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
23736ISO 14155:1996Clinical investigation of medical devicesAtcelts
74151ISO 10993-23:2021Biological evaluation of medical devices — Part 23: Tests for irritationAtcelts
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
93385ISO/PWI TS 26399Biological evaluation of medical devices – Guidance on the application of ISO 10993-1 throughout the medical device life cycleIzstrādē
93382ISO/PWI TR 26376Biological evaluation of medical devices – Information on biological equivalence in the application of ISO 10993-1Izstrādē
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