BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICROMAX SYSTEM CUTTERS

    MDR report key: 1191900 · Received September 30, 2008

    Report

    Report Number
    1045834-2008-00104
    Event Type
    Malfunction
    Date Received
    September 30, 2008
    Date of Event
    September 18, 2008
    Report Date
    September 30, 2008
    Manufacturer
    THE ANSPACH EFFORT, INC.
    Product Code
    ERL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CUTTER BROKE DURING USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICROMAX SYSTEM CUTTERS CUTTERS ERL THE ANSPACH EFFORT, INC. P-CRN NOT KNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA