BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR24000136-000

    MDR report key: 19709811 · Received July 9, 2024

    Report

    Report Number
    COR24000136-000
    Event Type
    No answer provided
    Date Received
    July 9, 2024
    Report Date
    May 30, 2024
    Product Code
    REK
    Report Source
    Manufacturer report
    Reporter Location
    MT, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1458987 REK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA