Registration number (WIID)Project No.TitleStatus
12987LVS CR 13217:2001Nomenclature system for medical devices for the purpose of regulatory data exchange - RationaleAtcelts
24145LVS CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
59550LVS EN ISO 15223-1:2017Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2016-12-15)Atcelts
39825LVS EN ISO 15225:2016Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016)Atcelts
21072LVS EN ISO 14971:2000/AC:2002Medical devices - Application of risk management to medical devices (ISO 14971:2000)Atcelts
64861LVS CEN/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
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
24145CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
21479LVS EN ISO 14971:2000/A1:2003Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AM1:2003)Atcelts
24838LVS EN 1041:2008Information supplied by the manufacturer of medical devicesAtcelts
Displaying 71-80 of 140 results.