BEUDAMED
    FDA Adverse Event Other Summary report: N

    SKYTRON

    MDR report key: 475031 · Received July 29, 2003

    Report

    Report Number
    1825014-2003-00003
    Event Type
    Other
    Date Received
    July 29, 2003
    Date of Event
    March 1, 2002
    Report Date
    July 25, 2003
    Manufacturer
    SKYTRON (DIV. OF KNW GROUP)
    Product Code
    FTD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SKYTRON SURGICAL LIGHT FTD SKYTRON (DIV. OF KNW GROUP) * *

    Patients

    Seq Age Sex Outcome Treatment
    1