Registration number (WIID)Project No.TitleStatus
24766LVS EN 980:2008Symbols for use in the labelling of medical devicesAtcelts
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
64029EN ISO 13485:2016/AC:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Atcelts
79260prEN ISO 20417Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024)Aptauja slēgta
68559LVS EN ISO 15223-1:2021Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)Standarts spēkā
69481LVS EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
66261LVS CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
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