The International Standard specifies requirements for oropharyngeal airways of plastics materials and/or rubber, including those with a reinforcement insert made of plastics materials and/or metal.
DIN EN ISO 5364:2011 Referenced Document
EN 1041 Information supplied by the manufacturer of medical devices*, 2013-09-01 Update
EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices*, 2024-04-19 Update
EN 980 Graphical Symbols for Use in the Labelling of Medical Devices
ISO 10993-1 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process*, 2018-08-01 Update
ISO 11607-1 Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1
ISO 7000 Graphical symbols for use on equipment — Index and synopsis*, 2019-07-12 Update
DIN EN ISO 5364:2011 history
2017DIN EN ISO 5364:2017 Anaesthetic and respiratory equipment - Oropharyngeal airways (ISO 5364:2016); German version EN ISO 5364:2016
2011DIN EN ISO 5364:2011 Anaesthetic and respiratory equipment - Oropharyngeal airways (ISO 5364:2008); German version EN ISO 5364:2011