Compact / Series 7600 Installation Procedure
1
Introduction
This manual describes the installation of the Compact / Series 7600 system
and a definition of the responsibilities and instructions for reporting, safety,
unpacking, moving and verifying system operation.
Responsibility
The customer must provide the labor and equipment necessary to unload the
system from the transport vehicle and move it to the final location. It is the
customer’s responsibility to obtain all permits necessary to meet all
requirements of state and local codes, regulations and ordinances with respect
to the installation and operation of the system.
A qualified service technician should perform the following:
•
Installation Report/Checklist (00-879038-03).Safety procedures should be
in effect at all times during the installation process. By law, complete
reports within 15 days from the date of assembly (installation).
•
Return the assembler's copy of the Report of Assembly of Diagnostic X-ray
(FDA form 2579), the Beam Alignment Radiographs (films), and the
Installation Report/Checklist to OEC Medical Systems, Inc., Attention:
Technical Support, in the stamped, manila envelope provided in the Field
Service Documentation Package.
•
Distribute the various remaining copies of the Report of Assembly of
Diagnostic X-ray (FDA form 2579), following the documentation instructions
included in the Field Service Documentation Package.
•
The OEC Medical Systems, Inc. Representative MUST sign the last page of
the Installation Report and Checklist, verifying Field Service acceptance of
the unit. If, for any reason, the installation remains incomplete, notify the
Hospital that the system is not yet ready for use.
Safety Procedures
Under no circumstances should the safety interlocks in the system be
bypassed, jumped or otherwise disabled. Never operate or store the system in
a location where conductive fluids such as water, saline solution, etc., can spill
on any part of the equipment unless you cover the system with a protective
waterproof draping.
NOTE:
All OEC Medical Systems, Inc. systems comply with International
Electrotechnical Commission safety standard IEC-601. Do not connect any
external device to the system that does not meet the requirements of IEC-601.
Only devices provided by or approved by OEC Medical Systems, Inc. should be
connected to the system.
Explosion Hazard
Never operate the system in the presence of flammable anesthetics or other
flammable or explosive liquids, vapors, or gases. Vapors and gases can ignite
by electrical arcs that can occur during the normal operation of switches, circuit
breakers, push-buttons and other circuit components.
Used and Refurbished C-Arms are Available from www.SharpMedical.com - Call us at 800-969-9800
An Independent C-Arm Service Provider. This PDF provided for research / historical purposes only.
