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

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    Filters Status: Injury ×

    ARCOS 18X150MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY 60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY / TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 15, 2014

    ARCOS DISTAL SCREW TI DIA5X50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS DISTAL SCREW TI DIA5X45MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY TYPE 1 TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 14, 2017

    ARCOS STS DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 23, 2017

    ARCOS MODULAR REVISION HIP SYSTEM STANDARD BROACH PROXIMAL BODY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·January 6, 2017

    ARCOS CON SZ A STD 50MM HA 0MM SZ A

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 26, 2021

    ARCOS CONE STANDARD BODY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 24, 2017

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 13, 2017

    ARCOS CON SZ C STD 60MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 18, 2019

    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

    ARCOS CON SZ A STD 70MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 21, 2018

    ARCOS 14X250MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 1, 2016

    ARCOS 17X190MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·December 5, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 13, 2017