BEUDAMED
    770 results · 21ms · Sources: EU EUDAMED, US FDA

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    ULTRA DRIVE 6MM PLUG PULLER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDX·July 20, 2022

    CONSOLE FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code DZI·July 2, 2015

    FOOT PEDAL FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code DZI·July 2, 2015

    HAND PIECE FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code ERL·June 12, 2015

    ULTRA DRIVE 7MM SPAGETTIBOHRER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDX·August 14, 2015

    FOOT PEDAL FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code JDX·September 2, 2015

    ULTRADRIVE III

    FDA Adverse Event
    Malfunction ·BIOMET SPORTS MEDICINE REDDING·Product code JDX·January 13, 2009

    HAND PIECE FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code JDX·April 7, 2014

    CEMENT REMOVAL HANDSET

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·December 18, 2017

    HAND PIECE FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code JDX·October 15, 2014

    GUIDE F/ACETAB+MEDULL-REAMING ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code JDX·October 28, 2014

    LED RING F/HANDLE F/PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code JDX·December 19, 2014

    SINGLE USE 8MM SCRAPER PROBE - 80MM - STERILE

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code JDX·April 28, 2021

    CEMENT REMOVAL HANDSET

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·June 3, 2021

    SINGLE USE 8MM PIERCER PROBE - STERILE

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code JDX·April 28, 2021

    HAND PIECE FOR PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JDX·November 18, 2014

    ULTRA DRIVE 9.5MM DISK DRILL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDX·October 8, 2014

    H+PIECE F/PIEZOELECTRIC SYSTEM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDX·October 2, 2014

    BONECUTTER OSTEOTOME HANDSET

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·April 15, 2021

    PIEZOSURGERY

    FDA Adverse Event
    Malfunction ·MECTRON S.P.A.·Product code JDX·May 10, 2022