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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.
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Technical
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Direction 5118962INS
Revision 4
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
Copyright ©2005
By General Electric Co.
Service/Operation Documentation
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.
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.
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
REGULATORY REQUIREMENTS
Manufacturer:
Place of Manufacturing:
Made in China
See the GEHC Myworkshop System to determine the status of this document.
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.
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
REVISION HISTORY
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.
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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.
3.3 Ground
Control for indicating radiation field by using light and aligning the bucky
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
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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.
Collimator
rating plate
System cable
Collimator ETL
certificate
Collimator cable
connector
Figure 3 Rear View of Collimator
4. Installation
Note: Only qualified personnel is permitted to unpack and install the collimator unit.
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.
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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.
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.
• 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
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.
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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
Note: The light field of the collimator shouldn’t be larger than 17inch × 17inch @ SID=1m (43cm ×
43cm).
2 3
Light Localizer
The light localizer is used to indicate the full field of the exposure area on the
cassette or directly on the patient.
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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.
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.
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.
14
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
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.
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.
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GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
16
• 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
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
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.
18
1
Figure 14 Collimator Lamp Exchange Cover
•
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.
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
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.
20
• 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.
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
7. Error Summary
Next table lists the summary of the errors handled in the collimator software.
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
DS7
J8
J7
DS13
J4
DS10
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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.
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
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ECLIPSE PROTEUS Collimator
GE Healthcare User Manual
REV 4 DIRECTION 5118962INS
Panel LCD
Collimator mechanics
W105
W106
W109
Interconnection
W101
board
W103 W101
Control board
W102
W104
W102
24
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DOC0328014, rev 1
Review Information:
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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:
Page 1 of 4
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DOC0328014, rev 1
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.
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
Page 2 of 4
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DOC0328014, rev 1
Consolidated Review Recommendation: (To be completed after Review Meeting. Mark with an X)
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.):
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DOC0328014, rev 1
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.
Page 4 of 4
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