GE Brivo OEC 715 Service Manual page 4

REGULATORY REQUIREMENTS
International Electrotechnical Commission (IEC), international standards organization, when
applicable.
Brivo OEC 715/Brivo OEC 785/Brivo OEC 865 complies with the regulatory requirements of the
following:
Council Directive 93/42/EEC concerning medical devices.
CE label affixed to the product testifies compliance to all requirements of the Directive.
The location of the CE
European Representative:
GE Medical Systems S.C.S.
Quality Assurance Manager
283 rue de la Minière
78530 BUC France
Tel: +33 1 30 70 40 40
2
Brivo OEC 715/785/865 Mobile C-Arm X-Ray Product Service Manual
label is described in this manual.
0459