Registration number (WIID)Project No.TitleStatus
12983CR 14230:2001Global medical device nomenclature for the purpose of regulatory data exchange (identical to ISO/TS 20225:2001)Atcelts
38536EN ISO 13485:2012/AC:2012Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009)Atcelts
64029LVS EN ISO 13485:2016/AC:2017Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Atcelts
39370LVS EN 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)Atcelts
18858LVS CR 14060:2003Medical device traceabilityAtcelts
64029EN ISO 13485:2016/AC:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)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
33578LVS EN ISO 13485:2003 /AC:2010Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009)Atcelts
12981LVS EN 1041:1998Information supplied by the manufacturer with medical devicesAtcelts
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