10,000 results · 116ms · Sources: EU EUDAMED, US FDA

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BECTON, DICKINSON & CO.

FDA registration
BECTON, DICKINSON & CO.·6 products·🇺🇸 United States

BECTON, DICKINSON & CO.

FDA registration
BECTON, DICKINSON & CO.·102 products·🇺🇸 United States

BECTON, DICKINSON & CO.

FDA registration
BECTON, DICKINSON & CO.·12 products·🇺🇸 United States

BECTON, DICKINSON & CO.

FDA registration
BECTON, DICKINSON & CO.·16 products·🇺🇸 United States

BECTON, DICKINSON AND CO.

FDA registration
BECTON, DICKINSON AND CO.·1 product·🇮🇪 Ireland

BECTON, DICKINSON & CO., (BD)

FDA registration
BECTON, DICKINSON & CO., (BD)·6 products·🇺🇸 United States

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO·Product code FMI·February 13, 2004

BECTON, DICKINSON AND CO

FDA Adverse Event
Malfunction ·*·Product code FMF·January 30, 2004

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMF·January 11, 2002

BECTON DICKINSON & CO

FDA Adverse Event
BECTON DICKONSON & CO.·Product code FMF·July 25, 2000

BECTON DICKINSON AND CO.

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMF·March 13, 2001

BECTON DICKINSON & CO.

FDA Adverse Event
Malfunction ·BECTON DICKINSTON & CO·Product code KZH·July 21, 1994

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO.·Product code FMI·April 30, 1998

BECTON, DICKINSON & CO.

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·March 16, 2009

BECTON DICKINSON AND CO.

FDA Adverse Event
Injury ·Product code FMI·February 14, 2019

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO·Product code FMF·June 8, 2001

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO.·Product code FMI·November 20, 1998

BECTON DICKINSON AND CO.

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO.·Product code FMF·December 4, 1998

BECTON DICKINSON & CO

FDA Adverse Event
Malfunction ·*·Product code FMF·November 14, 2002

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code OOI·October 30, 2023