Reģistrācijas numurs (WIID)Projekta Nr.NosaukumsStatuss
45367ISO 10993-16:2010Évaluation biologique des dispositifs médicaux — Partie 16: Conception des études toxicocinétiques des produits de dégradation et des substances relargablesAtcelts
64582ISO 10993-16:2017Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesStandarts spēkā
23955ISO 10993-17:2002Évaluation biologique des dispositifs médicaux — Partie 17: Établissement des limites admissibles des substances relargablesAtcelts
75323ISO 10993-17:2023Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituentsStandarts spēkā
88201ISO 10993-17:2023/Amd 1:2025Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1Standarts spēkā
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 10993-2:1992Évaluation biologique des dispositifs médicaux — Partie 2: Exigences concernant la protection des animauxAtcelts
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
Attēlo no 31. līdz 40. no pavisam 155 ieraksta(-iem).