BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VIRTUERF

    MDR report key: 17086200 · Received June 7, 2023

    Report

    Report Number
    MW5118261
    Event Type
    Injury
    Date Received
    June 7, 2023
    Date of Event
    May 6, 2022
    Manufacturer
    SHENB CO LTD.
    Product Code
    GEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    HI, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    VIRTUERF SEVERE FAT LOSS TO THE FACE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    270200 VIRTUERF ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI SHENB CO LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Female