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Norma o proyecto bajo la responsabilidad directa de ISO/TC 150/SC 6 Secretaría Etapa 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
90.60
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
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
90.60
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)
90.60
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
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
40.60
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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