BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3191495 · Received June 26, 2013

    Report

    Report Number
    3004493922-2013-01334
    Event Type
    Malfunction
    Date Received
    June 26, 2013
    Report Date
    May 30, 2013
    Manufacturer
    INVACARE SUZHOU
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER SAYS THE 9805P HYDRAULIC LIFT LOWERS WITH WEIGHT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    290031 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other