BEUDAMED
    75 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    MAXLOCK EXTREME

    FDA Adverse Event
    Injury ·ORTHOHELIX SURGICAL DESIGN·Product code HRS·January 5, 2012

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·July 10, 1997

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES·Product code HQL·July 28, 1997

    LAMITRODE 4

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 21, 2014

    PULSE GEN MODEL 106

    FDA Adverse Event
    Injury ·CYBERONICS - HOUSTON·Product code LYJ·May 7, 2018

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 12, 2017

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 12, 2017

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·September 17, 1997

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·April 8, 2013

    TACTICATH¿ QUARTZ CONTACT FORCE ABLATION CATHETER

    FDA Adverse Event
    Injury ·VENUSA DE MEXICO S.A. DE C.V.·Product code OAE·April 30, 2019

    CRTS SML SGA VLV

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·May 15, 2026

    MAXLOCK EXTREME SYSTEM Y PLATE

    FDA Adverse Event
    Injury ·TORNIER INC.·Product code HRS·June 21, 2016

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code GZB·October 27, 2017

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 26, 2007

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 26, 2007

    SURGICAL STAINLESS STEEL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAT·September 19, 2007

    CERTAS PLUS ELECTRONIC TOOL KIT

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·May 29, 2026

    HEARTMATE II LEFT VENTRICULAR ASSIST SYSTEM, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·September 25, 2018

    MITRACLIP SYSTEM STEERABLE GUIDE CATHETER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DRA·November 5, 2019

    UNKNOWN CERTAS PLUS VALVE

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·May 29, 2026