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

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    Filters FDA Adverse Event ×

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·April 28, 2006

    PICC

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD)·Product code DQO·May 15, 2006

    SABRE 2400 ESU

    FDA Adverse Event
    Malfunction ·CONMED ELECTROSURGERY·Product code GEI·July 25, 2006

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·November 8, 2006

    INSERTER-MEDIUM

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code LXH·August 9, 2016

    N595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT, INC.·Product code DQA·June 12, 2006

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·March 20, 2006

    VISION ICL IMPLANTABLE COLLAMER LENS

    FDA Adverse Event
    Injury ·STAAR SURGICAL·Product code HQL·June 30, 2006

    MED-EL COMBI-40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·June 9, 2006

    KINMX PLUS, SML TIB B/PL ASSY

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·October 18, 2006

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·May 2, 2006

    MADEX PROTECTIV PLUS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL M.D. INC.·Product code FOZ·October 10, 2006

    RENU WITH MOISTURE LOC

    FDA Adverse Event
    Injury ·BASUCH & LOMB·Product code LPN·August 1, 2006

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·February 1, 2007

    ANGIOCATH PERIPHERAL VENOUS CATHETER

    FDA Adverse Event
    Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·March 30, 2006

    CLARION

    FDA Adverse Event
    Injury ·ADVANCED BIONICS CORP.·Product code MCM·December 20, 2006

    N595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code DQA·November 27, 2006

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORP.·Product code MCM·June 5, 2006

    VITALITY AVT

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007

    10MM HEMASHIELD ARTERIAL CANNULA

    FDA Adverse Event
    Death ·ABIOMED, INC.·Product code DSQ·November 30, 2006