BEUDAMED
    FDA Adverse Event Other Summary report: N

    8010456-2006-00001

    MDR report key: 728808 · Received June 21, 2006

    Report

    Report Number
    8010456-2006-00001
    Event Type
    Other
    Date Received
    June 21, 2006
    Product Code
    LYT
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    SINCE THIS INSTRUMENT IS FAULTLESS AS TO ITS TECHNICAL FUNCTIONS, WE FEEL THAT NO CORRECTIVE OR PREVENTIVE ACTIONS HAVE TO BE TAKEN ON OUR PART. THE TIPS OF THE INSTRUMENT INVOLVED WERE POLISHED/REFURBISHED AND THE FORCEPS WERE RETURNED TO THE DISTRIBUTOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LYT

    Patients

    Seq Age Sex Outcome Treatment
    1