BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INSIGNIA PLUS

    MDR report key: 1042595 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-34046
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    March 3, 2008
    Report Date
    March 3, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DXY
    Removal / Correction Number
    Z0187-94/6
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INSIGNIA PLUS IMPLANTABLE PULSE GENERATOR DXY CARDIAC PACEMAKERS, INC 1297 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Required Intervention THE DEVICE 5024 LAT201 WAS USED DURING THE EVENT.| THE DEVICE 4269/266414 WAS IMPLANTED 25-FEB-1997