ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 26211 | ISO 10993-5:1999 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 25333 | ISO 10993-1:1997 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Atcelts |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
| 23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
| 22696 | ISO 10993-4:1992/DAmd 1 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Izstrādē |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 22694 | ISO 10993-15:2000 | Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys | Atcelts |
| 22693 | ISO 10993-14:2001 | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Standarts spēkā |
Displaying 131-140 of 154 results.