BEUDAMED
    6 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    MODULAR HEAD COCR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 31, 2017

    ACETABULAR SHELL REGENEREX POROUS TITANIUM CONSTRUCT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·May 31, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY/TYPE I TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 31, 2017

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 31, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 29, 2016