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
IEC 60417 Graphical symbols for use on equipment (DATABASE SNAPSHOT) ((SNAPSHOTS ARE NOT AVAILABLE FOR RETAIL PURCHASE))*, 2023-12-23 Update
IEC 60601-1-6 Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability*, 2023-12-23 Update
IEC 60601-1:2005 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
IEC 62366 Medical devices - Application of usability engineering to 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 14971 Medical devices — Application of risk management to medical devices — Amendment 1: Rationale for requirements*, 2019-12-10 Update
ISO 15223-1:2012 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
ISO 23328-2:2002 Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects
ISO 4135:2001 Anaesthetic and respiratory equipment - Vocabulary
ISO 5356-1 Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets*, 2015-03-01 Update
ISO 7000 Graphical symbols for use on equipment — Index and synopsis*, 2019-07-12 Update
ISO 80601-2-12:2011 Medical electrical equipment - Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
ISO 80601-2-13:2011 Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation
ISO 8185:2007 Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems
ISO 9360-1:2000 Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml
BS EN ISO 5367:2014 history
1970BS EN ISO 5367:2023 Anaesthetic and respiratory equipment — Breathing sets and connectors
2014BS EN ISO 5367:2014 Anaesthetic and respiratory equipment. Breathing sets and connectors