BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    REPICCI TIBIAL 37X6.5MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRY·April 20, 2015

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 18, 2018

    RECAP CMT FMRL HD RESUR 50M

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KXA·September 18, 2018

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 18, 2018

    RECAP CMT FMRL HD RESUR 50M

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KXA·September 18, 2018

    PALACOS R 1X40 SINGLE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 15, 2019

    UNKNOWN DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC..·Product code JWH·September 19, 2014

    REPICCI II UNICONDYLAR KNEE - REPICCI FMRL 54MM RM/LL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRY·May 18, 2017

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 17, 2015