Essential Performance - Medtronic LIFEPAK 12 Instrucciones De Uso

Declaración de conformidad/ Guía de compatibilidad
Guidance and Manufacturer's Declaration - Electromagnetic Emissions
Tabla 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
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage
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
Compliance Electromagnetic Environment - Guidance
Group 1 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.
Class B 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
Class A
purposes.
Complies
Instrucciones de uso del desfibrillador/monitor LIFEPAK 12