BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1018233-2000-00003

    MDR report key: 262160 · Received February 10, 2000

    Report

    Report Number
    1018233-2000-00003
    Event Type
    Injury
    Date Received
    February 10, 2000
    Date of Event
    October 21, 1999
    Report Date
    February 10, 2000
    Manufacturer
    C.R. BARD, INC.
    Product Code
    FEW
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FEW C.R. BARD, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1