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Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007)
60.60 Standard published
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type (ISO 81060-2:2018)
60.60 Standard published
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type - Amendment 1 (ISO 81060-2:2018/Amd 1:2020)
60.60 Standard published
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type - Amendment 2 (ISO 81060-2:2018/Amd 2:2024)
60.60 Standard published
Non-invasive sphygmomanometers - Part 3: Clinical investigation of continuous automated measurement type (ISO 81060-3:2022)
60.60 Standard published
Suction catheters for use in the respiratory tract (ISO 8836:2019)
60.60 Standard published
Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2017)
60.60 Standard published
Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008)
60.60 Standard published
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 (ISO 9360-1:2000)
60.60 Standard published
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001)
60.60 Standard published
Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process (ISO/FDIS 18562-1:2023)
60.55 Ratification completed (DOR)
Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 2: Tests for emissions of particulate matter (ISO/FDIS 18562-2:2023)
60.55 Ratification completed (DOR)
Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic substances (ISO/FDIS 18562-3:2023)
60.55 Ratification completed (DOR)
Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 4: Tests for leachables in condensate (ISO/FDIS 18562-4:2023)
60.55 Ratification completed (DOR)
Anaesthetic and respiratory equipment - Anaesthetic reservoir bags (ISO/FDIS 5362:2024)
60.55 Ratification completed (DOR)
Medical electrical equipment - Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment (ISO/FDIS 80601-2-79:2024)
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Medical electrical equipment - Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency (ISO/FDIS 80601-2-80:2024)
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Transportable liquid oxygen systems for medical use - Part 1: Common requirements and particular requirements for base units (ISO/DIS 18777-1:2024)
40.20 DIS ballot initiated: 12 weeks
