You are on page 1of 31

Document Information for: 5118962INS

Type Drawing Print


Name 5118962INS
Revision 4
State Release
ECO 2060691
Description This is the Eclispe Proteus Collimator user manual, including ope
Originator 305007780_yongtao__tan

File List
1. 5118962INS_s2_r1.pdf
2. 5118962INS_s2_r1.doc
3. 5118962INS_s1_r4.pdf
4. 5118962INS_s1_r4.doc
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Approval Information
See the GEHC Myworkshop System to determine the status of this document.

Person Action Date and Time


305006674_wusheng__yang Approved 06/25/2008 03:28:06 AM GMT
305007780_yongtao__tan Approved 06/24/2008 07:54:55 AM GMT

This page is generated automatically by the GEMS ePDM System


Printed documents are for Reference Only and may be out-of-date.
Check the database to ensure you have the correct revision.

Approved Document - 5118962INS_r4.pdf Page 1 of 31


GE Healthcare

Technical
Publications
Direction 5118962INS
Revision 4
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Eclipse Proteus Collimator


User Manual
See the GEHC Myworkshop System to determine the status of this document.

Copyright ©2005
By General Electric Co.
Service/Operation Documentation

Approved Document - 5118962INS_r4.pdf Page 2 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

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,
Medical Systems 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 everyone 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
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

available from NCRP Publications, 7910 Woodmont Avenue, Room 1016,


Bethesda, Maryland 20814, and of the International Commission on Radiation
Protection, and take adequate steps to protect against injury.

The equipment is sold with the understanding that the General Electric
Medical Systems, its agents, and representatives have no responsibility for
injury or damage which may result from improper use of the equipment.
Various protective material and devices are available. It is urged that such
materials or devices be used.
See the GEHC Myworkshop System to determine the status of this document.

CAUTION United States Federal law restricts this device to be used by or on the
order of a physician.

1
Approved Document - 5118962INS_r4.pdf Page 3 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

REGULATORY REQUIREMENTS

This product complies with the regulatory requirements of the following:

• FDA 21CFR (1020.30; 1020.31)


• UL 60601-1
• CSA C-22.2 No.601.1
• EN 60601-1
• IEC 601-1-2 ed 2 (EMC)
• IEC 601-1-3
• IEC 601-2-28

The following equipment classifications are applicable to the


product:
• Equipment classification with respect to protection from electric shock: Class 1
• Degree of protection from electric shock: Type B
• Equipment not suitable for use in the presence of a flammable anesthetic mixture
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

with air or with nitrous oxide;


• Mode of operation: Continuous with intermittent loading

Manufacturer:

GE Hualun Medical Systems Co. Ltd


No. 1, Yong Chang North Road, Economic & Technology Development Zone,
Beijing, PR China 100176

Place of Manufacturing:
Made in China
See the GEHC Myworkshop System to determine the status of this document.

The circuit diagrams, component part and calibration instruments


will be offered by supplier if there is a request

Approved Document - 5118962INS_r4.pdf Page 4 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

SAFETY
• THIS MANUAL IS AVAILABLE IN ENGLISH ONLY.
WARNING • IF A CUSTOMER OR ITS SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICE.
• FOR CONTINUED SAFE USE AND SERVICE OF THIS EQUIPMENT, FOLLOW
THE INSTRUCTIONS CONTAINED IN THIS SERVICE AND OPERATING MANUAL.
STUDY THIS MANUAL CAREFULLY BEFORE USING AND SERVICING THE
EQUIPMENT AND KEEP IT AT HAND FOR QUICK REFERENCE.
• THE COLLIMATOR MUST BE OPERATED BY QUALIFIED PERSONNEL AND
ONLY AFTER SUFFICIENT TRAINING.
• UNITED STATES FEDERAL LAW RESTRICTS THIS DEVICE TO USE BY OR ON
THE ORDER OF A PHYSICIAN.
• IF ANY SAFETY PROBLEM OCCUR, PLEASE STOP USING THIS DEVICE AND
CONTACT OUR SERVICE AT ONCE.
• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

PROVIDER, OPERATOR OR PATIANT FROM ELECTRIC SHOCK,MECHANICAL


OR OTHER HAZARDS
• TO AVOID ENVIRONMENTAL DAMAGE AND/ OR PERSONAL INJURY, DISPOSE
AND HANDLE THE COMPONENT ACCORDING TO THE LOCAL GOVERNMENT
REGULATIONS AND NATIONAL INDUSTRY STANDARDS
• EQUIPMENT SHALL NOT BE USED IN THE PRESENCE OF A FLAMMABLE
ANAESTHETIC MIXTURE WITH AIR OR WITH NITROUS OXIDE;

• ALWAYS BE ALERT TO SAFETY WHEN YOU OPERATE THIS EQUIPMENT. YOU


CAUTION MUST BE FAMILIAR ENOUGH WITH THE EQUIPMENT TO RECOGNIZE ANY
MALFUNCTIONS THAT CAN BE A HAZARD. IF A MALFUNCTION OCCURS OR A
SAFETY PROBLEM IS KNOWN TO EXIST, DO NOT USE THIS EQUIPMENT
See the GEHC Myworkshop System to determine the status of this document.

UNTIL QUALIFIED PERSONNEL CORRECT THE PROBLEM.


• ALWAYS HANDLE THE COLLIMATOR WITH CARE. ALWAYS USE THE
ORIGINAL PACKING WITH THE TRANSPORTATION SAFEGUARDS.

• DO NOT SCRATCH THE OUTPUT WINDOW.

• ONLY APPLY A POWER SUPPLY ON THE COLLIMATOR ACCORDING TO THE


TECHNICAL DESCRIPTION.

• SWITCH OFF THE POWER SUPPLY BEFORE TOUCHING CONNECTORS.

• DO NOT DRILL ANY ADDITIONAL HOLES IN THE COLLIMATOR.

3
Approved Document - 5118962INS_r4.pdf Page 5 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

REVISION HISTORY

REV DATE TYPE OF MODIFICATION

1 Sep 02, 2005 Creation of the document


2 Nov 02,2006 Correct laser set P/N
Change FRU from lamp subassembly to lamp
Update lamp exchange procedure
Add electrical board diagnosis
3 Dec 25,2007 Add 2383799 (Tube Flange), 5126970 (Tube Flange for Rad14) as
FRU
4 Jun 25 Add Al plate removable option
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 - 5118962INS_r4.pdf Page 6 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

TABLE OF CONTENTS
1. Introduction ........................................................................................................................................... 6
2. Collimator Description ......................................................................................................................... 6
3. Symbols ................................................................................................................................................... 6
3.1 Special Notices ............................................................................................................................... 6
3.2 Electrical Type ................................................................................................................................ 7
3.3 Ground ............................................................................................................................................ 7
3.4 Eclipse Proteus Collimator ........................................................................................................... 7
3.5 Laser Warning Label ...................................................................................................................... 7
3.6 Collimator Rating Plate.................................................................................................................. 8
4. Installation ............................................................................................................................................. 9
5. Operation .............................................................................................................................................. 12
5.1 Control Panel ................................................................................................................................ 12
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

5.2 Collimator Display ........................................................................................................................ 13


5.3 Bottom view of collimator ........................................................................................................... 13
5.4 Rotating the collimator ± 90° around the vertical axis ............................................................. 15
6. Maintanance ........................................................................................................................................ 15
6.1 Cleaning ........................................................................................................................................ 15
6.2 Periodic Maintanance .................................................................................................................. 15
6.3 FRU definition ............................................................................................................................... 15
6.4 FRU replace procedure................................................................................................................ 15
6.4.1 Replace whole collimator .................................................................................................................. 16
See the GEHC Myworkshop System to determine the status of this document.

6.4.2 Replace collimator control board .................................................................................................... 16


6.4.3 Replace collimator user interface board........................................................................................ 17
6.4.4 Replace collimator lamp .................................................................................................................... 18
6.4.5 Replace collimator bucky centering light...................................................................................... 20
6.4.6 Replace collimator LCD display....................................................................................................... 21
6.4.7 Replace collimator tape...................................................................................................................... 21
7. Error Summary.................................................................................................................................... 22
8. Repairing and Recycling .................................................................................................................... 23
9. Disposal ................................................................................................................................................. 23
10. Specifications .............................................................................................................................. 23
Appendix A: Cable Connection ................................................................................................................. 24
Appendix B: Electric interface between collimator and system .......................................................... 25

5
Approved Document - 5118962INS_r4.pdf Page 7 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

1. Introduction
This document describes how to install Eclipse Proteus collimator (GE part No.: 2379827) on Proteus
system, operate the collimator and replace the FRUs of Eclipse Proteus collimator.

2. Collimator Description
• Easy mounting on the tube flange
• Symmetric rectangular collimation
• Light to indicate exposure area
• Laser bucky light guarantees a sharp line light for all SIDs
• Large LCD display of the current SID and field size either in cm or inch
• CAN-Bus data interface
• Automatic SID-tracking
• Lead cone close to the source to shield off-focal radiation
• Simple rotating of the collimator at the tube (±90°) by means of a swiveling flange with stop in 0°
position
• Source image distance check by means of a measuring tape
• Manual operation via an user interface panel
• Two accessory rails
• This collimator is compatible with the following X-ray tubes or cones or DAP assemblies:
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Max 100
Varian Rad 21
Varian Rad 14
• Sinus Cone (GE part no. 2368910) could be used in this collimator by insert in the accessory rails
• PTW DAP could be incorporated inside the collimator

3. Symbols
Symbols used on this system and in its accompanying documents are shown and explained in this
section.

3.1 Special Notices


See the GEHC Myworkshop System to determine the status of this document.

Caution advises of an avoidable condition that could cause minor


CAUTION physical injury, or damage to equipment or data.

Warning advises of an avoidable condition that may allow or cause a


WARNING personal injury or the catastrophic destruction of equipment or data.

This symbol on the equipment means that the operating instructions


should be consulted to assure safe operation.

Approved Document - 5118962INS_r4.pdf Page 8 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

3.2 Electrical Type

Type B Equipment. Equipment providing a particular degree of protection


against electrical shock regarding leakage current and protective
grounding per IEC 601-1.

3.3 Ground

Functional Earth (ground) Terminal. Terminal directly connected to a


point of a measuring supply or control circuit or to a screening part which
is intended to be earthen for functional purposes.

Protective Earth (ground). Identifies any terminal that is intended for


connection of an external protective conductor to protect against
electrical shock in case of a fault.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

3.4 Eclipse Proteus Collimator

Control for indicating radiation field by using light and aligning the bucky

3.5 Laser Warning Label

注 意
激光辐射, 请勿直视
See the GEHC Myworkshop System to determine the status of this document.

最大输出功率 1mw
波 长 540~700nm
II 类激光产品

Figure 1 Laser Warning Label

7
Approved Document - 5118962INS_r4.pdf Page 9 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Figure 2 Laser Warning Label Location

3.6 Collimator Rating Plate


THE LABEL FOR THE ECLIPSE PROTEUS COLLIMATOR IS FOUND ON THE BACK PANEL
OF THE COLLIMATOR. THIS LABEL INCLUDES THE ETL MARK FOR THE COLLIMATOR.
SEE THE FOLLOWING SKETCH.
See the GEHC Myworkshop System to determine the status of this document.

Collimator
rating plate
System cable
Collimator ETL
certificate

Collimator cable
connector
Figure 3 Rear View of Collimator

Approved Document - 5118962INS_r4.pdf Page 10 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

4. Installation
Note: Only qualified personnel is permitted to unpack and install the collimator unit.

The collimator is designed for a focus flange distance of 80mm

Note: Before collimator is mounted, make sure one of the following flange (there are V notches along the
edge) is mounted on tube
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Figure 4 Collimator Flange for Max100 Figure 5 Collimator Flange for Rad 21 and Rad 14

Note: If the one of the following flange (there are U notches along the edge) is mounted on tube, remove
this one first, mount the related flange on tube.
See the GEHC Myworkshop System to determine the status of this document.

Previous Collimator Flange for Max100 Previous Collimator Flange for Rad 14, 21

The procedure to mount the tube flange is refered to Charpter 2 (mount the collimator) , Proteus Service
Manual (Direction 2273022-100).

Note: For MX100 X-ray tube, if the X-ray field and light field of Collimator are not aligned after mounting,
the performing of Job Card IST 032 “MX100 X-ray tube-Collimator Interface Plate Alignment” in Chapter
3, Proteus Service Manual (Direction 2273022-100), can calibrate and ensure the alignment of X-ray
field and light field of Collimator.

9
Approved Document - 5118962INS_r4.pdf Page 11 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Mounting Collimator
3 2

4
1
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Figure 6 Collimator Top View

Note: Before mounting the collimator, Be sure the collimator mounting flange is well
mounted on the tube.
Note: If the tube type is Rad14 or 21, mount the collimator on corresponding flange directly.
Note: If tube type is Max100, and the replaced collimator is Siemens unit, remove the lead
cup on tube side before new collimator installation
• Loosen the screw (1/ figure 6,), put the two clamps outwards to the max opening position.
• Put the Locking Tongue (3/figure 6) inside the holder
• Position the collimator on the X-ray tube.
Note: Be sure the Locking Tongue (3/figure 6) is inside the holder.
See the GEHC Myworkshop System to determine the status of this document.

Note: Apply grease supplied to collimator mount flange, the tube/collimator interface plate and
locking tongue (see picture below) for easy movement.

Apply grease on the


Apply grease inside surface of
underneath the adapter and the
flange edge locking tongue

• Put the two clamps closed. Make sure that collimator is properly connected with the flange.
Tighten the screw (1/figure 6) with torque of 5.6 Nm.

10

Approved Document - 5118962INS_r4.pdf Page 12 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

• Loosen the locking screw. Rotate the collimator to the


normal position when a click is heard. Tighten the locking
screw.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

• Turn the X-ray tube back into normal position.

CHECK THAT THE MOUNTING IS CORRECT BEFORE TURNING THE TUBE BACK TO
WARNING NORMAL POSITION.
• Loosen the X-ray tube. Use level gauge to check that the tube and collimator are in level
position, then fasten the tube by using trunion handle securely.
Note: For RAD 21 X-ray tube, there is no trunion handle. Just need to fasten clamp screws.
Apply locktite 242 to mount screws.
See the GEHC Myworkshop System to determine the status of this document.

• Connect the collimator cable (GE part No. 2258383).

• Fix the cable on the strain relief screw with M5 nut


• Mount the cable cover
Note: After measuring HVL of x-ray source, if the HVL is larger than requirement, deinstall
the collimator, remove 1 or 2 pieces of AL plate on the entrance of the collimator. Follow the
above steps to reinstall collimator.

11
Approved Document - 5118962INS_r4.pdf Page 13 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

5. Operation
During operation of the collimator unit ensure that it is not damaged due to collision and adhere to the
temperature range according to the specifications in this manual. Also refer to the safety section in this
manual for additional information regarding the operation of this product.

