Standard:
NEW DIN EN IEC 80601-2-59 VDE 0750-2-59:2024-03Medical electrical equipment Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening |
Standard:
DIN EN IEC 60601-2-43 VDE 0750-2-43:2024-02Medical electrical equipment Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures |
Draft:
E DIN EN IEC 60601-2-37 VDE 0750-2-37:2023-12Medical electrical equipment Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment |
Standard:
DIN EN IEC 61689 VDE 0754-3:2023-12Ultrasonics Physiotherapy systems – Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz |
Standard:
DIN EN 50527-2-3 VDE 0848-527-2-3:2023-12Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 2-3: Specific assessment for workers with implantable neurostimulators; |
Draft:
E DIN EN IEC 60601-2-20/A1 VDE 0750-2-20/A1:2023-10Medical electrical equipment Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators |
Standard:
DIN EN ISO 14708-4 VDE 0750-20-4:2023-09Implants for surgery – Active implantable medical devices Part 4: Implantable infusion pump systems |
Standard:
DIN IEC/TR 61390 VDE 0754-4:2023-09Ultrasonics Real-time pulse-echo systems – Test procedures to determine performance specifications |
Draft:
E DIN EN IEC 60601-2-2/A1 VDE 0750-2-2/A1:2023-05Medical electrical equipment Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories |
Draft:
E DIN EN IEC 60601-2-57 VDE 0750-2-57:2023-03Medical electrical equipment Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use |
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 80001-1 VDE 0756-1:2023-02Application of risk management for IT-networks incorporating medical devices Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software |
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 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 |