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 |
| 32086 | ISO 10993-4:2002 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
| 26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 69217 | ISO/TR 15499:2016 | Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process | Atcelts |
| 35978 | ISO/TS 10993-19:2006 | Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials | Atcelts |
| 18964 | ISO 10993-5:1992 | Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methods | Atcelts |
| 18963 | ISO 10993-4:1992 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
| 18973 | ISO 10993-12:1996 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 18969 | ISO 10993-8:2000 | Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
Displaying 61-70 of 155 results.