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

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    Filters Status: Injury ×

    GM HELIX ACQUA IMPLANT,TI,5.0X16

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·May 16, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 6, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 22, 2018

    GM DRIVE ACQUA IMPLANT 3.5X8 MM

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·August 29, 2018

    GM HELIX ACQUA IMPLANT 3.75X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    GM HELIX IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 29, 2018

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    GM HELIX ACQUA IMPLANT 3.5X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    GM DRIVE IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 20, 2018

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 11, 2013

    PFCSIG FLUT FEMROD 5DG12X125MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 8, 2011

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    PERF CON TIB BRG LRG 22X60

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    NON-POROUS PERF TIB TRAY-LGE

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    PERF ANAT TIBIAL STEM 120X14X5

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    PEDICLE SCREW PEDICLE SCREW 6X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018