User Guide for the

DRX‑Revolution Mobile X‑ray System

Publication No. AH9168

2022-01-07
Supersedes:
2021-11-01
All rights reserved. No part of this manual may be reproduced or copied in any form by any
means—graphic, electronic, or mechanical, including photocopying, typing, or information
retrieval systems—without written permission.
Notices and Conventions

The information herein is based on the experience and knowledge relating to the
subject matter gained by Carestream Health, Inc. prior to publication. No patent license
is granted by this information. Carestream Health reserves the right to change this
information without notice, and makes no warranty, express or implied, with respect to
this information. Carestream Health shall not be liable for any loss or damage,
including consequential or special damages, even if loss or damage is caused by
Carestream Health’s negligence or fault.

Note:
Notes provide additional information, such as expanded explanations, hints, or reminders.

Important:
Important highlights critical policy information that affects how you use this manual and this
product.

CAUTION:
Caution points out a potentially hazardous situation which, if not avoided, might cause minor
or moderate injury.

Authorized European Representative

Carestream Health France SAS

207, Rue de Bercy
75012 Paris
France

CAUTION:
Federal law restricts this device to sale by or on the order of a physician.

CAUTION:
If you witness or become aware of a potential safety issue with this equipment, take the
appropriate safety measures and report this to your Carestream Service representative
immediately.

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 Notices and Conventions

About this Guide

This User Guide contains content related to safety and regulatory information,
electromagnetic compatibility (EMC), and system hardware operation. Content related
to system software operation, including making exposures, is found in the online help.
Access the online help by using the Help button on the software screens.

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Contents

Notices and Conventions

About this Guide..............................................................................................................................-iv

1 Safety and Regulatory Information

Indications for Use.......................................................................................................................... 1-1
Manufacturer’s Responsibility........................................................................................................ 1-1
Usability...........................................................................................................................................1-2
Overview......................................................................................................................................... 1-3
Safety Symbols................................................................................................................................ 1-5
Radiation and X-ray System........................................................................................................... 1-7
Safety and Health Compliance.....................................................................................................1-11
Environmental Requirements.................................................................................................1-11
Conforming Safety Standards................................................................................................ 1-11
Cautions...................................................................................................................................1-12
Safe Operation Precautions....................................................................................................1-18
Preventing Unintentional Exposures..................................................................................... 1-18
Product Safety Classification.................................................................................................. 1-18
Acoustic Noise Emission..........................................................................................................1-19
Programmable Electric Medical Systems (PEMS) Intended to be Incorporated into an
IT Network...............................................................................................................................1-19
Disposal......................................................................................................................................... 1-20

2 Technical Specifications

3 EMC Standards
US and Canada EMC Statements................................................................................................... 3-1
Additional Warnings, Instructions and Information Required by IEC 60601-1-2:2014
(EN 60601-1-2:2015)........................................................................................................................3-2
Electromagnetic Emissions/Immunity............................................................................................ 3-4
Guidance and Manufacturer’s Declaration for Electromagnetic Emissions.......................... 3-4
Guidance and Manufacturer’s Declaration for Electromagnetic Immunity.......................... 3-5
Guidance and Manufacturer’s Declaration for Radio Frequency Immunity................................3-7

4 Wireless
DRX-Revolution Wireless Systems.................................................................................................. 4-1
National Usage Restrictions........................................................................................................... 4-2

5 System Components
Component Descriptions................................................................................................................ 5-1
Cart.................................................................................................................................................. 5-7

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 Primary and Secondary Monitors...................................................................................................5-9
Crane............................................................................................................................................. 5-10
Tube Head Assembly.....................................................................................................................5-11
Movements of the Boom, Column, Turntable, and Tube Head Assembly.................................5-12
Subcomponents............................................................................................................................ 5-13
Labels.............................................................................................................................................5-17

6 Operating the System

Unusual Conditions.........................................................................................................................6-1
Drive the Cart..................................................................................................................................6-2
Dock and Undock the Boom.................................................................................................... 6-4
Start Up the Cart and Log In.......................................................................................................... 6-5
Shut Down the Cart and Log Out.................................................................................................. 6-6

7 Additional System Information

Collision Stop Feature ...................................................................................................................7-1
Extra Focal Dimensions...................................................................................................................7-2
Packaging Material and Weight.................................................................................................... 7-3

8 Maintenance Information
Cleaning Instructions...................................................................................................................... 8-1
Clean the Monitors................................................................................................................... 8-3
Clean the Plastic Components..................................................................................................8-3
System Maintenance.......................................................................................................................8-5

9 Troubleshooting

10 Product Disclosure Table

Optional Parts

Hardware-Software Interfaces
Log in with a Proximity Badge for the First Time .......................................................................... -II
Emergency Stop................................................................................................................................ -II
Screen Saver..................................................................................................................................... -III
Logging Out at a Monitor...............................................................................................................-III
Battery Indicators............................................................................................................................ -IV
Drive Mode...................................................................................................................................... -VI

Publication History

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1 Safety and Regulatory Information

• For continued safe use of this equipment, follow the instructions in this operating
manual.
• Study this manual carefully before using the equipment and keep it at hand for
quick reference.

Indications for Use

The device is designed to perform radiographic x-ray examinations on all pediatric and
adult patients, in all patient treatment areas.

Manufacturer’s Responsibility
Although this equipment incorporates protection against X-radiation other than the
useful beam, practical design does not provide complete protection. Equipment design
does not compel the operator or assistants to take the necessary precautions; nor does
it prevent the possibility of improper use (authorized or unauthorized persons
carelessly, unwisely, or unknowingly exposing themselves or others to direct or
secondary radiation). Allow only authorized, properly trained personnel to operate this
equipment.
Be certain that all individuals authorized to use the equipment are aware of the
danger of excessive exposure to X-radiation.
This equipment is sold with the understanding that the manufacturer, its agents, and
its representatives do not accept any responsibility for overexposure of patients or
personnel to X-radiation.
Furthermore, the manufacturer does not accept any responsibility for overexposure of
patients or personnel to X-radiation generated by this equipment as a result of them
not following proper operating techniques or procedures.
No responsibility is assumed for any unit that has not been serviced and maintained in
accordance with the technical service manual, or that has been modified or tampered
with in any way.

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 Safety and Regulatory Information

Usability
The design and development of a diagnostic x-ray system incorporated a usability
engineering process in accordance with the standard IEC 60601-1-6: Medical Electrical
Equipment, Part 1-6: General requirements for basic safety and essential performance—
Collateral standard: Usability.
It is not possible or practical to resolve every potential usability issue without affecting
the intended use of the system. Therefore, some precautions must be observed. These
precautions appear throughout the manual.

Important:
Warning statements and the explanation of warning symbols marked on the equipment are
provided in this document.

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 Safety and Regulatory Information

Overview
The DRX-Revolution Mobile X-ray System is a mobile imaging system that incorporates
a self contained x-ray generator, image receptor, imaging display and software for
acquiring medical diagnostic images outside a standard x-ray room. It is a mobile
diagnostic system intended to generate and control x-rays for examination of various
anatomical regions.
The system is designed for use in all locations of a hospital or clinical site, including
patient rooms, operating rooms, emergency departments, trauma bays, Intensive Care
Units (ICU), and other patient treatment areas.
Personnel operating and maintaining the system should receive training and be
familiar with all aspects of operation and maintenance. To ensure safety, read the
Safety Information section carefully before using the system and observe all Cautions,
Importants, and Notes located throughout this manual and other manuals supplied
with the equipment.
From this point forward, all references to the DRX-Revolution Mobile X-ray System will
be referred to as “the system.”
The DRX-Revolution Mobile X-ray System is designed specifically for digital radiography
(DR) with Carestream detectors.
The system also offers:
• A high-power, 32 kW generator
• A maneuverable drive system
• X-ray tube positioning in five axes of motion
• A telescoping column for better visibility while driving
• Storage for detectors and supplies
• A touchscreen user interface

Intended Audience
The audience for this guide includes technologists, radiologists, service engineers, and
quality assurance technicians.

Training
This equipment is intended for use by appropriately trained and skilled radiological
health care professionals who have received specific training on the operation and use
of this equipment.

CAUTION:
Only qualified personnel may operate the system. Operation of the equipment by persons who
have not been trained or who are unfamiliar with the functions and controls of the system may
cause serious injury to the patient, serious injury to the operator, or equipment damage.

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 Safety and Regulatory Information

CAUTION:
Only allow trained x-ray personnel to operate the system.
For training in the operation of this equipment, contact Carestream Health, Inc.

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 Safety and Regulatory Information

Safety Symbols
The following symbols may be used for marking on this equipment:

Emergency Stop button

Follow the operating instructions

Warning—dangerous voltage

Dangerous voltage

Warning—ionizing radiation

Type B applied part

Direct current

Alternating current

Collimator light
H204_0008AC

Off (disconnect from the mains)

On (power connected to the mains)

Off (only for a part of the equipment)

On (only for a part of the equipment)

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 Safety and Regulatory Information

Caution

Non-ionizing radiation

Tether cable

Ethernet connection

USB connection

Protective earth (ground)

Transport position
>5º

Pinch point

Remove before clinical use

Medical Device: Any serious incident that may occur in relation

to this device should be reported to the manufacturer and the
national competent authority.

Model Number: Indicates the model number of the product.

Unique Device Identifier: Indicates a carrier that contains unique

device identifier information.

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 Safety and Regulatory Information

Radiation and X-ray System

Safety and General Compliance Information
Occupational workers associated with x-ray work must be familiar with the
recommendations of the Center for Devices and Radiological Health (CDRH), the
National Council on Radiation Protection (NCRP), the International Commission on
Radiation Protection (ICRP), and state and local regulations.
Be sure that all personnel authorized to operate the system are familiar with the
established regulations of the authorities named above. All personnel should be
monitored to ensure compliance with recommended procedures.
Current sources of information include:
• NCRP Report 147: Structural Shielding Design for Medical Imaging Facilities
• Current recommendations of the International Committee on Radiation Protection
• State or local requirements for radiation protection
Although exposure to high levels of x-radiation may pose a health risk, system x-ray
equipment does not pose any danger when properly used. Be certain all operating
personnel are properly educated concerning the hazards of radiation. Persons
responsible for the system must understand the safety requirements and special
warnings for x-ray operation. Review this manual and the manuals for each component
in the system to become aware of all safety and operation requirements.

CAUTION:
Ensure exposure parameters are properly adjusted within safety limits.

CAUTION:
Incorrect x-ray tube and collimator position could cause the x-ray field to be misaligned with the
receptor, resulting in unacceptable images.

CAUTION:
Materials between the tube and the patient may adversely affect the resulting image.

CAUTION:
It is recommended that the operator take the x-ray exposure from a distance not less than
2.0 m (6.5 ft) from the focal spot and the x-ray beam.

CAUTION:
Maximum Symmetrical Radiation Field: Full 43 x 43 cm (17 x 17 in.) coverage with the
collimator at a 100 cm SID.

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 Safety and Regulatory Information

Maximum Permissible Dose (MPD)

Various studies on the effects of x-radiation have provided a foundation for
establishing the maximum permissible dose of x-radiation to which an occupational
worker may be exposed. The results of these studies have been used by the NCRP and
the ICRP to develop recommendations for MPD. In addition, state or local regulators
also provide mandatory occupational exposure limits with which to comply.
Occupational Exposure Limits
Whole body: 5.0 rem/year
Extremity: 50.0 rem/year
Declared pregnant occupational worker: 0.5 rem/gestation period

Radiographic Performance

kVp range: 40–150 kVp

kVp accuracy: ± (5 % + 1) kVp, measured 5 ms after the beginning of the exposure

Ripple (kVp): ±5 % p–p over the full operating range (for ripple frequency ≥10
kHz)

Risetime (10– 90 %): < 2.0 ms (typically < 1.5 ms)

mAs accuracy: ± (10 % + 0.20) mAs: > 0.5 mAs

± (10 % + 0.5 mAs: 0.1 mAs–0.5 mAs

Coefficient of linearity: 0.1 (station to station) for exposures ≥ 25.0 mA or 3.2 ms

Coefficient of reproducibility: < 0.05 for kVp and mAs parameters

Radiation Protection
Because exposure to high levels of x-radiation may pose a health risk, operators must
ensure that they use all available methods to reduce their radiation dose to a level that
is As Low As Reasonably Achievable (ALARA). This includes protection from the primary
beam as well as scattered radiation. Protection from excessive amounts of exposure is
accomplished using a combination of engineering and administrative controls.
• Portable Barriers and Lead Aprons—Portable barriers and lead aprons may be
needed to protect personnel from scattered radiation if operators need to be in
close contact with the patient. Make sure that the shielding and aprons have
sufficient lead equivalence, as determined by a qualified Health or Medical
Physicist, and are maintained properly for maximum benefit.
• Procedures—Always follow the procedures of your institution to ensure proper
protection.

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 Safety and Regulatory Information

• Training—Medical equipment should be operated by trained personnel only. Most

regulatory agencies require that medical diagnostic procedures be done only by
properly licensed individuals. Consult your state or local agencies for more
information.
• Radiation Survey—Monitor the exterior of the x-ray facility (outside the primary
protective barrier) and control room periodically to ensure that dose rates meet
design objectives for allowable radiation exposures. A qualified Health or Medical
Physicist should use only calibrated equipment for this survey.
• Personal Monitoring—Monitor occupational workers that use x-ray equipment
for x-ray exposure to ensure that established controls are functioning properly and
procedures are being followed. Typically, film badges or similar devices are used.
Film badges use x-ray sensitive film enclosed in a holder that incorporates metal
filters of varying degrees of transparency to x-ray radiation. Even though this device
only measures the radiation reaching the area of the body on which it is worn, it
provides an indication of the amount of radiation received. Film badges can also be
used as area dosimeters on the outside perimeter of the x-ray facility and control
room to verify dose rates.
Film badges are available from a number of distributors. Consult your institution’s
Radiation Safety Officer for further information.

Important:
Use a source-to-skin distance as large as possible to keep the absorbed dose as low as
reasonably achievable. The Operator Console must be located where there is audio and visual
communication between the radiographer and the patient.

CDRH Compliance
The x-ray system complies with Department of Health and Human Services radiation
performance standards per Title 21 CFR, Chapter 1, Subchapter J.

Classification in Accordance with IEC 60601-1

Type of protection against Class I equipment/Internally powered

electrical shock:

Degree of protection against Type B protection against electrical shock

electrical shock:

Degree of protection against Ordinary protection

ingress of water:

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 Safety and Regulatory Information

Mode of operation: Continuous operation with intermittent loading

Flammable anesthetics: The system is not suitable for use in the presence of
flammable anesthetics or a mixture of flammable anesthetics
with air, nitrous oxide, or oxygen concentrations above
25 % at 101.3 kPa (14.7 psi) or partial pressures above
27.5 kPa (4.0 psi).

IEC/EN 60601-1-3 Compliance

The system is manufactured with radiation protection in accordance with IEC/
EN 60601-1-3:1994.

System/Component Electrical Rating

DRX-Revolution Mobile X-ray System Voltage: 100/120/200/220–240 V (ac)

Current: 15/12/9/8 A

Frequency: 50/60 Hz

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 Safety and Regulatory Information

Safety and Health Compliance

Environmental Requirements
This equipment and all components will perform to specifications when operated in
normal use under the least favorable combination of the following temperature,
humidity, and altitude specifications.

Environment

Relative Humidity In-use: 30– Storage: 10–86 % The receiving and storage
65 % non- non-condensing areas must be dry and able to
condensing provide the proper humidity
and temperature control
Atmospheric 70–106 kPa 70–106 kPa required for the equipment.
Pressure

Temperature In-use: 18– Storage: –

30 °C (64– 10 to 66 °C
86 °F) (14 to 150 °F)

Altitude Equivalent to maximum 3,048 m

atmospheric pressure

Conforming Safety Standards

USA ANSI/AAMI ES60601–1:2005 – Medical Electrical Equipment - Part 1: General

requirements

Canada CSA C22.2 No. 60601-1 CAN/CSA:2008 – Medical electrical equipment – Part 1:
General requirements for basic safety and essential performance

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 Safety and Regulatory Information

Europe EN 60601–1:2006 – Medical electrical equipment - Part 1: General requirements for

basic safety and essential performance

EN 60601–1-3:2008 – Medical electrical equipment - Part 1-3: General requirements

for basic safety and essential performance - Collateral Standard: Radiation protection
in diagnostic X-ray equipment

EN 60601–1–6:2007 – Medical electrical equipment - Part 1-6: General requirements

for basic safety and essential performance - Collateral standard: Usability

EN 60601-2–54:2009 – Medical electrical equipment - Part 2-54: Particular

requirements for the basic safety and essential performance of X-ray equipment for
radiography and radioscopy

International IEC 60601-1:2005 – Medical electrical equipment - Part 1: General requirements for
basic safety and essential performance

IEC 60601-1-3:2008 – Medical electrical equipment - Part 1-3: General requirements

for basic safety and essential performance - Collateral Standard: Radiation protection
in diagnostic X-ray equipment

IEC 60601-1-6:2006 – Medical electrical equipment - Part 1-6: General requirements

for basic safety and essential performance - Collateral standard: Usability

IEC 60601-2-54:2009 – Medical electrical equipment - Part 2-54: Particular

requirements for the basic safety and essential performance of X-ray equipment for
radiography and radioscopy

Cautions

General
The following are general safety precautions:
• Do not remove the covers for any purpose.
• Do not defeat or bypass built-in equipment safety features.
• Observe all cautions, stated or implied, in the procedures.
• Follow all safety labels on the equipment.

CAUTION:
This device must be maintained according to the directions in the Maintenance Information
section. Failure to maintain this equipment as directed may result in injury, equipment
malfunction, or unacceptable images.

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 Safety and Regulatory Information

CAUTION:
Pinch Hazard
Be careful not to pinch your fingers when working in the following areas:
• Boom dock
• Turn table
• When rotating the tube head backward

CAUTION:
Only a qualified authorized service provider should replace electrical and mechanical
components.

CAUTION:
Excessive use of the virtual keyboard may result in repetitive strain injury.

CAUTION:
The equipment is fragile and must be handled with care.

Important:
To keep foreign matter from getting on the machine, place a cover loosely over it when not in
use. Do not cover the vent holes on the sides of the panels.

CAUTION:
Do not drive the DRX-Revolution unless you are standing directly behind it using two hands.
Failure to do so may result in loss of control, causing serious injury or equipment damage.

H239_0034

CAUTION:
Only allow trained x-ray personnel to use the operator console.

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 Safety and Regulatory Information

Electro-mechanical/Equipment

>5º

The following are mechanical safety precautions:

• Do not operate the equipment with covers or access panels removed.
• Route cables properly to eliminate hazards from tripping.
• All 4 wheels must be kept on the same flat surface to prevent tipping.

CAUTION:
Retract the boom and place in a docked position anytime the cart is driven. Do not release the
boom from a locked position on a surface that slopes more than 3 °.

CAUTION:
When using the system, do not allow the top of the column cap assembly to come in contact
with any object.

CAUTION:
Do not operate this equipment outside of its operating environment limits. Doing this may
cause the equipment to malfunction.

CAUTION:
Exposures may be made with a tethered detector, but tethered exposures are not to be made
with the system plugged into the AC mains. The system can be plugged in while making
wireless exposures only.

CAUTION:
Exercise caution when replacing the detector battery. Dropping the battery may damage it.

CAUTION:
Do not attempt any repairs if the equipment fails to operate correctly. Immediately call a person
qualified and authorized to repair the equipment.

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 Safety and Regulatory Information

CAUTION:
Do not make any modifications to this machine. Doing so may result in personal injury or
damage to the machine.

CAUTION:
The system includes no user serviceable parts. Contact Carestream Health, Inc. for service
information.

X-ray/Radiation

WARNING:
This x-ray unit may be dangerous to patient and operator unless safe exposure factors,
operating instructions and maintenance are observed.

CAUTION:
Use of controls or adjustments or performance of procedures other than those specified herein
may result in hazardous radiation exposure.

CAUTION:
The user must pay attention to possible adverse effects from materials located in the x-ray
beam.

Electrical Shock and Flammability

CAUTION:
The system is not suitable for use in the presence of flammable anesthetics or a mixture of
flammable anesthetics with air, nitrous oxide, or oxygen concentrations above 25 % at
101.3 kPa (14.7 psi) or partial pressures above 27.5 kPa (4.0 psi).

Important:
Instructions are provided to indicate the type of attachment plug that should be used to
connect to the alternate voltage.

WARNING:
To avoid risk of electric shock, this equipment must only be connected to a supply mains with
protective earth.

DANGER:
Charge the system only in a well-ventilated area.

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 Safety and Regulatory Information

WARNING:
If a thunderstorm begins, unplug the power cord to prevent electrical shock and fire due to a
lightning strike. Users can operate the cart during a thunderstorm as long as the unit is indoors,
and not plugged in.

CAUTION:
Do not place a vessel that contains water or other liquid on the system. If liquid spills into the
system, first turn off the system’s main power switch, and then unplug the power cord.

Radiation and Magnetic Field Cautions

CAUTION:
The system produces ionizing radiation. Operators must meet all international, national, state,
and local requirements and regulations.

CAUTION:
This x-ray unit may be dangerous to patients and operators unless safe exposure factors and
operating instructions are observed.

WARNING:
No operator or other personnel shall stay behind the detector during x-ray exposure.

Cleaning

CAUTION:
Do not operate the equipment when cleaning the equipment.

CAUTION:
Do not spray cleaning or disinfecting solution directly onto the equipment. Moisten a cloth with
a 70 % isopropyl alcohol solution for use on plastics and enameled metal. Apply to patient
contact areas after each contact to prevent cross contamination.

CAUTION:
Isopropyl alcohol is a flammable solvent. Read and follow instructions in the Material Safety
Data Sheet (MSDS).
Do not use isopropyl alcohol when the system is running because it is flammable. If this is a
concern, remember that batteries always retain a charge.

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 Safety and Regulatory Information

CAUTION:
Do not immerse the equipment in liquid.

Caution Regarding Small-Object Image Handling

As with all digital imaging devices, there is the potential that some structures could
appear different in the digital image from an image created with an analog device—
such as a screen-film system—or with another digital device that has smaller individual
detector elements. These structures include small-detail structures, high-contrast edge
structures, and fine-line structures with a repeating pattern. For example, the edges of
a sharp-edged object may appear to have “stair-steps” when the object edge does not
have such structure. This is an effect of digital sampling.
For small-detail objects having a size on the same order of magnitude as an individual
pixel or smaller, the apparent contrast of that object can vary based on the position
relative to the individual detector element locations. For example, the contrast of a
single spherical object the same size as a pixel would have a dramatically different
appearance if the object were imaged directly overlying a detector element (highest
contrast) or placed at the intersection of four detector elements (lowest contrast).
Objects inherently smaller than individual pixels have a lower apparent contrast
because of the digital sampling of the analog radiation intensity signal over an area
larger than the small object. In each case, a lower apparent signal-to-noise can result in
reduced visibility of such objects.

Restrictions on Use
The user must make sure that any equipment used with the system does not
compromise the system patient contact rating.
The user is also responsible for safety and EMC compliance of any non-Carestream
Health recommended, installed, or supplied accessory equipment.
The use of accessory equipment and/or hardware not complying with the equivalent
product safety and EMC requirements of this product may lead to a reduced level of
safety and/or EMC performance of the system.
Consideration relating to the choice of accessory equipment used with this product
shall include:
• Use of the accessory in the patient’s vicinity.
• Evidence that the safety certification of the accessory has been performed in
accordance with applicable coordinated harmonized product safety standards per
IEC 60601-1-1.
• Evidence that applicable emission certification of the accessory has been performed.

CAUTION:
Observe all safety precautions recommended by the accessory equipment manufacturer in the
user documentation provided with the equipment.

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 Safety and Regulatory Information

The hardware specified for use with the system has been selected, tested, and verified
by Carestream Health, Inc. to meet the intended applications. All specified hardware
meets applicable regulatory agency requirements for those countries where it is
offered for sale with respect to its intended applications. Consult the user
documentation included with the equipment for specific information relating to
product safety and EMC compliance.

Safe Operation Precautions

Personnel operating and maintaining this equipment should be familiar with all aspects
of operation and maintenance. To ensure safety, read the DRX-Revolution Safety and
Regulatory information carefully before using the system and observe all caution,
important, and note statements located throughout the manual.

Important:
For continued safe use of this equipment, follow the instructions contained in this operating
manual.

Important:
Study this manual carefully before using the equipment and keep it at hand for quick reference.
The equipment must be used only by qualified personnel and only after training in the
specific operations. It is the operator's responsibility to ensure the safety of patients,
users, other personnel, and objects by visual observation, audio communication, proper
patient positioning, and use of the protective devices.
Thoroughly check that there is no interference or possibility of collision between the
patient and other equipment.
Maintain the equipment periodically to ensure continued safe use of the equipment.
Refer to the maintenance and safety recommendations.
The equipment must be repaired only by authorized service personnel.

Related information
Operating the System
Maintenance Information

Preventing Unintentional Exposures

When a patient is selected from the Worklist and the tube head is undocked but not
yet moved away from the console, it is possible to make an exposure by pressing the
prep/expose switch. To prevent unintentional exposures, do not handle the prep/
expose switch until you position the detector and tube head and are ready to acquire
an image.

Product Safety Classification

Product classification per IEC 60601-1, Class I equipment/Internally powered.

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 Safety and Regulatory Information

Acoustic Noise Emission

The sound pressure level is less than 70 db.

Programmable Electric Medical Systems (PEMS) Intended to

be Incorporated into an IT Network

CAUTION:
It is the user’s responsibility to take the necessary steps to ensure the integrity of their
IT network when interacting with Carestream medical systems. The following risks need to be
addressed:
• Connection of the PEMS to an IT network that include other equipment, could result in
previously unidentified risks to patients, operators or third parties. The requirements in
safety standard IEC 80001-1:2010, RISKS; NOTE 3 provides guidance to the responsible
party on how to identify, analyze and evaluate these risks.
• Subsequent changes to the IT network can introduce new risks and require additional
analysis; changes include:
• Changes in the IT network configuration
• Connection of additional items to the IT network
• Disconnecting items from the IT network
• Update of equipment connected to the IT network
• Upgrade of equipment connected to the IT network

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 Safety and Regulatory Information

Disposal

CAUTION:
This product contains lead in sealed lead-acid batteries, collimator and in the counterweight.
Disposal of components that contain these materials may be regulated due to environmental
conditions. For disposal or recycling information, contact your local authorities.

In the European Union, this symbol indicates that when the last user
wishes to discard this product, it must be sent to appropriate facilities for
recovery and recycling. See http://recycle.carestreamhealth.com for
additional information on the collection and recovery programs available
for this product.

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2 Technical Specifications

Components

Component Specification

Batteries • The battery life allows for driving 2.4 km (1.5 mi.) and
120 exposures without charging.
• When fully charged, the battery bank produces
240 V (dc) nominal.
• There are a total of 20 lead-acid batteries; each battery
has 12 V and 12 Ah capacity.
• Electronics to track battery health and to recharge the
batteries are included.

Cable The large cable, that extends from the front of the cart and
hangs on the lead apron hook, powers and controls the tube
head assembly.

Cart Docked speed (assumes new batteries):

• Forward 0 to 5.8 km/h (0 to 3.6mph) +/-15%
• Reverse 0 to 2.5 km/h (0 to 1.5 mph) +/-15%
Maximum weight: 558 kg (1232 lb)

Circuit breakers (2) On the left side (facing the drive handle) is a DC voltage
circuit breaker. This breaker controls all DC voltage power to
the PC, generator, monitor displays, motion systems, and
circuit boards.
On the right side is an AC voltage circuit breaker. This breaker
controls AC voltage to the cart when plugged into an outlet.
The AC voltage is used only for the battery charging system.
This circuit breaker has no effect when the cart is not
plugged in.

Collimator Projection radiography range of 40–150 kV. Single transverse

and longitudinal cross-hairs on the output aperture. Rotates
independently of the x-ray tube ±90 °. Accessory rails for the
use of a Dose Area Product (DAP) measurement chamber and
additional filters.

AH9168 2-1 2022-01-07

 Technical Specifications

Component Specification

Collimator field light and The collimator light field provides an average luminance of
visual aids ≥200 lux at 100 cm. Refer to CFR, Title 21, Volume 8,
1020.31, (d)(2)(ii).

Column Rotates ≥ ±270 ° from docked position

Desktop computer hardware • Processor: INTEL 10th Generation Processor minimum

platform
• OS: WINDOWS 10
• Memory: 16 GB minimum
• Up to 15000* images can be saved for retransmission or
reprocessing. Images can be protected; otherwise they
are reclaimed on a FIFO (first in, first out) basis. Images
can be saved to removable media; CD or USB drive.
*Based on 500 GB Solid State Drive
• WLAN antenna (wireless access point) or LAN cable
• Computerized diagnostics

Detectors and rechargeable • Space for storing and charging a 43 x 43 cm detector or

battery storage bins a 35x43 detector in landscape mode
• Space for storing one 35x43 grid with or without a
compatible digital, flat-panel detector
• Space for storing one 25 x 30 cm detector
• Space for storing and charging two detector batteries

Note:
A bin lock for the detectors and the in-bin charging are
optional.

AH9168 2-2 2022-01-07

 Technical Specifications

Component Specification

Generator • 32 kW x-ray generator (for exposures ≤20 ms)

• kV range: 40–150 kV
• mAs range: 0.1–320.0 mAs
• mA range: 25–400 mA (not user-selectable)

X-ray tube and tube • Tube range: 40–150 kV

movements
• Anode heat capacity: 300 kHU
• Focal spots: 0.6 and 1.2 mm
• Target angle: 14 °
• Angulation range (alpha): ≥ ±180 °
• Tilt range (tau): ≥ –20 to +90 ° (where zero = tube
pointing straight down)
When the boom arm is fully extended, the x-ray tube focal
spot is 1340 mm (52.8 in) from the column center.
When the boom arm is fully compressed, the x-ray tube
focal spot is 857 mm (33.7 in) from the column center.
When the column is fully extended vertically, the x-ray
tube focal spot is 2058.0 mm (81.0 in.) above the floor.
When the column is fully compressed, the x-ray tube focal
spot is 724.0 mm (28.5 in.) above the floor, but not over the
entire range of column rotation (beta).

Figure 1: Cart specifications

1341.70 mm
(52.80 in.)

2192.81 mm
(86.33 in.)

1390.00 mm
(54.72 in.)

866.81 mm
(34.13 in.)

1260.21 mm
H253_0025 (46.91 in.)

AH9168 2-3 2022-01-07

3 EMC Standards

US and Canada EMC Statements

Changes or modifications not expressly approved by Carestream Health, Inc. could void
the user’s authority to operate this equipment.

Note:
This equipment has been tested and found to comply with the limits for a Class A digital device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable
protection against harmful interference when the equipment is operated in a commercial
environment. This equipment generates, uses, and radiates radio frequency energy. If it is not
installed and used in accordance with the instruction manual, it may cause harmful interference
to radio communications. Operation of this equipment in a residential area is likely to cause
harmful interference, in which case the user will be required to correct the interference at his
own expense.
This device complies with part 15 of the FCC Rules. Operation is subject to the
following two conditions:
1. This device may not cause interference.
2. This device must accept any interference received, including interference that may
cause undesired operation.
This device complies with Industry Canada license–exempt RSS standard(s). Operation is
subject to the following two conditions:
1. This device may not cause interference.
2. This device must accept any interference, including interference that may cause
undesired operation of the device.
Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils
radio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes:
1. L'appareil ne doit pas produire de brouillage.
2. L'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même
si le brouillage est susceptible d'en compromettre le fonctionnement.

AH9168 3-1 2022-01-07

 EMC Standards

Additional Warnings, Instructions and

Information Required by IEC 60601-1-2:2014
(EN 60601-1-2:2015)
Additional Requirements for Marking on the Outside of ME Systems - Use Only
in a Shielded Location Special Environment.
Not applicable for Carestream products.

Instructions for Use - General

The Carestream System is intended to be used in a Professional Healthcare Facility
environment except near high frequency surgical equipment or outside the RF shielded
room of a medical equipment system for magnetic resonance imaging.
Carestream Systems have the following essential performance as defined in IEC
60601-1:
• All Carestream detectors: Image Retention.
• All Carestream products containing x-ray sources:
• Accuracy of Loading Factors
• Reproducibility of Generator Output
• Image Retention

WARNING:
Use of this equipment adjacent to or stacked with other equipment should be avoided because
it could result in improper operation. If such use is necessary, this equipment and the other
equipment should be observed to verify that they are operating normally.

WARNING:
Use of accessories, transducers and cables other than those specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and result in improper operation.

WARNING:
Portable RF communications equipment (including peripherals such as antenna cables and
external antennas) should be used no closer than 30 cm (12 inches) to any part of the DRX
detectors, including cables specified by the manufacturer. Otherwise, degradation of the
performance of this equipment could result.

Technical Description
Carestream Systems are considered group 1, Class A for conducted and radiated
emissions according to CISPR 11.

AH9168 3-2 2022-01-07

 EMC Standards

Note:
The emissions characteristics of this equipment make it suitable for use in industrial areas and
hospitals. If it is used in a residential environment (for which CISPR class B is normally required)
this equipment might not offer adequate protection to radio-frequency communication
services. The user might need to take mitigation measures, such as relocating or re-orienting
the equipment.

Requirements Applicable To Equipment That Transmits/

Receives Electromagnetic Energy For Operation
Systems using Carestream detectors transmit and receive wireless communications with
the following characteristics.

Frequency (MHz) Modulation Power

2412 -2462 See below 9.51 dBm

5180-5825 See below 11.83 dBm

Modulation: BPSK, QPSK, 16QAM, 64QAM, DBPSK, DQPSK, CCK

AH9168 3-3 2022-01-07

 EMC Standards

Electromagnetic Emissions/Immunity
1. Electromagnetic Compatibility Precautions:
Medical electrical equipment requires special precautions regarding
electromagnetic compatibility (EMC). Medical equipment must be installed and put
into service according to the EMC information provided.
2. Communications Equipment:
Portable and mobile radio frequency (RF) communications equipment can affect
medical electrical equipment EMC performance.
3. Replacement of cables, or accessories, other than those specified below with the
exception of transducers or cables sold by the equipment manufacturer as
replacement parts for internal components, may result in increased emissions or
decreased immunity of the medical equipment.
4. Cable and accessory information for the system:

Port/Cable Function User Cable Length

USB 1 Blue Tooth Customer NA

2 Keyboard/Mouse/DVD Service 1m

3 Keyboard/Mouse/DVD Service 1m

Ethernet 1 Hospital Uplink Customer 3m

Ethernet 1 Tethered Detector Link Customer / 3m

Service

Prep/Expose 1 Prep/Expose/Collimator Customer 3m

Hand Switch Light Controller

AC Power 1 Retractable --- 3m

Cord

5. Shielded Locations:
The system is fully compliant with the requirements of IEC 60601-1-2: 2007 without
being used in a shielded room.

Guidance and Manufacturer’s Declaration for

Electromagnetic Emissions
Carestream Systems are intended for use in the electromagnetic environment specified
below. The customer or the user of the Carestream System should assure that it is used
in such an environment.

AH9168 3-4 2022-01-07

 EMC Standards

Emissions Test Compliance Electromagnetic Environment—Guidance

RF emissions Group 1 Carestream Systems use RF energy only for their internal
function. Therefore, RF emissions are very low and are
CISPR 11 not likely to cause any interference in nearby electronic
equipment.

RF emissions Class A Carestream Systems are suitable for use in all

establishments other than domestic and those directly
CISPR 11 connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.

Harmonics emissions Class A Carestream Systems are suitable for use everywhere,
including those establishments directly connected to the
IEC 61000-3-2 public low-voltage power supply network that supplies
buildings used for domestic purposes.

Voltage fluctuations/ flicker Complies Carestream Systems are suitable for use everywhere,
emissions including those establishments directly connected to the
public low-voltage power supply network that supplies
IEC 61000-3-3 buildings used for an isolated AC backbone.

Guidance and Manufacturer’s Declaration for

Electromagnetic Immunity

Carestream Systems are intended for use in the electromagnetic environment specified below. The
customer or the user of the System should assure that it is used in such an environment.

Immunity Test IEC 60601 Compliance Electromagnetic

Environment—Guidance
Test Level Level

Electrostatic Discharge ± 8 kV contact ± 8 kV contact Floors should be wood,

(ESD) concrete, or ceramic tile. If
± 2 kV, ± 4 kV,± 6kV ± 2 kV, ± 4 kV,± 6kV
floors are covered with
EC 61000-4-2
± 8 kV, ± 15 kV air ± 8 kV, ± 15 kV air synthetic material, the
relative humidity should be
at least 30 %.

AH9168 3-5 2022-01-07

 EMC Standards

Electrical fast transient/ ± 2 kV for power ± 2 kV for power Mains power quality should
burst supply lines supply lines be that of a typical
IEC 61000-4-4 ± 1 kV for input/ ± 1 kV for input/ commercial or hospital
output lines output lines environment.

Surge ± 1 kV line to line ± 1 kV line to line Mains power quality should

be that of a typical
IEC 61000-4-5 ± 2 kV line to earth ± 2 kV line to earth
commercial or hospital
environment.

Voltage dips, short < 5 % UT < 5 % UT Mains power quality should

interruptions, and be that of a typical
voltage variations on (> 95 % dip in UT) for (> 95 % dip in UT) for commercial or hospital
power supply lines 0.5 cycle 0.5 cycle environment.
IEC 61000-4-11 40 % UT (60 % dip in 40 % UT (60 % dip in
UT) for 5 cycles UT) for 5 cycles Note:
Most components in the
70 % UT 70 % UT Carestream System are
(30 % dip in UT) for (30 % dip in UT) for powered from an
25 cycles 25 cycles uninterruptible power
supply
< 5 % UT < 5 % UT
(> 95 % dip in UT) for (> 95 % dip in UT) for
5 sec 5 sec

Power frequency 30 A/m 30 A/m Power frequency magnetic

fields should be at levels
(50/60 Hz) magnetic
characteristic of a typical
field
location in a typical
IEC 61000-4-8 commercial or hospital
environment.

Note:
UT is the mains (ac) voltage prior to application of the test level.

AH9168 3-6 2022-01-07

 EMC Standards

Guidance and Manufacturer’s Declaration for

Radio Frequency Immunity

All Carestream products are intended for use in the electromagnetic environment specified below. The
customer or the user of the system should assure that it is used in such an environment.

