BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3243272 · Received July 23, 2013

    Report

    Report Number
    9616091-2013-01287
    Event Type
    Malfunction
    Date Received
    July 23, 2013
    Report Date
    July 2, 2013
    Manufacturer
    INVAMEX
    Product Code
    IOR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A T420RDA MANUAL WHEELCHAIR HAD A BROKEN WELD ON THE RIGHT SIDE OF THE FRAME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    343257 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T420RDA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other