Registration number (WIID)Project No.TitleStatus
68576CEN ISO/TR 24971:2020Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020)Izstrādē
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
69482EN ISO 15223-1:2016/FprA11Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, including corrected version 2017-03)Izstrādē
70256EN 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)Izstrādē
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
71616EN ISO 80369-3:2016/A1:2022Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019)Izstrādē
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
72189-Guidance on the relationship between CEN ISO TR 20146: 2019 (Medical devices — Post-market surveillance for manufacturers) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices RegulationIzstrādē
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
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