Registration number (WIID)Project No.TitleStatus
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
40963CEN/CLC/TR 14060:2014Medical device traceability enabled by unique device identification (UDI)Atcelts
24416CEN ISO/TR 14969:2005Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004)Atcelts
66261CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
68576CEN ISO/TR 24971:2020Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020)Izstrādē
24145CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
64861CEN/TR 17223:2018Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices RegulationAtcelts
12987CR 13217:1998Nomenclature system for medical devices for the purpose of regulatory data exchange - RationaleAtcelts
18857CR 13825:2000Luer connectors - A report to CEN chef from the CEN forum task group "Luer fittings"Atcelts
18858CR 14060:2000Medical device traceabilityAtcelts
Displaying 1-10 of 139 results.