Registration number (WIID)Project No.TitleStatus
78991prEN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025)Aptauja
78992prEN ISO 10993-2Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO/DIS 10993-2:2024)Izstrādē
78988prEN ISO 10993-3Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025)Izstrādē
73021prEN ISO 10993-3 revBiological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive and developmental toxicityIzstrādē
31037prEN ISO 10993-4 revBiological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/NP 10993-4:2008)Izstrādē
80887prEN ISO 10993-4 revBiological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodIzstrādē
31980prEN ISO 10993-5Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Izstrādē
40814prEN ISO 10993-5 revBiological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Izstrādē
40661prEN ISO 10993-7 revBiological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsIzstrādē
77335prEN ISO 18969Clinical evaluation of medical devices (ISO/DIS 18969:2025)Aptauja
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