BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON MINO

    MDR report key: 4151839 · Received October 6, 2014

    Report

    Report Number
    1627487-2014-24253
    Event Type
    Injury
    Date Received
    October 6, 2014
    Date of Event
    September 9, 2014
    Report Date
    September 16, 2014
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    IT WAS REPORTED THE PT EXPERIENCES PERSISTENT PAIN AT THE IPG SITE. THE IPG IS NOT POSITIONED FLAT IN THE POCKET. SURGICAL INTERVENTION MAY TAKE PLACE AT A LATER DATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    622939 EON MINO SCS IPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 4665313

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Other IMPLANT DATE:| SCS LEAD, MODEL 3169 (4),| IMPLANT DATE:| SCS EXTENSION, MODEL 3343 (2),| SCS ANCHOR, MODEL 1192 (4),| IMPLANT DATE: