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

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    NEXGEN LCCK FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code JWH·December 17, 2015

    LEFT 16MM VARIABLE ANGLE SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·February 27, 2013

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·August 8, 2014

    SAGB QUICKCLOSE WITH VELOCITY* INJECTION PORT

    FDA Adverse Event
    Malfunction ·OBTECH MEDICAL SARL_·Product code LTI·February 16, 2011

    STEM EXTENSION STRAIGHT 24MM DIA X 100MM LENGTH(COMBINED LENGTH 145MM)

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 15, 2017

    NEXGEN LEGACY CONSTRAINED CONDYLAR KNEE ARTICULAR SURFACE WITH LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·August 3, 2016

    NEXGEN STEMMED PRECOAT TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·August 3, 2016

    ZIMMER NEXGEN ARTICUL

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·May 1, 2017

    NEXGEN LCCK ARTICULAR SURFACE WITH LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 7, 2017

    NEXGEN CR-FLEX PRECOAT FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 15, 2017

    NEXGEN STRAIGTH STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code NJL·April 13, 2017

    N-K FLEX ALL-POLY PATELLA

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 10, 2016

    NEXGEN LCCK ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 10, 2016

    NEXGEN A/P WEDGED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 10, 2016

    NEXGEN STRAIGHT STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code NJL·April 13, 2017

    NEXGEN FULL BLOCK TIBIAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·April 13, 2017