BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3020203 · Received March 25, 2013

    Report

    Report Number
    1531186-2013-01263
    Date Received
    March 25, 2013
    Report Date
    February 26, 2013
    Manufacturer
    UNKNOWN
    Product Code
    IOR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATED FRAME IS BENT ON THE RIGHT SIDE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    121446 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN V18RLR

    Patients

    Seq Age Sex Outcome Treatment
    1 Other