BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR22000080-000

    MDR report key: 14254839 · Received April 26, 2022

    Report

    Report Number
    COR22000080-000
    Event Type
    No answer provided
    Date Received
    April 26, 2022
    Report Date
    April 26, 2022
    Product Code
    LXE
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    105142 LXE

    Patients

    Seq Age Sex Outcome Treatment
    1