ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90742 | ISO/AWI 10993-13 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Izstrādē |
| 90743 | ISO/AWI 10993-14 | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Izstrādē |
| 23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
| 59992 | ISO 14155:2011/Cor 1:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1 | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 39360 | ISO 10993-10:2002/Amd 1:2006 | Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity — Amendment 1 | Atcelts |
| 18962 | ISO 10993-3:1992 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 18963 | ISO 10993-4:1992 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
Displaying 61-70 of 147 results.