BEUDAMED
    FDA Adverse Event Other Summary report: N

    NEUROSIGN

    MDR report key: 285423 · Received July 4, 2000

    Report

    Report Number
    8021774-2000-00002
    Event Type
    Other
    Date Received
    July 4, 2000
    Date of Event
    June 19, 2000
    Report Date
    July 3, 2000
    Manufacturer
    THE MAGSTIM COMPANY LTD.
    Product Code
    GXZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    ONE OF THE NEEDLE ELECTRODES BECAME DETACHED FROM ITS LEAD, RESULTING IN THE NEEDLE BEING LEFT IN THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEUROSIGN 30MM REUSEABLE NEEDLE ELECTRODE SET GXZ THE MAGSTIM COMPANY LTD. REUSEABLE NEEDLE ELECTRODE SET FOR NEUROSIGN 400 35283

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR Other