Agfa CR75, CR85 Digitizer - Service Manual
Agfa CR75, CR85 Digitizer - Service Manual
Agfa CR75, CR85 Digitizer - Service Manual
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
2nd Edition
CR 85-X CR 75.0
Type 5148/100 Type 5146/105
(as of SN ≥ 6000)
CONFIDENTIALITY NOTE:
Use, dissemination, distribution or reproduction of this document by unauthorized personnel is not permitted and may be unlawful.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
► Manufacturer
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
► Document History
► Chapter Overview
Chapter
Order List
0
About this Manual
2 Functional Description
6 Accessories
7 Field Modifications
9 Maintenance
10 Service Bulletins
11 Installation Planning 1 2 3
12 Glossary
► Explanation of notes
► Conventions
IMPORTANT:
The 2nd Edition of the Service Documentation for
CR 85-X Type 5148/100 and CR 75.0 Type 5146/105 , DD+DIS378.05E is valid for:
• CR 85-X – Type 5148/100
• CR 75.0 – Type 5146/105 (as of SN ≥ 6000)
Explanation:
The improved detector unit (light guide and photomultiplier) from CR 85-X Type
5148/100 is integrated in CR 75.0 and hence the new subtype CR 75.0 Type
5146/105 has been created.
The improvement is not available for:
• ADC Compact Plus Type 5146/100
• CR 75.0 Type 5146/101
• Centricity CR MP3510 Type 5146/200 and 201
The Digitizer CR 75.0 Type 5146/105 has been introduced in production and can be
distinguished from ADC Compact Plus Type 5146/100, CR 75.0 Type 5146/101 and
Centricity CR MP3510 Type 5146/200 and 201 by the type label:
• Type: 5146/105
• Serial Number SN: ≥ 6000
For the ADC Compact Plus Type 5146/100, CR 75.0 Type 5146/101 and
Centricity CR MP3510 Type 5146/200 and 201 only the
CR 75.0 Service Documentation, DD+DIS002.04E and Spare Part List,
DD+DIS007.04M must be used.
Reason The 2nd Edition of this Documentation has been released due to the fact that the
for the CR 85-X Service Documentation from now on is also valid for
2
nd
Edition
CR 75.0 Type 5146/105.
Only the layout of the Service Documentation and product specific safety notes have
been adapted. No other changes of the content have been made.
Product The CR 85-X Type 5148/100 digitizer is the follow-up model of the
Description CR 75.0 Type 5146/100 digitizer.
It has been designed for General Radiology environments and, particularly, for the
CR Mammography 1C Solution.
The main changes between CR 75.0 Type 5146/100 and
CR 85-X Type 5148/100 are:
• Acrylic light guide with glued PMT (PhotoMultiplier Tube) is used instead of
optical fibers.
Features of The CR 85-X Type 5148/100 (CR 75.0 Type 5146/105) scans the exposed
the CR image plate, converts the information into digital data and automatically transfers
Digitizer
the image to the image processing station for further processing and visualization.
The digitizer requires but little manual interaction. All you have to do, after exposure
and identification of the cassette, is to place it in the input buffer of the digitizer. You
can deposit up to 10 cassettes of different sizes simultaneously in the input buffer.
The Digitizer takes in the cassettes one by one. The Digitizer reads the demographic
data and routing information from the memory chip in the cassette, opens the
cassette, removes the image plate and scans the latent image by means of a
sweeping laser beam.
Once the image is digitized, the cassette is returned to the output buffer to be used
for new exposures. After a full Digitizer cycle, the plate has turned 180° in the
cassette.
Depending on the X-ray intensity which has affected the phosphor during the
exposure, more or less light will be emitted during laser scanning. The light is
converted into an electrical signal. This signal is then converted into a digital bit
stream.
Once converted into digital form, the digitized image is transferred to the image
processing station for further processing and visualization.
Intended This device must only be used to scan exposed X-ray cassettes, containing an
Use of the erasable image plate (IP).
Digitizer
This device is part of a system, consisting of X-ray cassettes with erasable phosphor
image plates, an identification station for the cassettes and a workstation where the
resulting digital image information is further processed and routed.
It is intended that this device is only operated in a radiological environment by
qualified staff.
Published by
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
This Generic Safety Directions document comprises the general safety relevant information including
relevant environmental and occupational safety instructions for the Service Engineer.
It is valid for all Agfa HealthCare Imaging Products and part of each Service Documentation as well as
Installation Planning document.
The latest version is available via MedNet, GSO Library path:
General Info => Agfa HealthCare => Publications => Service Manual
► Document History
► Referenced Documents
Document Title
Not applicable Not applicable
Edition 1, Revision 3
07-2009 printed in Germany Document Node ID: 11849633
eq_generic_safety_directions_e_template_v01
Agfa Company Confidential Copyright © 2009 Agfa HealthCare N.V.
DD+DIS238.06E Generic Safety Directions
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2009 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on the
equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
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LIST OF CONTENTS
1 DISCLAIMER......................................................................................................... 5
3 LABELS ................................................................................................................. 7
3.1 CE Mark................................................................................................... 7
3.2 System Labels ......................................................................................... 7
3.3 System Labels concerning Laser Radiation ............................................ 8
4 PRODUCT COMPLAINTS .................................................................................. 10
5 REFERENCES .................................................................................................... 10
6 INTENDED USE.................................................................................................. 11
12 COMPLIANCE..................................................................................................... 14
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24 RECYCLING ........................................................................................................27
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1 Disclaimer
Fitters, engineers and other persons who are not employed by or otherwise directly
affiliated with or authorized by Agfa HealthCare or one of its affiliates are directed to
contact one of the local offices of Agfa HealthCare or one of its affiliates before attempting
installation or service procedures.
No part of this document may be reproduced, copied, adapted or transmitted in any form
or by any means without the written permission of Agfa HealthCare.
Agfa HealthCare shall under no circumstances be liable for any damage arising from the
use or inability to use any information, apparatus, method or process disclosed in this
document.
Agfa HealthCare is not liable for resulting consequences, damages or injuries if you don’t
operate the product correctly or if you don’t have it serviced correctly.
Agfa HealthCare reserves the right to change the product, the characteristics and its
documentation without further notice to improve reliability, function or design.
NOTE:
In the United States, Federal Law stipulates that medical devices should only be sold to,
distributed and used by or by order of a licensed physician.
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2 Used Icons
INSTRUCTION:
If used in combination with the warning or caution sign: Indicates
a specific instruction, which if followed exactly, avoids the
subject of the warning or caution.
If used without warning or caution sign: Indicates an instruction
where it is important to follow literally as described.
IMPORTANT:
Highlights very important actions which have to be carried out to
prevent malfunction.
NOTE:
Indicates advice to facilitate the following step or action.
Highlights unusual points.
Indicates background information.
Can be used to explain or highlight displays of the
graphical user interface.
Is additional information without influence on the action or step!
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3 Labels
3.1 CE Mark
CE Mark This product carries the CE Mark. The CE Declaration (CE Conformity)
becomes invalid if the product is changed without explicit consent of the
manufacturer! This applies to all parts, not only to safety elements.
All system labels and software version number locations are referred to within this service
document in the appropriate section.
Enclosed an overview of common labels, according to ISO 3864.
This list is not complete.
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According to its classification, laser radiation can lead to eye and skin injuries.
Each laser source is classified from class 1 to class 4, based on standard
DIN EN 60825-1:2007.
The table below lists the meaning of the different laser classes. Note the detailed
instructions in the user manual and technical documentation.
conditions.
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4 Product Complaints
Any service person who has any complaints or has experienced any dissatisfaction in the
quality, durability, reliability, safety, effectiveness or performance of this product must
notify Agfa HealthCare by the Agfa HealthCare complaint procedure.
If the product malfunctions and may have caused or contributed to a serious injury of a
patient or an accident or if there are any hazards which may cause an accident
Agfa HealthCare must be notified immediately by telephone, fax or written
correspondence to the following address:
Agfa Service Support - local support addresses and phone numbers listed on:
www.agfa.com
5 References
Technical Documentation is available via MedNet (PDF) and your local Agfa HealthCare
support organisation (Paper).
Access to MedNet:
IntraNet: http://docs.agfanet/bu/mi/mednet/mednetcso.nsf
ExtraNet: http://extranet.agfa.com/bu/mi/mednet/mednetcso.nsf
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6 Intended Use
This Agfa HealthCare product should only be operated in a hospital or clinical radiological
environment by qualified staff.
It must only be operated according to its specifications and its intended use. Any
operation not corresponding to the specifications or intended use may result in hazards,
which in turn may lead to serious injuries or fatal accidents (for example electric shocks).
AGFA will not assume any liability whatsoever in these cases.
Make sure that the product is constantly monitored in order to avoid inappropriate
handling, especially by children.
The product must only be installed and put into operation under the specified conditions.
7 Intended User
This manual is written for Agfa trained Field Service Engineers and Clinical Application
Specialists, trained users of Agfa HealthCare products and trained diagnostic X–Ray
clinical personnel who have received proper training. Users are considered as the persons
who handle the equipment as well as the persons having authority over the equipment.
This Technical Documentation describes adjustments and routines which must only to be
performed by qualified technical personnel.
The Agfa (trained) Field Service Engineers and Clinical Application Specialists must have
received adequate Agfa HealthCare training on the safe and effective use of the product
and applicable environmental and occupational safety matters before attempting to work
with it. Training requirements may vary from country to country.
Agfa (trained) Field Service Engineers and Clinical Application Specialists must make
sure that training is received in accordance with local laws or regulations that have the
force of law.
Your local Agfa HealthCare representative can provide further information on training.
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Each Agfa (trained) Field Service Engineer and Clinical Application Specialist:
• Must make his or her personal contribution to improve safety and protect the
environment.
• When working on a customers site, has a duty to take reasonable care to avoid injury
to himself or herself or to others who may be affected by their acts or omissions.
• Is obligated to adhere strictly to regulations and instructions.
• Shall familiarise himself or herself with the provisions of the Agfa Healthcare
Health, Safety and Environment Policy and any specific rules or procedures relating to
occupational safety at work and the protection of the environment.
• Shall promptly report any near misses, accidents, incidents or dangerous occurrences
to their line manager and co-operate fully in any investigation.
• Shall co-operate with company management on matters relating to
health, safety and environment and, where appropriate, discuss with and / or assist
their manager in resolving matters relating to health, safety and environment.
• Shall ensure that any company equipment issued to them, or, for which they are
responsible, is correctly used and properly maintained.
• Shall wear protective equipment whenever instructed or if it is recommended to do so.
• Shall be responsible for good housekeeping in the area in which he or she is working.
• Shall report situations, which could put them at risk, on either company or
customers' premises, to their manager or supervisor; and, if warranted, directly and in
confidence, to the Health and Safety Co-ordinator, Global HSE Manager, or ultimately
to the Managing Director.
• Shall report any injuries, diseases or dangerous occurrences to his or her line
manager.
• Shall report any accidents, incidents or near misses to his or her line manager.
• Shall report any situation of which he or she is aware that is potentially dangerous.
• Shall comply with any health surveillance procedure instituted for his or her benefit or
for compliance with regulations.
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Agfa HealthCare equipment must only be used in combination with other Agfa HealthCare
equipment or components if these are expressly recognized by Agfa HealthCare as
compatible. A list of such equipment and components is available from Agfa HealthCare
service on request.
Changes or additions to the equipment must only be carried out by persons authorized to
do so by Agfa HealthCare. Such changes must comply with best engineering practice and
all applicable laws and regulations that have the force of law within the jurisdiction of the
hospital.
The Agfa HealthCare products are designed to communicate with other devices in the
hospital network using DICOM protocols.
INSTRUCTION:
Consult the Technical Documentation before making any connections to other equipment.
Consideration relating to the choice of accessory equipment shall include:
• Use of the accessory equipment in the patient vicinity.
• Evidence that the safety certification of the accessory equipment has been performed
in accordance with the appropriate IEC 60601-1 and IEC 60601-1-1 harmonized
national standard.
In addition all configurations must comply with the medical electrical systems standard IEC
60601-1-1. The party that makes the connections acts as system Configurer and is
responsible for complying with the systems standard.
If required, contact your local service organization.
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INSTRUCTION:
• Replace defective parts with Agfa HealthCare original spare parts.
• Use only tools and measuring instruments which are suitable for the procedure.
• Only approved Agfa HealthCare accessories must be used. For a list of compatible
accessories contact your local Agfa HealthCare organization or www.agfa.com.
12 Compliance
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• IEC 60601-1, Ed. 3: Medical electrical equipment - Part 1: General requirements for
basic safety and essential performance
Harmonization:
This document has been prepared to comply with Study Group 1 guidance document
of the Global Harmonization Task Force (GHTF) www.ghtf.org/ to assist development
of a consistent, harmonized definition for a medical device that could be used within a
global regulatory model and would offer significant benefits to the manufacturer, user,
patient or consumer, and to Regulatory Authorities and support global convergence of
regulatory systems.
IECEE CB SCHEME
The IECEE CB (Certification Body) Scheme is the world's first truly international system
for acceptance of test reports dealing with the safety of electrical and electronic products.
It is a multilateral agreement among participating countries and certification organizations.
Agfa has produced a CB test report and claims national certification in all other member
countries of the CB Scheme.
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Note:
This product has been tested and found to comply with the limits for a Class A
computing device pursuant to Subpart B of Part 15 of FCC Rules, which are designed to
provide reasonable protection against such interference when operated in a commercial
environment.
Operation of this equipment in a residential area is likely to cause interference.
The user will be required to take all necessary measures to correct the interference at
his own expense.
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• Under certain conditions the Agfa HealthCare product will show a display containing a
message. This message will show that either a problem or action has occurred or that
a requested action is required or cannot be performed. The user must read these
messages carefully they will provide information on what to do. This will be either
performing an action to resolve the problem or to contact the Agfa HealthCare
service organization. Details on the contents of messages can be found in this
Technical Documentation.
• All images created using any image technology can show artifacts which could be
confused with diagnostic information. If there is any doubt that the diagnostic
information could be corrupted, additional investigations must be performed to get
clear diagnostic information.
• Ventilation openings must not be covered.
• If you notice conspicuous noise or smoke, disconnect the product immediately from
the mains.
• Do not pour water or any other liquid over the device.
• If a system malfunction causes an emergency situation involving the patient, operating
personnel or any system component, activate the emergency stop for the system
concerned. All motor driven system movements will be stopped.
• Do not store any magnetic media near or on devices, which produce magnetic fields,
since stored data may be lost.
Explosive environment:
DANGER:
Risk of explosion.
Never operate this device in zones where there are flammable anesthetics or oxygen which
may cause an explosion.
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14 Radiation Protection
Only qualified and authorized personnel shall operate any X-Ray system. In this context
qualified means those legally permitted to operate this X-Ray equipment in the jurisdiction
in which the X-Ray equipment is being used, and authorized means those authorized by
the authority controlling the use of the X-Ray equipment. Full use must be made of all
radiation protection features, devices, systems, procedures and accessories.
Ionizing radiation can lead to radiation injuries if handled incorrectly. When radiation is
applied, the required protective measures must be complied with.
• Details about cleaning and disinfection or sterilization methods that may be used on
SYSTEM parts or ACCESSORIES that can become contaminated through contact
with the PATIENT or with body fluids, are referred to within the individual service
documents.
• Disconnect the power supply from the equipment prior to cleaning the equipment.
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• This system uses high voltage. Please consider the respective safety regulations.
• Electrical repairs and connections must only be performed by a qualified electrician.
• Mechanical repairs and connections must only be performed by a qualified technician.
• The safety directions for operation (see section 13) are also valid for all service
activities.
• During all service activities observe prescribed local and country-specific
requirements (e.g. occupational safety and accident prevention regulations).
• All existing screw connections must be tightened sufficiently firmly, but they may not
be overstressed when tightening. There must always be compliance with stated
torque values!
• Damaged or missing screws may be replaced only with the same screw types that
have the specified hardness rating. Unless a different value is listed in the
instructions, all Allen screws used must be hardness rated 8.8.
• All screws must be secured in accordance with the corresponding data.
If "Loctite" has to be used to secure screws, this is stated in the text.
• Any Agfa service PC or tool which is to be connected via RS232, RJ45, USB or other
interface to an Agfa device must not be connected to the mains but must be operated
on its internal battery or indirect supply (low voltage).
• When handling printed circuit boards (abbr.: PCBs) the following points must be
observed:
o Always switch off the equipment and unplug the power cord, before you
disconnect or connect cables on printed circuit boards.
o When working on PCBs, always wear an anti-static wrist strap. Never touch any
parts or components on PCBs with your bare fingers.
o PCBs have to be kept or transported in their protection bags. Never carry a
PCB without protection bag and walk on carpet or plastic floor covering
(electrostatic charge).
o Once the PCB is taken out of its protection bag, it has to be protected from
electrostatic charge by a grounded mat.
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The digitizer and the cassette storage shall be protected against X-ray radiation this way,
that the annual dose equivalent at the installation place will not exceed 1 mSv.
The film-screen system shall be protected against X-ray radiation this way, that the annual
dose equivalent at the installation place will not exceed 1 mSv.
INSTRUCTION:
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• The device complies with the EN 60601-1, 2006 standard for Information Technology.
This means that, although it is absolutely safe, patients may not come in direct contact
with the equipment. Therefore the operator console must be placed outside a radius
of 1.5 m around the patient.
R = 1.5m
1.5m
1.5m
Patient environment
• This device should be installed behind the institution firewall for network security and
anti-virus protection. No ongoing computer virus protection or network security for this
medical device is provided (e.g. a computer firewall). Network security and anti-virus
provisions are the ongoing responsibility of the user or institution.
Floor load:
CAUTION:
Heavy device may damage the floor covering.
Make sure that the floor covering is solid enough to stand the weight of the device.
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INSTRUCTION:
Prior to connecting the device to the mains:
• Compare the power requirements indicated on the type label with the available
power supply in the installation room.
• Check the service manual for the type of input voltage selection, manual or
automatic: If manual, select the appropriate voltage and fuses.
• Confirm to use the correct socket and plug for the required power supply.
• Check the equipment will work with the power supply available.
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INSTRUCTION:
• Always connect the associated monitor to the same Uninterruptible Power Source as
the PC.
• When different combinations of equipment are used in various medical environments
a potential difference (V) can exist between the protective earths in different localities.
If the protective earthing fails this potential difference can cause a HAZARD for the
OPERATOR or for the PATIENT.
• This Technical Documentation identifies the parts on which preventive inspection and
maintenance shall be performed by Agfa HealthCare service personnel, including the
periods to be applied.
• In general the device has to be switched off during service activities. Exception: If the
device is switched on to perform tests pay particular attention to any hazards due to
moving and rotating parts. Avoid lose clothing or finger traps. Switch off the device
immediately after the tests.
• Do not turn motors manually. If required, first disconnect the motor from the motor
control board.
• Make sure that the power cord does not show any signs of damage.
• After repair work always check that the integrated safety features are not overridden
or disconnected.
• If there is any visible damage to the machine casing do not hand-over the product to
the customer. First repair the machine casing.
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Replacing batteries:
WARNING:
Battery can explode, causing chemical burns.
INSTRUCTION:
NOTE:
On MedNet, GSO Library path "General Info => Agfa HealthCare => Publications =>
Service Manual" a form “IEC 62353:2007 Test Documentation” for CR Digitizers is
available, to be handed out to the responsible organization (Intranet Link / Extranet Link).
1
Responsible Organization:
Entity accountable for the use and maintenance of a medical equipment or a medical equipment system. The
accountable entity can be, for example, a hospital or an individual clinician.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
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INSTRUCTION:
• Strictly observe the warning notes in the service manual of devices emitting laser
radiation (See service manual chapter describing Safety Guidelines / General
Repair Instructions) and at the corresponding steps of instructions.
• Strictly observe the warning labels at the modules emitting laser light. For the
meaning of the labels refer to section 3.3 in this document.
• Do not look into the laser beam.
• Do not open modules containing a laser. Only open modules containing a laser if
explicitly instructed to do so.
• Do not keep tools in the laser beam unless explicitly instructed to do so.
• Make yourself familiar with the path of the laser light and the conditions, when the
laser beam is switched on. Refer to the Functional Description in the
corresponding service manual.
• Do not operate modules with laser outside the device.
Sharp edges:
CAUTION:
Sharp edges inside the device: Cut or abrasion possible.
Be careful at maintenance and replacement of parts.
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Secured screws:
CAUTION:
Opening screws secured by red lacquer may misalign important device
adjustments:
Do not open screws that are secured by red lacquer.
Replacing fuses:
Warning:
Replacing fuses by wrong type may lead to fire hazard!
Use only fuses of the exact value and characteristics stated in the service manual or on
the device.
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'Hazardous materials' is the designation for substances which can ignite or explode or
which are toxic, injurious to health, corrosive or irritating. The “Hazardous Material”
instructions must be read and the required protective measures must be complied with
when performing work to avoid health risks.
Their properties together with the hazards and protective measures connected with them
are identified clearly by symbols and described by the instructions appertaining to the
hazardous substances.
24 Recycling
Agfa HealthCare has Recycling Passports available for all equipment. The Recycling
Passport explains whether hazardous materials, special components and batteries are
present, where they are located and how they can be removed at the end of the life cycle.
The Recycling Passports are meant to be used as information for waste treatment
partners and companies that want to recycle end-of-life Agfa equipment.
To get a copy of the required Agfa HealthCare Recycling Passport please contact your
local Sales organization.
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25 Waste Disposal
AGFA HealthCare Field Service Personnel or its authorized affiliates are responsible for
the removal of Protected Health Information (PHI) patient data from devices, modules or
parts that are removed from the customer’s site. This also applies to the exchange of
spare parts, especially to parts that are returned to central warehouses for repair or
refurbishing. Examples for parts or modules that may contain Protected Health
Information (PHI) are: Computer hard disks, CD-ROMS, backup tapes, archive tapes.
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Chapter 1
HEALTHCARE Controls, Connections,
Imaging Services
and Setup Procedures
Document No: DD+DIS378.05E
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
Edition. Release Changes
Revision Date compared to previous Version 2.0:
2.1 06-2008 • Improved the installation workflow
for CR 85-X / CR 75.0
• Added the task codes to the task overviews.
• Added CR Mammo flatfield exposure and evaluation,
see section 9.3.
► Referenced Documents
Document Title
The Service Manuals of other CR system components are
listed in section 11 of this document.
Edition 2, Revision 1
06-2008 printed in Germany Document Node ID: 10027262
eq_01_setup_procedure_e_template_v05
Agfa Company Confidential Copyright © 2008 Agfa HealthCare N.V.
DD+DIS378.05E Controls, Connections, and Setup Procedures
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2008 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications
=> Service Manual) prior to attempting any operation, repair or
maintenance task on the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions"
and on the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
LIST OF CONTENTS
2.2.1 CCM-Tool..................................................................................................................................7
2.3 Compare voltage indicated on type label with available power supply.....................................8
NOTE:
• The Installation Checklist in the appendix of this chapter gives an overview
of all steps and guides through the complete installation process.
• The time required for the installation steps within this document
(target: 2 hours) should be entered in the service/installation report
under the respective task code.
This device must only be used to scan exposed X-ray cassettes, containing an
erasable image plate (IP).
• Digitizer
• X-ray cassettes with erasable phosphor image plates,
• An identification station for the cassettes and
• A processing station where the resulting digital image information is further
processed and routed.
Goal The purpose of this section is to list the required tasks before physical installation, to
guarantee a smooth digitizer installation.
TOOLS:
• Service PC
• Serial interface cable (RS-232) for connection between digitizer and Service PC
• Cu filter (spare part number*: CM+9 5155 1015 2)
Remark: The CU-filter is also part of the digitizer delivery.
• CD ROM with test images (spare part number*: CM+9 5145 3055 0)
• Screwdriver medium size
• Open end wrench (17 mm)
• Socket wrench (7 mm)
• Configuration file (adc.cpf) which you prepared beforehand (on a floppy disk)
• Empty floppy disk or USB-stick for storing machine specific data
• “Mammography Calibration Kit”, which is part of the digitizer delivery for
exclusive Mammography sites
* The last digit in the spare part number indicates the spare part revision at release of this
document. When ordering, the actual revision of the spare part is delivered.
2.2.1 CCM-Tool
The CCM-Tool is needed to create and modify the configuration file (adc.cpf) for the
CR 85-X and the other CR system components.
The latest version of the CCM-Tool is installed by default on the NX processing
station (Go to Start Æ Agfa Æ Service Æ CCM Tools).
If not yet done create and/or adapt the configuration file adc.cpf together with the
application specialist.
NOTE:
When integrating the digitizer into an existing network, it is strongly recommended to
create a CPF– file beforehand (see CR 85-X Service Manual, Chapter 11,
Installation Planning, checklist).
The "SHOW ERROR PROGRAM" with the "ERROR.MSG file" translates the
CR 85-X error codes into clear text.
The "SHOW ERROR PROGRAM" is a part of IMOS, the "ERROR.MSG file" is loaded
in the digitizer.
2.3 Compare voltage indicated on type label with available power supply
5148_Chap01_020.cdr
figure 1
NOTE:
The digitizer has an “auto switching” power supply built in. This adapts itself to the
input voltage. The input voltage has to be between 200/240 V (AC), 50/60 Hz.
Goal The purpose of this section is to make sure that the digitizer is ready to be installed.
Checking Shipment
5 min. mandatory INS 3.3
Completeness
5148_Chap01_018.cdr
figure 2
IMPORTANT:
If you notice transport damages, document them (e.g. take a photo) and contact
your local Sales representative.
(3) Check the completeness of the shipment by means of the bill of material
(number of pallets).
(4) Compare the labels on the boxes with the customer’s order list and
the shipping papers.
NOTE:
• The individual boxes inside must not be opened by the forwarder.
• For unpacking the machine and lifting it off the pallet, an area of
minimal 200 x 500 cm (78.8” x 197”) is required (see figure 3).
• If the available space at the installation site is limited, the machine can be
unpacked beforehand and rolled carefully to the final destination.
5148_Chap01_019.cdr
figure 3
(1) Check shipment completeness by comparing the delivery with the packing list
(part of the accessories box).
(2) In case it is not complete, inform the local sales representative. He will initiate
the required steps. Additionally note the missing items(s) in the
installation report.
Goal The purpose of this section is to introduce the digitizer controls and connectors.
(3) Keypad
4 2
(4) Service-Port to connect the
Service PC
(RS 232 - 25-pin D connector,
5148_Chap01_003.cdr
female D)
figure 5
Twisted Pair
5148_Chap01_006.cdr
figure 6
5148_Chap01_017.cdr
figure 7
Key Function
Emergency key to give an image the status ‘emergency’ when it is sent to the
image processing station.
Up key to move cursor one position up to previous entry field and to scroll
upwards or to increment digits in a numeric entry field.
Down key to move cursor one position down to next entry field and to scroll
downwards or to decrement digits in a numeric entry field.
Left key to scroll backwards through multiple choices within a field, to move
entry position in a numerical field in descending order (from right digit to left
digit) and to toggle between values in a field.
Right key to scroll forwards through multiple choices within a field, to move
entry position in a numerical field in ascending order (from left digit to right
digit) and to toggle between values in a field.
Goal This section describes the installation of the base plate and how to connect
the digitizer to the network.
NOTE:
When putting the digitizer at its final position, mind that network and mains cable are
sufficient in length.
The base plate is kept in place by the weight of the digitizer. Additionally, a
double sided adhesive tape can be used to fix the plate.
1.c
dr 2
02
p0
1_ 1
ha
8_C
4
51
2
1
figure 8
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
(2) Move the digitizer onto the base plate at the planned installation position.
Take care that the rollers are guided by the rail!
Move the digitizer gently to the stop.
5148_Chap01_022.cdr
figure 9
(3) Turn screws by hand to their stop, on both sides of the digitizer. Then use a
screwdriver and perform one more turn (A). Do not give more turns!
Put the plastic caps on the screws to protect them. (B)
5148_Chap01_023.cdr
figure 10
(4) Open the doors of the digitizer and mount the two adjustable feet
(part of the delivery) with two screws (7 mm socket wrench)
as shown below.
(5) Adjust the two feet with an open end wrench (17 mm), so that they
touch the floor.
5148_Chap01_004.cdr
17mm
figure 11
(1) Connect the network cable to the digitizer (not yet to the network wall outlet).
(2) Two different mains cables are delivered with the digitizer:
• USA/Japan: Nema 6-15 P
• Europe: CEE(7)VII 250 V/16 A
Connect the appropriate mains cable at the rear side of the digitizer,
(see figure 6).
(3) Plug in the mains cable at the wall outlet.
NOTE:
The digitizer has an automatic voltage selector. Voltage is adapted automatically
between 200 V and 240 V AC, as soon as the machine is switched on.
NOTE:
In case of any problems during the installation, consult chapter 3.3 (Troubleshooting).
CR 85-X
5148_Chap01_008.cdr
figure 13
Goal This procedure checks, whether all cassette formats available at the customer site
can be handled properly by the digitizer.
NOTE:
Perform at least one test cycle for each cassette format.
(1) Open Service menu on the local key pad of the digitizer.
(2) Select
<2 MAINTENANCE>
<3 Test and adjust cycle>
<4 Handling Cycle>.
1 Scan with transmission Service menu
2 Scan cycle - no image MAINTENANCE
3 Scan - no era, no img Test cycle
4 Handling cycle
5 Adjustment cycle X :cancel
:ok
5148_Chap01_009.cdr
figure 14
(3) Use up and down keys to enter number of handling cycle(s) and
confirm with .
Æ The handling cycle runs until all cassettes of the input buffer have been
processed.
Goal This section describes necessary software settings for the start-up of the digitizer.
(1) Open Key-Operator menu on the local key pad of the digitizer.
• Use the left and right keys to select the digit you want to change.
• Use the up and down keys to set the digit to the desired value.
Goal User interface messages are available in eleven languages. As default English is set.
To change the language of the digitizer user interface perform following procedure:
(1) Open Service menu on the local key pad of the digitizer.
(2) Select
<6 CONFIGURE>
<2 User terminal language>.
1 Local network ID Service menu
2 User terminal language CONFIGURE
3 Pre-check monitor
4 Alarm system
X :cancel
:ok
5148_Chap01_010.cdr
figure 15
(3) Use up and down keys to select user interface language from list
and confirm with .
Goal This procedure serves to integrate the digitizer into an existing network via a cpf-file.
(3) Open Service menu on the local key pad of the digitizer.
(4) Select:
<5 INSTALL data>
<6 CPF-File>.
1 Software Service menu
2 Machine specific data INSTALL
3 PMT settings (mfa/mfb)
4 Optics parameters
5 Scanner parameters X :cancel
6 CPF-File :ok
7 Language files
8 HW modification ID
5148_Chap01_011.cdr
figure 16
NOTE:
For VIPS and CR QS systems:
The cpf – file has to be installed on the digitizer and on the processing station.
For NX systems:
The cpf – file has to be installed only on the digitizer.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Goal This section describes the steps to set the digitizer into operation and to check the
technical image quality.
approx. 1 min.
Erasing Image Plates mandatory INS 9.2
per plate
NOTE:
The destinations, i.e. processing stations, intended for the digitizer, have to be put
into operation and must be obtainable via Ethernet.
(1) Open Service menu on the local key pad of the digitizer.
figure 17
(3) Check whether the processing station(s) is/are obtainable by sending a ping
to each destination.
(4) Open Key-Operator menu .
NOTE:
Before the hand over of the digitizer to the client all available image plates
must be erased.
figure 18
The hard disk of the digitizer contains samples showing the minimal required
image quality.
Send two flatfields (banding pattern and calibration pattern) to a printer
via service-menu.
(1) Open Service menu on the local key pad of the digitizer.
figure 19
(3) Compare the samples with the images you create in 9.3.2.
(1) Expose a flatfield and evaluate the image on the processing station
and the corresponding printer.
Criteria: homogenous field, no stripes or any artifacts.
(2) Have a new plate of every format exposed twice as follows:
Rotating
Anode x-ray tube
Cathode
51
48
_ 3. 6
.cd
r
(3) Place the cassette in length direction to the X-ray tube; see figure above.
Æ 1st exposure: dose: 10 µGy (1,142 mR)
(4) Select the following exposure parameters to obtain a dose of 10 μGy by using a
1.5 mm Cu-filter:
- 12 mAs
- 75 kVp
- 1.3 m (51,2”) distance and
- Large focus.
NOTE:
Please note that these are approximate values that may vary within the X-ray
devices to reach the specified dose of 10 µGy.
• On CR QS
Processing Station:
Select Substudy:
<Flat field>.
Confirm Exposure
class: <200>.
figure 21
• On NX
Processing Station:
Confirm Detector
Sensitivity: <200>.
figure 22
NOTE:
If the image quality does not reach the one of the sample printed in section 9.3.1, first
consult chapter 3.6, Adjustments and calibrations of the CR 85-X Service Manual,
then, in case this did not solve the problem, contact your support center.
NOTE:
In order to fix the Al-filter below the collimation window, a reliable adhesive
tape is required. Depending on the adhesive tape, a solvent may be required
for the cleaning of the X-ray source.
(4) Put in the cassette. Take care that the chest wall side is orientated to the front
of the X-ray source.
(5) Expose the cassette.
NOTE:
Perform one single exposure!
Rotation of cassette is not required.
• On CR QS Processing
Station:
Select Substudy:
<Flat field>.
<50>.
figure 24
NOTE:
If the image quality does not reach the one of the sample printed in section 9.3.1, first
consult chapter 3.6, Adjustments and calibrations of the CR 85-X Service Manual,
then, in case this did not solve the problem, contact your support center.
Confirming the
1 min. mandatory INS 10.1
Installation
(1) Open Service menu on the local key pad of the digitizer.
(2) Select
<2 MAINTENANCE>
<8 Confirm installation>.
1 SAL inspection Service menu
2 Calibration MAINTENANCE
3 Test and adjust cycle
4 Confirm maintenance
5 Confirm repair X :cancel
6 Clear infocounter :ok
7 Confirm modification
8 Confirm installation
5148_Chap01_015.cdr
figure 25
(1) Open left front door of the digitizer and insert floppy disk or plug in storage
medium.
(2) Open Service menu on the local key pad of the digitizer.
(3) Select
<3 Save data>
<2 Machine specific data>.
1 Info counter file Service menu
2 Machine specific data SAVE
3 Service report
4 Session files
5 CPF-File X :cancel
6 Alarm log file :ok
5148_Chap01_016.cdr
figure 26
S/N: <XXX>
Date: <date>
Software- ACP_xxxx
version:
figure 27
(1) Dispose of all packing material (depending on the country, by the forwarding
agent or by the hospital).
(2) Fill out the installation report delivered with the device and send it by to the
regional service manager.
(3) Hand over the CR System to the application specialist.
NOTE:
For detailed information on the installation of CR devices refer to the respective
documentation on MedNet GSO Library:
12 Installation Checklist
No. Step See OK
section
Prerequisites for Installation (Task Code: PRI)
1. Checking installation site prerequisites. 2.1
2. Checking and adapting the configuration file. 2.2
3. Compare voltage indicated on type label with 2.3
available power supply.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
This document explains the functional principle including the functions of the individual
assemblies always under normal conditions without any problems (nominal functional
sequence).
Furthermore it describes the structure and function of specific individual assemblies.
► Document History
► Referenced Documents
Document Title
n.a. n.a.
Edition 2, Revision 1
10-2008 printed in Germany Document Node ID: 10028252
eq_02_functional_e_template_v06
Agfa Company Confidential Copyright © 2008 Agfa HealthCare N.V.
DD+DIS378.05E Functional Description
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2008 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
LIST OF CONTENTS
1.1.3 Digitizers (CR 85-X / CR 75.0 / ADC Compact Plus / CR 35-X / CR 25.0 / ADC Solo) ..........7
3 CASSETTES ..........................................................................................................................13
3.1 CR MD4.0 General Cassette ..................................................................................................13
4.5.1 cPCI-Rack (CR 75.0 Type 5146/105 up to SN 6499, CR 85-X Type 5148/100 up to SN
3999) .......................................................................................................................................25
4.5.2 cPCI Rack (CR 75.0 Type 5146/105 as of SN 6500, CR 85-X Type 5148/100 as of SN
4000) .......................................................................................................................................28
7 CALIBRATION PRINCIPLE....................................................................................................56
7.1 IP Center Calibration (BOL/BOS Adjustment) ........................................................................56
7.1.2 BOS.........................................................................................................................................56
The ADC cassette is the “container” for the image plate. During the handling outside the
Digitizer (e.g. exposing the plate) the image plate is in the cassette. It is only opened
inside the Digitizer.
The ADC cassette has an internal chip card which holds the cassette, patient,
examination and routing data belonging to a certain X-ray exposure. The data put
together are called demographic data.
The image plate takes the place of the X-ray film in a conventional system. It receives
the X-Ray radiation and “stores” a latent image. The image plates can be reused
thousands of times. The actual restriction of utilization is the mechanical robustness.
The Identification Tablet is used to write the cassette, patient, examination and routing
data to the cassette chip. This data can be entered manually or by retrieving the data
from a Hospital or Radiology Information System (HIS/RIS).
Writing and reading is done by means of radio frequency in a contact less manner.
1.1.3 Digitizers (CR 85-X / CR 75.0 / ADC Compact Plus / CR 35-X / CR 25.0 / ADC Solo)
The Digitizer reads the latent image in the image plate. After the ADC cassette is
exposed and identified it is inserted into the Digitizer. The Digitizer reads the data on the
cassette chip, opens the cassette, takes out the image plate and scans it.
The latent image on the image plate is stimulated by means of a laser beam to emit light
according to X-ray exposure.
The data from the cassette chip is used to set the scan parameters correctly (e.g. speed
class, image plate size, etc.) for this individual X-ray exposure.
The emitted light is converted into voltage and then digitalized into a 12/14bit, square
root compressed raw image. This image is transmitted together with the chip data on the
fly via Ethernet to the Processing Station. A backup of that image is made on the internal
hard disk in parallel to retransmit the image in case of transmission problems. The output
format of the Digitizer is DICOM SCU-CR.
After scanning / transmitting is finished the image plate is erased with very bright light to
make it ready for the next exposure. It is put back into the cassette and a status flag on
the cassette chip is set from “EXPOSED” to “ERASED”. The cassette is returned to the
user and is ready for the next examination.
1.1.4 CR Workstations
QS Server Station
The ADC QS 2.0.x/2.1.x (Quality System) Server Station is a Windows NT4.0 based
Workstation with the ADC Quality-System software installed.
The Server Station receives the raw image from the Digitizer. Every incoming image
runs through an image processing. The processed images are stored on the internal
hard disk(s) of the Server station. The Server station only provides short term storage.
The final archiving must be realized either by hardcopies or a PACS.
The Server station decodes the routing data and sends the image data to the selected
destinations (e.g. Printer, PACS).
A Softcopy can be sent to an Archive with 8 or 12 bit. To print a Hardcopy a 8 bit format
is used.
For the Server station a lot of licensed software options (e.g. Annotation, Print
Composer, etc.) exist.
X-ray device
ID-tablet - CRUS
ADC Cassette
with image
plate inside
ID-Data
Digitizer
CR QS
Server/Client
or NX Workstation
Archive Station
5148_reg02_006.cdr
Printer
figure 1
2 Image Plates
The CR plate can be identified by the plate type and sensitivity code printed
on the back.
The image plate lying in the cassette consists of five different layers:
3
2 Phosphor layer 4
3 Anti-halo layer, blue
5
4 Support P.E.T, white
5 Laminate
figure 2
figure 3
CAUTION:
Wrong screen cleaner may damage the Image plate.
Do not use the AGFA CR phosphor plate cleaner to clean the
CR MM3.0 Mammo image plates. Use PROSAT wipers instead.
* The last digit in the order number indicates the spare part revision at release of
this document. When ordering, the actual revision of the spare part is delivered.
3 Cassettes
The principle function of the digitizer is close connected to the structure of the
CR Cassettes. The digitizer accepts only CR Cassettes. All other cassettes,
e.g. ADC 70, are refused.
NOTE:
For system preparation please refer to chapter 3.6 of this manual.
NOTE:
The cassette must always be inserted into the digitizer in the correct orientation to
make it possible to identify and handle the cassette!
Legend figure 4:
1 2 3
1 ADC label
2 ID-Chip carries demographic data
4
3 Label showing size of Image Plate
4 Sliders to prevent from usage in film handling 5
devices
5 Metal label – silver dot – identifies an
ADC Cassette
6
6 ADC Image Plate (gray surface up, white
surface down) 4
figure 4
The ADC label and the label, showing the size of the contained image plate, are put on
for the identification by the user.
The metal label is detected by the digitizer to identify the cassette as an ADC cassette.
For protection against electrostatic charging and mechanical damage the inner lining of
the cassette is made of felt.
Specification
To improve the image quality with Full Leg Full Spine (FLFS) images
a FLFS CR Cassette was introduced.
Identification
The FLFS CR Cassettes are with exception of two major differences identical to the
current standard ADC Cassette (35 cm x 43 cm).
The differences are:
• Reduced backscatter protection (minus 1.5 cm at locking and
hinge side)
• Specific FLFS labeling
figure 5
Format
The FLFS Cassette is available in format 35 cm x 43 cm.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Specification
Identification
figure 6
Formats
The CR Mammo Cassette contains a CR Mammo image plate. This type of image plate
has a special phosphor layer which results in reduced noise and increased sharpness.
The cassette is equipped with a positioning mechanism in order to ensure the chest
wall distance to the image plate.
Identification
figure 7
Formats:
The CR Mammo Cassette is available in two formats:
• 18 cm x 24 cm
• 24 cm x 30 cm
Specification
The CR Mammography cassettes and Image Plates were revised to improve
functionality. For more information refer to DD+DIS233.08E (Service Bulletin No. 37).
(Intranet link / Extranet link)
Identification
The cassette is labeled with “Mammo” on both sides.
The cassette is pre-initialized as a Mammo Cassette. If the cassette is not identified
proceed as described in chapter 3.4 of the CR Mammo Solution Manual.
figure 8
Formats:
The revised CR Mammo Cassette is available in two formats:
• 18 cm x 24 cm
• 24 cm x 30 cm
Specification
The CR MD4.2 Extremities system is foreseen for X-ray images of the distal extremities
and adjacent joints (hands and feet) and provides a spatial scan resolution of 50 µm.
Initialization:
• Scan size: 18 x 24 or 24 x 30 cm
• Scan resolution: Very high resolution
The CR MD4.2 Extremities cassettes can only work when digitizer software ACP_4005
or higher is installed on the CR 85-X.
Identification
CR MD4.2 Extremities cassettes can be recognized by the code label:
“Extremities - code XX”
The light green dots are dedicated only to the CR MD4.2 Extremities cassette.
This makes it easy to distinguish the cassette from others when stored in a rack.
a b
1 silver dot
Extremities - code XX 1 green dot
5156_dis307.05_001.cdr
Cassette formats
2 green dots 18 x 24 cm or 24 x 30 cm
Formats
New CR MD4.2 Extremities cassettes (available formats 18 x 24 cm and
24 x 30 cm) are delivered with the appropriate initialization:
• Scan size: 18 x 24 or 24 x 30 cm
• Scan resolution: Very high resolution
Input Buffer
Power Unit
Output Buffer
cPCI-Rack
Cassette Unit 1 / 2
IP Transport Unit Prescan
Rotation Unit
Optic Module
Erasure Unit
figure 10
figure 11
The Input Buffer has a capacity of 10 cassettes which can be queued in front of the
feed gate. The first cassette is detected and the machine cycle starts. To transport the
cassette inside the digitizer the transport belt (1) shifts the cassette, the feed gate
opens and the RF-tag reader reads out the ID- and image specific data.
After the data is read out, the transport roller of the cassette module takes over the
movement of the cassette.
4
3
figure 12
The power supply of the Power Unit is a single phase System, means the cable
connection is a common inlet connector for non-heating apparatus.
The supply voltage for the Power Unit is automatically detected in the range of
200 – 240 V (AC), 50/60Hz. Therefore for installation it is not necessary to change any
setting manually, but has to be checked before the first use.
If the interlock switch is active, all the power supplies of mechanical parts and the laser
are interrupted, for safety during service interventions. The power supply of the
cPCI-Rack is placed in the rack itself, so e.g. software updates can be done although
the right door of the power unit is open and the interlock switch is active.
The Multi Supply Board (MS-Board) controls the mechanical periphery of the digitizer
and protects the stepper motor cards. The supply voltage is detected by the board and
errors are displayed by LEDs.
The following components are controlled by the IO-Bus of the board:
The two vacuum pumps with two magnetic valves on the IP transport units, the parking
position function by using solenoids at the IP transport unit postscan, the fan of the
erasure unit and of the power unit and the voltage selection between 200 V, 208 V and
230/240 V.
LEDs on the inner side of right door at the power unit show the status of the supply
voltages of the power unit:
GS100-MULTI-
Supply-BD
5146_reg02_008.cdr
figure 13
Additional LEDs are visible if right door and power unit housing is open:
D19 – D32 red LEDs are corresponding to stepper motor fuses where they are placed
next to. The stepper motor supply is protected with a fuse on every stepper motor
board itself (12 in total). The status is shown with a green LED on the side of the power
unit (see figure 12).
D 33 green LED is corresponding to the fuse (Si13) of power supply of simple switcher,
which is placed next to the fuse.
Normal status:
The status of the LEDs, after switching on the digitizer with active interlock switch and
without any error, is:
Example:
figure 14
The Erasure-Control-Board controls five transformers to supply the erasure lamps with
power. The lamps are controlled in pairs, so one transformer supplies two lamps. Also
the temperature of the erasure unit is controlled, if the detected temperature is lower
than 85 °C (185 °F), the erasure process can start.
If the temperature is higher than 85 °C (185 °F), the process is delayed until
temperature has dropped below 75 °C (167 °F).
During the delay the erasure unit fan cools the module.
The failure of a lamp is detected by the current sense board, which is also part of the
power unit and is connected to the Erasure-Control-Board.
figure 15
The Output Buffer has a capacity of 10 cassettes. The transport rollers at the gate
move the cassette outside. To avoid blocking a lever (1) pushes the cassette aside
which rests in the buffer.
The cassettes which are released are monitored. After the last one the machine cycle
stops.
4.5 cPCI-Rack
4.5.1 cPCI-Rack (CR 75.0 Type 5146/105 up to SN 6499, CR 85-X Type 5148/100 up to
SN 3999)
7
6
5
4
3 2
figure 16
The CPU (Central Processing Unit) called OBERON board is based on a Power PC
and is working with an operating system called Portex. The interfaces to the service
and the Ethernet are placed on the front plane.
Service:
Connector (female) to Service
Interface (RS232)
figure 17
The Scan Master Board controls the main functions of the digitizer which are related to
the image data acquisition. The board has to support two operating levels, low
resolution and high resolution. Therefore timing, frequency and converters need to be
controlled.
Polygon Control:
Controls via the Polygon the deflection
Connector (female)
of the laser beam on the image plate,
to Polygon
controls the rotational speed and
detects the facets.
RF-Tag Reader Control:
Controls the transmitter and receiver
Connector (male)
signals for reading out demographic
to RF-Reader
data of the ADC Cassette.
User terminal Control:
Controls the user terminal via a 20 mA
Connector (female)
interface.
to User terminal
Connector (female) IO-BUS Control:
to IO-Bus Provides the IO-BUS with power and
is connected via eight data lines and
three control lines to the IO-BUS.
2
3
figure 19
NOTE:
The new cPCI Rack does not contain a floppy drive.
The Revive board controls the main functions of the digitizer. The board has to support
two operating levels, low resolution and high resolution. Therefore timing, frequency
and converters need to be controlled.
Connector
Fast Ethernet Controller:
(female) to RJ45 connector, Fast Ethernet with
Photomultiplier 10 to 100 Mbit/s.
Tub
Connector to RF-Tag Reader Control:
Fast Ethernet Controls the transmitter and receiver signals for
reading out demographic data of the ADC
Connector Cassette.
(male) to RF-
Reader
Service:
Connector Service communication port
(female) to
Service Polygon Control:
Interface Controls via the Polygon the deflection of the
(RS232) laser beam on the image plate, controls the
rotational speed and detects the facets.
Connector
(female) to
Polygon USB-Port:
Standard USB Port for USB Memory Sticks Type
USB-port A (Standard)
Connector
(female) to User terminal Control:
User terminal Controls the user terminal via a 20 mA interface.
Connector
(male) to Laser IO-BUS Control:
Diode Module Provides the IO-BUS with power and is connected
Connector via eight data lines and three control lines to the
(female) to IO- IO-BUS.
Bus
Laser diode Module Control:
Controls the power supply of the laser diode of
the laser module, controls the power switch of the
laser diode, controls Begin-of-Line Signal and
Laser-Power-Monitor board.
figure 20
Green LEDs to
monitor power supply
5146_reg02_014.cdr
figure 21
During normal operation the LEDs monitor 5.1 V and 3.3 V voltage levels.
The power supply of the cPCI Rack is not interrupted by the interlock switch. This
independent supply makes it possible to update software or work out other actions at
the rack while both doors of the digitizer are open.
The gray rectangle in the partition map marks the directories which are only necessary
for remote control via http access.
Directories and
Partitions Files Annotations
subdirectories
*.BAT batch and
C: *.SYS
STARTUP.COM
system files
*.PRG program files
ERROR.MSG error message files
*.ESX tables
*.GIF
IMAGES *.JPG
*.TBL tables
*.SHD calibration files
*.SWP sweep curve
*.TEMP
temporary files
HTTPTEMP.OUT
E:
FLATFLD CONTROL.DAT
IMAGE.DAT
FLATFLD2 CONTROL.DAT
IMAGE.DAT
figure 22
4
2
3
figure 23
The Cassette Unit 1 or 2, depends on which one is at the input buffer, fixes and holds
the cassette during the IP is taken out and scanned. An opener mechanism for the
cassette is also part of each unit. The Cassette Units 1and 2 together are supported
and turned by the rotation unit.
On the inner side of each of the Cassette Units is a 5fold stepper motor board placed,
which controls the motors of the corresponding unit.
1
2
figure 24
1 Vacuum unit
2 Suction arms
3 Guide plate
The IP transport robot takes the IP out of the cassette and leads it along the guide
plate to the optic module. The transport robot is guided in the frame of the unit.
51
46
_re
g0
2_
01
8.C
DR
2
figure 25
1 Rotational drive
2 Stepper motor board
The rotation unit rotates the Cassette Units by 180° to bring the empty cassette from
the input side to the output side, for putting back the scanned and erased image plate
inside the cassette.
figure 26
The function of the scan module is to stimulate a two dimensional, X-ray exposed
phosphor image plate with laser energy. Out of the blue light, which is emitted by the
phosphor, a digital image is generated.
The stimulation of the image plate is done pixel by pixel. Therefore the laser beam is
moved. The laser power on the focal plane is 50 mW + 5 %. The movement in the x-
axis is achieved by a rotating polygon mirror (fast scan direction) which is part of the
optical path. The movement in the y-axis is done mechanically by transporting the
image plate (slow scan direction) with two pairs of rolls.
The Scan mode 2 µs is used for 35 cm x 43 cm high resolution scanning.
A 1 µs scan mode has been established already in ADC Compact Plus for
35 x 43 cm cassettes standard resolution.
This principle has been enhanced in CR85-X to small formats < 35 x 43 cm.
Consequently, the throughput increases because of reduced scan time.
The 1 µs scan mode option can be switched on in the key operator menu.
Laser Diodes
The optic module contains a monochromatic anamorph scan optic where the laser
beam is modified. The light source which is stimulating the image plate is a red laser
diode, with a wavelength from 650 nm to 670 nm and a maximal output of 80 mW
(see 1 in figure below), which results in 50 mW laser power on the surface of the image
plate. The increase and decrease time of the laser power is shorter than 20 μs. The
beam of the laser diode has a spot diameter of 60 µm on the scan surface.
3
2
Fa
s ts
ca
4 nd
ire
c tio
51
n
48
_c
ha
p2
_0
02
.cd
r
figure 27
1 Laser beam
2 Mirror for deflecting a small part of the laser energy to 3
3 Sensor for power sense and regulation of the laser energy
4 Polygon
Polygon
The Polygon (see 4 in figure above) has 6 facets, each with a mirror. It is turned by a
DC motor which is clock pulsed from the scanning hardware. Pixel times between 2.5
and 0.6 µs can be reached, but for scanning are two times used, 1 and 2 µs.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
5148_02_007.cdr
figure 28
The detector module consists of an acrylic light collection module, an optical filter and a
photomultiplier module (PMM).
The acrylic light collection module, the optical filter and the PMM are cemented
together in order to obtain the maximum available light collection efficiency.
The acrylic light collection unit consists of an acrylic light guide, a collection mirror and
a mechanical mount supporting simple exchange of the detector module.
The aim of this development is to provide high image quality for EUREF compliance
with a detector that can be integrated in a digitizer with maximum similarity to the
CR 75.0 digitizer. The image quality is increased by improved light collection efficiency
with an acrylic light guide.
3
4
figure 29
The lamps are controlled by the erasure control board and the CS board. The lamps
are controlled during work in pairs and also the power supply of 12 V is generated via
5 single transformer. By initialization of the digitizer every lamp is controlled separately.
For erasing the image plate a power input of in total 1000 Watt with 230 V / 50 Hz is
present.
The erasure unit fan (placed in the cPCI Rack) is switched on from the MS board at the
same time the lamps are switched on. After the last scanned and erased image plate
the fan is running a certain time for cooling down the unit.
The lamps are already switched on for 0.5 s before the IP reaches the erasure window.
The speed the IP is transported past the erasure unit is varied between image plate
begin and end for optimized homogeneity – dependent on speed class and format
(Erasure energy per time is determined by means of the demographic data). An image
plate format of 35 x 43 cm is transported centered past the erasure front glass.
The maximal distance from image plate to erasure front glass is 20 mm + 5 mm.
Erasing process is not taking place if scan is in progress or the temperature switch is
detecting to high values and interrupts for a cooling delay.
figure 30
1 Guide plate
2 Rocker for parking position
3 Suction arms
4 Vacuum unit
The IP transport robot leads the IP along the guide plate and puts the IP back to the
cassette in the cassette unit.
The transport robot is guided in the frame of the unit. To move the suction arms back in
working position without a conflict with the next IP coming out of the scanner, the robot
is moved in a parking position.
figure 31
figure 32
figure 33
figure 34
figure 35
figure 36
figure 37
figure 38
5146_REG02_030.CDR
figure 39
figure 40
figure 41
figure 42
5148_Chap02_008.CDR
figure 43
figure 44
figure 45
figure 46
figure 47
figure 48
figure 50
figure 51
6 Software Architecture
The Diagnostics Software is a tool which helps to find defective parts in the digitizer.
A dialog with requests and questions via the display guides you through the test of a
module.
All components of a module (light barriers, boards, motors, valves, mechanics…) are
checked during a test. If the result is satisfying, the module is working in a normal
operating mode. If a problem is detected a problem description and a repair proposal
comes up on the display.
Input buffer and R/F-TAG Opens input door and moves cassette to
position 'silver dot detection'; tests R/F-Tag
reading and writing.
Identified cassette 35 x 43 cm is for this test
needed!
The Software of the digitizer allows access from the Internet to the service level of the
machine. The access via a graphic User Interface (ADC web pages) is part of the
service concept. The web pages follow the structure of the User Terminal.
Access via web pages guarantees a convenient and fast service by making use of
standard tools. The usage of different ports for these ways allows working
simultaneously with FTP, HTTP, and TelNet.
Spare parts which are sent with a floppy, need to be included in the system via
software. The floppy e.g. of the optic module contains specific settings of production
calibration and data of the spare part. This information need to be installed after the
spare part is mounted in the digitizer. For other spare parts sent with a floppy only the
information for the info counter is included.
10-2008
Cassette Unit Optic Module
DD+DIS378.05E
Edition 2, Revision 1
figure 52
Demographic Data Image Data
Data Flow
10
cPCI Unit
Service PC
cPCI Backplane
Legend:
Harddisk
RAM Image Data
Partition C:
Demographic
Data
Partition D: Raw Data (to
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Proc. Station)
Lowpass Filter
Functional Description
Partition E: CPU
ARIEL
I/V converter
IP data
Cassette data Conversion of
Exposure emitted light
Destination into current
Patient
5146_reg02_056.cdr
figure 53
7 Calibration Principle
There are two different calibrations to work out with the CR85-X in the field:
The IP center calibration adjusts two different scan signal settings in one process, the
begin of line (BOL) signal for the fast scan direction and the begin of scan (BOS)
signal for slow scan direction. Both signals in combination are responsible for the area
which is scanned and where pixels are created.
7.1.1 BOL
The BOL sensor is a pin diode placed in the optic module. It controls the switching off
and on of the laser. The sensor is beside the IP, therefore the laser beam hits the
sensor before the IP. Out of the defined distance between the sensor and the border of
the IP the moment of reading out the pixel lines on the IP is set.
7.1.2 BOS
The BOS sensor is a long distance light barrier which is placed at the bottom part of the
scan unit. The light barrier gives the signal to start the scan process in slow scan
direction. When the IP reaches the sensor it is detected and then passes a fixed
distance to the begin of scan line, then the scan process starts.
5146_reg02_059.cdr
A number of lines of a flat field image are averaged and scaled to the maximum pixel
value. All the lines need to be in a certain range to make the calibration successful, if
not the error is displayed at the user terminal.
The y-axis of the coordinate system shows the Scan Average Level (SAL) which is the
digital value (gray scale) of a pixel and is one of the criteria for a successful calibration.
The x-axis shows the number of pixels.
NOTE:
Scan average level (SAL) values have been converted into SAL log or PVI log
from NX 2008 Workstation Software on.
For details please refer to Service Bulletin No. 07 (Intranet link / Extranet link).
CR85-X
Type 5148 / 100
CR75.0
Type 5146 / 100 (Up to SN < 6000)
Type 5146 / 105 (As of SN ≥ 6000)
► Please note
* Access the document by entering the document ID in the Agfa HealthCare Library search window,
or follow the direct link.
Edition 1, Revision 2
05-2011 printed in Germany Document Node ID: 27652068
service_bulletin_cover_e_template_v02
Agfa Company Confidential Copyright © 2011 Agfa HealthCare N.V.
DD+DIS099.09E Software / Hardware Compatibility
This page is intentionally left blank to enable print out of even and odd pages on duplex printers.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin. CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
1 SAFETY DIRECTIONS.............................................................................................................4
1.1 General .....................................................................................................................................4
1.3 To be considered with mechanical Tests of Stepper Motor controlled Drive Units .................4
1 Safety Directions
1.1 General
With every repair work check the following points visually:
Do not
activate! Repairs in progress!
Location:......................
Repairs in
progress. Sign must only be removed by:
..................
figure 1
figure 2
WARNING:
Laser beam! Risk of serious eye damage!
Avoid direct and indirect eye contact.
Do not open the optic module.
Do not hold any tools in the laser beam - risk of reflection.
figure 3
DANGER:
Risk of injury from moving parts of rotation drive.
The rotation drive turns very quickly!
Keep hair, hand and clothing clear when machine is running with the doors open.
figure 4
The power supply for all electronic components, except the PCI-Rack, is interrupted
when the Digitizer is opened. The PCI-Rack remains energized in order to allow file
uploads/downloads.
WARNING:
If the safety switch is overridden with a service key there are risks of injuries.
Keep your hair, hands and garments away from the device.
Remove service key before the device is handed over to the customer.
Laser beam! Risk of serious eye damage!
Avoid direct and indirect eye contact with the laser beam.
Do not hold any tools in the laser beam - risk of reflection.
Consider that the service key must be removed again before the doors are closed.
After use of the service key, the function of the safety switch has to be checked.
CAUTION:
Static discharge! Electrical components may be destroyed:
For the repair on electrical components, wear a grounding strap (CM+9 9999 0830 0)
around the wrist and connect the other end of this strap on a grounded conducting metal
piece.
Since there is a frequent problem with electrical components which are destroyed by
static discharge, protective measures must be taken to avoid this problem. For the
repair on electrical components it is necessary to wear the grounding strap around the
wrist and connect the other end of this strap on a position of the frame which is free of
lacquer.
Be attentive, that the frame is grounded!
CAUTION:
Transportation parts can damage the product.
Remove all transportation parts prior to first operation.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp.
Check that both adjustable feet are touching the ground before removal of the scan unit.
CAUTION:
Wrong screen cleaner may damage the Image plate.
Do not use the AGFA CR phosphor plate cleaner to clean the CR MM3.0 Mammo
image plates. Use PROSAT wipers instead.
WARNING:
Poor image quality caused by incorrect cassette initialization.
Initialize the cassette/plate as described in the corresponding user manual.
CAUTION:
Image quality may be inadequate when using wrong cassettes:
Only cassettes with both labels “CR MD4.2 Extremities” and “Extremities code XX”
must be used for the Extremities application
(XX depends on the plate sensitivity SAL).
Other cassettes must not be used.
WARNING:
Risk of electric shock!
Switch off the digitizer before performing any service interventions at the digitizer.
CAUTION:
Do not try to unscrew the screw in the left upper position (see arrow)!
It is secured by lacquer.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp.
Check that both adjustable feet are touching the ground before removal of the scan unit.
WARNING:
Risk of electric shock!
Make sure that the digitizer is switched off, before you remove the optic module.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp.
Check that both adjustable feet are touching the ground before removal of the scan
unit.
CAUTION:
Risk of damage!
Photomultiplier and light collector are glued and must be treated as one component.
WARNING:
Risk of electric shock!
Switch off the digitizer and disconnect the machine from the mains.
Safety instructions for electronical parts see Chapter 3.1
DANGER:
Risk of injury from moving parts of rotation drive.
The rotation drive turns very quickly!
Keep hair, hand and clothing clear when machine is running with the doors open.
CAUTION:
Risk of damaging the scan unit.
Do not remove the scan rollers. Clean the scan rollers in place by moving the slow scan
motor manually.
CAUTION:
Risk of damage when using wrong cleaning method.
Do not use any fluid for cleaning of the inner side of the large glass plate since it is
coated with a gelatin layer.
CAUTION:
Wrong screen cleaner may damage the Image plate.
Do not use the AGFA CR phosphor plate cleaner to clean the CR MM3.0 Mammo
image plates. Use PROSAT wipers instead.
WARNING:
Poor image quality caused by incorrect cassette initialization.
Initialize the cassette/plate as described in the corresponding user manual.
Type B equipment:
Indicates that the CR 85-X complies with the limits for type B equipment.
Provides a connection between the CR85-X and the potential equalization busbar of the
electrical system as found in medical environments. This plug should never be unplugged
before the power is turned off and the power plug has been removed.
Intergrounding connector:
Provides a connection between the Digitizer and other equipment which might exhibit
minor ground potential differences. These differences may degrade the quality of
communication between different equipment. Never remove connections to this terminal.
Provides a connection between the Digitizer and the protective earth of the mains. Do not
remove this connection, because this will have a negative influence on the leakage
current.
Power on
Power off:
Note that the power cord has to be disconnected from the wall outlet in order to
disconnect the unit entirely from the mains.
CAUTION:
Precautions for use in USA only:
Make sure that the circuit is single-phase center-tapped, if the Digitizer is connected to a
240 V / 60 Hz source instead of a 120 V / 60 Hz source.
5148_Chap3.1_004.CDR
5148_Chap3.1_004
figure 5
The warning label (see figure 6) is placed in the upper left corner of the front side of the
input buffer; details see figure 7.
3mm
5mm
Feed Gate
WARNING:
The erasure unit is hot - up to 200 °C: Risk of burns.
Avoid contact with the Erasure Unit.
Observe the relevant sticker on the Erasure Unit. (see figure 8)
200 c
CAUTION.
Photomultplier is fragile: Risk of damage.
Care must be taken. (see figure 9)
5148_Chap3.1_003
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
2 Service PC (Standard)
Service PC connection: at a RS232 interface beside the mains switch of the ADC
Digitizer.
The optical fiber has been omitted, but the presence of the laser beam can still be
validated by visual inspection through the opened input rollers.
Mind the safety instructions for laser radiation.
4.1.2 Prerequisites
(1) Make sure that the digitizer you want to examine is switched on and you can
access it remotely.
(2) Open your web browser.
(3) Enter the IP address of the digitizer in the URL address field of your browser.
(4) You will be asked to enter a user name and a password. If you do not know the
proper password, please contact GSC Munich.
Æ Result: HTML pages will open with the Welcome Page on your screen.
Plus
Plus
The software display shows an ADC Compact Plus instead of a CR 85-X. This has no
impact from a technical point of view.
Show Info Device Info Typical info on the device, e.g. type.
Device Status Emulates the User Interface; shows the User
Terminal in current status.
User Terminal Messages Like Device Status
Error Messages Shows a history of errors that occurred
during operation, latest error on top.
Network Info Shows network info, e.g. hostname,
IP address.
Test Report Shows and reports history on performed
local service interventions on device. Latest
on top.
Info Counter Shows detailed info on device,
e.g. SW-version, serial number,
modifications.
Scanner Shows calibration lines in graphic format for
various resolutions
(mainly for production purposes).
NOTE:
When selecting files for downloads, these files are first zipped and copied to the
download area (adc_c:\dl\). From the download area, the zip-files can be downloaded
to a directory of your HDD.
IMPORTANT:
The changes confirmed under Local Network ID and
User Terminal Language are activated immediately.
IMPORTANT:
The following item Advanced Access allows access via the command line. It is for
advanced users only. Protective mechanisms are no longer in force.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
Checkpoint 2
Cassette unit
Checkpoint 3
Rotation unit
Checkpoint 7
Postscan transp. Checkpoint 1
Input buffer
Checkpoint 4
Prescan transp.
Checkpoint 6 & Vacuum
Erasure unit
Checkpoint 5
Scanner
figure 1
The reports are checked by the Diagnostic Software for the selected module. The
procedure is not visible on the display of the digitizer only results, problem
descriptions and repair proposals are displayed.
NOTE:
The error numbers of the internal reports are not identical to the error codes shown on
the display.
Ok
Test if X positioning
lightbarrier of motor
M513 is interrupted Error xxxx ocurred when
testing X positioning light
Ok barrier of motor M513
Test if 0 positioning
lightbarrier of motor
Ok M514 is clear Error xxxx ocurred when
testing 0 positioning light
barrier of motor M514
Ok
Test if X positioning
lightbarrier of motor
M514 is interrupted Error xxxx ocurred when
testing X positioning light
barrier of motor M514
Waking up RF-tab reader
Wake up RF-tag reader
failed
Ok
Order RF-tag reader to
Order RF-tag reader to Reading data from tag Cancelling of waiting for
read data from tag failed a new tag failed
Ok
Order RF-tag reader to Writing data to tag failed Ok
write data back to tag
Ok
CASMODCON
ROTCON
Ok
Ok
Ok
Ok
Ok
Ok
Ok
Stopping input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Lift of cassette module x Moving down lift of
is being moved down cassette module x failed
Ok
Unclamping cassette of Unclamping cassette of
cassette module x cassette module x failed
Ok
Ok
Opening cassette in Opening cassette in
module x module x failed
Ok
Closing cassette in Closing cassette in
module x module x failed
Ok
Unclamping cassette in Unclamping cassette in
module x module x failed
Ok
Moving up lift of cassette Moving up lift of cassette
module x module x failed
Ok
Lift of cassette module x
is moved up
Ok
Test connections of
rotation module
Test if clear and interrupt
Move rotation unit home Moving rotation unit functionality of 0
home failed positioning lightbarrier
Ok of motor Mxxx
Ok
Initialize rotation module Initialization of rotation
module failed
Ok
Ok
Test connections of
prescan module
Initializing prescan
module
Test connections of
cassette module Ok
Ok
Unclamp clamper of Unclamping clamper of
cassette module x cassette module x failed
Ok
Move up lift of Moving up lift of
cassette module x cassette module x failed
Ok
Move home belt of Moving home belt of
cassette module x cassette module x failed
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Start input rolls of Starting input rolls of
cassette module x cassette module x failed
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
O
Move down lift of Moving down lift of
cassette module x cassette module x failed
Ok
Unclamping cassette of Unclamping cassette of
cassette module x cassette module x failed
Ok
Clamp cassette of Clamping cassette of
cassette module x cassette module x failed
Ok
Open cassette of Opening cassette of
cassette module x cassette module x failed
Ok
Ok
Start of moving up
prescan robot failed
Ok
Prescan robot started
to move up
Ok
Ok
Ok
Finishing cycle of Finishing cycle of
prescan module prescan module failed
Ok
Ok
Unclamp clamper of Could not unclamp
cassette module x cassette of cassette
module x
Ok
Move up lift of Could not move up lift of
cassette module x cassette module x
Subprogram VACUUM:
Switch off vacuum pump
prescan/postscan
module
Ok
Ok
Ok
Switch on vacuum
pump prescan/postscan
module
Ok
Ok
Ok
Ok
Ok
Ok
User interference:
remove tube
Ok
Test connections of
slow scan module
Ok
Stopping slowscan
rollers failed
Ok
Ok
Move scanner motors Moving scanner motors Moving home pre-align Moving home pre-align
to home position into to home position slow scan drive slow scan drive failed
failed
Test connections of
erasure unit
Ok
Test transformer 1
Ok
Test transformer 2
Ok
Test transformer 3
Ok
Test transformer 4
Ok
Test transformer 5
Ok
LAMPS
Subprogram LAMPS :
Ok
Test connections of
postscan module
Initializing postscan
module
Timeout
Timeoutwhen
whentesting
testingXifif
Timeout when testing X if positioning lightbarrier
puls lightbarrier of of
positioning lightbarrier of motor M403 is interrupted
subnode 2 of GS414 is
motor M400 is clear Test if lightbarrier GS414 interrupted
is interrupted
Error xxxx ocurred when Error xxxx ocurred when
testing X positioning light testing
testingXpulspositioning light
lightbarrier
barrier of motor M400 Ok ofbarrier
subnode2of motor M403
of GS414
is clear isisinterrupted
interrupted
Move home suction
motor of postscan
Ok module
Ok
Ok
Test connections of
rotation module
Test connections of
cassette module x
Ok
Unclamp clamper of Unclamping clamper of
cassette module x cassette module x failed
Ok
Move up lift of Moving up lift of
cassette module x cassette module x failed
Ok
Move home belt of Moving home belt of
cassette module x cassette module x failed
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Start input rolls of Starting input rolls of
cassette module x cassette module x failed
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Move down lift of Moving down lift of
cassette module x cassette module x failed
Ok
Open cassette of Opening cassette of
cassette module x cassette module x failed
Ok
Ok
Close opener of Could not close cassette
cassette module x of cassette module x
Ok
Unclamp clamper of Could not unclamp
cassette module x cassette of cassette
module x
Ok
Move up lift of Could not move up lift of
cassette module x cassette module x
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Start input rolls of Starting input rolls of
cassette module x cassette module x failed
Ok
Stop input rolls of Stopping input rolls of
cassette module x cassette module x failed
Ok
Move down lift of Moving down lift of
cassette module x cassette module x failed
Ok
Unclamping cassette of Unclamping cassette of
cassette module x cassette module x failed
Ok
Clamp cassette of Clamping cassette of
cassette module x cassette module x failed
Ok
Open cassette of Opening cassette of
cassette module x cassette module x failed
Ok
VACUUM
Ok
Waiting for postscan Postscan robot did not
robot to reach upper reach upper position
position
Ok
Ok
Ok
Ok
Ok
Ok
Test connections of
cassette module x
Ok
Unclamp clamper of Could not unclamp
cassette module x cassette of cassette
module x
Ok
Move up lift of Could not move up lift of
cassette module x cassette module x
Ok
Test connections of
cassette module x
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
GS IOB-SIN-5Step Boards:
CM+9 9499 8120 3
1 8
LJGS210sn2.cdr
2/B4-E5
JL 2 JL2
1 8
LJGS210sn1.cdr
1 8
LJGS260sn2.cdr
2/F4-H5
JL2 JL2
1 8
LJGS260sn1.cdr
1 8
LJGS610sn2.cdr
6/D3-H3
JL2 JL2
1 8
LJGS610sn1.cdr
GS IOB-SIN-Step Boards
CM+9 9499 8140 4
2 Fuses Overview
NOTE:
All fuses are slowbow fuses.
