BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRIDENT CROSSFIRE INSERT - UNKNOWN OD

    MDR report key: 1252183 · Received November 24, 2008

    Report

    Report Number
    2249697-2008-00378
    Event Type
    Injury
    Date Received
    November 24, 2008
    Report Date
    October 31, 2008
    Product Code
    KWB
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRIDENT CROSSFIRE INSERT - UNKNOWN OD IMPLANT KWB NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention