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Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)
Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)
Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)
gehealthcare.com
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Page 2
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
LEGAL NOTES
TRADEMARKS
All other products and their name brands are the trademarks of their respective holders.
COPYRIGHTS
All Material, Copyright © 2013 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written permission
of General Electric Company, Inc.
IMPORTANT PRECAUTIONS
LANGUAGE
ПРЕДУПРЕЖДЕНИЕ ТО В А УП Ъ ТВ А Н Е ЗА РА Б О ТА Е Н А Л И Ч Н О С А М О Н А А Н ГЛ И Й С КИ ЕЗИ К.
(BG) А КО Д О С ТА В Ч И КЪ Т Н А УС Л УГА ТА Н А КЛ И ЕН ТА И ЗИ С КА ЕЗИ К,
РА З Л И Ч ЕН О Т А Н ГЛ И Й С КИ , ЗА Д Ъ Л Ж ЕН И Е Н А КЛ И ЕН ТА Е Д А О С И ГУРИ
П РЕ В О Д .
Н Е И ЗП О Л ЗВ А Й ТЕ О Б О РУД В А Н ЕТО П РЕД И Д А С ТЕ С Е КО Н С УЛ ТИ РА Л И
И Р А ЗБ РА ЛИ УП Ъ ТВ А Н ЕТО З А РА Б О ТА .
Н ЕС П А ЗВ А Н ЕТО Н А ТО В А П Р ЕД УП РЕЖ Д Е Н И Е М О Ж Е Д А Д О В ЕД Е Д О
Н А РА Н Я В А Н Е Н А Д О С ТА В Ч И КА Н А УС ЛУГА ТА , О П ЕРА ТО РА И Л И
П А Ц И ЕН Т В РЕЗ УЛ ТА Т Н А ТО КО В УД А Р И Л И М ЕХА Н И Ч Н А И Л И Д РУГА
О П А С Н О С Т.
警告 本维修手册仅提供英文版本。
(ZH-CN) 如果维修服务提供商需要非英文版本,客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前,不得进行维修。
忽略本警告可能对维修人员,操作员或患者造成触电、机械伤害或其他形式的伤害。
このサービスマニュアルには英語版しかありません。
(JA) サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業
者の責任で行うものとさせていただきます。
このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでくださ
い。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、
感電や機械的又はその他の危険により負傷する可能性があります。
(KO) 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우, 번역 서비스를 제공하는 것
은 고객의 책임입니다.
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write “Damage
In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed
for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage
MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after
receipt, and the contents and containers held for inspection by the carrier. A transportation
company will not pay a claim for damage if an inspection is not requested within this 14 day period.
Call GEHC Global Parts 1-800-548-3366 and select option 8, immediately after damage is found.
At this time be ready to supply name of carrier, delivery date, consignee name, freight or express
bill number, item damaged and extent of damage.
Complete instructions regarding claim procedure are found in Section S of the Policy And
Procedures Bulletins.
14 July 1993
IMPORTANT...X-RAY PROTECTION
X-ray equipment, if not properly used, may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. The General Electric Company, Healthcare
Group, will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements as published in NCRP Reports available from NCRP Publications, 7910 Woodmont
Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on
Radiation Protection, and of any other local authorities, and take adequate steps to protect against
injury.
The equipment is sold with the understanding that the General Electric Company, Healthcare
Group, its agents, and representatives have no responsibility for injury or damage which may result
from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be used.
CAUTION Danger of explosion if battery is incorrectly replaced. Replace only with the same or equivalent type
Risk of recommended by the manufacturer. Discard used batteries according to the manufacturer’s
Explosion instructions.
Revision History
Page 16
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
Preface
Publication Conventions
Standardized conventions for representing information is a uniform way of communicating information to a
reader in a consistent manner. Conventions are used so that the reader can easily recognize the actions or
decisions that must be made. There are a number of character and paragraph styles used in this publication to
accomplish this task. Please become familiar with them before proceeding forward.
It’s important that you read and understand hazard statements, and not just ignore them.
Section 1.0
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and style for
safety communications reflected in this publication represents the harmonization of IEC/ISO 3864 and ANSI
Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential hazards.
Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety
information. Text (Hazard) styles are applied to the paragraph contents that are applicable to each specific
safety statement.
Preface Page 17
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
NOTICE - Indicates information or a company policy that relates directly or indirectly to the safety of
personnel or protection of property. This signal word is associated directly with a hazard or hazardous
situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.' It can include:
• Destruction of a disk drive
• Potential for internal mechanical damage, such as to a X-ray tube
Page 18 Preface
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
Section 2.0
Publication Conventions
2.1 General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose,
Example, Comment or Note) are used to identify important but non-safety related information. Text styles
are also applied to text within each paragraph modified by the specific prefix.
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location. The
document part number and revision number appears in every header on every page. Odd numbered page
footers indicate the current chapter, its title and current page number. Even page footers show the current
section and its title, as well as the current page number.
Preface Page 19
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
2.3 Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that’s either
screen input and output. Mono-spaced fonts, such courier, are used to indicated text direction. When you type
at your keyboard, you are generating computer input. Occasionally you will see the math operator “greater-
than” and “less-than” symbols used to indicate the start and finish of variable output. When reading text
generated by the computer, you are reading it as computer generated output. In addition to direction,
characters are italicized (e.g. italics) to indicate information specific to your system or site.
Example: Fixed This paragraph’s font represents computer generated screen “fixed” output.
Output Its output is fixed from the sense that it does not vary from application
to application. It’s the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example: This paragraph’s font represents computer screen output that is
Variable Output “variable”. It’s used to represent output that varies from application to
application or system to system. Variable output is sometimes found placed
between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed This paragraph’s font represents fixed input. It’s computer input that is
Input typed-in via the keyboard. Typed input that does not vary from application
to application or system to system. Fixed text the user is required to
supply as input. For example: cd /usr/3p
Example: This paragraph’s font represents computer input that can vary from
Variable Input application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or soft button,
switch or key. Physical hardware, such as buttons and switches, are called hard keys because they are hard
wired or mechanical in nature. A keyboard or on/off switch would be a hard key. Software or computer
generated buttons are called soft keys because they are software generated. Software driven menu buttons are
an example of such keys. Soft and hard keys are represented differently in this publication.
Example: Hard A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style that uses
Keys both over and under-lined bold text that is bold. This is a hard key.
Example: Soft Whereas the computer MENU button that you would click with your mouse or touch with your hand uses
Keys over and under-lined regular text. This is a soft key.
