GE MEDICAL SYSTEMS - KRETZTECHNIK RAFT VOLUSON® 730PRO / 730PROV (BT´04)
D
IRECTION KTI105947, REVISION 2 SERVICE MANUAL
8-2 Section 8-2 - Ultrasound Application Software (UIS) Installation Procedure
8-1-2 Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GEMS policy states that body fluids must be properly removed from any part or equipment prior to
shipment. GEMS 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
and 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 what 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 purpose and must be
transported as a hazardous material.
Section 8-2
Ultrasound Application Software (UIS) Installation Procedure
8-2-1 Introduction
8-2-2 Manpower
One Person, 20 min.
8-2-3 Tools
System DVD
8-2-4 Preparations
Before performing the Software Update/Upgrade:
A.) make sure that all system functions are working correct
B.) check the current Software Version and installed Options
NOTICE
It is possible to update the Ultrasound Application Software via the UPDATE button in the System Setup
SERVICE page; see: Section 8-2-5 on page 8-5.
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