BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ARGON PATIENT MONITORING SET

    MDR report key: 89042 · Received May 2, 1997

    Report

    Report Number
    1625425-1997-90025
    Event Type
    Injury
    Date Received
    May 2, 1997
    Date of Event
    March 28, 1997
    Manufacturer
    *
    Product Code
    FLN
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *