BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEUROVISION COBRA 3-PLATE EMG ET TUBE ENDOTRACHEAL TUBE

    MDR report key: 19722077 · Received July 10, 2024

    Report

    Report Number
    MW5157195
    Event Type
    Injury
    Date Received
    July 10, 2024
    Date of Event
    July 8, 2024
    Manufacturer
    NEUROVISION MEDICAL PRODUCTS, INC.
    Product Code
    ETN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NEUROVISION COBRA 3-PLATE EMG ET TUBE WAS PLACED, BUT IMMEDIATELY BECAME KINKED AND TIDAL VOLUMES COULD NOT BE DELIVERED. TUBE WAS REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2385367 NEUROVISION COBRA 3-PLATE EMG ET TUBE ENDOTRACHEAL TUBE STIMULATOR, NERVE ETN NEUROVISION MEDICAL PRODUCTS, INC. LTE7003PS 052024B

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Female Required Intervention