ISO/TC 194
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
88201 | ISO 10993-17:2023/DAmd 1 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1 | Aptauja slēgta |
88199 | ISO/DIS 10993-3 | Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity | Aptauja |
86799 | ISO/DIS 10993-11 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Aptauja |
21225 | ISO 10993-1:1992/Cor 1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1 | Atcelts |
18969 | ISO 10993-8:2000 | Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
37875 | ISO 10993-1:2003 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Atcelts |
18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
44908 | ISO 10993-1:2009 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process | Atcelts |
55441 | ISO/TR 15499:2012 | Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process | Atcelts |
Displaying 31-40 of 146 results.