Page 20 Preface
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 6 INSTALLATION MANUAL
Table of Contents
Preface
Publication Conventions ..................................................................................................... 17
Section 1.0
Safety & Hazard Information........................................................................................ 17
1.1 Hazard Messages ............................................................................................................................ 17
1.2 Text Format of Signal Words ......................................................................................................... 17
1.3 Symbols and Pictorials Used .......................................................................................................... 18
Section 2.0
Publication Conventions................................................................................................. 19
2.1 General Paragraph and Character Styles ........................................................................................ 19
2.2 Page Layout .................................................................................................................................... 19
2.3 Computer Screen Output/Input Text Character Styles ................................................................... 20
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) ........................................................ 20
Section 1.0
Lock-Out & Tag-Out (LOTO)
1.1 System Power
Title(s) of Employees Authorized to Perform LOTO: Those trained in Lockout Tagout (LOTO)
Title(s) of Affected Employees and How to Notify: Hospital Personnel; notified by verbal
communication.
POTENTIAL PERFORM LOTO BEFORE PERFORMING SERVICE OF ANY KIND. See Section 1.0 on
ELECTRICA page 29.
L SHOCK
Follow the steps below to ensure that your system powers up safely, properly and reliably.
Potential for PDU tap settings must match input voltage else there is potential for equipment damage.
Equipment
Damage
4.) System startup is complete when applications screen is displayed on workstation computer.
3.) Now tag and lock out facility power to the system, if you wish to perform service. See Section 1.2 on
page 30.
Section 4.0
Equipment Safety - Electrostatic Discharge (ESD)
A sudden discharge of static electricity from your finger or other conductor can destroy static-sensitive
devices or microcircuitry. Often the spark is neither felt nor heard, but damage occurs. An electronic device
exposed to electrostatic discharge (ESD) might not appear to be affected at all and can work perfectly
throughout a normal cycle. The device can function normally for a while, but it has been degraded in the
internal layers, reducing its life expectancy.
Networks built into many integrated circuits provide some protection, but in many cases, the discharge
contains enough power to alter device parameters or melt silicon junctions.
Relative Humidity
Event 55% 40% 10%
Walking across carpet 7,500 V 15,000 V 35,000 V
Walking across vinyl floor 3,000 V 5,000 V 12,000 V
Motions of bench worker 400 V 800 V 6,000 V
Removing bubble pack from PCB 7,000 V 20,000 V 26,500 V
Packing PCBs in foam-lined box 5,000 V 11,000 V 21,000 V
Many electronic components are sensitive to ESD. Circuitry design and structure determine the degree of
sensitivity. The following packaging and grounding precautions are necessary to prevent damage to electric
components and accessories.
• Transport products in static-safe containers, such as tubes, bags, or boxes to avoid hand contact.
• Protect all electrostatic parts and assemblies with conductive or approved containers or packaging.
• Keep electrostatic sensitive parts in their containers until they arrive at static-free stations.
• Place items on a grounded surface before removing them from their container.
• When handling or touching a sensitive component or assembly, ground yourself by touching the chassis.
• Avoid contact with pins, leads, or circuitry.
• Place reusable electrostatic-sensitive parts from assemblies in protective packaging or conductive foam.
3 2 4
7
8
1 Arm 5420592
3 Detector 5436666
4 Tube 5331186
5 Console 5429246
7 Workstation 5810000-A
8 Monitor 5414707
Page 36 -
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 INSTALLATION MANUAL
Section 1.0
Installation
2 Uncrate, Inventory and move them to room People Required: 2 Minutes to Complete: 60
Collect Product Locator Cards and store in a secure location.
Uncrate and Inventory subbox.
Plan route and transport equipment to room.
2 System cabinet positioning and fix Arm People Required: 2 Minutes to Complete: 10
Take out cabinet to the designed position.
fix and position Arm according to designed position
3 Detector component installation and cable connection People Required:2 Minustes to Complete:55
Take out detector housing from shipping container.
Install detector housing to the U-Arm.
Connect and routing cables
Install ion chambor(optional)
install detector.
install the grid(optional)
Take out Tube support, tube and collimator from shipping container.
Install the tube support to the U-Arm
Put the tube on the tube support
Connect the collimator to the tube
Connect and routing cables
Lead is used in this system to provide required radiation shielding, such as in tube, collimator, please pay
attention and do not touch it directly.
Item # Item
3.) Cable shield clamps installed and tightened (how many?, where?).
4.) All mounting bolts installed and tightened (floor and wall).
13.) List of any installation drawing deviations (all deviations should be signed by customer
and reviewed by the installation specialist).
Warning labels
Rating plates
28.) Has system documentation (paper and CDROM) been given to the customer?
29.) Is the hospital scheduling system (HIS/RIS) configured? Does the modality display
MWL (Modality WorkList) responses successfully?
30.) Are printers configured and printer calibrations done on ALL printers?
31.) Are PACS configured and SMPTE and/or test images pushed to system for successful
display (be sure burn/no burn is properly set for PACS)?
32.) Has local physics inspection been completed. Some states/sites may not allow use of
system for patients until this is done.
33.) Has backup of pristine system been performed? (Patient Data Base as well as total
system backup)
Installation checklist
Red
If the center of the preventive tilting label is GREEN, it means the system is OK without any tilting during
shippment.
If the center of the preventive tilting label is RED, it means the system is not OK with tilting during shipment.
Please open the crates to check system carefully.
Green
Section 1.0
Arm Component
1.1 Unpacking and Positioning
• Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for
against the packing list.
• Check the mechanical conditions and external appearances of all parts for possible damages or missing
items.
• The distribution center or factory must be notified immediately for any damage or shortage of parts.
Note: Take out the Operator and Service Documents and CD. Read Manuals carefully before system installation
and calibration.
2.) Remove the top and side of shipping container, and Arm is bound on it. See Figure 5-2.
Figure 5-2 Table Crate with top and side plate Removed
4.) Take out the wood fixtures and metal fixtures in the crate.
5.) Use the service tool to move the U-Arm to the position.
4.) Remove the bolt and axle from the ring in the transport cart.
6.) Remove out the bolts from the cart box to take out the lifting rope
7.) Insert the bolt to the hole in the bottom of the column.
8.) Insert the axle trough the hole in the top of the column.
9.) Set the two ropes crossingly from one side in the bottom bolt to another side in the top
axle
carrier
* Draw out the pin and Strench out the lifting hook to the number 3 position.
Pin
11.) Adjust the lifting arm height by hold the bar up and down to lift the U-arm off to the
transport cart.
hold the
bar
12.) Block the bottom of the column to the bar on the cart.
14.) Bundle up the Arm and cart together. put the hook under the cart to avoid scrape.
Slide
* Put up the tripot and fix it to the column by tightening a bolt with a wrench.
* make the bottom of the column off the ground by the bar across the cart.
* Remove off the foldable crane and push the U-arm into or out of the elevator then.
* When reach to the position, connect the foldable crane to the ring on the column and
put down the tripot.
19.) Using the foldable crane to make the column stand on the position.
20.) Lift up the U-Arm off the ground and rotate the column to front
21.) Pull down the lift arm by screw the knob on the foldable crane to disconnect the crane with
the ring on the column.
Knob
6.) Pull the arm down the ground and return to the front.
7.) Move the other crate and take out the system accessories
3.) Insert the pin hydrant though the column and install the fixed plate to both side of the column.for
safety concern. For Brivo XR575P, the column cover need to be removed firstly.
4.) Use a center punch or marking pen to mark the location of the 5 mounting holes at the notch of the
column base.
2.2 Installation
1.) Screw off the Lock/Release handle of detector housing from the U-Arm
3.) Direct the plate on the detector housing to the detent on U-Arm.
5.) Make the detector vertical to the floor by release the handle to rotate the detector housing.
Lock
Release
Note: When the detector housing is vertical to the arm, the detent will be in fixed position.
6.) To balance the U-Arm, install the tube support.
Tube support
U-Arm
Figure 5-15 screw off the back cover of detector housing (before)
Figure 5-16 screw off the back cover of detector housing (after)
3.) Insert cables (5428934, 5428629, 5428859, 5433031) from the back of U-arm into detector
housing.And leave the cables out of the detector housing about600mm.
5.) Connect the receptacle plug(5433031 to Grid-in SW) into the micro switch of grid in/out.
6.) Put the cable(5433031 to button) in the wire slot under the detector housing.
8.) Slide in the Ion chambor with the cable inside the housing firstly.
d.) Screw off the nuts and fix the ground cables on the U-Arm
b.) Move off the block and relax the four clamps
Ground Cable
5428859
14.) Route the cables between the detector housing and U-Arm
15.) Wear the cables sleeve.
Section 3.0
X-ray Tube and Collimator
3.1 Unpacking
• Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for
against the packing list.
• Check the mechanical conditions and external appearances of all parts for possible damages or missing
items.
• The distribution center or factory must be notified immediately of any damage or shortage of parts.
1.) Loosen the screws on the tube arm, install the tube fork into it, and screw it tightly. And mount the cable
2.) Loosen the screws of the upper clamp of tube fork, and remove the upper clamp of tube fork.
3.2 Installation
1.) Put the tube on the tube support.
Notice the tube installation direction. If the direction is wrong, the tube focal spot will be
inaccurate, and the tube may be falling down if the clamps are loose.
4.) Rotate the tube support 180 degrees to make the flank up.
2.) Route the cable(5428663,5428666,5428637) through cable support to the tube side.
3.) Prior to the connection of the high-voltage cables, remove the old silicone compound on the plug
surfaces with clean dry cloth and check to verify there are as cracks, flaws, or traces of creeping
discharge on the surfaces.
Note: When the traces of creeping discharge are found, be sure to replace the defective parts. (Grinding off the
traces only will not be effective.)
4.) Coat the tip of the cable plugs with the silicone compound about five to seven grams, that is, to the extent
the tip is hidden under the heaped up compound. At this time, the side of the cable plug should not be
greased.
5.) Remove the cap covered the socket of the tube housing and wipe the inside softly with a clean dry cloth.
DO NOT use any chlorinated solvents to clean any parts.
6.) Connect the anode and cathode HV cables (2269002-5) to the X-ray tube.
Check the polarity of HV cables carefully, and DO NOT connect the two HV cables reversedly.
Connect the HV cables in the correct polarity with sufficient care not to produce clearance
between the cable plug flange and the cable socket at the insertion of the plugs. Presence of such
clearance or incomplete silicone compound coating will cause creeping discharge and normal
operation of tube will be disturbed.
7.) Tighten the high-voltage cables solidly to the sockets of the tube housing by the threaded cable flange.
Figure 5-47 Cable connection from spine board to tube side button.
Cable clip
Section 5.0
Cabinet Electrical Connections
For details, please refer to System Schematics and Drawings in Service Manual and Pre-Installation Manual.
Note: The handle on each side of the cabinet only used to lift off the cover. Don’t move the cabinet by the
two handles.
HV cable 5393036
Jedi X-ray On
Lmp Cable
5432235
IF board to Jedi
Cable 5428664
Ion Chambor(AEC1)
cable 5437495
Tube Rotator
cable 5428666
IF Board:
IF powercable to PDU
5428661,
IF board to Jedi
able 5428664,
IF board to Spine
board cable 5428632,
IF board to PC RS232
,
cable 5428628.
IF broad to Console
cable 5428630,
Room-door open switch
cable 5432234
J2+J3:
PC power cable 5428622
Chapter 6 - Workstation
Section 1.0
Computer
1.) Placement
2.) Connections(USB/PS2)
5428622
5428628
5428629
cable connected to
monitor
Section 2.0
Mouse and Keyboard
1.) Placement
2.) Connections (USB/PS2)
Section 4.0
LCD Monitor
1.) Placement
2.) Connections
a.) Video (DVI)
b.) Power & Ground
3.) Rotate the Arm to horizontal position. Adjust the SID from 100mm to 180mm to make judge.
4.) Make sure the bias of the center is less than 5 mm, and make sure the collimator beam can align the
center point of the detector mark.
5.) If the requirements above cannot be met, adjust the four screws on the tube fork and insert iron plates
into the tube support to align the collimator.
1.) When all position between 180mm and 100 mm are up or down, adjust four screws of
number 1 as illustrated in Figure 8-4 Align Collimator
2.) When the position is tilt left or right, adjust four screws of number 2 as illustrated in Figure
8-4 Align Collimator
3.) When the position is tilt up or down, relax two screws of number 3 as illustrated in Figure
8-4 Align Collimator,screw the two little bolts of number 4 as illustrated in Figure 8-4 Align
Collimator
1 3
Notch
the position
of wo little
4 olts
6.) Rotate the Arm to 90 degree and conduct collimator alignment under above way.
2.) Mount on the top cover on it with the three screws. And cover the top plate to it.
top plate
Item # Item
3.) Cable shield clamps installed and tightened (how many, where).
4.) All mounting bolts installed and tightened (floor and wall).
Chapter 15 - Counterweight
Purpose: The counterweight has been finished before delivery. It usually don’t need to do
this step in fields. Just in case the equipment can’t keep level , adjust the weight of either
side of the Arm and the back of the column under the instructions in this chapter to balance
the equipment.
1.) If the Arm can’t be level in 0°, add or reduce the counterweights in either side of the Arm.
counterweight
counterweight
2.) If the column tilts foreward or backward, move the Arm to top position, open the counterweight
cover on the back of the column, add or reduce the counterweights.
1.2 Table
5456538 CASTOR 4
5457304 Tabletop 1
5456538 5457304
5429246 5439061
5448740
1.5 PDU
5393037
5435234
5393036
5224265
5435236
5443099
5398369
5435232 5443496
1.5.2 U-Arm
5439844 Spring 1
5447915 Brake 1
5457298 Bearing 8
5458808 Handle 1
5430961
5443085
5458806
5446298
5444677 5458808
5448732
5439843
5447916 5447915
5435327
5461879
5445536 5430959
5452427
5444763
5428769
5452377
5394097
5453213
5456202
5446299
5459299
5458807
5443085
5458080
5439844
1.6.1 Introduction
This Section provides information for the identification of Renewal Parts for the JEDI 50 R 1T
generator.
