Registration number (WIID)Project No.TitleStatus
78991prEN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic evaluation for degradation products and leachables (ISO/DIS 10993-16:2025)Aptauja slēgta
78812prEN ISO 21762Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025)Aptauja slēgta
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025)Aptauja slēgta
60724EN ISO 10993-16:2017Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2016)Standarts spēkā
67767EN ISO 10993-17:2023Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)Standarts spēkā
77939EN ISO 10993-4:2017/A1:2025Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2017/Amd 1:2025, Corrected version 2025-04)Standarts spēkā
60723EN ISO 10993-15:2023Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO/DIS 10993-15:2018)Standarts spēkā
60725EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Évaluation biologique (ISO/DIS 10993-18:2018)Standarts spēkā
67187LVS EN ISO 10993-10:2023Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021)Standarts spēkā
9493LVS EN ISO 10993-7:2009Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)Standarts spēkā
Displaying 131-140 of 195 results.