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© Bosch Healthcare Solutions GmbH 55Instrucciones de uso
Fabricante
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10 Fabricante
Bosch Healthcare Solutions GmbH
Stuttgarter Str. 130
71332 Waiblingen, Germany
Correo electrónico: info@vivatmo.com
Internet: www.vivatmo.com
11 Anexo
11.1 Compatibilidad electromagnética
Información importante relativa a la compatibilidad electromagnética (CEM)
Por la presente, Bosch Healthcare Solutions GmbH, declara que el tipo de equipo radioeléctrico Vivatmopro se ajusta a la
Directiva 2014/53/UE. El texto completo de la declaración UE de conformidad está disponible en la dirección Internet siguiente:
https://www.vivatmo.com/en/service-support/additional-information.html
Vivatmopro portátil satisface la norma EN60601-1-2: 2015 con el fin de evitar situaciones de inseguridad del producto.
Dicha norma regula los niveles de inmunidad frente a las interferencias electromagnéticas y los valores máximos de emisión
electromagnética para equipos médicos. Vivatmopro está fabricado por la empresa y satisface las directrices estándar y la
declaración del fabricante acerca de las emisiones electromagnéticas EN60601-1-2: 2015 tanto en términos de inmunidad como
de emisiones y, por lo tanto, no necesita ningún servicio ni mantenimiento en relación con la CEM y la ESD a lo largo de su vida
útil. Las bases Vivatmopro cuya fecha de fabricación sea anterior al 1de noviembre de 2018 satisfacen la norma EN61326-
1: 2013 en relación con la CEM. Para consultar la declaración del fabricante respecto a la CEM, visite www. vivatmo. com.
55


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