BEUDAMED
    FDA Adverse Event Other Summary report: N

    OLYMPUS

    MDR report key: 504595 · Received December 11, 2003

    Report

    Report Number
    8010047-2003-10108
    Event Type
    Other
    Date Received
    December 11, 2003
    Report Date
    November 13, 2003
    Manufacturer
    OLYMPUS OPTICAL CO. LTD.
    Product Code
    EOQ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    UNKNOWN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OLYMPUS BRONCHOSCOPE EOQ OLYMPUS OPTICAL CO. LTD. BF-P240 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other