Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992); German version EN 30993-1:1994— 12 стр.
Biological evaluation of medical devices; part 3: tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:1992); German version EN 30993-3:1993— 8 стр.
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994); German version EN 30993-6:1994— 10 стр.
Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995); German version EN ISO 10993-10:1995— 27 стр.
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:1996); German version EN ISO 10993-12:1996— 10 стр.
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007); German version EN ISO 10993-12:2007— 24 стр.
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002+Amd.1:2006); German version EN ISO 10993-10:2002+A1:2006— 69 стр.
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003); German version EN ISO 10993-3:2003— 25 стр.
Biological evaluation of medical devices - Part 5: Tests for cytotoxicity: in vitro-methods (ISO 10993-5:1999); German version EN ISO 10993-5:1999— 8 стр.
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007); German version EN ISO 10993-6:2007— 28 стр.
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997); German version EN ISO 10993-16:1997— 8 стр.
