BEUDAMED
    209 results · 47ms · Sources: EU EUDAMED, US FDA

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    FLO GARD 6301 BY TRAVENOL

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FRN·April 25, 1997

    FLO-GARD 6301 DUAL CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 25, 1997

    SELOX JT 45

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO·Product code DTB·February 20, 2008

    PALL PURECELL REO HIGH EFFICING RAPID FLOW

    FDA Adverse Event
    Injury ·PALL MEDICAL·Product code CAK·May 16, 2005

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·March 19, 2002

    ATLANTIS SR PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP·Product code DQO·April 15, 2009

    LIFELINK

    FDA Adverse Event
    Injury ·LIFELINK·Product code MCV·August 24, 2005

    AVE GFX OTW CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ARTERIAL VASCULAR ENGINEERING, INC.·Product code MAF·April 23, 1999

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 24, 2006

    OMEGA 4.75MM PEEK KNOTLESS ANCHOR SYSTEM, DOUBLE-DOUBLE

    FDA Adverse Event
    Injury ·STRYKER ENDOSCOPY-SAN JOSE·Product code MBI·February 26, 2020

    KIT IMPLANTABLE SLIM TIP LEAD, 90CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·June 26, 2020

    KIT IMPLANTABLE SLIM TIP LEAD, 90CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·June 26, 2020

    ENDEAVOR RESOLUTE RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·November 22, 2011

    NC QUANTUM APEX BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·December 18, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·September 18, 2006

    PROMUS PREMIER?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 18, 2013

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·May 13, 2015

    THERMOCOOL® SMARTTOUCH® BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·October 14, 2016

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 28, 2012

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 14, 2014