Draft:
E DIN EN IEC 80601-2-77/A1 VDE 0750-2-77/A1:2023-03Medical electrical equipment Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment |
Standard:
DIN EN IEC 60601-2-1 VDE 0750-2-1:2022-12Medical electrical equipment Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV |
Standard:
DIN EN ISO 14708-2 VDE 0750-20-2:2022-12Implants for surgery – Active implantable medical devices Part 2: Cardiac pacemakers |
Standard:
DIN EN ISO 14708-3 VDE 0750-20-3:2022-12Implants for surgery – Active implantable medical devices Part 3: Implantable neurostimulators |
Standard:
DIN EN ISO 14708-5 VDE 0750-20-5:2022-12Implants for surgery – Active implantable medical devices Part 5: Circulatory support devices |
Standard:
DIN EN ISO 14708-6 VDE 0750-20-6:2022-12Implants for surgery – Active implantable medical devices Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators) |
Standard:
DIN EN ISO 14708-7 VDE 0750-20-7:2022-12Implants for surgery – Active implantable medical devices Part 7: Particular requirements for cochlear and auditory brainstem implant systems |
Standard:
DIN EN IEC 63203-101-1 VDE 0750-30-1:2022-12Wearable electronic devices and technologies Part 101-1: Terminology |
Standard
withdrawn: DIN EN IEC 63203-204-1 VDE 0750-31-1:2022-12Wearable electronic devices and technologies Part 204-1: Electronic textile – Test method for assessing washing durability of leisurewear and sportswear e-textile systems |
Draft:
E DIN IEC 63310 VDE 0750-34-5:2022-12Functional performance criteria for robots used in AAL connected home environment
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Standard:
DIN EN IEC 63203-406-1 VDE 0750-35-406-1:2022-12Wearable electronic devices and technologies Part 406-1: Test method for measuring surface temperature of wrist-worn wearable electronic devices while in contact with human skin |
Standard:
DIN EN 60601-1 VDE 0750-1:2022-11Medical electrical equipment Part 1: General requirements for basic safety and essential performance |
Standard:
DIN EN IEC 60601-2-21 VDE 0750-2-21:2022-11Medical electrical equipment Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
Draft:
E DIN EN IEC 80601-2-26/A1 VDE 0750-2-26/A1:2022-11Medical electrical equipment Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalograph |
Draft:
E DIN EN IEC 60601-2-39 VDE 0750-2-39:2022-11Medical electrical equipment Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment |
Standard:
DIN EN ISO 80601-2-13 VDE 0750-2-13:2022-10Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
Draft:
E DIN EN IEC 60601-2-16 VDE 0750-2-16:2022-10Medical electrical equipment Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
Standard:
DIN EN IEC 60601-2-22 VDE 0750-2-22:2022-10Medical electrical equipment Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment |
Standard:
DIN EN IEC 60601-2-35 VDE 0750-2-35:2022-10Medical electrical equipment Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use |
Draft:
E DIN EN IEC 60601-2-40 VDE 0750-2-40:2022-10Medical electrical equipment Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment |