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

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    Filters FDA Adverse Event ×

    DELTA CER HEAD 12/14 32MM +1

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code LZO·March 13, 2013

    SM BONE FASTAK, TAPERED NEEDLE W/#2-0 FIBERWIRE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·February 25, 2011

    ADVANCED VENOUS ACCESS CATHETER

    FDA Adverse Event
    Other ·EDWARDS LIFESCIENCES, PR·Product code DQO·February 14, 2008

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 8, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019

    TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 26, 2018

    TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 26, 2018

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·October 8, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 8, 2019

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019