BEUDAMED
    9 results · 51ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    STIMQ NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC·Product code GZF·December 30, 2020

    FREEDOM NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZB·December 8, 2021

    FREEDOM NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZB·October 25, 2021

    STIMQ PERIPHERAL NERVE STIMULATOR SYSTEM

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·October 28, 2024

    WEARABLE ANTENNA ASSEMBLY

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·March 4, 2021

    WEARABLE ANTENNA ASSEMBLY

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·March 4, 2021

    STIMQ PERIPHERAL NERVE STIMULATOR SYSTEM

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·January 21, 2025

    PERIPHERAL NERVE STIMULATOR

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·January 11, 2022

    SPINAL CORD STIMULATOR

    FDA Adverse Event
    Malfunction ·STIMWAVE TECHNOLOGIES INC.·Product code GZB·October 30, 2019