BEUDAMED
    2,297 results · 24ms · Sources: EU EUDAMED, US FDA

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    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·June 27, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·June 27, 2013

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·November 19, 2004

    EASYTRAK

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·November 9, 2004

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·January 8, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 24, 2011

    IMPLANTABLE PACEMAKER PULSE-GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DXY·August 12, 2023

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code LWS·August 12, 2023

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code NIK·August 12, 2023

    AOL COMPLETE MOISTURE PLUS

    FDA Adverse Event
    Other ·AOM·Product code LPN·November 22, 2006

    IMPLANTABLE PACEMAKER PULSE-GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DXY·August 12, 2023

    GELFOAM STERILE SPONGE

    FDA Adverse Event
    Injury ·PHARMACIA & UPJOHN, INC.·Product code LMF·August 17, 1999

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·March 10, 2011

    THERMOGARD

    FDA Adverse Event
    Malfunction ·COMMED CORP·Product code GEI·July 1, 2003

    DEX COM SEVEN - SYSTEM SENSOR

    FDA Adverse Event
    Injury ·DEX COM·Product code MDS·November 12, 2008

    STEFFEE VSP SPINAL IMPLANT

    FDA Adverse Event
    Injury ·AOMED CORP.·Product code MCV·December 5, 1994

    LANDMARK MIDLINE I.V. CATHETER

    FDA Adverse Event
    Injury ·MENLO COM·Product code FOZ·April 9, 1993

    BIO INSTABILITY DRILL BIT 2.1MM

    FDA Adverse Event
    Malfunction ·COMMED LINVATEC·Product code HTW·November 13, 2006

    TEM/COM (DISTRIBUTED BY O/METER)

    FDA Adverse Event
    Injury ·TEM COM·Product code FLK·February 5, 2001