BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LINOX SMART S DX 65/17

    MDR report key: 4822138 · Received June 5, 2015

    Report

    Report Number
    1028232-2015-01950
    Event Type
    Injury
    Date Received
    June 5, 2015
    Date of Event
    December 5, 2013
    Report Date
    May 8, 2015
    Manufacturer
    BIOTRONIK SE & CO. KG
    Product Code
    NVY
    PMA / PMN Number
    P980023
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE IS CURRENTLY NOT AVAILABLE FOR ANALYSIS. NO CONCLUSION CAN BE DRAWN AT THIS TIME. THE INVESTIGATION WILL BE RE-OPENED SHOULD ADDITIONAL DATA BECOME AVAILABLE.

    Description of Event or Problem · 1

    WE WERE NOTIFIED BY A HOSPITAL THAT THIS LEAD WAS EXPLANTED FOR AN UNKNOWN REASON. THERE WERE NO ADVERSE PATIENT EVENTS REPORTED. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THIS FILE WILL BE UPDATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    363971 LINOX SMART S DX 65/17 ICD LEAD NVY BIOTRONIK SE & CO. KG 365501

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Hospitalization