BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR20000149-000

    MDR report key: 10181490 · Received June 22, 2020

    Report

    Report Number
    COR20000149-000
    Event Type
    No answer provided
    Date Received
    June 22, 2020
    Report Date
    June 22, 2020
    Product Code
    GEX
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    641365 GEX

    Patients

    Seq Age Sex Outcome Treatment
    1