9 8
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

2
3

5
7 4 7
Figure 7 Collimator Front Panel
See the GEHC Myworkshop System to determine the status of this document.

(1) Locking screw for ±90º of the collimator around the center beam axis. The collimator stops only
in 0° and ±90º position.
(2) Adjusting knob for format height collimation (Turning to the left closes the collimator, turning to
the right opens the collimator)
(3) Adjusting knob for format width collimation (Turning to the left closes the collimator, turning to the
right opens the collimator)
(4) X-ray field illumination (light localizer) and bucky centering light on/off. Cutoff also performed
automatically via a time switch.
(5) Measuring tape grip for SID measurement
- Take reading at bottom edge of collimator.
- The measuring tape has both a cm and an inch graduation
(6) In manual or auto collimator mode, M button for resetting last exposure format used when
current blade width and height are larger than last setting.
(7) Two accessory rails
(8) +,-key: I SID adjusting
- Press “+” key in manual collimator mode,
Collimator SID is set to 100cm, 150cm, and 180cm.
- Press “- “key in manual collimator mode,
Collimator SID is set to 180cm, 150cm, and 100cm.
(9) No use

12

Approved Document - 5118962INS_r4.pdf Page 14 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Note: The light field of the collimator shouldn’t be larger than 17inch × 17inch @ SID=1m (43cm ×
43cm).

If the lamp of the light localizer remains illuminated for a longer


WARNING period of time, the holder may heat up. The maximum acceptable
light on/off ratio is 1 to 1 (one minute on to one minute off)

5.2 Collimator Display


1

2 3

Figure 8 Collimator Display


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

(1) Operating mode:


PBL = with automatic format collimation system
Manual = without automatic format collimation system
(2) Display of width and height of collimated x-ray field
(3) Display of Source-Image Distance (SID)

ELECTROSTATIC DISCHARGE MAY CAUSE THE DISPLAY ON THE FRONT


WARNING OF THE COLLIMATOR TO GO BLANK. THE SYSTEM POWER MUST BE
CYCLED VIA THE CONSOLE ON/OFF SWITCH TO RECOVER.

5.3 Bottom view of collimator


See the GEHC Myworkshop System to determine the status of this document.

On/Off switch for light localizer and Bucky


centering light

Bucky centering light

Centering cross for positioning

Locking spring for accessories


Figure 9 Bottom View of Collimator

Light Localizer

The light localizer is used to indicate the full field of the exposure area on the
cassette or directly on the patient.

13
Approved Document - 5118962INS_r4.pdf Page 15 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

• The light localizer is switched on or off by pushing button (4/figure 7) on the control panel.
- Automatic cut out is also performed via an internal time switch.

• The blade will move a little when switch on or off the light localizer. It’s normal to keep the same
field size of light and x-ray beam.

• The light localizer and Bucky centering light cannot be switched separately.

• Light field dimension check:


- Power on lamp by pushing the button(4/figure 7) on the control panel to make the light field
visible. Use a ruler or tape to measure the height and width of light field.

Centering Cross

The centering cross is used to indicate the longitudinal and transverse center of the
exposure field on the cassette or directly on the patient.
• Centering cross is projected by the light localizer.

Bucky centering light


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

The bucky centering light provides the axis mark for longitudinal centering which is
lined up with the centering mark on the handle of the cassette loading device.

• The bucky centering light, which is a laser beam, is switched on or off together with light localizer
by pushing button (4/figure 7) on the control panel.
- Automatic cutout is also performed via an internal time switch.
LASER Radiation
WARNING Peak power < 1mW / Wave Length 650 nm / Class II LASER Product
Do not stare into beam!
When you switch on the Linear LASER Light Localizer, take care that no
person looks directly into the LASER to avoid eye injuries or impaired
vision.
See the GEHC Myworkshop System to determine the status of this document.

Accessory rails and Locking spring


• The Accessory rails provide a way to insert the compensating filters, template and cone, etc.
To ensure product safety use only accessories with the following
CAUTION specifications:
• Maximum weight: 7 kg
• Plug-in metrics: width 177.5-0,5 mm
depth 177.5-0,5 mm
• The locking spring locks the inserted accessory in place to prevent them from falling out
• To remove an accessory from the collimator, the locking spring must be pressed in before the
compensating filter, templates etc., can be removed.
When applying the accessories such as compensating filters, templates
CAUTION and cone, please pay attention to ensure the accessories to be supported
securely and reliably by the accessory rails.
Otherwise, the incorrect and unsafe insertion of the accessories may result
in the falling down and lead to possible injure to the human body or
instruments.

14

Approved Document - 5118962INS_r4.pdf Page 16 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

5.4 Rotating the collimator ± 90° around the vertical axis


• Loosen the locking screw (1/figure 7) on the collimator to release the 0° lock-in position of the
collimator.
• The max rotated angle of collimator is ± 90°
• Grasp the collimator with both hands and rotate it by the desired angle to the required direction.

Rotating the collimator to the 0° lock-in position


• Grasp collimator with both hands and turn it to the 0° lock-in position.
• Tighten the locking screw (1/figure 7) on the collimator

Always grasp the collimator in such a way that hand can be neither pinched
WARNING
nor crushed between the collimator and other parts of the system.

6. Maintanance

The collimator contains no user serviceable components. Do not attempt to


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

WARNING disable these components or remove any trim covers. Refer service to
qualified service personnel.

6.1 Cleaning
This equipment should be cleaned frequently. Using a clean cloth moistened slightly with a
good mild cleaner to clean the surfaces of the equipment. Do not use cleaners or solvents of
any kind as they may dull the finish or blur the lettering.

6.2 Periodic Maintanance


No periodic maintenance, calibration is needed for this equipment.

6.3 FRU definition


See the GEHC Myworkshop System to determine the status of this document.

1) Whole collimator 2379827


2) Collimator control board 2383312
3) Collimator user interface board 2383313
4) Collimator lamp 2377082
5) Collimator bucky centering laser 2383804
6) LCD display 2385357
7) Collimator tape 2383805
8) Tube Flange 2383799
9) Tube Flange for Rad14 5126970
Note: When replace Failed Siemens collimator with 2379827, please order a tube flange
(2383799 for Max100 or 5126970 for Rad14) together with new collimator.

6.4 FRU replace procedure

Before replace the FRU, make sure the collimator is powered off, otherwise
WARNING it may result in injury to the service provider from electric shock or other
hazards, or damage to the collimator.

15
Approved Document - 5118962INS_r4.pdf Page 17 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

6.4.1 Replace whole collimator

6.4.1.1 Replace the Siemens collimator AL10F


• Dismount the defective collimator from the tube
• Dismount the old flange from tube
• Mount the new flange. The procedure to mount the tube flange is refered to Charpter 2, Proteus
Service Manual (Direction 2273022-100)
• Mount the new collimator on tube flange. Refer to chapter 4, Collimator installation

6.4.1.2 Replace the Eclipse collimator


• Dismount the defective collimator from the tube
• Mount the new collimator on tube flange. Refer to chapter 4, Collimator installation

6.4.2 Replace collimator control board


6.4.2.1 Removing the defective control board
• Open the collimator front cover by loosening the 2 screws, one is on the top of the collimator,
the other is at the bottom.

User interface board Control board


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.

Figure 10 Collimator Electrical Boards

• Unplug all the cables of the control board

16

Approved Document - 5118962INS_r4.pdf Page 18 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Figure 11 Collimator Control Board


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

• Loosen the 4 screws which are used to fix the control board
6.4.2.2 Mounting the new control board
• Mount the new control board with the 4 screws
• Reconnect all the cables
• Close the front cover and fix the 2 screws

6.4.3 Replace collimator user interface board

6.4.3.1 Removing the defective user interface board


• Open the collimator front cover by loosening the 2 screws, one is on the top of the collimator,
the other is at the bottom.
• Unplug all the cables of the user interface board
See the GEHC Myworkshop System to determine the status of this document.

• Unhook the front cover and put it down

17
Approved Document - 5118962INS_r4.pdf Page 19 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Figure 12 Collimator User Interface Board


• Remove the knob on front panel
Loosen the screws from the knob hole

Figure 13 Collimator Control Knob

Take off the knobs


Using an 11 mm hex wrench, remove the securing nuts on the encoder shafts and take
off the snap rings.
• Loosen the 4 screws which are used to fix the user interface board
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

6.4.3.2 Mounting the new user interface board


• Remove the securing nuts and snap rings from the encoders shaft on the new user interface
board.
• Mount the new user interface board with the 4 screws
• Mount the securing nuts and snap rings on the new user interface board
• Place the knobs on the encoder shafts and secure them using the 1.5 Allen wrench. When
the knobs are turned, they must not scratch against the front panel.
• Install the front cover on collimator
• Reconnect all the cables
• Close the front cover and fix the 2 screws

6.4.4 Replace collimator lamp


See the GEHC Myworkshop System to determine the status of this document.

Only the lamp offered by GEHL with the holder can be used as
WARNING replaced part. Otherwise it may cause issue of light illuminance,
edge contrast or light/x-ray field alignment.

6.4.4.1 Removing the defective lamp


• Move the collimator right cover (1/figure14 ) and the shielding for lamp mounting hole
(2/figure14 ).

18

Approved Document - 5118962INS_r4.pdf Page 20 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

1
Figure 14 Collimator Lamp Exchange Cover

• Unplug the connector of the lamp

If the lamp of the light localizer remains illuminated for a longer


WARNING
period of time, the holder may heat up. Wait for lamp to cool to avoid
skin burns.


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Loosen 2 mouning screws of the lamp assembly from the hole on rear side of the collimator
and remove the defective lamp assembly from the right side of the collimator, see Figure15.

Lamp exchange Hole


See the GEHC Myworkshop System to determine the status of this document.

Figure 15 Collimator Lamp Exchange


• Loosen 4 screws of lamp support, take out the failed lamp. See Figure 16.

