ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 37544 | ISO 10993-1:1997/CD Amd 1 | Biological evaluation of medical devices — Part 1: Evaluation and testing — Amendment 1 | Izstrādē |
| 64581 | ISO/PWI 10993-13 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Izstrādē |
| 84512 | ISO/FDIS 10993-1 | Biological evaluation of medical devices — Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process | 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 |
| 85514 | ISO/CD 18969 | Clinical evaluation of medical devices | 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 |
| 91724 | ISO/NP 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 |
Displaying 111-120 of 146 results.