IEC 60601 Maximum Power

Immunity Test Tested
Test Level (W)

For ac power cable 3 V (rms) 0.15 MHz, 80 MHz

conducted disturbances by
RF fields IEC 61000-4-6 6 V (rms) In ISM bands between
0.15 and 80 MHz

For enclosure port radiated 3 V (rms) 80 MHz to 2700 MHz

RF fields IEC 61000-4-3

Proximity fields from RF 27 v/m 1.8 385

wireless equipment
28 v/m 2 450

9 v/m 0.2 710, 745, 780 MHz

28 v/m 2 810, 870, 930 MHz

28 v/m 2 1720, 1845, 1970 MHz

28 v/m 2 2450 MHz

9 v/m 0.2 5240, 5500, 5785 MHz

Interference may occur in the vicinity of equipment marked with the following symbol:

AH9168 3-7 2022-01-07

4 Wireless

DRX-Revolution Wireless Systems

• CARESTREAM System Detector
• D-LINK DAP 2553, ARUBA 214 or ARUBA 505 wireless access point (WAP)
• RF IDeas Model RDR–80_82AKU proximity badge reader
• Code Corp. Model CR2701 bar code reader
• RAYTEC BT Dongle MDT50Q USB adapter
• SPARKLAN WPEA-251N(BT) or INTEL AX201, BT5 (non-Vpro) WLAN module
• CARESTREAM Remote Exposure Switch
Refer to the appropriate manufacturer documentation for wireless regulatory
declarations.

Wireless certification (for Brazil)

Incorporates product approved by Anatel under number 04099-13-01728.
Certificação sem fio (para o Brasil)
Incorpora produto homologado pela Anatel sob número 04099-13-01728.

Carestream System Detectors

• Radio Frequency Exposure Declaration—See the Safety and Regulatory information
in the user guide of the detector.
• Intentional Radiator Wireless Compliance to Regulatory Requirements—See the the
Safety and Regulatory information in the user guide of the detector.

AH9168 4-1 2022-01-07

 Wireless

National Usage Restrictions

Refer to the appropriate manufacturer documentation for European Union wireless
regulatory declarations.

AH9168 4-2 2022-01-07

5 System Components

While most of the external parts will be intuitive to an experienced radiographer,

please review the parts diagrams in this guide to become familiar with the naming
conventions used.

Related references
Optional Parts

Related information
Technical Specifications

Component Descriptions

Component Description

Detector battery storage and The cart provides storage and charging space for two DRX
charging batteries.

Bins Storage bins are located in the back of the cart. See Detector.

Boom The boom is an extendable, horizontal arm that holds the

tube head assembly, two boom handles, and the boom dock
tube.
If the boom is undocked, the software will prevent the
system from being driven on a surface that slopes more than
3 °.

CAUTION:
Do not hang clothing or place any object on the boom.

Brakes See: Bumper, Column, Drive handle, E-Stop.

AH9168 5-1 2022-01-07

 System Components

Component Description

Bumper The bumper on the front of cart is touch sensitive. Forward

motion is prevented when the bumper touches an obstacle.
To move the system after coming into contact with an
object, release the drive handle, then squeeze it while
pulling the cart back. You will be able to back up the
cart at a reduced speed. To resume normal back-up speed,
release and squeeze the handle again.

Cart The cart exterior includes a drive handle, storage bins, prep/
expose switch, wheels, bumper, LEDs and other light
indicators, primary touchscreen monitor, boom dock receiver,
proximity badge reader option, and bar code reader option.
Inside, the cart contains batteries, a generator, circuitry, and
motors.

Collimator The collimator includes an LED that creates a light field,

which represents the area on the patient to be x-rayed, two
control knobs on either side to operate the horizontal and
vertical shutter openings, and a collimator brake release.

Column The column is an extendable, motor-assisted, vertical

component that lifts and lowers the boom. The column
rotates right or left on a turntable 270 ° in each direction. To
release the brake and raise the column or extend the boom,
grip either or both of the collimator handles, or either boom
handle, press and hold the button on the back of the
handle(s), and lift or pull.

CAUTION:
When using the system, do not allow the top of the column
cap assembly to come in contact with any object.

Connectors See Power components.

Crane The crane includes the turntable, column, and boom.

AH9168 5-2 2022-01-07

 System Components

Component Description

Detector, upper storage bins, The top bin provides storage and optional in-bin charging for
tether, and lock a 43x43 detector or 35x43 detector in landscape mode. The
middle bin provides storage for a 35x43 grid with or without
a compatible digital, flat-panel detector and the bottom bin
provides storage for a 25x30 detector.
To store the grid or detector, slide it straight into the bin so
that it seats securely.
For security, these bins can be configured with an optional
bin lock. After an operator logs in, the bin lock is
automatically released. To manually lock the bins, slide the
lock to the side.
If the power goes off, an emergency bin release and a
detector tether are available. To operate the emergency bin
release, insert the end of a paper clip into the pin hole to the
left of the lock.
Compatible detectors can be used wirelessly or tethered.

DANGER: Electrical Hazard

If the system is plugged into an AC mains, exposures can not
be taken while the detector is tethered.

Docking tube and docking The docking tube on the boom fits inside of the docking
receiver receiver on the cart to lock the tube head assembly and
crane. To release the tube from the receiver, press the buttons
on the back of the boom or collimator handles and lift.

Drive handle The drive handle steers and powers the drive wheels,
allowing the cart to be self-propelled. Release the handle to
engage the brake and stop the cart from moving.
The cart may be driven at normal speeds if it is unplugged
from the wall socket, is locked in the docked position, and an
operator is logged in.
If the tube head is undocked, the cart may be driven at
reduced speeds.
If the power goes off, there is an emergency brake release so
the cart can be manually moved by the operator. To release
the emergency brake, press the small button on the inside of
the left power handle side panel.
If the operator is not logged in, the cart is immovable unless
the emergency brake release is pressed, which allows the
user to manually push the cart when the power is off.

AH9168 5-3 2022-01-07

 System Components

Component Description

E-Stop (Emergency Stop) There are two red emergency stop knobs: one on the x-ray
knobs tube and one on the cart. Press the knob to disable all drive
motors. To release, turn the knob in the direction of the
arrow.

Ethernet cable An Ethernet cable is used to connect to the hospital network,

RIS, and PACS. The cable can be stored on the system when
it is not being used.

Filter There is a slot on the collimator for a dual filter for added
filtration. One filter is supplied to calibrate the compatible
detector. You can also use your own filter. The filter can be
stored on the back of the cart in the pocket on the lower
right as you face the drive handle.

Lead apron hook A hook in the front of the column provides a place to carry a
user-supplied lead apron. The apron hook is compatible with
a normal coat hanger to hold aprons open when hanging.

Power components Power components include cords (including the main,

battery-charging, retractable cord); a generator; USB,
network, and tether connectors, in-bin charging, batteries,
motors, AC voltage and DC voltage circuit breakers, a
network cable, and a wireless access point. The batteries
support the full functionality of the mobile cart without being
plugged into a wall. There are separate electronic control
boards for the cart, crane, and battery.

Power status indicators A column of small green LED lights on the top left of the cart
indicate the charging status of the main battery.

PREP/EXP indicator When the Prep/Expose light is green, it indicates that all
systems are ready to take an x-ray image. When it is yellow,
an x-ray image is being taken.

PREP/EXP unit This unit includes a tethered exposure control with a two
stage prep/expose button on top and a collimator light
control on the side. A wireless exposure control is also
available as an option.

CAUTION:
The prep/expose cable can be a trip hazard when in use.
With use, the cable can stretch and cause a hazard when
stored on the system.

AH9168 5-4 2022-01-07

 System Components

Component Description

Protective bags Storage space is provided for detector bags. Protective bags
can be used to cover the detector during patient exams.
Clean bags may reduce the possibility of spreading
contaminants among patients.

Proximity card reader The optional proximity card reader scans an RFID badge to
identify the operator for login security. Carestream offers
optional proximity badges if needed, or you can use your
own. Badges need to be configured to enable the unit.

Shelves for holding the There are two shelves for holding the detector in place while
detector in place while inserting and removing the detector from a bag:
bagging
• One shelf is located inside each detector slot. The
detector can be partially lifted from the bin (about three-
quarters of the way out) and held in place on top of the
shelf while a bag is put on or taken off.
• Another shelf is at the bottom of the primary monitor,
below the drive handle. The detector can be leaned
against the side of the shelf and over the drive handle,
while the bag is put on or taken off.

Touchscreen monitors (2)

Important:
Carestream products utilize touchscreen monitors. Any
interaction with the monitors, intentional or unintentional,
will induce an action on the screen.
A primary touchscreen, 48.26 cm (19.00 in.) is permanently
positioned on top of the cart. A secondary touchscreen,
21.00 cm (8.40 in.) is situated on the tube head assembly.The
monitors display the PC-based software application that
manages image acquisition, manipulation, and delivery in a
health network. Both monitors display the detector battery
life so the operator can see if the detector has enough
battery charge prior to acquiring an image.
Hospital supplied external HDMI monitor can be used with
the system using the optional HDMI connector. A medical
grade (certified to IEC 60601-1, etal) display must be used.

AH9168 5-5 2022-01-07

 System Components

Component Description

Tube head assembly The tube head assembly is the entire unit located at the end
of the boom. It includes the x-ray tube, collimator, secondary
monitor, and handles on the boom and collimator for
movement. The secondary monitor allows the operator to
change techniques and views at the tube head assembly. The
angle of the x-ray tube is displayed on the secondary
monitor.The two buttons on the front of the boom handle
and the back of the collimator handles allow you to undock,
move up and down, and rotate around the column. The front
buttons on the collimator handles allow you to rotate the
tube head in any direction (x, y, z).
The tube head assembly must be docked when the cart is
being driven. If it is undocked, it can be moved, but speed is
reduced.
If the system is on a surface that slopes more than 3 °, the
boom can not be undocked.

USB connectors USB connectors are located on the front of the cart. If the
network is not functioning, an image can be delivered from
the DRX-Revolution to a PACS using a USB device.

Wheels There are two rear motorized drive wheels and two front
caster wheels. Each of the rear wheels is controlled by a
separate motor, which is activated when you press the left,
right, or both sides of the handle.

X-ray tube Maximum Anode Heat Content = 300 kHU. Normal

operation of the DRX-Revolution is considered 125 images in
a 24-hour period.The tube has two focal spot sizes ~0.6 and
1.2 mm.
• The smaller focal spot size allows better image detail for
smaller patients/anatomy.
• The larger spot size allows for use of higher tube limit
(higher allowable maximum voltage) for better image
quality when imaging larger patients.

Other Optionally supports DAP with automatic population

Related references
Drive the Cart
Subcomponents

AH9168 5-6 2022-01-07

 System Components

Cart

9 10

11
7

12
5

13
3

2 14

H253_0017_C1

1 Detector battery charging and storage bin1 8 Storage

2 Detector battery charging and storage bin 2 9 Power status indicators

3 Storage bin for 25 x 30 cm detector 10 Drive handle

4 Storage bin for 35 x 43 grid holder 11 Built-in bar code reader (optional)

5 Storage bin for 35 x 43 or 43 x 43 detector 12 Prep/Expose switch and collimator light

in-bin charging (optional) switch

6 Emergency brake release (inside the drive 13 Bag holder storage (protective bags for
handle side panel) detector)

7 Proximity badge scanner (optional) 14 Storage

AH9168 5-7 2022-01-07

 System Components

2
1

2
12
3

5
11

10

9 7
8
H253_0019_C1

1 Boom dock receiver

2 Emergency stop (2)

3 Primary monitor

4 Retractable AC voltage power cord (optional)

5 Bumper sensor

6 Front caster (2)

7 AC voltage circuit breaker

The DC voltage circuit breaker is in the same location on the opposite side.

8 Motorized drive wheel (2)

9 Drive handle side panel

10 Optional bar code reader

11 Tape measure

12 Secondary monitor/tube head display

AH9168 5-8 2022-01-07

 System Components

Primary and Secondary Monitors

1
H253_0021_C1

1 Primary monitor

2 Secondary monitor

AH9168 5-9 2022-01-07

 System Components

Crane
1

2
8

H253_0024_C1 5

1 Boom

2 Lead apron hook

3 Cable (power and controls)

4 Column

5 Turntable

6 USB storage

7 Boom handle (2)

8 Yoke

AH9168 5-10 2022-01-07

 System Components

Tube Head Assembly

10

8
5
7
6
H253_0022_C1

1 X-ray tube head 6 One button on the back of each

collimator handle to release the tube
head from its docking position, so you
can raise and rotate the column

2 Emergency stop 7 Collimator blade controls (two on each

side of tube head assembly)

3 Secondary monitor display 8 Boom dock tube

4 Collimator handle (one on each side) 9 Boom handle (one on each side)

A button on the front of each handle

can be used to release the brake on
the collimator to allow for rotational
movement

5 Collimator light switch 10 Boom handle buttons (one on each

handle) to release the tube head from
its docking position, so you can raise
and rotate the column

AH9168 5-11 2022-01-07

 System Components

Movements of the Boom, Column, Turntable,

and Tube Head Assembly

3
H253_0023_C1

1 Column

2 Boom

3 Turntable

AH9168 5-12 2022-01-07

 System Components

Subcomponents
The following photos show details of some of the subcomponents that are not easily
seen in other illustrations.

Boom Docking Mechanism

The view on the left displays the boom dock in the docked position. The view on the
right shows the boom dock receiver.

H253_0012 H253_0013

Power Display Indicators

A photo of the power display indicators (below) includes the round Ready/Prep light
above. An explanation of the changing indicators and other symbols on this panel
follows.

AH9168 5-13 2022-01-07

 System Components

What is illuminated What it means Notes

7 green lights The battery is fully All image techniques are

charged. All exam types available.
are available.

4–6 green lights Normal operating mode All image techniques are
available.

H253_0010 3 yellow lights The batteries are low A minimum of two yellow
on power. lights must be illuminated
to take an image, and the
image must not require
high technique.

1 red light The batteries are Take cart to charge station.

extremely low on
power. Batteries must
be charged for further
exams.

Blinking battery symbol The battery must be Take cart to charge station.
charged for further
exams.

Blinking green lights The battery is charging. When fully charged, the
lights will stop blinking.

Battery and plug The DC circuit breaker Turn on the DC circuit

symbol are alternately is turned off. breaker to use the system.
blinking

Nothing The cart is turned off You can still drive the cart.
and not plugged in.

Plug symbol The cart is plugged in. Motion is inhibited.

Wireless Prep/Expose Switch

CAUTION:
Multiple units with the infrared (IR) remote prep/expose switch (1) should not be used in the
same area.

AH9168 5-14 2022-01-07

 System Components

H253_0018_C1

CAUTION:
Do not pair remote prep/expose switch to multiple machines.
Both wired and wireless pre/expose switches are active.

Brake Release on Boom Handle

A brake release switch on each boom handle allows you to move the column up and
down and the turntable around.

H253_0020

AH9168 5-15 2022-01-07

 System Components

USB, Network, and Tether Connectors

2
3

H253_0026_C1

1 USB 3.0 connector for Service

Note:
An additional USB 2.0 connector is located at the base of the boom dock.

2 USB 3.0 connector for the optional 2D bar code reader

3 USB 3.0 connector for Service

4 HDMI connector (optional)

5 Hospital uplink network connector

6 Detector tether connector

AH9168 5-16 2022-01-07

 System Components

Labels
System Label Locations
9
10
11
1

3,4,5,6

2
H253_0024_C2 1

1 Pinch point label

2 AC voltage circuit breaker label (The DC voltage circuit breaker label is in the same
location on the opposite side.)

3 System data plate

4 Generator label

5 X-ray tube label

6 Collimator label

7 Retractable power cord (optional)

8 Emergency Stop label (2)

9 Ionizing radiation label

10 Transport position warning label

11 Follow the instructions label

Note:
The label locations as shown display the external labels with pertinent information from the
manufacturers.

AH9168 5-17 2022-01-07

 System Components

System Data Plate Sample

10
2
1

7
4

P/N XXXXXX REV A

O ffic ial Prod uc t N ame ( Jap an e se , if re quired )
O ffic ial Prod uc t N ame ( Ch in ese , if req uired )

50
THIS PRODUCT COMPLIES WITH 21 CFR CHAPTER 1, SUBCHAPTER J
O ffi cial Produc t Name ( En g lish)

150 Verona Street, Rochester, NY 14608 USA

Ꮁḹ䏃1510 ো㄀ಯǃϗᐶ䗮⫼ॖ᠓
Ϟ⍋Ꮦ⌺ϰᮄऎ䞥ḹߎষࡴᎹऎ
䫤⦖ Ϟ⍋ ए⭫఼ᴤ᳝䰤݀ৌ
SN

Carestream Health, Inc.

Manufactured:

Made in China by

Ё೑ࠊ䗴
MODEL
SC

11

1 Official product name

2 Service code and serial number

3 Manufactured date

4 Model type as required / consistent with product safety test reports

5 Voltage range, rated frequency in hertz and amps / consistent with product safety
test reports: V = volts, Hz = hertz, A = amperes

6 Symbols for product safety, EMC, and CE marking

7 SFDA Registration number

8 SFDA Product Standard number

9 Compliance statement according to FDA requirements for radiation emitting

products.

10 Label manufacturer registration number and material specification

11 Manufacturer

AH9168 5-18 2022-01-07

 System Components

Detector Weight Limit Label

CAUTION:
Since the detector is not a patient support device, it must be placed on a suitable surface, such
as a table or a floor, before applying patient weight. The weight label indicates the acceptable
limits of use that will not damage the detector. To prolong the life of the detector and minimize
potential internal detector damage, observe the following weight restrictions:
• The load limit applied to a single 4 cm (1.6 in.) point is 114 kg (250 lb.)
• The load limit distributed evenly over the detector area is 170 kg (375 lb.)

AH9168 5-19 2022-01-07

6 Operating the System

This chapter includes basic directions for driving the cart, docking and undocking the
boom, logging on and off, and unusual operating conditions.

Related references
Safe Operation Precautions

Unusual Conditions

Important:
Immediately stop using the equipment and call your authorized Service Representative if you
notice any abnormal conditions. Hazards may exist if the equipment is used in an abnormal
condition.
Some examples are:
• Loose screws or components
• Abnormal noises
• Broken handles or parts
• Drift of column or tube assembly
• Difficulty of motion
• Malfunctioning switches
• Abnormal driving behavior
• Erratic touchscreen behavior
To facilitate repair if a failure occurs, provide specific information to the service
representative. Note any unusual events prior to the failure, the type of procedure in
progress, and specific failure information.

Important:
If you witness or become aware of a potential safety issue with this equipment, take the
appropriate safety measures and report this to your authorized Service Representative.

AH9168 6-1 2022-01-07

 Operating the System

Drive the Cart

Start Squeeze the drive handle to release the brake before pushing or pulling the
cart. The boom must be docked in order to drive it at full speed. It can be
moved when undocked, but its speed is reduced by half.
If the system is on a surface that slopes more than 3 °, the boom can not
be undocked.
If the boom is undocked the software will prevent the system from being
driven on a surface that slopes more than 3 °.

Stop Release the drive handle to activate the brake.

CAUTION:
Do not park or leave the system unattended on an incline. The unit may
roll.