* Fuse quality was changed from T 1A to T 2.5A because of too high current load.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
No. 49 (CR 75.0) DD+DIS028.07E.
Edition 2, Revision 1
09-2008 printed in Germany Document Node ID: 10030943
eq_03-5_replacements_e_template_v06
Agfa Company Confidential Copyright © 2008 Agfa HealthCare N.V.
Repair and Service
DD+DIS378.05E Replacements / Repair Procedures
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2008 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
LIST OF CONTENTS
1 SAFETY NOTE.........................................................................................................................5
2 REPLACEMENTS AT THE ERASURE UNIT...........................................................................5
2.1 Removing the Erasure Unit.......................................................................................................5
5.3 Replacing the 5fold Stepper Motor Board at the Scan Unit....................................................19
5.5.3 Installing the new Photomultiplier Module (PMM) with Light Collector ...................................32
5.6 Removing the Scan Unit completely from the Digitizer ..........................................................36
1 Safety Note
WARNING:
Risk of electric shock!
Switch off the digitizer before performing any service interventions at the digitizer.
Required tools:
N.a.
Required time:
Approximately 15 min
Removal:
figure 1
figure 2
figure 3
NOTE:
The glass bulbs of the new lamps must be clean. Use a soft cloth; do not touch with
bare fingers.
figure 4
figure 5
Re-installation:
Required tools:
Socket wrench 7 mm
Required time:
Approximately 10 minutes
Removal:
IMPORTANT:
Do not try to unscrew the screw in the left
upper position (see arrow in figure 6)!
It is secured by lacquer.
figure 6
figure 7
Re-installation:
(1) Plug the cable of the new fan in the
erasure fan unit (see figure 7).
(2) Insert the fan.
(3) Fasten the three screws (marked
with white circles with a socket
wrench 7mm (see figure 6).
NOTE:
For replacing the vacuum pump of the IP transport unit – postscan, it is necessary to
take the complete frame out of the digitizer.
Required tools:
Socket wrench (5.5 mm)
Required time:
Approximately 20 minutes
Removal:
figure 8
figure 9
figure 10
figure 11
figure 12
figure 13
Re-installation:
(1) Follow the steps of Removal in reverse order.
Required tools:
N.a.
Required time:
Approximately 10 minutes.
Removal:
(1) Unplug both plugs.
figure 14
NOTE:
By repositioning the transport unit take care of the guiding bar on the bottom of the
digitizer.
figure 15
Re-installation:
(1) Push the transport unit in the digitizer.
(2) Plug in the 2 plugs.
Required tools:
Socket wrench 5,5 mm
Required time:
Approximately 20 minutes.
Removal:
(1) Remove the IP-transport unit from
the machine.
(2) Move the robot manually to the top
of the frame.
figure 16
figure 17
figure 18
Re-installation:
(1) Follow the steps of Removal in reverse order.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp. Check that both adjustable feet
are touching the ground before removal of the scan unit.
Required tools:
Screwdriver
Required time:
Approximately 5 minutes
Removal:
(1) Unlock the scan unit by loosening
two screws (1) - only half a turn.
Scan Unit
figure 19
Re-installation:
(1) Push the scan unit until it stops.
(2) Fasten the two screws
(see figure 20).
5.3 Replacing the 5fold Stepper Motor Board at the Scan Unit
Required tools:
N.a.
Required time:
Approximately 15 minutes
Removal:
Slide out the scan unit as described in section 5.2, page 18.
NOTE:
Wear a grounding strap (spare part number*: CM+9 9999 0830 0) when touching the
stepper motor board.
* The last digit in the spare part number indicates the spare part revision at release of this document.
When ordering, the actual revision of the spare part is delivered.
5146_Chap3.5_008.cdr
figure 20
5148_Chap3.5_009.CDR
figure 21
Re-installation:
(1) Follow the steps of Removal in
reverse order.
WARNING:
Risk of electric shock!
Make sure that the digitizer is switched off, before you remove the optic module.
IMPORTANT:
There are no serviceable parts inside the
optic module.
Do not open sealed parts of the module.
figure 22
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp. Check that both adjustable feet
are touching the ground before removal of the scan unit.
* The last digit in the spare part number indicates the spare part revision at release of this document.
When ordering, the actual revision of the spare part is delivered.
Required tools:
• Socked wrench 5,5 mm
• Allen key 4 mm
Required time:
Approximately 30 minutes
Removal:
(1) Unlock the scan unit by loosening
two screws 1 - only half a turn.
Scan Unit
figure 23
5146_Chap3.5_050.cdr
figure 24
NOTE:
Locking clips prevent the plug from working loose.
5146_Chap3.5_008.cdr
figure 25
5148_Chap3.5_005.cdr
figure 26
5146_Chap3.5_020.cdr
figure 27
5148_Chap3.5_006.cdr
figure 28
5148_Chap3.5_030.cdr
figure 29
Re-installation:
(1) Insert the new optic module by 2
1
using the two handles: make sure
that both centering pins
(1-2) have engaged.
(5) An IP center calibration and a shading calibration must be done after the
installation (see chapter 3.6).
NOTE:
In case that a digitizer with new cPCI-Rack and USB is used (CR 85-X SN ≥ 4000;
CR 75.0 SN ≥ 6500), copy the floppy disk to a USB memory stick.
, (3) Select
<5 INSTALL data>*
<4 Optics parameters>.
(4) The system requests:
- to compare the S/N on the optic module and the S/N stored on the
floppy disk.
After confirmation the parameters are loaded.
The serial number of the exchange part is automatically entered in the
info counter file under "HW Replacement history" together with date and
counter stamp.
- to update the backup
(5) Make an IP center calibration, see chapter 3.6.
(6) Make a shading calibration of all formats, see chapter 3.6.
(7) Update the backup to save the calibration data.
(8) Select
<3 SAVE data>*
<2 Machine specific data>.
(9) Follow the on-line instructions.
(10) Enter the serial number of the Digitizer on the label of the
optic module floppy disk.
(11) Check the image quality with flatfield exposures (if available, also with test
sheet), see chapter 3.6.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp. Check that both adjustable feet
are touching the ground before removal of the scan unit.
Required tools:
• Allen key 2,5 mm
• Allen key 7 mm
• Screwdriver
Required time:
Approximately 30 minutes
Removal:
(1) Unlock the scan unit by loosening
two screws (1) - only half a turn.
Scan Unit
figure 31
5146_Chap3.5_020.cdr
figure 32
5148_Chap3.5_006.cdr
figure 33
5148_Chap3.5_030.cdr
figure 34
5148_Chap3.5_013.CDR
figure 35
CAUTION:
Risk of damage!
Photomultiplier and light collector are glued and must be treated as one component.
Removal:
4
(1) Loosen the four
Allen screws at the corners of the 3
5148_Chap3.5_060.cdr
figure 36
5148_Chap3.5_063.cdr
figure 37
figure 38
5146_Chap3.5_064.cdr
figure 39
figure 40
5146_Chap3.5_066.cdr
figure 41
5146_Chap3.5_069.cdr
figure 42
5.5.3 Installing the new Photomultiplier Module (PMM) with Light Collector
Re-installation:
(1) Install the new PMM, put in with left
side ahead.
5146_Chap3.5_070.cdr
figure 43
figure 44
5146_Chap3.5_064.cdr
figure 45
figure 46
5148_Chap3.5_060.cdr
figure 47
5148_Chap3.5_063.cdr
figure 48
(8) Re-install the light-well and the optic module in reverse order as described
above.
(10) Push scan unit back into the digitizer and tighten the fastening screws.
(3) Select
<5 INSTALL data>*
<3 PMT settings (mfa/mfb)>.
CAUTION:
Risk of injury when removing the scan unit!
To remove the scan unit safely, use the digitizer ramp. Check that both adjustable feet
are touching the ground before removal of the scan unit.
Required tools:
Allen key 3 mm
Required time:
Approximately 20 minutes
5148_Chap3.5_003.CDR
figure 49
Removal:
(1) Unlock the scan-unit by removing the locking device (3 mm Allen key).
(2) Remove the ramp of the scan unit; it is hidden behind the left side panel.
(3) Hook the ramp into the gaps between the two feet of the digitizer.
(4) Let the scan unit slide onto the ramp.
figure 50
5146_Chap3.5_008.cdr
figure 51
5148_Chap3.5_011.CDR
3 4
figure 52
Required tools:
n.a.
Required time:
Approximately 20 minutes (excluding tasks named in 5.7)
Re-installation:
(1) Unpack the new scan unit as described in the enclosed Installation Instructions.
(2) For sending back the old scan unit use the packing of the new one and follow
the unpacking instructions in reverse order.
NOTE:
Mind to fill out the Defect Label in a correct and detailed way for the
old scan module!
figure 53
(4) Re-install
- the PMM with light collector and dust-brush,
- the light-well
- the optic module
- and the 5fold stepper motor board in reverse order as described above.
(2) Install the mfa / mfb parameters from the enclosed floppy disk via the Service
Menu at the user terminal.
NOTE:
In case that a digitizer with new cPCI-Rack and USB is used (CR 85-X SN ≥ 4000;
CR 75.0 SN ≥ 6500), copy the floppy disk to a USB memory stick.
(3) Select
<5 INSTALL data>*
<3 PMT settings (mfa/mfb)>
(4) Install the optics specific data from the enclosed floppy disk via the Service
Menu at the user terminal.
(5) Select
<5 INSTALL data>*
<4 Optics parameters>
(6) Install the scanner parameters from the enclosed floppy disk via the Service
Menu at the user terminal.
(7) Select
<5 INSTALL data>*
<5 Scanner parameters>
(10) Select
<3 SAVE data>*
<2 Machine specific data>
(12) Enter the serial number of the Digitizer on the label of the
photomultiplier floppy disk.
(13) Check the image quality with flatfield exposures (if available, also with test
sheet), see chapter 3.6.
Required tools:
Socket wrench 7 mm
Required time:
Approximately 30 minutes
figure 54
figure 55
figure 56
figure 57
figure 58
figure 59
figure 60
figure 61
figure 62
NOTE:
Take care that the screws cannot fall into the digitizer.
12
figure 63
13
figure 64
Re-installation:
(1) Re-install the cassette unit in reverse order as described in 6.1 - 6.3.
WARNING:
Risk of electric shock!
Switch off the digitizer and disconnect the machine from the mains.
Safety instructions for electronical parts see Chapter 3.1 and Generic Safety Directions
for HealthCare and Imaging Products.
Required tools:
Screwdriver
Required time:
Approximately 30 minutes (including Software installation)
NOTE:
In order to avoid any damage at the storage board, replace the HDD very cautiously.
NOTE:
Always use the Antistatic wrist strap when working inside the digitizer.
Removal:
(1) Open the front doors. The cPCI-rack
with the storage board (1) is placed
in the frame of the left door.
figure 65
figure 66
NOTE:
These are captive screws. They cannot be removed completely.
figure 67
figure 68
1 Storage board
2 Connector
3 Terminal rail
4 Ribbon cable for hard disk
5 Ribbon cable for floppy disk
6 Hard disk
7 Floppy disk drive
8 Connector
figure 69
figure 70
NOTE:
Hold the hard disk firmly in one hand (see figure 70), while you remove the four round-
head screws with a mid-size screw driver.
figure 71
Re-installation:
(1) To install the new hard disk follow the instructions in reverse order.
NOTE:
For installation instructions of the software on a virgin hard disk refer to the enclosure
delivered with the software. The software can be downloaded from:
MEDNET GSO => Computed Radiography => CR Digitizer => CR 85-X =>
Freeware => CR 85-X - Software - Device Software - ACP_5007
WARNING:
Risk of electric shock!
Switch off the digitizer and disconnect the machine from the mains.
Safety instructions for electronical parts see Chapter 3.1 and Generic Safety Directions
for HealthCare and Imaging Products.
Required tools:
Screwdriver
Required time:
Approximately 20 minutes (including installation)
NOTE:
• In order to avoid any damage at the storage board,
replace the HDD very cautiously.
• Always use the Antistatic wrist strap when working inside the digitizer.
Removal:
(1) Open the front doors of the digitizer.
The cPCI-rack with the storage
board (A) is placed in the frame of
the left door.
figure 72
NOTE:
It is sufficient to loosen the Allen screws.
It is not necessary to remove them
completely.
figure 73
NOTE:
Do not pull the cable itself. Always pull the
plug.
figure 74
figure 75
figure 76
Re-installation:
(1) Connect the Power and the IDE-
cable at the ordered hard disk.
NOTE:
Push it in opposite direction of the board
connections. Be carefull with the cables,
they should not get stuck on the revive
board.
(3) Connect power and IDE cables of
the hard disk with the rack
(see figure 74).
NOTE:
For installation instructions of the software on a virgin hard disk refer to the enclosure
delivered with the software. The software can be downloaded from:
MEDNET GSO => Computed Radiography => CR Digitizer => CR 85-X =>
Freeware
Required tools:
Screwdriver
Required time:
Approximately 10 minutes
Removal:
(1) Open the front doors. The new
cPCI-rack with the storage board
(A) is placed in the frame of the left
door. The fan is placed on top of the
new cPCI-rack.
figure 77
figure 78
figure 79
Re-installation:
(1) Replace the defect fan with ordered fan.
(2) Fasten the 3 screws on top of the fan to fix the fan to the bracket.
(3) Remount the bracket into the digitizer.
(4) Fasten the 2 screws of the bracket.
(5) Connect the power cable.
(6) Close the front doors.
Required tools:
Screwdriver
Required time:
Approximately 15 minutes
Removal:
(1) Remove the revive board like described in 8.1.
(2) Remove the hard disk from the defective revive board.
Re-installation:
(1) Install the hard disk into the new revive board (according to 8.1).
NOTE:
The replacement of the revive board does not require a new installation of the
digitizer software.
Required tools:
Screwdriver
Required time:
Approximately 15 min.
Removal:
(1) Open the front doors. The power supply (A)
with the storage board is placed in the frame
of the left door.
(2) Loose the 4 allen screws
(see circles in figure 79).
Pull out the power supply cautiously.
A
NOTE:
The 4 Allen screws coming with the spare part
power supply can be used, but are only alternative
screws.
figure 80
Re-installation:
(1) Remount the new power supply.
(2) Fasten the 4 screws.
(3) Close the front doors of the digitizer.
Required tools:
Screwdriver
Required time:
Approximately 15 min.
Removal:
(1) Open the front doors. The cPCI-rack
is placed in the frame of the left
door. A B
figure 81
Re-installation:
(1) Connect the grey cable to the
external right side of the new rack
(see figure 81).
(2) Mount the new cPCI-rack.
(3) Fasten the 6 screws of the rack.
(4) Remount revive board, Power
Supply and fan as described in 8.1,
8.2 and 8.4.
(5) Connect any connectors to the
sockets.
(6) Close the front doors of the digitizer.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
DD+DIS174.08E CR 85-X Service Bulletin # 06: “Announcement of Digitizer
Software ACP_5007”
Edition 2, Revision 1
09-2008 printed in Germany Document Node ID: 10026934
eq_03-6_adjustments_e_template_v06
Agfa Company Confidential Copyright © 2008 Agfa HealthCare N.V.
Repair and Service
DD+DIS378.05E Adjustments and Calibrations
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2008 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
LIST OF CONTENTS
3 CALIBRATIONS .....................................................................................................................18
3.1 Possible Reasons for a Calibration.........................................................................................18
4 BACKUP .................................................................................................................................47
Adjustments Calibrations
see section 2 see section 3
Guiding Plate
see 2.2
IP Center
Calibration
see 3.2
Suction Cups
see 2.3
Shading
Adjustment Cycle Calibration
see 2.4 see 3.3
5148_Chap03.6_028.cdr
figure 1
2 Mechanical Adjustments
REQUIRED TIME:
Approximately 30 min.
2.1.1 General
For orientation the two modules of the Cassette Unit are marked with stickers
“Module 1” and “Module 2” on the front side. Adjustment needs to be done if the light
barrier flag is misadjusted and as a result the suction cups do not suck the IP properly.
Carry out this adjustment only if it is sure that the rotation unit is misadjusted, see
check in section 2.1.3. Normally the light barrier flag is pre-adjusted in production and
secured by a positioning bracket.
DANGER:
Risk of injury from moving parts of rotation drive.
The rotation drive turns very quickly! Keep hair, hand and clothing clear
when machine is running with the doors open.
OK
OK
figure 2
figure 3
5148_Chap01_011.cdr
figure 4
(4) Select <2 Cassette module 1> 1 Input buffer & R/F tag Service menu
2 Cassette module 1 Mech.modules
resp. <3 Cassette module 2> 3 Cassette module 2
The selected cassette module will be 4 Rotation Unit
5 Prescan transp. + vac. X :cancel
moved in input position. 6 Scanner :ok
7 Postscan transport
(5) Press confirm key .
5148_Chap01_012.cdr
figure 5
5148_Chap01_013.cdr
figure 6
:ok
-> : exit
5148_Chap01_014.cdr
figure 7
5148_Chap01_015.cdr
figure 8
Service menu
(9) Press confirm key . DIAGNOSTICS
Cassette mod.
5148_Chap01_016.cdr
figure 9
5148_Chap3.6_001.CDR
figure 10
Fine check of ideal position D istan ce 1 = D ista nce 2
2
1
Distance 1 = Distance 2 if flag is
adjusted correctly
(see figure 11).
5145_109.02_aa.CDR
figure 11
The movement of the flag is approximately equal to the difference of the middle axis of
the cassette modules to the hole in the frame (e.g. if cassette module 1 is 2 mm too far
left, move the flag on cassette module 2 for 2 mm to the left side).
A
figure 12
NOTE:
Make sure that the position of both cassette modules are correct before you perform
an Adjustment Cyle (see 2.4 of this Chapter).
REQUIRED TIME:
Approximately 30 min.
2.2.1 General
If a guiding plate is not in perfect
position the IP may be misguided.
The robot carriage cannot insert the
IP in the cassette correctly.
figure 13
1 2 3
Guiding plate too far left: Guiding plate too far right: Guiding plate correct:
IP will miss the cassette IP will miss the cassette IP will enter the cassette
Cassette
IP
Guiding plate
figure 14
(3) Put the suction cups of the robot carriage in upward position.
figure 15
(5) During the last 10 cm of the upward movement the space between the
white plastic gearwheel and the guiding plate has to be examined.
(6) While the robot carriage is being moved to the very top the plastic gear wheel
comes very close to the guiding plate.
fi
gure 16
(8) If the guiding plate touches the plastic gear wheel, touch the bottom ledge of
the guiding plate and move the guiding plate away from the plastic gear wheel.
(9) If the space between guiding plate and plastic gear wheel is more than 2 mm,
touch the bottom ledge of the guiding plate and move the guiding plate towards
the plastic gear wheel.
(10) When the perfect space is reached (1 or 2 mm), fix one screw at the front of the
ledge and check the distance again.
(12) Repeat readjustment until the screws are fixed and the perfect space
is reached.
REQUIRED TIME:
Approximately 30 min.
Problems with insufficient vacuum at the image plate can be caused by non parallel
suction cups. To check if the suction cups are parallel, work out the following steps:
(2) The robot needs to be in lowest position at the transport unit and in
horizontal alignment.
figure 17
figure 18
REQUIRED TIME:
Approximately 30 min.
An adjustment cycle is necessary to define the position of the suction cups and the
return position of the IP.
NOTE:
• Before an adjustment cycle is carried out, make sure that both cassette modules
of the rotation unit are adjusted correctly (see section 2.1 of this Chapter).
• Shown display menus are based on Software Version ACP_4105 and may vary
with further Software updates.
1 INFO
(2) Select <2 MAINTENANCE>. 2 MAINTENANCE
Service menu
OVERVIEW
3 SAVE on floppy
4 SHOW error
5 INSTALL from floppy X :cancel
6 CONFIGURE :ok
7 DIAGNOSTICS
8 CHECKS
5148_Chap01_017.cdr
figure 19
1 SAL inspection
(3) Select 2 Calibration
Service menu
Maintenance
<3 Test and adjust cycle>. 3 Test and adjust cycle
4 Confirm maintenance
5 Confirm repair X :cancel
6 Clear infocounter :ok
7 Confirm modification
8 Confirm installation
5148_Chap01_018.cdr
figure 20
5148_Chap01_034.cdr
figure 21
figure 22
2 mm
figure 23
figure 24
1 INFO
(9) Select <2 MAINTENANCE>. 2 MAINTENANCE
Service menu
OVERVIEW
3 SAVE on floppy
4 SHOW error
5 INSTALL from floppy X :cancel
6 CONFIGURE :ok
7 DIAGNOSTICS
8 CHECKS
5148_Chap01_017.cdr
figure 25
1 SAL inspection
(10) Select 2 Calibration
Service menu
Maintenance
<3 Test and adjust cycle>. 3 Test and adjust cycle
4 Confirm maintenance
5 Confirm repair X :cancel
6 Clear infocounter :ok
7 Confirm modification
8 Confirm installation
5148_Chap01_018.cdr
figure 26
5148_Chap01_021.cdr
figure 27
(12) Carry out two cycles without changing the adjustment, because the second
time the other Cassette Module is picking up the IP.
(14) If the position is ok, repeat the procedure <4 Handling Cycle> three times
with a cassette format 35 x 43 cm and three times with 18 x 24 cm.
If the position is not ok, you have to find a compromise for both units. Move the
stop plate corresponding to the IP position but remember, it will also affect the
other unit. Redo (8) to (14) until the position is for both units ok (see above).
(15) Create a new backup floppy to save the settings for the vertical adjustment.
3 Calibrations
NOTE:
Make sure that the used IPs are dry, clean and do not have artifacts such as
scratches or contamination.
IMPORTANT:
If an IP-center calibration is necessary, always perform a shading calibration
afterwards.
Details
Calibration When
see
* only on 24 x 30 cm and 18 x 24 cm cassette formats. The white border is present only on one side of the image.
REQUIRED TIME:
Approximately 30 min.
NOTE:
The GenRad X-ray source and the Mammography X-ray source require
different prerequisites.
Do not use GenRad X-ray source with Al-filter or Mammography X-ray source
with Cu-filter!
NOTE:
For Mammography X-ray source, in order to fix the Al-filter below the collimation
window, a reliable adhesive tape is necessary. Depending on the adhesive tape,
a solvent may be required for the cleaning of the X-ray source. Make sure the tape
is not getting in the optical path of the X-rays.
Verification 3.4
figure 28
in figure 29.
51
48
_3
. 6.c
dr
figure 30
NOTE:
Best use a dosimeter to measure the dose!
NOTE:
The exposure of the Mammo cassette with a Mammography X-ray source is only
applicable for the Mammography IP-center calibration.
Goal Expose at least the half of the cassette (tube side up), which lies opposite to the
chestwall side, see figure 31.
Exposed area
(= 1/2 of cassette)
cassette
(with tube side up)
(chestwall side)
figure 31
(2) Check that the appropriate window is selected according to the bucky size.
If both, the 18 x 24 cm and the 24 x 30 cm, buckies are available, the smallest cassette
format (18 x 24 cm) has to be used with the largest bucky size (24 x 30 cm). For this
purpose refer to column 1 of the following table.
If only one bucky size is available (cassette format is then identical to the bucky size)
refer to column 2 of the following table.
Column 1: Column 2:
(3) Select the following exposure Select the following exposure
parameters: parameters:
- 20 mAs - 2 x 10 mAs
- 28 kV - 28 kV
- Molybdenium source / Molybdenium - Molybdenium source / Molybdenium
filter (Mo/Mo) filter (Mo/Mo)
- Large focus - Large focus
(5) Place the cassette on the bucky: Place the cassette on the bucky:
- With tube side up - With tube side up
- Horizontally centered - With a slight offset in horizontal
direction.
Move the cassette vertically towards
the bucky chestwall, so that the rear Move the cassette vertically towards
half (opening side) of the cassette is bucky chestwall, so that the rear half
in the middle of the collimation (opening side) of the cassette is in
window. the collimation window.
bucky
figure 33
figure 32
(6) Fix the Al-filter below the collimation Fix the Al-filter below the collimation
window and make sure the tape is window and make sure the tape is
not getting in the optical path of the not getting in the optical path of the
X-rays. X-rays.
(7) Expose the cassette. Expose the cassette.
Perform one single exposure!
Rotation of cassette is not required.
(8) n.a. Remove the Al-filter.
Column 1: Column 2:
(9) n.a. Leave the cassette on the bucky with
tube side up.
Move the cassette horizontally to the
other side of the bucky and vertically
towards bucky chestwall, so that the
rear half (opening side) of the cassette
is in the collimation window.
The marked area
in figure 34 must be within the
collimation window.
bucky
collimation window
cassette
(chestwall)
figure 34
(13) Clean the X-ray source with a solvent. Clean the X-ray source with a solvent.
NOTE:
Close the doors of the digitizer during calibration.
(5) If the right format is detected the calibration starts automatically and you
can skip step (6).
(9) figure 37
(8) Press confirm key .
(9) Perform a shading calibration (see section 3.3) and finally a verification
(see section 3.4).
Information on Details
Reason
the Display see
Check • Flatfield was not used.
collimation and • A defective IP was used (with scratches in slow-
optics 3.2.4.1
scan direction).
NOTE:
The Scan Average Level (SAL) is the digital 12 bit value (gray scale) of a pixel and is
one of the criteria for a successful calibration. The SAL values during a calibration
must be in a range of approximately 730 to 4095.
3.2.4.1 Check collimation and optics (dynamic range bigger than 1:2)
5148_Chap03.6_035.cdr
figure 38
(3) If the failure message pops up again, press the escape key .
Check if the the photomultiplier floppy was installed properly after a PMT
replacement.
Check if the backup floppy was installed properly after a software installation
including hard disk formatting.
Install the corresponding floppy if necessary.
Redo the calibration.
(3) If the failure message pops up again, press the escape key .
Check if the the photomultiplier floppy was installed properly after a PMT
replacement.
Check if the backup floppy was installed properly after a software installation
including hard disk formatting.
Install the corresponding floppy if necessary.
Redo the calibration.
REQUIRED TIME:
Approximately 60 min.
* The last digit in the spare part number indicates the spare part revision at release of this
document. When ordering, the actual revision of the spare part is delivered.
NOTE:
The GenRad X-ray source and the Mammography X-ray source require
different prerequisites.
Do not use GenRad X-ray source with Al-filter or Mammography X-ray source
with Cu-filter!
NOTE:
For Mammography X-ray source, in order to fix the Al-filter below the collimation
window, a reliable adhesive tape is necessary. Depending on the adhesive tape, a
solvent may be required for the cleaning of the X-ray source. Make sure the tape is not
getting in the optical path of the X-rays.
Verification 3.4
figure 39
NOTE:
The GenRad X-ray source can be used for both, the GenRad and the Mammo,
calibration procedure.
figure 40.
51
48
_3
. 6.c
dr
figure 41
NOTE:
Best use a dosimeter to measure the dose!
3.3.2.2 Exposure of the “CR Mammo Calibration Kit” Cassette for a Mammography
X-ray source
NOTE:
The exposure of the “CR Mammo Calibration Kit” cassette with a Mammography
X-ray source is only applicable for the Mammography shading calibration.
(2) Fix the Al-filter below the collimation window and check that the appropriate
window is selected according to the bucky size.
Make sure the tape is not getting in the optical path of the X-rays.
NOTE:
Perform one single exposure!
Rotation of cassette is not required.
NOTE:
Close the doors of the digitizer during calibration.
Selection
Exposure
on the Details
Application Type Remarks
User see
(X-ray source)
Interface
GenRad 1 GenRad GenRad - Use the biggest GenRad 3.3.3.1
fast* (default cassette available (35x43 cm)
2 GenRad selection) - Use Cu-filter
slow
Mammo 3 Mammo GenRad - Use the biggest GenRad 3.3.3.2
(recommended cassette available (35x43 cm)
if available) - Use Cu-filter.
NOTE:
If the Mammo application is not activated:
- A Mammo shading calibration with a GenRad cassette can be performed, anyway.
- A Mammo shading calibration with a Mammo Cassette can not be performed.
figure 43
(3) If the right format is detected the calibration starts automatically and you
can skip step (4).
(4) If the wrong format is detected a Format is smaller than Service menu
warning message will be recommended! Calibration
displayed. Shading
Shading calibration will
- Press the confirm key to only be valid for X :cancel
start the calibration with the calibrated format and :ok
wrong format, or smaller ones.
5148_Chap01_027.cdr
figure 45
- Press the escape key to
stop calibration.
Remove the cassette and
press confirm key .
(7) Redo the calibration for the next application, shown on the display. Continue with
section 3.3.2.
When an application has been calibrated successfully, the remark “o.k.” will be
shown next to the application on the display (see figure 42)
When all 3 applications (GenRad fast, GenRad slow and Extremity) have been
performed continue with the Mammo application (see section 3.3.3.2).
(8) Perform verification (see section 3.4), after all applications have
been calibrated.
(1) Choose one of the 2 possible Select exposure type. Service menu
exposure types. Calibration
1 GenRad Shading
2 Mammo
X :cancel
:ok
5148_Chap03.6_025.cdr
figure 47
figure 48
(3) If the right format is detected the calibration starts automatically and you
can skip step (4).
(4) If the wrong format is detected a Format is smaller than Service menu
warning message will be recommended! Calibration
displayed. Shading
Shading calibration will
- Press the confirm key to only be valid for X :cancel
start the calibration with the calibrated format and :ok
wrong format, or smaller ones.
5148_Chap01_027.cdr
figure 50
- Press the escape key to
stop calibration.
Remove the cassette and
press confirm key .
IMPORTANT:
Ensure that the "CR Mammography calibration kit" cassette is used for
the following steps!
figure 52
(3) If the right format is detected the calibration starts automatically and you
can skip step (4).
(4) If the wrong format is detected a Format is smaller than Service menu
warning message will be recommended! Calibration
displayed. Shading
Shading calibration will
- Press the confirm key to only be valid for X :cancel
start the calibration with the calibrated format and :ok
wrong format, or smaller ones.
5148_Chap01_027.cdr
figure 54
- Press the escape key to
stop calibration.
Remove the cassette and press
the confirm key .
(7) Perform verification (see section 3.4), after all applications have
been calibrated.
Information on Details
Reason
the Display see
Underexposed • The exposure conditions were wrong
(e.g. the dose was too low).
• The filter was not positioned correctly.
• The photomultiplier floppy was not installed properly 3.3.4.1
after a photomultiplier (PMT) replacement.
• The backup floppy was not installed properly after a
software installation including hard disk formatting.
Overexposed • The exposure conditions were wrong
(e.g. the dose was too high).
• The filter was not positioned correctly.
• The photomultiplier floppy was not installed properly 3.3.4.2
after a PMT replacement.
• The backup floppy was not installed properly after a
software installation including hard disk formatting.
Dust detected • Dust is present on the IP.
3.3.4.3
• Flatfield was not used.
Check coll. and • Flatfield was not used.
optics • Collimation was used.
3.3.4.4
• A defective IP was used (with scratches in slow-
scan direction).
Modality is • GenRad:
vignetting - Flatfield was not used.
- A defective IP was used.
- The collimation was used. 3.3.4.5
(Warning
message only) • Mammography:
- Flatfield was not used.
- A defective IP was used.
NOTE:
The Scan Average Level (SAL) is the digital 12 bit value (gray scale) of a pixel and is
one of the criteria for a successful calibration. The SAL values during a calibration
must be in a range of approximately 730 to 4095.
figure 56
(3) If the failure message pops up again, press the escape key .
Check if the the photomultiplier floppy was installed properly after a PMT
replacement.
Check if the backup floppy was installed properly after a software installation
including hard disk formatting.
Install the corresponding floppy if necessary.
Redo the calibration.
figure 57
IMPORTANT:
For Mammography X-ray source, even if the dose has to be
decreased due to overexposure, the settings must not fall below
50 mAs and 0.5 s.
(3) If the failure message pops up again, press the escape key .
Check if the the photomultiplier floppy was installed properly after a PMT
replacement.
Check if the backup floppy was installed properly after a software installation
including hard disk formatting.
Install the corresponding floppy if necessary.
Redo the calibration.
(4) Check if the exposure parameters have been the same as shown on the display.
(6) Check on the IP the presence of scratches in slow scan direction and of dust.
Look for another IP which is dry, clean and immaculate.
3.3.4.4 Check collimation and optics (dynamic range bigger than 1:2)
figure 58
In case the Mammo exposure type was selected and the above actions do not
show success:
- Look for the Mammography X-ray source with the smallest heel effect.
- Redo the calibration with this X-ray source and use the same bucky size
as for the first exposure.
figure 59
5148_Chap03.6_002.cdr
figure 60
(7) If the above actions do not show success and in case the Mammo exposure type
was selected:
- Look for the Mammography X-ray source with the smallest heel effect.
- Redo the calibration with this X-ray source and use the same bucky size
as for the first exposure.
(8) If the warning message still pops up, and still in case the Mammo exposure type
was selected, the following workaround is possible:
- Take a flatfield as evidence that the collimation area of the X-ray source does
not fit with the IP position in the bucky.
- Explain the problem to the customer and ask him to call the X-ray supplier for
a service intervention.
- Carry out a final calibration after the service intervention on the X-ray source.
NOTE:
In this workaround the left and the right 3 mm of the image are not shading
calibrated. It is the customer’s responsibility to use this workaround and to handle
the mismatch of cassette position and beam collimation.
NOTE:
The calibration verification is always taking place after the shading calibration was
performed. There is no sense to perform the IP-center calibration verification before
the shading calibration procedure is done.
(1) Expose a cassette with a regular flatfield, to check the image quality of each used
application as described in the following table:
On CR QS Processing Station:
figure 61
On NX Processing Station:
figure 62
On CR QS Processing Station:
figure 63
On NX Processing Station:
figure 64
(3) Insert the cassette into the Digitizer.
(4) Print the image with a window setting of 1.2 (level setting leaves unchanged).
(5) Check the image quality of the flatfield for absence of any stripes and large area
inhomogenities (shading calibration) and for absence of lateral borders (IP-center
calibration).
(6) Start the backup to save the new calibration parameters (see section 4).
4 Backup
(1) Update the backup storage media to save the new machine specific data
(calibration, PD-factor).
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
CR 85-X
Type 5148/100
CR 75.0
Type 5146/100 (Up to SN < 6000)
Type 5146/105 (As of SN ≥ 6000)
* Previously supplied software versions (prior to version ACP_4005) are no more listed in this document.
► Document History
► Referenced Documents
Document Title
DD+DIS233.08E CR Mammography Solution, Service Bulletin No. 37
Edition 1, Revision 0
07-2010 printed in Germany Document Node ID: 12099766
eq_standard_e_template_v07
Agfa Company Confidential Copyright © 2010 Agfa HealthCare N.V.
DD+DIS207.10E Repair and Service
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright 2010 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
LIST OF CONTENTS
1.2 Changes in Service and Customer functionality since Software Version ACP_5102 ..............4
2.2 Changes in Service and Customer functionality since Software Version ACP_5007 ..............5
Software was adapted in order to avoid issues during the sensitivity adjustment done in
the production line.
Mammo cassettes are not closed while turning the cassette module with the
empty cassette. This prevents possible damage of the fleece of the new type
of Mammography cassettes.
In the screen which is displayed after a shading calibration failed, was no option
to skip this menu. Now the <Chancel> bottom is available to skip this screen.
Support of the new revive-racks for CR 85-X with USB interface instead of
floppy disk drive.
HQ_0511110001: Improved handling of RF-Tags. The software will not write
anymore data in protected sectors of the RF-Tag.
New screens of the shading calibration are translated in the different languages
(Version ACPL5007 of the language floppy).
New version of operating system “portex 2006.02”
Modified menu:
o Specific terms like “floppy“ are replaced by e.g. “storage medium”.
o New version of language files
Support of the new revive-racks for CR 85-X with USB interface instead
of floppy disk drive.
Modified calibration procedure:
o IP-Center and Shading calibration is also possible with cassettes
exposed on mammography X-ray modalities.
Modified user interface (Service Menu):
o Service menus for calibrations are adapted to the menus of
CR 25.0 / CR 35-X.
o Improved shading calibration screens
o New version of language files
o Specific terms like “floppy” are replaced by e.g. “storage medium” or “data”.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
A Identification Diagrams
100
500
100
400
600
MC101
GS204
GS314
ST319
1 8
M212
JL1
GS202
G S206
Si1 GS100
Si2
Si3
Si4
Si6
Si7
TR106 Si8
Si9
S103 Si10
Si11
M101 Si12
Si13
GS102
TR105
GS104
S102
TR104
TR103
TR102 5 1 46 0 7af.cd r
TR101
8
JL1
G S210
JL2
1
1
G S220
G S230 G S216
G S214 M 205
M 202
M 201
M 203
M 204
G S222
G S226
G S224
5 14 60 7a k.cd r
G S228
8
JL1
GS260
JL2
1
1
GS270
GS280 GS266
GS265 M210
M207
M206
M208
M209
GS278
GS276
GS274
5 14 60 7 al.cd r
GS277
M701
M300
GS302
GS304
GS300
GS310
GS312 GS306
MG422
JL1 GS420
1
5 1 4 60 7a j.cd r
GS434
GS432
M403 GS426
GS424 M402
GS428
1 JL1 8
MG411
GS402
MG402
GS406
MG401
GS404
JL1 1
GS412
M400 GS410
GS414 GS408 M401
GS416
GS418
8 JL1 1
JL1
1 8
GS514 GS510
GS518
M514
GS516
M513 GS512
GS532
JL1
GS536
1
GS538
GS540
JL1
1 8
GS552
M516
GS554
GS560
GS562
GS556 GS558 M515 GS564
514607ao.cdr
1 JL1 8
GS570 GS568
GS566
8
JL2
JL1
GS610
1
1
GS620
GS622 GS616
GS612
M622
M702
M612
5148_Chap04_001.CDR
13.1 Diagram
M621
GS628
GS618
GS614 GS626
5148_Chap04_002.CDR
LA7
LA8
LA9
LA10
LA1
LA2
LA3
LA4
LA5
LA6
B Circuit Diagrams of
CR 85-X (CR 75.0 Type 5146/105) Digitizer
The Circuit Diagrams (Sheets 1-7) can be found on the following pages.
ST5
*3/3
INPUT N N1 1 1 11 12 1 1 7 8 1 1 1/3
BU132
3 4
Netz
1 1 3 3/3
Last
BU876
appliance inlet 250VAC 1 BU3-02A
BU134
ST110
10A BU123 BU130
IEC 320 22
BU122 1 21 1
L L1 1
13.0
VAC
2/6 2 8 208VAC
2 2
MA120 MA122 MA123 7 13
3/6 3 200VAC
/CPCI_RACK.1H 15
MA_DOOR_LEFT
13.0
VAC
4/6 4 6 3.2AT 0V
17
3 1 B9911095-V
2 3 3 1 BU2 ST102 TR102
1/6 1 9 230VAC 11
/CPCI_RACK.2A 1 2 2 1
POWER_RACK
13.0
1 1
VAC
BU105 ST105 2/6 2 8 208VAC
7 13
3/6 3 200VAC BU112 ST113
15
1 1
13.0
2 2
VAC
ERASURE_DRILLED
ST6 BU135 4/6 4 6 3.2AT 0V 3 3
1/2 1 4 4
2/2 2 17 5 5
3 D42 RED 200V D14 RED SI1-12 OK 6 6 3
B9911095-V 7 7
BU3 ST104 TR103
1/6 1 9 230VAC 11 8 8
BU136 9 9
13.0
ST5 D14 YELLOW +24V
VAC
X #25 D42 YELLOW 208V 10 10
#0/27 2/6 2 8 208VAC
/PRE_POST_TRANSPORT_UNIT.1H
Prescan
GND-5
D42 GREEN 230V D14 GREEN +5V 13
3/6 3 7 200VAC /ERASE_UNIT_700.3A
15
1 GND5 ST129 BU1 BU2 ST103
13.0
4 4/12 4/12 4
VAC
ST122 BU5
X
#25
ST3 BU113 BU137 ST4 4/6 4 6 3.2AT 0V 3 3/12 3/12 3
#0/27 *5/5 *5 *5 *5/5
/PRE_POST_TRANSPORT_UNIT.1D 12 12/12 12/12 12
Postscan GND_2 17 6 6/12 6/12 6
2 2/12 2/12 2
GND2 SI12 T1A D32 B9911095-V 11 11/12 11/12 11
BU4 ST106 TR104
1/6 1 9 230VAC 11 9 9/12 9/12 9
ST115 BU4 GS428-PRE-SUCTION-BD 1/12
1 1/12 1
13.0
+40V 1 1/9
VAC
SI11 T1A D29 7 7/12 7/12 7
+40V 2 2/9 2/6 2 8 208VAC 10 10/12 10/12 10
/INPUT_and_OUTPUTBUFFER.6C GND 4 4/9 GS434-PRESCAN-SLED-BD
SM_Outbuffer GND 13
4 5 5/9 SI10 T1A D28 3/6 3 7 200VAC 4
15
+40V 3 3/9 GS412-POSTSC-SUCT-BD
13.0
VAC
/CASSETTE_UNIT.6A GND 6 6/9 SI9 T1A D27 6 3.2AT
Cas_Rotation 4/6 4 0V
GND 7 7/9 GS418-POST-SLED-BD BU102 ST1
Signale 8 8/9 SI8 T1A D26 17 *20 #20/22
/ERASE_UNIT_700.5A
Erasure_Fan +24V 9 9/9
GS202-ROTATION-BD
B9911095-V
SI7 T1A D25 BU5 ST107 TR105 GS104 CURRENT-SENSE
ST116 BU3 1/6 1 9 230VAC 11 F8.5155.6440.x
+40V 1 1/4 GS552-OUTBUFF-PUSH-BD
13.0
VAC
/INPUT_and_OUTPUTBUFFER.6D GND 2 2/4 SI6 T1A D24
Inbuff_Belt 2/6 2 8 208VAC
+40V 3 3/4 GS556-OUTBUFF-ROLL-BD
/INPUT_and_OUTPUTBUFFER.6F GND 4 4/4 13
Inbuff_Door SI5 T1A D23 3/6 3 7 200VAC
15
GS532-INBUFF-DOOR-BD
13.0
VAC
SI4 T1A D22 4/6 4 6 3.2AT 0V
1 +40V 2 GND CASS_1
BU115 ST4 GS510-INBUFF-BELT-BD
3 +40V 4 GND CASS_2 17
*4 *4/4
/CASSETTE_UNIT.1A SI3 T2,5A D21 ST2 BU101
5 Cass_Unit1_2 GS610-5FOLD-ST-SCAN #20/22 *20 #20
5
SI2 T2,5A D20
GS260-5FOLD-ST-CASS2
ST117 BU2 ST3 BU114
1 +40V 2 GND *2 *2/2 SI1 T2,5A D19 1/6 1 11 15
/SCAN_OPTIC_UNIT.1F
SM_Scan GS210-5FOLD-ST-CASS1 230VAC /16
30VAC
2/6 2 10 208VAC
3/6 3 9 200VAC
SI13 T2,5A D33 Green POWER-UNIT-FAN
BU103 ST1 4/6 4 T6.3A 0V 18
+24V ST2 BU120 7
IO_MSB *26 *26/26 /19
#26 ALARM WHITE
3/3 3
S
/INPUT_and_OUTPUTBUFFER.6D TR106
GND BLACK GS102 ERASURE-CTRL-DB B9911091-V
2
2/3 2
F8.5155.6410.x
1/3 1 +24V RED
1
GS100 M-S-BOARD
*26/26
F8.5146.4893.x M101
ST1
BU6
We reserve all rights in this document and in the informa-
1/3
3/3
tion contained therein. Reproduction, use or disclosure
to third parties without express authority is strictly
6
6
BU104
*26
ST114
1
DATE NAME
CIRCUIT DIAGRAM Project
USER 2.11.05 Leith.
APPR.
CR85 5148
(1)
NORM Sheet name: POWER_UNIT / 100
forbidden.
