BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FLEXTEND IS-1 BI POSITIVE FIX 45CM

    MDR report key: 1043202 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33439
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 11, 2008
    Report Date
    February 11, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DTB
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXTEND IS-1 BI POSITIVE FIX 45CM IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4086 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 89 YR Required Intervention THE DEVICE 1296/130150 WAS IMPLANTED 26-JAN-2006| THE DEVICE 4087/251859 WAS IMPLANTED 26-JAN-2006| THE DEVICE 4135/244182 WAS IMPLANTED 11-FEB-2008| THE DEVICE 4136/282594 WAS IMPLANTED 11-FEB-2008