Registration number (WIID)Project No.TitleStatus
60725LVS EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)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
9484LVS EN ISO 10993-2:2000Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
22132LVS EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirementsAtcelts
69998LVS EN ISO 10993-2:2023Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)Standarts spēkā
68925LVS EN ISO 10993-23:2021Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)Standarts spēkā
78993LVS EN ISO 10993-23:2021/A1:2025Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/Amd 1:2025) 
9495LVS EN ISO 10993-3:2003Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
31978LVS EN ISO 10993-3:2009Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)Atcelts
30398LVS EN ISO 10993-3:2015Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)Standarts spēkā
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