BEUDAMED
    10,000 results · 58ms · Sources: EU EUDAMED, US FDA

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    KWP

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWQ·January 6, 2014

    KWP

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code HSB·January 8, 2024

    KWP, MNH, MNI

    FDA Adverse Event
    Injury ·ALPHATEC SPINE INC·Product code KWP·August 13, 2015

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWP·April 7, 2016

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·October 4, 2017

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·October 30, 2017

    ORTHOSIS,PEDICLE SPINAL FIXATION

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·December 8, 2015

    CD HORIZON® BALLAST¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·February 6, 2024

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 25, 2015

    REVERE

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code KWQ·January 30, 2017

    6.0MM TI HARD ROD 300MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNH·March 8, 2013

    2520274-2013-05265

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MNI·September 4, 2013

    CREO

    FDA Adverse Event
    Malfunction ·GLOBUS MEDICAL, INC.·Product code MNH·February 29, 2024

    CREO

    FDA Adverse Event
    Malfunction ·GLOBUS MEDICAL, INC.·Product code MNH·February 29, 2024

    MIS SINGLE INNER SETSCW

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·January 5, 2024

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·September 21, 2016

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNH·April 4, 2014

    COCR DD ROD 3.5-5.5 X 600

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code NKG·November 15, 2021

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MNH·January 28, 2014