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In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices
99.60 Withdrawal effective
Graphical symbols for use in the labelling of medical devices
99.60 Withdrawal effective
Graphical symbols for use in the labelling of medical devices
99.60 Withdrawal effective
Graphical symbols for use in the labelling of medical devices
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)
99.60 Withdrawal effective
Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000)
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 11137-2:2012)
99.60 Withdrawal effective
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)
99.60 Withdrawal effective
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006/Amd 1:2014)
99.60 Withdrawal effective
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/Amd 1:2014)
99.60 Withdrawal effective
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)
99.60 Withdrawal effective