ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 75323 | ISO 10993-17:2023 | Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents | Standarts spēkā |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 64582 | ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Standarts spēkā |
| 45367 | ISO 10993-16:2010 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 68937 | ISO 10993-15:2019 | Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys | Standarts spēkā |
| 22694 | ISO 10993-15:2000 | Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys | Atcelts |
| 22693 | ISO 10993-14:2001 | Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics | Standarts spēkā |
| 44050 | ISO 10993-13:2010 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Standarts spēkā |
| 22692 | ISO 10993-13:1998 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
Displaying 121-130 of 154 results.