BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NONE

    MDR report key: 1191783 · Received September 30, 2008

    Report

    Report Number
    1045834-2008-00103
    Event Type
    Malfunction
    Date Received
    September 30, 2008
    Date of Event
    September 15, 2008
    Report Date
    September 30, 2008
    Manufacturer
    THE ANSPACH EFFORT
    Product Code
    ERL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NEURO-TIP BROKE DURING SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE ERL THE ANSPACH EFFORT CRANI-A

    Patients

    Seq Age Sex Outcome Treatment
    1 NA