BEUDAMED
    FDA Adverse Event Summary report: N

    DAILY ACTIVITY ASSIST DEVICES

    MDR report key: 3811757 · Received May 15, 2014

    Report

    Report Number
    1531186-2014-01787
    Date Received
    May 15, 2014
    Report Date
    December 9, 2013
    Manufacturer
    PINGHU WEIFENG MATERIAL TECHNOLOGY
    Product Code
    IKX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    LEG BUCKLED WHEN THE END USER SAT ON THE TRANSFER BENCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    289339 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX PINGHU WEIFENG MATERIAL TECHNOLOGY 98071

    Patients

    Seq Age Sex Outcome Treatment
    1 Other