Registration number (WIID)Project No.TitleStatus
68937ISO 10993-15:2019Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysStandarts spēkā
88200ISO 10993-23:2021/Amd 1:2025Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1: Additional in vitro reconstructed human epidermis modelsStandarts spēkā
86868ISO/DIS 21762Medical devices utilizing non-viable human materials — Risk managementAptauja slēgta
85514ISO/DIS 18969Clinical evaluation of medical devicesAptauja slēgta
88206ISO/DIS 10993-16Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachablesAptauja slēgta
86799ISO/DIS 10993-11.2Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAptauja
68936ISO 10993-1:2018Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processAtcelts
21225ISO 10993-1:1992/Cor 1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1Atcelts
72766ISO 10993-7:2008/Amd 1:2019Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infantsAtcelts
31723ISO 14155-1:2003Clinical investigation of medical devices for human subjects — Part 1: General requirementsAtcelts
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