Registration number (WIID)Project No.TitleStatus
32013prEN ISO 13485 revMedical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)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
32010EN 20594-1:1993/prA2Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)Izstrādē
77025prEN ISO 18250-7Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 7: Connectors for intravascular infusionIzstrādē
77026prEN ISO 18250-8Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 8: Citrate-based anticoagulant solution for apheresis applicationsIzstrādē
32009prEN ISO 15225 revNomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000)Izstrādē
71616EN ISO 80369-3:2016/A1:2022Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019)Izstrādē
64227EN ISO 80369-3:2016/prA2Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 2 (ISO 80369-3:2016/DAmd 2:2017)Izstrādē
28643prEN 15546-2Small bore connectors for liquids and gases in healthcare applications - Part 2 - Connectors for respiratory applicationsIzstrādē
Displaying 131-140 of 140 results.