Proper driving position

and procedure to drive
the cart

H239_0034

CAUTION:
Do not drive the system unless you are standing directly behind it using two
hands. Failure to do so may result in loss of control causing serious injury or
equipment damage.
To move the cart forward or reverse, stand behind the cart with both hands
on either side of the drive handle. Squeeze the handle to release the brake,
and gently push or pull using the motor to power the drive wheels.

CAUTION:
The system is quiet, make sure people are aware or your presence when
driving the system. If using a hanger for the lead apron, check that your full
line of visibility is not diminished or obscured

AH9168 6-2 2022-01-07

 Operating the System

Turn right or left To turn right, apply more pressure to the left side of the drive handle with
your left hand, and less pressure with your right hand. To turn left, do the
opposite.

Control speed The cart will keep pace with your walking speed.

CAUTION:
Driving the cart with one hand is not recommended. Doing so may cause the cart to go into
reverse quickly and erratically.

H239_0037

Hand Placement

CAUTION:
Grasp only the drive handle of the cart with both hands when driving in any direction. Do not
hold the side cover and the handle to drive the cart. Doing so may cause the cart to go into
reverse quickly and erratically.

AH9168 6-3 2022-01-07

 Operating the System

Dock and Undock the Boom

Dock
CAUTION:
To ensure patient safety, the boom must be docked before doing
any of the following:
• Powering On
• Powering Off
• Deactivating the Emergency Stop (E-Stop) button (twist and
pull)
Fully compress the boom, align the boom dock tube over the boom
dock receiver, and lower the crane until it locks in place.

Important:
Make sure the boom is fully compressed before attempting to
dock. When the tube head is docked, the display is turned off. If a
secondary monitor exists, it displays the Patient Worklist.

Undock To release the crane lock and raise the boom dock from the
receiver, press the boom brake release buttons behind the boom
handle or collimator handles. The primary monitor automatically
“wakes up” when the tube head is raised.

AH9168 6-4 2022-01-07

 Operating the System

Start Up the Cart and Log In

Prerequisites:
Make sure that the cart has been parked, docked, and plugged into a wall socket to
recharge the batteries.

DANGER: Electrical Hazard

Make sure that your hands are dry before touching the electrical components.

1. Grasp the plug housing and carefully pull it from the power outlet.

Note:
When you disconnect the power cable, it may “wake up” the primary monitor; then there
is no need to touch the screen.

Important:
Do not allow the cord to snap back into the system. Doing so may damage the cord.
2. Slowly pull the cord until you no longer hear the audible clicks. Continue to hold
the plug and control the speed of the cord as it retracts into the system.
3. Touch the monitor screen the tube head assembly to “Wake up” the system
The system “wakes up” and the Login screen is displayed.
4. To log in, either type your user name and password on the display, or swipe your ID
badge over the proximity reader.

AH9168 6-5 2022-01-07

 Operating the System

Shut Down the Cart and Log Out

DANGER: Electrical Hazard

Make sure that your hands are dry before touching the electrical components.

1. When you have completed your exams, dock the boom and return the cart to its
parking/recharging location.
2. Hold the plug at the cart and gently pull out enough of the power cord to place the
plug fully into an AC voltage wall socket.
3. Continue to pull the cord until you hear one of eight audible clicks.

Important:
If the cord does not remain extended, allow it to retract back into the system and then
repeat this step.

CAUTION:
Do not trip on the cord.
4. After a predetermined time, the system automatically enters a screen saver mode,
cuts power to the monitor light, and logs you out.

Note:
You remain logged in until another radiographer logs in or until the system automatically logs
you out.

AH9168 6-6 2022-01-07

7 Additional System Information

Collision Stop Feature

Table 1: Drive System

Motor Drive Two independent drive motors provide

forward/reverse drive and directional control.

Collision Sensing Frontal and Lateral

AH9168 7-1 2022-01-07

 Additional System Information

Extra Focal Dimensions

X-RAY TUBE (XRR-3336X) X-RAY TUBE (XRR-3336X)

G G
21.0 mm C C 21.0 mm C C
80.0 mm (0.8 in.) 80.0 mm (0.8 in.)
(3.1 in.)
A
24.0 mm 29.5 mm (3.1 in.)
A
22.0 mm D 33.5 mm
(0.9 in.) D D B 178.5 mm D B 162.5 mm
(1.2 in.) F (0.9 in.) (1.3 in.) F
(7.0 in.) (6.5 in.)
39.0 mm 39.0 mm
(1.5 in.) (1.5 in.)

76.8 mm 69.9 mm
(3.0 in.) (2.7 in.)
1000.0 mm 1000.0 mm
(39.4 in.) (39.4 in.)

101.0 mm 430.0 mm 101.0 mm 116.0 mm 430.0 mm 116.0 mm

(4.0 in.) (16.9 in.) (4.0 in.) (4.6 in.) (16.9 in.) (4.6 in.)
I H I I H I
A A

H253_0029 H253_0028

A Distance from the focal spot to the collimator mounting flange surface

B Distance from the near-focus shutter opening to the mounting flange surface

C The maximum opening size of shielded x-ray tube port

D The maximum opening size of near-focus shutters

E The maximum size of far-focus shutters

F The distance from the focal spot to the far-focus shutters

G Focal spot position

H Primary x-ray field

I Extra focal radiation

AH9168 7-2 2022-01-07

 Additional System Information

Packaging Material and Weight

Packaging Weight

Total Packaging Material 165.47 kg (364.80 lb)

Metal 2.63 kg (5.80 lb)

Plastic (Foam) 1.27 kg (2.80 lb)

Plastic (LDPE) 1.45 kg (3.20 lb)

Wood 160.12 kg (353.00 lb)

AH9168 7-3 2022-01-07

8 Maintenance Information

Related references
Safe Operation Precautions
Cautions

Cleaning Instructions
See the Cautions section for information on cleaning precautions.
Use only the approved cleaning/disinfecting solutions.

Solution Note

METREX CAVIWIPES 1 Do not use on the digital grid holder accessory

Oxivir Tb Do not use on prep/expose switch

PDI SANI-CLOTH AF3 Do not be use on the digital grid holder accessory

PDI SANI-CLOTH

CLOROX Healthcare Wipes

CLOROX Hydrogen Peroxide

PDI SUPER SANI-CLOTH

CLINELL Wipes Do not use on the digital grid holder accessory

System Exterior
To ensure that the system continues to provide quality performance, clean the exterior
periodically.

CAUTION:
Do not let any liquid drip into the cart or its components.
Do not use volatile cleaning agents like ammonia. These may degrade or discolor the system.
Do not use a regular vacuum because it generates static electricity that can damage the system.
You can use a battery-powered vacuum on the exterior except for on the touchscreen monitors.

AH9168 8-1 2022-01-07

 Maintenance Information

Follow the instructions for cleaning each of these components:

• Monitors
• Detector/grid
• Plastic components
• Metal column

Patient Contact Areas

After each exam, clean the areas of the system that contact the patient.

CAUTION:
Do not operate the equipment when you are cleaning patient contact areas.

Monitors
A touchscreen monitor is a prime target for dust, fingerprints, and bacteria. At the
same time, a touchscreen monitor is very sensitive, so proper cleaning is important to
maximize its performance and prolong its life.

Hardware

CAUTION:
Do not operate the equipment when you are cleaning the hardware.
Do not immerse the equipment in liquid.

Detector
See the detector’s user guide for instructions on cleaning the detector.

Plastic Components
All of the components are plastic except for the touchscreen monitors and the painted
column and boom.
Never use abrasive cleaning products such as abrasive sponges, steel wool pads,
abrasive powdered cleaners, or harsh detergents. Plastic surfaces are easily scratched.
This can ruin the finish.
Do not use glass cleaner on plastic. While the damage may not be immediately visible,
over time, glass cleaners leave the plastic with an appearance that doesn't appear to be
clean. Instead, use sponges, soft cloths, and mild detergents when cleaning plastic.

Metal Column and Boom

Handle the painted metal column with care to avoid striking any object, which may
chip the paint.
You can clean the column using any of these methods:

AH9168 8-2 2022-01-07

 Maintenance Information

• Use a battery-powered vacuum with a soft nozzle to remove the dust and dirt.
Pay particular attention to corners and side grooves, where buildup of dirt and
residue can occur.
• Wash the surface with a soft, lint-free cloth moistened with warm water and a mild
liquid detergent.

Note:
Trisodium phosphate (TSP) is made specifically to remove grease and grime from painted
surfaces without harming the finish.
• Use a solution of 70 % isopropyl alcohol on a clean, soft cloth.

Clean the Monitors

Prerequisites:
Power Off the system.
Either a screen cleaner kit with antistatic wipes or a soft, lint-free cloth with 70 %
isopropyl alcohol is required.

Important:
Do not spray any liquids directly onto the screen. Use gentle pressure while cleaning and do not
use a paper towel because it may scratch the screen.

1. Prepare the wipe or cloth, depending on the cleaning materials you are using:
» Spray a small amount of cleaning solution on a wipe.
» Wet a soft, lint-free or microfiber cloth with 70 % isopropyl alcohol. Make sure
the cloth is damp but not wet.
2. Wipe the screen in a gentle motion with the wipe or cloth.
3. If necessary, finish cleaning the screen with a dry, lint-free cloth to wipe away any
moisture.

Clean the Plastic Components

Prerequisites:
Power Off the cart.
Lint-free or antistatic dust cloths are required.
Water and 70 % isopropyl alcohol is required.

AH9168 8-3 2022-01-07

 Maintenance Information

CAUTION:
Do not attempt to clean inside the machine or remove the plastic panels.
Do not use aerosol sprays directly on or over the machine.

1. Moisten the lint-free or antistatic cloth with 70 % isopropyl alcohol and water.
2. Wipe the system panels, handles, bins, knobs, and wheels.
If necessary, you can use lint-free foam swabs moistened with alcohol or water to
clean hard-to-reach areas.
3. Wipe away any moisture left from cleaning with a dry, lint-free or antistatic cloth.

AH9168 8-4 2022-01-07

 Maintenance Information

System Maintenance

CAUTION:
Do not attempt mechanical or electrical repair of the system. Contact your authorized
Carestream Service Representative if any unit does not perform to your satisfaction.
Avoid safety risks, performance issues, and unplanned downtime with regularly
scheduled inspection, calibration, and maintenance checks. The equipment must be
maintained in good operating order at all times to provide safe conditions for
operating personnel and patients. It must also be maintained to prevent possible loss
of patient or image data. To ensure continued safe performance of x-ray equipment, it
is the owner's responsibility to supply or arrange for a periodic maintenance program.
After installation, perform maintenance on the system per the schedule below. The
system must be serviced and repaired only by your authorized Carestream Service
Representative.

Maintenance Schedule

Component Maintenance Initial 6-month 12-month

General Visual inspection X X

Clean all system components X X

Perform system functional testing X

(such as Acceptance and Compliance
tests)

X-ray generator X-ray tube (filament) calibration X X

• X-ray generator Mechanical/electrical inspection X X

• Cart
Functional checks X X
• Column
• Boom
• Tube head
• Electrical/
Batteries

Users should perform the following maintenance periodically or as needed:

• Clean the equipment.
• Recalibrate the touchscreen.
• Run an x-ray calibration on the detector array monthly or as prompted by the
software.

AH9168 8-5 2022-01-07

 Maintenance Information

Safety and Functional Checks

Contact your authorized Service Representative to perform safety and functional
checks:
• 6 months after installation
• 12 months after installation
• Annually thereafter

Reporting Unusual Conditions

Report any unusual noise, difficulty of motion, malfunctions, or other problems with
the equipment immediately.
To facilitate repair if a failure occurs, provide specific information to the service
representative. Note any unusual events prior to the failure, the type of procedure in
progress, and specific failure information.

Battery Service Life

• The service life of the system’s lead acid batteries is significantly reduced if they are
deeply discharged multiple times or left in a partially charged state for extended
periods of time.
• If you limit the depth of discharge and keep the batteries fully charged whenever
possible, it maximizes battery life.
• To keep the batteries fully charged, plug the system into a live AC circuit and place
the AC circuit breaker in the On position after every use.
• Plug the system in whenever it is not in use for more than 10 minutes. The system
may be left plugged in indefinitely.
• If the unit will not be used for more than two hours, and it is not possible to plug it
in, first fully charge the system, then shut the system down. This preserves the
battery charge and extends the battery life.
• If the system will be stored for more than 30 days and not charged during this time,
contact your authorized Service Representative for long-term storage instructions.

Replacing the Batteries

CAUTION:
The cart batteries need to be replaced periodically. The batteries contain lead and pose a hazard
to the environment and human health if not disposed of properly. Due to the toxicity of lead,
the U.S. EPA Resource Conservation and Recovery Act (RCRA) and state solid and hazardous
waste authorities consider a spent lead-acid battery a regulated waste. The customer must treat
this battery as a hazardous waste if it is not recycled. A recycling infrastructure is widely
available in the U.S. to manage this battery type.

AH9168 8-6 2022-01-07

 Maintenance Information

Disposal

In the European Union, this symbol indicates that when the

last user wishes to discard this product, it must be sent to
the appropriate facilities for recovery and recycling. Contact
your local authorized representative for additional
information.
See http://recycle.carestreamhealth.com for
additional information on the collection and recovery
programs available for this product.

CAUTION:
This product contains lead. Disposal of components that contain these materials are regulated
due to environmental conditions. For disposal or recycling information, contact your local
authorities.

CAUTION:
The flat panel display in this system contains mercury. Disposal is regulated due to
environmental considerations. Return the equipment to the manufacturer for proper disposal.
For recycling and disposal options in the European Union, visit the European Portable
Battery Association (EPBA) web site at http://www.epbaeurope.net. In other areas,
contact local or regional solid waste authorities for recycling/disposal guidance.

Important:
Contact your authorized Service Provider for service and replacement.

AH9168 8-7 2022-01-07

9 Troubleshooting

Problem Recommended Action

The system does not start up. 1. Check the battery level indicators.
2. Make sure all applicable switches (circuit breakers) on the
system are on.
If the problem persists, contact your authorized service
provider.

During startup, one of the tasks in the Power Off and then power On the system. If the failure occurs
Startup screen does not start. again, contact your authorized service provider.

The operator console powers On Power Off and then power On the system. If the blocking error
successfully but reports a blocking occurs again, contact your authorized service provider.
error.

The operator console powers On Power Off and then power On the system. If the problem
successfully but the application does persists, contact your authorized service provider.
not start.

You cannot log in. Make sure you are using the correct login and password. Note
that passwords are case sensitive.
Check with your System Administrator or Key Operator.
If the problem persists, contact your authorized service
provider.

None of the motorized movements are Check that there is not an E-Stop button engaged.
working.

Service and Support

For technical support in the United States and Canada, contact the Center of Excellence
(COE) at 1-800-328-2910.
For regions outside the United States and Canada, contact your local Shared Service
Center (SSC).
General customer support for U.S. and Canada:
Carestream Health, Inc.

AH9168 9-1 2022-01-07

 Troubleshooting

150 Verona Street

Rochester, NY, USA 14608
1-800-431-7278
Elsewhere in the world, contact Carestream Health, Inc. in your country.

AH9168 9-2 2022-01-07

10 Product Disclosure Table

AH9168 10-1 2022-01-07

Optional Parts

Note:
Some DRX-Revolution models do not support all of these parts and tools.

Tools
• 2D bar code reader
• Dose Area Product (DAP)
• Wireless remote exposure switch
• Detector bin lock
• In-bin charging
• RFID badge reader

AH9168 I 2022-01-07
Hardware-Software Interfaces

Important:
For information about using the tube head software and a guide to the icons displayed on tube
head screens, access the system software online help from the primary monitor. Tube head
software topics are located in the contents pane.

Note:
The tube head display is not available on some DRX-Revolution models.

AH9168 I 2022-01-07
 Hardware-Software Interfaces

Log in with a Proximity Badge for the First Time

Prerequisites:
You have a user account set up in the system.

1. Log in to the system using your user name and password.

2. Select System Menu > User Settings > Register Badge.
3. Scan your badge by swiping it across the badge reader (1).

H253_0027_C1

4. Wait for the beep.

A dialog window displays a message that your badge is not registered and asks if
you want to register it to the current login account.
5. Select Yes.
6. If prompted, type your password.
7. Verify that the registration was successful by logging out and then selecting
Badge Authentication from the desktop.
8. Swipe your badge over the badge reader and confirm log in.

Emergency Stop
The Emergency Stop (E-Stop) indicator displays on the screen if the user activates it. The
indicator disappears when the cart begins to move again.

AH9168 II 2022-01-07
 Hardware-Software Interfaces

Screen Saver
Touching a monitor and using any part of the cart, such as driving or using the prep/
expose switch, resets the screen saver timer and the auto logout timer. This prevents
the system from automatically logging out a technologist while they drive to a
patient’s room.

Note:
• To save power, the power to the primary monitor is disabled when the tube head assembly
is docked. You cannot see the primary monitor when the tube head is docked.
• On systems with secondary monitors, there is no screen saver for the secondary monitor.
Instead, the cart cuts power to the backlight on this monitor to save battery life. The system
is activated by touching the secondary monitor.

Logging Out at a Monitor

Note:
Some system models do not include a secondary monitor on the tube head.
A technologist can log out of the system from either the primary monitor or the
secondary monitor, if the system has one.
Select System Menu > Shut Down or Sign Out > Sign Out.

AH9168 III 2022-01-07

 Hardware-Software Interfaces

Battery Indicators
Detector Battery Indicator
A detector battery indicator displays the charge of the battery installed in the selected
detector. If no detector is selected, an empty placeholder is displayed. It also indicates
when the battery is being charged by showing a detector with tether. Touch this or any
other battery indicator on the control panel to display the Battery and Charging
screen.

Description

Detector battery status

Cart Battery Indicator

A cart battery indicator displays the charge of the batteries that run the console
computer and the wheels. It also indicates when the battery is being charged (plugged
in).

Description

Cart battery charging

No cart battery power

25 % of cart battery power remaining

AH9168 IV 2022-01-07
 Hardware-Software Interfaces

Description

Cart battery charging, 50 % power

Cart battery status unknown

50 % of cart battery power remaining

AH9168 V 2022-01-07
 Hardware-Software Interfaces

Drive Mode

Drive-only mode

The Key Operator can configure driving as follows:

• Allow driving only when the user is logged into the system.
• Allow driving, without logging in, by touching the Drive icon.
• Allow driving, without logging in, by touching the Drive icon and entering the
drive code.

AH9168 VI 2022-01-07
Publication History

Version Date Changes

A 2019-07-22 Initial release

B 2020-03-10 • Updated CE mark and

copyright information.
• Updated address of
Authorized Representative
(European Union).
• Added Medical Device
symbol

C 2021-10-14 Updated:
• Technical Specifications
• Labels
• DRX-Revolution Wireless
Systems
• National Usage Restrictions
• Component Descriptions
• Operating the System
• Additional Information
• Optional Parts

AH9168 I 2022-01-07
 Publication History

Version Date Changes

D 2021-11-01 Added Model Number to Safety

Symbols

E 2022-01-07 • Added UDI to Safety

Symbols
• Added Preventing
Unintentional Exposures
to the Safety and Health
Compliance section
• Updated the DRX-Revolution
Wireless Systems section
• Updated Drive the Cart
section

AH9168 II 2022-01-07
Carestream Health, Inc.
150 Verona Street
Rochester, NY, USA 14608
© Carestream Health, Inc., 2022
Made in USA.
CARESTREAM is a trademark of Carestream Health.
Pub. No. AH9168
Rev. E

“Rx only”