BEUDAMED
    FDA Adverse Event Summary report: N

    DAILY ACTIVITY ASSIST DEVICES

    MDR report key: 3840345 · Received May 30, 2014

    Report

    Report Number
    1531186-2014-02012
    Date Received
    May 30, 2014
    Date of Event
    February 26, 2014
    Report Date
    February 27, 2014
    Manufacturer
    UNKNOWN
    Product Code
    ILS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATED THAT THE SEAT ON A 6500-BHD COMMODE HAS CRACKED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    318594 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS UNKNOWN 6500-BHD

    Patients

    Seq Age Sex Outcome Treatment
    1 Other