Registration number (WIID)Project No.TitleStatus
56669ISO 10993-1:2009/Cor 1:2010Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1Atcelts
36403ISO/TS 20993:2006Biological evaluation of medical devices — Guidance on a risk-management processAtcelts
37875ISO 10993-1:2003Biological evaluation of medical devices — Part 1: Evaluation and testingAtcelts
55064ISO 10993-7:2008/Cor 1:2009Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — 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
44908ISO 10993-1:2009Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processAtcelts
39205ISO 10993-4:2002/Amd 1:2006Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1Atcelts
32086ISO 10993-4:2002Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodAtcelts
18971ISO 10993-10:1995Biological evaluation of medical devices — Part 10: Tests for irritation and sensitizationAtcelts
35331ISO 10993-12:2002Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
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