This part of ISO 14708 is applicable to active implantable medical devices intended for electrical stimulation of the central or peripheral nervous system. This part of ISO 14708 is also applicable to all non-implantable parts and accessories of the devices as defined in Clause 3. The tests that are specified in this part of ISO 14708 are type tests intended to be carried out on a sample of a device to show compliance, and are not intended to be used for the routine testing of manufactured products.
ANSI/AAMI/ISO 14708-3:2008 history
1970ANSI/AAMI/ISO 14708-3:2017 Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
2008ANSI/AAMI/ISO 14708-3:2008 Implants for surgery - Active implantable medical devices - Part 3: Implantable neurostimulators