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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• 3D Imaging Devices

• Acid Fuchsin Stain (FDA Code: IDF / 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.

• Acridine Orange Stain (FDA Code: IDC / 864.1850)

• Advanced inverted microscope

• Advanced Microscope Objective

• Aerobic Transport System (FDA Code: JTW / 866.2900) A microbiological specimen collection and transport device is a specimen collecting chamber intended for medical purposes to preserve the viability or integrity of microorganisms in specimens during storage of specimens after their collection and during their transport from the collecting area to the laboratory. The device may be labeled or otherwise represented as sterile. The device aids in the diagnosis of disease caused by pathogenic microorganisms.

• Agar Plate Test

• Agar Tube Test

• Alcohol Containing Fixative (FDA Code: LDZ / 864.4010)

• Alcohol Pad (FDA Code: LKB)

• Alcohol Swabs

• Allergen and Vaccine Delivery System (FDA Code: LDH)

• Allergy Syringe

• Allergy Syringe Organizer

• Allergy Syringes/Trays

• Amino Acid Assay Culture Media (FDA Code: JRZ / 866.2350) A microbiological assay culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes to cultivate selected test microorganisms in order to measure by microbiological procedures the concentration in a patient's serum of certain substances, such as amino acids, antimicrobial agents, and vitamins. The concentration of these substances is measured by their ability to promote or inhibit the growth of the test organism in the innoculated medium. Test results aid in the diagnosis of disease resulting from either deficient or excessive amounts of these substances in a patient's serum. Tests results may also be used to monitor the effects of the administration of certain antimicrobial drugs.

• Anaerobic Glove Box (FDA Code: JTM / 866.2120) An anaerobic chamber is a device intended for medical purposes to maintain an anaerobic (oxygen free) environment. It is used to isolate and cultivate anaerobic microorganisms.

• Anaerobic Identification Kit Test (FDA Code: JSP / 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.

• Anaerobic Transport Culture Media (FDA Code: JSL / 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.

• Anaerobic Transport System (FDA Code: JTX / 866.2900)

• Analyte Specific Reagents, Asr Reagents (FDA Code: MVU / 864.4020) Analyte specific reagents (ASR's) are antibodies, both polyclonal and monoclonal, specific receptor proteins, ligands, nucleic acid sequences, and similar reagents which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens. ASR's that otherwise fall within this definition are not within the scope of subpart E of this part when they are sold to:

• Anesthesia

• Anesthesia Conduction Kit (FDA Code: CAZ / 868.5140) An anesthesia conduction kit is a device used to administer to a patient conduction, regional, or local anesthesia. The device may contain syringes, needles, and drugs.

• Anesthesia Equipment

• Anesthesia Equipment

• Anesthesia Inhalation Fluids

• Anesthesia Monitor

• Anesthesia Ring

• Anesthesia Workstation

• Anesthetic Conduction Catheter (FDA Code: BSO / 868.5120) An anesthesia conduction catheter is a flexible tubular device used to inject local anesthetics into a patient and to provide continuous regional anesthesia.

• Anesthetic Conduction Needle with/without Introducer (FDA Code: BSP / 868.5150) An anesthesia conduction needle is a device used to inject local anesthetics into a patient to provide regional anesthesia.

• Angiographic Injector Controller (FDA Code: DQF / 870.1670) A syringe actuator for an injector is an electrical device that controls the timing of an injection by an angiographic or indicator injector and synchronizes the injection with the electrocardiograph signal.

• Anti-GBM Antibodies Test Kids

• Antibiotic Assay Culture Media (FDA Code: JSA / 866.2350)

• Antibiotic Sensitivity Disc Dispenser

• Antibiotics & Antimicrobials

• Antibodies Stain Sets

• Antidiabetics

• Antimicrobial Susceptibility Test Culture Media (FDA Code: JSO / 866.1700) A culture medium for antimicrobial susceptibility tests is a device intended for medical purposes that consists of any medium capable of supporting the growth of many of the bacterial pathogens that are subject to antimicrobial susceptibility tests. The medium should be free of components known to be antagonistic to the common agents for which susceptibility tests are performed in the treatment of disease.

• Antimicrobial Susceptibility Test Disc (FDA Code: JTN / 866.1620) An antimicrobial susceptibility test disc is a device that consists of antimicrobic-impregnated paper discs used to measure by a disc-agar diffusion technique or a disc-broth elution technique the in vitro susceptibility of most clinically important bacterial pathogens to antimicrobial agents. In the disc-agar diffusion technique, bacterial susceptibility is ascertained by directly measuring the magnitude of a zone of bacterial inhibition around the disc on an agar surface. The disc-broth elution technique is associated with an automated rapid susceptibility test system and employs a fluid medium in which susceptibility is ascertained by photometrically measuring changes in bacterial growth resulting when antimicrobial material is eluted from the disc into the fluid medium. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.

• Antimicrobial Susceptibility Test Powder (FDA Code: JTT / 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.

• Antimycobacterial Susceptibility Test Powders (FDA Code: MJA / 866.1640)

• Antisera, Control for Non-Treponemal Test (FDA Code: GMP / 866.3820)

• Antistick Syringe (FDA Code: MEG / 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.

• Approved Chemotherapy Containers

• Artery Catheter

• Assisted Reproduction Labware (FDA Code: MQK / 884.6160) Assisted reproduction labware consists of laboratory equipment or supplies intended to prepare, store, manipulate, or transfer human gametes or embryos for in vitro fertilization (IVF), gamete intrafallopian transfer (GIFT), or other assisted reproduction procedures. These include syringes, IVF tissue culture dishes, IVF tissue culture plates, pipette tips, dishes, plates, and other vessels that come into physical contact with gametes, embryos or tissue culture media.

• Athletic Elastic Wraps and Tapes

• Auramine O Stain (FDA Code: KJK / 864.1850)

• Auto Inverted Microscope