Registration number (WIID)Project No.TitleStatus
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 slēgta
85514ISO/DIS 18969Clinical evaluation of medical devicesAptauja
88206ISO/DIS 10993-16Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachablesAptauja
36403ISO/TS 20993:2006Biological evaluation of medical devices — Guidance on a risk-management processAtcelts
18964ISO 10993-5:1992Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methodsAtcelts
44789ISO 10993-6:2007Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
Displaying 31-40 of 155 results.