BEUDAMED
    FDA Adverse Event Other Summary report: N

    CONMED DISPERSIVE ELECTRODE

    MDR report key: 507944 · Received January 5, 2004

    Report

    Report Number
    1317214-2003-00071
    Event Type
    Other
    Date Received
    January 5, 2004
    Date of Event
    December 3, 2003
    Report Date
    December 5, 2003
    Manufacturer
    CONMED CORP
    Product Code
    JOS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    "IT WAS REPORTED THAT" PT SHOWED BLISTERING AFTER PAD WAS REMOVED. PAD WAS ON THE LEFT THIGH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED DISPERSIVE ELECTRODE DISPERSIVE ELECTRODE JOS CONMED CORP NA 0305271

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other CITRAZIN OINTMENT