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Diasys Diagnostic Systems

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Web: http://www.diasys-diagnostics.com
E-Mail:
Address: Alte Straße 9, Holzheim 65558, Germany
Phone: +49-(6432)-9146-0 | Fax: +49-(6432)-9146-32 | Map/Directions >>
 
 

Profile: Diasys Diagnostic Systems develops and assembles diagnostic systems. We are an ISO certified company. Our products include instruments, immunoturbidimetric tests, controls, calibrators, clinical chemistry, OEM and ecoline. Our immunoturbidimetric tests are available with long calibration stability and high prozone limit. Our instrument includes biosensor, photometric, random access, and poc diabetes analyzer.

The company is ISO 13485:2003, ISO 9001:2000 certified.

1 to 50 of 52 Products/Services (Click for related suppliers)  Page: [1] 2 >> Next 50 Results
• Albumin
• Albumin Reagent Set
• Alpha-Ketobutyric Acid and NADH (FDA Code: JMK / 862.1380)
A hydroxybutyric dehydrogenase test system is a device intended to measure the activity of the enzyme alpha-hydroxybutric dehydrogenase (HBD) in plasma or serum. HBD measurements are used in the diagnosis and treatment of myocardial infarction, renal damage (such as rejection of transplants), certain hematological diseases (such as acute leukemias and megaloblastic anemias) and, to a lesser degree, liver disease.
• Antistreptolysin-Titer/Streptolysin O Reagent (FDA Code: GTQ / 866.3720)
• Auto LDL-Cholesterol, automated analyzer test kits
• Blood Albumin Detector
• 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
• Clinical Colorimeter (FDA Code: JJQ / 862.2300)
A colorimeter, a photometer, or a spectrophotometer for clinical use is an instrument intended to measure radiant energy emitted, transmitted, absorbed, or reflected under controlled conditions. The device may include a monochromator to produce light of a specific wavelength.
• 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.
• Creatinine Microalbumin Reagent Strips
• Diagnostic Kits, AST (SGOT)
• Discrete Photometric Chemistry Analyzer (FDA Code: JJE / 862.2160)
A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.
• 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.
• Fatty Acids Titrimetric (FDA Code: JLH / 862.1290)
A fatty acids test system is a device intended to measure fatty acids in plasma and serum. Measurements of fatty acids are used in the diagnosis and treatment of various disorders of lipid metabolism.
• Gamma-Glutamyl Transpeptidase Kinetic Method (FDA Code: JQB / 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.
• 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
• Iron
• 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.
• 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).
• 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)
• Lipoprotein(A) Test System (FDA Code: MSM / 862.1475)
• Lipoproteins Turbidimetric Method Test (FDA Code: JHN / 862.1475)
• Microalbumin Immunoturbidimetric Test kit
• Microalbuminuria Testing Kits
• 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.
• Prealbumin Antiserum (FDA Code: JZJ / 866.5060)
A prealbumin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the prealbumin (a plasma protein) in serum and other body fluids. Measurement of prealbumin levels in serum may aid in the assessment of the patient's nutritional status.
• 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.
• Serum Albumin Detection Kit
• 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.
• Total Protein Turbidimetric Test (FDA Code: JGQ / 862.1635)
• Triglycerides
• 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.
• Triglycerides Lipase Hydrolysis/Glycerol Kinase Enzyme Test (FDA Code: CDT / 862.1705)
• Triglycerides Monitoring Kits

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