Draft:
E DIN EN IEC 60601-2-21/A1 VDE 0750-2-21/A1:2022-05Medical electrical equipment Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
Draft:
E DIN EN IEC 60601-2-34 VDE 0750-2-34:2022-05Medical electrical equipment Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment |
Draft:
E DIN EN 60601-2-45/A2 VDE 0750-2-45/A2:2022-05Medical electrical equipment Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices |
Draft:
E DIN EN IEC 60601-2-50/A1 VDE 0750-2-50/A1:2022-05Medical electrical equipment Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment |
Standard:
DIN EN IEC 80601-2-26 VDE 0750-2-26:2022-04Medical electrical equipment Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs |
Draft:
E DIN EN IEC 60601-2-46 VDE 0750-2-46:2022-04Medical electrical equipment Part 2-46: Particular requirements for the basic safety and essential performance of operating tables |
Draft:
E DIN EN IEC 60601-2-75/A1 VDE 0750-2-75/A1:2022-03Medical electrical equipment Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment |
Draft:
E DIN IEC 63168-1 VDE 0750-34-1:2022-03Cooperative multiple systems in connected home environments – AAL functional safety requirements of electronic safety-related systems Part 1: General requirements for design and development |
Draft:
E DIN IEC 63168-2 VDE 0750-34-2:2022-03Cooperative multiple systems in connected home environments – AAL functional safety requirements of electronic safety-related systems Part 2: Concept phase of product design |
Draft:
E DIN IEC 63168-3 VDE 0750-34-3:2022-03Cooperative multiple systems in connected home environments – AAL functional safety requirements of electronic safety-related systems Part 3: Product development |
Draft:
E DIN IEC 63168-4 VDE 0750-34-4:2022-03Cooperative multiple systems in connected home environments – AAL functional safety requirements of electronic safety-related systems Part 4: Production, operation, modification and supporting process |
Standard:
DIN EN 60601-1-12 VDE 0750-1-12:2022-02Medical electrical equipment Part 1-12: General requirements for basic safety and essential performance – Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment |
Standard:
DIN EN 60601-1-2 VDE 0750-1-2:2022-01Medical electrical equipment Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests |
Standard:
DIN EN 60601-1-8 VDE 0750-1-8:2021-12Medical electrical equipment Part 1-8: General requirements for basic safety and essential performance – Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
Standard:
DIN EN 60601-1-11 VDE 0750-1-11:2021-12Medical electrical equipment Part 1-11: General requirements for basic safety and essential performance – Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |
Standard:
DIN EN 60601-1-6 VDE 0750-1-6:2021-11Medical electrical equipment Part 1-6: General requirements for basic safety and essential performance – Collateral standard: Usability |
Standard:
DIN EN 60601-1-10 VDE 0750-1-10:2021-11Medical electrical equipment Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers |
Draft:
E DIN EN ISO 80601-2-12 VDE 0750-2-12:2021-11Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators |
Standard:
DIN EN 60601-1-3 VDE 0750-1-3:2021-10Medical electrical equipment Part 1-3: General requirements for basic safety and essential performance – Collateral Standard: Radiation protection in diagnostic X-ray equipment |
Draft:
E DIN EN 60601-2-3/A2 VDE 0750-2-3/A2:2021-10Medical electrical equipment Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment |