BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEUROMARK RADIOFREQUENCY PROBE

    MDR report key: 24134115 · Received January 21, 2026

    Report

    Report Number
    MW5182584
    Event Type
    Injury
    Date Received
    January 21, 2026
    Date of Event
    January 5, 2026
    Report Date
    January 15, 2026
    Manufacturer
    NEURENT MEDICAL LIMITED
    Product Code
    GEI
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    302667 NEUROMARK RADIOFREQUENCY PROBE ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI NEURENT MEDICAL LIMITED NMK00301

    Patients

    Seq Age Sex Outcome Treatment
    1