BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HAMILTON MEDICAL, INC.

    MDR report key: 317518 · Received February 23, 2001

    Report

    Report Number
    2937708-2001-00001
    Event Type
    Malfunction
    Date Received
    February 23, 2001
    Date of Event
    December 4, 2000
    Manufacturer
    HAMILTON MEDICAL, INC.
    Product Code
    CBK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    7102 HAMILTON MEDICAL, INC. VEOLAR VENTILATOR CBK HAMILTON MEDICAL, INC. VEOLAR

    Patients

    Seq Age Sex Outcome Treatment
    1