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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ISO 5841-2:2000 [Withdrawn]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
ISO 5841-2:2014
Implants for surgery -- Cardiac pacemakers -- Part 2: Reporting of clinical performance of populations of pulse generators or leads
60.60
ISO 5841-3:2000 [Withdrawn]
Implants for surgery -- Cardiac pacemakers -- Part 3: Low-profile connectors (IS-1) for implantable pacemakers
95.99
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ISO 10310:1995 [Withdrawn]
Neurosurgical implants -- Marking and packaging of implantable neural stimulators
95.99
ISO/TS 10974:2012 [Withdrawn]
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
90.92
ISO/FDIS 14117 [Under development]
Active implantable medical devices -- Electromagnetic compatibility -- EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
50.00
ISO 14708-1:2000 [Withdrawn]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
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
90.20
ISO 14708-2:2005 [Withdrawn]
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
90.92
ISO/DIS 14708-2 [Under development]
Implants for surgery -- Active implantable medical devices -- Part 2: Cardiac pacemakers
40.99
ISO 14708-3:2008 [Withdrawn]
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/NP 14708-4 [Under development]
Implants for surgery -- Active implantable medical devices -- Part 4: Implantable infusion pumps
10.99
ISO 14708-5:2010
Implants for surgery -- Active implantable medical devices -- Part 5: Circulatory support devices
90.92
ISO/DIS 14708-5 [Under development]
Implants for surgery -- Active implantable medical devices -- Part 5: Circulatory support devices
40.20
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)
90.92
ISO/DIS 14708-6 [Under development]
Implants for surgery -- Active implantable medical devices -- Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)
40.99
ISO 14708-7:2013
Implants for surgery -- Active implantable medical devices -- Part 7: Particular requirements for cochlear implant systems
90.92
ISO/FDIS 14708-7 [Under development]
Implants for surgery -- Active implantable medical devices -- Part 7: Particular requirements for cochlear and auditory brainstem implant systems
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
IEC/DIS 60601-2-31 [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