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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
Website
www.bd.com/en-us
LinkedIn
linkedin.com/company/bd1
Facebook
facebook.com/BectonDickinsonandCo
Email
[email protected]
Phone
1-844-823-5433
PRRC Contact
Paul Dellow
EUDAMED SRN
US-MF-000018910
FDA FEI Number
1213809
DUNS Number
—

Catalogue (227)

Page 2 of 5
DeviceModel / ReferenceRegistriesClassStatus
Bd Emerald Saf-T Single Use, Hypodermic K121283
FDA 510(k)
Class IIActive
BD SoloShot Mini Syringe/ BD Auto Disable Syringe K201234
FDA 510(k)
Class IIActive
Bd Veritor System For The Rapid Detection Of Flu A+b K120049
FDA 510(k)
Class IIActive
BD Vacutainer® Citrate Blood Collection Tubes K240455
FDA 510(k)
Class IIActive
BD Phoenix™ Automated Microbiology System K250344
FDA 510(k)
Class IIActive
Bd Autoshield Duo Pen Needle K110703
FDA 510(k)
Class IIActive
BD Vacutainer® Eclipse™ Blood Collection Needle K243207
FDA 510(k)
Class IIActive
BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel K214122
FDA 510(k)
Class IIActive
BD FlowSmart Set, MiniMed Pro-Set K160651
FDA 510(k)
Class IIActive
BD Epilor Syringe K210983
FDA 510(k)
Class IIActive
0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe K231161
FDA 510(k)
Class IIActive
BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle K210978
FDA 510(k)
Class IIActive
BD Ultra-Fine™ Insulin Syringe, BD Ultra-Fine™ II Insulin Syringe, BD Insulin Syringes with the BD Ultra-Fine™ needle and BD Insulin Syringes with Micro-Fine™ IV Needle K170386
FDA 510(k)
Class IIActive
BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) K250059
FDA 510(k)
Class IIActive
BD Eclipse Hypodermic Needle K161170
FDA 510(k)
Class IIActive
BD BACTEC™ Myco/F Lytic Culture Vials K222559
FDA 510(k)
Class IActive
Bd Recykleen Sharps Collectors K112774
FDA 510(k)
Class IIActive
BD SafeAssist K161553
FDA 510(k)
Class IIActive
Bd Veritor (tm) System For Rapid Detection Of Rsv K132456
FDA 510(k)
Class IActive
BD Plastipak™ Syringe K251350
FDA 510(k)
Class IIActive
Onclarity™ Self-Collection Kit K260184
EUDAMEDFDA 510(k)
Class IIActive
BD PureHub Disinfecting Cap K193190
FDA 510(k)
Class IIActive
BD Veritor™ System Flu A+B Assay K132693
FDA 510(k)
Class IIActive
Bd Max(tm) Enteric Bacterial Panel;bd Max(tm) Instrument K140111
FDA 510(k)
Class IIActive
Bd Veritor(tm) System For Rapid Detection Of Flu A+b K112277
FDA 510(k)
Class IIActive
Bd Directigen Ex Flu A+b K101461
FDA 510(k)
Class IIActive
BD Vaginal Panel K243725
FDA 510(k)
Class IIActive
BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes K260128
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
BD BACTEC Plus PRIME Aerobic/F Culture Vials K120994
FDA 510(k)
Class IActive
BD MiniDraw™ Capillary Blood Collection System with BD MiniDraw™ SST™ Capillary Blood Collection Tube K230391
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets K223243
EUDAMEDFDA 510(k)
Class IIActive
Bd Viper Lt System K140447
FDA 510(k)
Class IIActive
BD Nano 2nd Gen Pen Needle K212015
FDA 510(k)
Class IIActive
Bd Ctgctv2 K210585
FDA 510(k)
Class IIActive
BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube K160657
EUDAMEDFDA 510(k)
Class IIActive
Bd Max Ct/Gc/Tv, Bd Max Instrument K151589
FDA 510(k)
Class IIActive
BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes K252040
FDA 510(k)
Class IIActive
BD Insulin Syringe K190054
FDA 510(k)
Class IIActive
BD PhaSeal Optima Closed System Transfer Device K181221
FDA 510(k)
Class IIActive
BD Nano 2nd Gen Pen Needle K213156
FDA 510(k)
Class IIActive
BD FACSLyric Flow Cytometer (3-1, 4-2, 4-2-2, 4-3-3 and 4-3-5 optical configurations), BD FACSDuet Sample Preparation System, BD FACS Universal Loader, BD FACSuite Clinical software, BD Multitest 6-Color Assay Modules, BD Multitest 4-Color Assay Modules, BD FACSFlow Sheath Fluid, BD CS&T Beads, BD FC Beads 7-Color Kit K201814
FDA 510(k)
Class IIActive
BD Vacutainer Eclipse Signal Blood Collection Needle K170824
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
BD MAX Enteric Viral Panel K220607
FDA 510(k)
Class IIActive
BD Cathena Safety IV Catheter K172506
FDA 510(k)
Class IIActive
BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) K233986
FDA 510(k)
Class IIActive
BD Single Use, Hypodermic Syringe K172670
FDA 510(k)
Class IIActive
Bd Veritor System For The Rapid Detection Of Flu A+b K132692
FDA 510(k)
Class IIActive
BD MAX Enteric Viral Panel, BD MAX Instrument K181427
FDA 510(k)
Class IIActive
BD Vacutainer UltraTouch Push Button Blood Collection Set K212724
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
BD BBL™ Sensi-Disc™ Lefamulin 20µg (LMU-20) K230651
FDA 510(k)
Class IIActive

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