Registration number (WIID)Project No.TitleStatus
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
74437ISO/TR 24971:2020Medical devices — Guidance on the application of ISO 14971Standarts spēkā
85462ISO 80369-6:2025Small bore connectors for liquids and gases in healthcare applications — Part 6: Connectors for neural applicationsStandarts spēkā
69126IEC/TR 62366-2:2016Medical devices — Part 2: Guidance on the application of usability engineering to medical devicesStandarts spēkā
67942ISO/TR 20416:2020Medical devices — Post-market surveillance for manufacturersStandarts spēkā
50733IEC 80369-5:2016Small-bore connectors for liquids and gases in healthcare applications — Part 5: Connectors for limb cuff inflation applicationsStandarts 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
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
67284ISO 18250-1:2018Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methodsStandarts spēkā
Displaying 1-10 of 114 results.