ISO 14708-5:2010
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ISO 14708-5:2010
52779

Status : Withdrawn

This standard has been revised by ISO 14708-5:2020

Abstract

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.

General information

  •  : Withdrawn
     : 2010-02
    : Withdrawal of International Standard [95.99]
  •  : 1
     : 47
  • ISO/TC 150/SC 6
    11.040.40 
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