BEUDAMED
    FDA Adverse Event Other Summary report: N

    GOBED II

    MDR report key: 1891009 · Received November 1, 2010

    Report

    Report Number
    9680128-2010-00246
    Event Type
    Other
    Date Received
    November 1, 2010
    Date of Event
    September 30, 2010
    Report Date
    September 30, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK