BEUDAMED
    FDA Adverse Event Other Summary report: N

    NASAL SCOPE

    MDR report key: 1180453 · Received October 1, 2008

    Report

    Report Number
    MW5008478
    Event Type
    Other
    Date Received
    October 1, 2008
    Date of Event
    September 25, 2008
    Report Date
    October 1, 2008
    Product Code
    EOB
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    REPORTER REPORTS THAT AFTER HAVING HIS NOSE SCOPED HE NOW EXPERIENCES COLD AIR ON THE LEFT SIDE OF HIS NOSE WHEN HE INHALES, UNABLE TO SLEEP AND FEELS THAT HIS NASAL PASSAGES ARE STRETCHED AND THAT THERE MAY BE TISSUE DAMAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NASAL SCOPE NONE EOB

    Patients

    Seq Age Sex Outcome Treatment
    1 NA