Regulatory Requirement - GE LOGIQ 200 PRO Series Quick Start Manual

Regulatory Requirement

This product complies with regulatory requirements of the following European Directive
93/42/EEC concerning medical devices
This Quick Start Guide is a reference for the LOGIQ
version of the 0.0 software for the LOGIQ
t
200 PRO Series. It applies to all
t
200 PRO Series.
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–Europe
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Solingen GERMANY