BEUDAMED
    FDA Adverse Event Summary report: N

    QED

    MDR report key: 2564685 · Received May 1, 2012

    Report

    Report Number
    2564685
    Date Received
    May 1, 2012
    Date of Event
    September 29, 2011
    Report Date
    February 20, 2012
    Manufacturer
    SUN NUCLEAR CORPORATION
    Product Code
    LHO
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    9UPON REMOVAL OF DOSING DIODES FROM PATIENT'S SKIN, A BLISTER WERE NOTED AT THE SITE OF ONE OF THE DIODES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QED DOSIMETER, RADIATION, DIODE DETECTOR LHO SUN NUCLEAR CORPORATION QED SCATTER 11300-2 *

    Patients

    Seq Age Sex Outcome Treatment
    1 18 YR