Registration number (WIID)Project No.TitleStatus
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
9484EN ISO 10993-2:1998Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:1992)Atcelts
22132EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006)Atcelts
69998EN ISO 10993-2:2022Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)Standarts spēkā
68925EN ISO 10993-23:2021Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)Standarts spēkā
78993EN ISO 10993-23:2021/prA1Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/DAmd1:2024)Izstrādē
9495EN ISO 10993-3:2003Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)Atcelts
31978EN ISO 10993-3:2009Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)Atcelts
30398EN ISO 10993-3:2014Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO/DIS 10993-3:2011)Standarts spēkā
9496EN ISO 10993-4:2002Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)Atcelts
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