ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 26211 | ISO 10993-5:1999 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Atcelts |
| 53468 | ISO 10993-12:2012 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 35978 | ISO/TS 10993-19:2006 | Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials | Atcelts |
| 41106 | ISO 10993-18:2005 | Biological evaluation of medical devices — Part 18: Chemical characterization of materials | Atcelts |
| 22692 | ISO 10993-13:1998 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 36403 | ISO/TS 20993:2006 | Biological evaluation of medical devices — Guidance on a risk-management process | Atcelts |
| 59992 | ISO 14155:2011/Cor 1:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1 | Atcelts |
Displaying 61-70 of 146 results.