BEUDAMED
    FDA Adverse Event Other Summary report: N

    DUPEN EPIDURAL CATHETER

    MDR report key: 16231 · Received June 14, 1994

    Report

    Report Number
    16231
    Event Type
    Other
    Date Received
    June 14, 1994
    Date of Event
    June 13, 1994
    Report Date
    June 14, 1994
    Manufacturer
    DAVOL, INC.
    Product Code
    BSO
    Report Source
    User Facility report
    Reporter Location
    IN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    INITIAL INSERTION OF CATHETER 10/28/93. REMOVAL OF CATHETER DONE IN SURGERY. PT'S PHYSICIAN STATED CATHETER REMOVAL NECESSARY DUE TO PT'S NONCOMPLIANCE, WOULD DISCONNECT CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DUPEN EPIDURAL CATHETER Implant EPIDURAL CATHETER BSO DAVOL, INC. 60290-2 36AD1871

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Other