BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BEI MEDICAL SYSTEMS

    MDR report key: 508024 · Received October 17, 2003

    Report

    Report Number
    508024
    Event Type
    Malfunction
    Date Received
    October 17, 2003
    Date of Event
    April 1, 2003
    Report Date
    October 1, 2003
    Manufacturer
    BOSTON SCIENTIFIC CORP
    Product Code
    MNB
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BEI MEDICAL SYSTEMS HYDRO THERMABLATOR MNB BOSTON SCIENTIFIC CORP * *

    Patients

    Seq Age Sex Outcome Treatment
    1 34 YR