FRU name
Inverter PW Assembly
2187001 Part number for
Inverter Capa Assembly ordering
2203900
> Uninstall the back cover of the detector housing and relax the four clips.
> Uninstall the left part of detector housing, and disconnect the E-stop cable.
> Put out the receptable plug from the Grid-in switch.
> Remove the Grid-in switch on detector housing.
2.) Reinstall the new Grid-in switch.
1.) Reinstall the new Grid-in switch to the detector housing.
2.) Connect the receptable plug to the Grid-in switch.
3.) Put back the patient barrier to the detector housing.
4.) Remove LOTO and energize the system.
5.) Clean the site.
2.) Reinstall
1.) Install the new power supply
2.) Install back the topbox
3.) Remove LOTO and energize the system.
4.) Clean the site.
2.) Reinstall
1.) Install the new power supply
2.) Install back the topbox
3.) Remove LOTO and energize the system.
4.) Clean the site.
2.) Reinstall
1.) Install the new board
2.) Install back the cover
3.) Remove LOTO and energize the system.
4.) Clean the site.
Potential for Data Loss. Archive all protocols, patient files, and backup calibration and
configuration data. It's recommended that a system backup be performed prior to any
installation, upgrade or restoration of software. The installation of software can destroy
existing files, including patient, calibration and configuration files. You might have to
configure and calibrate your system, if you do not have a good backup to restore!
Purpose: Files within the workstation PC and other subsystems need to be saved, if system
software is reload, upgraded or becomes corrupt. After system installation or in the event a
subsystem failure occurs, saved files can be restored in their original condition and location.
2.2 Procedure1
1.) From the application desktop, click on the Service Tools icon.
4.) Click on the plus sign preceding the System folder ICON, in the navigation frame.
5.) Click on Backup link.
1.
Note: USB Backup cannot be stopped and do not remove USB drive during Backup.
9.) When backup is complete, you will see “System backup success" in the status bar.
10.) Remove and label CD((include current date and time)).
11.) Exit SUIF
3.2 Procedure
Potential for Data Loss. DICOM configuration information is not part of the backup. All
DICOM information should be kept written down and kept with system information. Use it
later to manually reconfigure DICOM, after the restore is completed.
4.) Click on the plus sign preceding the System folder ICON, in the navigation frame.
5.) Click on Restore link,
6.) Select the media type by clicking on one of the media type buttons.
8.) Click on the down-arrow in the drop down box to display a drop down list of items.
3.2 Consumables
• Empty/blank CD-R: 2
3.3 Safety
II.) Select Preferences first and then Protocols, from the menu.
III.) Insert a blank CD into the CD tray and close.
III.) entering the Worklist screen and clicking the icon of image management,this is
2.) To see the status of the exams being copied, click on located at the
Do not press the RESET button on the Console, unless you are instructed to.
a.) Load Linux Operating System (OS) software.
I.) Place the Linux Operating System DVD into the PC.
II.) Press and hold the RESET button for at least 3 seconds. You will hear a short beep,
and the system will begin to shut down and later reboot.
III.) When a ring is heard,the PC “splash” screen is displayed, press <F9> as instructed
on the screen.
IV.) When the Boot Device Menu is displayed, select to boot from "Optical Drive" and
press the <Enter>key.
V.) When the "Boot: "appears, type: GEHCXR and then press the <Enter>key.
VI.) Be patient, it takes approximately 15 minutes for the Linux Operating System
software to load.
VII.)Remove the Linux Operating System DVD from the PC and close the CD/DVD drive
drawer.
b.) Load Application Software
I.) Insert the Applications CD into the CD/DVD drive.
II.) Open the CDROM, and run the "autorun" file once. It will reboot for installing the
Graphics driver.
III.) After entering the system, open the CDROM and run the "autorun" file again.
IV.) Select “Brivo XR575” for Brivo XR575 model or "Brivo XR515" for Brivo XR515 model
as the product configuration to install Software.
V.) Click the Install tab.
VI.) When the installation of applications software is complete, "Installation is complete"
appear on the screen.
VII.)Click OK.
VIII.)Click [REBOOT]
IX.) The system will reboot and pop up the login screen.
X.) Remove the Applications CD from the CD/DVD drive.
For Brivo XR515 system, 192.168.1.1 and 192.168.1.45 has been used by Magic PC eth0 and
Detector. If these IP addresses also used in hospital network, we need to change Magic PC eth0
and Detector IP. So, if system IP conflict with 192.168.1.1 and 192.168.1.45, please follow the
below procedure.
2. Type:
su
#superxr
d.) Click on the plus (+) sign preceding the System folder icon in the navigation frame.
e.) Click on the [ Restore] link.
i.) Click on the arrow that points down, in the drop-down box, to display a list of items that
can be selected.
m.) Press and hold the RESET button for 3 seconds. You will hear a short beep.
You will now re-initialize the system to recognize the restored calibration and
configuration files
n.) Log into the system, when prompted.
o.) Open the Service Desktop.
p.) From the SUIF home page. verify that your current configuration accurately describes the
number of Detectors you have installed. The software load automatically defaults to one
Detector, unless you have done a successful restore and system reset.
8.) Backup System Calibration and Configuration files.
9.) Restore Protocol Data Base
a.) Be assure the system language config are the same with the backuped database. From
the Worklist screen, click the Service Tools icon. The Service Tools screen appears.
Worklist screen
b.) Select [Preferences] and then [ Protocols] .
c.) Insert the CD with the saved protocols database into the CD/DVD drive.
d.) Click the [Retrieve] button.
a.) Use the [CD1] button to open the CD tray on the PC.
b.) Select Eject CD from the drop-down list. The CD/DVD drive tray will open.
c.) Place the CD with the images onto the tray and close.
d.) Click the [CD1] on the top left corner of the screen. The exam list updates to now show
you the images stored on the CD.
e.) Select the exams you wish to retrieve. using the mouse.
f.) Click the [Local] button as the destination (located on the lower left corner of the screen).
g.) A message appears: Images will be copied to the selected exam. Images will not
automatically be removed from the source exam.
h.) Click [OK] , when it appears.
* If there is a problem and the exams cannot be copied to the selected network host:
1.) A message appears: The network destination is not responding. If the problem
persists contact your network administrator.
2.) Click OK to close the message.
3.) Try copying the exams at a later time.
* To see the status of the exams being copied:
1.) Click [Transfer Log] at the bottom of the Image Management screen.
2.) The Transfer Log screen appears.
3.) Click the [Close] button to close the screen and return to the Image Management
screen.
11.) Reload any applicable software patches.
12.) Re-checkout Insite.
13.) Congratulations, you're finished. Unless, you're installing a new system. Then proceed on to
Parameters Definition
Site Name Name of specific location (Hospital, clinic...) where system is installed
(64 characters maximum)
Parameters Definition
Contact Person Name Customer or person responsible for maintenance of equipment. One
line, and 64 characters maximum.
