Profile: Beckman Coulter, Inc. is a manufacturer of biomedical testing instrument systems, tests & supplies that simplify and automate laboratory processes. Spanning the biomedical testing continuum from medical research & clinical trials to laboratory diagnostics and point-of-care testing, we provide essential biomedical information. GenomeLab is a family of solutions that identifies & removes the bottlenecks in the study of genetics, with the ultimate goal of identifying disease targets for therapy. We also render in vitro diagnostics systems to hospital laboratories. Our Hemoccult® ICT is the latest and most advanced fecal occult blood test (FOBT) in our Hemoccult product line. An immunochemical FOBT (iFOBT) with high specificity and sensitivity, Hemoccult ICT is clinically proven to detect bleeding associated with more cancers & polyps than traditional guaiac-based FOBTs. Because of its superior specificity for lower GI bleeding, Hemoccult ICT is an ideal screening tool for colorectal cancer (CRC), and this specificity also reduces the number of false positive test results.

The company was founded in 1934, has revenues of > USD 1 Billion, has ~10100 employees and is ISO 9000, ISO 9001, ISO 9002, CE certified.

FDA Registration Number: 2050012

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• 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.

• Isoenzymes Fluorometric Method (FDA Code: JHX / 862.1215)

• Isoenzymes NAD Reduction/NADH Oxidation (FDA Code: CGS / 862.1215)

• Isotonic Solution (FDA Code: JCE / 864.4010)

• Lab Automation Systems

• Lab Setup/design Consultants

• Lab Troponin I Kit, ELISA

• Labeled Medical Laboratory Equipment (FDA Code: LXG / 862.2050) General purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use.

• Laboratory Automation Systems

• Laboratory Automation Workstation

• Laboratory Centrifuges, Floor

• Laboratory Chart Recorder

• Laboratory Coagulation Analyzers

• Laboratory Densitometer

• Laboratory Hematology Analyzers

• Laboratory Liquid Dispenser

• Laboratory pH Electrode

• Laboratory Plasticware, Centrifuge Tubes

• Laboratory Pump

• Laboratory Refrigerators

• Labware, Centrifuge Tube

• Labware, Diluter

• Labware, Pipette Tip

• Labware, Test Tube Rack(CODE: RNT)

• Lacrimal Dilators and Probes

• Lactate Dehydrogenase 4-dinitrophenylhydrazine 2 (FDA Code: CER / 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.

• Lactate Dehydrogenase NAD Reduction/NADH Oxidation (FDA Code: CFJ / 862.1440)

• Lactic Acid Enzymatic Method (FDA Code: KHP / 862.1450) A lactic acid test system is a device intended to measure lactic acid in whole blood and plasma. Lactic acid measurements that evaluate the acid-base status are used in the diagnosis and treatment of lactic acidosis (abnormally high acidity of the blood).

• Laser Scanning Confocal Microscope

• Laser-Based Point Scanning Confocal Microscopes

• Latex Based Reagent Kit, Rheumatoid Factor

• 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.

• Lecithin/Sphingomyelin Ratio Electrophoretic Method (FDA Code: JHH / 862.1455) A lecithin/sphingomyelin ratio in amniotic fluid test system is a device intended to measure the lecithin/sphingomyelin ratio in amniotic fluid. Lecithin and sphingomyelin are phospholipids (fats or fat-like substances containing phosphorus). Measurements of the lecithin/sphingomyelin ratio in amniotic fluid are used in evaluating fetal maturity.

• Light Sources Microscope Light Source

• Lipase Photometric Enzymatic Lipase-Esterase Test (FDA Code: CHI / 862.1465) A lipase test system is a device intended to measure the activity of the enzymes lipase in serum. Lipase measurements are used in diagnosis and treatment of diseases of the pancreas such as acute pancreatitis and obstruction of the pancreatic duct.

• Lipids Test Kits

• Lipoprotein Low-Density Test System (FDA Code: MRR / 862.1475)

• Lipoproteins Electrophoretic Separation Test (FDA Code: JHO / 862.1475)

• Lipoproteins Microdensitometry Method Test (FDA Code: JHL / 862.1475)

• Lipoproteins Nephelometric Method Test (FDA Code: JHQ / 862.1475)

• Lipoproteins Turbidimetric Method Test (FDA Code: JHN / 862.1475)

• Liquid Chromatography Column (FDA Code: DPM / 862.2260) A high pressure liquid chromatography system for clinical use is a device intended to separate one or more drugs or compounds from a solution by processing the mixture of compounds (solutes) through a column packed with materials of uniform size (stationary phase) under the influence of a high pressure liquid (mobile phase). Separation of the solutes occurs either by absorption, sieving, partition, or selective affinity.

• Liquid Chromatography Equipment

• Liquid Gel Chromatography

• Luteinizing Hormone Radioimmunoassay (FDA Code: CEP / 862.1485) A luteinizing hormone test system is a device intended to measure luteinizing hormone in serum and urine. Luteinizing hormone measurements are used in the diagnosis and treatment of gonadal dysfunction.

• Macro Pipette

• 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).

• Male Hormone Test Kits

• Manual Microplate Washers

• Manual Platelet Counter (FDA Code: GLG / 864.6160) A manual blood cell counting device is a device used to count red blood cells, white blood cells, or blood platelets.