BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARGON PATIENT MONITORING SDT

    MDR report key: 96592 · Received June 2, 1997

    Report

    Report Number
    1625425-1997-90054
    Event Type
    Malfunction
    Date Received
    June 2, 1997
    Manufacturer
    MAXXIM MEDICAL ARGON DIVISION
    Product Code
    DRS
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TUBING DISCONNECTED FROM HUB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARGON PATIENT MONITORING SDT PVC MONITORING LINE DRS MAXXIM MEDICAL ARGON DIVISION * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *