BEUDAMED
    82 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LAG SCREWDRIVER RETENTION ROD

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·April 11, 2018

    CABLE

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·May 2, 2019

    INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·July 16, 2015

    EIGHT-PLATE GUIDED GROWTH SYSTEM SCREW, 24MM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HWC·March 20, 2009

    PILLAR SPACER SYSTEM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code MAX·June 3, 2014

    FORZA

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code MAX·April 24, 2014

    PILLAR SPACER SYSTEM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code MAX·June 3, 2014

    ORTHOFIX BONE GROWTH STIMULATOR 5212

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code LOF·November 22, 2017

    ORTHOFIX

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code JDW·July 11, 2003

    DYNAMIC AXIAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code JDW·June 7, 2007

    ISKD INTRAMEDULLARY SKELETAL KINETIC DISTRACT

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·June 29, 2007

    EIGHT PLATE SCREW, 32MM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HRS·June 29, 2007

    ISKD INTRAMEDULLARY SKELETAL KINETIC DISTRACT

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·November 13, 2008

    ISKD INTRAMEDULLARY SKELETAL KINETIC DISTRACT

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·October 10, 2007

    EIGHT-PLATE GUIDED GROWTH SYSTEM SCREW, 32MM

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HWC·December 10, 2008

    ORTHOFIX STANDARD CD MODULE

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code JEC·February 11, 2003

    PILLAR SPACER SYSTEM

    FDA Adverse Event
    Injury ·ORTHOFIX INC·Product code MAX·August 4, 2011

    ISKD INTRAMEDULLARY SKELETAL KINETIC DISTRACT

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·April 14, 2009

    ISKD INTRAMEDULLARY SKELETAL KINETIC DISTRACT

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code HSB·April 20, 2009

    TRUE/LOK WIRE 1.8MM WIRE WITH CENTRAL OLIVE

    FDA Adverse Event
    Injury ·ORTHOFIX INC.·Product code LXT·May 28, 2009