BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 773281 · Received September 6, 2006

    Report

    Report Number
    MW4004237
    Date Received
    September 6, 2006
    Report Date
    September 6, 2006
    Manufacturer
    DAL-075
    Product Code
    GZJ
    Report Source
    Voluntary report
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    CONCERNS REGARDING POSSIBLE ADULTERATED PRODUCT BEING DISTRIBUTED BY NEURO RESOURCE GROUP (NRG), A REGISTERED MEDICAL DEVICE MFR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * TENS UNIT GZJ DAL-075 * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *