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GE LOGIQ E9 Service Manual

GE LOGIQ E9
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GE
D
IRECTION 5535208-100, REV. 2 LOGIQ E9 SERVICE MANUAL
8 - 4 Section 8-2 - Warnings and important information
8-2-3 Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GE Healthcare policy states that body fluids must be properly removed from any part or equipment prior
to shipment. GE Healthcare employees, as well as customers, are responsible for ensuring that parts/
equipment have been properly decontaminated prior to shipment. Under no circumstance should a part
or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils
or an ultrasound Probe). The purpose of the regulation is to protect employees in the transportation
industry, as well as the people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that “items that were saturated and/or
dripping with human blood that are now caked with dried blood; or which were used or intended
for use in patient care” are “regulated medical waste” for transportation purposes and must be
transported as a hazardous material.
8-2-4 Manpower - When two persons are needed
These replacement procedures require two persons:
Casters Replacement
The rest of the replacement procedures can be carried out by one person.

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GE LOGIQ E9 Specifications

General IconGeneral
TypeUltrasound System
3D/4D ImagingYes
Transducer Ports4 active ports
ConnectivityDICOM, USB, Ethernet
ApplicationsAbdominal, Vascular, Musculoskeletal, Small Parts, Urology, Pediatric, Cardiac, Obstetrics/Gynecology
TransducersLinear, Convex, Phased Array, Volume
Doppler ModesColor Doppler, Power Doppler, Pulsed Wave Doppler, Continuous Wave Doppler
ElastographyYes
Advanced FeaturesB-Flow, Volume Navigation
PortabilityCart-based system
Display19-inch high-resolution LCD monitor

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