19
Approved Document - 5118962INS_r4.pdf Page 21 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Figure 16 Lamp Exchage

6.4.4.2 Mounting the new lamp assembly


• Mount the new lamp into lamp support.
• Mount the new lamp assembly on collimator
• Reconnect the connector of the lamp
• Mount the right cover of the collimator and the shielding for lamp mounting hole
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

To avoid damage the lamp, do not touch the bulb or inside of the reflector
CAUTION with bare hands.
See the GEHC Myworkshop System to determine the status of this document.

6.4.5 Replace collimator bucky centering light

20

Approved Document - 5118962INS_r4.pdf Page 22 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Figure 17 Collimator Bucky Centering Light Mounting


6.4.5.1 Removing the defective bucky centering laser equipment
• Open the collimator front cover.
• Unplug the connector (1/figure 17) of bucky centering laser equipment
• Loosening the mounting screws, Remove the laser equipment (2/figure 17) from the laser
support
6.4.5.2 Mounting the new bucky centering laser equipment
• Insert the laser equipment into the support, fix the screw
• Reconnect the connector to user interface board
6.4.5.3 Align the laser beam with light field
• Power on the collimator
• Set SID=1m, FOV=200mmX200mm
• Verify if laser line is at the transverse center of the light field
• Adjust 2 mounting screws until the laser beam deviation to the center of the light field < 2mm
• Close the front cover and fix it with the 2 screws
6.4.6 Replace collimator LCD display
6.4.6.1 Removing the defective LCD display
• Open the collimator front cover.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

• Remove the user interface board, referring to 6.2.3.1. The LCD display is now visible.
• Loosen the 4 screws which are used to fix the LCD module
See the GEHC Myworkshop System to determine the status of this document.

Figure 18 Collimator LCD Module

6.4.6.2 Mounting the new LCD display


• Mount the new LCD module with the 4 screws
• Mount the user interface board, referring to 6.2.3.2
• Reconnect all the plugs
• Close the front cover and fix the 2 screws

6.4.7 Replace collimator tape


• Open the collimator front cover
• Remove the defective tape from the tape holder
• Put the new tape in the holder

21
Approved Document - 5118962INS_r4.pdf Page 23 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

• Close the front cover with the 2 screws

Figure 19 Collimator Tape


State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

7. Error Summary
Next table lists the summary of the errors handled in the collimator software.

Error Code Description Recommended Reactions


Z00 Collimator UIF board error Restart system; if fail again, Change UIF board (FRU 2383313)
Z01 Collimator Control Board error Restart system; if fail again, Change control board(FRU
2383312)
Z02 Collimator Control board error Dismiss the error, check the local connection cable
Z03 Collimator UIF Error Dismiss the error, check the local connection cable
Z04 Collimator local Check the local connection cable, then restart system; if still fail,
communication error change the boards(FRU 2383312,2383313)
Z05 Collimator LCD error Change the LCD (FRU 2385357)
See the GEHC Myworkshop System to determine the status of this document.

Z06 Collimator Blade out of limit Restart the system.


Z10 Collimator internal error Reset collimator; if fail again, change collimator (FRU 2379827)
Z11 Collimator internal error Reset collimator; if fail again, change collimator (FRU 2379827)
Z14 Collimator Homing Error Reset collimator; if fail again, change collimator (FRU 2379827)

If the lamp cannot be switched on when push the lamp button on front panel, refer to the following
trouble shooting.
1. Open the collimator front cover, assure stable cable connection on J4, J7 and J8 of user interface board.
2. Push ‘lamp’ button to light on lamp. Check the LED indicator status (DS7, DS10, DS13), as shown in
Figure 20

Indicator
Error Recommended Reactions
DS13 DS10 DS7
on - - Lamp failure Exchange lamp (FRU 2377082)
off on on UIF board failure Exchange lamp (FRU 2377082)
off off - System lamp power failure Check power supply unit on system side
Exchange UIF board; if failure remains, change whole
off - off UIF board or UIF panel failure
collimator (FRU 2379827)

22

Approved Document - 5118962INS_r4.pdf Page 24 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

DS7

J8

J7

DS13

J4
DS10
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Figure 20 Collimator User Interface Board

8. Repairing and Recycling


In the interest of complying with legal requirements concerning the environmental compatibility of our
products (protection of natural resources, avoidance of waste) we endeavor to reuse parts and to return
them to the production cycle. The failed components could be returned to GE Hualun Medical systems. We
guarantee the functioning, quality and life of these parts by taking extensive quality assurance measures,
just as for factory-new components.

9. Disposal
Lead is used in Eclipse Proteus collimator as blade material.
To avoid environmental damage and/ or personal injury, dispose and handle the component according to
See the GEHC Myworkshop System to determine the status of this document.

the local government regulations and national industry standards.

