BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IOCTRODE

    MDR report key: 3052623 · Received April 2, 2013

    Report

    Report Number
    1627487-2013-06124
    Event Type
    Injury
    Date Received
    April 2, 2013
    Date of Event
    March 11, 2013
    Report Date
    March 11, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    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 INFO RELATED TO THE PT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 3 OF 4. REF MFR REPORTS: 1627487-2013-06122, 1627487-2013-06123, 1627487-2013-06125.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    133718 IOCTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3189 3628737

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Required Intervention IMPLANT DATE:| SCS EXTENSION: MODEL 3386 (X2)| SCS IPG: MODEL 3716| IMPLANT DATE: