BEUDAMED
    FDA Adverse Event Other Summary report: N

    GOBED+

    MDR report key: 1901185 · Received November 10, 2010

    Report

    Report Number
    9680128-2010-00292
    Event Type
    Other
    Date Received
    November 10, 2010
    Date of Event
    October 17, 2010
    Report Date
    October 17, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT NO POWER TO THE BED. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK