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Becton, Dickinson and Company

United States·US-MF-000018910

Last updated September 17, 2026

About

At BD, we seek to usher in a new era of healthcare by bringing medical products, capabilities and solutions to every corner of the world.

From the manufacturer's own website. Source

What Becton, Dickinson and Company makes

Becton, Dickinson and Company manufactures a range of medical devices including microbiology systems (BD Phoenix™ Automated Microbiology System), rapid diagnostic tests (BD Veritor System for SARS-CoV-2, BD VERITOR SYSTEM FOR THE RAPID DETECTION OF FLU A+B), insulin syringes (BD U-500 INSULIN SYRINGE), blood collection tubes (BD Vacutainer® K2 EDTA Blood Collection Tubes), IV catheter systems (BD Nexiva Closed IV Catheter System), and flow cytometry systems (BD FACSPresto System).

The company's portfolio includes devices classified under Class A, Class B, Class I, Class II, Class III, and Class IIa, and is listed in regulatory registries including eudamed, fda_510k, and fda_pma. Becton, Dickinson and Company is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Becton, Dickinson and Company manufacture?

Becton, Dickinson and Company produces a diverse range of medical devices including microbiology systems like the BD Phoenix™ Automated Microbiology System, rapid diagnostic tests such as the BD Veritor System for SARS-CoV-2 and flu detection, insulin syringes, blood collection tubes like BD Vacutainer® K2 EDTA, IV catheter systems, and flow cytometry systems.

Where is Becton, Dickinson and Company based?

Becton, Dickinson and Company is based in the United States, with operations spanning multiple countries to deliver medical products and solutions globally.

Which regulatory registries list Becton, Dickinson and Company's devices?

The company's devices are listed in several regulatory registries including eudamed, fda_510k, and fda_pma, ensuring compliance with regulatory requirements in different markets.

How are Becton, Dickinson and Company's devices classified?

The company manufactures devices across various risk classifications including Class A, Class B, Class I, Class II, Class III, and Class IIa, reflecting the different levels of regulatory control based on device risk and intended use.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
1, Becton Drive, Franklin Lakes, New Jersey, United States
Phone
1-844-823-5433
PRRC Contact
Paul Dellow
EUDAMED SRN
US-MF-000018910
FDA FEI Number
1213809
DUNS Number
—

Catalogue (227)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
Bbl 221082
EUDAMEDFDA UDI
Class AActive
Difco 225441
EUDAMEDFDA UDI
Class BActive
Bbl 220959
EUDAMEDFDA UDI
Class AActive
BD PhoenixSpec 441355
EUDAMEDFDA UDI
Class AActive
Bbl 212537
EUDAMEDFDA UDI
Class AActive
Viper 441360
EUDAMED
Class AActive
Phoenix 246015
EUDAMEDFDA UDI
Class AActive
Bbl 297252
EUDAMEDFDA UDI
Class AActive
Bbl 212523
EUDAMEDFDA UDI
Class AActive
Bbl 221669
EUDAMEDFDA UDI
Class AActive
Bbl 240938
EUDAMEDFDA UDI
Class BActive
Bbl 212528
EUDAMEDFDA UDI
Class AActive
Bbl 221714
EUDAMEDFDA UDI
Class AActive
Bbl 221392
EUDAMEDFDA UDI
Class AActive
Difco 226591
EUDAMEDFDA UDI
Class BActive
Bbl 299486
EUDAMEDFDA UDI
Class AActive
Vacutainer 364815
EUDAMEDFDA UDI
Class IActive
Difco 222361
EUDAMEDFDA UDI
Class BActive
BD Onclarity™ HPV Assay P160037
FDA PMA
Class IIIActive
Bbl 231749
EUDAMEDFDA UDI
Class AActive
Difco 229471
EUDAMEDFDA UDI
Class BActive
Bbl 212527
EUDAMEDFDA UDI
Class AActive
Bbl 240958
EUDAMEDFDA UDI
Class BActive
Bbl 221815
EUDAMEDFDA UDI
Class AActive
Difco 229701
EUDAMEDFDA UDI
Class BActive
Difco 228171
EUDAMEDFDA UDI
Class BActive
Bbl 221196
EUDAMEDFDA UDI
Class AActive

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