BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AXONICS

    MDR report key: 14640190 · Received June 8, 2022

    Report

    Report Number
    3002968685-2022-00055
    Event Type
    Malfunction
    Date Received
    June 8, 2022
    Date of Event
    May 17, 2022
    Report Date
    June 8, 2022
    Manufacturer
    AXONICS MODULATION TECHNOLOGIES, INC
    Product Code
    EZW
    UDI-DI
    10810005340141
    PMA / PMN Number
    P180046
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    THE PATIENT UNDERWENT AN EXPLANT SURGERY DUE TO LEAD MIGRATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    894631 AXONICS NEUROSTIMULATOR EZW AXONICS MODULATION TECHNOLOGIES, INC 1201 10810005340141

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown