BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARGON PATIENT MONITORING KIT

    MDR report key: 85373 · Received April 18, 1997

    Report

    Report Number
    1625425-1997-90012
    Event Type
    Malfunction
    Date Received
    April 18, 1997
    Manufacturer
    MAXXIM MEDICAL ARGON DIV.
    Product Code
    FLN
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TUBING DISCONNECTED FROM THE STOPCOCK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARGON PATIENT MONITORING KIT 6" EXT LINE W/STOPCOCK FLN MAXXIM MEDICAL ARGON DIV. * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *