BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CAPSUREFIX NOVUS

    MDR report key: 1013368 · Received March 10, 2008

    Report

    Report Number
    2649622-2008-00970
    Event Type
    Malfunction
    Date Received
    March 10, 2008
    Date of Event
    May 17, 2007
    Manufacturer
    MEDTRONIC PUERTO RICO, INC.
    Product Code
    DTB
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CAPSUREFIX NOVUS IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 5076 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Required Intervention AT501 IMPLANTABLE PULSE GENERATOR