BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FLEXTEND IS-1 BI POSITIVE FIX

    MDR report key: 1253973 · Received November 11, 2008

    Report

    Report Number
    2124215-2008-40800
    Event Type
    Injury
    Date Received
    November 11, 2008
    Date of Event
    September 18, 2008
    Report Date
    September 18, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    DTB
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXTEND IS-1 BI POSITIVE FIX IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4087 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR Required Intervention THE DEVICE 1297/295109 WAS IMPLANTED 30-APR-2004| THE DEVICE 4086/156010 WAS IMPLANTED 30-APR-2004| THE DEVICE 4136/283229 WAS IMPLANTED 19-SEP-2008| THE DEVICE S602/571654 WAS IMPLANTED 19-SEP-2008