Sheet 1
© AGFA
F1.5148.4003.0
#26
0 21957 8.21.05 of 7 SH
/CPCI_RACK.2H
A B C D E F G H
IO_Cass_Units
Cass_Unit1_2
PE8
XL200
F8.8360.7000.x F8.9499.6580.x F8.9499.4630.x F8.5100.7460.x F8.9499.6540.x F8.9499.5880.x F8.9499.6540.x F8.9499.6540.x F8.8360.7000.x F8.9499.6580.x F8.9499.4630.x F8.5100.7460.x F8.9499.6540.x F8.9499.4630.x F8.9499.6540.x F8.9499.6540.x
#26
1 GS226 -CASS1- GS228 -CASS1- GS222 -CASS1- GS216 -CASS1- GS230 -CASS1- GS224 -CASS1- GS214 -CASS1- GS220 -CASS1- GS276 -CASS2- GS277 -CASS2- GS278 -CASS2- GS266 -CASS2- GS280 -CASS2- GS274 -CASS2- GS265 -CASS2- GS270 -CASS2- 1
BU201
BU200 ST200
XL201
SWITCH OPEN-0-LS IN-DET-LS IN-DET-LS CLAMP-LS CLAMP-0-LS LIFT-0-LS BELT-0-LS SWITCH OPEN-0-LS IN-DET-LS IN-DET-LS CLAMP-LS CLAM-LS- LIFT-0-LS BELT-0-LS
8
7
6
5
4
3
2
1
PE9
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
*3/3
*4/4
*3/3
*4/4
8
7
6
5
4
3
2
1
ST201
GND
GND
PE10
GND
GND
+40V
+40V
+40V
+40V
XL202
BU209
BU210
BU212
BU243
BU242
BU213
BU214
BU215
BU216
BU238
BU248
BU246
*3
*4
*4
BU250
BU252
BU211
*4
*4
*4
#2*4
*4
*4
*3
BU240
*4
#2*4
*4
*4
*4
*4
#6
#4
#4
#4
#4
#4
#6
#4
#4
#4
#4
ST204
BU203
BU245
BU241
BU251
BU217
BU239
BU249
BU220
BU221
BU222
BU223
BU237
BU247
BU219
BU218
#6
#6
*4
*4
*4
*4
*4
*4
*4
*4
*4
*4
*4
*4
9
8
7
6
5
4
3
2
1
#26
BU866
ST51 ST39
ST8
ST40 ST2 ST38 ST51 ST39 ST40 ST2 ST38
ST8
#4/6
ST11
#4/6
#6/8
#4/6
#4/6
ST1
#4/6
#4/6
ST37
#4/6
#4/6
#4/6
ST11
#4/6
#6/8
#4/6
#4/6
ST1
#4/6
#4/6
ST37
#4/6
#4/6
#26ST203
BU208
9
8
7
6
5
4
3
2
1
BU236
XL203
ST12 ST12
*26 #26 *26/26 *26 *26/26
#26
PE7
2 2
ST205 BU1 ST206 BU1
1
3 2 2/2 2 2/2
JL1
JL1
JL2
JL2
12345678 12345678 12345678 12345678
GS260
GS210 5FOLD-ST-CASS2
5FOLD-ST-CASS1 CASSETTE_MODUL 1 F8.9499.8120.X
CASSETTE_MODUL 2
F8.9499.8120.x
ST35
ST35
ST14
ST17
ST24
ST33
ST34
ST14
ST17
ST24
ST33
ST34
*4/4
*4/4
*4/4
*4/4
*4/4
*4/4
*4/4
*4/4
*4/4
*4/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
1/4
2/4
3/4
4/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
4/4
3/4
2/4
1/4
1/4
2/4
3/4
4/4
200MA7
BU225 BU226 BU227 BU228 BU229 BU253 BU254 BU255 BU256 BU257
200MA17
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
200MA15
200MA5
ST4-01A-ADAP-V
ST4-01A-ADAP-V
ST4-01A-ADAP-V
ST4-01A-ADAP-V
ST4-01A-ADAP-V
4
3
2
4
3
2
1
ST4-01A-ADAP-V
3 3
BU231
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
BU230 BU262
4
3
2
1
BU232 BU258 BU260
A1
A4
A3
A2
A1
A4
A3
A2
A4
A3
A2
A1
A2
A1
A4
A3
A4
A3
A2
A1
A1
A4
A3
A2
ST236 ST237 ST238 ST260 ST262
ST258
B4
B3
B2
B1
B1
B4
B3
B2
B1
B2
B3
B4
B1
B4
B2
B1
B3
B4
B3
B2
B4
B3
B1
B2
BU233 BU234 BU235 BU261 BU263
BU259
4
3
2
1
200MA13
200MA19
200MA3
200MA11
200MA1
4
3
2
1
4
3
2
1
4
3
2
1
4
3
2
1
200MA9
4
3
2
1
200MA18
200MA2
200MA14
200MA20
200MA12
200MA16
200MA10
200MA8
200MA4
200MA6
4 4
GNWT
GNWT
GNWT
YEWT
GNWT
YEWT
GN
GN
GN
GN
GN
YEWT
GNWT
GNWT
YEWT
YEWT
YEWT
YE
YE
GN
YE
YE
YE
YE
YE RD YE RD YE RD YE RD
BK BK BK BK BK BK
OR BKWT BKWT OR BKWT OR BKWT BKWT OR BKWT
M BR M RDWT
RD (1)
M RD
RDWT
M BR M RDWT
RD
M BR M RD
RDWT
M RD
RDWT
M BR M RD
RDWT
M201-CASS1-ROLLER-MOT M204-CASS1-OPENER-MOT M202-CASS1-LIFT-MOT M205-CASS1-BELT-MOT M203-CASS1-CLAMP-MOT M206-CASS2-ROLLER-MOT M209-CASS2-OPEN-MOT M207-CASS2-LIFT-MOT M210-CASS2-BELT-MOT M208-CASS2-CLAMP-MOT
F8.5145.4524.x F8.5120.5165.x F8.5120.5165.x F8.5120.5165.x F8.5120.5165.x F8.5145.4524.x F8.5120.5165.x F8.5120.5165.x F8.5120.5165.x F8.5120.5165.x
5
5
F8.5145.9010.x
BU264 GS206 -ROTAT-0-POS-LS
ST1
IO_ROTATION *26 *26/26 ST2 BU267 BU269 ST1
/CPCI_RACK.1H #26
#4/6 *4 #4 *4 #4/6
BU265 ST4
1+40V 1 1/5
Cas_Rotation #3/5
/POWER_UNIT.4A JL1
2 GND 5 5/5
We reserve all rights in this document and in the informa-
tion contained therein. Reproduction, use or disclosure
BU266 12345678
4 4/4
to third parties without express authority is strictly
YE RD 3 3/4 F8.9499.6770.x 6
6 2 2/4 ST5 GS204 -ROT-WORKPOS-LS
1 1/4 DATE NAME
OR ST3 BU268 BU270 ST1 CIRCUIT DIAGRAM Project
GS202 #4/6 *4 #4 *4 #4/6 USER 2.11.05 Leith.
M BR
200MA22 200MA21
-ROTATION-BD APPR.
CR85 5148
M212-ROTATION-DRIVE F8.9499.8140.X NORM Sheet name: CASSETTE_UNIT / 100
F8.5145.4574.x
forbidden.
Sheet 2
© AGFA
0 21957 F1.5148.4003.0 of 7 SH
/POWER_UNIT.2A
MA_DOOR_LEFT
MA121
M300
CPCI-RACK-FAN
ST1 BU868
M BU5
*3/3
BU1
*3/3
*26/26 *26 #26 IO_OUTBUFF
/INPUT_and_OUTPUTBUFFER.6C
1 ST2 BU869 1
2 1 *26 IO_ROTATION
*26/26 #26
ST308 BU309 ST1 BU1 /CASSETTE_UNIT.6A
1 1 1 1/2 BU305
ST3
2 2 2 2/2 *26/26 *26 IO_OPTICS
BU6 ST1 #26 /SCAN_OPTIC_UNIT.1F
#48/50 #48/50
ST4
*26/26 BU306 IO_8_INBUFF
#26 /INPUT_and_OUTPUTBUFFER.6F
*26
ST5 BU307
ST307 *26/26 *26 #26 IO_POSTSCAN
/PRE_POST_TRANSPORT_UNIT.
GS306 BU1
CPCI-POWER #25 #25/27 BU308
#26 ST6
*26/26 *26 IO_Cass_Units
#26 #26 /CASSETTE_UNIT.1A
BU310 MC300 BU311 26
L 1 SCHIRM 26/27
ST7 BU7
L L1 SHIELDING *26/26 *26 IO_PRESCAN
#26 /PRE_POST_TRANSPORT_UNIT.
BU312 BU322 ST3
POWER_RACK PE 3A 1 1 1/4
/POWER_UNIT.2A 250VAC 2/4 GS314 IOBUS-DISTRIB.
BU313 3 3/4 3J4 F8.9499.6020.x
2 N 1 4 4/4 #135/137 2
N N1
BU323
PE103 1
3J1
#135/137
BU4 ST304
3 1/17 1 bk 3
2/17 2 br
8/17 8 rd
9/17 9 or
10/17 10 ye
15/17 15 gn
3/17 3 bk
4/17 4 br
7/17 7 rd PM_1
11/17 11 or /SCAN_OPTIC_UNIT.1E
2J4 BU2 12/17 12 ye
#135/137 #135/137
14/17 14 gn
5/17 5 bk
6/17 6 br
13/17 13 rd
16/17 16
17/17 17 (1)
300MA2
BU6 ST306
#10/11 #10 POLYGON_CTRL
/SCAN_OPTIC_UNIT.1E
4 BU302 300MA3 4
ST2
#9/11 #9 #10 RF_READER
2J1 BU1 /INPUT_and_OUTPUTBUFFER.6F
#135/137 #135/137 10
10/11
BU3 ST303
#9/10 #9 LCD
/INPUT_and_OUTPUTBUFFER.6B
BU5 ST305
#25/27 #25 #26
26/27 26 SCHIRM
SHIELDING
ST2 BU314 BU317 ST1 ST1 BU301
#34/36 *34 (34) *34 #34/36 #25/27 #25
300MA4
26 #26 LD_MODULE
26/27 /SCAN_OPTIC_UNIT.1F
ST1 BU315
1/4 1 ST319
GS304 2/4 2 GS310 SCAN-CTRL-MASTER
FLOPPY F8.5146.1460.x
5 L7.8506.9520.x BU320
1 A1 B1 5
2 A2 B2
3 A3 B3
ST1 BU316 ST310 ST318 BU3 ST1 BU321
1/4 1
BU318
1 1/4 *8/8 *8
4 A4 B4 ETHERNET
1J4 P4 (8) 5 A5 B5
2/4 2 1 1 2 2/4 #135/137 #135/137
2 2 6 A6 B6
3/4 3 3 3/4
3 3 7 A7 B7
4/4 4 4 4/4
4 4 8 A8 B8
8/11 8 5
tion contained therein. Reproduction, use or disclosure
6
6
Sheet 3
© AGFA
0 21957 F1.5148.4003.0 of 7 SH
/POWER_UNIT.
/CPCI_RACK.2H
A B C D E F G H
Prescan
IO_POSTSCAN
Postscan
IO_PRESCAN
#26
ST401 BU401
*26 *26 ST403 BU425
#25 #26
#25 *26 *26
1 1
SUCT. GND 17
SUCT. GND 4
SUCT. +40V 16
#26
BU424 ST402
BU400 ST400 SUCT. +40V 3
26 GND4 1 26 26
26
(1) SLED GND 15
GND3 GND_4
GND_3 GND
SLED 2
ST715 BU857 BU400 ST400 BU424 ST402
*10 #26 #25 #25 #25 #25 SLED +40V 14 #16 #25 #25 #25
#3
*10 S4557 X SLED +40V 1
S4554
XL402
1 1/4
24
9
4
11
25
3
1
#26
12
13
22
11
23
3/4
16
3/4
15
10
17
14
1 #26 #26 BU452
1 2/4 2/4
7 and 20
7 and 20
6 and 19
5 and 18
6 and 19
5 and 18
1
8 and 21
8 and 21
GND
GND
ST409 ST714
GND
GND
+40V
+40V
+40V
+40V
ST4-01A-ADAP-V ST4-01A-ADAP-V
PE104
BU462
PE105 27 27 BU427 BU450
2 2
PE3
#2 1 A1 B1 1 GS401 SOL-VALE-POST 28 28 1 A1 B1 1 +24V
GS422 SOL-VALE-PRE
SUCT.
SUCT.
SUCT.
SUCT.
29 29
SLED
SLED
SLED
SLED
#2 2 A2 B2 2 SOLENOIDE_VALVE 2 A2 B2 2 GND SOLENOID_VALVE
3 A3 B3 3 F7.0424.2164.0 30 30 3 A3 B3 3 +24V
1
PE2
#2 F7.0424.2164.0
#2 4 A4 B4 4 31 31 4 A4 B4 4 GND
(1)
32 32
BU855 BU460 33 33
XL727
3 3
POINDS-LEFT-LS POINDS-RIGHT-LS
POINDS-MG-RIGHT
HU-24-F-24V-V HU-24-F-24V-V
MG401 POINS-MG-LEFT MG402
ST406 ST407 BU446 #2
BU445 1 1 F8.5145.4524.x
1 1 #2
2 2 PRE-SUCT-DRIVE
2 2 M402
4 4
BR
M
GND
+40V
ST1 BU431 ST1 BU856 OR
27 and 28
29 and 30
#4/6 *4 #4/6 *4
BU436
2
4
RD YE
GS424 GS426
#4
400MA6
F8.5145.4524.x F8.9499.5880.x F8.9499.5880.x BU2
POST-SUCT-DRV ST2
*4
ST4
1/5
2/5
4/5
5/5
#4/6
12345678
M400
#2
BR *4 #4/6
#4
M BU435 ST5 BU437
GND
ST1
2 +40V
JL1
BU415
#52
PE4
#4/6 *4 #4/6 *4 2/4 2
27 and 28
29 and 30
RD YE 4/4 4
GS408 F8.9499.8140.x
400MA2
GS410
#4
4/5
5/5
#4/6 F8.5145.4574.x
XL403
12345678
#52 #2
2/4 2 ST1 BU438 ST1 BU439 #2
PE5
GND
3/4 3 #4/6 *4 #4/6 *4 OR
+40V
GS412 POSTSC-SUCT-BD
BU443
4/4 4
4
F8.9499.8140.x
31 and 32 GS430 GS432
XL401
RD YE
#4
400MA1 F8.9499.5880.x F8.9499.5880.x
400MA8
BU440 ST2
F8.5145.4574.x
ST4
*4
1/5
2/5
4/5
5/5
33 and 34 #4/6
12345678
POST-SLED-DRV
M401 PRE-SLEDPOS-LS PRESC-SLED-0-LS BU441 ST3
*4 #4/6
#4
BR BU442 ST5 BU444
ST1 BU417 ST1 BU418 #2
#2
M *26
ST1
*26/26 1/4 1
JL1
#26
GND
F8.9499.5880.x RD YE
F8.9499.5880.x
We reserve all rights in this document and in the informa-
400MA4
BU419 ST2
tion contained therein. Reproduction, use or disclosure
*4 400MA7
ST4
1/5
2/5
4/5
5/5
#4/6
to third parties without express authority is strictly
12345678
2/4 2
GS418 POST-SLED-BD 3/4 3 APPR.
CR85 5148
POSTSLED F8.9499.8140.x 4/4 4
NORM Sheet name: PRE_POST_TRANSPORT_UNIT / 100
forbidden.
400MA3 Sheet 4
© AGFA
0 21957 F1.5148.4003.0 of 7 SH
GS554 -OUTBUFF GS562 -OBUFF- GS560 -OBUFF- GS564 -OUTBUFF GS518 -INBUFF- GS516 -INBUFF- GS514 -INBUFF- GS540 -CASS-DOT-DETECT GS534 -INBUFF- GS530 GS538 -RF-TAG-
-PUSH-LS CASS-DET CASS-DET -ROLL-LS BELT-LS CASS-DET CASS-DET F8.9499.6940.X DOOR-LS ANTENNA
EMERGENCY-NODE
1 F7.0486.1318.X F7.0486.1316.X 1
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
#4/6
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
ST1
*4/4
*4/4
*26/26
BU500
BU501
BU504
*4
*4
BU503
*4
*4
BU506
*4
BU507
*4
BU508
*4
BU509
*4
BU510
*4
ST1
#2
#2
BU511
*26
#4
#4
#4
#4
#4
#26
BU515
BU512
BU513
BU514
BU516
BU517
#4
*4
*4
#6
#6
*4
*4
ST2
#6/8
ST2
#4/6
ST2
#4/6
ST3
#4/6
ST2
#4/6
ST2
#6/8
ST2
#4/6
2 GS532 -INBUFF- 2
DOOR-BD
F8.5145.4410.X
GS558 -OBUFF-
12345678
12345678
12345678
12345678
#4/6
#4/6
ST1
ST1
BU1
*6/6
BU531 ST3
BU518
*4 #4/6
BU530
JL1
JL1
*4
*4
JL1
JL1
ST1
BU529
#4
ST3
ST502
*4
*6
GS552 -OUTBUFF- BU519 GS556 -OUTBUFF- GS510 -INBUFF- #4/6 #4
ST3
#4/6 *4
PUSH-BD ROLL-BD ST7 BELT-BD
F8.9499.8140.X F8.9499.8140.X BU872 F8.9499.8140.X
1/4 1 ST7 BU873
3 1/4 1 3
ST5
ST5
2/4 2 2/4 2
*26/26
*26/26
*26/26
*26/26
3/4 3 3/4 3
ST5
ST4
ST1
ST4
ST1
*5/5
ST4
ST1
ST5
ST4
ST1
4/4
3/4
2/4
1/4
5/5
1/5
4/4
3/4
2/4
1/4
1/5
5/5
4/4
3/4
2/4
1/4
1/5
5/5
4/4
3/4
2/4
1/4
4/4 4 4/4 4
BU534
BU520
500MA3
BU521
500MA5
BU525 BU528
BU522
*26
4
3
2
1
4
3
2
1
*5
BU533
*26
4
3
2
1
1
BU527
*26
4
3
2
1
BU526
*26
BU532
BU523 5 1 BU524
500MA1
500MA7
GND
GND
ST503
+40V
+40V
*6
1
2
(26)
2
1
(26)
#52
500MA8
500MA2
BU1
*6/6
500MA6
500MA4
(5) GS536 -RF-TAG-
READER
GNWT
GNWT
YEWT
YEWT
GN
YE
F7.0486.1315.X
GN
YE
YE RD YE RD
4 4
5
4
3
2
1
ST5-01A-ADAP-V
BK BK
*20/20
OR BKWT BKWT OR
B5 A5
B4 A4
B3 A3
B2 A2
B1 A1
ST500
ST504
ST1
M M
*26
BR M RDWT
RD
M RDWT
RD
BR
M516 -OUTB.
PUSH-DRV 5 1 M515 -OUTB. M514 -INBUFF- M513 -IBUFF-
GND
GND
BU535
+40V
+40V
*20
ST506
F8.5145.4580.x F85145.4580.x F8.5145.4524.x
GND_1
GND1
GND1
#10
ST4
*2/2
S30
GS568
ST1 BU536 BU537 ST5
DISPLAY LCD-MOD *20/20 *20 *20 #20/22
(20)
5 ST2
F8.8377.3202.X 5
ST1
F8.8377.1450.X
-TERMINAL-BD
-LCD-
1/14
2/14
3/14
GS566
#52
6/14
9/14
10/14
11/14
12/14
13/14
14/14
ST544
#4/14
*26
ST11
1/8
2/8
3/8
4/8
5/8
6/8
7/8
8/8
We reserve all rights in this document and in the informa-
BU544
*26
tion contained therein. Reproduction, use or disclosure
6
#26
IO_8_INBUFF
IO_OUTBUFF
SM_Outbuffer
RF_READER
Inbuff_Door
Inbuff_Belt
DATE NAME
IO_MSB
#26
APPR.
CR85 5148
INPUT_and_OUTPUTBUFFER / 100
/POWER_UNIT.6A
Sheet name:
/POWER_UNIT.5A
NORM
/POWER_UNIT.5A
/CPCI_RACK.4H
/POWER_UNIT.4A
/CPCI_RACK.1H
/CPCI_RACK.1H
/CPCI_RACK.4H
forbidden.
Sheet 5
© AGFA
0 21957 F1.5148.4003.0 of 7 SH
6
5
4
3
2
1
A
A
F8.5146.2750.X
ST1 1/17 1
bk
B
B
2/17 2 br
rd
8/17 8
9/17 9 or
10/17 10
ye
GS620 OPTICS_MODULE
F8.5148.2250.X
15/17 15 gn
3/17 3
bk
GS622 PM-TUBE 1
4/17 4 br
rd
7/17 7
11/17 11 or
12/17 12
ye
14/17 14 gn
5/17 5
bk
6/17 6 br
13/17 13
rd
16/17 16 (1)
17/17 17 (1)
600MA2
BU600 MA14
#15
ST1
*8/8 *8 (8)
C
C
ST2 BU601
#25/27 #25 #25 #26
26/27 26 Schirm
SHIELDING
GND 2
+40V 1
ST601
2/2
1/2
BU1
-BU1
GS610
BU2-02A
BU2-02A
F8.9499.8120.x
D
D
12345678
JL2
5FOLD-ST-SCAN
YE
M
M612
SUBNODE 1
RD
F8.5145.4524.x
GS612
ST14
POST-ALIGN-DRV
BU715 BU713 BU618
4 4 4 4 4/4
BR
OR
3 B4 A4 3 3 3 3/4
F8.9499.6540.x
2 B3 A3 1 2/4
X2 X2
1 B2 A2 2 1 1 1/4
B1 A1 600MA13 600MA12 ST19
600MA7 600MA6 #4/6
ST15
POST-ALIGN-LS
ST4-01A-ADAP-V
ST603 *4/4 ST21 BU619 BU603 ST1
#4/6 *4 #4 *4 #4/6
E
E
ST18
F8.9499.6540.x
600MA5
YE #2/4
/CPCI_RACK.3H
M
GS614 POST-IP-DET-LS
PM_1
M702
BU611 BU604
RD
F8.5146.2510.x
ST17 #4/6 *4 *4 #4/6
BU615
SLOWSCAN-DRV
4 4/4 /CPCI_RACK.4H
ST11 POLYGON_CTRL
BR
OR
3 3/4 #4/6
2 2/4
1 1/4 /CPCI_RACK.5H
LD_MODULE
/POWER_UNIT.5A
SM_Scan
ST12 BU612
*26/26 *26 #26 #26
/CPCI_RACK.1H
IO_OPTICS
F
F
ST30
*2/2
0
F8.9499.4630.X
IDX
600MA11 S4759
BU871
GS626 BEGIN-O-SCAN-LS
ST1
21957
YE
#2*4 #4/6
ST1
Change-NR
M
M622
F8.5145.4524.x
RD
600MA10 ST23
PRE-ALIGN-DRV
BU718
4 4/4
BR
OR
DATE
3 3/4
2 2/4
1 1/4
F8.9499.4640.X
ST24
G
NAME
*4/4
S4758
USER
APPR.
NORM
#6/8 #6 #4 *4 #4/6
ST1
DATE
2.11.05
YE
ST39
GS616
Leith.
#4/6
M
NAME
WT
M621
600MA8 ST40
F8.5146.2635.x
BU721
BU720
ROLL-LIFT-DRV
4 4 4 4/4
BL
RD
ROLL-LIFT-DRV
3 B4 A4 3 3 3/4
CR85
ST1
M621 alter Stand
2 B3 A3 2 2 2/4 #4/6
1 B2 A2 1 1 1/4
Sheet name:
PRE-ALIGN-LS
Replacement for
B1 A1 BU602 BU605
ST2 ST1
ST33 #4/6 *4 #4 *4 #4/6
H
87654321
ST34
JL1
*4/4 ST37
SUBNODE 2 #4/6
F1.5148.4003.0
ST35
SCAN_OPTIC_UNIT
F8.9499.6540.x
of
Sheet 6
5148
/ 100
4
3
2
1
Project
6
5
7 SH
A B C D E F G H
TR5
1
TR4 1
TR3
ST701 BU701
TR2
1 1
2 2
3 3 TR1
4 4
5 5
6 6
2 7 7 2
8 8
9 9
10 10
LA1 LA2 LA3 LA4 LA5 LA6 LA7 LA8 LA9 LA10
ST703 BU703
1 1
2 2
3 3
4 4
5 5
3 6 6 3
7 7
ERASURE_DRILLED 8 8
/POWER_UNIT.3H 9 9
10 10
11 11
12 12
13 13
14 14
15 15
16 16
17 17
18 18
19 19
20 20
ERASURE-UNIT
4 4
ST702 BU702
4 4
3 3
12 12
6
2
6
2 ADAPTER
11 11
9 9
1 1
7 7
10 10
M701-ERASURE-UNIT-FAN
1 ST704 BU704 +24V red
5 M701
1 1 5
1
Erasure_Fan 3 GND black
/POWER_UNIT.4A
M
2 2
2
2 ALARM white
3 3
S
GND BLUE
We reserve all rights in this document and in the informa-
tion contained therein. Reproduction, use or disclosure
ALARM WHITE
to third parties without express authority is strictly
6
6
DATE NAME
CIRCUIT DIAGRAM Project
USER 2.11.05 Leith.
APPR.
CR85 5148
NORM Sheet name: ERASE_UNIT_700 / 100
forbidden.
Sheet 7
© AGFA
0 21957 F1.5148.4003.0 of 7 SH
CR 85-X CR 75.0
Type 5148/100 Type 5146/101/105
Internal update: 4
CONFIDENTIALITY NOTE:
Use, dissemination, distribution or reproduction of this document by unauthorized personnel is not permitted and may be unlawful.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Manufacturer
Agfa HealthCare N.V
Published by
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
WARNING:
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
WARNING:
INSTRUCTION:
• Replace defective parts with Agfa HealthCare original spare parts.
• Use only tools and measuring instruments which are suitable for the procedure.
• Only approved Agfa HealthCare accessories must be used. For a list of
compatible accessories contact your local Agfa HealthCare organization or
www.agfa.com.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO Library.
Document History
NOTE:
Agfa reserves the right to deliver compatible parts or alternative parts.
Prices to the original order may differ.
Contact
Spare Parts ordering
Europe [email protected]
Overseas [email protected]
Worldwide [email protected]
NOTE:
For Recycling Information please refer to:
http://intra.agfanet/cd/ep/ehs.nsf
Contents
AUSGABEPUFFER
OUTPUT BUFFER
RESERVE DE SORTIE EINGABEPUFFER
PAGE 10 - 15 INPUT BUFFER
RESERVE D'ENTREE
PAGE 16 - 21
TÜR LINKS
DOOR LHS
PORTE A GAUCHE
PAGE 36 - 37
CPCI-RACK, REVIVE RACK
CPCI-RACK, REVIVE RACK TÜR RECHTS, LEISTUNGSEINHEIT
CPCI-RACK, REVIVE RACK DOOR RHS, POWER UNIT
PAGE 38 - 41 PORTE A DROITE, BLOC DE PUISSANCE
PAGE 42 - 45
KASSETTENTEIL
CASSETTE PART
PARTIE CASSETTE
PAGE 22 - 35 ROTATIONSANTRIEB
ROTATION DRIVE
COMMANDE ROTATIVE
LÖSCHEINHEIT
PAGE 76 - 77
ERASURE UNIT
UNITE D'EFFACEMENT
PAGE 46 - 47
KASSETTEN
CASSETTES
CASSETTES
PAGE 80 - 101
FOLIENTRANSPORT, EINGABE
IP TRANSPORT, INPUT
TRANSPORT DE L'ECRAN, ENTREE
FOLIENTRANSPORT, AUSGABE PAGE 54 - 59
IP TRANSPORT, OUTPUT
TRANSPORT DE L'ECRAN, SORTIE SCANMODUL
PAGE 48 - 53 SCAN UNIT
MODIFIKATIONSBAUGRUPPEN / ZUBEHÖR MODULE SCAN
MODIFICATION KITS / ACCESSORIES PAGE 60 - 75
KIT DE MODIFICATION / ACCESSOIRE
PAGE 78 - 79 5148_chap05_INHALT.cdr
02
19*
17*
01*
18
D2853
D635
D6426
D3088
16*
02 03
07*
X
15*
05
08*
13 09*
14*
Detail X D6408
D6426
06
04 11*
12* 10*
12*
5148_chap05_01_m.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
(GS 314)
06
05 (GS 204) 02
07
(St319)
04
D708
08
D117
D5682 03
03
D5682
D117
5148_chap05_03.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01 02
D217
D2514
D217
D2853
07
02
06
(GS 564)
04
(M515)
05 03
5146_chap05_04.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
(M516)
02
D579
D2514
02
D2861
03
(GS562) (GS560)
04
06 (GS554)
05
D6522
D6522
05 5148_chap05_05.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
08
01
(GS 552)
02
10
05 04
03
01
(GS 556)
02
09
07 08
03
(GS 558)
06
04
5148_chap05_06.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
02
05 D2513
(GS518)
D2763
D2861
D417
D2514
D2861
D2514
D579
D6522
03
04
(M514)
D372
5148_chap05_07.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
06
01
04
03
(GS512) 10
09
05 07 08
(GS510)
(GS516)
02 04
D6522 (GS514)
04
5148_chap05_08.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
16 01
(GS530) 02
(GS534) 03
15 04
(M513)
D333
12
D579 D369
D2514
D542
14
(GS532)
13 10
12
08 09
11
04
07
05
(GS540)
06
(GS536, GS538) D2513
D369
5148_chap05_09.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05
D6522 D6522 (M202)
(M207)
D579
5141
D2681
04
01
D6522
D3154
03 D333
(GS214)
(GS265)
02
D6522
5148_chap05_10.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
06
04
05*
03
02
(GS220, GS270)
01*
(M205, M210)
5148_chap05_11.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
06
(M204)
(M209)
01
05
03
02
(GS228)
(GS277)
04
5148_0100_12.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01 (M201)
(M206)
02
05
(GS230)
(GS280) 04
03
D3083
D2995
D320
07
D377
06
D6522
(M203)
(M208)
5148_chap05_13.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
02 (GS216)
(GS266)
04
05
06
07 09
07
08
(GS226, GS276)
07
5148_chap05_14.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
02 03 04 05 03 06 07 08
12 11 10 09
(GS210, GS260)
5148_chap05_15.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05
04
06
03* 09*
02
01
08
07*
5148_chap05_16.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
D5682
D117 D706
02 04
(M701)
D5682
D117
D2681
D335
D6522
03
01
D706
5148_chap05_17.CDR
DOOR LHS
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
DOOR LHS
01
(M300)
02
04
03
(GS302)
(GS304)
05
09
(GS300)
08
(GS312)
06
07 (GS306)
(GS310)
CR85-X
Type 5148/100 (up to SN <4000)
CR75.0
Type 5146/101
Type 5144/105 (up to SN <6500) 5148_chap05_18.CDR
CPCI-RACK
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
CPCI-RACK
01
02
07**
03
06
05 04
REVIVE RACK
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
REVIVE RACK
05 D5682
D117
D703 07
D706
06
02
(M101)
03
(TR106) 04*
01
D321 D854
D855 D865
D539
5148_chap05_20.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
04
(S103)
05 09
12
(GS104)
01
(S102)
07
07 08
(GS100)
02
06 10
02, 03
11
(GS102)
10 06 5148_chap05_21.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01 05
06
08
D221 07
D353
D81 D221 07
02
03
04
09
10
11
5148_chap05_22.CDR
ERASURE UNIT
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
ERASURE UNIT
01*
02
(GS401, GS402)
10
D542
12 03
D2514
04
D706
D540
D6426
D2514
D2861
11 (GS401, GS402)
ONLY FOR DEVICES
WHICH ARE LOCATED
HIGHER THAN 2000M
ABOVE SEE LEVEL
(SEE SB DD+DIS276.07E)
08
(MG402)
08
(MG401)
D6426
D2514
09
05
07 D542
(GS406)
07 06
(GS404)
5148_chap05_23.CDR
12 CM+9042421640 MAGNETVENTIL
SOLENOID VALVE
ELECTROVANNE
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
02
10
(GS412) 03
D372
D2514
D579
12
(GS414 / 04 (M401)
GS416)
D372
D2514
D579
10
(GS418)
11 06
09
07
05
08
5148_chap05_24.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
03 (GS410)
D372 03
02 D2514
D579
01 (GS408)
04
06
07
09
08
07
05 12 06
11
(M400)
D372
D2514
D579
05
10
10
5148_chap05_25.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01*
02
D6424
D2514
D2861
03
(GS422)
(GS420) 05
07
D706
D2514
04
D542
D6426 (GS422)
06 (GS420)
ONLY FOR DEVICES WHICH ARE LOCATED
HIGHER THAN 2000M ABOVE SEE LEVEL
(SEE SB DD+DIS276.07E) 5148_chap05_26.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05
10
D372
D2514
D579
11
04 (GS428)
(GS430) 07
(GS432) (M403)
D372
D2514
D579
11
(GS434)
12 02
09
03
08
06
01
5148_chap05_27.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05 (GS424)
D372 05
D2514
D579
10 (GS426)
04
09
02
06
01
07
06
08 03 02
11
(M402)
D372
D2514
D579
08
12
12
5148_chap05_28.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05
02
(GS610)
04
01
(GS620)
03
(GS622)
CR85-X
Type 5148/100
CR75.0
Type 5146/105 (as of SN 6000) 5148_chap05_29.cdr
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
05
02
(GS622)
(GS620)
03
04
(GS610)
01
CR75.0
Type 5146/101 (up to SN < 6000) 5148_chap05_30.CDR
1 CM+9047913370 LEITERPLATTENHALTER
PCB HOLDER
CARTE FIXATION
2 CM+9514622504 PMT-MODUL - (GS622) - (TYPE 5146/101 ONLY)
PMT MODULE - (GS622) - (TYPE 5146/101 ONLY)
MODULE PMT - (GS622) - (TYPE 5146/101 ONLY)
3 CM+9514827003 OPTIKBAUGRUPPE - (GS620) CR75.0
OPTIC MODULE - (GS620)
ENSEMBLE OPTIQUE - (GS620)
Type 5146/101 (up to SN <6000)
4 CM+9949981300 GS IOB-SIN-5STEP - (GS610)
5 FOLD MOTOR CONTROLLER PCB - (GS610)
CI IOB-SIN-5STEP - (GS610)
5 CM+9514621070 VERKLEIDUNG
PLASTIC COVER
PLASTIC COVER
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
03
06
02
05
D3252 D2763
01
04 D2513
D2851 D2763
01
D369
D3252
CR85-X
04 D2851
Type 5148/100 D2851
CR75.0 D3252
Type 5146/105 (as of SN 6000) 04 5148_chap05_31.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
03
02
D3252 D2763
05
04 D2513
D2851 D2763
05
D369
D3252
04 D2851
D2851
D3252
04
CR75.0
Type 5146/101 (up to SN < 6000)
5148_chap05_32.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
D5681
03 D2778
04
02
D444
D2765 01
(M702)
06
(GS612)
05
CR85-X (M612)
Type 5148/100
CR75.0
Type 5146/105 (as of SN 6000)
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
04
D5681
06 D2778
(GS612)
09
02
D444
D2765
05 03
(M612) (M702)
08
D2443
01
D3008
07
D579
D2514
CR75.0 D542
Type 5146/101 (up to SN < 6000)
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
02
05
02
04
(GS616)
06
01
03
(M622)
5148_chap05_35.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
04
(M621)
05
03
(GS618)
06 09
06
07
(GS626)
(GS628)
D6522
D2514
D2853
02
03 01
(GS614)
08
5148_chap05_36.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
06
06
D2873
D2514
D579 05
(GS202)
04
02
(GS206)
D706
D4338
07
01
(M212)
03
5148_chap05_37.CDR
ROTATION DRIVE
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
ROTATION DRIVE
01 02
04
03
06
07 CM+9514565502 (1x)
05
CM+9514571252 (1x)
5148_chap05_38_M.cdr
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
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= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
02*
03* 01*
04
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13 12
15
17 07
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5146_chap05_54.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
02*
03* 01*
04
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14
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13 12
15
17 07
16
18
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10
11
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08 10
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5146_chap05_54.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01*
02
03*
12 04*
11 10
13
15 05
14
16
07
08
09
10 09
06 08
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5148_chap05_50.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01*
02
03*
12 04*
11 10
13
15 05
14
16
07
08
09
10 09
06 08
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5148_chap05_50.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01
02*
11 03*
10 09
12
14 04
13
15
06
07
08
09 08
05 07
06
5148_chap05_53.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
02*
03* 01*
04
05*
14
06*
13 12
15
17 07
16
18
09
10
11
12 11
08 10
09
5146_chap05_54.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01*
02
03*
12 04*
11 10
13
15 05
14
16
07
08
09
10 09
06 08
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5148_chap05_50.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
01*
02
03*
12 04*
11 10
13
15 05
14
16
07
08
09
10 09
06 08
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5148_chap05_50.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
03*
02* 01* 04
05*
12
06
13 07
14
09
10
11
06
11
08 10
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5148_chap05_042.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
03*
02* 01* 04
05*
12
06
13 07
14
09
10
11
06
11
08 10
09
5148_chap05_042.CDR
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
• Number of machines
• Extension of the service area
• Local service structure (centralized / decentralized)
• Stockpilling
Type Overview
This spare parts list is valid for the following machine type(s):
Accessory Overview
Following accesssories are separately available:
► Document History
► Referenced Documents
Document Title
Not applicable
Edition 4, Revision 1
12-2010 printed in Germany Document Node ID: 32047827
so_standard_e_template_v07
Agfa Company Confidential Copyright © 2010 Agfa HealthCare N.V.
DD+DIS025.05E CR User Station
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D – 81539 München
Germany
Copyright © 2010 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
Agfa and the Agfa rhombus are trademarks of Agfa-Gevaert N.V., Belgium,
or its affiliates.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the “Generic Safety Directions” document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the “Generic Safety Directions” and on
the product.
LIST OF CONTENTS
1 INTRODUCTION ......................................................................................................................5
2 SAFETY INSTRUCTIONS........................................................................................................7
2.1 General Safety Instructions.......................................................................................................7
5 TROUBLESHOOTING............................................................................................................26
5.1 Isolating Transformer ..............................................................................................................26
5.2 ID Tablet..................................................................................................................................27
8 INSTALLATION PLANNING...................................................................................................28
8.1 Dimensions .............................................................................................................................28
8.4.2 ID Tablet..................................................................................................................................31
1 Introduction
The CR User Station (CRUS) is an operating console that facilitates the work of the
radiographer. It is suitable for all CR environments: centralized, decentralized or
personal CR solutions.
It has been designed in line with the look and feel of the range of the new generation
digitizers, combining with the digitizers to form a “whole”. It provides a professional way
of delivering an integrated solution for computer equipment in Agfa’s CR offering.
Figure 1
NOTE:
• For all required information concerning digitizers, where the CRUS is attached
to, please refer to the relevant Service Documentation:
• CR 25.0: DD+DIS071.04E
• CR 35-X: DD+DIS219.06E
• CR 75.0: DD+DIS002.04E
• CR 85-X DD+DIS378.05E
2 Safety Instructions
Figure 2
• Make sure that the two safety caps are mounted on top of the right side rollers in
case of stand-alone CRUS (this means that the CRUS is not connected to a
CR 25.0/CR 35-X Digitizer), as shown below.
Figure 3
Pay attention to the warning label at the rear side of the CRUS:
Check power selection before connecting to mains
Figure 4
In combination with a digitizer the isolating transformer assures that the digitizer still
complies with EN 60601-1-1 medical, electrical systems.
The CR User Station bears the CE mark and fully complies with the
CE Directive 89/336/EEC and with the federal code of the United States, bearing on:
• Emission and immunity according to EN 60601-1-2, for emissions the
equipment complies with EN 55011 class A (CISPR 11).
This is a Class A product. In a domestic environment this product may
cause radio interference in which case the user may be required to take
adequate measures.
• Emissions according to 47 CFR part 15 subpart B, Class A.
This equipment has been tested and found to comply with the limits for a
Class A digital device, pursuant to part 15 of the FCC Rules. These limits
are designed to provide reasonable protection against harmful
interference when the equipment is operated in a commercial environment. This
equipment generates, uses, and can radiate radio frequency energy and, if not
installed and used in accordance with the instruction manual, may cause harmful
interference to radio communications. Operation of this equipment in a residential
area is likely to cause harmful interference in which case the user will be required to
correct the interference at his own expense.
• Radio-parameters of the ID Tablet according to ETS 300330.
3 Installation Instructions
NOTE:
The actions described in this section apply only, if the CRUS is installed as stand-
alone device.
Skip this section if you want to dock it to a CR 25.0 / CR 35-X digitizer.
Figure 5
Figure 6
Figure 7
Figure 8
Figure 11
Figure 12
Figure 13
NOTE:
By default, a rack for the Barco monitor is installed.
If you have a Barco monitor, go directly to step (2).
If you have another monitor, exchange the rack before proceeding
with step (2). The exchange of the rack for the NEC monitor is
described in section 3.9.
Figure 14
(3) Adjust the monitor according to
section 3.10.
Figure 15
(1) Put the ID-Tablet back to its place and fix the Phillips screw
(see Figure 8, page 11).
(2) Connect the USB cable coming from the ID-Tablet to a free USB port of the PC.
Figure 17
100 V: 6.3 AT
120 V 5.0 AT
230 V 2.5 AT
240 V 2.5 AT
Figure 18
Figure 19
Figure 20
20
100
2 01
240
Figure 21
Figure 22
(1) Connect the network cable of the digitizer to the hub of the CRUS.
NOTE:
If you want to dock the CRUS to a CR 25.0 digitizer, continue with section 3.8.
Result The installation of the CRUS as a stand-alone device is finished. Connect it to the
mains.
Figure 23
Figure 24
Figure 25
Figure 26
Figure 27
Figure 29
Figure 30
Figure 31
NOTE:
The monitor rack, the bearing and the
washers can easily fall down!
Be careful when removing the axis.
Figure 32
Figure 33
NOTE:
If the monitor rack is not fixed properly, it
may tilt unwanted.
Check that the hole of the retainer (see
circle) and the form of the axis fit smoothly
together.
Figure 35
Figure 34
Figure 36
Figure 37
Figure 38
Figure 39
Adjust the inclination of the monitor by using the lever at the rear side:
NOTE:
The lever is a quick-fix system: Its fixed or loose position can be changed when it is
pulled (lever free, see Figure 40).
There is no need to open the Allen screw at the axis for the adjustment of the monitor.
lever lever
(2) Loosen lever by turning counter-
free locked
clockwise.
Figure 40
Result The individual components of the CR User Station are ready for use now.
4 Functional Description
Monitor (*)
Keyboard (*)
ID Tablet
Cassette storage
Inside:
- Isolating transformer
- PC (*)
- UPS (*)
- Network Switch (*)
Figure 41
3
store 2
exposed
cassette
store
scanned
and erased
cassette
4
Figure 42
• Up to five exposed cassettes are stored in the upper side storage racks (1).
• The exposed and identified cassettes are inserted directly into the digitizer or, if the
digitizer is busy, stored in the top storage rack (3).
• The scanned and erased cassettes waiting to be used again are stored in the lower
side storage rack (4).
In order to save time it is also possible to use the CRUS for Direct ID.
• For this an exposed but unidentified cassette is inserted into the digitizer.
• By entering the cassette, the digitizer reads the cassette information of the RF Tag
and a communication to the CRUS is opened.
• The digitizer starts scanning the IP and sends an ID Data Request Message to the
CRUS. On the monitor of the CRUS the ID window pops up and the ID data have to
be entered.
• After the user completed the information at the CRUS, it is sent back to the digitizer.
The communication channel is closed afterwards.
5 Troubleshooting
WARNING:
Fire hazard:
Only use fuses of the exact value and characteristics stated above.
5.2 ID Tablet
Figure 44
For the current Spare Parts List refer to MedNet GSO Library.
7 Maintenance
8 Installation Planning
8.1 Dimensions
193 (75”)
5 (2”)
43 (17”) 45 (18”) 100 (40”)
5 (2”)
Digitizer
64 (25”)
75 (30”)
200 (77”)
120 (47”)
Figure 45
64 (25”)
Digitizer
200 (77”)
127 (48”)
Figure 46
Weight • 53 kg (empty)
• Approx. 100 kg (fully equipped)
Operating Conditions
Temperature 10°C – 30°C
Change of temperature 0.5°C / min.
Humidity 15% RH to 80% RH
Type Label
The type label is at the rear side of the CRUS.
Figure 48
Figure 47
8.4 Connections
CRUS
Primary:
100 V 6,3 A, slow blow
120 V 5,0 A, slow blow
230 – 240 V 2,5 A, slow blow
CR 25.0
Operating voltage:
230 V / 240 V + 10%
120 V + 10%
100 V + 10%
Mains Fuse Protection
Europe 16 A, slow blow
USA & Japan 15 A, slow blow
8.4.2 ID Tablet
Local and International wiring regulations must be observed. Check all supplies and
voltages, currents, trips and fuses with the hospital facilities department or their
engineers.
CR User Station
Type 5157/100
Internal update: 4
CONFIDENTIALITY NOTE:
Use, dissemination, distribution or reproduction of this document by unauthorized personnel is not permitted and may be unlawful.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Manufacturer
Agfa HealthCare N.V
Published by
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright © 2011 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V., Belgium,
or its affiliates.
WARNING:
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
WARNING:
INSTRUCTION:
• Replace defective parts with Agfa HealthCare original spare parts.
• Use only tools and measuring instruments which are suitable for the procedure.
• Only approved Agfa HealthCare accessories must be used. For a list of
compatible accessories contact your local Agfa HealthCare organization or
www.agfa.com.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO Library.
Document History
NOTE:
Agfa reserves the right to deliver compatible parts or alternative parts.
Prices to the original order may differ.
Contact
Spare Parts ordering
Spare Parts ordering
Europe
Europe [email protected]
[email protected]
Overseas
Overseas [email protected]
[email protected]
Worldwide [email protected]
Worldwide [email protected]
NOTE:
For Recycling
Recycling of theInformation
electronicplease refer to:waste equipment will ensure safety
and electrical
of human health and the environment.
For information about electronic and electrical waste equipment disposal,
http://intra.agfanet/cd/ep/ehs.nsf
recovery and collection points, please contact your local waste disposal service
or producer / distributor of this equipment.
If your equipment contains removable batteries or accumulators please dispose
of these separately according to local regulations.
Contents
LEISTUNGSEINHEIT
POWER UNIT
MODULE DE PUISSANCE
PAGE 12 - 13
GESTELL
FRAME
CHÂSSIS
PAGE 6 - 7
ID STATION - AB FN 10.000
ID STATION - AS OF SN 10.000
ID STATION - A PARTIR DE NS 10.000
PAGE 10 - 11
08
06
05
09
07
04
03*
02
01
5157_chap05_01.CDR
FRAME
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
FRAME
01*
07
08
04 06
02
05 05
03
5157_chap05_02.CDR
ID STATION - UP TO SN 10.000
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
ID STATION - UP TO SN 10.000
01*
05
04
03
02
5157_chap05_03.CDR
ID STATION - AS OF SN 10.000
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
ID STATION - AS OF SN 10.000
02
01
03, 04, 05
5157_chap05_04.CDR
POWER UNIT
= Assembly
D = Standard part. For order please refer to the separate spare parts list for standard parts "DD+DIS011.93M".
* = Spare part standardly is not kept in stock, extended delivery time is possible.
99 = Spare Part is not shown in Exploded Views.
POWER UNIT
• Number of machines
• Extension of the service area
• Local service structure (centralized / decentralized)
• Stockpilling
• Not available
Type Overview
This spare parts list is valid for the following machine type(s):
Accessory Overview
Following accesssories are separately available:
• Not available
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Preceding Bulletin Release of ACPL1004 Language Files for Digitizer User
Interface of CR 85-X, DD+DIS088.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
LIST OF CONTENTS
See chapter 3.8 of the service manual for the software release information.
1.2 CR Applications
Digitizer software ACP_4007 can be used for the following
CR applications:
• General Radiography (GenRad),
• Mammography (Mammo),
• General Radiography 50 µm (Extremities), and
• Full Leg – Full Spine (FLFS)
SN = 1017, 1019, 1021, 1023, 1025, 1026, 1027, 1029, 1030, 1031,
1032, 1036, 1047, 1052 and 1060
SN > 1069
REQUIRED TOOLS:
You need max. 8 empty formatted floppy disks with 1.44 MB capacity each:
• one for the backup of site specific data and
• 7 for the preparation of the installation set of floppy disks
if you obtained the digitizer software from MedNet.
9 pins 25 pins
figure 1
REQUIRED TIME:
• approximately 30 minutes for the software upgrade or
• approximately 60 minutes for the installation on the blank hard disk.
3 Installation Procedure
3.1 Making Installation Floppy Disks
Execute these actions if you downloaded the digitizer software from MedNet.
Skip them if you obtained the software via the spare parts supply.
(2) Extract all files from ACP_4007.zip into an empty folder on the service PC.
NOTE:
For each of these folders, a floppy disk with the same name is created in the following
steps.
(3) Insert an empty floppy disk.
(4) Select the floppy drive entry (A:) in the Windows Explorer.
(6) Select tab General and enter the corresponding folder name,
e.g. HDFORMAT.
(8) Copy the contents of the folder (e.g. HDFORMAT) from the service PC to the
floppy disk.
(9) Remove the floppy disk from the drive and label it with the folder name, e.g.
HDFORMAT.
(10) Repeat steps (3) to (9) for the other five floppy disks.
Result Now you have the required installation set of floppy disks.
(2) Enter the Service menu on the digitizer keypad and select
Save on floppy / Machine specific data.
NOTE:
In the rare case that a backup floppy cannot be generated in this way, obtain the
out-of-factory backup data using this link:
http://intra.agfanet/BU/MI/MEDNET3.NSF/EN/factorybackupftp.htm
(1) Enter the Service menu on the digitizer keypad and select
Install from floppy / Software.
(3) Close the front door and switch off/ on the digitizer.
Wait until the system is ready.
(1) Enter the Service menu on the digitizer keypad and select
Install from floppy / Software.
(2) Insert the floppy disk labeled PORTEX1 into the disk drive of the digitizer.
(4) Wait until the control LED of the floppy disk drive is off.
(6) Insert the floppy disk labeled PORTEX2 into the disk drive of the digitizer.
(8) Wait until the control LED of floppy disk drive is off.
NOTE:
Do not insert any other floppy disk!
WAITING TIME:
Wait approx. 2 minutes.
The files of the Portex operating system are installed.
(11) Insert the floppy disk labeled ACP4007_1_3 into the disk drive of the digitizer.
(13) Wait until the control LED of floppy disk drive is off.
(15) Insert the floppy disk labeled ACP4007_2_3 into the disk drive of the digitizer.
(17) Wait until the control LED of floppy disk drive is off.
(19) Insert the floppy disk labeled ACP4007_3_3 into the disk drive of the digitizer.
(21) Wait until the control LED of floppy disk drive is off.
WAITING TIME:
Wait approx. 2 minutes.
The system extracts the ACP_4007 software.
(24) Close the front door and switch off/ on the digitizer.
Result Normally, the digitizer performs its self test and afterwards changes its state to Ready.
Proceed with section 3.7.
If the digitizer does not perform the self test, the software installation was not successful.
The cause is a corruption of the file system on the hard disk.
Perform the installation according to section 3.5.
NOTE:
This procedure must be carried out only if the hard disk of the digitizer is corrupted or
has been replaced by a blank one.
In this case the hard disk must be formatted using the installation disk HDFORMAT.
(2) Connect your service PC to the RS232 port at the cPCI rack.
(4) Create a new connection and select your serial port (e.g., COM1).
(5) Set terminal settings to 9600 baud, Xon/Xoff, no parity, 8 bit, 1 stop bit.
(7) Insert the floppy disk labeled HDFORMAT into the disk drive of the
cPCI rack.
(9) Confirm partitioning/formatting of the hard disk on your terminal with ‘y’.
(12) Insert the floppy disk labelled PORTEX2 into the disk drive of the digitizer.
NOTE:
Do not insert any other floppy disk!
(19) Insert the floppy disk labeled ACP4007_1_3 into the disk drive of the digitizer.
(23) Insert the floppy disk labeled ACP4007_2_3 into the disk drive of the digitizer.
(27) Insert the floppy disk labeled ACP4007_3_3 into the disk drive of the digitizer.
(35) Enter the Service menu on the digitizer keypad and select
Install from floppy / Machine specific data.
NOTE:
Without restoring the device-specific parameters, an operation of the digitizer is
impossible.
(37) Restore the test image files from CD (CM+9 5145 3055 0) to the directory
E:\testimg on the digitizer.
(38) Generate the CPF file with the QS, the VIPS or the CCM tool. Please refer to the
service documentation, chapter 1, for details.
(39) Enter the Service menu on the digitizer keypad and select
Install from floppy / CPF-File.
(43) Close the front door and switch digitizer power off/ on.
Result The digitizer performs its self test and afterwards changes its state to Ready. Proceed
with section 3.7.
NOTE:
ACPL1004 language files are installed ex factory on following digitizers. Then a
installation of the ACPL1004 language files is not necessary.
• CR 85-X Type 5148/100: SN ≥ 1937 , CW 15/2007
• CR 75.0 Type 5146/105: SN ≥ 6031 , CW 15/2007
To install ACPL1004 language files and to change the language of the digitizer user
interface perform following procedure:
(2) Open Service menu on the local key pad of the digitizer.
(3) Choose
<INSTALL from floppy>
<language files>
(5) Insert floppy disk with ACPL1004 language files at disk drive of cPCI-Rack and
confirm with <;> on the local key pad.
(6) After a short while following message appears on the Service menu:
<Please remove the floppy and press ;>
NOTE:
Skip action (1) if the previous software version was ACP_1201 or higher.
(3) Refresh your backup by following the guidelines of Service Menu topic Save on
floppy / Machine specific data.
NOTE:
If the version of the previous software was less than ACP_1007, perform IP Center and
Shading calibrations. Please refer to the service documentation, chapter 3.6.
NOTE:
If you use the digitizer for Mammography applications, enable “Mammo” manually in the
Service Menu of the digitizer.
(1) Enter the Service menu on the digitizer keypad and select
Info / Device info.
Result If the entry Software is equal to ACP_4007, the software installation was successful.
Otherwise repeat the installation and closely follow the instructions in section 3.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
n.a. n.a.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
TABLE OF CONTENT
The following modifications of CR 85-X Type 5148/100 and CR 75.0 Type 5146/105
(as of SN ≥ 6000) are listed in chronological order, the latest modification on top of the
list.
SB – Service Bulletin
Reason A modified vacuum pump has been introduced for the use of the
digitizer on sites between 2000 m and 4000 m above sea level.
Product(s) & The High Altitude Vacuum Pump is not part of series production and
Serial only available as upgrade kit for new installations or already installed
Number(s) digitizers as well as spare part for the replacement of modified
vacuum pumps, which are defective.
Part • Upgrade Kit “High Altitude Vacuum Pump for CR 75.0/CR 85-X”
Number(s) ABC Code: EZKFF
• Spare part “High Altitude vacuum pump”,
CM+9 5148 6230 0
Referenced • Service Bulletin No. 04, DD+DIS278.07E
Document(s)
• Enclosure - Replacement Instructions: High Altitude Vacuum
Pump for Use on Sites between 2000 m and 4000 m above Sea
Level, DD+DIS151.07E
Reason User interface language files have been released to ensure that
messages in the digitizer user interface are available in several
languages. Eleven languages can be used with the release of
ACPL1004 language files.
Product(s) & CR 85-X Type 5148/100:
Serial
SN ≥ 1937 , CW 15/2007
Number(s)
4 Modification of cPCI-Rack
Reason The power supply unit has been modified to enable the use of hard
disks with higher voltage input.
The modified power supply unit is RoHS compliant.
Product(s) & SN ≥ 1666 , CW 05/2007
Serial
Number(s)
Part Following spare parts have been modified:
Number(s) • Spare part “cPCI-Rack, CM+9 5146 1400 6
• Spare part “cPCI-Rack assembled”, CM+9 5146 1405 7
• Spare part “PCI power supply”, CM+9 5146 1430 2
Referenced n.a.
Document(s)
Reason The fixation of the 5-fold stepper motor board has been changed by
introducing new clips to prevent bending of the board.
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
Edition 2, Revision 0
CR 85-X CR 75.0
Type 5148/100 Type 5146/105
(as of SN ≥ 6000)
CONFIDENTIALITY NOTE:
Use, dissemination, distribution or reproduction of this document by unauthorized personnel is not permitted and may be unlawful.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
LIST OF CONTENTS
2.2 Inside.......................................................................................................................................11
4 COMPLETION OF MAINTENANCE.......................................................................................22
1 General Information
NOTE:
These maintenance instructions must be considered confidential.
To ensure quality and functional reliability of the system all the points listed below
(minimum maintenance points) must be carried out.
• The maintenance points have been arranged in a chronologically suitable order to
make the work routines as efficient as possible.
The sequence of the maintenance points in the checklist (see appendix of this
chapter) is identical with these maintenance instructions.
• If there is a detailed description for a certain maintenance point in the service
documentation, this will be noted in the column "details".
• During the maintenance procedure always consider the safety instructions, see
TECHNICAL DOCUMENTATION chapter 1/1.
• Please check if it is necessary to include country specific regulations as additional
maintenance points!
NOTE:
Only for Systems with DRA Contract (Direct Remote Access):
In systems with DRA Contract the infocounters are checked and evaluated in regular
intervals by the GSC. If there is an indication of an upcoming defect, this is noted in the
DRA Report and sent to the respective NSO with instructions for measures possibly
required on the machine.
Therefore we recommend to contact your NSO about this subject before maintenance, in
order to perform these recommended measures in addition to the "must" maintenance
points.
2.1 Diagnostics
2.1.1 Questioning of the Customer
• Ask the customer for any problem that appeared since the last maintenance.
"\D_\infocounter\0\infocounter.txt" figure 1
Evaluation of infocounters.txt
2.2 Throughput For throughput most important are the cycles per day.
They usually count between 50 and 200.
3.3 Hardware By comparing the status of the device with the available
Modification History “Field Modifications”, chapter 7, the exact hardware
status can be determined.
4.6 Laser Power Check that laser power is constant: no more than 1 mW
difference in between two entries. If the value is higher,
run diagnostic software and
scan & signals and check laser diode module.
Evaluation of infocounters.txt
What to check in the Comment
infocounter
5.3 Retries Retries lead to less throughput of the device. If the
fraction of retries exceeds 1%, compare with frequent
error codes.
5.7 Error History Check errors since last maintenance, how often they
appeared as well as the CBF (cycles between failures) of
these errors. This gives an overview of the current status
of the machine.
Compare frequently occurring errors with the error list in
chapter 3.3, and take actions.
5.8 Error List Relatives Troubleshoot these errors using the technical
and documentation, chapter 3.3, “Troubleshooting”.
5.9 Error List Total
• Flashlight
(1) Check overall condition of the machine – outside and inside – for obvious changes
or damage.
2.2 Inside
• Vacuum cleaner
• Lint free cloth
• Dust brush
• Roller (CM+9 5145 9100 0)
• Toothed belt (CM+9 5145 5195 0)
5146_reg02_000cdr
figure 2
• Soft cloth
• Air filter (CM+9 5146 1799 2)
figure 3
5146_reg09_007.cdr
figure 4
• Vacuum cleaner
• Soft cloth
• Air filter (CM+9 5146 1799 2)
51 4
51
2E
C. C
D R
figure 5
Air Filter (3) Clean the grid of the fan with a soft
cloth.
5146_reg09_01
figure 6
• Soft cloth
• ADC Cleaner (if not available, use water)
• Discharge brush (CM+9 5145 2442 1)
(2) Clean the scan rollers on prescan and postscan side with ADC Cleaner.
CAUTION:
Risk of damaging the scan unit.
Do not remove the scan rollers. Clean the scan rollers in place by moving the slow scan
motor manually.
figure 7
• Soft cloth
• Dust brush
• ADC Cleaner (if not available, use water)
• 1 set of 10 pieces 100 W halogen erasure lamps:
Philips CAPSULEline Pro (CM+9 0450 6582 0)
5146_reg09_003.cdr
figure 8
Lamps (3) Remove the complete erasure unit.
CAUTION:
Risk of damage when using wrong cleaning method.
Do not use any fluid for cleaning of the inner side of the large glass plate since it is
coated with a gelatin layer.
4 3 5
5146_reg02_021.cdr
figure 9
NOTE:
Do not touch the lamps with bare fingers!
Use a dry, soft cloth to insert the lamp.
2.9 Cassettes
NOTE:
The digitizer needs the aluminum label to recognize ADC cassettes.
CAUTION:
Wrong screen cleaner may damage the Image plate.
Do not use the AGFA CR phosphor plate cleaner to clean the CR MM3.0 Mammo
image plates. Use PROSAT wipers instead.
WARNING:
Poor image quality caused by incorrect cassette initialization.
Initialize the cassette/plate as described in the corresponding user manual.
NOTE:
Repeat this procedure for all formats on site!
• Flatfield
(2) Print the flatfields "Calibration" and "Banding" via the Processing Station (window
setting of 0.6, without changing the level setting).
Rotating
(3) Expose a new image plate: Anode x-ray tube
Cathode
• Place the cassette in length
direction to the
X-ray tube, see figure 11.
NOTE:
Notice, that all exposure parameters are approximate values.
NOTE:
Make sure that the outlined areas are filled in as shown in the example.
(5) Insert the cassette into the digitizer and print the image on a printer with a window
setting of 0.6 without changing the level setting.
figure 12
figure 13
NOTE:
If there are still unacceptable effects, please contact the Support Center.
figure 14
NOTE:
If there are still unacceptable effects please contact the Support Center.
figure 15
NOTE:
If there are still unacceptable effects please contact the Support Center.
4 Completion of Maintenance
Published by
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
1 Maintenance Checklist
NOTE:
Maintenance must be carried out according to the maintenance instructions
DIS020.07E
Transport Units • Check position of suction cups and clean them with
ADC cleaner
Remarks:
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
..........................................................................................................................................
............................................................. .........................................................
Date / Signature Service Technician Customer
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Please note
Service Bulletins are not part of the Service Manual for Download.
Edition 2, Revision 0
03-2008 printed in Germany Document Node ID: 23230986
service_bulletin_cover_e_template_v01
Agfa Company Confidential Copyright © 2008 Agfa HealthCare N.V.
DD+DIS378.05E Service Bulletins
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
Edition 2, Revision 2
CR 85-X CR 75.0
Type 5148/100 Type 5146/105
(as of SN ≥ 6000)
CONFIDENTIALITY NOTE:
Use, dissemination, distribution or reproduction of this document by unauthorized personnel is not permitted and may be unlawful.
DOCUMENT CONTROL NOTE:
The controlled version of this document resides on MedNet. Any printed copy of this document is uncontrolled.
Edition 2, Revision 2
04-2009 printed in Germany Document Node ID: 10031648
eq_11_install-planning_e_template_v07
Agfa Company Confidential Copyright © 2009 Agfa HealthCare N.V.
1 2 3
DD+DIS021.07E Installation Planning
► Manufacturer
Agfa HealthCare N.V.
Publisher
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright 2009 Agfa HealthCare N.V.
All rights reserved.
Technical modifications reserved.
AGFA and the Agfa-Rhombus are trademarks of Agfa HealthCare N.V.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
NOTE:
To verify the latest version of single documents and of Service Manuals refer to the
Document Type ‘Order List’ in the GSO library.
This document contains all planning data including the required measures to be carried
out on site prior to the machine delivery.
This chapter is divided into:
Construction planning data
Technical connection and performance data
Safety instructions, listing of certificates
► Document History
► Referenced Documents
Document Title
Not applicable Not applicable
LIST OF CONTENTS
6 SPECIFICATIONS ............................................................................................................... 11
6.1 Type Definition ...................................................................................................................11
7 ELECTRICAL CONNECTIONS............................................................................................ 14
7.1 External Fuse Protection ....................................................................................................14
8 SYSTEM INTEGRATION..................................................................................................... 16
8.1 Required Network Parameters............................................................................................16
8.2 CPF-file..............................................................................................................................19
9.2 Certificates.........................................................................................................................20
1 Installation Planning-Checklist
# Step Goal Section Okay
1. Ask the Agfa sales representative A installation date can be scheduled -
for a contact person in the with the customer.
hospital.
2. Make yourself familiar with the To see in which environment the 2
System Overview. digitizer will be installed.
3. Make yourself familiar with the Basic information, to see whether 3
scope of delivery. additional, site specific material for
installation might be required.
4. Make yourself familiar with the To be able to order required 4
available accessories. accessories before the installation.
5. Have a look at the machine To be able to check, whether the 5.1
dimensions. digitizer fits in the desired installation
place.
6. Check the required free space To see whether enough free space for 5.2
around the digitizer. repair and maintenance is available.
7. Check the required transport path Transport to the installation site, 5.3
of the digitizer. unpacking and taking the machine off
the pallet must be done by the carrier.
8. Make yourself familiar with the To have all digitizer parameters 6
digitizer specifications. available which might be required for
people who are in involved in
installation and operation of the
digitizer.
9. Compare the required ambient To prevent installation of the digitizer 6.4
and climatic conditions with the in an inappropriate environment,
condition at the installation place. leading to functional faults.
10. Make an appointment with the To be able to initiate all required 7
house electrician or the prerequisites in advance to allow
authorized electrician and check proper electrical connections.
the required electrical
connection.
11. Organize the required network To have all parameters in advance, to 8.1
parameters to hook up the prevent a delay during installation.
digitizer in the existing network.
12. Make an appointment with the The cpf-file has to be created with the 8.2
clinical application specialist. clinical application specialist.
13. Have a look at the digitizer safety To have the safety standards and 9
standards and regulations. regulations for which the printer is
tested available in case they are
requested by the hospital
administration.
14. Confirm the installation To be sure that all required pre- Last
readiness. installation conditions are fulfilled. Page
NOTE:
This document describes the Installation Planning of the Digitizers
CR 85-X Type 5148/100
CR 75.0 Type 5146/105 (as of SN ≥ 6000).
2 System Overview
rk
two
ne
on
ly
5148_chap11_002_new
Figure 1
3 Scope of Delivery
CR user station
PACS station (archive) with diagnostic viewing station
Lead glass shield to protect from scatter radiation in case the CR user station is
installed in the X-ray room
High Altitude Vacuum Pump for use on sites between 2000 m and 4000 m above
Sea Level (ABC Code: EZKFF)
93 cm (36.64 In)
3 cm
68 cm (26.79 In)
Figure 3
84 cm (33.09 In)
A
61 cm (24.03 In)
Digitizer
106 cm (47.76 In)
Figure 4
Make sure that it is possible to transport the digitizer through all hallways and doors up
to the installation site:
Dimensions
5148_Chap01_019.cdr
Figure 5
Weight
NOTE:
Once the machine is unpacked, it can be moved to the installation site on four
mounted rollers.
Make sure that the floor covering is solid enough to stand the weight of the digitizer.
6 Specifications
Digitizer Type
CR 85-X 5148/100
CR 75.0 5146/105 (as of SN ≥ 6000)
Scan Technology
Red laser diode 6 facetted polygon scanner
Resolution Up to 10 lp/mm
Greyscale levels 4096 (12 bit)
Throughput ≤ 115 IPs / hour depending on size and
application
200 Day
4.000 Month
50.000 Year
Relative Humidity 15 % to 80 %
Light Tightness
NOTE:
The digitizer must not be operated in direct sunlight exposure.
Magnetic Fields
Floor Conditions
Emissions
Noise Level During scanning: max. 65 dB (A),
stand-by mode / idle: max. 46 dB (A)
7 Electrical Connections
Ensure the availability of power socket close to the installation location (approx. 1m
distance maximum).
The UTP network cable is 5 m (197”) long (2 x RJ45 connection).
Single phase connection, operable on 50 Hz and 60 Hz.
The digitizer has an automatic voltage selector. Voltage is adapted automatically as
soon as the machine is switched on. The selected voltage is displayed on a LED at the
inner side of the right door.
Two cables are included as standard delivery:
USA/Japan: Nema 6-15 P
Europe: CEE(7)VII 250 V/16 A
Network
Interfaces Ethernet port with RJ45 socket.
10/100 MBit/s, half duplex:
- CR 75.0 Type 5146 / 105 up to SN < 6500
- CR 85-X Type 5148 / 100 up to SN < 4000
Ethernet port with RJ45 socket.
10/100 MBit/s, full duplex:
- CR 75.0 Type 5146 / 105 as of SN ≥ 6500
- CR 85-X Type 5148 / 100 as of SN ≥ 4000
Serial Port RS232 for Service interface.
NOTE:
The USB port of the digitizer does not accept all types of USB stick.
USB Memory Stick must support USB version 1.1.
8 System Integration
ACTION:
Collect the network parameters from a hospital IT representative and note it in the
table below.
Therefore ask the hospital IT-Manager to define and provide settings for the
network environment for all Agfa components that have to be configured:
Digitizer Parameters:
1
ADC (VIPS) Processing Station. * Station name appears in the USER interface.
2
or ADC Preview Station.
ID-Station Parameters:
8.2 CPF-file
NOTE:
When integrating the digitizer into an existing network, it is necessary to create a
CPF– file beforehand.
NOTE:
For detailed information see ADC System Components
(DD+DIS198.00E, Chapter 6.2)
DOCUMENTATION:
ADC Application Manual Chapter 11 – Description of the CCM Tool 1.1.07,
DD+DIS181.03E.
ADC System Components Chapter 6.2, DD+DIS198.00E
SOFTWARE:
Following Service Programs are required and have to be installed on the Service PC
or the PC of the ID / Preview Station.
CCM Tool and documentation (necessary to create the configuration file
adc.cpf):
MedNet GSO Library:
Computed Radiography CR Accessories ADC System Components
Freeware ADC System Components - Software - CCM Tool 1.1.07 plus
documentation
The CCM - Tool is needed to create and modify the configuration file (adc.cpf)
for the CR 85-X and the other ADC System Components.
9 Safety Regulations
9.2 Certificates
The CR 85-X Type 5148/100 and CR 75.0 Type 5146/105 (as of SN ≥ 6000):
are in compliance with EG regulation 93/42/EEC (Medical device directive).
comply with:
The general safety regulations:
- EN 60601-1: 1990 + A1: 1993 + A2: 1995
- IEC 601-1: 1988 + A1:1991 + A2: 1995
- IEC 60601-1-1: 2000/ EN 60601-1-1:2001
- IEC 60601-1-2: 2001
- UL 2601-1 Second Edition
- CAN/CSA 22.No.601.1-M90
It is hereby certified that the CR 85-X Type 5148/100 and CR 75.0 Type 5146/105
(as of SN ≥ 6000) have interference suppression according to EN 55011: 1998 Class B
as well as FCC Rules CR47 Part 15 Class B (North-America).
This page is intentionally left blank to enable print out of even and odd pages on duplex printers.
In order to guarantee an effectice and smooth installation process within the targeted time frame,
the following tasks of the checklist below must be carried out prior to the installation of the device.
Check and discuss all the required measures for the installation by means of this checklist.
Remarks on the individual items can be noted on the back of the list.
After completion please hand out this checklist to your local Agfa representative:
Remarks:______________________________________________________________________
______________________________________________________________________________
______________________________________________________________________________
CR 85-X
Type 5148/100
CR 75.0
Type 5146/105
(as of SN ≥ 6000)
► Document History
► Referenced Documents
Document Title
Service Bulletin CR 75.0 Type 5146/105 (as of SN ≥ 6000) introduced,
DD+DIS028.07E
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" document
(see MEDNET GSO => General Info => Agfa HealthCare => Publications =>
Service Manual) prior to attempting any operation, repair or maintenance task on
the equipment.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and
on the product.
1 Glossary