Registration number (WIID)Project No.TitleStatus
9472EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
9489LVS EN ISO 10993-15:2003Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
32002LVS EN ISO 10993-16:2009Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)Atcelts
9487LVS EN ISO 10993-13:2000Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesAtcelts
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
24852LVS EN ISO 10993-12:2008Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsAtcelts
27092EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
31979LVS EN ISO 10993-4:2009Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)Atcelts
40624LVS EN ISO 10993-10:2013Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)Atcelts
9481EN ISO 10993-7:1995Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995)Atcelts
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