BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BARD UROLOGICAL CATHETER

    MDR report key: 419269 · Received September 27, 2002

    Report

    Report Number
    1018233-2002-00029
    Event Type
    Injury
    Date Received
    September 27, 2002
    Date of Event
    May 29, 2002
    Report Date
    September 27, 2002
    Manufacturer
    *
    Product Code
    FEW
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD UROLOGICAL CATHETER UROLOGICAL CATHETER FEW * * *

    Patients

    Seq Age Sex Outcome Treatment
    1