Electromagnetic Compatibility Guidance
LIFEPAK 1000 Defibrillator Operating Instructions G-1
©2018 Physio-Control, Inc.
ELECTROMAGNETIC EMISSIONS
The LIFEPAK
®
1000 defibrillator is intended for use in the electromagnetic environment specified
below. The customer or the user of the LIFEPAK 1000 defibrillator should ensure that the device
is used in such an environment.
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 1 Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
Emissions Test Compliance Electromagnetic Environment - Guidance
RF emissions
CISPR 11
Group 1 The LIFEPAK 1000 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 LIFEPAK 1000 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
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