BEUDAMED
    FDA Adverse Event Other Summary report: N

    COR23000256-000

    MDR report key: 18385743 · Received December 22, 2023

    Report

    Report Number
    COR23000256-000
    Event Type
    Other
    Date Received
    December 22, 2023
    Report Date
    December 21, 2023
    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
    632402 MKB

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other