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

101 to 150 of 186 Products/Services (Click for related suppliers)  Page: 1 2 [3] 4

• Intrinsic Factor Blocking Antibody Radioassay (FDA Code: LIG / 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.

• IOL Delivery Systems

• Isoenzymes Colorimetric Method (FDA Code: JHY / 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.

• IV Fluids

• IV Medication Delivery Systems, volumetric infusion pumps

• IV Stand Accessories, Multi-Infusion Pump

• Jejunal Feeding Tubes

• Jejunostomy Catheter

• Jejunostomy Feeding Tube

• Lancet Devices

• Laparoscopy Kit (FDA Code: FDE / 876.1500) An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

• Latex Free Sterile Surgical Gloves

• Latex Sterile Microsurgical Gloves

• Malecot Catheters (FDA Code: FEW / 876.5090) A suprapubic urological catheter and accessories is a flexible tubular device that is inserted through the abdominal wall into the urinary bladder with the aid of a trocar and cannula. The device is used to pass fluids to and from the urinary tract. This generic type of device includes the suprapubic catheter and tube, Malecot catheter, catheter punch instrument, suprapubic drainage tube, and the suprapubic cannula and trocar.

• Microbiology Diagnostic Device (FDA Code: LIB / 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.

• MicroThinr Surgical Gloves

• MRI Infusion Pump Systems, Infusion System Accessories

• Multifocal Intraocular Lens (FDA Code: MFK / 886.3600) An intraocular lens is a device made of materials such as glass or plastic intended to be implanted to replace the natural lens of an eye.

• Nasogastric Tube Holder

• Nasogastric Tubes (FDA Code: BSS / 876.5980) A gastrointestinal tube and accessories is a device that consists of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding of the alimentary tract. This device may incorporate an integral inflatable balloon for retention or hemostasis. This generic type of device includes the hemostatic bag, irrigation and aspiration catheter (gastric, colonic, etc.), rectal catheter, sterile infant gavage set, gastrointestinal string and tubes to locate internal bleeding, double lumen tube for intestinal decompression or intubation, feeding tube, gastroenterostomy tube, Levine tube, nasogastric tube, single lumen tube with mercury weight balloon for intestinal intubation or decompression, and gastro-urological irrigation tray (for gastrological use).

• Nasogastric Weighted Feeding Tubes

• Neisseria DNA Reagents (FDA Code: LSL / 866.3390)

• Neoprene Latex Free Surgical Gloves

• Nonnarcotic Analgesics

• Nucleic Acid Amplification Test for Chlamydia (FDA Code: MKZ / 866.3120) Chlamydia serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to chlamydia in serum. Additionally, some of these reagents consist of chlamydia antisera conjugated with a fluorescent dye used to identify chlamydia directly from clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusChlamydia and provides epidemiological information on these diseases. Chlamydia are the causative agents of psittacosis (a form of pneumonia), lymphogranuloma venereum (a venereal disease), and trachoma (a chronic disease of the eye and eyelid).

• Ocular Surgery Irrigation Device (FDA Code: KYG / 886.4360) An ocular surgery irrigation device is a device intended to be suspended over the ocular area during ophthalmic surgery to deliver continuous, controlled irrigation to the surgical field.

• Ophthalmic Aberrometer (FDA Code: NCF / 886.1760) An ophthalmic refractometer is an automatic AC-powered device that consists of a fixation system, a measurement and recording system, and an alignment system intended to measure the refractive power of the eye by measuring light reflexes from the retina.

• Ophthalmic Aspiration 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.

• Ophthalmic Cannula (FDA Code: HMX / 886.4350)

• Ophthalmic Excimer Laser System (FDA Code: LZS)

• Ophthalmic Knife (FDA Code: HNN / 886.4350)

• Ophthalmic Manual Trephine (FDA Code: HRH / 886.4350)

• Ophthalmic Refractometer (FDA Code: HKO / 886.1760)

• Ophthalmic Suturring Needle (FDA Code: HNM / 886.4350)

• Oral Analgesics

• Orthopedic Surgical Gloves

• Otic Solutions

• Over-The-Counter Blood Glucose Test System (FDA Code: NBW / 862.1345) A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.

• P.V.C Infant Feeding Tubes

• Patient Controlled Analgesia (PCA) Infusion Pump (FDA Code: MEA / 880.5725) An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.

• PCA Pumps, Infusion Pump

• Pediatric Nasogastric Feeding Tubes

• PEG Feeding Tubes/Kits

• Percutaneous Endoscopic Gastrostomy Kit

• Peripheral Dilatation Catheter

• Peristaltic Infusion Pump (FDA Code: FRN / 880.5725)

• Phacoemulsification Systems

• Phacofragmentation Unit (FDA Code: HQC / 886.4670) A phacofragmentation system is an AC-powered device with a fragmenting needle intended for use in cataract surgery to disrupt a cataract with ultrasound and extract the cataract.

• Phenobarbital Fluorescence Polarization Immunoassay Test (FDA Code: LGQ / 862.3660) A phenobarbitol test system is a device intended to measure phenobarbital, an antiepileptic and sedative-hypnotic drug, in human specimens. Measurements obtained by this device are used in the diagnosis and treatment of phenobarbital use or overdose and in monitoring levels of phenobarbital to ensure appropriate therapy.

• Pipetting and Diluting Station (FDA Code: JQW / 862.2750) A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.