BEUDAMED
    7,846 results · 35ms · Sources: EU EUDAMED, US FDA

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    MPQ-42

    FDA 510(k)
    FDA Class 2 ·Radiology

    Macroplastique Implants

    FDA UDI
    Uroplasty, Inc.·08717591240266·Soft tissue bulking agent indicated for transur...

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Injury ·UROPLASTY, LLC·Product code LNM·June 10, 2016

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY LLC·Product code LNM·October 14, 2016

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·March 2, 2018

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·February 16, 2018

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·February 16, 2018

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·April 25, 2019

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Injury ·UROPLASTY, LLC·Product code LNM·March 13, 2018

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·May 9, 2019

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·March 9, 2018

    MACROPLASTIQUE IMPLANTS

    FDA Adverse Event
    Malfunction ·UROPLASTY, LLC·Product code LNM·April 25, 2019

    ITREL 3

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 11, 2016

    PALMAZ MEDIUM ON POWERFLEX PLUS

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code FGE·May 16, 2007

    X-CORE

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code MPQ·September 8, 2025

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·NUVASIVE, INCORPORATED·Product code MPQ·November 4, 2020

    UNKNOWN

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code MPQ·February 2, 2011

    HEIGHT EXPANSION DRIVER

    FDA Adverse Event
    Malfunction ·K2M, INC.·Product code MPQ·December 13, 2021

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·June 4, 2014

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 4, 2014