Standard:
DIN IEC/TR 60601-4-5 VDE 0750-4-5:2022-06Medical electrical equipment Part 4-5: Guidance and interpretation – Safety-related technical security specifications |
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 60601-2-46 VDE 0750-2-46:2022-04Medical electrical equipment Part 2-46: Particular requirements for the basic safety and essential performance of operating tables |
Anwendungsregel:
VDE-AR-E 2750-300 Anwendungsregel:2022-04Digital qualification in the health sector Basics |
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 ISO 21388 VDE 0753-388:2022-01Acoustics - Hearing aid fitting management (HAFM) (ISO 21388:2020); |
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 IEC 63240-1 VDE 0754-5-1:2021-12Active assisted living (AAL) reference architecture and architecture model Part 1: Reference architecture |
Standard:
DIN IEC 63240-2 VDE 0754-5-2:2021-12Active assisted living (AAL) reference architecture and architecture model Part 2: Architecture model |
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 |
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 |