ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
| 18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 18962 | ISO 10993-3:1992 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 22694 | ISO 10993-15:2000 | Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys | Atcelts |
| 18960 | ISO 10993-1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests | Atcelts |
| 25333 | ISO 10993-1:1997 | Biological evaluation of medical devices — Part 1: Evaluation and testing | Atcelts |
| 18961 | ISO 10993-2:1992 | Biological evaluation of medical devices — Part 2: Animal welfare requirements | Atcelts |
| 26211 | ISO 10993-5:1999 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 56669 | ISO 10993-1:2009/Cor 1:2010 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1 | Atcelts |
Displaying 51-60 of 159 results.