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.

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This part of ISO 14708 specifies general requirements for active implantable medical devices to provide basic assurance of safety for both patients and users. To minimize the likelihood of a device being misused, this part of ISO 14708 also details comprehensive

Sep 17, 2018 · 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...

ISO 14708 consists of the following parts, under the general title Implants for surgery ? Active implantable medical devices: Part 1: General requirements for safety, marking and for information to be provided by the manufacturer. Part 2: Cardiac pacemakers. Part 3: Implantable neurostimulators. Part 4: Implantable infusion pumps.

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.

This part of ISO 14708 specifies requirements that are generally applicable to active implantable medical devices. NOTE 1 For particular types of active implantable medical devices, these general requirements are supplemented or modified …

ISO 14708-1 Second edition 2014-08-15 Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer