BEUDAMED
    2,346 results · 26ms · Sources: EU EUDAMED, US FDA

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    XIA 3 TITANIUM BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-FRANCE·Product code MNI·May 23, 2017

    THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER INC·Product code LPB·June 24, 2024

    THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 24, 2024

    UNK_SMART TOUCH UNIDIRECTIONAL

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 23, 2025

    ETM FLUSH CUT DISTAL-END CUTTER WITH SAFETY HOLD

    FDA Adverse Event
    Injury ·ORMCO CORPORATION·Product code EKD·December 9, 2016

    NI

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. AG ORTHOPAEDIC DIVISION·Product code EKD·February 26, 2010

    VISIONAIRE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV·Product code EKD·February 11, 2010

    ADSN TISS FCPS 4-3/4 1X2

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code EKD·June 26, 2014

    INDIANA TOME

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code EKD·January 31, 2002

    INDIANA TOME

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code EKD·May 12, 1999

    MALLET

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code EKD·May 15, 2013

    SECURITY BLADE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPAEDICS·Product code EKD·October 25, 2005

    INSTRUMENT, MANUAL, SURGICAL

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code EKD·October 28, 2005

    VISIONAIRE TIBIA GI

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code EKD·March 17, 2011

    MOPS

    FDA Adverse Event
    Injury ·Product code EKD·September 14, 2021

    INDIANA TOME

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code EKD·June 17, 1998

    JACOBSON MICRO MOSQ 5 CV

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code EKD·December 24, 2014

    OMFS010-002 AND OMFS010-003

    FDA Adverse Event
    Malfunction ·UNK·Product code EKD·November 9, 2016

    INDIANA TOME SYSTEM

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code EKD·April 4, 2008

    FEM RASP TRIAL CO/FJD T11

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code EKD·July 20, 2018