BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR20000124-000

    MDR report key: 10083518 · Received May 22, 2020

    Report

    Report Number
    COR20000124-000
    Event Type
    No answer provided
    Date Received
    May 22, 2020
    Report Date
    May 19, 2020
    Product Code
    GEX
    Report Source
    Manufacturer report
    Reporter Location
    DA
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    545061 GEX

    Patients

    Seq Age Sex Outcome Treatment
    1