Regulatory Requirement
LOGIQ E9 complies with regulatory requirements of the following European
Directive 93/42/EEC concerning medical devices.
This manual is a reference for the LOGIQ E9. It applies to Version R4 software for
the LOGIQ E9 ultrasound system.
0459
GE Healthcare
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
Summary of Contents for LOGIQ E9
Page 8: ...i 6 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
Page 12: ...i 10 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
Page 126: ...Performing an Exam 2 40 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
Page 202: ...After the Exam is Over 3 76 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
Page 250: ...Safety 4 48 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
Page 254: ...Index 4 LOGIQ E9 User Guide Direction 5454884 100 English Rev 1 ...
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