Contact Person Phone Two lines, and 64 characters maximum per line
Contract Expiration* Licensed Inhouse Service Contract number expiration date; created
by GE Healthcare. (64 characters maximum)
Default Gateway 16 characters maximum Note: If the customer site does not have a
default gateway, use the default value loaded upon installation. The
field cannot be empty.
Parameter Definition
Time Zone Allows the user to choose time zone according to site.
System Clock Allows the user to set the system clock according to site needs.
Data Display Format Allows the user to change/set system date display format. The Date
format is defined as MM-DD-YYYY (default) or DD-MM-YYYY.
Time Display Format Allows the user to change/set system time display format. The time
Format may be kept in a 24 hour format (Military) or 12 hour AM/PM
format: (hh:mm:ss (AM/PM)). The default value is Military
Parameter Definition
Application Language Defines the language used for applications screens. The default
value is English. For the site the chinese application wanted, the
Chinese should be selected.
QAP Timeout This item determines the interval between QAP test in days. Used to
inform system users that a QAP interval has expired and a QAP test
should be performed. The default value is 7 days.
Screen Blank Timeout Used to set the period of inactivity (where no user inputs and
processing activity occurs) in which screen blanking can begin. This
feature functions to prolong the life of the monitor, thus preventing a
burn-in. Time is selected in minutes. The default value is 15 minutes.
(4 characters maximum)
Image Mask Adjustment Adjusts the mask that is applied to the acquired image from the
detector. It affect Raw and Processed images.
Parameter Meaning
Parameter Meaning
Remove Patient Orientation This was a Non-purchased option. Please select Yes.
DICOM Tag
3.5 Insite
To configure the system for insite connectivity via broadband or modem.
Please refer to please refer to the Chapter Login Administration in Operator Manual for this setup.
on page 184 for operation steps.
Note: Note: Exit service user interface and reboot system after completion of Insite checkout /
configuration activities.
The following worksheets should be used to capture and archive your system’s DICOM
configuration for future reference. Records configuration information in the work sheets that follows.
Place worksheets in a safe place so that they may be referenced in the future if needed.
Host Label = = =
Network Address = = =
Port Number = = =
Query Retrieve = = =
Storage Commitment = = =
Comments = = =
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
General Comments:
- Supports Clear and Blue Film. If medium selected (Clear, Paper) does not match the
printer, the job will be queued until the correct film is loaded.
- AGFA layouts are specific to maximum printable area layouts. Please consult the AGFA
technical representative to install custom layouts
- Only 14x17 film was tested with this printer.
- Trim is not supported by this printer
Note: Avoid print job failures by having printer vendor ensure that the Confirmation Level (DICOM
Connectivity) at the printer is set to ?? (accept all). Failure to set this level on the printer will result
in failed print jobs
14 x 17 1:1 P 2411
14 x 17 1:2 P 9001
14 x 17 2:1 P 9000
14 x 17 2:2 P 9002
14 x 17 1:1 L 2511
14 x 17 1:2 L 9003
14 x 17 2:1 L 9004
14 x 17 2:2 L 9005
11 x 14 1:1 P 9014
11 x 14 1:2 P 9102
11 x 14 2:1 P 9103
11 x 14 2:2 P 9104
11 x 14 1:1 L 9018
11 x 14 1:2 L 9202
11 x 14 2:1 L 9203
11 x 14 2:2 L 9204
8 x 10 1:1 P 9006
8 x 10 1:2 P 9009
8 x 10 2:1 P 9008
8 x 10 2:2 P 9010
8 x 10 1:1 L 9007
8 x 10 1:2 L 9012
8 x 10 2:1 L 9011
8 x 10 2:2 L 9013
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
14 x 17 1:1 P 2411
14 x 17 1:2 P 9001
14 x 17 2:1 P 9000
14 x 17 2:2 P 9002
14 x 17 1:1 L 2511
14 x 17 1:2 L 9003
14 x 17 2:1 L 9004
14 x 17 2:2 L 9005
11 x 14 1:1 P 9014
11 x 14 1:2 P 9102
11 x 14 2:1 P 9103
11 x 14 2:2 P 9104
11 x 14 1:1 L 9018
11 x 14 1:2 L 9202
11 x 14 2:1 L 9203
11 x 14 2:2 L 9204
8 x 10 1:1 P 9006
8 x 10 1:2 P 9009
8 x 10 2:1 P 9008
8 x 10 2:2 P 9010
8 x 10 1:1 L 9007
8 x 10 1:2 L 9012
8 x 10 2:1 L 9011
8 x 10 2:2 L 9013
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
Note: ONLY 14 x 17 film should be used with this printer. Any other film size used may print films with
incorrect measurements
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Polarity NORMAL
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
Slide formats
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Smooth Factor 15
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2 1:2 only valid for portrait 2:1 only
valid for landscape
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Smooth Factor 15
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2 1:2 only valid for portrait 2:1 only
valid for landscape
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Smooth Factor 15
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2 1:2 only valid for portrait 2:1 only
valid for landscape
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
Pixel Depth 12
Smooth Factor 40
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer Check at least one (1on1) or
more as desired
Slide formats
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator,eg : PRINT_SCP sure to check on-site
Port Number Enter value given by Site Network Port numbers may be site specific,
Administrator, eg: 104 be sure to check on-site
Pixel Depth 12
Trim NO
Polarity NORMAL
Slide formats
Once logged in, you will have full access to system features and operation you are entitled to by
permissions.
xrusers- Users with these privileges are allowed access to all system features and operation.
insite - Gives complete control over protocols and user accounts. The insite account includes all of
the privileges defined for a typical Radiologist account. The difference is that the insite account can
also create and maintain user accounts.
User accounts must be created after system installation or whenever system software is installed
or re-installed.
Log into the Digital system with User ID insite, enter the password ******, for Admin/Service
privileges.
Use Emergency login unless you have a valid account set up.
• log in with Admin Privileges
If you have administrator privileges, when you log in you are asked if you to perform
administrative tasks or scan. Do not click the button next to the Enter administrator screen, if
you only want to scan.
• Manual Logout
1.) Move the cursor to a blank area on the screen.
2.) Right-click and select Lock Screen from the menu.
please refer to the Chapter Login Administration in Operator Manual for this setup.
11.1.1 Preliminaries
1.) Insert the Class “M” service media into the host PC prior to starting the SUIF.
2.) From the applications desktop, click on the tools icon.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now displayed.
3.) Enter the IP address of your system or the gateway IP address as defined by the facilities
network administrator.
4.) Click [Apply] button.
11.2.1 Summary
1.) Click on [Hour] and [Minute] fields of idm_send_data task and select an hour and minute from
the pull down lists that the system is normally “on” (typically between 9am and 5pm). After each
selection, click [Yes] on the Data has been modified. Please confirm it message.
