Registration number (WIID)Project No.TitleStatus
60721LVS EN ISO 10993-1:2021Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-11)Standarts spēkā
60214EN ISO 22442-2:2015Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2015)Atcelts
60213EN ISO 22442-1:2015Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015)Atcelts
60133EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
60133LVS EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
40815EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
40815LVS EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
40814prEN ISO 10993-5 revBiological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Izstrādē
40661prEN ISO 10993-7 revBiological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsIzstrādē
40624EN ISO 10993-10:2013Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
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