BEUDAMED
    327 results · 64ms · Sources: EU EUDAMED, US FDA

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    MANSFIELD EP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code DYB·November 10, 1999

    DISPOSABLE SUTURE PLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code FHQ·December 10, 2010

    ROTAGLIDE LUBRICANT

    FDA Adverse Event
    Injury ·BOSTON ONE SCIENTIFIC·Product code MCX·June 9, 2011

    COAPTITE

    FDA Adverse Event
    Injury ·BIOFORM MEDICAL, INC.·Product code LNM·June 16, 2007

    DISPOSABLE SUTURE PLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code GCJ·December 7, 2010

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·October 27, 2021

    COAPTITE

    FDA Adverse Event
    Death ·BIOFORM MEDICAL, INC.·Product code LNM·June 20, 2006

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·June 4, 2009

    PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

    FDA Adverse Event
    Death ·COVIDIEN·Product code FGE·June 24, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·July 10, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·July 1, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·July 10, 2019

    ZIMMON PANCREATIC STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 1, 2020

    GEENEN PANCREATIC STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·October 1, 2020