Registration number (WIID)Project No.TitleStatus
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
18962ISO 10993-3:1992Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
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
22692ISO 10993-13:1998Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
32162ISO 10993-3:2003Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
18964ISO 10993-5:1992Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methodsAtcelts
35978ISO/TS 10993-19:2006Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materialsAtcelts
18961ISO 10993-2:1992Biological evaluation of medical devices — Part 2: Animal welfare requirementsAtcelts
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