• Filter:

  •  
  •  
  •  
  •  
Standard and/or project under the direct responsibility of ISO/TC 150/SC 6 Secretariat Stage ICS
ISO 5841-2:2000
Implants for surgery — Cardiac pacemakers — Part 2: Reporting of clinical performance of populations of pulse generators or leads
95.99
ISO 5841-2:2014
Implants for surgery — Cardiac pacemakers — Part 2: Reporting of clinical performance of populations of pulse generators or leads
90.20
ISO 5841-3:2000
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers
95.99
ISO 5841-3:2000/Cor 1:2003
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers — Technical Corrigendum 1
95.99
ISO 5841-3:2013
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers
90.93
ISO 10310:1995
Neurosurgical implants — Marking and packaging of implantable neural stimulators
95.99
ISO/TS 10974:2012
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
95.99
ISO/TS 10974:2018
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
90.92
ISO 11318:2002
Cardiac defibrillators — Connector assembly DF-1 for implantable defibrillators — Dimensions and test requirements
90.93
ISO 14117:2012
Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
95.99
ISO 14117:2019
Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
60.60
ISO 14708-1:2000
Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
95.99
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
90.92
ISO 14708-2:2005
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
95.99
ISO 14708-2:2012
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
95.99
ISO 14708-2:2019
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
60.60
ISO 14708-3:2008
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
95.99
ISO 14708-3:2017
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
60.60
ISO 14708-4:2008
Implants for surgery — Active implantable medical devices — Part 4: Implantable infusion pumps
90.92
ISO 14708-5:2010
Implants for surgery — Active implantable medical devices — Part 5: Circulatory support devices
90.92
ISO 14708-6:2010
Implants for surgery — Active implantable medical devices — Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)
95.99
ISO 14708-6:2019
Implants for surgery — Active implantable medical devices — Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)
60.60
ISO 14708-7
Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear and auditory brainstem implant systems
60.00
ISO 14708-7:2013
Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear implant systems
90.92
ISO/CD 14708-4
Implants for surgery — Active implantable medical devices — Part 4: Implantable infusion pump systems
30.60
ISO/FDIS 14708-5
Implants for surgery — Active implantable medical devices — Part 5: Circulatory support devices
50.00
ISO/TR 21900:2018
Guidance for uncertainty analysis regarding the application of ISO/TS 10974
60.60
ISO 27185:2012
Cardiac rhythm management devices — Symbols to be used with cardiac rhythm management device labels, and information to be supplied — General requirements
90.93
ISO 27186:2010
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices - Dimensional and test requirements
90.92
ISO/CD 27186
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices - Dimensional and test requirements
30.99
IEC/FDIS 60601-2-31
Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
50.20

No matching records found. Please try changing the filter settings.