BEUDAMED
    290 results · 41ms · Sources: EU EUDAMED, US FDA

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    NUVASIVE SPINOUS PROCESS PLATE SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code KWP·October 12, 2011

    NEURAL INTEGRITY MONITORING SPINE SYSTEM

    FDA Adverse Event
    Other ·WARSAW ORTHOPEDIC INC.·Product code ETN·July 27, 2009

    NUVASIVE SPINOUS PROCESS PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code PEK·November 14, 2011

    NUVASIVE SPINOUS PROCESS PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code PEK·November 14, 2011

    UNK - CONSTRUCTS: ANTERIOR CERVICAL LOCKING PLATE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KWQ·May 22, 2023

    MAZOR X SYSTEM

    FDA Adverse Event
    Malfunction ·MAZOR ROBOTICS LTD·Product code OLO·December 19, 2025

    ES2 INTEGRATED BLADE SCREW SIZE L 6.5X45MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·September 29, 2020

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 18, 2013

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·April 16, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 13, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·April 13, 2015

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 10, 2014

    ES2 INTEGRATED BLADE SCREW SIZE L 6.5X50MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·December 29, 2020

    LEOPARD 9MM VBR IMPLANT

    FDA Adverse Event
    Injury ·DEPUY SPINE·Product code JDN·November 7, 2003

    VALLEYLAB

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·August 9, 2018

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 1, 2014