Registration number (WIID)Project No.TitleStatus
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
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
18858LVS CR 14060:2003Medical device traceabilityAtcelts
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
64029EN ISO 13485:2016/AC:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Atcelts
67368EN ISO 20417:2021Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)Atcelts
22133LVS EN ISO 13485:2003Medical devices - Quality management systems - System requirements for regulatory purposesAtcelts
28921LVS EN ISO 13485:2003 /AC:2007Medical devices - Quality management systems - Requirements for regulatory purposesAtcelts
31251EN ISO 80369-1:2010Small bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2010)Atcelts
24145LVS CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
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