BEUDAMED
    10,000 results · 181ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    NEXGEN ALL POLY PATELLA

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·September 7, 2018

    NEXGEN ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 7, 2018

    NEXGEN STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·September 7, 2018

    NEXGEN CR-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·September 7, 2018

    MEDTRONIC SPINAL CORD STIMULATOR (NOT IN PROTOCOL)

    FDA Adverse Event
    Other ·Product code LGW·September 16, 2009

    MODULAR ANALYTICS CORE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 22, 2008

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·January 25, 2008

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·August 10, 2007

    ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT

    FDA Adverse Event
    Injury ·A.I.D.D LONGFORD·Product code MMI·June 20, 2022

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·October 28, 2024

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 18, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code NIQ·September 17, 2003

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·June 6, 2007

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 17, 2014

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 18, 2014

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·September 3, 2014

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 18, 2014

    DYNASTY(R) COCR LINER

    FDA Adverse Event
    MICROPORT ORTHOPEDICS INC.·Product code JDL·March 28, 2016

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·November 30, 2016

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·November 30, 2016