BEUDAMED
    FDA Adverse Event Other Summary report: N

    PRECISION MEDICAL

    MDR report key: 591082 · Received April 11, 2005

    Report

    Report Number
    2523148-2005-00002
    Event Type
    Other
    Date Received
    April 11, 2005
    Date of Event
    March 22, 2005
    Report Date
    March 22, 2005
    Manufacturer
    PRECISION MEDICAL INC.
    Product Code
    CAN
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FLOW METER BLOEW APART HITTING THE EKG TECHNICIAN IN THE FACE AND THE HAND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION MEDICAL REGULAR/FLOWMETER CAN PRECISION MEDICAL INC. 1600M 0800

    Patients

    Seq Age Sex Outcome Treatment
    1 *