Service Manuals, User Guides, Schematic Diagrams or docs for : CANON Medical CXDI-50 Canon CXDI-50 X-Ray - Service manual (2003)

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                                                                     Printed by Canon Inc.
                                                                       Oct. 2003 Rev.02




         CXDI-1 System


            CXDI-50G
               Service Manual




                            Canon Inc. Japan
Copyright (C) Canon Inc. Medical Technical Service Dept. All rights Reserved.
                                                         Manual Control No.         : BY8-2257-0E2
                                                         Name of Product            : CXDI-50G
                                                         Distribution Control No.
                                                         Issued on


                         Service Manual Introduction
This service manual belongs to a series of after-service guides Canon Inc. publishes as part of
its comprehensive product quality guarantee program.

This service manual consists of seven chapters; General Information, Installation Guide, Feature
Information, Repair Guide, Parts Catalog, Troubleshooting and Service Manual Report.

If the product undergoes a large modification, a new service manual of revised edition will be
sent to you. In other cases, service manual report will be sent to you updates the manual.

Note 1:

This service manual is published by Canon Inc. in accordance with Article 6 (Furnishing
the Referent Materials) of the Service Assignment Contract it has concluded with your
company.

Note 2:

This service manual property of Canon Inc. and the company may seek to have it returned,
depending on circumstances. You are expected to keep it until then.

Note 3:

You inquiries, suggestions etc. about the contents of this service manual should be
addressed to:

          Medical Products Technical Service Dept.
          Canon Inc. Utsunomiya Optical Products Operations
          20-2 Kiyohara-Kogyodanchi, Utsunomiya-shi, Tochigi-ken 321-3292
          JAPAN
                          Caution Regarding Service
This product was precisely assembled under strict manufacturing process control. There
are several hazardous locations inside of this product. Careless work while the cover is
removed can result in pinching fingers or cause electrical shock. Please perform the work
with the following important points in mind:

1. Setup, Repair and Maintenance

  In order to ensure safety, the best performance, setup, repair and maintenance work can only
  be performed by the technicians received the service training specified by Canon Inc. If there
  are order required certificates or restrictions specified by the law or ordinances, those
  regulations of the country must be observed.

2. Removing the external cover

  When removing the cover during maintenance, repair, etc., perform the work after switching
  the power off. Never touch the device with wet hands, as there is a risk of electric shock.

3. Fuse

  When replacing the fuse, first, resolve the reason of failure and then replace the fuse with the
  specified type. Never use a fuse other than the specified type.

4. Connecting the grounding wire

  The provided ground wire must be connected to the ground terminal indoors. make sure that
  the device is properly grounded.

5. Alternation prohibition

  Never modify the medical device in any way.

6. Waste control

  The service provider is responsible for the disposal of used service parts, packing material,
  etc. resulting from the setup, repair or maintenance of the medical device However, the
  customer is responsible for the disposal of the medical device. Disposal activities must
  follow the regulations (=specially controlled industrial waste) of the country where the
  device is used.
                          Caution regarding the setup
According to the "IEC60601-1-1:2000", devices installed in the patient environment are
restricted to "electric medical devices conforming to IEC60601-1".

The Control PC, operation unit, and the magnetic card reader, etc. options that are parts of the
CXDI-C3S are classified under the data processing device standard (IEC60950), therefore these
items should not be installed in the patient environment. Otherwise the Control PC is only
classified in CXDI-C3S.
The patient environment described below is an example cited from the "IEC60601-1-1:2000" 

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