Registration number (WIID)Project No.TitleStatus
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
73915ISO 14117:2019Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devicesStandarts spēkā
54472ISO 14117:2012Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devicesAtcelts
31511ISO 11318:2002Cardiac defibrillators — Connector assembly DF-1 for implantable defibrillators — Dimensions and test requirementsStandarts spēkā
18357ISO 10310:1995Neurosurgical implants — Marking and packaging of implantable neural stimulatorsAtcelts
86249IEC/DIS 80601-2-31Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power sourceAptauja slēgta
72452IEC 60601-2-31:2020Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power sourceStandarts spēkā
Displaying 51-57 of 57 results.