BEUDAMED
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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

    NEUROFORM MICRODELIVERY STENT SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code NJE·March 23, 2007

    SELOX JT 45

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

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 23, 2008

    PALL PURECELL REO HIGH EFFICING RAPID FLOW

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

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·July 10, 2008

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 23, 2026

    [RE,O;EME 0 (3.5) 75CM HR26 9M)

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GAW·December 12, 2014

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE

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

    IAB : 8FR - 40 CC

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·April 9, 2009

    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

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 30, 2006

    CS100 INTRA-AORTIC PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·March 28, 2014

    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

    RESTORE ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 13, 2016

    KIT IMPLANTABLE SLIM TIP LEAD, 90CM

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