BEUDAMED
    FDA Adverse Event Summary report: N

    GOBED+

    MDR report key: 1883458 · Received October 21, 2010

    Report

    Report Number
    9680128-2010-00181
    Date Received
    October 21, 2010
    Date of Event
    September 21, 2010
    Report Date
    September 21, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE IS NOT WORKING PROPERLY. 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