BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3790320 · Received May 5, 2014

    Report

    Report Number
    9616091-2014-00818
    Event Type
    Malfunction
    Date Received
    May 5, 2014
    Date of Event
    April 3, 2014
    Report Date
    April 3, 2014
    Manufacturer
    INVAMEX
    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

    DEALER STATED THAT THE LEFT SIDE FRAME ON A T422RDA WHEELCHAIR IS BROKEN AT A REAR WELD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    266508 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T422RDA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other