Registration number (WIID)Project No.TitleStatus
64582ISO 10993-16:2017Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesStandarts spēkā
23955ISO 10993-17:2002Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesAtcelts
75323ISO 10993-17:2023Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituentsStandarts spēkā
88201ISO 10993-17:2023/DAmd 1Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1Aptauja slēgta
41106ISO 10993-18:2005Biological evaluation of medical devices — Part 18: Chemical characterization of materialsAtcelts
64750ISO 10993-18:2020Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management processStandarts spēkā
18961ISO 10993-2:1992Biological evaluation of medical devices — Part 2: Animal welfare requirementsAtcelts
36405ISO 10993-2:2006Biological evaluation of medical devices — Part 2: Animal welfare requirementsAtcelts
78866ISO 10993-2:2022Biological evaluation of medical devices — Part 2: Animal welfare requirementsStandarts spēkā
74151ISO 10993-23:2021Biological evaluation of medical devices — Part 23: Tests for irritationStandarts spēkā
Displaying 31-40 of 146 results.