Registration number (WIID)Project No.TitleStatus
22693ISO 10993-14:2001Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramicsStandarts spēkā
36406ISO 10993-5:2009Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityStandarts spēkā
55064ISO 10993-7:2008/Cor 1:2009Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Technical Corrigendum 1Standarts spēkā
63448ISO 10993-4:2017Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodStandarts spēkā
86799ISO/DIS 10993-11Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAptauja slēgta
86868ISO/DIS 21762Medical devices utilizing non-viable human materials — Risk managementAptauja
36403ISO/TS 20993:2006Biological evaluation of medical devices — Guidance on a risk-management processAtcelts
44789ISO 10993-6:2007Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
18964ISO 10993-5:1992Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methodsAtcelts
35978ISO/TS 10993-19:2006Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materialsAtcelts
Displaying 31-40 of 154 results.