Profile: Abaxis, Inc supplies point of care blood analyzers to the medical market. We are an ISO 9001 certified company. We offer products to military, physician offices, hospitals, urgent care clinics and oncology clinics. We provide technology, tools and services that support medical practices. Our Piccolo® is a compact clinical chemistry system designed for near-patient testing. Our Piccolo® panels are configured to aid in disease diagnosis or monitor disease treatment. The Piccolo xpressT is the next generation compact, portable on-site analyzer designed to deliver test results quickly and easily.

The company was founded in 1989, has revenues of USD 25-50 Million, has ~260 employees and is ISO 9001 certified. NASDAQ:ABAX (SEC Filings)

FDA Registration Number: 2939693

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• Glucose Test Kits

• High Capacity Floor Model Centrifuges

• High Performance Microcentrifuges

• Immuno Chemistry Analyzers

• Immunoassay Equipment, Immunochemistry Analyzers

• Inorganic Phosphorus Phosphomolybdate (FDA Code: CEO / 862.1580) A phosphorus (inorganic) test system is a device intended to measure inorganic phosphorus in serum, plasma, and urine. Measurements of phosphorus (inorganic) are used in the diagnosis and treatment of various disorders, including parathyroid gland and kidney diseases, and vitamin D imbalance.

• Instruments, Blood Gas & Electrolytes

• Instruments, Immunoassays

• Laboratory Centrifuges, Floor

• Lactate Dehydrogenase NAD Reduction/NADH Oxidation (FDA Code: CFJ / 862.1440) A lactate dehydrogenase test system is a device intended to measure the activity of the enzyme lactate dehydrogenase in serum. Lactate dehydrogenase measurements are used in the diagnosis and treatment of liver diseases such as acute viral hepatitis, cirrhosis, and metastatic carcinoma of the liver, cardiac diseases such as myocardial infarction, and tumors of the lung or kidneys.

• LDL & VLDL Precipitation, Cholesterol Via Esterase-Oxidase (FDA Code: LBS / 862.1475) A lipoprotein test system is a device intended to measure lipoprotein in serum and plasma. Lipoprotein measurements are used in the diagnosis and treatment of lipid disorders (such as diabetes mellitus), atherosclerosis, and various liver and renal diseases.

• Lipid Analyzers

• Lipid Panel and Triglyceride Analyzers

• Lipids Test Kits

• Magnesium Photometric Method Test (FDA Code: JGJ / 862.1495) A magnesium test system is a device intended to measure magnesium levels in serum and plasma. Magnesium measurements are used in the diagnosis and treatment of hypomagnesemia (abnormally low plasma levels of magnesium) and hypermagnesemia (abnormally high plasma levels of magnesium).

• Micro and Benchtop Centrifuges Refrigerated Centrifuges

• Micro Ultracentrifuges

• Microcentrifuges Non-Refrigerated

• Microhematocrit Centrifuges

• Microhematocrit, Mini Centrifuges

• MiniFuge Microcentrifuges

• Mobile Equipment & Service Parts

• Mobile Equipment & Services

• Mobile Equipment Accessories

• Multi Analyte Control (FDA Code: JJY / 862.1660) A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• Multi Analyte Mixture - Calibrator (FDA Code: JIX / 862.1150) A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also 862.2 in this part.)

• Nadh Oxidation/Nad Reduction (FDA Code: CKA / 862.1030) An alanine amino transferase (ALT/SGPT) test system is a device intended to measure the activity of the enzyme alanine amino transferase (ALT) (also known as a serum glutamic pyruvic transaminase or SGPT) in serum and plasma. Alanine amino transferase measurements are used in the diagnosis and treatment of certain liver diseases (e.g., viral hepatitis and cirrhosis) and heart diseases.

• Patient Monitoring Accessories

• Patient Monitoring Device Spare Parts

• Patient Monitoring Devices

• Patient Monitoring Installation Service

• Personal Mini Microcentrifuges

• Point-of-care Testing, Blood Gas Kits

• Potassium Colorimetry Tetraphenyl Borate Test (FDA Code: CEJ / 862.1600) A potassium test system is a device intended to measure potassium in serum, plasma, and urine. Measurements obtained by this device are used to monitor electrolyte balance in the diagnosis and treatment of diseases conditions characterized by low or high blood potassium levels.

• Potassium Ion Specific Electrode (FDA Code: CEM / 862.1600)

• Preparative Ultracentrifuges

• Purple Bromcresol Albumin Dye-Binding Test (FDA Code: CJW / 862.1035) An albumin test system is a device intended to measure the albumin concentration in serum and plasma. Albumin measurements are used in the diagnosis and treatment of numerous diseases involving primarily the liver or kidneys.

• Pyrex Test Tubes

• Refrigerated Microcentrifuges

• Rimmed Glass Test Tubes

• Scientific Microcentrifuges

• Scientific Microhematocrit Centrifuges

• Sodium Ion Specific Electrode (FDA Code: JGS / 862.1665) A sodium test system is a device intended to measure sodium in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of aldosteronism (excessive secretion of the hormone aldosterone), diabetes insipidus (chronic excretion of large amounts of dilute urine, accompanied by extreme thirst), adrenal hypertension, Addison's disease (caused by destruction of the adrenal glands), dehydration, inappropriate antidiuretic hormone secretion, or other diseases involving electrolyte imbalance.

• Test Kits, Lipids

• Test Tubes

• Total Protein Biuret Method (FDA Code: CEK / 862.1635) A total protein test system is a device intended to measure total protein(s) in serum or plasma. Measurements obtained by this device are used in the diagnosis and treatment of a variety of diseases involving the liver, kidney, or bone marrow as well as other metabolic or nutritional disorders.

• Triglycerides Colorimetric Method Test (FDA Code: JGY / 862.1705) A triglyceride test system is a device intended to measure triglyceride (neutral fat) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of patients with diabetes mellitus, nephrosis, liver obstruction, other diseases involving lipid metabolism, or various endocrine disorders.

• Tube Microhematocrit Centrifuge

• 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.

• Urea Nitrogen Photometric Urease Test (FDA Code: CDN / 862.1770) A urea nitrogen test system is a device intended to measure urea nitrogen (an end-product of nitrogen metabolism) in whole blood, serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of certain renal and metabolic diseases.