BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLUM A+ DRIVER NEW 8

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·October 18, 2012

    NEXGEN STEMMED TIBIAL BROACH IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LXH·February 21, 2014

    LDR SPINE ROI-A INTERBODY FUSION DEVICE

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MAX·August 6, 2010

    BIOMET VANGUARD PATELLA COMPONENTS

    FDA Adverse Event
    Injury ·.·Product code JWH·July 13, 2017

    BIOMET VANGUARD COMPLETE KNEE SYSTEM TIBIAL BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 12, 2017

    BIOMET REGENEREX TIBIAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·July 13, 2017

    BIOMET MCK MAXIMUM CONGRUENT KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 12, 2017