BEUDAMED
    1,046 results · 64ms · Sources: EU EUDAMED, US FDA

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    EQUINOX

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·April 24, 2020

    3003135857-2007-00030

    FDA Adverse Event
    Product code CBK·June 27, 2007

    3003135857-2007-00028

    FDA Adverse Event
    Product code CBK·June 27, 2007

    3003135857-2007-00025

    FDA Adverse Event
    Malfunction ·Product code CBK·May 24, 2007

    3003135857-2007-00024

    FDA Adverse Event
    Product code CBK·June 1, 2007

    NI

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code DTR·June 22, 2006

    STROLLER

    FDA Adverse Event
    Injury ·Product code BYJ·May 7, 2021

    LIBERATOR 60

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code BYJ·March 3, 2023

    SARA 3000

    FDA Adverse Event
    Malfunction ·MEDIBO MEDICAL PRODUCTS NV·Product code FSA·July 25, 2012

    VISIONAIRE 5

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code CAW·May 14, 2020

    D-100 IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·June 13, 2006

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 19, 2014

    PNEUPAC VENTIPAC WITH ALARMS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL PM, INC.·Product code CBK·January 15, 2008

    VISIONAIRE

    FDA Adverse Event
    Injury ·Product code CAW·March 11, 2021

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·February 13, 2012

    ECLIPSE

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·November 1, 2018

    CVS HEALTH

    FDA Adverse Event
    Injury ·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·March 13, 2020

    O-ARM 1000 IMAGING SYSTEM 3RD EDITION

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 16, 2016

    COULTER ® LH750

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·December 8, 2010

    MARK 5 NUVO

    FDA Adverse Event
    Malfunction ·NIDEK MEDICAL PRODUCTS, INC.·Product code CAW·October 24, 2012