Registration number (WIID)Project No.TitleStatus
40384ISO 10993-12:2007Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
45557ISO 14155:2011Clinical investigation of medical devices for human subjects — Good clinical practiceAtcelts
45367ISO 10993-16:2010Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
86799ISO/DIS 10993-11Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAptauja slēgta
88199ISO/DIS 10993-3Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicityAptauja slēgta
65918ISO/TR 10993-22:2017Biological evaluation of medical devices — Part 22: Guidance on nanomaterialsStandarts spēkā
68936ISO 10993-1:2018Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processStandarts spēkā
71150ISO/TR 21582:2021Pyrogenicity — Principles and methods for pyrogen testing of medical devicesStandarts spēkā
75323ISO 10993-17:2023Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituentsStandarts spēkā
72766ISO 10993-7:2008/Amd 1:2019Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infantsStandarts spēkā
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