Registration number (WIID)Project No.TitleStatus
9485-Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residualsIzstrādē
9483-Biological evaluation of medical devices - Methods of testing for degradation productsIzstrādē
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9475EN 30993-3:1993Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:1992)Atcelts
9479EN 30993-4:1993Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:1992)Atcelts
9472EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
9480EN 30993-6:1994Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994)Atcelts
9477EN ISO 10993-10:1995Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995)Atcelts
9501EN ISO 10993-10:2002Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002)Atcelts
23724EN ISO 10993-10:2002/A1:2006Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006)Atcelts
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