Diazyme Laboratories

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Web: http://www.diazyme-ga.com
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Address: 12889 Gregg Ct., Poway, California 92064, USA
Phone: +1-(858)-455-4768 | Fax: +1-(858)-455-3701 | Map/Directions >>
 
 

Profile: Diazyme Laboratories develops uniform diagnostic products for clinical and research use. We are an ISO certified company. Our enzymatic tHcy assay is based on a novel assay principle that assesses the co-substrate conversion product. Our uric acid enzymatic test kit helps in the determination of uric acid in serum or urine. Our creatine amidinohydrolase catalyzes the hydrolytic reaction converting creatine to sarcosine and urea. The enzyme is purified from a microorganism & weight of the enzyme is approximately 67,000. It is useful for the enzymatic assay of creatine and creatinine when coupled with other related enzymes.

FDA Registration Number: 2032900

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• 5'-Nucleotidase 5-AMP-Phosphate Release (Colorimetric Test) (FDA Code: CED / 862.1520)
A 5'-nucleotidase test system is a device intended to measure the activity of the enzyme 5'-nucleotidase in serum and plasma. Measurements of 5'-nucleotidase are used in the diagnosis and treatment of liver diseases and in the differentiations between liver and bone diseases in the presence of elevated serum alkaline phosphatase activity.
• Adenosine Deaminase Test Kit
• Amylase
• Amylase Inhibitors
• Amylase Starch
• Apolipoproteins (FDA Code: MSJ / 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.
• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 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.
• Auto LDL-Cholesterol, automated analyzer test kits
• Bile Acids Cholyglycine Radioimmunoassay (FDA Code: KWW / 862.1177)
A cholylglycine test system is a device intended to measure the bile acid cholylglycine in serum. Measurements obtained by this device are used in the diagnosis and treatment of liver disorders, such as cirrhosis or obstructive liver disease.
• 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.
• Bilirubin Enzymatic Method Test (FDA Code: JFM / 862.1110)
• Carbon Dioxide (CO2) Test Kit
• Carbon-Dioxide Enzymatic (FDA Code: KHS / 862.1160)
A bicarbonate/carbon dioxide test system is a device intended to measure bicarbonate/carbon dioxide in plasma, serum, and whole blood. Bicarbonate/carbon dioxide measurements are used in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance.
• Chloride Enzymatic Test Kit
• Creatinine
• Creatinine Enzymatic Method Test (FDA Code: JFY / 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.
• Creatinine Microalbumin Reagent Strips
• Creatinine Test Kit, enzymatic
• Creatinine Test Kit, liquid reagents
• Cystatin C Assay Kit
• Cystatin C Test (FDA Code: NDY / 862.1225)
• 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.
• Enzymatic Homocysteine Test Kit
• Enzymatic Method Potassium System Test (FDA Code: MZV / 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.
• Enzymatic Method Sodium Test System (FDA Code: MZU / 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.
• Gamma-GT
• Glycated Serum Protein Enzymatic Test Kit
• Glycosylated Hemoglobin Assay Test (FDA Code: LCP / 864.7470)
A glycosylated hemoglobin assay is a device used to measure the glycosylated hemoglobins (A1a, A1b, and A1c) in a patient's blood by a column chromatographic procedure. Measurement of glycosylated hemoglobin is used to assess the level of control of a patient's diabetes and to determine the proper insulin dosage for a patient. Elevated levels of glycosylated hemoglobin indicate uncontrolled diabetes in a patient.
• HDL Precipitation Method (FDA Code: LBR / 862.1475)
• LDL & VLDL Precipitation Method (FDA Code: LBR / 862.1475)
• LDL & VLDL Precipitation, Cholesterol Via Esterase-Oxidase (FDA Code: LBS / 862.1475)
• Lipase Assay Kit
• 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 (a) Assay Kit
• Lipoprotein-Associated Phospholipase A2 Immunoassay Test System (FDA Code: NOE / 866.5600)
A low-density lipoprotein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the low-density lipoprotein in serum and other body fluids. Measurement of low-density lipoprotein in serum may aid in the diagnosis of disorders of lipid (fat) metabolism and help to identify young persons at risk from cardiovascular diseases.
• Lithium
• Lithium Atomic Absorption (FDA Code: JII / 862.3560)
A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to assure that the proper drug dosage is administered in the treatment of patients with mental disturbances, such as manic-depressive illness (bipolar disorder).
• Lithium Enzymatic Test Kit
• Low Density Lipoprotein (FDA Code: DFC / 866.5600)
• 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.)
• Pancreatic Amylase
• Potassium Enzymatic Test Kit
• Primary Calibrator (FDA Code: JIS / 862.1150)
• Quantitative Kinetic Determination Of Amylase Kit
• Salivary Amylase
• Secondary Calibrator (FDA Code: JIT / 862.1150)
• Serum Amylase
• Sodium Enzymatic Test Kit
• Total Bile Acids Test Kit
• 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.

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