BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FINELINE II STEROX BIPOLAR IS-1 PASSIVE STEROID RV 52 CM

    MDR report key: 1681485 · Received May 7, 2010

    Report

    Report Number
    2124215-2010-09139
    Event Type
    Injury
    Date Received
    May 7, 2010
    Date of Event
    March 31, 2010
    Report Date
    May 7, 2010
    Manufacturer
    CPI - DEL CARIBE
    Product Code
    DTB
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FINELINE II STEROX BIPOLAR IS-1 PASSIVE STEROID RV 52 CM IMPLANTABLE LEAD DTB CPI - DEL CARIBE 4456 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Other