Medical Device Directive
Definium AMX 700 X-Ray System
5161515-1EN
Rev. 6 (10 February 2008)
i
Operator Manual
© 2008 General Electric Company. All rights reserved.
Medical Device Directive
Documentation, trademark and the software are copyright reserved. Under the copyright laws, the
documentation may not be photocopied, reproduced, translated, or reduced by any electronic machine
to a readable form, in whole or part, without the prior written permission of General Electric Company.
The original language of this manual is English.
The General Electric Company reserves the right to revise this manual and to make changes in the
content of it without notify any person of such revision or changes.
European registered place of business:
GE Medical Systems Europe
Quality Assurance Manager
BP 34
F 78533 BUC CEDEX
Green QSD 1990 Standard issued by MDD (Medical Devices Directorate, Department of Health, UK).
Medical Device Good Manufacturing Practice Manual issued by the FDA (Food and Drug Administration,
Department of Health, USA).
Underwriters' Laboratories, Inc. (UL), an independent testing laboratory.
Canadian Standards Association (CSA).
International Electrotechnical Commission (IEC), international standards organization, when applicable.
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