BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2020394-2006-00007

    MDR report key: 663259 · Received January 6, 2006

    Report

    Report Number
    2020394-2006-00007
    Event Type
    Injury
    Date Received
    January 6, 2006
    Date of Event
    November 15, 2005
    Report Date
    December 9, 2005
    Product Code
    DTK
    Report Source
    Manufacturer report
    Reporter Location
    FL, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DTK GFPH3268

    Patients

    Seq Age Sex Outcome Treatment
    1