BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SETROX S 45

    MDR report key: 1020565 · Received March 28, 2008

    Report

    Report Number
    1028232-2008-00311
    Event Type
    Injury
    Date Received
    March 28, 2008
    Date of Event
    February 15, 2008
    Report Date
    February 28, 2008
    Manufacturer
    BIOTRONIK GMBH AND CO.
    Product Code
    DTB
    PMA / PMN Number
    P950037
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    PER MDRF, THIS SYSTEM WAS REMOVED DUE TO INFECTION. ALSO REMOVED: LUMAX 340 DR-T, MDR 1028232-2008-00289. LINOX SD 65/16, MDR 1028232-2008-00299.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SETROX S 45 PACER LEAD DTB BIOTRONIK GMBH AND CO. 350973

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization