BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SUCTION COAGULATOR

    MDR report key: 842210 · Received April 20, 2007

    Report

    Report Number
    2242056-2007-00001
    Event Type
    Injury
    Date Received
    April 20, 2007
    Date of Event
    February 26, 2007
    Report Date
    April 18, 2007
    Manufacturer
    ALTO DEVELOPMENT CORP., D/B/A A&E MEDICAL CORP.
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUCTION COAGULATOR SUCTION CAUTERY GEI ALTO DEVELOPMENT CORP., D/B/A A&E MEDICAL CORP. NA 087C

    Patients

    Seq Age Sex Outcome Treatment
    1 4 YR Required Intervention