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DIN EN 60601-2-34 ; VDE 0750-2-34:2015-01
Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment (IEC 60601-2-34:2011); German version EN 60601-2-34:2014
Edition
2015-01
DIN EN IEC 80601-2-26 ; VDE 0750-2-26:2022-04
Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs (IEC 80601-2-26:2019); German version EN IEC 80601-2-26:2020
Edition
2022-04
DIN EN IEC 80601-2-26 Berichtigung 1 ; VDE 0750-2-26 Berichtigung 1:2022-06
Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs (IEC 80601-2-26:2019/COR1:2021); German version EN IEC 80601-2-26:2020/AC:2021-10
Edition
2022-06
DIN EN IEC 60601-2-43 ; VDE 0750-2-43:2024-02
Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures (IEC 60601-2-43:2022); German version EN IEC 60601-2-43:2023
Edition
2024-02
Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures (IEC 60601-2-43:2022); German version EN IEC 60601-2-43:2023; Corrigendum 1
Edition
2024-07
DIN SPEC 91365
Needle Puncture Testing
Edition
2018-09
DIN 58953-9
Sterilization - Sterile supply - Part 9: Use of re-usable sterilization containers
Edition
2024-03
DIN EN ISO 80601-2-80
Medical electrical equipment - Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency (ISO/DIS 80601-2-80:2023); German and English version prEN ISO 80601-2-80:2023
Edition
2023-07
DIN EN 301839
Ultra Low Power Active Medical Implants (ULP-AMI) and associated Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz - Harmonised Standard covering the essential requirements of article 3.2 of the Directive 2014/53/EU (Endorsement of the English version EN 301 839 V2.1.1 (2016-04) as German standard)
Edition
2016-09
DIN EN 62083
Medical electrical equipment - Requirements for the safety of radiotherapy treatment planning systems (IEC 62083:2009); German version EN 62083:2009
Edition
2011-01