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Abbott Laboratories

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Web: http://www.abbott.com
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Address: 100 Abbott Park Road, Abbott Park, Illinois 60064-3500, USA
Phone: +1-(847)-937-6100 | Map/Directions >>
 
 

Profile: Abbott Laboratories is a diversified health care company which discovers, develops, manufactures and markets innovative products & services that span the continuum of care from prevention, diagnosis to treatment & cure. We focus on advancing medical science & the practice of health care with expertise in the therapeutic areas of diabetes, pain management, respiratory infections, HIV/AIDS, men & women's health, pediatrics and animal health. Our product Similac® Isomil® DF is ideal for dietary management of diarrhea to help firm loose and watery stools in infants older than 6 months & toddlers. It is the first and only infant formula to contain added dietary fiber (soy) specifically for diarrhea management. It is clinically shown to be effective in the management of antibiotic-induced diarrhea. Two carbohydrates, mainly corn syrup and sucrose are added to maximize absorption & minimize the risk of malabsorption. Our product juven® is a targeted therapeutic nutrition that helps build and maintain lean body mass & support healing.

The company has ~5000 employees. NYSE:ABT (SEC Filings)

FDA Registration Number: 1451914

151 to 186 of 186 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 3 [4]
• Polyurethane Feeding Tubes
• Powder-Free Latex Surgical Gloves
• Powder-Free Synthetic Surgical Gloves
• Powdered Exam Gloves and Latex Surgical Gloves
• Powered Surgical Laser Instrument (FDA Code: GEX / 878.4810)
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.
• Product Development, Hand-held Infusion Pump Controller
• Product Development, Infusion Pumps
• Radiation Resistant Surgical Gloves
• Rewetting Drops
• Rigid Gas-Permeable Contact Lens (FDA Code: MRC / 886.5918)
A rigid gas permeable contact lens care product is a device intended for use in the cleaning, conditioning, rinsing, lubricating/rewetting, or storing of a rigid gas permeable contact lens. This includes all solutions and tablets used together with rigid gas permeable contact lenses.
• Slide Warming Table (FDA Code: IEG / 864.3010)
Tissue processing equipment consists of devices used to prepare human tissue specimens for diagnostic histological examination by processing specimens through the various stages of decalcifying, infiltrating, sectioning, and mounting on microscope slides.
• Soft Lens Accessories (FDA Code: LPN / 886.5928)
A soft (hydrophilic) contact lens care product is a device intended for use in the cleaning, rinsing, disinfecting, lubricating/rewetting, or storing of a soft (hydrophilic) contact lens. This includes all solutions and tablets used together with soft (hydrophilic) contact lenses and heat disinfecting units intended to disinfect a soft (hydrophilic) contact lens by means of heat.
• Spikeable Enteral Feeding Bag
• Sterile, Infant Feeding Tubes
• Surgical Gloves
• Surgical Ophthalmic Cannula (FDA Code: HMX / 886.4350)
A manual ophthalmic surgical instrument is a nonpowered, handheld device intended to aid or perform ophthalmic surgical procedures. This generic type of device includes the manual corneal burr, ophthalmic caliper, ophthalmic cannula, eyelid clamp, ophthalmic muscle clamp, iris retractor clip, orbital compressor, ophthalmic curette, cystotome, orbital depressor, lachrymal dilator, erisophake, expressor, ophthalmic forcep, ophthalmic hook, sphere introducer, ophthalmic knife, ophthalmic suturing needle, lachrymal probe, trabeculotomy probe, cornea-sclera punch, ophthalmic retractor, ophthalmic ring (Flieringa), lachrymal sac rongeur, ophthalmic scissors, enucleating snare, ophthalmic spatula, ophthalmic specula, ophthalmic spoon, ophthalmic spud, trabeculotome or ophthalmic manual trephine.
• Synthetic Surgical Gloves
• Syringe Infusion Pump
• Syringe/Needle Combos
• Tears Lubricating Eye Drops
• Theophylline Fluorescence Polarization Immunoassay Test (FDA Code: LGS / 862.3880)
A theophylline test system is a device intended to measure theophylline (a drug used for stimulation of the muscles in the cardiovascular, respiratory, and central nervous systems) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of theophylline overdose or in monitoring levels of theophylline to ensure appropriate therapy.
• Thyroid Stimulating Hormone Radioimmunoassay (FDA Code: JLW / 862.1690)
A thyroid stimulating hormone test system is a device intended to measure thyroid stimulating hormone, also known as thyrotrophin and thyrotrophic hormone, in serum and plasma. Measurements of thyroid stimulating hormone produced by the anterior pituitary are used in the diagnosis of thyroid or pituitary disorders.
• Topical Anesthetics
• Total Thyroxine Non-Radiolabeled Enzyme Immunoassay (FDA Code: KLI / 862.1700)
A total thyroxine test system is a device intended to measure total (free and protein bound) thyroxine (thyroid hormone) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of thyroid diseases.
• Total Triiodothyronine Radioimmunoassay (FDA Code: CDP / 862.1710)
A total triiodothyronine test system is a device intended to measure the hormone triiodothyronine in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of thyroid diseases such as hyperthyroidism.
• U.V. Method, CPK/Isoenzymes (FDA Code: JHW / 862.1215)
A creatine phosphokinase/creatine kinase or isoenzymes test system is a device intended to measure the activity of the enzyme creatine phosphokinase or its isoenzymes (a group of enzymes with similar biological activity) in plasma and serum. Measurements of creatine phosphokinase and its isoenzymes are used in the diagnosis and treatment of myocardial infarction and muscle diseases such as progressive, Duchenne-type muscular dystrophy.
• Ultrasonic Lens Removal Systems
• Urinary Ketones, Nitroprusside Test (FDA Code: JIN / 862.1435)
A ketones (nonquantitative) test system is a device intended to identify ketones in urine and other body fluids. Identification of ketones is used in the diagnosis and treatment of acidosis (a condition characterized by abnormally high acidity of body fluids) or ketosis (a condition characterized by increased production of ketone bodies such as acetone) and for monitoring patients on ketogenic diets and patients with diabetes.
• Urine Dip Stick Chemistries
• Urine Screening Kit (FDA Code: JXA / 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.
• Used Infusion Pumps
• Viscoelastic Surgical Aid (FDA Code: LZP / 886.4275)
An intraocular fluid is a device consisting of a nongaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment.
• Viscosurgical Devices (Viscoelastics)
• Vitamin B12 Radioimmunoassay (FDA Code: CDD / 862.1810)
A vitamin B12test system is a device intended to measure vitamin B12in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of anemias of gastrointestinal malabsorption.
• Vitrectomy Cutters (FDA Code: MLZ / 886.4150)
A vitreous aspiration and cutting instrument is an electrically powered device, which may use ultrasound, intended to remove vitreous matter from the vitreous cavity or remove a crystalline lens.
• Volumetric Infusion Pumps

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