10. Specifications

Description Specification
Dimensions (L x W x H) [mm] 330 x 210 x 180
Weight [kg] 10 ± 0.5
Angle of rotation around central beam axis [°] ± 90
Maximum FOV [cm] @ SID = 100cm 50 x 50
Minimum FOV [cm] @ SID = 180cm 4.5 x 4.5
Power supply: DC input voltage [V] 24 ± 10%
Max. DC input current [A] 2
AC input voltage [V] 37 ± 10%
Max. AC input current [A] 7
Lamp type Philips 12999: 12v, 50W

23
Approved Document - 5118962INS_r4.pdf Page 25 of 31
ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Temperature: Operation [°C] 5 ≤ T ≤ 40


Transport and storage [°C] -40 ≤ T ≤ 70
Humidity: Operation [%] 10 ≤ T ≤ 90, non-condensing
Storage [%] 5 ≤ T ≤ 95, non-condensing
Pressure: Operation [hPa] 650≤ T ≤ 1013
Storage [hPa] 525 ≤ T ≤ 1013
Total filtration >=1.5 mm Al at 100 kV
Leakage radiation (150kV, 4mA) <0.5 mGy/ h
Rectangular blade positioning accuracy ±2mm@SID=1m
Rectangular blade positioning repeatability ±1mm@SID=1m
FOV accuracy ±5mm@SID=1m
Tape display accuracy ±5mm@SID=1m

Appendix A: Cable Connection


Eclipse Proteus Collimator Interconnection
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Panel LCD
Collimator mechanics
W105

W106

From system Bucky


0 W107
W11
laser
W001 X1 W1
11
User I/F board
W108
Light unit
Rectangular
Blade unit
See the GEHC Myworkshop System to determine the status of this document.

W109

Interconnection

W101
board

W103 W101

Control board
W102
W104
W102

Sub-System motor Mechanics conn. System conn. Board


Sub-System optical sensor Electrical&user I/F conn. X1 System connector Cable

24

Approved Document - 5118962INS_r4.pdf Page 26 of 31


ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS

Appendix B: Electric interface between collimator and system


Eclipse Proteus collimator is connected to system with system connector. Signal definition as below,
includes CAN bus for communication and 3 power supply input: 12VDC ± 10% with a maximum current of
150 mA for the CAN interface, 24VDC ± 10% with a maximum current of 2A for collimator motor and 37
VAC ± 10% with a maximum current of 10A for the light localizer.

Pin Connection Signal


pin 1 Power supply motor +24VDC
pin 2 Power supply motor 0VDC
pin 3 Ground Ground
pin 4 N.C. N.A.
pin 5 CAN Data NEG CAN
pin 6 CAN Data POS CAN
pin 7 Power supply light +37VAC
pin 8 Ground Ground
pin 9 N.C. N.A.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

pin 10 N.C. N.A.


pin 11 Power supply light 0VAC
pin 12 Ground Ground
pin 13 Power supply CAN 0VDC
pin 14 Power supply CAN +12VDC
pin 15 N.C. N.A.
pin 16 Ground Ground
See the GEHC Myworkshop System to determine the status of this document.

25
Approved Document - 5118962INS_r4.pdf Page 27 of 31
DOC0328014, rev 1

g GE Healthcare China Beijing

High Impact Inspection Log for Design review


This Template can be used to formally document Reviews of: Requirements Specifications, Verification Plans and Procedures, Validation Plans and procedures, Hardware Design, Software design, SEEA, FMEA, FTA,etc…

Review Information:
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Review Topic: Eclipse Proteus Collimator User Manual Review

Workproduct Name: Eclipse Proteus Program / Project: Eclipse Proeus


Author: Tan Yongtao
Facilitator: Log Return Date: Dec 25, 2007
Original Revision: Rev 3, ver 1 Log Return Yongtao.tan@geahk.ge.com
Location:
After Review Revision: Rev 3, ver 2 Review Date:
Workproduct Beijing Review Location:
Location:
See the GEHC Myworkshop System to determine the status of this document.

List of Mandatory Reviewers ( To be filled before the review. Minimum 2 reviewers, including 1 independent reviewer):
Role: Name: Function: Signature
Optional if reviewer accepted as is or w/conditions or if
reviewer signs final document.
Mandatory for all other cases
Independent Lin Mei Application Specialist
Reviewer:

Independent Zhao Shiming Service Engineer


Reviewer:

Note: All the signature will be done on ePDM.

Page 1 of 4
Approved Document - 5118962INS_r4.pdf Page 28 of 31
DOC0328014, rev 1

g GE Healthcare China Beijing

Defect Logs:
Reviewers Finding Classifications Author Resolution Codes
D - Major Defect. The content of the Workproduct is faulty or wrong. F – Fix. The author acknowledges the defect and intends to execute the
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

actions described in Author’s Intended Actions to fix the defect.


I - Issue. The content of the Workproduct is unclear or may be missing material. S – SPR. The finding has been escalated and will be resolved through the
SPR process. Put SPR number in Author’s Intended Actions.
T - Trivial Defect. A defect needing no discussion such as misspellings, cut-paste errors, etc. ? – Discuss. The author wishes to discuss the finding at the review
meeting prior to assigning a resolution code.
E – Enhancement. The content of the Workproduct is acceptable, but the reviewer sees room for D – Duplicate. The finding is a duplicate of a previous finding.
improvement.
N - No Action. No action is required to resolve the finding.
4 – Closed. Accepted by all reviewers for implementation, (if applicable).
Location Convention:

# Initials Location Findings Finding Author’s Intended Action Res


See the GEHC Myworkshop System to determine the status of this document.

Class Code 4
1 ZSM overall Ensure all FRU parts your defined should be E Yes, all the FRUs are orderable and have been N
ordered stored in warehouse
2 ZSM overall Identify the items for PM(Planned maintenance E Has been mentioned in section 6.2 N
3 ZSM Page 22 Trouble shooting items which is related with the E Added in section 7 F
error code and FRU part

Reviewer Summary (to be filled by reviewers and compiled by the author):

Returned Attended Recommendation


Log? Meeting? (mark with an X, See definitions below)
Reviewer Name Initials (Yes, No) (Yes, No) Accept Accept With Accept With Revise and Re-
As Is Conditions Verification Inspect
Zhao Shiming ZSM Y N X
Lin Mei LM N N X

following sheets to be filled out by Author

Page 2 of 4
Approved Document - 5118962INS_r4.pdf Page 29 of 31
DOC0328014, rev 1

g GE Healthcare China Beijing

Consolidated Review Recommendation: (To be completed after Review Meeting. Mark with an X)

X Accept As Is - No changes needed, no verification needed, review is complete


Accept With Conditions - Fix the defects, no verification needed
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

Accept With Verification - Fix the defects, one or more reviewers have requested to review the reworked document
Revise And Re-inspect - Fix the defects and repeat review process (ie. re-review)

SPR Summary (List SPR Numbers used as resolution actions, if not applicable, mark NA.):

SPR’s Generated from Escalation of Review Defects (Resolution Code = S).


SPR ID SPR headline
NA
See the GEHC Myworkshop System to determine the status of this document.

Review Log Instructions


1. Author Prepares the Review Package and Notification:
Fill in the Workproduct and review meeting information required in the Review Information section.
Identify the required reviewers and place their names and titles in the List of Mandatory Reviewers section.
Specify a location identification convention for findings on the Defect Log page.
Place the Workproduct under review in the location indicated in the Review Information section. The Original Revision need to be archived.
Notify reviewers and provide them with a copy of the prepared review log. Retain a master copy of the review log for consolidation and metrics collection.
2. Reviewer Response
Review the Workproduct.
Log findings in the Review Log prepared by the Author. Use the convention specified by the Author to give location information.
For each finding enter your initials, location of finding, description of the finding, and classification of finding (in accordance with definitions given in the table).
Record review resolution recommendation in Reviewer Summary table, according to definitions given in the Consolidated Review Recommendation table.
Record the time you spent reviewing the Workproduct and filling in the review log in the Reviewer Summary table.
Return an electronic copy of the review log to the author by the date and to the location given in the Review Information section.
3. Author Consolidates Review Logs
Consolidate all of the returned review log findings into one Defect Log. Sort the consolidated log by finding location.
Consolidate all of the returned review log Review Summary sections into one table.
Evaluate each finding and record your intended actions in the Author’s Intended Action column.

Page 3 of 4
Approved Document - 5118962INS_r4.pdf Page 30 of 31
DOC0328014, rev 1

g GE Healthcare China Beijing


Assign an applicable Resolution Code according to definitions given in the Table heading
Distribute a copy of the consolidated Review Log to the reviewers prior to the Review Meeting.
4. Review Meeting. (The purpose of the review meeting is to determine if the Author’s Intended Actions for each finding is adequate. )
A facilitator leads in systematically reviewing each finding to ensure there is consensus on finding classification, adequacy of Author’s intended action, and
resolution code. A 4 column is provided to indicate that Intended actions are agreed. It is recommended that findings marked with a ? code be addressed first.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.

At the end of the review meeting, the facilitator leads the team in determining a consolidated review recommendation, according to definitions given the table.
5. Review Resolution
The Author records the consolidated review recommendation in the Consolidated Review Recommendation section.
The Author updates finding classification, author’s intended actions, and resolution codes in the consolidated review log per the results of the review meeting. All
findings given a ? - Discuss resolution code prior to the review meeting shall be given a final resolution code.
The Author reworks the Workproduct per the Author’s Intended Actions.
The Author updates the consolidated review log to indicate completion of action items.
The Author distributes the reworked Workproduct to those reviewers that requested to verify the reworked Workproduct.
The Author makes a hard copy of the completed consolidated review log and obtains signatures of reviewers who requested verification.
If resolution of any review finding exceeds two weeks after the review meeting, the unresolved findings shall be escalated by converting them into SPRs. Record
the SPR number in the Author’s Intended Action and assign an SPR resolution code to each escalated finding. The review may be closed after all unresolved
findings have been escalated to SPR’s.
When all findings are resolved, the Author gets the approval of final Workproduct (if required) and archives final Workproduct, along with this HII file.
See the GEHC Myworkshop System to determine the status of this document.

6. Defects Found in Other Workproducts


If a finding reveals a defect in a Workproduct other than the Workproduct under review, the finding shall be resolved by converting it into an SPR. Record the
SPR number in the Author’s Intended Action and assign an SPR resolution code to the finding.

Page 4 of 4
Approved Document - 5118962INS_r4.pdf Page 31 of 31

You might also like