BEUDAMED
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    Filters FDA Adverse Event ×

    ARSENAL PETITE LAPIDUS PLATE, R

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

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·September 2, 2009

    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

    OLSEN

    FDA Adverse Event
    Other ·OLSEN MEDICAL·Product code GEI·March 12, 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

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 4, 2011

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

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

    TIMAX

    FDA Adverse Event
    Malfunction ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 15, 2009

    TIMAX

    FDA Adverse Event
    Malfunction ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 15, 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

    UNK

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·November 18, 2009

    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

    SYMPHONY

    FDA Adverse Event
    Malfunction ·ELA MEDICAL, S.A.S.·Product code DXY·March 11, 2009

    HTA PROCERVA PROCEDURE SET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MNB·October 13, 2009

    NI

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