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

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    INTRACATH W/WIRE STYLET

    FDA Adverse Event
    Injury ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code DQO·August 11, 1997

    INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·April 19, 1997

    INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·April 29, 1997

    ANGIOCATH

    FDA Adverse Event
    Injury ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·May 7, 1997

    INSYTE-W

    FDA Adverse Event
    Injury ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·April 9, 1997

    INSYTE AUTO GUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·May 22, 1997

    INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·April 29, 1997

    INSYTE AUOTGUARD

    FDA Adverse Event
    Injury ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·April 29, 1997

    NOVALON IV CATHETER/NEEDLE UNIT

    FDA Adverse Event
    Injury ·BECTON DICKINSON VASCULAR ACCESS, INC.·Product code FOZ·January 12, 1998

    Becton Dickinson Ireland Limited

    Authorized representative
    🇮🇪 Ireland·21 Manufacturers

    LIVERTY TIPS ACCESS SET

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

    Becton Dickinson Distribution Center N.V.

    Importer
    🇧🇪 Belgium·28 Manufacturers

    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 8F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; NAUTILUS DELTA Tip Confirmation System (Includes: Netbook with Pre-loaded Software, Patient Module, and ECG Cable) Product Usage: Is an implantable access device designed to provide repeated access to the vascular system.

    FDA Recall
    Completed ·Bard Peripheral Vascular Inc·Product code LJT·June 25, 2018