BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STIMUPLEX

    MDR report key: 12664573 · Received October 20, 2021

    Report

    Report Number
    12664573
    Event Type
    Malfunction
    Date Received
    October 20, 2021
    Date of Event
    September 27, 2021
    Report Date
    September 30, 2021
    Product Code
    BXN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ANESTHESIA PROVIDERS ARE HAVING A HARD TIME SEEING THIS NEEDLE WHEN USING ULTRASOUND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1565295 STIMUPLEX STIMULATOR, NERVE, BATTERY-POWERED BXN 20H06

    Patients

    Seq Age Sex Outcome Treatment
    1