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ISO 14708-7:2013

Implants for surgery -- Active implantable medical devices -- Part 7: Particular requirements for cochlear implant systems

General information
Withdrawn from 20.12.2019
Directives or regulations
None

Standard history

Status
Date
Type
Name
20.12.2019
Main
08.01.2013
Main
ISO 14708-7:2013 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.
The tests that are specified in ISO 14708-7:2013 are type tests and are to be carried out on samples of a device to show compliance.
ISO 14708-7:2013 is also applicable to non-implantable parts and accessories of the devices.
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