BEUDAMED
    FDA Adverse Event Summary report: N

    1049092-1996-00017

    MDR report key: 50493 · Received November 12, 1996

    Report

    Report Number
    1049092-1996-00017
    Date Received
    November 12, 1996
    Date of Event
    August 24, 1996
    Product Code
    MDZ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1