BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·November 1, 2024

    EPOLY 36MM RLC LNR MROM SZ25

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 25, 2020

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·MEDTRONIC PHYSIO-CONTROL CORP.·Product code LDD·March 21, 2002

    AUTO SUTURE MULTIFIRE ENDO GIA 30-2.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GCJ·June 29, 2000

    DURA DURATION A/P TIB LG 11

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HSH·August 28, 1998

    ZIMMER VITAMIN-E ELEVATED LINER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code OQI·September 9, 2016

    BIOMET 360 TIBIAL TRAY WITH LOCKING BAR AND SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 19, 2017

    VNGD SSK 360 FEMUR L 67.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 20, 2021