BEUDAMED
    334 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    EIGHT-PLATE GUIDED GROWTH SYSTEM SCREW, 24MM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code HWC·April 20, 2009

    EXTERNAL BONE GROWTH STIMULATOR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LOF·May 15, 2007

    CERVICAL STIM CERVICAL FUSION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LOF·March 27, 2007

    MODULAR 5/8 RING, 200MM, TL-HEX

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code KTT·February 9, 2017

    CONSTRUX MINI PEEK VBR SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MQP·November 29, 2016

    FORZA IMPLANT INSERTER

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MDM·December 16, 2016

    PHOENIX MIS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code NKB·August 17, 2015

    CENTURION POCT SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code KWP·August 28, 2015

    CONSTRUX - PEEK VBR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MQP·August 5, 2015

    SPINE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MNI·September 30, 2015

    SFS II PARALLEL ROD CONNECTORS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code MNI·February 1, 2012

    TRUELOK RING FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXT·January 26, 2012

    INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code HSB·February 18, 2012

    FIREBIRD (PHOENIX)

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code NKB·January 20, 2012

    SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code MNI·February 6, 2012

    INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code HSB·January 3, 2012

    TRUELOK RING FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXT·January 20, 2012

    POSTERIOR CERVICAL SYSTEM (ASCENT POCT)

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code KWP·February 24, 2012

    FIREBIRD SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code NKB·February 1, 2012

    SFS SECOND GENERATION CROSS CONNECTOR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code MNI·January 20, 2012