BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SUNETICS

    MDR report key: 13358746 · Received January 25, 2022

    Report

    Report Number
    MW5106987
    Event Type
    Injury
    Date Received
    January 25, 2022
    Date of Event
    January 21, 2022
    Report Date
    January 22, 2022
    Manufacturer
    SUNETICS INTERNATIONAL MARKETING GROUP, LLC
    Product Code
    OAP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    HEADACHES. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36434 SUNETICS LASER, COMB, HAIR OAP SUNETICS INTERNATIONAL MARKETING GROUP, LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 33 YR Female