BEUDAMED
    417 results · 43ms · Sources: EU EUDAMED, US FDA

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    UNKNOWN MEDIUM PRESSURE FLOW CONTROL VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·April 3, 2013

    SYNCHROMED 2

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LKK·July 17, 2009

    NEUROBLATE SYSTEM

    FDA Adverse Event
    Injury ·MONTERIS MEDICAL·Product code GEX·June 18, 2021

    INTELLIVUE MX400 PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·January 5, 2018

    21 GAUGE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·April 22, 2024

    HEARTMATE 2

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·April 10, 2019

    DURAGEN 4X5 1 PACK CE

    FDA Adverse Event
    Injury ·INTEGRA - PRINCETON·Product code GXQ·July 17, 2024

    CATHETER IV AUTOGUARD 20 GA

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD·Product code FOZ·January 16, 2018

    CAVITRON SELECT W/RESERVOIR G123

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·March 3, 2023

    ALARIS PUMP MODULE

    FDA Adverse Event
    Death ·CAREFUSION·Product code FRN·July 5, 2019

    COVIDEN SHILEY ENDOTRACEAL TUBE

    FDA Adverse Event
    Injury ·MEDTRONIC (COVIDEN) / COVIDIEN·Product code BTO·November 12, 2021

    BD EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·April 15, 2025

    4.0MM OPEN CONNECTOR CLOSURE TOP

    FDA Adverse Event
    Injury ·Product code KWP·December 1, 2015

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·November 8, 2012

    MEDSYSTEM III

    FDA Adverse Event
    CAREFUSION·Product code FRN·October 29, 2012

    CAVITRON 300 SERIES G310SCLR(DNA)

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·April 28, 2025

    LUMAX 540 DR-T

    FDA Adverse Event
    Death ·BIOTRONIK SE & CO. KG·Product code MRM·July 25, 2013

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code QBJ·March 22, 2022

    HEARTWARE HVAD

    FDA Adverse Event
    Injury ·Product code DSQ·November 1, 2021

    NEUROMONITOR BASIC KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC/MEDOS S.A·Product code GWM·May 15, 2007