DIN EN ISO 14708-2 VDE 0750-20-2:2022-12

Implants for surgery – Active implantable medical devices

Part 2: Cardiac pacemakers

DIN EN ISO 14708-6 VDE 0750-20-6:2022-12

Implants for surgery – Active implantable medical devices

Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)

DIN EN ISO 14708-7 VDE 0750-20-7:2022-12

Implants for surgery – Active implantable medical devices

Part 7: Particular requirements for cochlear and auditory brainstem implant systems

DIN EN 45502-1 VDE 0750-10:2016-02

Implants for surgery – Active implantable medical devices

Part 1: General requirements for safety, marking and for information to be provided by the manufacturer;

DIN EN 45502-2-3 VDE 0750-10-3:2010-07

Active implantable medical devices

Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems;

An english translation of this document is available.

DIN EN 45502-2-2 VDE 0750-10-2 Berichtigung 1:2009-09

Corrigendum to DIN EN 45502-2-2 (VDE 0750-10-2):2008-10;

DIN EN 45502-2-2 VDE 0750-10-2:2008-10

Active implantable medical devices

Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators);

DIN EN 45502-2-1 VDE 0750-10-1:2004-08

Active implantable medical devices

Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers);

DIN EN 45502-1 VDE 0750-10:1998-07

Active implantable medical devices

General requirements for the safety, marking and information to be provided by the manufacturer;