Registration number (WIID)Project No.TitleStatus
18963ISO 10993-4:1992Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodAtcelts
23955ISO 10993-17:2002Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesAtcelts
32217ISO 14155-2:2003Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plansAtcelts
18962ISO 10993-3:1992Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
39360ISO 10993-10:2002/Amd 1:2006Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity — Amendment 1Atcelts
59992ISO 14155:2011/Cor 1:2011Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1Atcelts
22695ISO 10993-16:1997Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
35331ISO 10993-12:2002Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
18960ISO 10993-1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of testsAtcelts
18972ISO 10993-11:1993Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAtcelts
Displaying 101-110 of 147 results.