ISO/TC 194
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
64580 | ISO 10993-9:2019 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Standarts spēkā |
44049 | ISO 10993-9:2009 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
26212 | ISO 10993-9:1999 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | Atcelts |
18969 | ISO 10993-8:2000 | Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological tests | Atcelts |
55064 | ISO 10993-7:2008/Cor 1:2009 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Technical Corrigendum 1 | Standarts spēkā |
72766 | ISO 10993-7:2008/Amd 1:2019 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infants | Standarts spēkā |
34213 | ISO 10993-7:2008 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Standarts spēkā |
18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
Displaying 81-90 of 146 results.