ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 35980 | ISO/WD TS 10993-21 | Biological evaluation of medical devices — Part 21: Guidelines for the preparation of standards for the biological evaluation of medical devices | Izstrādē |
| 86248 | ISO/PWI TS 10993-22 | Biological evaluation of medical devices — Part 22: Guidance on nanomaterials | Izstrādē |
| 45651 | ISO/AWI TS 29741 | Biological evaluation of medical devices — Development of tolerable intake values for Di(2-ethylhexyl)phthalate (DEHP) | Izstrādē |
| 42997 | ISO/CD 10993-1 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Izstrādē |
| 64744 | ISO/PWI 10993-17 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Izstrādē |
| 85211 | ISO/PWI 10993-5 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Izstrādē |
| 89238 | ISO/AWI 8250 | Cleanliness of medical devices — Process design and test methods | Izstrādē |
| 41176 | ISO/PWI 14155-1 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Izstrādē |
| 91724 | ISO/AWI TS 25364-4 | Analytical chemistry matters associated with ISO 10993-18 — Part 4: Critical aspects of extract viability in extractables and leachables testing using non-targeted analysis (NTA) | Izstrādē |
| 64751 | ISO/NP TS 10993-19 | Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials | Izstrādē |
Displaying 141-150 of 156 results.