Registration number (WIID)Project No.TitleStatus
66700EN ISO 13485:2016/AC:2018Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
75110EN ISO 14971:2019/A11:2021Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
39364LVS EN ISO 80369-3:2016Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016)Standarts spēkā
73639EN ISO 80369-20:2024Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods (ISO 80369‑20:2024)Standarts spēkā
79260EN ISO 20417:2026Medical devices - Information to be supplied by the manufacturer (ISO 20417:2026)Standarts spēkā
76512EN ISO 80369-6:2025Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neural applications (ISO 80369-6:2025)Standarts spēkā
64555EN 80369-5:2016/AC:2017-02Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applicationsStandarts spēkā
77231EN ISO 15223-1:2021/A1:2025Medical 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 specific (ISO 15223 1:2021/Amd 1:2025)Standarts spēkā
63920EN ISO 14971:2019Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
71616LVS EN ISO 80369-3:2016/A1:2023Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019)Standarts spēkā
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