BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    MDR report key: 1914015 · Received December 3, 2010

    Report

    Report Number
    6000034-2010-00755
    Event Type
    Injury
    Date Received
    December 3, 2010
    Date of Event
    November 9, 2010
    Report Date
    August 8, 2011
    Manufacturer
    COCHLEAR LTD.
    Product Code
    MCM
    PMA / PMN Number
    970051
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    PER PATIENT'S SURGEON, THE DEVICE WAS EXPLANTED IN (B)(6) OF 2010 (SPECIFIC DATE UNKNOWN); IT IS UNKNOWN IF THE PATIENT WAS REIMPLANTED WITH ANOTHER DEVICE. (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4). IMPLANTED DEVICE REMAINS.

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    PER THE CLINIC, THE PATIENT DEVELOPED MENINGITIS RESULTING IN HOSPITALIZATION AND THE DECISION TO EXPLANT THE DEVICE. EXPLANTATION IS PLANNED, BUT HAS NOT OCCURRED AS OF THE DATE OF THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM MCM, PRODUCT CODE: MCM MCM COCHLEAR LTD. CI24R (CS) N/A

    Patients

    Seq Age Sex Outcome Treatment
    1 11 YR Hospitalization| L| R