BEUDAMED
    FDA Adverse Event Other Summary report: N

    OPTI-PLAST XT PTA DILATION CATHETER

    MDR report key: 940270 · Received August 31, 2004

    Report

    Report Number
    2020394-2004-00093
    Event Type
    Other
    Date Received
    August 31, 2004
    Date of Event
    August 4, 2004
    Report Date
    August 6, 2004
    Manufacturer
    BARD PERIPHERAL VASCULAR, INC.
    Product Code
    LIT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OPTI-PLAST XT PTA DILATION CATHETER PTA BALLOON DILATION CATHETER LIT BARD PERIPHERAL VASCULAR, INC. * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *