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Becton, Dickson & Co.,


Web: http://www.bd.com/us
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

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• Positive and Negative Febrile Antigen Control Serum (FDA Code: GSN / 866.3085)
• Preparative Ultracentrifuges
• Pressure Monitoring Kit
• Primarily Semen Quality Analyzers
• Procedure Kits & Packs
• Programmable Slide Stainers
• Propagating Transport Culture Media (FDA Code: JSN / 866.2390)
A transport culture medium is a device that consists of a semisolid, usually non-nutrient, medium that maintains the viability of suspected pathogens contained in patient specimens while in transit from the specimen collection area to the laboratory. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.
• Protected Disposable Scalpels
• Pulmonary Artery Catheters
• Punctal Irrigation Cannulas
• Pyrex Test Tubes
• Quality Control Slide (FDA Code: LJG / 866.2660)
A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.
• Racked Non-Sterile Non-Barrier Multi-Channel Pipette Tips
• Racked Non-Sterile Non-Barrier Pipette Tips
• Radiology Needles
• Rapid Microbiology Detection System
• Rapid Plasma Reagin (RPR) Test Kits
• Reagent/Device, Inoculum Calibration (FDA Code: LIE / 866.1640)
An antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.
• Real Time Nucleic Acid Amplification System (FDA Code: OOI / 862.2570)
• Red Blood Cell Storage Solutions
• Red Cell Lysing Fluid (FDA Code: GGK / 864.8540)
A red cell lysing reagent is a device used to lyse (destroy) red blood cells for hemoglobin determinations or aid in the counting of white blood cells.
• Refractive Surgery kits
• Refrigerated Microcentrifuges
• Refurbished Hematology Analyzers
• Removable Skin Staple (FDA Code: GDT / 878.4760)
A removable skin staple is a staple-like device intended to connect external tissues temporarily to aid healing. It is not absorbable.
• Renal Surgical Devices Percutaneous Stone Extractors
• Research Inverted System Microscope
• Respiratory Syncytial CF Antigen (FDA Code: GQG / 866.3480)
Respiratory syncytial virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to respiratory syncytial virus in serum. Additionally, some of these reagents consist of respiratory syncytial virus antisera conjugated with a fluorescent dye (immunofluorescent reagents) and used to identify respiratory syncytial viruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of respiratory syncytial virus infections and provides epidemiological information on diseases caused by these viruses. Respiratory syncytial viruses cause a number of respiratory tract infections, including the common cold, pharyngitis, and infantile bronchopneumonia.
• Respiratory Syncytial Virus (RSV) Test Kits
• Reticulocyte Stain (FDA Code: GJH / 864.1850)
Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.
• Retinal Thickness Analyzer
• Reusable Aspiration and Injection Needle (FDA Code: GDM / 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.
• Reusable Glass Syringes
• Reusable Medical Sterilization Containers
• Reusable Needles
• Reusable Syringes
• Reuseable Polycarbonate Dome without Diaphragm
• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775)
A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis.
• Rimmed Glass Test Tubes
• Robotic Glove Aids
• Rocking Microplate Shakers
• Safranin Stain (FDA Code: HZS / 864.1850)
• Salmonella Spp Antigen (FDA Code: GRL / 866.3550)
• Salmonella Spp Antiserum (FDA Code: GRM / 866.3550)
• Scalpel Blade (FDA Code: GES / 878.4800)
• Scalpel Handle (FDA Code: GDZ / 878.4800)
• Scalpels
• Scientific Microcentrifuges
• Scientific Microhematocrit Centrifuges
• Scientific Microscope Objectives

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