2.) Click on [Hour] and [Minute] fields of idm task and select an hour and minute from the pull down
lists to schedule 5 minutes before the idm_send_data task. After each selection, click [Yes] on
the “Data has been modified. Please confirm it" message.
3.) When idm and idm_send_data hour and minute selections are complete, click on [Apply] to
finalize the schedule updates. Click [Yes] on the Are you sure you want to apply changes?
message.
4.) Close the ProDiags utility browser by clicking on [Close] from the upper left browser window
pull down menu.
11.2.2 Procedure
Use the following sequence to update the scheduled time (Hour and Minute) of the idm and
idm_send_data tasks:
1.) ProDiags idm_send_data Task
a.) Click on the idm_send_data task Hour field.
b.) From the pull down list, select an hour that the system is normally “ON” (typically between
09:00 and 17:00).
c.) On the “Data has been modified. Please confirm it” pop-up message, click on [YES].
d.) Click on the idm_send_data task Minute field.
e.) From the pull down list, select a minute .
f.) On the Data has been modified. Please confirm it pop-up message, click on YES.
2.) ProDiags idm Task
b.) [DISABLE INSITE] - Selecting this button will remove the system configurations that have
been configured during a previously successful checkout.
Note: Open a terminal window and manually remove the sclink.cfg file if necessary from the ~insite
directory.
c.) [AUTO CHECKOUT] - This button can only be used if a sclink.cfg already file exists, (i.e.,
meaning the site has completed a checkout using the [CHECKOUT NOW] button. [AUTO
CHECKOUT] will run ConfigLink, dial the AutoSC, queue a task with the AutoSC to dial
back, and wait for the AutoSC to dial back and leave a file /tmp/autocheckout. The IIP
Configuration Tool will wait only 10 minutes for the for the file to appear. Typically, the
AutoSC will call back in 5-6 minutes.
3.) Wait 10 seconds after the InSite Checkout is complete before touching any workstation buttons
and proceeding with the next step. (The workstation automatically reloads the browser after
InSite configuration is completed. Failure to wait before proceeding will cause the system to
“hang” )
4.) Reset System. A system reset is necessary after exiting Service User Interface for
configuration parameters to be established for use in applications.
1. Insure that insite Checkout is done successfully. Below icon will appear in the lower right
corner of screen.
7. Please contact related GE OLE and wait for remote connection from GE OLE.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now
displayed.
Page 194 Section 13.0 - Configuring In-House Service (Advanced Service Mode)
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 CONFIGURATION
4.) On the SUIF, click on Configuration Tab.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now displayed
(see ).
4.) Verify the Home screen displays Advanced Service at the top of the page.
5.) On the SUIF, press the Configuration ICON.
Page 196 Section 13.0 - Configuring In-House Service (Advanced Service Mode)
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 CALIBRATION
Be patient when executing commands. Text status messages are generally displayed in status line,
whenever a calibration icon is selected. If you are uncertain whether a command is being executed,
check the status line first. Repeated attempts to execute a command may require you to exit the
SUIF and re-enter to gain control again.
Calibrations must be performed in the order shown on the left hand side of the calibration tab. The
calibration summary screen only displays the date that a specific calibration was last performed.
You must always calibrate your system before it can be used and remember to restart your system
after the calibration to active the calibration.
The system must be rebooted if changes are made to calibrations files. This includes the creation
of new calibrations and/or the restoration of calibration files. Applications software running on this
system only reads calibration files during workstation boot-up. Any changes after boot-up are not
detected by the applications software.
To change the Measurement System, open the Service Desktop and select Configuration/General/
Measurement System. Click on [English] or [Metric] to select.
1.5 The use of Collimator(XS-1D) tape (Note the difference between SID and
OID)
In the calibration, you need to use collimator tape to measure SID. In the case to measure SID, you
need to consider the effect of OID (Object Image distance) .
To measure the SID when Uarm is at the 90 degree postion, you can use the collimator tape to
measure the distance from tube to patient and record it as length A. Then the SID = length A + OID.
To measure the SID when Uarm is at the 0 degree postion, you can use the collimator tape to
measure the distance from tube to table top and record it as length B. Then the SID = length B +
Table OID.
3.1 REQUIREMENTS
1.) Use the focal spot of the tube specified in the table See Table 21-3,
2.) The operating tube voltage and current should be monitored all exposures during this
operation.
3.) The anode rotation should be utilized at normal speed (3000 or 3600 min-1).
4.) Do not exceed either the generator or the tube ratings.
SF 40 50 50 2
40 50 10 2
40 200 50 2
40 200 10 2
80 50 50 2
80 50 10 2
80 200 50 2
80 200 10 2
120 50 50 2
120 50 10 2
120 200 50 2
120 200 10 2
LF 40 50 50 2
40 50 10 2
40 200 50 2
40 200 10 2
80 50 50 2
80 50 10 2
80 200 50 2
80 200 10 2
120 50 50 2
120 50 10 2
120 200 50 2
120 200 10 2
4.2.2 Procedure
Note: It is important that the Grid be removed. If the grid is left in during calibration, the CF value
will be higher than normal. The normal value for CF is approximately 1.2, whereas the value
when the grid is left in is approximately 1.7.
1.) Follow the on-screen instructions as presented by the tool.
Mechanical risk. Be care of collimator collision. Remember to take flat panel phantom off
from collimator before system power off or reset.
5.4 Procedure
There are three steps for calibrating an Image Detector. All three steps must be completed in the
following order: Bad Pixel Calibration, Pixel Gain Variation Calibration and CF Measurement.
You are required to do the following:
1.) Follow the on-screen instructions as presented by the tool.
2.) Install the flat field phantom.
3.) Execute Bad Pixel Calibration refer to the screen instruction.
4.) Execute Gain Calibration refer to the screen instruction.
No-Burn Burn-on-Send
Table 21-5 Results from the Simplified and Additional Tests Sections
WC = / /
WW = / /
5 DICOM Header on PACS (Image 1 No-Burn)?
VOI-LUT
Tags(Yes/No
WC = / /
WC = / /
7 Values Displayed on PACS Viewer (Image 1)?
WW = / /
WC = / /
Additional 8 Values Displayed on PACS Viewer (Image 6)?
Tests WW = / /
Mechanical risk. Be care of collimator collision. Remember to take flat panel phantom off
from collimator befor system power off or reset.
2.) Click [Quality Control Tools] and [Acquisition] sequently to open QAP screen.
1.3 Exposure/Acquisition
select Exposure/Acquisition folder to see the diagnostics item.
1.3.1 Generator
select the Generator folder to see the Generator diagnostic
1.3.1.1 Rotation
select the Rotation in the Generator folder to see the Rotation Function Test, as per the
procedures to finish the diagnostics.
