Registration number (WIID)Project No.TitleStatus
20264EN 45502-1:1997Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturerAtcelts
20264LVS EN 45502-1:1997Active implantable medical devices - Part 1: General requirements for safety, marking and information to be provided by the manufacturer 
20265LVS EN 45502-2-1:2004Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)Atcelts
20265LVS EN 45502-2-1:2005Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)Standarts spēkā
20267LVS EN 45502-2-2:2008Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)Standarts spēkā
20268LVS EN 45502-2-3:2010Active implantable medical devices -- Part 2-3: Particular requirements for cochlear and auditory brainstem implant systemsStandarts spēkā
20269prEN 45502-2-XImplantable neurostimulatorsIzstrādē
20270prEN 45502-2-XImplantable infusion pumpsIzstrādē
35624LVS EN 45502-1:2015Implants for surgery - Active implantable medical devices - Part 1: General requirements for safety, marking and for information to be provided by the manufacturerStandarts spēkā
53984LVS EN 45502-2-2:2008 /AC:2009Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)Standarts spēkā
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