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

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    Filters Status: Death ×

    PLUM INFUSION PUMP

    FDA Adverse Event
    Death ·ABBOTT LABORATORIES·Product code FRN·July 30, 2004

    PCA II PUMP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE (SG)·Product code MEA·August 22, 2001

    3M

    FDA Adverse Event
    Death ·SMITH'S MEDICAL MD, INC.·Product code FPA·December 23, 2004

    CORFLO-ULTRA NG

    FDA Adverse Event
    Death ·CORPAK MEDSYSTEMS, INC.·Product code FPD·August 26, 1996

    SPECTRUM IQ IV PUMP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 1, 2021

    DRAGER EVITA

    FDA Adverse Event
    Death ·DRAGER, INC.·Product code CBK·June 2, 1999

    KIWI OMNICUP TRACTION FORCE

    FDA Adverse Event
    Death ·CLINICAL INNOVATIONS·Product code HDB·May 8, 2018

    RELAY NBS PRO THORACIC STENT-GRAFT

    FDA Adverse Event
    Death ·BOLTON MEDICAL, INC.·Product code MIH·June 11, 2021

    ACS MULTI-LINK DUET CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·GUIDANT VASCULAR INTERVENTION·Product code MAF·April 27, 1999

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE (SG)·Product code FRN·March 13, 2002

    PULMONETICS LTV 950

    FDA Adverse Event
    Death ·PULMONETICS SYSTEMS·Product code CBK·July 31, 2008

    PATIENT WORN DEVICE

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code DSI·December 16, 2008

    SIMPLEX P RADIOPAQUE UNIT

    FDA Adverse Event
    Death ·HOWMEDICA INC.·Product code LOD·February 10, 1999

    J & J

    FDA Adverse Event
    Death ·CORDIS·Product code NIQ·March 11, 2004

    COOK

    FDA Adverse Event
    Death ·COOK CARDIOLOGY·Product code MAF·September 11, 1997

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Death ·NORTH HAVEN - USS·Product code GDW·June 18, 2008

    FLEXIFLO III ENTERNAL NUTRITION PUMP

    FDA Adverse Event
    Death ·ROSS PRODUCTS DIVISION ABBOTT LABORATORIES·Product code LZH·January 8, 1998

    NAVIGATION SYSTEM (DEVICE AVAILABLE)

    FDA Adverse Event
    Death ·COVIDIEN, INC.·Product code EOQ·May 11, 2015

    INTROFLEX PERCUTANEOUS SHEATH INTRODUCER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DYB·October 19, 2005

    FRESENIUS USA

    FDA Adverse Event
    Death ·FRESENIUS USA·Product code FID·April 10, 2003