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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

151 to 200 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
• Clinical Sample Concentrator (FDA Code: JJH / 862.2310)
A clinical sample concentrator is a device intended to concentrate (by dialysis, evaporation, etc.) serum, urine, cerebrospinal fluid, and other body fluids before the fluids are analyzed.
• Clinical Specular Microscopes (FDA Code: NQE / 886.1850)
An AC-powered slitlamp biomicroscope is an AC-powered device that is a microscope intended for use in eye examination that projects into a patient's eye through a control diaphragm a thin, intense beam of light.
• Clip Removal Instrument (FDA Code: HBQ / 882.4200)
A clip removal instrument is a device used to remove surgical clips from the patient.
• Clip Surgical Applier (FDA Code: GDO / 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.
• Clostridium Difficile Rapid Toxin A Test
• Clostridium difficile Test Kits
• Clostridium Difficile Toxin Reagent (FDA Code: LLH / 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.
• Closure for Specimen Tubes
• Co2 Water Jacketed Incubators
• Coagulation Analyzers (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.
• Coagulation Lab Testing
• Compact Anesthesia Monitor
• Compact Microhematocrit Centrifuge
• Compact Microplate Shakers
• Computer Assisted Semen Analyzers
• Confocal Microscope Objectives
• Conmed Electrosurgery
• Containers
• Continuous Flush Catheter (FDA Code: KRA / 870.1210)
A continuous flush catheter is an attachment to a catheter-transducer system that permits continuous intravascular flushing at a slow infusion rate for the purpose of eliminating clotting, back-leakage, and waveform damping.
• Controls
• Controls for Diagnostic Equipment
• Cortical Cleaving Hydrodissector
• Corynebacterium Diphtheriae Virulence Strip (FDA Code: KFI / 866.3140)
• Creatinine Test Kit, liquid reagents
• Crystal Violet
• Culture Media Supplements (FDA Code: JSK / 866.2450)
A supplement for culture media is a device, such as a vitamin or sugar mixture, that is added to a solid or liquid basal culture medium to produce a desired formulation and that is intended for medical purposes to enhance the growth of fastidious microorganisms (those having complex nutritional requirements). This device aids in the diagnosis of diseases caused by pathogenic microorganisms.
• Culture Plate
• Culture Reagents NZY Broth
• Culture Reagents, Pen-Strep
• Culture Reagents, SOC Media
• Cultured Animal and Human Cells (FDA Code: KIR / 864.2280)
Cultured animal and human cells are in vitro cultivated cell lines from the tissue of humans or other animals which are used in various diagnostic procedures, particularly diagnostic virology and cytogenetic studies.
• Cytocentrifuge (FDA Code: IFB / 864.3300)
A cytocentrifuge is a centrifuge used to concentrate cells from biological cell suspensions (e.g., cerebrospinal fluid) and to deposit these cells on a glass microscope slide for cytological examination.
• Cytokeratins (FDA Code: LYE / 866.5550)
An immunoglobulin (light chain specific) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques both kappa and lambda types of light chain portions of immunoglobulin molecules in serum, other body fluids, and tissues. In some disease states, an excess of light chains are produced by the antibody-forming cells. These free light chains, unassociated with gamma globulin molecules, can be found in a patient's body fluids and tissues. Measurement of the various amounts of the different types of light chains aids in the diagnosis of multiple myeloma (cancer of antibody-forming cells), lymphocytic neoplasms (cancer of lymphoid tissue), Waldenstrom's macroglobulinemia (increased production of large immunoglobulins), and connective tissue diseases such as rheumatoid arthritis or systemic lupus erythematosus.
• Cytological Preservative (FDA Code: LEA / 864.4010)
• Cytology Cervical Spatula (FDA Code: HHT / 884.4530)
An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:
• Cytomegalovirus Enzyme Linked Immunoabsorbent Assay (FDA Code: LFZ / 866.3175)
Cytomegalovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to cytomegalovirus in serum. The identification aids in the diagnosis of diseases caused by cytomegaloviruses (principally cytomegalic inclusion disease) and provides epidemiological information on these diseases. Cytomegalic inclusion disease is a generalized infection of infants and is caused by intrauterine or early postnatal infection with the virus. The disease may cause severe congenital abnormalities, such as microcephaly (abnormal smallness of the head), motor disability, and mental retardation. Cytomegalovirus infection has also been associated with acquired hemolytic anemia, acute and chronic hepatitis, and an infectious mononucleosis-like syndrome.
• Cytometry Software
• Data Processing Module for Clinical use (FDA Code: JQP / 862.2100)
A calculator/data processing module for clinical use is an electronic device intended to store, retrieve, and process laboratory data.
• Densitometers Accessories
• Diabetes Care
• Diabetes Take Home Kit (FDA Code: OSS)
• Diabetic Monitoring
• Diagnostic Aids
• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)
An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.
• Diagnostic Kits and Reagents, AST (GOT) and Starter Reagent
• Diagnostic Kits and Reagents, AST (GOT) Liquidplus Reagent
• Diagnostic Kits and Reagents, Ovulation Fern Test Kits
• Differential Cell Counter (FDA Code: GKZ / 864.5220)
An automated differential cell counter is a device used to identify one or more of the formed elements of the blood. The device may also have the capability to flag, count, or classify immature or abnormal hematopoietic cells of the blood, bone marrow, or other body fluids. These devices may combine an electronic particle counting method, optical method, or a flow cytometric method utilizing monoclonal CD (cluster designation) markers. The device includes accessory CD markers.
• Digital Microcentrifuges
• Digital Thermometers

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