BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 36074 · Received August 20, 1996

    Report

    Report Number
    1928508-1996-00002
    Event Type
    Other
    Date Received
    August 20, 1996
    Date of Event
    July 22, 1996
    Manufacturer
    *
    Product Code
    FYH
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *