Registration number (WIID)Project No.TitleStatus
69481EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
39366EN ISO 80369-6:2016Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neuraxial applications (ISO/IEC/DIS 80369-6:2014)Standarts spēkā
66261LVS CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
76512LVS EN 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
79260LVS EN ISO 20417:2026Medical devices - Information to be supplied by the manufacturer (ISO 20417:2026)Standarts 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
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
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
75110EN ISO 14971:2019/A11:2021Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
39370EN ISO 80369-7:2017Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01)Atcelts
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