BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ARGON PATIENT MONITORING KIT

    MDR report key: 82284 · Received March 25, 1997

    Report

    Report Number
    1625425-1997-90002
    Event Type
    Malfunction
    Date Received
    March 25, 1997
    Manufacturer
    ARGON MEDICAL
    Product Code
    FLN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARGON PATIENT MONITORING KIT PATIENT MONITORING KIT FLN ARGON MEDICAL * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *