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 |
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 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 IEC 61326-2-6 VDE 0843-20-2-6:2022-11Electrical equipment for measurement, control and laboratory use – EMC requirements Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical 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 |
Standard:
DIN CEN ISO/TS 20342-10 VDE V 0750-2-52-10:2022-10Assistive products for tissue integrity when lying down Part 10: Guide to cleaning, disinfecting, and care of polyurethane APTI covers |
Draft:
E DIN EN IEC 80601-2-58 VDE 0750-2-58:2022-10Medical electrical equipment Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
Standard:
DIN EN IEC 80601-2-77 VDE 0750-2-77:2022-10Medical electrical equipment Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment |
Draft:
E DIN IEC/TS 63219 VDE V 0754-7:2022-10Active Assisted Living (AAL) System Development Requirements for AAL Service Providers |
Draft:
E DIN EN IEC 60601-2-33 VDE 0750-2-33:2022-09Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
Standard:
DIN EN IEC 60601-2-19 VDE 0750-2-19:2022-08Medical electrical equipment Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators |
Standard:
DIN EN IEC 60601-2-50 VDE 0750-2-50:2022-08Medical electrical equipment Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment |
Draft:
E DIN EN ISO 20342-1 VDE 0750-2-52-1:2022-08Assistive products for tissue integrity when lying down Part 1: General requirements |