BEUDAMED
    FDA Adverse Event Injury Summary report: N

    8022247-2002-00042

    MDR report key: 410402 · Received July 31, 2002

    Report

    Report Number
    8022247-2002-00042
    Event Type
    Injury
    Date Received
    July 31, 2002
    Date of Event
    December 3, 2001
    Report Date
    July 23, 2002
    Product Code
    KXK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KXK 1990028

    Patients

    Seq Age Sex Outcome Treatment
    1