Registration number (WIID)Project No.TitleStatus
40444EN 1041:2008+A1:2013Information supplied by the manufacturer of medical devicesAtcelts
24145LVS CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
28921EN ISO 13485:2003/AC:2007Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)Atcelts
40585EN ISO 80369-1:2018Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2018)Atcelts
39370EN ISO 80369-7:2017Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01)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
24145CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
12985LVS EN ISO 15225:2001Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
21479EN ISO 14971:2000/A1:2003Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AM1:2003)Atcelts
21072EN ISO 14971:2000/AC:2002Medical devices - Application of risk management to medical devices (ISO 14971:2000)Atcelts
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