BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AXONICS

    MDR report key: 14079251 · Received April 11, 2022

    Report

    Report Number
    3002968685-2022-00031
    Event Type
    Injury
    Date Received
    April 11, 2022
    Date of Event
    March 18, 2022
    Report Date
    April 11, 2022
    Manufacturer
    AXONICS MODULATION TECHNOLOGIES, INC
    Product Code
    EZW
    UDI-DI
    10810005340141
    PMA / PMN Number
    P180046
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    THE COMPANY WAS MADE AWARE THAT A PATIENT HAD FALLEN ON THEIR IMPLANT SITE WHICH RESULTED IN PAIN. THE PHYSICIAN PERFORMED A LEAD REVISION TO RESOLVE THE ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    132735 AXONICS NEUROSTIMULATOR EZW AXONICS MODULATION TECHNOLOGIES, INC 1201 10810005340141

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown