Registration number (WIID)Project No.TitleStatus
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)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
32004LVS EN ISO 10993-18:2009Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
60721EN ISO 10993-1:2020Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO/DIS 10993-1:2017)Atcelts
30062EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2008)Atcelts
32001LVS EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
31978LVS EN ISO 10993-3:2009Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)Atcelts
9501EN ISO 10993-10:2002Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002)Atcelts
22132EN ISO 10993-2:2006Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006)Atcelts
40624LVS EN 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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