BEUDAMED
    FDA Adverse Event Other Summary report: N

    CONMED CORPORATION

    MDR report key: 232408 · Received July 9, 1999

    Report

    Report Number
    232408
    Event Type
    Other
    Date Received
    July 9, 1999
    Date of Event
    June 1, 1999
    Report Date
    July 9, 1999
    Manufacturer
    CONMED CORP
    Product Code
    KMK
    Report Source
    User Facility report
    Reporter Location
    CT, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DARK SKINNED FEMALE HAS DARKENED (IMPRINT) PIGMENTATION ON FOREARM DUE TO DEVICE USED WITH IV ADMINISTRATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION VENI-GUARD TM IV DRESSING KMK CONMED CORP 705-4431 2004-03-9903051

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other