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Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2002/Amd 1:2006)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:1999)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)
99.60 Withdrawal effective
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)
99.60 Withdrawal effective
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006)
99.60 Withdrawal effective
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013)
99.60 Withdrawal effective
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006)
99.60 Withdrawal effective
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006, corrected version 2006-08-01)
99.60 Withdrawal effective