Profile: Egyptian Co. For Biotechnology develops and manufactures in vitro diagnostic reagents for clinical chemistry, serology, coagulation tests, and blood group reagents. We offer reagents for all biochemical tests done by manual and automation techniques in clinical chemistry. Our serology products include kits for Anti-Streptolysin O, C-reactive protein, & IgM rheumatoid factor for diagnosis in rheumatology. Our products for infectious diseases include Widal set for S.typhi & S.paratyphi, and kits for Brucella abortus and melitensis. Our coagulation test products include kits for determination of PT and APTT in the patient's plasma, which are supplied with normal and abnormal control plasma for calibration and quality control.
FDA Registration Number: 3005739565
US Agent: N/a / N/a
39 Products/Services (Click for related suppliers)
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| • Alkaline Phosphatase (ALP) (FDA Code: JCJ / 864.7660) A leukocyte alkaline phosphatase test is a device used to identify the enzyme leukocyte alkaline phosphatase in neutrophilic granulocytes (granular leukocytes stainable by neutral dyes). The cytochemical identification of alkaline phosphatase depends on the formation of blue granules in cells containing alkaline phosphatase. The results of this test are used to differentiate chronic granulocytic leukemia (a malignant disease characterized by excessive overgrowth of granulocytes in the bone marrow) and reactions that resemble true leukemia, such as those occuring in severe infections and polycythemia (increased total red cell mass). |
| • Alt/Sgpt Diazo (FDA Code: CJJ / 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. |
| • ALT/SGPT Vanillin Pyruvate Test (FDA Code: CKC / 862.1030) |
| • Antistreptolysin-Titer/Streptolysin O Reagent (FDA Code: GTQ / 866.3720) |
| • Bilirubin and Conjugates Colorimetric Azo-Dyes Test (FDA Code: JJB / 862.1115) A urinary bilirubin and its conjugates (nonquantitative) test system is a device intended to measure the levels of bilirubin conjugates in urine. Measurements of urinary bilirubin and its conjugates (nonquantitative) are used in the diagnosis and treatment of certain liver diseases. |
| • Brucella Spp Agglutination Antigen (FDA Code: GSO / 866.3085) |
| • Brucella Spp Fluorescent Antisera (FDA Code: GSM / 866.3085) |
| • Cholesterol Colorimetric Test (FDA Code: CGO / 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. |
| • Cholesterol Ferric Ion-Sulfuric Acid (FDA Code: CHD / 862.1175) |
| • Colorimetric SGPT Test (FDA Code: CKD / 862.1030) |
| • Complement Protein (FDA Code: DHL / 866.4100) A complement reagent is a device that consists of complement, a naturally occurring serum protein from any warm-blooded animal such as guinea pigs, that may be included as a component part of serological test kits used in the diagnosis of disease. |
| • Copper Diethyldithiocarbamate (Colorimetric) (FDA Code: JKZ / 862.1190) A copper test system is a device intended to measure copper levels in plasma, serum, and urine. Measurements of copper are used in the diagnosis and treatment of anemia, infections, inflammations, and Wilson's disease (a hereditary disease primarily of the liver and nervous system). Test results are also used in monitoring patients with Hodgkin's disease (a disease primarily of the lymph system). |
| • Copper Oxalydihydrazide (Spectroscopic) (FDA Code: JKY / 862.1190) |
| • Creatine Conversion To Creatinine (FDA Code: JLA / 862.1210) A creatine test system is a device intended to measure creatine (a substance synthesized in the liver and pancreas and found in biological fluids) in plasma, serum, and urine. Measurements of creatine are used in the diagnosis and treatment of muscle diseases and endocrine disorders including hyperthyroidism. |
| • Creatine Kinase (FDA Code: JLB / 862.1210) |
| • Entamoeba Histolytica & Rel Spp Antigen (FDA Code: GMO / 866.3220) |
| • Enzymatic Esterase-Oxidase, Cholesterol (FDA Code: CHH / 862.1175) |
| • 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. |
| • Gamma-Glutamyl Transpeptidase Isoenzymes Electrophoretic (FDA Code: JQA / 862.1360) |
| • Gamma-Glutamyl Transpeptidase Kinetic Method (FDA Code: JQB / 862.1360) |
| • 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) |
| • Leukocyte Alkaline Phosphatase Test (FDA Code: GHD / 864.7660) |
| • Lowry Colorimetric Total Protein method (FDA Code: JGP / 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. |
| • Nadh Oxidation/Nad Reduction (FDA Code: CKA / 862.1030) |
| • Phosphohexose Isomerase Glucose-6-Phosphate (Colorimetric) (FDA Code: JNE / 862.1570) A phosphohexose isomerase test system is a device intended to measure the activity of the enzyme phosphohexose isomerase in serum. Measurements of phosphohexose isomerase are used in the diagnosis and treatment of muscle diseases such as muscular dystrophy, liver diseases such as hepatitis or cirrhosis, and metastatic carcinoma. |
| • Phosphohexose Isomerase Nad Reduction (U.V.) (FDA Code: KLJ / 862.1570) |
| • Protein /Albumin Turbidimetric Method (FDA Code: JIQ / 862.1645) A urinary protein or albumin (nonquantitative) test system is a device intended to identify proteins or albumin in urine. Identification of urinary protein or albumin (nonquantitative) is used in the diagnosis and treatment of disease conditions such as renal or heart diseases or thyroid disorders, which are characterized by proteinuria or albuminuria. |
| • Salmonella Spp Antigen (FDA Code: GRL / 866.3550) |
| • Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase (FDA Code: CFH / 862.1440) |
| • TLC Chromatographic Separation Triglyceride Test (FDA Code: CEA / 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. |
| • Total Protein Biuret Method (FDA Code: CEK / 862.1635) |
| • Total Protein Refractometric Test (FDA Code: JGR / 862.1635) |
| • Total Protein Turbidimetric Test (FDA Code: JGQ / 862.1635) |
| • Triglycerides Colorimetric Method Test (FDA Code: JGY / 862.1705) |
| • Triglycerides Fluorometric Method Test (FDA Code: JGW / 862.1705) |
| • Triglycerides Lipase Hydrolysis/Glycerol Kinase Enzyme Test (FDA Code: CDT / 862.1705) |
| • Triglycerides Turbidimetric Method (FDA Code: JGX / 862.1705) |
| • Urinary Protein/Albumin Nonquantitative Test System (FDA Code: JIR / 862.1645) |