BEUDAMED
    197 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ARSENAL PETITE LAPIDUS PLATE, R

    FDA Adverse Event
    Injury ·TRILLIANT SURGICAL·Product code HRS·April 3, 2020

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·February 11, 2009

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH. LTD.·Product code HQL·July 2, 2009

    ACRYSOF TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD / HUNTINGTON·Product code MJP·November 11, 2009

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code JDI·October 6, 2008

    NEXGEN STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER·Product code JWH·June 20, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·May 20, 2009

    TIMAX

    FDA Adverse Event
    Injury ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·September 23, 2010

    AXIUM DETACHABLE COIL

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code HCG·May 26, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·June 21, 2009

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·May 19, 2009

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·March 19, 2009

    SYBRONPRO TL

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·February 17, 2009

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·May 20, 2009

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·January 19, 2009

    BLADELESS VP 5MM W/ FIXATION

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GCJ·February 20, 2009

    REPLY DR

    FDA Adverse Event
    Injury ·SORIN BIOMEDICA CRM S.R.L.·Product code DXY·October 19, 2009

    SAGB QUICK CLOSE

    FDA Adverse Event
    Injury ·OBTECH MEDICAL SARL·Product code LTI·June 19, 2009

    ELEVATE ANTERIOR

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·February 25, 2010

    FOLEY STANDARD 3-WAY 22FR. 30ML BALLOON

    FDA Adverse Event
    Injury ·ROCHESTER MEDICAL CORP.·Product code EZL·November 30, 2009