BEUDAMED
    10,000 results · 83ms · Sources: EU EUDAMED, US FDA

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    BIOFLO PICC WITH ENDEXO AND PASV VALVE TECHNOLOGY

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code LJS·September 21, 2020

    BARD

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LRO·June 4, 2004

    POWERPICC

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code LJS·October 1, 2021

    POWER PORT PORTACATH

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·February 28, 2019

    BARD ACCESS SYSTEMS

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code DQO·June 8, 2007

    POWER PORT IMPLANTABLE ACCESS PORT

    FDA Adverse Event
    Other ·BARD ACCESS SYSTEMS·Product code LJT·September 25, 2012

    POWERPICC HF CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code LJS·August 6, 2025

    SHERLOCK 3CG+ TCS

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJS·November 7, 2023

    BARD ACCESS SYSTEMS

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code DYB·July 31, 2002

    DOME TITANIUM SINGLE LUMEN PORT

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code LJT·September 17, 2012

    IMPLANTABLE POWERPORT MRI AIRGUARD CHRONOFLEX

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEM, INC.·Product code LJT·September 21, 2018

    MRI SINGLE LUMEN ACCESS

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·August 31, 1993

    PORT-A-CATH BARD POWER PORT DUO MRI

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJT·April 29, 2021

    8 FRENCH IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·BARD ACCESS·Product code LJT·March 17, 2016

    POWERPORT IMPLANTABLE PORT

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJT·July 9, 2019

    BROVIAC VASCULAR ACCESS CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code DQO·July 24, 1996

    DIALYSIS CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD)·Product code LFJ·February 7, 2006

    RETRO SAFETRAC 28CM

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code MSD·June 12, 2013

    M.R.I. ULTRA SLIMPORT IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 6F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·August 17, 2021

    POWERPICC

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code LJS·June 2, 2021