BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REDIGUARD IAB CATHETER

    MDR report key: 180989 · Received August 5, 1998

    Report

    Report Number
    1217435-1998-00232
    Event Type
    Injury
    Date Received
    August 5, 1998
    Date of Event
    May 16, 1998
    Report Date
    July 14, 1998
    Manufacturer
    BARD VASCULAR SYSTEM
    Product Code
    DSP
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REDIGUARD IAB CATHETER INTRA AORTIC BALLOON DSP BARD VASCULAR SYSTEM NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1