BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HAMILTON MEDICAL, INC.

    MDR report key: 297084 · Received September 21, 2000

    Report

    Report Number
    2937708-2000-00003
    Event Type
    Malfunction
    Date Received
    September 21, 2000
    Date of Event
    September 15, 2000
    Manufacturer
    HAMILTON MEDICAL, INC.
    Product Code
    CBK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HAMILTON MEDICAL, INC. VENTILATOR CBK HAMILTON MEDICAL, INC. GALILEO *

    Patients

    Seq Age Sex Outcome Treatment
    1