BEUDAMED
    FDA Adverse Event Other Summary report: N

    IN TOUCH ZU

    MDR report key: 1410726 · Received July 2, 2009

    Report

    Report Number
    9680128-2009-00051
    Event Type
    Other
    Date Received
    July 2, 2009
    Date of Event
    June 3, 2009
    Report Date
    June 3, 2009
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PT FOOT LEFT SIDERAIL WAS ALLEGEDLY NOT RAISING AND LOWERING PROPERLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN TOUCH ZU HOSP BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP 2141000000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA