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Life-support policy, Apc three-phase systems – American Power Conversion PD150G6F User Manual

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150kW InfraStruXure PDU—Operation and Configuration

69

Life-Support Policy

APC Three-Phase Systems

American Power Conversion Corporation (APC) and its affiliates and subsidiaries worldwide do not
recommend the use of any of their products in life-support applications where failure or malfunction
of the APC product can be reasonably expected to cause failure of the life-support device or to
significantly affect its safety or effectiveness. APC does not permit the use of any of its products in
direct patient care. APC will not knowingly sell its products for use in such applications unless the
life-support system or direct patient care device is part of a whole facility/building into which the
UPS is integrated, and unless APC receives, in writing, assurances satisfactory to APC that:

a. The UPS system will be configured in a manner that will provide N+1 power redundancy to

the critical load,

b. The end-user customer assumes all risks and signs the APC System Configuration and Use

Form, and

c. The customer and operators of the APC UPS system agree to indemnify and hold APC and

its affiliates and subsidiaries harmless for any and all claims arising out of the systems use in
such applications.

The term life-support device includes but is not limited to neonatal oxygen analyzers, nerve
stimulators (whether used for anesthesia, pain relief, or other purposes), autotransfusion devices,
blood pumps, defibrillators, arrhythmia detectors and alarms, pacemakers, hemodialysis systems,
peritoneal dialysis systems, neonatal ventilator incubators, ventilators (for adults and infants),
anesthesia ventilators, infusion pumps, and any other devices designated as “critical” by the

U.S. FDA

.

Hospital-grade wiring devices and leakage current protection may be ordered as options on many

APC UPS

systems.

APC

does not claim that units with these modifications are certified or listed as

hospital-grade by

APC

or any other organization. Therefore these units do not meet the requirements

for use in direct patient care.

This manual is related to the following products: