Regulatory Requirement
This product complies with regulatory requirements of the following European
Directive 93/42/EEC concerning medical devices.
First CE Marked in 2017.
This manual is a reference for the Versana Essential ultrasound system. It applies
to all revisions of the R1.x.x software for the Versana Essential ultrasound system.
GE
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Ultraschall Deutschland GmbH & Co. KG
Beethovenstrasse 239
Postfach 11 05 60
D-42655 Solingen GERMANY
TEL: 49 212.28.02.208; FAX: 49 212.28.02.431
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