Filter :
Standard and/or project under the direct responsibility of ISO/TC 150/SC 6 Secretariat Stage ICS
ISO 5841-2:2000 [Withdrawn]
Implants for surgery — Cardiac pacemakers — Part 2: Reporting of clinical performance of populations of pulse generators or leads
95.99
Implants for surgery — Cardiac pacemakers — Part 2: Reporting of clinical performance of populations of pulse generators or leads
90.60
ISO 5841-3:2000 [Withdrawn]
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers
95.99
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers — Technical Corrigendum 1
95.99
Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers
90.93
ISO 10310:1995 [Withdrawn]
Neurosurgical implants — Marking and packaging of implantable neural stimulators
95.99
ISO/DIS 10974 [Under development]
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
40.60
ISO/TS 10974:2012 [Withdrawn]
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
95.99
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
90.92
Cardiac defibrillators — Connector assembly DF-1 for implantable defibrillators — Dimensions and test requirements
90.93
ISO 14117:2012 [Withdrawn]
Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
95.99
Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
90.93
ISO 14708-1:2000 [Withdrawn]
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
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/CD 14708-1 [Under development]
Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
30.99
ISO 14708-2:2005 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
95.99
ISO 14708-2:2012 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
95.99
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
90.93
ISO 14708-3:2008 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
95.99
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
90.92
ISO/AWI 14708-3 [Under development]
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
20.00
ISO 14708-4:2008 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 4: Implantable infusion pumps
95.99
Implants for surgery — Active implantable medical devices — Part 4: Implantable infusion pump systems
60.60
ISO 14708-5:2010 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 5: Circulatory support devices
95.99
Implants for surgery — Active implantable medical devices — Part 5: Circulatory support devices
90.92
ISO 14708-6:2010 [Withdrawn]
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
Implants for surgery — Active implantable medical devices — Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)
90.93
ISO 14708-7:2013 [Withdrawn]
Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear implant systems
95.99
Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear and auditory brainstem implant systems
90.93
Guidance for uncertainty analysis regarding the application of ISO/TS 10974
90.93
ISO/AWI 24965 [Under development]
EMC for exocardiac implantable cardioverter defibrillators
20.00
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 [Withdrawn]
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices - Dimensional and test requirements
95.99
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices — Dimensional and test requirements
90.92
ISO 27186 [Under development]
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices — Dimensional and test requirements
60.00
Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
90.92
IEC/DIS 80601-2-31 [Under development]
Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
40.60

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