Registration number (WIID)Project No.TitleStatus
64582ISO 10993-16:2017Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesStandarts spēkā
55614ISO 10993-3:2014Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityStandarts spēkā
86868ISO/DIS 21762Medical devices utilizing non-viable human materials — Risk managementAptauja slēgta
88206ISO/DIS 10993-16Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachablesAptauja slēgta
85514ISO/DIS 18969Clinical evaluation of medical devicesAptauja slēgta
86799ISO/DIS 10993-11.2Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAptauja
32217ISO 14155-2:2003Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plansAtcelts
23955ISO 10993-17:2002Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesAtcelts
31723ISO 14155-1:2003Clinical investigation of medical devices for human subjects — Part 1: General requirementsAtcelts
18963ISO 10993-4:1992Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodAtcelts
Displaying 31-40 of 157 results.