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ISO 14708-5:2010

Implants for surgery -- Active implantable medical devices -- Part 5: Circulatory support devices

General information
Withdrawn from 12.05.2020
Directives or regulations
None

Standard history

Status
Date
Type
Name
12.05.2020
Main
26.01.2010
Main
ISO 14708-5:2010 specifies requirements for safety and performance of active implantable circulatory support devices. It is not applicable to extracorporeal perfusion devices, cardiomyoplasty, heart restraint devices and counter-pulsation devices, such as extra- or intra-aortic balloon pumps.
ISO 14708-5:2010 specifies type tests, animal studies and clinical evaluation requirements.
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