BEUDAMED
    FDA Adverse Event Injury Summary report: N

    THE MORPH DEVICE

    MDR report key: 19343507 · Received May 16, 2024

    Report

    Report Number
    MW5155091
    Event Type
    Injury
    Date Received
    May 16, 2024
    Report Date
    May 13, 2024
    Manufacturer
    UNKNOWN
    Product Code
    BWK
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    APRN USED MORPH DEVICE FOR CHRONIC PAIN MANAGEMENT WHICH LED TO STROKE. THERAPEUTIC NEUROMODULATION SYSTEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1616045 THE MORPH DEVICE STIMULATOR, ELECTRO-ACUPUNCTURE BWK UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Disability| H