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GE LOGIQ P7 Service Manual

GE LOGIQ P7
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GERAFT LOGIQ P9/P7
D
IRECTION 5604324, REVISION 11 DRAFT (JANUARY 24, 2019) SERVICE MANUAL
8-6 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.
Refer to Section 1-3-10 "Returning/Shipping System, Probes and Repair Parts" on page 1-15.
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.

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GE LOGIQ P7 Specifications

General IconGeneral
BrandGE
ModelLOGIQ P7
CategoryMedical Equipment
LanguageEnglish

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