Registration number (WIID)Project No.TitleStatus
80820EN ISO 10993-5:2009/A11:2025Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicityStandarts spēkā
22089EN ISO 10993-5:2009Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Standarts spēkā
9497EN ISO 10993-5:1999Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Atcelts
77939EN ISO 10993-4:2017/A1:2025Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2017/Amd 1:2025, Corrected version 2025-04)Standarts spēkā
40815EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/DIS 10993-4:2015)Atcelts
65727EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Standarts spēkā
31979EN ISO 10993-4:2009Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)Atcelts
23327EN ISO 10993-4:2002/A1:2006Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2002/Amd 1:2006)Atcelts
9496EN ISO 10993-4:2002Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)Atcelts
78988EN ISO 10993-3:2026Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/FDIS 10993-3:2026)Izstrādē
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