GE SENOGRAPHE DMR+ Technical Publications page 7

GE Medical Systems
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CAUTION
REGULATORY REQUIREMENTS
This product complies with the regulatory requirements of the following:
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Council Directive 93/42/EEC concerning medical devices: the
to the product testifies compliance to the Directive.
For a system, the location of the CE marking label is described in the system manual.
European registered place of business:
GE Medical Systems Europe
Quality Assurance Manager
BP 34
F 78533 BUC CEDEX France
Tel: +33 (0)1 30 70 40 40
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Medical Device Good Manufacturing Practice Manual issued by the FDA (Food and
Drug Administration, Department of Health, USA).
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Underwriters' Laboratories, Inc. (UL), an independent testing laboratory.
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Canadian Standards Association (CSA).
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International Electrotechnical Commission (IEC), international standards organiza-
tion, when applicable.
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USA/HHS:
United States Federal law restricts this device to use by or on the order of a
physician.
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General Electric Medical Systems is ISO 9001 and EN 46001 certified.
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The original document was written in English.
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SENOGRAPHE DMR+
om 5128689-2-100
label affixed
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