ISO/TC 210
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
38421 | IEC 62304:2006 | Medical device software — Software life cycle processes | Standarts spēkā |
65624 | IEC/TR 80002-3:2014 | Medical device software — Part 3: Process reference model of medical device software life cycle processes (IEC 62304) | Standarts spēkā |
69336 | ISO/TS 11633-1:2019 | Health informatics — Information security management for remote maintenance of medical devices and medical information systems — Part 1: Requirements and risk analysis | Standarts spēkā |
73316 | IEC 80369-5:2016/Cor 1:2017 | Small-bore connectors for liquids and gases in healthcare applications — Part 5: Connectors for limb cuff inflation applications — Technical Corrigendum 1 | Standarts spēkā |
63179 | IEC 62366-1:2015 | Medical devices — Part 1: Application of usability engineering to medical devices | Standarts spēkā |
61895 | ISO 18250-3:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 3: Enteral applications | Standarts spēkā |
80906 | ISO/CD 5137 | Maintenance management program for medical equipment | Standarts spēkā |
64686 | IEC 62304:2006/Amd 1:2015 | Medical device software — Software life cycle processes — Amendment 1 | Standarts spēkā |
86270 | ISO 15223-1:2021/Amd 1:2025 | Medical 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 specific | Standarts spēkā |
69126 | IEC/TR 62366-2:2016 | Medical devices — Part 2: Guidance on the application of usability engineering to medical devices | Standarts spēkā |
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