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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

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General

Type	Ultrasound System
3D/4D Imaging	Yes
Transducer Ports	4 active ports
Connectivity	DICOM, USB, Ethernet
Applications	Abdominal, Vascular, Musculoskeletal, Small Parts, Urology, Pediatric, Cardiac, Obstetrics/Gynecology
Transducers	Linear, Convex, Phased Array, Volume
Doppler Modes	Color Doppler, Power Doppler, Pulsed Wave Doppler, Continuous Wave Doppler
Elastography	Yes
Advanced Features	B-Flow, Volume Navigation
Portability	Cart-based system
Display	19-inch high-resolution LCD monitor