Registration number (WIID)Project No.TitleStatus
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
38319EN ISO 10993-6:2016Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/DIS 10993-6:2014)Standarts spēkā
78989LVS EN ISO 10993-12:2021/A1:2025Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - Amendment 1 (ISO 10993-12:2021/Amd 1:2025)Standarts spēkā
69998LVS EN ISO 10993-2:2023Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)Standarts spēkā
27051LVS EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)Standarts spēkā
32000LVS EN ISO 10993-14:2009Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Standarts spēkā
Displaying 141-150 of 195 results.