Appendix A Guidance And Manufacturer's Declarations; Table 10: Guidance And Manufacturer's Declaration - Electromagnetic Emissions - For All Medical Electrical Equipment And Medical Electrical Systems - Adaptec Sensica UO Instructions For Use Manual

Sensica™ UO System for ICU Instructions for Use, Model No. SCCS-1001, ver. 1001
Guidance and Manufacturer's Declarations
Table 10: Guidance and Manufacturer's Declaration - Electromagnetic Emissions –
for all Medical Electrical Equipment and Medical Electrical Systems
The Sensica™ UO System for ICU is intended for use in the electromagnetic environment
specified below. The customer or the user of the Sensica™ UO System for ICU should assure
that it is used in such an environment.
Emissions Test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage
fluctuations/flicker
emissions
IEC 61000-3-3
P/N 005-0175 Rev A
Appendix A
Compliance
Group 1
Class A
Class A
Complies
Adaptec Medical Devices
Electromagnetic Environment - Guidance
The Sensica™ UO System for ICU uses RF
energy only for its internal function. Therefore,
its RF emissions are very low and are not likely
to cause any interference in nearby electronic
equipment.
The Sensica™ UO System for ICU is suitable for
use in all establishments other than domestic
and those directly connected to the public low-
voltage power supply network that supplies
buildings used for domestic purposes.
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