ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 86247 | ISO/CD TS 20324 | Generation of medical device extracts for chemical analysis to support toxicological risk assessment | Izstrādē |
| 86246 | ISO/DIS 10993-2 | Biological evaluation of medical devices — Part 2: Animal welfare requirements | Izstrādē |
| 90037 | ISO/WD TS 25364 | Discovery, Identification and Quantification of Medical Device Extractables and Leachables via Non-Target Analysis (NTA) — Analytical Chemistry Matters Associated with ISO 10993-18 | Izstrādē |
| 22696 | ISO 10993-4:1992/DAmd 1 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Izstrādē |
| 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 |
| 90932 | ISO/CD TS 25364-3 | Analytical chemistry matters associated with ISO 10993-18 — Part 3: Instrumental and human requirements for evaluating organic medical device extractables and leachables via Non-Targeted Analysis (NTA) | Izstrādē |
| 90746 | ISO/AWI 22442-3 | Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents | Izstrādē |
| 93386 | ISO/PWI 10993-5 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Izstrādē |
| 93384 | ISO/PWI TR 26398 | Biological evaluation of medical devices - Information on the use of clinical data in the application of ISO 10993-1 | Izstrādē |
Displaying 41-50 of 155 results.