BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MORPHEUS, 8

    MDR report key: 19894605 · Received August 1, 2024

    Report

    Report Number
    MW5157943
    Event Type
    Injury
    Date Received
    August 1, 2024
    Date of Event
    August 25, 2023
    Report Date
    July 30, 2024
    Manufacturer
    INMODE LTD.
    Product Code
    GEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MORPHEUS 8 SKIN TREATMENT WHICH HAS LED TO FACIAL FAT LOSS, I WAS TOLD AT START OF TREATMENT THAT WOULD NOT HAPPEN. TODAY LOOKING FOR FAT LOSS TREATMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    384662 MORPHEUS, 8 ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI INMODE LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Female MULTIVITAMIN