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Standard and/or project under the direct responsibility of ISO/TC 150/SC 6 Secretariat | Stage | ICS |
---|---|---|
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
|
90.20 | |
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
|
90.60 | |
Neurosurgical implants — Marking and packaging of implantable neural stimulators
|
95.99 | |
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
|
30.99 | |
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
|
90.60 | |
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
|
90.20 | |
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 | |
Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
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30.60 |
|
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
|
95.99 | |
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
|
95.99 | |
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
|
90.20 | |
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 | |
Implants for surgery — Active implantable medical devices — Part 3: Implantable neurostimulators
|
20.00 | |
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 | |
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
|
60.60 | |
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)
|
90.20 | |
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
|
90.20 | |
Guidance for uncertainty analysis regarding the application of ISO/TS 10974
|
90.93 | |
Cardiac rhythm management devices — Symbols to be used with cardiac rhythm management device labels, and information to be supplied — General requirements
|
90.93 | |
Cardiac rhythm management devices — Symbols to be used with cardiac rhythm management device labels, and information to be supplied — General requirements
|
30.98 | |
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 | |
Active implantable medical devices — Four-pole connector system for implantable cardiac rhythm management devices — Dimensional and test requirements
|
40.20 | |
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 | |
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 |
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