BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL WALKER, ROLLATOR

    MDR report key: 3821591 · Received May 20, 2014

    Report

    Report Number
    1531186-2014-01850
    Date Received
    May 20, 2014
    Date of Event
    March 20, 2014
    Report Date
    April 7, 2014
    Manufacturer
    JUNCHENG
    Product Code
    ITJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    THE DEALER ALLEGES IT IS PULLING TO THE LEFT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    299925 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ JUNCHENG 6240-5F

    Patients

    Seq Age Sex Outcome Treatment
    1 Other