ISO 14708-2:2012 specifies requirements that are applicable to those active implantable medical devices intended to treat bradyarrhythmias.
The tests that are specified in ISO 14708-2:2012 are type tests, and are to be carried out on samples of a device to show compliance.
ISO 14708-2:2012 is also applicable to some non-implantable parts and accessories of the devices.
Revises
ISO 14708-2:2005
WITHDRAWN
ISO 14708-2:2012
95.99
Withdrawal of Standard
3 sht 2019
PUBLISHED
ISO 14708-2:2019
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