93/42/EEC Commission communication in the framework of the implementation of the Council Directive 93/42/EEC concerning medical devices (Text with EEA relevance; Publication of titles and references of harmonised standards under the directive)
EN 1041 Information supplied by the manufacturer of medical devices
EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices*， 2023-12-23 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 11712 Anaesthetic and respiratory equipment — Supralaryngeal airways and connectors*， 2023-10-01 Update
ISO 15223-1 Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1
ISO 4135:2001 Anaesthetic and respiratory equipment - Vocabulary
ISO 7000 Graphical symbols for use on equipment — Index and synopsis*， 2019-07-12 Update
ISO/TR 11991 Guidance on airway management during laser surgery of upper airway
BS EN ISO 5364:2016 history
2016BS EN ISO 5364:2016 Anaesthetic and respiratory equipment. Oropharyngeal airways
2011BS EN ISO 5364:2011 Anaesthetic and respiratory equipment. Oropharyngeal airways