Becton, Dickson & Co.,

Address: One Becton Drive, Franklin Lakes, New Jersey 07417, USA
Phone: +1-(201)-847.6800 | Map/Directions >>

Profile: Becton, Dickinson & Co., manufactures and distributes a broad range of medical supplies, devices, laboratory equipment and diagnostic products. Our product BD Soluvia™ is a prefillable microinjection system that is integrated with a tiny BD™ microneedle. It allows a drug or vaccine to be accurately delivered intradermally. This has proven to offer a simple, reliable delivery method. The dermal layer contains a dense network of lymphatic vessels feeding local lymph nodes, resulting in rapid & efficient therapeutic response. It also contains a high concentration of potent immune cells that play a key role to initiate the immune response following vaccination.

The company has revenues of USD 10-25 Million, has ~1600 employees and is ISO 9000, CE certified. NYSE:BDX (SEC Filings)

FDA Registration Number: 1119779

501 to 550 of 716 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 3 4 5 6 7 8 9 10 [11] 12 13 14 15 >> Next 50 Results
• Non-Refrigerated Centrifuges
• Non-Selective and Differential Culture Media (FDA Code: JSH / 866.2320)
A differential culture medium is a device that consists primarily of liquid biological materials intended for medical purposes to cultivate and identify different types of pathogenic microorganisms. The identification of these microorganisms is accomplished by the addition of a specific biochemical component(s) to the medium. Microorganisms are identified by a visible change (e.g., a color change) in a specific biochemical component(s) which indicates that specific metabolic reactions have occurred. Test results aid in the diagnosis of disease and also provide epidemiological information on diseases caused by these microorganisms.
• Non-Selective and Non-Differential Culture Media (FDA Code: JSG / 866.2300)
A multipurpose culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes for the cultivation and identification of several types of pathogenic microorganisms without the need of additional nutritional supplements. Test results aid in the diagnosis of disease and also provide epidemiological information on diseases caused by these microorganisms.
• Non-Sterile Absorbent Tipped Applicator (FDA Code: KXF / 880.6025)
An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.
• Non-Sterile Barrier Pipette Tips
• Non-Treponemal Antigen (FDA Code: GMQ / 866.3820)
• Nuclear Intensity & Percent Positivity Operator Intervention Immunohistochemistry Image Analysis Automated Microscope (FDA Code: NQN / 864.1860)
Immunohistochemistry test systems (IHC's) are in vitro diagnostic devices consisting of polyclonal or monoclonal antibodies labeled with directions for use and performance claims, which may be packaged with ancillary reagents in kits. Their intended use is to identify, by immunological techniques, antigens in tissues or cytologic specimens. Similar devices intended for use with flow cytometry devices are not considered IHC's.
• Nucleic Acid Amplification Test for Chlamydia (FDA Code: MKZ / 866.3120)
Chlamydia serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to chlamydia in serum. Additionally, some of these reagents consist of chlamydia antisera conjugated with a fluorescent dye used to identify chlamydia directly from clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusChlamydia and provides epidemiological information on these diseases. Chlamydia are the causative agents of psittacosis (a form of pneumonia), lymphogranuloma venereum (a venereal disease), and trachoma (a chronic disease of the eye and eyelid).
• Nucleus Hydrodissector
• Obstetric Anesthesia Set (FDA Code: KNE / 884.5100)
An obstetric anesthesia set is an assembly of antiseptic solution, needles, needle guides, syringes, and other accessories, intended for use with an anesthetic drug. This device is used to administer regional blocks (e.g., paracervical, uterosacral, and pudendal) that may be used during labor, delivery, or both.
• One-Piece Scalpel (FDA Code: GDX / 878.4800)
A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
• Operating Microscope Filters, Fixed filters
• Operating Microscope Filters, Two-position filter
• Operating Room Scrub Brush (FDA Code: GEC / 878.4800)
• Operator Intervention Automated Image Analysis Microscope (FDA Code: NOT / 864.1860)
• Ophthalmic Tests
• Ophthalmology Culture Reagents Agar
• Ophthalmology Culture Reagents LB Agar Plates
• Papain (FDA Code: IBF / 864.4400)
Enzyme preparations are products that are used in the histopathology laboratory for the following purposes:
• Pathogenic Neisseria Culture Media (FDA Code: JTY / 866.2410)
A culture medium for pathogenicNeisseria spp. is a device that consists primarily of liquid or solid biological materials used to cultivate and identify pathogenicNeisseria spp. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusNeisseria, such as epidemic cerebrospinal meningitis, other meningococcal disease, and gonorrhea, and also provides epidemiological information on these microorganisms.
• Patient Data Management Computer
• PCA Syringe Pump
• Percutaneous Nephroscopy PCNL, Percutaneous Stone Extractors
• Peritoneal Shunt (FDA Code: KPM / 876.5955)
A peritoneo-venous shunt is an implanted device that consists of a catheter and a pressure activated one-way valve. The catheter is implanted with one end in the peritoneal cavity and the other in a large vein. This device enables ascitic fluid in the peritoneal cavity to flow into the venous system for the treatment of intractable ascites.
• Personal Mini Microcentrifuges
• Petri Dish Desk Holder
• Petri Dish Dispenser
• Petri Dish Spreaders
• Petri Dishes
• Petri Dishes & Nutrient Agar Kit
• pH Buffer (FDA Code: JCC / 864.4010)
• Phaco Slit Knife
• Phacoemulsification Surgery, Cortex Extractors
• Phlebotomy Needles & Tourniquets
• Pipette Tip Disposal Box
• Pipetter
• Pipetting and Diluting Station (FDA Code: JQW / 862.2750)
A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.
• Pipettors, Pipettes
• Piston Syringe (FDA Code: FMF / 880.5860)
A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.
• Plasma Protein Analyzers
• Platelet Aggregation Reagents (FDA Code: GHR / 864.5700)
An automated platelet aggregation system is a device used to determine changes in platelet shape and platelet aggregation following the addition of an aggregating reagent to a platelet-rich plasma.
• Platelet Agitators, Platelet Incubators
• Platewash Microplate Washer
• POC Cardiac Marker Analyzers
• POC Cardiac Marker Analyzers, RAMP System
• POC Coagulation Analyzers (PT and INR)
• Point-of-care (POC) Coagulation Analyzers
• Point-of-Care (POC) Diagnostic Devices
• Polyethylene Tubing Adapter
• Portable Inverted Microscope

 Edit or Enhance this Company (9150 potential buyers viewed listing,  1343 forwarded to manufacturer's website)
Browse Category   |   Alphabetical Products   |   ALL 25,000 Suppliers
HomeBuyAdd FREE ListingAdvertise Medical CompanyMedical Portal