ISO 14708-1:2014

Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer

Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer

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Referenced standards

EN 50061:1988EN 60068-2-64:1994IEC 60068-2-14:2009IEC 60068-2-27:2008IEC 60068-2-47:2005IEC 60068-2-64:2008IEC 60601-1:2005IEC 62127-1:2007ISO 1ISO 10993-1:2009ISO 10993-9:2009ISO 7000:2014ISO 8601:2004ISO/TS 10974:2012
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ISO 14708-1:2014

Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer

Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer

ISO 14708-1:2014 specifies requirements that are generally applicable to active implantable medical devices.

The tests that are specified in ISO 14708 are type tests and are to be carried out on samples of an active implantable medical device to show compliance.

ISO 14708-1:2014 is applicable not only to active implantable medical devices that are electrically powered but also to those powered by other energy sources (for example by gas pressure or by springs).

ISO 14708-1:2014 is also applicable to some non-implantable parts and accessories of the active implantable medical devices.

Edition2014
Standard Part No1
Published Date2014
Published ByInternational Standardization Organisation
Page Count57