Regulatory Requirement
This product complies with regulatory requirements of the following European
Directive 93/42/EEC concerning medical devices
This manual is a reference for the LOGIQ 500 MD MR3 Plus. It applies to all
versions of 4.2 software for the LOGIQ 500.
GE Medical Systems
GE Medical Systems: Telex 3797371
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Medical Systems Ċ Europe: Tel: +49 (0) 212 28 02 208
Beethovenstraße 239, Postfach 11 05 60, D-42655 Solingen
GERMANY
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