BEUDAMED
    10,000 results · 113ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    BECTON, DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FMF·April 10, 2020

    BECTON, DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FMF·April 10, 2020

    BECTON, DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FMF·April 10, 2020

    BECTON DICKINSON & COMPANY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMF·December 20, 2024

    BECTON DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·June 23, 2004

    BECTON, DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code JKA·January 23, 2024

    BECTON,DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD.·Product code JKA·March 18, 2026

    BECTON DICKINSON AND COMPANY (BD)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMF·May 26, 2010

    BD-BECTON DICKINSON AND COMPANY

    FDA Adverse Event
    Malfunction ·BD·Product code FMF·May 18, 2006

    BD EXTENSION SET SMALLBORE TUBING FILTER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FPA·July 26, 2023

    BD PRECISION GLIDE NEEDLE / INJECTION

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FMI·February 21, 2019

    BD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMF·September 28, 2011

    SPINNING SPIROS CLOSED MALE LUER, RED CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·November 1, 2018

    BD STERILE 50 ML LUER-LOK TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 13, 2020

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 11, 2022

    ECLIPSE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMI·October 14, 2011

    ALARIS PCA MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code MEA·February 22, 2017

    3ML, 5ML, AND 10ML SYRINGES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 29, 2024

    BD 3ML SYRINGE LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMF·August 29, 2018

    BD ALARIS EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·September 13, 2023