BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASPEN SURGICAL SYSTEMS

    MDR report key: 93290 · Received May 23, 1997

    Report

    Report Number
    1720159-1997-00023
    Event Type
    Injury
    Date Received
    May 23, 1997
    Date of Event
    April 29, 1997
    Report Date
    May 23, 1997
    Manufacturer
    ASPEN LABORATORIES, INC.
    Product Code
    GEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL SYSTEMS SUCTION COAGULATOR GEI ASPEN LABORATORIES, INC. SUCTION COAGULATOR 97AHP002

    Patients

    Seq Age Sex Outcome Treatment
    1 * Life Threatening VALLEY LAB ESU