Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9617032

FEI Number

3002806485

Entity Name

Becton, Dickinson & Company (BD)

City/State/Country

Plymouth Devon, GB

Establishment Address

BELLIVER INDUSTRIAL ESTATE, Belliver Way, Plymouth Devon PL6 7BP, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Becton Dickinson and Company (Owner Number: 9922032)

Owner / Operator Contact Address

One Becton Drive, Franklin Lakes, NJ 07417, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K013971

PMA Number

N/A

All Registered Proprietary Names

BD Vacutainer® K2EDTA Blood Collection Tubes BD Vacutainer® K3EDTA Blood Collection Tubes PAXgene Blood RNA System BD Preset and BD A-Line Arterial Blood Collection Syringes BD Vacutainer® Barricor Lithium Heparin Plasma Blood Collection Tube BD Vacutainer(R) Urine Cup BD VACUTAINER NO ADDIT FALCON SPECIMEN COLLECTION PRODUCTS BD Vacutainer® Plus Plastic Round Bottom Tube with Preservative for Urinalysis BD Vacutainer® Plus Plastic Conical Bottom Tube with Preservative for Urinalysis BD Vacutainer Histology Specimen Container FALCON CONTAINERS FLUID COLLECTION BAG BD A-Line BD Preset Eclipse BD Vacutainer® Plus Serum Tubes BD Vacutainer® Plus K2EDTA Tubes BD Vacutainer® SST¿ Glass Tubes BD Vacutainer® SST¿ II Advance Tubes BD Vacutainer® SST¿ Plus Tubes BD Vacutainer® K2EDTA Blood Collection Tubes PAXGENE BLOOD RNA SYSTEM BD Vacutainer® Push Button Blood Collection Set with Pre-Attached Holder BD Vacutainer® Push Button Blood Collection Set PAXgene® Blood DNA Tube BD Vacutainer® Push Button UltraTouch Blood Collection Set BD Vacutainer® Push Button UltraTouch Blood Collection Set with Pre-Attached Holder BD Whole Blood Tube K2EDTA BD Vacutainer EDTA Tubes BD Vacutainer Plus Plastic BD Vacutainer Plastic Citrate Tube Buffered Sodium Citrate Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIM	Tubes, Vacuum Sample, With Anticoagulant	Clinical Chemistry	Class 2	862.1675	2023-09-26
NTW	System, Blood Collection, Rna Stabilization, Rna Purification, Rt-Pcr Molecular Diagnostic Test	Immunology	Class 2	866.4070	2011-11-15
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2026-04-17
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2016-09-23
KDT	Container, Specimen Mailer And Storage, Sterile	Pathology	Class 1	864.3250	1994-09-13
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2005-04-06
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2021-05-26
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2007-12-26
GIM	Tubes, Vacuum Sample, With Anticoagulant	Clinical Chemistry	Class 2	862.1675	2024-04-24
NTW	System, Blood Collection, Rna Stabilization, Rna Purification, Rt-Pcr Molecular Diagnostic Test	Immunology	Class 2	866.4070	2016-07-15
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2023-05-17
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2023-05-17
PJE	Blood/Plasma Collection Device For Dna Testing	Clinical Chemistry	Class 2	862.1675	2024-04-24
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2022-04-06
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2022-04-06
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2007-12-26
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2007-12-26

Official Correspondent

No official correspondent registered.

US Agent Details

Nathan Carrington Business: Becton Dickinson and Company Email: nate.carrington@bd.com Phone: (317) 6455190

Related Public Records

Same Entity

Becton Dickinson and Company

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
9680577	BECTON DICKINSON GMBH	HEIDELBERG Baden-Wurttemberg, DE
3003916417	BECTON DICKINSON IND. CIRURGICAS LTDA.	CURITIBA Parana, BR
3036495171	BD Biosciences San Diego	San Diego, CA, US
3015292643	BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES	San Diego, CA, US
3010141591	BD Kiestra B.V.	Drachten Fryslan, NL

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K945777	Smiths Industries Medical Systems, Inc.	PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES	1994-12-22
K221518	Np Medical	NP Medical nCompass Extension Set with Stabilizing Base	2022-11-03
K953474	Medikmark, Inc.	IV START KIT	1995-10-02
K972493	Nipro Medical Corp.	NIPRO DISPOSABLE SOLUTION INFUSION SET	1997-09-18
K982672	Baxter Healthcare Corp	COLLEAGUE PUMP SYRINGE ADAPTER SET	1998-09-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0022-2009	Becton Dickinson and Company	1	BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.
Z-0030-2014	Perkin Elmer Health Sciences, Inc.	2	Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.
Z-0010-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.

Similar Registrations

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2029015	Sterigenics U.S., LLC	Ontario, CA, US
3013557562	CBR ENTERPRISE LIMITED	Hong Kong, HK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9617032. Last updated year: 2026. Please use registration number 9617032 when referencing this establishment in official correspondence.