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
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
69481EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
69481LVS EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
73639LVS EN ISO 80369-20:2024Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods (ISO 80369‑20:2024)Standarts spēkā
67368LVS EN ISO 20417:2021Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021,Ccorrected version 2021-12)Standarts spēkā
71616LVS EN ISO 80369-3:2016/A1:2023Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019)Standarts spēkā
Displaying 91-100 of 142 results.