Registration number (WIID)Project No.TitleStatus
21225ISO 10993-1:1992/Cor 1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1Atcelts
83916ISO/TS 11796:2023Biological evaluation of medical devices — Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devicesAtcelts
55614ISO 10993-3:2014Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
18971ISO 10993-10:1995Biological evaluation of medical devices — Part 10: Tests for irritation and sensitizationAtcelts
56669ISO 10993-1:2009/Cor 1:2010Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1Atcelts
18962ISO 10993-3:1992Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
35977ISO 10993-11:2006Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAtcelts
18969ISO 10993-8:2000Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological testsAtcelts
55441ISO/TR 15499:2012Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
23736ISO 14155:1996Clinical investigation of medical devicesAtcelts
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