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14. Declaración de conformidad de EMC
INFORMACIÓN SOBRE COMPATIBILIDAD ELECTROMAGNÉTICA
Tabla 1
Para todos los EQUIPOS y SISTEMAS MÉDICOS ELÉCTRICOS
Declaración de directrices y fabricación: emisiones electromagnéticas
El BG 17 está diseñado para usarse en el ambiente electromagnético especificado a continuación.
El cliente o usuario del BG 17 debe asegurarse de que se use en un ambiente como el descrito.
Prueba de emisiones Conformidad Ambiente electromagnético: directrices
Emisiones de
radiofrecuencia (RF)
CISPR 11
Grupo 1
El BG 17 utiliza energía de radiofrecuencia solo para su fun-
cionamiento interno. Por lo tanto, sus emisiones de radio-
frecuencia son muy bajas y no son susceptibles de causar
interferencia a equipos electrónicos cercanos.
Emisiones de
radiofrecuencia (RF)
CISPR 11
Clase B
Tabla 2
Para todos los EQUIPOS y SISTEMAS MÉDICOS ELÉCTRICOS
Declaración de directrices y fabricantes: inmunidad electromagnética
El BG 17 está diseñado para usarse en el ambiente electromagnético especificado a continuación.
El cliente o usuario del BG 17 debe asegurarse de que se use en un ambiente como el descrito.
Prueba de
INMUNIDAD
Nivel de prueba
IEC 60601
Nivel de
conformidad
Ambiente electromagnético: directrices
Descarga electros-
tática (ESD)
IEC 61000-4-2
± 6 kV contacto
± 8 kV aire
± 6 kV contacto
± 8 kV aire
Los pisos deberán ser de madera, con-
creto o losetas de cerámica. Si los pisos
están cubiertos con material sintético, la
humedad relativa deberá ser de por lo
menos 30 %.
Frecuencia de
potencia (50/60 Hz)
campo magnético
IEC 61000-4-8
3 A/m 3 A/m
Los campos de potencia magnética deben
estar a niveles característicos de un lugar
típico en un ambiente comercial o de hos-
pital típico.
30


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