BEUDAMED
    FDA Adverse Event Other Summary report: N

    SKYTRON

    MDR report key: 957522 · Received April 23, 2007

    Report

    Report Number
    1825014-2007-00004
    Event Type
    Other
    Date Received
    April 23, 2007
    Report Date
    April 16, 2007
    Manufacturer
    SKYTRON, DIV. THE KMW GROUP
    Product Code
    FQO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SKYTRON SURGICAL TABLE FQO SKYTRON, DIV. THE KMW GROUP 3600B *

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR