BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DEFLECTABLE ORTHOGONAL CATHETER

    MDR report key: 222534 · Received April 30, 1999

    Report

    Report Number
    2020638-1999-00011
    Event Type
    Malfunction
    Date Received
    April 30, 1999
    Date of Event
    January 27, 1999
    Report Date
    March 30, 1999
    Manufacturer
    CORDIS WEBSTER INC.
    Product Code
    DRF
    Product Problem
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEFLECTABLE ORTHOGONAL CATHETER DIAGNOSTIC CATHETER DRF CORDIS WEBSTER INC. DEFL. 7FR, 16P, D TYPE 708492

    Patients

    Seq Age Sex Outcome Treatment
    1 Other