BEUDAMED
    9 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OSSEOTITE® IMPLANT 4 X 15MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·July 9, 2021

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·May 16, 2022

    COMP RVS TRAY CO 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    ARCOM XL 44-36 STD HMRL BRNG RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 15, 2014

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·September 17, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 29, 2013

    BIOMET TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 2, 2018