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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) (ISO 14708-6:2019); German version EN ISO 14708-6:2022
Edition
2022-12
DIN EN 60601-2-4 ; VDE 0750-2-4:2021-09
Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators (IEC 60601-2-4:2010 + A1:2018); German version EN 60601-2-4:2011 + A1:2019
Edition
2021-09
DIN EN 50527-2-2 ; VDE 0848-527-2-2:2019-11
Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-2: Specific assessment for workers with cardioverter defibrillators (ICDs); German version EN 50527-2-2:2018
Edition
2019-11
DIN EN ISO/IEEE 11073-10103
Health informatics - Device interoperability - Part 10103: Nomenclature, implantable device, cardiac (ISO/IEEE 11073-10103:2025); English version EN ISO/IEEE 11073-10103:2025
Edition
2025-12
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; German version EN 45502-1:2015
Edition
2016-02
DIN EN 60601-2-27 ; VDE 0750-2-27:2015-04
Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment (IEC 60601-2-27:2011 + Cor.:2012); German version EN 60601-2-27:2014
Edition
2015-04
CSA ISO/IEC TR 20017
Information technology - Radio frequency identification for item management - Electromagnetic interference impact of ISO/IEC 18000 interrogator emitters on implantable pacemakers and implantable cardioverter defibrillators (Adopted ISO/IEC TR 20017:2011, first edition, 2011-12-15)
Edition
2014-03-01
CAN/CSA-C22.2 No. 60601-2-4-12
Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators (Adopted IEC 60601-2-4:2010, third edition, 2010-12, consolidated with amendment 1:2018, with Canadian deviations)
Edition
2019
CAN/CSA-C22.2 No. 60601-2-27-11
Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment
Edition
2011-11-01
CAN/CSA-C22.2 No. 60601-2-34-12
Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment
Edition
2012-06-01
