BEUDAMED
    FDA Adverse Event Summary report: N

    DAILY ACTIVITY ASSIST DEVICES

    MDR report key: 2912465 · Received January 12, 2013

    Report

    Report Number
    1531186-2013-00176
    Date Received
    January 12, 2013
    Report Date
    January 12, 2013
    Manufacturer
    LERADO GLOBAL
    Product Code
    ILS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    MDR DECISION DATE: (B)(6). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. DEALER STATES THE LOCK WILL NO LONGER LOCK IN PLACE. MDR FILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    19252 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS LERADO GLOBAL UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other