Registration number (WIID)Project No.TitleStatus
33578EN ISO 13485:2003/AC:2009Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009)Atcelts
24416LVS CEN ISO/TR 14969:2005Medical devices - Quality mangement systems - Guidance on the application of ISO 13485:2003Atcelts
18856LVS EN ISO 14971:2003Medical devices - Application of risk management to medical devices Medical devices - Application of risk management to 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
39825LVS EN ISO 15225:2016Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016)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
12988EN 980:2003Graphical symbols for use in the labelling of medical devicesAtcelts
21726EN ISO 15225:2000/A1:2004Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange - Amendment 1 (ISO 15225:2000/A1:2004)Atcelts
18856EN ISO 14971:2000Medical devices - Application of risk management to medical devices (ISO 14971:2000)Atcelts
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