Registration number (WIID)Project No.TitleStatus
64750ISO 10993-18:2020Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management processStandarts spēkā
88199ISO/DIS 10993-3Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicityAptauja
86799ISO/DIS 10993-11Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAptauja
18967ISO 10993-7:1995Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsAtcelts
18966ISO 10993-6:1994Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
35331ISO 10993-12:2002Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
22695ISO 10993-16:1997Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesAtcelts
23736ISO 14155:1996Clinical investigation of medical devicesAtcelts
18962ISO 10993-3:1992Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
32217ISO 14155-2:2003Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plansAtcelts
Displaying 31-40 of 146 results.