Registration number (WIID)Project No.TitleStatus
69126IEC/TR 62366-2:2016Medical devices — Part 2: Guidance on the application of usability engineering to medical devicesStandarts 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
85462ISO 80369-6:2025Small bore connectors for liquids and gases in healthcare applications — Part 6: Connectors for neural applicationsStandarts spēkā
73007IEC 62366-1:2015/Amd 1:2020Medical devices — Part 1: Application of usability engineering to medical devices — Amendment 1Standarts spēkā
67944ISO/IEC Guide 63:2019Guide to the development and inclusion of aspects of safety in International Standards for medical devicesStandarts spēkā
86275ISO/TS 5137:2026Medical device maintenance management programme for healthcare delivery organizations (HDO)Standarts spēkā
67284ISO 18250-1:2018Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methodsStandarts spēkā
88714ISO 20417:2026Medical devices — Information to be supplied by the manufacturerStandarts spēkā
87600ISO/TS 24971-2:2026Medical devices — Guidance on the application of ISO 14971 — Part 2: Machine learning in artificial intelligenceStandarts spēkā
42343ISO 15223-2:2010Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validationStandarts spēkā
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