BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 500581 · Received November 25, 2003

    Report

    Report Number
    1221826-2003-00026
    Event Type
    Other
    Date Received
    November 25, 2003
    Date of Event
    October 28, 2003
    Manufacturer
    *
    Product Code
    FGB
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FGB * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *