BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 3024209 · Received March 27, 2013

    Report

    Report Number
    1531186-2013-01304
    Date Received
    March 27, 2013
    Report Date
    February 28, 2013
    Manufacturer
    JUMAO MEDICAL EQUIPMENT
    Product Code
    IOR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PROVIDER STATES SEAT GUIDE IS BROKEN. MDR FILE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    125943 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V20RLR

    Patients

    Seq Age Sex Outcome Treatment
    1 Other