ISO 14708-7:2019
2019-12
Resumen
This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via electrical stimulation of the auditory pathways. Devices which treat hearing impairment via means other than electrical stimulation are not covered by this document.
The tests that are specified in this document are type tests and are to be carried out on samples of a device to show compliance.
This document is also applicable to non-implantable parts and accessories of the devices (see NOTE).
The electrical characteristics of the implantable part are determined by either the appropriate method detailed in this document or by any other method demonstrated to have an accuracy equal to, or better than, the method specified. In the case of dispute, the method detailed in this document applies.
NOTE A device that is commonly referred to as an active implantable medical device can in fact be a single device, a combination of devices, or a combination of a device or devices and one or more accessories. Not all of these parts are required to be either partially or totally implantable, this document specifies those requirements of non-implantable parts and accessories which could affect the safety or performance of the implantable part.
Informaciones generales
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Estado: PublicadoFecha de publicación: 2019-12
Versión corregida (en): 2020-05
Versión corregida (fr): 2020-05Etapa: Norma Internacional en proceso de revisión sistemática [90.20] -
Edición: 2Número de páginas: 68
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Comité Técnico :ISO/TC 150/SC 6ICS :11.040.40
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Ciclo de vida
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Anteriormente
RetiradaISO 14708-7:2013
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Ahora
