BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ESPRIT

    MDR report key: 1830984 · Received September 7, 2010

    Report

    Report Number
    1000165971-2010-00886
    Event Type
    Injury
    Date Received
    September 7, 2010
    Date of Event
    August 12, 2010
    Report Date
    August 20, 2010
    Manufacturer
    SORIN BIOMEDICA CRM S.R.L.
    Product Code
    NVZ
    PMA / PMN Number
    P950029
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ON 09/07/2010, THIS EVENT CONCERNS A DEVICE THAT WAS MANUFACTURED AND USED OUTSIDE THE UNITED STATES. ANALYSIS IS PENDING.

    Description of Event or Problem · 1

    CONNECTION ISSUES DURING THE IMPLANTATION PROCEDURE; THEREFORE THE DEVICE WAS NOT IMPLANTED. ANOTHER PACEMAKER WAS SUBSEQUENTLY IMPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ESPRIT NVZ SORIN BIOMEDICA CRM S.R.L. ESPRIT SR 2440

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention