Medizintechnik

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  • Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2020 + AMD1:2023); German version EN IEC 60601-2-50:2021 + A1:2023

    Standard [CURRENT] 2024-09

    DIN EN IEC 60601-2-50:2024-09; VDE 0750-2-50:2024-09

    Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2020 + AMD1:2023); German version EN IEC 60601-2-50:2021 + A1:2023

    These particular requirements set out safety requirements for infant phototherapy equipment, but alternate methods of compliance with a specific clause by demonstrating equivalent safety will not ...

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  • Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025); German and English version prEN ISO 21762:2025

    Draft standard 2025-10

    DIN EN ISO 21762:2025-10 - Draft

    Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025); German and English version prEN ISO 21762:2025

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  • Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis (Adopted IEC 60601-2-41:2021, third edition, 2021-09, with Canadian deviations)

    Standard [CURRENT] 2023-03-01

    CSA C22.2 No. 60601-2-41:2023-03-01

    Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis (Adopted IEC 60601-2-41:2021, third edition, 2021-09, with Canadian deviations)

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  • Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment (Adopted IEC 60601-2-39:2018,third edition, 20187-04, with Canadian deviations)

    Standard [CURRENT] 2023-01-01

    CSA C22.2 No. 60601-2-39:2023-01-01

    Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment (Adopted IEC 60601-2-39:2018,third edition, 20187-04, with Canadian deviations)

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  • Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems

    Standard [CURRENT] 2022-08-01

    CSA Z7396.1:2022-08-01

    Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems

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  • Traditional Chinese medicine - Air extraction cupping device

    Draft standard 2026-09

    ISO/FDIS 19611:2026-09 - Draft

    Traditional Chinese medicine - Air extraction cupping device

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  • Traditional Chinese medicine - General requirements for smokeless moxibustion devices

    Standard [NEW] 2026-09

    ISO 21366:2026-09

    Traditional Chinese medicine - General requirements for smokeless moxibustion devices

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  • Medical devices utilizing non-viable human materials - Risk management

    Draft standard 2025-09

    ISO/DIS 21762:2025-09 - Draft

    Medical devices utilizing non-viable human materials - Risk management

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  • Traditional Chinese medicine - Procedure for reporting indoor air quality when combusting moxibustion devices

    Pre-standard 2026-10

    ISO/TS 22358:2026-10

    Traditional Chinese medicine - Procedure for reporting indoor air quality when combusting moxibustion devices

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  • Traditional Chinese medicine - Vocabulary for device - Part 1: Moxibustion device

    Pre-standard 2026-08

    ISO/TS 25144-1:2026-08

    Traditional Chinese medicine - Vocabulary for device - Part 1: Moxibustion device

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