1 2 3 4 5 6 7 8
A 12VDC A
24VDC
12VDC
24VDC
DIRECTION 5429484 -CA-1EN, REVISION 1
B B
220VAC
RS232 Spine USB
Board
C RS232/12VDC
C
Magic PC
(HP Z400)
Display VGA
Collimator
Section 1.0 System Schematics
card
Xray Tube
Grid
Detector
Note: Only
for 575-P
Ion-Chamber
D Monitor D
9DF
Detector housing
E-Stop PS2
E
USB Keyboard
0(WKHUQHW
Mouse
HV+/-
Rotor
Barcode
USB
E Reader E
Hospital
Network
Ethernet
F F
RS232 220VAC
220VAC
AEC1 Hand
57
9 SW
Pwr PDU 380Vac
Ctrl RT
G IF G
JEDI Xray On lamp E-Stop E Power-On
E
Board TM E Reset
(50kW)
6:VLJQDO
Door lock
Hospital Door For electrical scheme with detail Cable
3P Power
Chapter 23 - Schematics and Drawings
1 2 3 4 5 6 7 8
Page 221
SCHEMATICS
Page 222
GE HEALTHCARE
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SCHEMATICS
Page 223 Chapter 23 - - Schematics and Drawings
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5429130ADW_r2.pdf Page 2 of 3
Section 3.0 Cable Assembly
SCHEMATICS DIRECTION 5429484 -CA-1EN, REVISION 1
GE HEALTHCARE
Section 1.0 - System Schematics Page 224
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5429130ADW_r2.pdf Page 3 of 3
SCHEMATICS DIRECTION 5429484 -CA-1EN, REVISION 1
GE HEALTHCARE
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
Chapter 24 Troubleshooting
1.) From the application desktop, click on the Service Tools icon.
2.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now
displayed.
4.) In the left frame, click on the page icon associated with the diagnostic you wish to execute. For
details,refer to Chapter 22 - System Diagnositcs
4.) select the appropriate font family,style, specially the size and press “OK” button. the new font
size for the Chinese input tool will be applied.
Page 226 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
Section 3.0 Positioner Troubleshooting
5 3 4
2 2
5/
GE Title or job number /
10/18/2012
Limit block
Steel rope
SID Adjustment
Chain and
pulley
Chain and
pulley
Brake
Carriage
Slide way Carriage
Limit block
Slide way
Arm 8/
GE Title or job number /
10/18/2012
Detent
U1/U2 Angle
meter
Column
Detent
Page 228 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
Tube Rotation
Detent
Handle
U1 Tube Support
with Handle
Detector Tilting
Emergency Detent
stop switch
Limit Board
Slot for
Grid
Rotation
U-arm shaft
handle
Lock Handle
Patient
barrier
V/H indicator
for Detector
Detector
Grid-in
Ion-chamber Sensor
11 /
GE Title or job number /
10/18/2012
Handle
Lock castor
Page 230 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
With the service key installed, error messages in the system error log area automatically linked to
the enhanced messages. The complete set of enhanced error messages is contained in a single
If you aren’t sure what programming options have been set, or if you want the factory default
settings restored, scan the “Factory Default Settings”.
Page 232 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
that “your “bar code is readable.
2.) If the scanner still can’t read the sample bar codes, scan “All Symbologies”.
5.2 Console
When power is first applied to the console, firmware inside the unit turns ON all of the LEDs for 2
seconds and then turns them OFF (LED ON sequence). If the LEDs don’t turn ON and OFF after
power-up, the console needs to be replaced.
5.3.1 No Picture
• The signal cable should be completely connected to the display card/computer.
• The display card should be completely seated in its slot.
• Check the Vacation Switch should be in the ON position.
• Front Power Switch and computer power switch should be in the ON position.
• Check to make sure that a supported mode has been selected on the display card or system
being used.
• Check the monitor and your display card with respect to compatibility and recommended
settings.
• Check the signal cable connector for bent or pushed-in pins.
• Check the signal input, “INPUT 1” or “INPUT 2”.
5.3.6 LED on monitor is not lit (no green or amber color can be seen)
Power Switch should be in the ON position and power cord should be connected.
5.3.8 No Video
• If no video is present on the screen, turn the Power button off and on again.
• Make certain the computer is not in a power-saving mode (touch the keyboard or mouse).
Page 234 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
Section 7.0 Engineering Toolkit
Problem: There are no software tools available if the PC hangs.
Solution/Workaround: There is a hot-key that will allow you to open an engineering user interface
to help diagnose an issue.
Here is the procedure to access this engineering GUI:
1.) Press <Ctrl>+<Shift>+ <F5>.
2.) The following GUI will popup on the screen your mouse cursor is currently on (Left or Right):
<a> Enter insert mode, the characters typed in will be inserted after the current cursor
position. If you specify a count, all the text that had been inserted will be repeated
that many times.
<i> Enter insert mode, the characters typed in will be inserted before the current cursor
position. If you specify a count, all the text that had been inserted will be repeated
that many times.
<r> Replace one character under the cursor. Specify count to replace a number of
characters
<u> Undo the last change to the file. Typing u again will re-do the change.
<x> Delete character under the cursor. Count specifies how many characters to delete.
The characters will be deleted after the cursor.
Table 24-2
<A> Append at the end of the current line. I Insert from the beginning of a line. O
(letter oh) Enter insert mode in a new line above the current cursor position.
<a> Enter insert mode, the characters typed in will be inserted after the current
cursor position. A count inserts all the text that had been inserted that many
times.
<i> Enter insert mode, the characters typed in will be inserted before the current
cursor position. A count inserts all the text that had been inserted that many
times.
<o> Enter insert mode in a new line below the current cursor position.
The QAP results files and images can be found in the following location:
relay:relay 192.227.61.116 23
Page 236 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
GEHC/CTT Linux 4.3.8
login: insite
Password:
Welcome InSite
Password: 4$xray
/export/home/insite/server/htdocs/suif/iq
[xruser@magic iq]$ cd en
[xruser@magic iqst]$ ls
Table WS
[xruser@magic Table]$ ls
200502280838P_Details.txt
200502280838P_iqst_Bad_Pixel.jpg
200502280838P_iqst_Conversion_Factor.jpg
200502280838P_iqst_Global_BNU.jpg
200502280838P_iqst_Local_BNU.jpg
200502280838P_iqst_Noise_Power_Spectrum.jpg
200502280838P_iqst_Physical_Test.jpg
200502280838P_iqst_Relative_DQE.jpg
200502280838P_iqst_SNR_Non_Unif.jpg
200502280838P_iqst_System_MTF.jpg
200502280838P_IQST.txt
200502280838P_QAP.txt
Image200502280838Pcomposite.img
Image200502280838Pflatfield1.img
Image200502280838Pflatfield2.img
Imagetimestamp
timestamp
Each time the QAP is run, 15 files are created. Three text result files (details.txt, IQST.txt, and
QAP.txt), nine graphical result jpg file types, and three image files (two flat field and one composite).
The only image files retained are for the last two QAP runs.
In addition, there are two time stamp files “timestamp” which documents when the QAP tests ran,
and “Imagetimestamp”, which documents when the last two sets of QAP images were created).
Page 238 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 EMC CONFORMANCE STATEMENT
The equipment comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC standards
for medical devices.
These equipments generate, use, and can radiate radio frequency energy. These
equipments may cause radio frequency interference to other medical and non-
medical devices and radio communications.
To provide reasonable protection against such interference, each product
complies with the radiated emission standard limits as per CISPR11 Group1
Class A standard limits.
However, there is no guarantee that interference will not occur in a particular
installation.
If these equipments are found to cause interference (which may be determined by
turning the equipment on and off), the user (or qualified service personnel) should
attempt to correct the problem by one or more of the following measure(s):
• Reorient or relocate the affected device(s)
• Increase the separation between the equipment and the affected device (see
recommended separation distances)
• Power the equipment from a source different from that of the affected device
• Consult the point of purchase or service representative for further suggestions
Use of accessories, transducers, cables and other parts other than those
specified by the manufacturer of this equipment may result in increased emissions
or decreased immunity of the equipment.
The manufacturer is not responsible for any interference caused by using other
than recommended interconnect cables or by unauthorized changes or
modifications to these equipments. Unauthorized changes or modifications could
void the users' authority to operate the equipment.
All interconnect cables to peripheral devices must be shielded and properly
grounded, except when technologically prohibited. Use of cables not properly
shielded and grounded may result in the equipment causing radio frequency
interference.
Each product is intended for use in non-domestic environments, and not directly
connected to the Public Mains Network that supplies buildings used for domestic
purposes.
The compatible accessories must be used within the recommended operating
conditions outlined in the operation manuals. In addition to calibration and warm-
up, other devices must be reset before and after use to ensure accurate dose
measurements. Sustained exposure to electromagnetic fields (exceeding the test
conditions) may cause false measurements. Failure to follow the recommended
These equipments comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC
standards for medical devices.
Each product is suitable to be used in an electromagnetic environment, as per the
limits & recommendations described in the tables hereafter:
• Emission Compliance level & limits (Table 25-1).
• Immunity Compliance level & recommendations to maintain equipment clinical
utility (see Table 25-2 and Table 25-3).
Note: These systems comply with above mentioned EMC standard when used
with supplied cables.If different cable lengths are required, contact a qualified
service representative for advice.
Voltage dips, short < 5% UT (> 95% dip in UT) 0% UT for 5 sec. Mains power quality should be that of a typical
interruptions and for 0.5 cycle. commercial or hospital environment. If the user
voltage variations on 40% UT , (60% dip in UT) of the system requires continued operation
power supply input for 5 cycles. during power mains interruptions, it is
lines, IEC 61000-4-11 70% UT , (30% dip in UT) recommended that the system be powered from
for 25 cycles. an un-interruptible power supply or a battery.
< 5% UT, (> 95% dip in
UT) for 5 cycles
Power frequency (50/60 3 A/m 3 A/m Power frequency magnetic fields should be at
Hz) magnetic field, levels characteristic of a typical location in a
IEC 61000-4-8 typical commercial or hospital environment.
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,
objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,
AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment
due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which each
product is used exceeds the applicable RF compliance level above, each product should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating each product.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distances between portable and mobile RF communications equipment and products
Each product is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of each product can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and each product as recommended below, according to the maximum output power of the
communications equipment.
Separation distance according to frequency of transmitter m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Rated Maximum Output Power (P)
of Transmitter Watts (W)
These equipments comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC
standard for medical devices and with radio frequency emission requirements per
CISPR11 Group1 Class A standard limits. The system is intended for use in
hospitals.
Do not use devices which intentionally transmit RF Signals (Cellular Phones,
Transceivers, or Radio Controlled Products) in the vicinity of this equipment as it
may cause performance outside the published specifications. Keep the power to
these types of devices turned off when near this equipment.
Adhering to the distance separation recommended in Table 25-4, between 150 kHz
& 2.5 GHz, will reduce disturbances recorded at the image level but may not
eliminate all disturbances. However, when installed and operated as specified
herein, the system will maintain its essential performance including safe X-Ray
acquisition and patient positioning, proper error reporting, and integrity of
patient and image data.
For example, a 1W mobile phone (800 MHz to 2.5 GHz carrier frequency) shall be
put 2.3 meters apart from the system (in order to avoid image interference risks).
These systems comply with above mentioned EMC standard when used with
supplied cables up to maximum lengths referenced in the system Pre-Installation
manual. In order to minimize interference risks, the following requirements shall
apply.
The system should not be used adjacent to or stacked with other equipment; if
adjacent or stacked use is necessary, the system should be tested and verified in
order to ensure normal operation in the configuration in which it will be used.
Consult qualified personnel regarding device/system configurations.
Not applicable.
In order to avoid interference on the system, static field limits from the surrounding
environment are specified.
Static field is specified less than <1 Gauss around the unit.
Users familiar with these concepts can use Integration Statements as an aid to
determine what level of integration this product supports with other systems and
what clinical and operational benefits such integration might provide.
The use of these IHE Integration Statements, by itself, it is not sufficient to ensure
that interoperation will be successful. The user needs to proceed with caution and
ensure that a qualified systems' integration (such as that provided by GE's IT
Professional Services) address at least four issues:
• Integration - The integration of any system into an integrated department or
enterprise requires an analysis of the applications requirements. The design of a
solution that integrates GE systems with non-GE systems is the user's
responsibility and should not be underestimated. Special care should be
exercised in defining the expected workflow, the special conditions, and the
clinical practice to be supported to ensure a safe and effective operation.
• Validation - Testing the complete range of possible interactions between any
GE system and non-GE system, before the integration is declared operational,
should not be overlooked. Therefore, the user should ensure that any non-GE
provider accepts full responsibility for all validation required for their connection
with GE systems. This includes the accuracy of the data once it has crossed the
interface and the stability of the data for the intended applications. Such a
Chapter 26 - Integrating the Healthcare Enterprise (IHE) Integration Statement Page 247
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 IHE
validation is required before any clinical use (diagnosis and/or treatment) is
performed.
• Future Evolution - GE understands that the IHE Technical Framework and the
underlying communication standards will evolve to meet the user's growing
requirements. GE is actively involved in the development of the IHE Technical
Framework and the underlying standards.Such evolutions may require changes to
already installed systems. In addition, GE reserves the right to discontinue or
make changes to product features including those reflected by this IHE Integration
Statement. The user should ensure that any non-GE system that connects with
GE systems also plans for the future evolution of IHE. Failure to do so will likely
result in the loss of function and/or connectivity as the IHE Integration profiles
evolve and GE Products are enhanced to support these changes.
Galaxy
GE Healthcare All
Brivo XR515
This product implements all transactions required in the IHE Technical Framework to support the IHE
Integration Profiles, Actors and Options listed below:
Actors Implemented Options Implemented
Integration Profiles Implemented
DICOM ge.com/dicom