Registration number (WIID)Project No.TitleStatus
44908ISO 10993-1:2009Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processAtcelts
37875ISO 10993-1:2003Biological evaluation of medical devices — Part 1: Evaluation and testingAtcelts
18970ISO/TR 10993-9:1994Biological evaluation of medical devices — Part 9: Degradation of materials related to biological testingAtcelts
36405ISO 10993-2:2006Biological evaluation of medical devices — Part 2: Animal welfare requirementsAtcelts
72766ISO 10993-7:2008/Amd 1:2019Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infantsAtcelts
68936ISO 10993-1:2018Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processAtcelts
65052ISO/TR 10993-33:2015Biological evaluation of medical devices — Part 33: Guidance on tests to evaluate genotoxicity — Supplement to ISO 10993-3Atcelts
21225ISO 10993-1:1992/Cor 1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1Atcelts
39360ISO 10993-10:2002/Amd 1:2006Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity — Amendment 1Atcelts
39205ISO 10993-4:2002/Amd 1:2006Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1Atcelts
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