User Manual

Appendix H
Electromagnetic Compatibility Guidance
LIFEPAK 20e Defibrillator/Monitor Operating Instructions H-1
©2006-2013 Physio-Control, Inc.
Canadian Standard ICES-003 Declaration
Note: This section applies only if a CodeManagement Module is attached to the LIFEPAK 20e defibrillator/
monitor.
This Class B digital apparatus complies with Canadian ICES-003.
This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the
following two conditions: 1) this device may not cause interference, and 2) this device must accept any
interference, including interference that may cause undesired operation of the device.
Essential Performance
The LIFEPAK 20e defibrillator/monitor maintains safe and effective performance of the defibrillation therapy
and patient monitoring functions when operated in the electromagnetic environment specified in Tables 2
through 4.
Table 1
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
The LIFEPAK 20e defibrillator/monitor is intended for use in the electromagnetic environment specified below.
The customer or the user of the LIFEPAK 20e defibrillator/monitor should ensure that the defibrillator/monitor is
used in such an environment.
Emissions Test Compliance Electromagnetic Environment - Guidance
RF emissions
CISPR 11
Group 1 The LIFEPAK 20e defibrillator/monitor 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 20e defibrillator/monitor 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
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies