Registration number (WIID)Project No.TitleStatus
37957LVS EN ISO 13485:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
68576LVS CEN ISO/TR 24971:2020Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020)Standarts spēkā
73006LVS EN ISO 80369-2:2024Small-bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for respiratory applications (ISO 80369-2:2024)Standarts spēkā
39364EN ISO 80369-3:2016Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016)Standarts spēkā
66261LVS CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
66261CEN ISO/TR 20416:2020Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020)Standarts spēkā
70256LVS EN ISO 80369-7:2021Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021)Standarts spēkā
69481LVS EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)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
67368LVS EN ISO 20417:2021Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021,Ccorrected version 2021-12)Standarts spēkā
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