Registration number (WIID)Project No.TitleStatus
64763ISO/WD 10993-7Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsIzstrādē
64780ISO/WD TS 29741Biological evaluation of medical devices — Development of tolerable intake values for Di(2-ethylhexyl)phthalate (DEHP)Izstrādē
64887ISO/TR 37137:2014Cardiovascular biological evaluation of medical devices — Guidance for absorbable implantsStandarts spēkā
65052ISO/TR 10993-33:2015Biological evaluation of medical devices — Part 33: Guidance on tests to evaluate genotoxicity — Supplement to ISO 10993-3Standarts spēkā
65918ISO/TR 10993-22:2017Biological evaluation of medical devices — Part 22: Guidance on nanomaterialsStandarts spēkā
68426ISO 10993-11:2017Biological evaluation of medical devices — Part 11: Tests for systemic toxicityStandarts spēkā
68936ISO 10993-1:2018Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processStandarts spēkā
68937ISO 10993-15:2019Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysStandarts spēkā
68938ISO/NP TS 10993-20Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devicesIzstrādē
69217ISO/TR 15499:2016Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
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