BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM304 M-SERIES W/ZOOM

    MDR report key: 1875029 · Received October 13, 2010

    Report

    Report Number
    1831750-2010-02805
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 14, 2010
    Report Date
    September 14, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE TOP SIDE RAIL WAS BROKEN AND RIGHT HANDLE BROKEN. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM304 M-SERIES W/ZOOM STRETCHER, WHEELED, POWERED INK STRYKER CORP., MEDICAL DIV 1025 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK