BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VITA VVIR

    MDR report key: 292600 · Received July 11, 2000

    Report

    Report Number
    6000095-2000-00001
    Event Type
    Injury
    Date Received
    July 11, 2000
    Date of Event
    March 28, 2000
    Manufacturer
    VITATRON MEDICAL B.V.
    Product Code
    LWR
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    MAGNET RATE OF 45, NO TELEMETRY REPORTED

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITA VVIR IMPLANTABLE PULSE GENERATOR LWR VITATRON MEDICAL B.V. 310 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 000 Other