BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EXPRO ELITE

    MDR report key: 1032549 · Received April 18, 2008

    Report

    Report Number
    MW5006344
    Event Type
    Injury
    Date Received
    April 18, 2008
    Date of Event
    February 28, 2008
    Report Date
    April 18, 2008
    Manufacturer
    ABBOTT VASCULAR - CARDIAC THERAPIES
    Product Code
    MMX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    ATTORNEY

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EXPRO ELITE NONE MMX ABBOTT VASCULAR - CARDIAC THERAPIES 1011897-25 07/W14200

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Hospitalization