Registration number (WIID)Project No.TitleStatus
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
12985LVS EN ISO 15225:2001Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
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
24416CEN ISO/TR 14969:2005Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004)Atcelts
38595EN ISO 14971:2012Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)Atcelts
18856EN ISO 14971:2000Medical devices - Application of risk management to medical devices (ISO 14971:2000)Atcelts
12987CR 13217:1998Nomenclature system for medical devices for the purpose of regulatory data exchange - RationaleAtcelts
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