BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SEXTRUS 4135

    MDR report key: 1033745 · Received April 25, 2008

    Report

    Report Number
    1028232-2008-00450
    Event Type
    Injury
    Date Received
    April 25, 2008
    Date of Event
    February 20, 2008
    Report Date
    March 27, 2008
    Manufacturer
    BIOTRONIK GMBH AND CO.
    Product Code
    DTB
    PMA / PMN Number
    P950037
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BOSTON SCIENTIFIC (BSC) CRM RECEIVED INFO THAT THIS RIGHT ATRIAL (RA) LEAD 4135 DISLODGED. THE LOCAL REP NOTED THE LEAD WOULD BE REPOSITIONED THE FOLLOWING DAY. NO ADVERSE PT EFFECTS WERE REPORTED. THE IMPLANT DATE IS UNAVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SEXTRUS 4135 PACER LEADS DTB BIOTRONIK GMBH AND CO. 358744

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Hospitalization