BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 477390 · Received August 6, 2003

    Report

    Report Number
    2021898-2003-00111
    Event Type
    Other
    Date Received
    August 6, 2003
    Report Date
    July 8, 2003
    Manufacturer
    MEDTRONIC NEUROSURGERY
    Product Code
    JXG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    EG
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THE SURGEON REPORTED THAT THE PRODUCT WAS NOT WORKING PREOPERATIVELY. NO FURTHER INFO IS AVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK CENTRAL NERVOUS SYSTEM FLUID SHUNTS AND COMPONENTS JXG MEDTRONIC NEUROSURGERY * *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN