Registration number (WIID)Project No.TitleStatus
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
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
74131LVS EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
74131EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
60723EN ISO 10993-15:2023Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)Standarts spēkā
60725EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)Standarts spēkā
22089LVS EN ISO 10993-5:2009Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Standarts spēkā
65481LVS EN ISO 22442-2:2021Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)Standarts spēkā
60133EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
77933prEN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025)Aptauja slēgta
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