BEUDAMED
    1,233 results · 54ms · Sources: EU EUDAMED, US FDA

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    GÜNTHER TULIP VENA CAVA FILTER JUGULAR APPROACH

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·February 3, 2017

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·April 7, 2014

    EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·June 23, 2025

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·September 15, 2014

    LIFESTENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code NIP·August 12, 2021

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·June 23, 2015

    ARROW

    FDA Adverse Event
    Injury ·ARROW INT'L, INC.·Product code DQO·May 30, 2000

    RUNWAY CLS4 6F

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·July 15, 2020

    PERQCATH 3 FR S/L W/GW I

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code DQO·September 7, 2001

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·June 24, 2015

    BARD LIFESTREAM COVERED STENT

    FDA Adverse Event
    Injury ·CLEARSTREAM TECHNOLOGIES LTD·Product code PRL·October 31, 2024

    SYNERGY 2

    FDA Adverse Event
    Injury ·MANSFIELD BOSTON SCIENTIFIC CORP·Product code LOX·July 5, 1996

    AXIUM PRIME BRPL HLX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·January 26, 2022

    INTELLISPACE CARDIOVASCULAR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code LLZ·May 29, 2026

    ACS RX MULTILINK 3.0 X15MM

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEM·Product code MAF·March 24, 1998

    MI,5F,40CMAT,7CMSMT

    FDA Adverse Event
    Injury ·VASCULAR SOLUTIONS LLC·Product code DYB·May 8, 2024

    TRAPEASE FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·March 7, 2014

    OPTION ELITE RETRIEVABLE VENA CAVA FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code DTK·October 18, 2022

    AMPLATZER PICCOLO

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MAE·July 1, 2024

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·June 24, 2015