Registration number (WIID)Project No.TitleStatus
69998EN ISO 10993-2:2022Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)Standarts spēkā
73021prEN ISO 10993-3 revBiological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicityIzstrādē
74131EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
74131LVS EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
75596prEN ISO 10993-1Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO/DIS 10993-1:2024)Izstrādē
75885prEN ISO 10993-7Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024)Izstrādē
76054prEN ISO 8250Cleanliness of medical devices -- Process design and test methodsIzstrādē
77182prEN ISO 14155Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024)Izstrādē
77335prEN ISO 18969Clinical evaluation of medical devicesIzstrādē
77391prEN ISO 10993-6Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/DIS 10993-6:2024)Izstrādē
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