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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

301 to 350 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
• Glycosylated Hemoglobin Analyzer System
• Graduated Liquid Medication Container (FDA Code: KYW / 880.6430)
A Liquid medication dispenser is a device intended for medical purposes that is used to issue a measured amount of liquid medication.
• Gram Negative Identification Panel (FDA Code: LQM / 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.
• Gram Positive Identification Panel (FDA Code: LQL / 866.2660)
• Grams Iodine Stain (FDA Code: HYI / 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.
• Guidewire Catheter (FDA Code: DQX / 870.1330)
A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.
• Haematology and Immunoassay Analyzers
• Haemophilus Influenza Antiserum (FDA Code: GRP / 866.3300)
• Hand Cleaners & Disinfectants
• Hand-held Microplate Washer
• Helical Stone Extractors
• Helicobacter pylori (H. pylori) IgG antibodies kit
• Hematocrit Analyzers
• Hematocrit Centrifuge (FDA Code: GKG / 864.6400)
A hematocrit measuring device is a system consisting of instruments, tubes, racks, and a sealer and a holder. The device is used to measure the packed red cell volume in blood to determine whether the patient's total red cell volume is normal or abnormal. Abnormal states include anemia (an abnormally low total red cell volume) and erythrocytosis (an abnormally high total red cell mass). The packed red cell volume is produced by centrifuging a given volume of blood.
• Hematocrit Tube Rack (FDA Code: GHY / 864.6400)
• Hematology Analyzers
• Hematology Instruments and Reagents
• Hematology Quality Control Mixture (FDA Code: JPK / 864.8625)
A hematology quality control mixture is a device used to ascertain the accuracy and precision of manual, semiautomated, and automated determinations of cell parameters such as white cell count (WBC), red cell count (RBC), platelet count (PLT), hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC).
• Hematology Reagents
• Hematology Reagents and Kits
• Hematology Reagents and Kits Hemoglobin A1C (Glycohemoglobin)
• Hematology Reagents and Supplies
• Hemocytometer (FDA Code: GHO / 864.6160)
A manual blood cell counting device is a device used to count red blood cells, white blood cells, or blood platelets.
• Hemoglobin A1c Analyzers
• Hemoglobin Analyzer System
• Hemoglobin Analyzers
• Herpes Simplex Virus (HSV2) Medical Diagnostic Kit
• High Capacity Floor Model Centrifuges
• High Performance Microcentrifuges
• High Resolution Microscope Video Cameras
• Histology Crystal Violet Stain (FDA Code: ICF / 864.1850)
• Histopathology Reference Laboratory
• Human IGFBP-3 ELISA Kit
• Human/Horse/Rabbit Coagulase Plasma (FDA Code: JTL / 866.2160)
Coagulase plasma is a device that consists of freeze-dried animal or human plasma that is intended for medical purposes to perform coagulase tests primarily on staphylococcal bacteria. When reconstituted, the fluid plasma is clotted by the action of the enzyme coagulase which is produced by pathogenic staphylococci. Test results are used primarily as an aid in the diagnosis of disease caused by pathogenic bacteria belonging to the genusStaphylococcus and provide epidemiological information on disease caused by these microorganisms.
• Humidity Analyzer
• Hypodermic Injections, Syringes
• Hypodermic Syringes
• Hypodermic Syringes, Reusable
• I.V. Flush Syringes
• I.V. Start Kits (FDA Code: LRS / 880.5200)
• IFA Antibody Antigen Respiratory Syncytial Virus (FDA Code: LKT / 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.
• Immuno Chemistry Analyzers
• Immuno Turbidmetric Chemical Analyzers
• Immunoassay Analyzers
• Immunoassay Equipment, Immunochemistry Analyzers
• Immunochemistry Analyzers
• Immunohistochemistry Reagents And Kits (FDA Code: NJT / 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.
• Immunology Laboratories
• Immunoturbidimetric Analyzers
• Immunoturbidmetric analyzers

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