BEUDAMED
    66 results · 32ms · Sources: EU EUDAMED, US FDA

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    OPUS SPEEDSTITCH SUTURE DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EQUINOXE PRIMARY SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·August 25, 2022

    MODIFICATION TO THERMAL ANGEL

    FDA 510(k)
    FDA Class 2 ·Hematology

    PHACOFRAGMENTATION SYSTEM MEGATRON

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    36MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 13, 2016

    UNKNOWN EXCEED HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 5, 2016

    UNKNOWN RECAP 48MM HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 16, 2016

    36MM 12/14 TPR FEM HEAD -4 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    EXCEED ABT M2A-36 MOD HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    EXCEED ABT RINGLOC-X SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·July 20, 2017

    M2A MOD HD COCR DIA28/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·December 23, 2015

    32MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 16, 2016

    RECAP/MAGNUM ACETABULAR SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 15, 2017

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 27, 2020

    EXCEED ABT M2A-36 MOD HEAD -3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 1, 2016

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 27, 2019

    ECHOTIP ULTRA

    FDA Adverse Event
    Malfunction ·COOK MEDICAL, ENDOSCOPY·Product code FCG·April 5, 2013

    EXCLAIM 8 SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 31, 2011

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019