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GSO ISO 80601-2-70:2024
ISO 80601-2-70:2020
Gulf Standard
Medical electrical equipment — Part 2-70: Particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment
GSO ISO 80601-2-90:2024
ISO 80601-2-90:2021
Gulf Standard
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment
GSO ISO 23368:2024
ISO 23368:2022
Gulf Standard
Anaesthetic and respiratory equipment — Low-flow nasal cannulae for oxygen therapy
GSO ISO 80601-2-69:2024
ISO 80601-2-69:2020
Gulf Standard
Medical electrical equipment — Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment
GSO ISO 23372:2024
ISO 23372:2022
Gulf Standard
Anaesthetic and respiratory equipment — Air entrainment devices
GSO ISO 23371:2024
ISO 23371:2022
Gulf Standard
Anaesthetic and respiratory equipment — Cuff pressure indication, control and regulation devices
GSO ISO 80601-2-13:2024
ISO 80601-2-13:2022
Gulf Standard
Medical electrical equipment — Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation
GSO ISO 26825:2024
ISO 26825:2020
Gulf Standard
Anaesthetic and respiratory equipment — User-applied labels for syringes containing drugs used during anaesthesia — Colours, design and performance
GSO ISO 21917:2023
ISO 21917:2021
Gulf Standard
Anaesthetic and respiratory equipment — Voice prostheses
GSO ISO 80601-2-85:2023
ISO 80601-2-85:2021
Gulf Standard
Medical electrical equipment — Part 2-85: Particular requirements for the basic safety and essential performance of cerebral tissue oximeter equipment
GSO ISO 9360-2:2023
ISO 9360-2:2001
Gulf Standard
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
GSO ISO/TS 81060-5:2023
ISO/TS 81060-5:2020
Gulf Standard
Non-invasive sphygmomanometers — Part 5: Requirements for the repeatability and reproducibility of NIBP simulators for testing of automated non-invasive sphygmomanometers