GANSHORN PowerCube-Ergo User manual

GANSHORN Medizin Electronic GmbH Service Manual Ref.No. 03 140 0 046
PowerCube-Ergo-CASE_ENG_rev.02, 23.11.2012 Preface, page 1 of 8
PowerCube-Ergo
Cardiopulmonary function testing
Service Manual
Ref.No. 03 140 0 046, rev.02
Valid for PowerCube-Ergo-SSO / CASE
- ENGLISH -
2004

GANSHORN Medizin Electronic GmbH Service Manual Ref.No. 03 140 0 046
PowerCube-Ergo-CASE_ENG_rev.02, 23.11.2012 Preface, page 2 of 8
Table of Contents
Preface
Chapter 1: Safety Regulations
Chapter 2: System Description
Chapter 3: Disassembly
Chapter 4: Circuit Diagrams and Board Layouts
Chapter 5: Software
Chapter 6: Troubleshooting, Checks and Adjustments
Chapter 7: Spare Parts
Appendix A: Allocation of Ergo-Parameters
Appendix B: Working Procedure AA MTK 70_03 for PowerCube-Ergo-
SSO
Appendix C: Checklist PP MTK 70_03 for PowerCube Ergo-SSO

GANSHORN Medizin Electronic GmbH Service Manual Ref.No. 03 140 0 046
PowerCube-Ergo-CASE_ENG_rev.02, 23.11.2012 Preface, page 3 of 8
Preface
Contact Addresses
Warranty
Copyright
Documentation
Valid for
Related Documents
Copyright
Revision History
General Notes
Update
Intended Use, Documentation Purpose, Target Group, and Safekeeping
System Description
Intended Use
Documentation Purpose
Target Group
Requirements for Installation, Maintenance and Service
Requirements for Maintenance and Service Personnel
Definitions
Danger
Warning
Caution
Action Instructions / Operating Steps
Lists
Cross Reference
Cross Reference to possible LF8 Settings
Keys and Buttons
Equipment Identification
Equipment Symbols
Acronyms

GANSHORN Medizin Electronic GmbH Service Manual Ref.No. 03 140 0 046
PowerCube-Ergo-CASE_ENG_rev.02, 23.11.2012 Preface, page 4 of 8
Preface
Contact addresses Distributed by:
Manufacturer and publisher
Ganshorn Medizin Electronic GmbH
Industriestr. 6-8
97618 Niederlauer
Germany
Tel. [phone]
Fax [phone]
[email protected]
www.ganshorn.de
Warranty
Only original GANSHORN parts may be utilized that have been listed in this documentation and in
complementary documentation and that have been inspected and approved by GANSHORN.
If non-original parts are used in GANSHORN devices, GANSHORN does not guarantee the safe
operation and functioning of its products. In that case, the GANSHORN guarantee expires.
No guarantee claims can be made in the case of damage resulting from utilization of non-original parts in
GANSHORN devices.
GANSHORN regards itself as responsible for its products concerning safety, reliability, precision, and
function only if:
Assembly, installation, expansion, modification, adjustment, changes, and
repairs have been carried out by GANSHORN or authorized GANSHORN
partners
The GANSHORN product has been employed in accordance with the operator
instructions
The GANSHORN product has been employed in accordance with the intended
use.
GANSHORN is liable for the function capability, but not for the absolute lack of defects of its software
programs. GANSHORN is only liable for the function capability of its software that is used with
GANSHORN systems.
GANSHORN does not guarantee the flawless functionality of GANSHORN software programs in
connection with any external software programs, and does not accept liability for malfunctions and/or
their consequences.
For the detailed terms of warranty see your purchase contract or your dealer contract.
Copyright
All rights are reserved and retained by the manufacturer for products, circuits, processes, software
programs, names, trademarks, and patents.
GE Medical Systems Information
Technologies, Inc.
8200 West Tower Avenue
Milwaukee, WI 53223 USA
Tel: [phone]
800.558.5120 (USA)
Fax: [phone]

GANSHORN Medizin Electronic GmbH Service Manual Ref.No. 03 140 0 046
PowerCube-Ergo-CASE_ENG_rev.02, 23.11.2012 Preface, page 5 of 8
Documentation
Ref.No. 03 140 0 046
Valid for.: PowerCube-Ergo-SSO, Ref.No. 03 337 0 210 and 03 337 0 238,
Rev. D and higher
Related documents:
Operating Instruction manual LF8
Operating Instruction manual PowerCube-Ergo
Copyright 2012, GANSHORN Medizin Electronic GmbH
Revision history
The release number changes with every update for this documentation
General Notes
All GANSHORN documents correspond to the state of the underlying safety standards at the time of
printing.
All illustrations in this documentation are provided as examples only. They may not necessarily reflect
your equipment setup or data displayed. All pictured GANSHORN products and screen displays can
deviate, due to technical changes.
All rights, including reprints, copying, and those from translation remain reserved by the publisher.
No part of this documentation may be reproduced in any form whatsoever or copied using electronic
reproduction systems without the publisher’s express written permission.
Update
This documentation is also regularly reviewed. Changes, technical improvements, as well as any
typographical errors are taken into consideration in each following issue.
Technical changes/modifications made on the devices after the issue date are not contained in this
documentation.
Changes/modifications performed on GANSHORN products that affect the hardware and software must
be documented in a Medical Device Book.
The operator must be accordingly trained concerning the changes/modifications. This must subsequently
be documented in the Medical Device Book.
In the case of non-observance, the manufacturer is not liable.
Release date:
Release number:
Comment:
11 February 2009
Release 01/2009
Index a
Initial release
09 March 2009
Release 01/2009
Index b
Preface, modification of front cover
07 October 2009
Rev.01
Change of the release number
Change of the ref. number system
Revision of the English translation
Modifications to REV.D (board layouts chapter 4)
Modifications to Installation Assistant (chapter 5)
Update Appendix B and D
23 November 2012
Rev 02
Update of the rear and front panels of the
PowerCube according to IEC 60601-1 3rd Edition
and review of contents