BEUDAMED
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    BARD PERIPHERAL VASCULAR INC.

    FDA Adverse Event
    BARD PERIPHERAL VASCULAR, INC.·Product code DTK·April 3, 2013

    BARD PERIPHERAL VASCULAR INC

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR INC·Product code LIT·March 7, 2006

    IMPLANTED HICKMAN CATHETER

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code LJT·July 29, 2010

    CATHETER CENTRAL VENOUS 4.2FR 90CM 1 LUMEN 2 CONNECTOR BROVIAC

    FDA Adverse Event
    No answer provided ·BARD PERIPHERAL VASCULAR, INC.·Product code LJS·May 4, 2022

    ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIO·July 27, 2022

    FLUENCY PLUS ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code PFV·October 29, 2019

    LIVERTY TIPS ACCESS SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code DYB·November 24, 2025

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F-7F

    FDA Adverse Event
    Malfunction ·CORDIS SANTA CLARA·Product code MGB·April 26, 2019

    GORE VIABAHN VBX BALLOON EXPANDABLE ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIO·February 15, 2019

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code PDU·January 7, 2021

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code MIH·July 16, 2018

    MERIDIAN FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 26, 2016

    FLAIR ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code MIH·December 2, 2016

    CROSSER CTO RECANALIZATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 19, 2016

    ULTRAVERSE 014 PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 8, 2016

    GHIATAS LOCALIZATION WIRE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code GAA·November 9, 2016