (oC) conversion to degrees F: (oF) = (oC * 9/5) + 32

NOTICE SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF
-10 TO +50 degrees C. or +60 degrees C, DEPENDING ON THE TYPE OF PROBE. WHEN
EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN
ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
Refer to the Table in section 2-2-1-1 on page 2-2 to determine the needed settlement time.

2-2-5 Time and manpower requirements

Site preparation takes time. Begin Pre-installation checks as soon as possible, if possible, six weeks
before delivery, to allow enough time to make any changes.

CAUTION HAVE TWO PEOPLE AVAILABLE TO DELIVER AND UNPACK THE LOGIQ E9.
ATTEMPTS TO MOVE THE LOGIQ E9 CONSIDERABLE DISTANCES OR ON AN INCLINE BY ONE
PERSON COULD RESULT IN INJURY OR DAMAGE OR BOTH.

2-6 Section 2-2 - General console requirements

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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.
Purchaser responsibility includes:

• Procuring the materials required.

• Completing the preparations before delivery of the LOGIQ E9.
• Paying the costs for any alterations and modifications not specifically provided in the sales contract.

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 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 LOGIQ E9 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 machine. 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 LOGIQ E9
reliability.

Chapter 2 Site preparations 2-7

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-2 Required facility needs

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 system.

The LOGIQ E9 will function on Voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt
power, 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.

Sites with a mains power system without a defined Neutral:

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.

• Dedicated single branch power outlet of adequate amperage (see: Table 2-5 on page 2-5) meeting
all local and national codes which is located less than 2.5 m (8 ft.) from the LOGIQ E9’s proposed
location
• Door opening is at least 76 cm (30 in) wide.
• Proposed location for LOGIQ E9 is at least 0.46 m (18 inches) from the wall or objects for cooling.
• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with
peripheral within 1 m (3.2 ft.) of the LOGIQ E9 to connect cables.
• Power outlets for other medical equipment and gel warmer.
• Power outlets for test equipment within 1 m (3.2 ft.) of LOGIQ E9.
• Clean and protected space to store transducers (in their cases or on a rack).
• Material to safely clean probes (done with a plastic container, never metal).

2-8 Section 2-3 - Facility needs

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-3 Desirable features

In addition to the Floor Plan Suggestions shown in Figure 2-1 and Figure 2-2, a nearby waiting room and a Receptacle for Bio–hazardous Waste,
like used probe sheaths is suggested. Grid represents 305 x 305 mm (1 x 1 foot).

2-3-4 Minimal floor plan suggestions

Figure 2-1 Floor Plan Suggestion 4.27 x 5.18 m (14 x 17 foot)

10 11 15
12

9 1

PW
X Z
CW
M CF
Elas to

Bo dy Pa ttern Zoom
El li ps e B
3D /4D

Co mmen t
Au to
L R

C lea r

16
2 3 4 5 13 14

7
1

17

18

Floor Plan Suggestion 4.27 x 5.18 m (14 x 17 foot) Key

Item Description Item Description

1. Secretaries or Doctors Desk 2. File Cabinet

3. Film Viewer 4. Counter Top

5. 6. Overhead Lights Dimmer - Dual Level Lighting (bright

Counter Top and Sink with hot and cold water
and dim)

7. Emergency Oxygen 8. Suction Line

Dedicated Power Outlet - Circuit Breaker protected and

9. LOGIQ E9 10.
easily accessible

457 mm (18 inches) distance of LOGIQ E9 from wall or

11. Network Interface 12.
objects

13. Stool 14. Footswitch

15. Storage for Linens and Equipment 16. Examination Table – 1930 x 610 mm (76 x 24 inches)

17. Lavatory and Dressing Room 18. Door – at least 762 mm (30 inches)

Chapter 2 Site preparations 2-9

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-4 Minimal floor plan suggestions (cont’d)

Figure 2-2 Floor Plan Suggestion 2.44 x 3.05 m (8 x 10 foot)

4 5
2 3

11
10
9

E las to
8

1
12

Cl ea r

Co mmen t

M
CW
X
Bo dy Pa ttern
El li pse

PW
Y
e
13

Z oom
3D /4D

CF
Z
L

B
7

R
Au to
6 14
1

Floor Plan Suggestion 2.44 x 3.05 m (8 x 10 foot) Key

Item Description Item Description

1. Door – at least 762 mm (30 inches) 2. Film Viewer

3. Counter Top, Sink with hot and cold water and Supplies 4. Linen Supply
Storage

5. Probes/Supplies 6. Examination Table – 1930 x 610 mm (76 x 24 inches)

7. Footswitch 8. Stool

9. LOGIQ E9 10. External Peripherals

11. Dedicated Power Outlet - Circuit Breaker protected and 12. Network Interface
easily accessible

13. 457 mm (18 inches) distance of LOGIQ E9 from wall or 14. GE Cabinet for Software and Manuals
objects

2 - 10 Section 2-3 - Facility needs

GE HEALTHCARE
DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-5 Networking setup requirements

2-3-5-1 Stand alone scanner (without network connection)

None.

2-3-5-2 Scanner connected to hospital’s network

Supported networks:

• 10/100/1000 Mbps Ethernet network connection

• Up to 300 Mbps WLAN (option)

2-3-5-3 InSite Requirements

Need internet access available to be able to connect to Insite ExC.

2-3-5-4 Purpose of the DICOM network function

DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote printers. As an added benefit, transferring
images in this manner frees up the on-board LCD and peripherals, enabling viewing to be done while
scanning continues. With DICOM, images can be archived, stored, and retrieved faster, easier, and at
a lower cost.

2-3-5-5 DICOM option setup requirements

To configure the LOGIQ E9 to work with other network connections, the site’s network administrator
must provide information to complete the form in Figure 2-3 "Worksheet for DICOM Network
Information" on page 2-12. Ensure that there are no spaces in any field of the form.

Entries must include:

• A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ E9.
• The IP addresses for the default gateway and other routers at the site for ROUTING
INFORMATION.
• The host name, IP address, port and AE Title for each device the site wants connected to the
LOGIQ E9 for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and the
revision of the device, is also included. This information may be useful for troubleshooting.

For connectivity setup information, refer to the current revision of the LOGIQ E9 Basic User Manual.

Chapter 2 Site preparations 2 - 11

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2-3-5-5 DICOM option setup requirements (cont’d)

Figure 2-3 Worksheet for DICOM Network Information

LOGIQ E9

Host Name IP Address . . . Local Port

AE Title Net Mask . . .

Network
Speed Default Gateway . . .

DHCP

DICOM APPLICATION

OTHER
NAME MAKE/ AE TITLE IP PORT
CONFIGURATION

Store 1 __Raw Data

. . . __Allow Multiframe
__Structured
Reporting
Compression_______

Store 2
__Raw Data
. . . __Allow Multiframe
__Structured
Reporting
Compression_______

Store 3
__Raw Data
. . . __Allow Multiframe
__Structured
Reporting
Compression_______
DICOM
Print Vendor: ___________
. . . Print Size: _________
Medium: ___________
Copies: ___________
Orientation: ________
Color ______________

Worklist . . .

Storage Associated
. . .
Commit Storage AE
_____________

DICOM . . .
MPPS

2 - 12 Section 2-3 - Facility needs