BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZYNEX

    MDR report key: 2543062 · Received March 22, 2012

    Report

    Report Number
    1723686-2012-00006
    Event Type
    Other
    Date Received
    March 22, 2012
    Date of Event
    February 27, 2012
    Report Date
    March 22, 2012
    Manufacturer
    ZYNEX MEDICLA INC.
    Product Code
    GZJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    PT REPORTED THAT HE RECEIVED A BLISTER ON HIS SKIN FORM ONE OF THE 4 ELECTRODES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZYNEX TENS ELECTRICAL STIMULATOR GZJ ZYNEX MEDICLA INC. NEXWAVE

    Patients

    Seq Age Sex Outcome Treatment
    1 Other