BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONTAK RENEWAL 4 RF

    MDR report key: 1043408 · Received May 8, 2008

    Report

    Report Number
    2124215-2008-33237
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 6, 2008
    Report Date
    February 6, 2008
    Manufacturer
    CARDIAC PACEMAKERS, INC
    Product Code
    NIK
    Removal / Correction Number
    Z-0863-05
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONTAK RENEWAL 4 RF IMPLANTABLE CHF GENERATOR NIK CARDIAC PACEMAKERS, INC H230 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention THE DEVICE H230/ WAS IMPLANTED