BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    MDR report key: 5855478 · Received August 8, 2016

    Report

    Report Number
    6000034-2016-01589
    Event Type
    Injury
    Date Received
    August 8, 2016
    Date of Event
    July 20, 2016
    Report Date
    August 17, 2016
    Manufacturer
    COCHLEAR LTD
    Product Code
    MCM
    PMA / PMN Number
    P970051
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    AUDIOLOGIST

    Narratives

    Additional Manufacturer Narrative · 0

    THIS REPORT IS SUBMITTED BY COCHLEAR LIMITED (MANUFACTURER) ON BEHALF OF COCHLEAR AMERICAS. REGISTRATION NUMBER 3009092818 AND EXEMPTION NUMBER E2016011. THIS REPORT IS FILED ON AUGUST 09, 2016. H3 OTHER TEXT : DEVICE NOT RETURNED TO MANUFACTURER.

    Additional Manufacturer Narrative · 0

    THIS REPORT IS SUBMITTED BY COCHLEAR LIMITED (MANUFACTURER) ON BEHALF OF COCHLEAR AMERICAS. REGISTRATION NUMBER 3009092818 AND EXEMPTION NUMBER E2016011 THIS REPORT IS FILED AUGUST 23, 2016. (B)(4).

    Description of Event or Problem · 0

    PER THE CLINIC, THE PATIENT EXPERIENCED NEUROFIBROMATOSIS TYPE 2, RESULTING IN THE DECISION TO EXPLANT THE DEVICE. THE DEVICE WAS EXPLANTED ON (B)(6) 2016, THERE ARE NO PLANS TO REIMPLANT THE PATIENT WITH A NEW DEVICE AS OF THE DATE OF THIS REPORT AUGUST, 09, 2016.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    506371 NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM MCM MCM COCHLEAR LTD CI24RE (CA) NA

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Required Intervention