AGFA DRYSTAR 5302 5366 User manual

HEALTHCARE
Imaging Services Service Manual
Document No: DD+DIS150.05E
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 0
09-2015 Printed in Germany
DRYSTAR 5302
Type 5366/100/300/400/500
Agfa Company Confidential
Document ID: 31598501
Service_Manual_standard_e_template_v01
Copyright © 2015 Agfa HealthCare N.V.

DD+DIS150.05E Service Manual
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. 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 2015 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.
All other trademarks mentioned in this document are held by Agfa HealthCare N.V. or
the respective owners and are used in an editorial fashion with no intention of
infringement.
Nothing contained in this legal notice nor in any text in this document shall be
construed as granting by implication, estoppel or otherwise, any license or right to use
any of the trademarks, service marks, trade names or logos appearing in this document
without the express prior written consent of their respective owner.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" prior to attempting any operation, repair or
maintenance task on the equipment.
Refer to Document ID 11849633,
anetAgfa Intr
/
Agfa Portal via Internet
.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
IMPORTANT:
The installation and service of the product(s) described herein is to be performed
by qualified personnel who are employed by Agfa HealthCare N.V or one of its affiliates
or who are otherwise authorized by Agfa HealthCare N.V. or one of its affiliates to
provide such services.
Edition 1, Revision 0 DRYSTAR 5302 Page 2 of 2
09-2015 Type 5366/100/300/400/500 Agfa Company Confidential

HEALTHCARE
Imaging Services Generic Safety Directions
Document No: DD+DIS238.06E
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5
04-2014 printed in Germany
Agfa Company Confidential
Document Node ID: 11849633
eq_generic_safety_directions_e_template_v01
Copyright © 2014 Agfa HealthCare N.V.
Generic Safety Directions
for Agfa HealthCare Imaging Products
►Purpose of this Document
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.
►Document History
Edition.
Revision Release Date Changes compared to previous Version 1.4:
1.5 04-2014
Corrected link to Global Harmonization Task Force. See
section 12.
Added reference to user manual safety directions when
operating the device or system. See section 13.
Added safety note for cleaning and disinfection. See
section 15.
Added reference to the user manual for cleaning
instructions. See section 15.
Added safety note in case of power ON and cover
removed. See section 16.
Added safety note to check tension before working at the
powered-off device. See section 16.
Added note to combine release system components only.
Refer to section 18.
Added recommendation to use the supplementary
protective earth connection as additional safety measure,
if available. See section 18.
►Referenced Documents
Document Title
Not applicable Not applicable

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 2 of 30
►Manufacturer
Agfa HealthCare N.V.
Published by
Agfa-Gevaert HealthCare GmbH
Tegernseer Landstraße 161
D - 81539 München
Germany
Copyright 2014 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.
All other trademarks mentioned in this document are held by Agfa HealthCare N.V. or the
respective owners and are used in an editorial fashion with no intention of infringement.
Nothing contained in this legal notice nor in any text in this document shall be construed
as granting by implication, estoppel or otherwise, any license or right to use any of the
trademarks, service marks, trade names or logos appearing in this document without the
express prior written consent of their respective owner.
WARNING:
Improper operation or service activities may cause damage or injuries.
INSTRUCTION:
(1) Read the "Generic Safety Directions" prior to attempting any operation, repair or
maintenance task on the equipment.
Refer to Document ID 11849633,
anetAgfa Intr
/
Agfa Portal via Internet
.
(2) Strictly observe all safety directions within the "Generic Safety Directions" and on
the product.
04-2014 Agfa Company Confidential

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 3 of 30
04-2014 Agfa Company Confidential
LIST OF CONTENTS
1DISCLAIMER......................................................................................................... 5
2USED ICONS ........................................................................................................ 6
3LABELS ................................................................................................................. 7
3.1 CE Mark................................................................................................... 7
3.2 Labels ...................................................................................................... 7
3.3 Labels concerning Laser Radiation ......................................................... 8
4PRODUCT COMPLAINTS .................................................................................. 10
5REFERENCES .................................................................................................... 10
6INTENDED USE.................................................................................................. 11
7INTENDED USER ............................................................................................... 11
8QUALIFICATIONS FOR OPERATION AND SERVICE TASKS.......................... 11
9ENVIRONMENTAL AND OCCUPATIONAL SAFETY INSTRUCTIONS............. 12
10 CONNECTIONS TO OTHER EQUIPMENT ........................................................ 13
11 ACCESSORIES AND SPARE PARTS................................................................ 14
12 COMPLIANCE..................................................................................................... 14
13 SAFETY DIRECTIONS FOR OPERATION......................................................... 17
14 RADIATION PROTECTION ................................................................................ 18
15 SAFETY DIRECTIONS FOR CLEANING AND DISINFECTION......................... 18
16 GENERAL SAFETY DIRECTIONS FOR SERVICE ACTIVITIES ....................... 19
17 SAFETY DIRECTIONS FOR INSTALLATION PLANNING ACTIVITIES ............ 21
18 SAFETY DIRECTIONS FOR INSTALLATION ACTIVITIES................................ 23
19 SAFETY DIRECTIONS FOR MAINTENANCE AND REPAIR ACTIVITIES ........ 25
20 SAFETY DIRECTIONS FOR REMOTE SERVICE ACTIVITIES ......................... 28

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 4 of 30
04-2014 Agfa Company Confidential
21 SAFETY DIRECTIONS FOR TRANSPORT AND SHIPMENT OF SPARE
PARTS, ACCESSORIES AND DEVICES............................................................28
22 SAFETY DIRECTIONS CONCERNING MODIFICATIONS.................................28
23 SAFETY DIRECTIONS CONCERNING HAZARDOUS MATERIALS .................28
24 RECYCLING ........................................................................................................29
25 WASTE DISPOSAL .............................................................................................29
26 ERASING PROTECTED HEALTH INFORMATION (PHI) ...................................30

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 5 of 30
1 Disclaimer
The installation and service of equipment described herein is to be performed by qualified
personnel who are employed by Agfa HealthCare or one of its affiliates or who are
otherwise authorized by Agfa HealthCare or one of its affiliates to provide such services.
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 makes no warranties or representation, expressed or implied, with
respect to the accuracy, completeness or usefulness of the information contained in this
document and specifically disclaims warranties of suitability for any particular purpose.
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.
04-2014 Agfa Company Confidential

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 6 of 30
2 Used Icons
Icon Signal Word and Situation
CAUTION: Possible dangerous situation: Light injuries or damage
to the equipment described in the manual and/or damage to any
other equipment or goods and/or environmental pollution can be the
consequence.
WARNING: Dangerous situation: Potential serious injury to a user,
engineer, patient or any other person and possible mistreatment of
patients can be the consequence.
DANGER: Direct, immediate danger: Death or heavy injuries can
be the consequence.
INSTRUCTION:
Indicates an instruction where it is important to follow the described
actions literally.
IMPORTANT:
Highlights very important actions which have to be carried out to
prevent malfunction.
NOTE:
Indicates advice to facilitate the following step or action
without having a direct influence on the step or action.
Highlights unusual points.
Indicates background information.
Can be used to explain or highlight displays of the graphical
user interface.
04-2014 Agfa Company Confidential

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 7 of 30
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.
3.2 Labels
For the meaning of the labels in and on the product refer to:
The corresponding product or system User Manuals and
The figure below, with a list of possible service activity related labels and their
meaning. To prevent injuries or damage to the equipment, follow the instructions
on the label or the related service instructions.
Hot surface
High voltage Hand injuries Do not touch Protective earth
connection
Laser radiation Magnetic field Ionizing radiation
04-2014 Agfa Company Confidential

DD+DIS238.06E Generic Safety Directions
DOCUMENT CONTROL NOTE:
The controlled version of this document is available from the Agfa HealthCare Library. Any printed copy of this document is uncontrolled.
Edition 1, Revision 5 Generic Safety Directions for HealthCare Imaging Products Page 8 of 30
3.3 Labels concerning Laser Radiation
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.
Class # Meaning Example Label
Class 1: Not dangerous to the human eye, even
when using optical instruments. Can
nevertheless produce irritating effects,
especially with low ambient light
conditions.
CLASS 1 LASER PRODUCT
Class 1 M: Not dangerous to the human eye if no
optical instruments (magnifying glass or
binocular) are used.
Can nevertheless produce irritating
effects, especially with low ambient light
conditions.
CLASS 1M LASER PRODUCT
DO NOT VIEW DIRECTLY WITH
OPTICAL INSTRUMENTS
LASER RADIATION
Class 2: Dangerous to the human eye for
intentional staring into the beam.
Not dangerous for short term exposure
< 0,25 seconds.
Using optical instruments does not
increase the risk of eye injury.
Can even for short term exposure < 0,25
seconds produce dazzling and irritating
effects, especially with low ambient light
conditions.
CLASS 2 LASER PRODUCT
DO NOT STARE INTO BEAM
LASER RADIATION
04-2014 Agfa Company Confidential