Registration number (WIID)Project No.TitleStatus
73733FprEN ISO 80369-1Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO/FDIS 80369-1:2025)Izstrādē
32013prEN ISO 13485 revMedical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)Izstrādē
77231EN ISO 15223-1:2021/prA1Medical 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/DAM 1:2024)Izstrādē
72189-Guidance on the relationship between CEN ISO TR 20146: 2019 (Medical devices — Post-market surveillance for manufacturers) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices RegulationIzstrādē
81349prCEN ISO/TR 20416 revMedical devices — Post-market surveillance for manufacturersIzstrādē
32011EN 1707:1996/prA1Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittingsIzstrādē
70256EN ISO 80369-7:2021Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021)Izstrādē
80075prCEN ISO/TS 24971-2Medical devices — Guidance on the application of ISO 14971 — Part 2: Machine learning in artificial intelligenceIzstrādē
66179prEN ISO 80369-3 revSmall-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016)Izstrādē
66700EN ISO 13485:2016/AC:2018Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Izstrādē
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