BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3840927 · Received May 30, 2014

    Report

    Report Number
    1531186-2014-02001
    Date Received
    May 30, 2014
    Report Date
    April 16, 2014
    Manufacturer
    JUMAO MEDICAL EQUIPMENT
    Product Code
    IOR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4) STATED THAT THE LEFT REAR CAMBER TUBE ON A (B)(4) VERANDA WHEELCHAIR IS CAUSING THE WHEEL TO RUB AGAINST THE CHAIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    318045 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V20RFR

    Patients

    Seq Age Sex Outcome Treatment
    1 Other