ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 18963 | ISO 10993-4:1992 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
| 21225 | ISO 10993-1:1992/Cor 1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1 | Atcelts |
| 23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
| 75138 | ISO/TS 10993-19:2020 | Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials | Atcelts |
| 44049 | ISO 10993-9:2009 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
| 26211 | ISO 10993-5:1999 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 44789 | ISO 10993-6:2007 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Atcelts |
| 36403 | ISO/TS 20993:2006 | Biological evaluation of medical devices — Guidance on a risk-management process | Atcelts |
| 55064 | ISO 10993-7:2008/Cor 1:2009 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Technical Corrigendum 1 | Atcelts |
Displaying 71-80 of 156 results.