ISO/TC 194
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
40384 | ISO 10993-12:2007 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
45557 | ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice | Atcelts |
45367 | ISO 10993-16:2010 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
86799 | ISO/DIS 10993-11 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja slēgta |
88199 | ISO/DIS 10993-3 | Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity | Aptauja slēgta |
65918 | ISO/TR 10993-22:2017 | Biological evaluation of medical devices — Part 22: Guidance on nanomaterials | Standarts spēkā |
68936 | ISO 10993-1:2018 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process | Standarts spēkā |
71150 | ISO/TR 21582:2021 | Pyrogenicity — Principles and methods for pyrogen testing of medical devices | Standarts spēkā |
75323 | ISO 10993-17:2023 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents | Standarts spēkā |
72766 | ISO 10993-7:2008/Amd 1:2019 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infants | Standarts spēkā |
Displaying 111-120 of 146 results.