ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 64581 | ISO/PWI 10993-13 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Izstrādē |
| 83711 | ISO/PWI 10993-20 | Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing 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 |
| 64763 | ISO/WD 10993-7 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | 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 |
| 90930 | ISO/CD TS 25364-1 | Chemical Characterization of Medical Devices — Part 1: Identification of Organic Extractables in Non-Targeted Analysis (NTA) | 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 |
Displaying 101-110 of 155 results.