BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3123080 · Received May 21, 2013

    Report

    Report Number
    1531186-2013-02184
    Date Received
    May 21, 2013
    Report Date
    April 24, 2013
    Manufacturer
    HENYI ENTERPRISE
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATED THAT THE 9099P HYDRAULIC PUMP WILL NOT HOLD THE LOAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    224855 NON AC-POWERED PATIENT LIFT 880.5510 FSA HENYI ENTERPRISE 9099P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other