BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR24000290-000

    MDR report key: 20612313 · Received November 5, 2024

    Report

    Report Number
    COR24000290-000
    Event Type
    No answer provided
    Date Received
    November 5, 2024
    Report Date
    October 22, 2024
    Product Code
    GEX
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1092625 GEX

    Patients

    Seq Age Sex Outcome Treatment
    1 NA