BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BASIC CONFIGURATION MODEL ST104

    MDR report key: 1972313 · Received December 30, 2010

    Report

    Report Number
    1831750-2010-05403
    Event Type
    Malfunction
    Date Received
    December 30, 2010
    Date of Event
    December 6, 2010
    Report Date
    December 6, 2010
    Manufacturer
    STRYKER CORP, MED DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE HYDRAULICS AND THE GAS SPRING ARE OUT OF FUNCTION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BASIC CONFIGURATION MODEL ST104 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MED DIV ST104BASIC NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA