BEUDAMED
    FDA Adverse Event Other Summary report: N

    2431314-1998-00001

    MDR report key: 193188 · Received October 21, 1998

    Report

    Report Number
    2431314-1998-00001
    Event Type
    Other
    Date Received
    October 21, 1998
    Date of Event
    May 6, 1997
    Product Code
    IYT
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1