BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR22000171-000

    MDR report key: 15455156 · Received September 19, 2022

    Report

    Report Number
    COR22000171-000
    Event Type
    No answer provided
    Date Received
    September 19, 2022
    Report Date
    September 19, 2022
    Product Code
    MKB
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    565572 MKB

    Patients

    Seq Age Sex Outcome Treatment
    1 NA