BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMITRODE 4

    MDR report key: 3133674 · Received May 20, 2013

    Report

    Report Number
    1627487-2013-04645
    Event Type
    Injury
    Date Received
    May 20, 2013
    Date of Event
    April 23, 2013
    Report Date
    April 23, 2013
    Manufacturer
    ST. JUDE MEDICAL, NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Product Problem
    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

    DEVICE 4 OF 4. REFERENCE MFR REPORT: 1627487-2013-04595. REFERENCE MFR REPORT: 1627487-2013-04596. REFERENCE MFR REPORT: 1627487-2013-04597.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    223156 LAMITRODE 4 SCS LEAD LGW ST. JUDE MEDICAL, NEUROMODULATION 3240 3253248

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Required Intervention SCS EXTENSION: MODEL 3346| IMPLANT DATE: