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About This Item

 

Full Description

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.

 

Document History

  1. ISO 14708-7:2019


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

    • Most Recent
  2. ISO 14708-7:2013

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

    • Historical Version