BEUDAMED
    11 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEXGEN FEMORAL COMPONENT OPTION FOR CEMENTED USE ONLY SIZE E LEFT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    PERSONA ARTICULAR SURFACE WITH HINGE POST EXTENSION SIZE E 20 MM HEIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    PERSONA ARTICULAR SURFACE WITH SEGMENTAL HINGE POST SIZE E 20 MM HEIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021

    RIGHT SIZE E CEMENTED OPTION FEMORAL COMPONENT FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2023

    NEXGEN FEMORAL AUGMENTS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018

    NEXGEN FEMORAL AUGMENTS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018

    RICHARD ALLEN SURGICAL NEEDLE

    FDA Adverse Event
    Other ·ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·February 21, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·February 15, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 7, 2014

    NEXGEN ROTATING HINGE KNEE FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·February 4, 2018

    NEXGEN STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018