Registration number (WIID)Project No.TitleStatus
64750ISO 10993-18:2020Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management processStandarts spēkā
41106ISO 10993-18:2005Biological evaluation of medical devices — Part 18: Chemical characterization of materialsAtcelts
88201ISO 10993-17:2023/DAmd 1Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1Aptauja slēgta
75323ISO 10993-17:2023Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituentsStandarts spēkā
23955ISO 10993-17:2002Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesAtcelts
64582ISO 10993-16:2017Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesStandarts spēkā
45367ISO 10993-16:2010Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
22695ISO 10993-16:1997Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
68937ISO 10993-15:2019Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysStandarts spēkā
22694ISO 10993-15:2000Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
Displaying 111-120 of 146 results.