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International Bio-Analytical Industries, Inc.

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Web: http://www.ibilabs.com
E-Mail:
Address: 3495 North Dixie Hwy. Unit # 8, Boca Raton, Florida 33431, USA
Phone: +1-(561)-826-0061 | Fax: +1-(561)-892-8450 | Map/Directions >>
 
 

Profile: International Bio-Analytical Industries, Inc. manufactures uranyl acetate, uranyl nitrate, uranium oxide and other fine specialty uranium compounds for medical purposes. Uranyl acetate, uranyl nitrate and uranium tetra fluoride are available in a kilogram & smaller quantities to companies & institutions both nationally & internationally.

The company was founded in 1994, has revenues of USD 1-5 Million, has ~40 employees and is ISO 9001, CE certified.

FDA Registration Number: 2032134

1 to 50 of 74 Products/Services (Click for related suppliers)  Page: [1] 2 >> Next 50 Results
• Acetaminophen Colorimetry Test (FDA Code: LDP / 862.3030)
An acetaminophen test system is a device intended to measure acetaminophen, an analgestic and fever reducing drug, in serum. Measurements obtained by this device are used in the diagnosis and treatment of acetaminophen overdose.
• Acid Phosphatase, Thymolphthalein Monophosphate Test (FDA Code: CKE / 862.1020)
An acid phosphatase (total or prostatic) test system is a device intended to measure the activity of the acid phosphatase enzyme in plasma and serum.
• Albumin
• Albumin Reagent Set
• Alkaline Picrate Creatinine Colorimetric Method (FDA Code: CGX / 862.1225)
A creatinine test system is a device intended to measure creatinine levels in plasma and urine. Creatinine measurements are used in the diagnosis and treatment of renal diseases, in monitoring renal dialysis, and as a calculation basis for measuring other urine analytes.
• Amylase Catalytic Method Test (FDA Code: JFJ / 862.1070)
An amylase test system is a device intended to measure the activity of the enzyme amylase in serum and urine. Amylase measurements are used primarily for the diagnosis and treatment of pancreatitis (inflammation of the pancreas).
• Amylase Starch-Dye Bound Polymer Test (FDA Code: CIW / 862.1070)
• Ast/Sgot Nadh Oxidation/Nad Reduction (FDA Code: CIT / 862.1100)
An aspartate amino transferase (AST/SGOT) test system is a device intended to measure the activity of the enzyme aspartate amino transferase (AST) (also known as a serum glutamic oxaloacetic transferase or SGOT) in serum and plasma. Aspartate amino transferase measurements are used in the diagnosis and treatment of certain types of liver and heart disease.
• Auto LDL-Cholesterol, automated analyzer test kits
• Bilirubin Diazo Colorimetry Test (FDA Code: CIG / 862.1110)
A bilirubin (total or direct) test system is a device intended to measure the levels of bilirubin (total or direct) in plasma or serum. Measurements of the levels of bilirubin, an organic compound formed during the normal and abnormal distruction of red blood cells, if used in the diagnosis and treatment of liver, hemolytic hematological, and metabolic disorders, including hepatitis and gall bladder block.
• Blood Albumin Detector
• Bromcresol Green Dye-Binding, Albumin (FDA Code: CIX / 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.
• Calcium Cresolphthalein Complexone Test (FDA Code: CIC / 862.1145)
A calcium test system is a device intended to measure the total calcium level in serum. Calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany (intermittent muscular contractions or spasms).
• Chloride Test System (FDA Code: CHJ / 862.1170)
A chloride test system is a device intended to measure the level of chloride in plasma, serum, sweat, and urine. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.
• Cholesterol
• Cholesterol (Single reagent)
• Cholesterol and Triglycerides Kits
• Cholesterol Home Testing Kits
• Cholesterol Monitor Kit
• Cholesterol Rapid Liquid Reagent
• cholesterol self-test kit
• Cholesterol Test Kits
• Cholesterol Testing and Cholesterol Monitoring Kits
• Colorimetric Uric Acid Test (FDA Code: KNK / 862.1775)
A uric acid test system is a device intended to measure uric acid in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of numerous renal and metabolic disorders, including renal failure, gout, leukemia, psoriasis, starvation or other wasting conditions, and of patients receiving cytotoxic drugs.
• Creatinine Microalbumin Reagent Strips
• Diagnostic Kits, AST (SGOT)
• Differential Rate Kinetic Method, Isoenzymes (FDA Code: JHS / 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.
• Enzymatic Esterase-Oxidase, Cholesterol (FDA Code: CHH / 862.1175)
A cholesterol (total) test system is a device intended to measure cholesterol in plasma and serum. Cholesterol measurements are used in the diagnosis and treatment of disorders involving excess cholesterol in the blood and lipid and lipoprotein metabolism disorders.
• Gamma-Glutamyl Transpeptidase Colorimetric Method (FDA Code: JPZ / 862.1360)
A gamma-glutamyl transpeptidase and isoenzymes test system is a device intended to measure the activity of the enzyme gamma-glutamyl transpeptidase (GGTP) in plasma and serum. Gamma-glutamyl transpeptidase and isoenzymes measurements are used in the diagnosis and treatment of liver diseases such as alcoholic cirrhosis and primary and secondary liver tumors.
• Gaseous Phase Oxygen Gas Analyzer (FDA Code: CCL / 868.1720)
An oxygen gas analyzer is a device intended to measure the concentration of oxygen in respiratory gases by techniques such as mass spectrometry, polarography, thermal conductivity, or gas chromatography. This generic type of device also includes paramagnetic analyzers.
• Glucose Oxidase, Glucose (FDA Code: CGA / 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.
• Haemogloblin Iron Testing Kits
• HDL Cholesterol
• HDL Precipitation Method (FDA Code: LBR / 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.
• Home Microalbumin Testing Kit
• Human Microalbumin Kit
• 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.
• Iron
• Iron Binding Capacity Bathophenanthroline (FDA Code: JQF / 862.1415)
An iron-binding capacity test system is a device intended to measure iron-binding capacity in serum. Iron-binding capacity measurements are used in the diagnosis and treatment of anemia.
• Iron Reagent (FDA Code: CFM / 862.1410)
An iron (non-heme) test system is a device intended to measure iron (non-heme) in serum and plasma. Iron (non-heme) measurements are used in the diagnosis and treatment of diseases such as iron deficiency anemia, hemochromatosis (a disease associated with widespread deposit in the tissues of two iron-containing pigments, hemosiderin and hemofuscin, and characterized by pigmentation of the skin), and chronic renal disease.
• 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 Method (FDA Code: LBR / 862.1475)
• LDL Cholesterol
• LDL Cholesterol Reagent
• 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.
• Lipoprotein Low-Density Test System (FDA Code: MRR / 862.1475)
• Magnesium Ion Specific Electrode (FDA Code: CFA / 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).
• Magnesium Photometric Method Test (FDA Code: JGJ / 862.1495)
• Microalbumin Immunoturbidimetric Test kit
• Microalbuminuria Testing Kits

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