BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INSYTE AUTOGUARD SHIELDED IV CATHETER

    MDR report key: 518583 · Received March 25, 2004

    Report

    Report Number
    1710034-2004-00009
    Event Type
    Injury
    Date Received
    March 25, 2004
    Date of Event
    February 9, 2004
    Report Date
    February 20, 2004
    Manufacturer
    BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.
    Product Code
    FOZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INSYTE AUTOGUARD SHIELDED IV CATHETER INTRAVASCULAR FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *