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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• Auto LDL-Cholesterol, automated analyzer test kits

• Auto Reader of Overnight Microorganism Identification System (FDA Code: LRH / 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.

• Automated Antimicrobial Susceptibility Test System (FDA Code: LON / 866.1645) A fully automated short-term incubation cycle antimicrobial susceptibility system is a device that incorporates concentrations of antimicrobial agents into a system for the purpose of determining in vitro susceptibility of bacterial pathogens isolated from clinical specimens. Test results obtained from short-term (less than 16 hours) incubation are used to determine the antimicrobial agent of choice to treat bacterial diseases.

• Automated Blood Cell Diluting Apparatus (FDA Code: GKH / 864.5240) An automated blood cell diluting apparatus is a fully automated or semi-automated device used to make appropriate dilutions of a blood sample for further testing.

• Automated Cell Counter (FDA Code: GKL / 864.5200) An automated cell counter is a fully-automated or semi-automated device used to count red blood cells, white blood cells, or blood platelets using a sample of the patient's peripheral blood (blood circulating in one of the body's extremities, such as the arm). These devices may also measure hemoglobin or hematocrit and may also calculate or measure one or more of the red cell indices (the erythrocyte mean corpuscular volume, the mean corpuscular hemoglobin, or the mean corpuscular hemoglobin concentration). These devices may use either an electronic particle counting method or an optical counting method.

• Automated Cell Washer

• Automated Cervical Cytology Slide Reader (FDA Code: MNM)

• Automated Chemiluminescent Immunoassay Analyzers

• Automated Coagulation Analyzer (FDA Code: GKP / 864.5400) A coagulation instrument is an automated or semiautomated device used to determine the onset of clot formation for in vitro coagulation studies.

• Automated Colorimetric Microbial Detection System

• Automated Cytology Slide Processor (FDA Code: MKQ)

• Automated Enzyme Immunoassay Analyzers

• Automated Hematology Analyzers

• Automated Immunoassay Analyzers

• Automated Liquid-phase Binding Immunoassay Analyzer

• Automated Microbial Detection System

• Automated Microplate Washer

• Automated Semen Analyzers

• Automated Slide Stainer (FDA Code: KPA / 864.3800) An automated slide stainer is a device used to stain histology, cytology, and hematology slides for diagnosis.

• Automated Tissue Processor (FDA Code: IEO / 864.3875) An automated tissue processor is an automated system used to process tissue specimens for examination through fixation, dehydration, and infiltration.

• Automated Urine Cell Analyzer

• Automated Urine Chemistry Analyzers

• Automated Urine Chemistry Reagent Strip Analyzer

• Automated Western Blot Analyzer

• Automatic Clinical Chemistry and Immunoturbidimetric Analyzers

• B Lymphocyte Marker Assay (FDA Code: LJD / 864.5220)

• B-Hemoglobin Analyzer

• B. Parapertussis Agglutinating Antisera (FDA Code: GOW / 866.3065)

• B. Parapertussis Antigen (FDA Code: GOT / 866.3065)

• B. Parapertussis Antiserum (FDA Code: JRW / 866.3065)

• B. Pertussis Agglutinating Antisera (FDA Code: GOY / 866.3065)

• B.Pertussis Antigen (FDA Code: GOX / 866.3065)

• Bacteria Characterization Test

• Bacterial Diagnostic Test

• Bags, Wraps & Tubing

• Beam-Scanning Confocal Microscope

• Benchtop Microcentrifuges

• Benchtop Ultracentrifuges

• Binkhorst Hooked Cannula

• Binkhorst Irrigating Cannula

• Binocular and Trinocular Inverted Microscopes

• Biochemistry Analyzers

• Biomedical Devices

• Blades

• Blood Analyzer Reagents

• Blood Bank Emergency ID System

• Blood Banking, Platelet Incubators

• Blood Cell Diluent (FDA Code: GIF / 864.8200) A blood cell diluent is a device used to dilute blood for further testing, such as blood cell counting.

• Blood Collect Tubes

• Blood Collection Lancet (FDA Code: FMK / 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.