Registration number (WIID)Project No.TitleStatus
69336ISO/TS 11633-1:2019Health informatics — Information security management for remote maintenance of medical devices and medical information systems — Part 1: Requirements and risk analysisStandarts spēkā
86270ISO 15223-1:2021/Amd 1:2025Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specificStandarts spēkā
69126IEC/TR 62366-2:2016Medical devices — Part 2: Guidance on the application of usability engineering to medical devicesStandarts spēkā
74437ISO/TR 24971:2020Medical devices — Guidance on the application of ISO 14971Standarts spēkā
50733IEC 80369-5:2016Small-bore connectors for liquids and gases in healthcare applications — Part 5: Connectors for limb cuff inflation applicationsStandarts spēkā
67942ISO/TR 20416:2020Medical devices — Post-market surveillance for manufacturersStandarts spēkā
67284ISO 18250-1:2018Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methodsStandarts spēkā
74038ISO 80369-3:2016/Amd 1:2019Small-bore connectors for liquids and gases in healthcare applications — Part 3: Connectors for enteral applications — Amendment 1Standarts spēkā
61895ISO 18250-3:2018Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 3: Enteral applicationsStandarts spēkā
63179IEC 62366-1:2015Medical devices — Part 1: Application of usability engineering to medical devicesStandarts spēkā
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