Registration number (WIID)Project No.TitleStatus
88201ISO 10993-17:2023/DAmd 1Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1Aptauja slēgta
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
21225ISO 10993-1:1992/Cor 1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1Atcelts
18969ISO 10993-8:2000Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological testsAtcelts
37875ISO 10993-1:2003Biological evaluation of medical devices — Part 1: Evaluation and testingAtcelts
18967ISO 10993-7:1995Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsAtcelts
26212ISO 10993-9:1999Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsAtcelts
44908ISO 10993-1:2009Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processAtcelts
55441ISO/TR 15499:2012Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
Displaying 31-40 of 146 results.