BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 7, 2010

    HEMOSPLIT, 14.5 FR, STANDARD KIT, 19 CM, STRAIGHT

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code MSD·December 4, 2012

    SYNCHROMED II

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

    IMPLANTABLE DRUG INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·November 7, 2024