ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 93385 | ISO/PWI TS 26399 | Biological evaluation of medical devices – Guidance on the application of ISO 10993-1 throughout the medical device life cycle | Izstrādē |
| 93386 | ISO/PWI 10993-5 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Izstrādē |
| 64763 | ISO/WD 10993-7 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 83711 | ISO/PWI 10993-20 | Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devices | Izstrādē |
| 91188 | ISO/CD 25695 | Medical devices utilizing bioengineered biological substances — Application of risk management | Izstrādē |
| 83092 | ISO/CD 8250 | Cleanliness of medical devices — Process design and test methods | Izstrādē |
| 83972 | ISO/PWI 10993-12 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Izstrādē |
| 18972 | ISO 10993-11:1993 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity | Atcelts |
| 18960 | ISO 10993-1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests | Atcelts |
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
Displaying 61-70 of 157 results.