Registration number (WIID)Project No.TitleStatus
66700LVS EN ISO 13485:2016/AC:2018Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
66261LVS CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
39363EN 80369-5:2016Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applicationsStandarts spēkā
66261CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
39364EN 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
24145LVS CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesStandarts spēkā
37957EN ISO 13485:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
68559EN ISO 15223-1:2021Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)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
63920EN ISO 14971:2019Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
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