Physio-Control LIFEPAK CR Plus - Manual (Page 73)

LIFEPAK CR Plus and LIFEPAK EXPRESS Defibrillator Operating Instructions D-1
©2009-2010 Physio-Control, Inc.
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Electromagnetic Compatibility Guidance
Essential Performance
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators maintain safe and effective performance of the
defibrillation therapy and patient monitoring functions when operated in the electromagnetic environment
specified in Tables 2 through 4.
Limitations Affecting Immunity to Electromagnetic Disturbances
The level of protection from electromagnetic disturbances is limited by several factors, including requirements
for protection from third-party defibrillators, patient safety isolation, and maintenance of adequate
signal-to-noise ratios for processing patient signals.
Table D-1 Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators are intended for use in the electromagnetic
environment specified below. The customer or the user of the defibrillator should ensure that the defibrillator is
used in such an environment.
Emissions Test Compliance Electromagnetic Environment - Guidance
RF emissions
CISPR 11
Group 1 The defibrillator 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.
RF emissions
CISPR 11
Class B The defibrillator is suitable for use in all establishments,
including domestic establishments and those directly connected
to the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Not Applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not Applicable