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

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    BAYER LIGAND PLUS 1, 2, 3 CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Endo GIA

    FDA UDI
    Covidien LP·10884523002836·Universal Articulating Loading Unit

    VERTEX-DENTAL B.V.

    FDA registration
    VERTEX-DENTAL B.V.·12 products·🇳🇱 Netherlands

    EGIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·April 30, 2015

    POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SCREENERS METHAMPHETAMINE TEST, DRUGSCREEN DIP METHAMPHETAMINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    C21617 DE LIFE SYSTEMS $PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 24, 2013

    ENDO GIA

    FDA Adverse Event
    Malfunction ·SURGICAL·Product code GDW·September 9, 2025

    ENDO GIA

    FDA Adverse Event
    Malfunction ·SURGICAL·Product code GDW·September 9, 2025

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·May 24, 2024

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·April 2, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 9, 2011

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·April 16, 2008

    CP82200 I MIRANDOLA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·April 6, 2012

    CP85341 FR PARIS

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

    EMORY/CL/KNNSTN ATLANTA GA1

    FDA Adverse Event
    Other ·SORIN GROUP USA·Product code DWF·August 19, 2010

    DUKE UNIV DURHAM NC 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DWF·July 15, 2011

    COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA SRL·Product code KFM·November 23, 2016

    COBE CARDIOVASCULAR REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    SORIN GROUP ITALIA·Product code KFM·February 29, 2016

    REVOLUTION CENTRIFUGAL BLOOD PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·July 20, 2018