BEUDAMED
    1,874 results · 48ms · Sources: EU EUDAMED, US FDA

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    ORTHOFIX FORZA-PTC / ORTHOFIX

    FDA Adverse Event
    Malfunction ·ORTHOFIX·Product code MAX·June 6, 2017

    MINIRAIL LENGTHENER

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code JDW·March 4, 2011

    VERONAIL

    FDA Adverse Event
    Other ·ORTHOFIX SRL·Product code JDS·November 5, 2008

    DRILL BIT D.4,8 MM L.240 MM TIN COATED - QUICK CONNECT

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·October 9, 2018

    OOSTEOTITE BONE SCREW 200/50 MM SHAFT D 6 MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HWC·March 5, 2013

    FITBONE INTRAMEDULLARY LENGTHENING NAIL TAA1180-F-245

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·September 14, 2023

    JPS SS LOCKING SCREW L70MM DOUBLE START THREAD D5.0MM STERILE

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HRS·February 13, 2024

    JPS SS NON-LOCKING SCREW L32MM DOUBLE START THREAD D4.5MM STERILE

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HRS·February 13, 2024

    JPS SS LOCKING SCREW L65MM DOUBLE START THREAD D5.0MM STERILE

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HRS·February 13, 2024

    SINGLE USE 8MM PIERCER PROBE - STERILE

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·March 27, 2018

    LONG EXTENSION REDUCER BAR FOR SINGLE USE PROBES

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·March 27, 2018

    HANDSET FOR OSCAR II

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·March 27, 2018

    COMPRESSION DISTRACTION UNIT LONG

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

    COMPRESSION DISTRACTION UNIT LONG

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

    COMPRESSION DISTRACTION UNIT LONG

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

    ORTHOFIX

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

    ORTHOFIX

    FDA Adverse Event
    Injury ·ORTHOFIX·Product code HWC·December 21, 2001

    ORTHOFIX

    FDA Adverse Event
    Malfunction ·ORTHOFIX·Product code HWC·August 6, 2009

    ORTHOFIX

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HTW·November 27, 2024

    ORTHOFIX

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code JDO·April 17, 2018