BEUDAMED
    FDA Adverse Event Other Summary report: N

    3019090-1998-00001

    MDR report key: 171940 · Received June 4, 1998

    Report

    Report Number
    3019090-1998-00001
    Event Type
    Other
    Date Received
    June 4, 1998
    Date of Event
    May 8, 1998
    Product Code
    EYD
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1