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

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    Filters FDA Adverse Event ×

    MAXLOCK EXTREME

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

    MUSCULOSKELETAL

    FDA Adverse Event
    Other ·MFT·Product code HWC·December 15, 2006

    AFT

    FDA Adverse Event
    Other ·MFT·Product code MBP·August 1, 2007

    AFT - 1 DIVERTED TUBE

    FDA Adverse Event
    Other ·MFT·Product code MBP·February 25, 2008

    ACRYSOF

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

    CRIT-LINE BLOOD CHAMBER

    FDA Adverse Event
    Malfunction ·CONCORD MFT·Product code KOC·April 30, 2014

    BD Q-SYTE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.·Product code FMF·July 21, 2009

    ACRYSOF

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

    CANNULA, 8MM, REGULAR, IS2000

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·September 21, 2007

    LAMITRODE 4

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

    PARKER BATH

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code ILM·September 23, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·February 17, 2011

    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

    AUTO SUTURE SURGITIE

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code MFT·January 6, 1998

    85" TEXIUM SET 20DP INLINE DP 1 YSITE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 11, 2021

    ACRYSOF

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

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., MEDREL·Product code MHY·December 7, 2006

    DBX

    FDA Adverse Event
    Malfunction ·MUSCULOSKELETAL TRANSPLANT FOUNDATION, INC.·Product code MQV·February 4, 2020