BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3840346 · Received May 30, 2014

    Report

    Report Number
    9616091-2014-00966
    Event Type
    Malfunction
    Date Received
    May 30, 2014
    Date of Event
    April 9, 2014
    Report Date
    April 16, 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 ALLEGES THE LEFT FOOTPLATE BROKE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    318362 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4X22RDA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other