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  • Vitalograph Respiratory Lung Monitor

    Vitalograph Respiratory Lung Monitor

    Vitalograph lung monitor is a easy to use home monitoring device which records lung function parameters

    Easy to use device for monitoring of lung function parameters for those with respiratory conditions including cystic fibrosis and transplant patients. The lung monitor measures FEV1, FEV6 & the ratio with electronic and hard copy reports. The device is simple to use and stores over 200 test sessions.

    • For simple, accurate lung function monitoring at home
    • Measures FEV1, FEV6 and the ratio
    • Displays % of personal best FEV1
    • Large, easy to read display
    • Electronic record – no need for record cards
    • Automatically stores best values in a test session
    • Quality of blow indicator
    • Suitable for multi-subject use in clinic with Vitalograph Bacterial Viral Filters (eco BVF)
    • Uses long life AAA batteries
    • Language independent
    • Meets ATS/ERS:2005 Spirometry Guidelines
    Product Vitalograph lung monitor
    Model Number 4000
    Part Number 40500, 40400, 40750, 40950
    Description Vitalograph lung monitor, Vitalograph lung monitor usb, Vitalograph lung monitor bluetooth, Vitalograph lung monitor serial
    Parameters Displayed FEV1, FEV6 , FEV1/FEV6 ratio and FEF
    Memory FEV1, FEV6 , FEV1/FEV6 ratio and FEF
    Quality of Blow Indicator Yes
    Accuracy Better than +/- 3%
    Range 0 - 9.99 L BTPS
    Sensor Stator rotor
    Flow Impedance Better than 0.15 kPa/L/s at 14 L/s
    Power Supply AAA batteries
    Display Custom liquid crystal display
    Size 113 x 63 x 48mm
    Weight 55g net
    Performance standards ISO 26782:2009
    ISO 23747:2007
    ATS/ERS Guidelines 2005
    Operating Temperature Range 17 - 37°C
    Management Zones Factory set 3 zones
    Green/Yellow threshold 95%
    Yellow/Red threshold 90%
    Zones may be changed by the user And number of zones increased to 4
    Safety Standards IEC 60601-1:2005
    Medical Safety Standard Medical Devices Directive 93/42/EEC
    Designed and manufactured to following QA/GMP standards ISO 13485:2003
    FDA 21CFR820
    CMDR

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