Customer Service:
Mon - Fri: 8:30 am - 6 pm EST

 Historical

ISO 14708-5:2010

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

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.


Content Provider
International Organization for Standardization [ISO]


Others Also Bought

IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package
IEC 60601-1 and IEC 60601-1-2 Medical Electrical Equipment Package
IEC 60529 Ed. 2.2 b:2013
Degrees of protection provided by enclosures (IP Code)
ANSI/AAMI HE75:2009 (R2013) (ANSI/AAMI HE 75:2009 (R2013))
Human factors engineering - Design of medical devices
ANSI Logo

As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

CUSTOMER SERVICE
NEW YORK OFFICE
ANSI HEADQUARTERS