BEUDAMED
    FDA Adverse Event Summary report: N

    DAILY ACTIVITY ASSIST DEVICES

    MDR report key: 3734604 · Received April 8, 2014

    Report

    Report Number
    1531186-2014-01232
    Date Received
    April 8, 2014
    Date of Event
    January 1, 2014
    Report Date
    March 10, 2014
    Manufacturer
    UNKNOWN
    Product Code
    IKX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SEAT OF THE SHOWER CHAIR IS CRACKED IN THE FRONT BETWEEN THE LEGS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    210626 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX UNKNOWN 9780

    Patients

    Seq Age Sex Outcome Treatment
    1 70 Other