Tabelle H-1 Guidance And Manufacturer's Declaration - Electromagnetic Emissions; Essential Performance - Medtronic lifepak 12 Gebrauchsanweisung

Konformitätserklärung/Richtlinien zur elektromagnetischen Verträglichkeit
Guidance and Manufacturer's Declaration - Electromagnetic Emissions
Table H-1
®
The LIFEPAK 12 defibrillator/monitor system is intended for use in the electromagnetic environment
specified below. The customer or the user of the LIFEPAK 12 defibrillator/monitor system should ensure
that the device is used in such an environment.
Emissions Test Compliance
RF emissions Group 1
CISPR 11
RF emissions Class B
CISPR 11
Harmonic Class A
emissions
IEC 61000-3-2
Voltage Complies
fluctuations/
flicker emissions
IEC 61000-3-3

Essential Performance

The LIFEPAK 12 defibrillator/monitor system 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.
H-2
Electromagnetic Environment - Guidance
The LIFEPAK 12 defibrillator/monitor system 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 LIFEPAK 12 defibrillator/monitor system 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.
LIFEPAK 12 Defibrillatoren/Monitore Gebrauchsanweisung