BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEROCEL WIPE AND WICK AND CORNEAL LIGHTSHIELD

    MDR report key: 4850293 · Received June 11, 2015

    Report

    Report Number
    MW5043100
    Event Type
    Other
    Date Received
    June 11, 2015
    Date of Event
    March 25, 2015
    Report Date
    June 11, 2015
    Manufacturer
    BEAVER-VISITEC INTERNATIONAL
    Product Code
    MDM
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PROD WAS USED AS UNINTENDED. PLAN WAS TO USE GELFOAM AND SUTURE PT CLOSED WITH F/U DAYS LATER WITH REMOVAL. "WIPE WITH WICK AND CORNEAL LIGHT SHIELD" WAS IMPLANTED ACCIDENTALLY DUE TO SIMILARITIES IN APPEARANCE. REASON FOR USE: NORMAL USE IS AN INSTRUMENT WIPE, WAS IMPLANTED INSTEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    381011 MEROCEL WIPE AND WICK AND CORNEAL LIGHTSHIELD MEROCEL WIPE AND WICK AND CORNEAL LIGHTSHIELD MDM BEAVER-VISITEC INTERNATIONAL

    Patients

    Seq Age Sex Outcome Treatment
    1 12 MO