Registration number (WIID)Project No.TitleStatus
88695ISO/CD 14708-1Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturerIzstrādē
88697ISO/PWI 14117Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devicesIzstrādē
88698ISO/PWI 14708-2Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakersIzstrādē
25298ISO 14708-1:2000Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturerAtcelts
39507ISO 5841-3:2000/Cor 1:2003Implants for surgery — Cardiac pacemakers — Part 3: Low-profile connectors (IS-1) for implantable pacemakers — Technical Corrigendum 1Atcelts
57580ISO 14708-7:2013Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear implant systemsAtcelts
54472ISO 14117:2012Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devicesAtcelts
52427ISO 14708-6:2010Implants for surgery — Active implantable medical devices — Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)Atcelts
41942ISO 14708-4:2008Implants for surgery — Active implantable medical devices — Part 4: Implantable infusion pumpsAtcelts
18357ISO 10310:1995Neurosurgical implants — Marking and packaging of implantable neural stimulatorsAtcelts
Displaying 21-30 of 57 results.