AVL Medical Instruments (Japan)

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Address: 5-3-20 Toranomon, Minato-ku, Tokyo 105-0001, Japan
Phone: +81-(03)-5776-6781 | Fax: +81-(03)-5776-6787 | Map/Directions >>
 
 

Profile: AVL Medical Instruments (Japan) provides automatic electrolyte analyzers, blood gas analyzers and blood collecting sets.

The company has revenues of USD 10-25 Million, has ~1300 employees and is ISO 9001, CE certified.

45 Products/Services (Click for related suppliers)  
• 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 Hematin (FDA Code: GGF / 864.7500)
A whole blood hemoglobin assay is a device consisting or reagents, calibrators, controls, or photometric or spectrophotometric instrumentation used to measure the hemoglobin content of whole blood for the detection of anemia. This generic device category does not include automated hemoglobin systems.
• 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).
• Arterial Blood Sampling Kit (FDA Code: CBT / 868.1100)
An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations. The kit may include a syringe, needle, cork, and heparin.
• Automated Hematocrit Instrument (FDA Code: GKF / 864.5600)
An automated hematocrit instrument is a fully automated or semi-automated device which may or may not be part of a larger system. This device measures the packed red cell volume of a blood sample to distinguish normal from abnormal states, such as anemia and erythrocytosis (an increase in the number of red cells).
• Automated Hemoglobin System (FDA Code: GKR / 864.5620)
An automated hemoglobin system is a fully automated or semi-automated device which may or may not be part of a larger system. The generic type of device consists of the reagents, calibrators, controls, and instrumentation used to determine the hemoglobin content of human blood.
• Blood Gas Analyzers
• Blood Gas and Ph Electrode Measurement (FDA Code: CHL / 862.1120)
A blood gases (PCO2, PO2) and blood pH test system is a device intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. Measurements of blood gases (PCO2, PO2) and blood pH are used in the diagnosis and treatment of life-threatening acid-base disturbances.
• Blood Gas/pH analyzer
• Blood Oxyhemoglobin Concentration Analyzer
• Blood Phase Oxyhemoglobin Concentration Analyzer (Non-Indwelling, Oxygen)
• Calcium Ion Specific Electrode (FDA Code: JFP / 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).
• Carbon-Monoxide Oxyhemoglobin/Carboxyhemoglobin Curve Test (FDA Code: JKS / 862.3220)
A carbon monoxide test system is a device intended to measure carbon monoxide or carboxyhemoglobin (carbon monoxide bound to the hemoglobin in the blood) in blood. Measurements obtained by this device are used in the diagnosis and treatment of or confirmation of carbon monoxide poisoning.
• Carboxyhemoglobin Assay (FDA Code: GHS / 864.7425)
A carboxyhemoglobin assay is a device used to determine the carboxyhemoglobin (the compound formed when hemoglobin is exposed to carbon monoxide) content of human blood as an aid in the diagnosis of carbon monoxide poisoning. This measurement may be made using methods such as spectroscopy, colorimetry, spectrophotometry, and gasometry.
• Chloride Ion Specific Electrode (FDA Code: CGZ / 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.
• Clearing Agent (FDA Code: KEM / 864.4010)
• 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.
• Complement C3 (FDA Code: CZW / 866.5240)
A complement components immunological test system is a device that consists of the reagents used to measure by immunochemical techniques complement components C1q, C1r, C1s, C2, C3, C4, C5, C6, C7, C8, and C9, in serum, other body fluids, and tissues. Complement is a group of serum proteins which destroy infectious agents. Measurements of these proteins aids in the diagnosis of immunologic disorders, especially those associated with deficiencies of complement components.
• 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.
• Dry and Liquid Heparin Arterial Blood Sampling Kits
• Electrolyte Chemistry Analyzer
• Electrolyte Control (FDA Code: JJR / 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.
• General Purpose Reagent (FDA Code: LDT)
• 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.
• Indwelling Blood Phase Oxyhemoglobin Concentration Analyzer (FDA Code: JED / 868.1120)
An indwelling blood oxyhemoglobin concentration analyzer is a photoelectric device used to measure, in vivo, the oxygen-carrying capacity of hemoglobin in blood to aid in determining the patient's physiological status.
• Ion Selective Electrode (FDA Code: JJP / 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.
• 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).
• Lithium Flame Photometer (FDA Code: JIH / 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).
• 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).
• Multi Analyte Control (FDA Code: JJY / 862.1660)
• 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.)
• Neonatal Total Bilirubin Test System (FDA Code: MQM / 862.1113)
A bilirubin (total and unbound) in the neonate test system is a device intended to measure the levels of bilirubin (total and unbound) in the blood (serum) of newborn infants to aid in indicating the risk of bilirubin encephalopathy (kernicterus).
• Non-Indw Blood Phase Carboxyhemoglobin Gas Analyzer
• Opiates Enzyme Immunoassay Test (FDA Code: DJG / 862.3650)
An opiate test system is a device intended to measure any of the addictive narcotic pain-relieving opiate drugs in blood, serum, urine, gastric contents, and saliva. An opiate is any natural or synthetic drug that has morphine-like pharmocological actions. The opiates include drugs such as morphine, morphine glucoronide, heroin, codeine, nalorphine, and meperedine. Measurements obtained by this device are used in the diagnosis and treatment of opiate use or overdose and in monitoring the levels of opiate administration to ensure appropriate therapy.
• Oxyhemoglobin (FDA Code: GGZ / 864.7500)
• pH Buffer (FDA Code: JCC / 864.4010)
• Potassium Ion Specific Electrode (FDA Code: CEM / 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.
• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)
A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.
• Sodium Ion Specific Electrode (FDA Code: JGS / 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.
• Thermostated Cuvette (FDA Code: JRI / 862.2050)
• Transcutaneous BP Oxyhemoglobin Concentration Analyzer
• Urea Nitrogen Ion Specific Electrode (FDA Code: CDS / 862.1770)
A urea nitrogen test system is a device intended to measure urea nitrogen (an end-product of nitrogen metabolism) in whole blood, serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of certain renal and metabolic diseases.
• Urinary Enzymatic Method (FDA Code: JIL / 862.1340)
A urinary glucose (nonquantitative) test system is a device intended to measure glucosuria (glucose in urine). Urinary glucose (nonquantitative) measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, hypoglycemia, and hyperglycemia.
• Whole Blood Hemoglobin Determination Test (FDA Code: KHG / 864.7500)
• Whole Blood Oximeter (FDA Code: GLY / 864.7500)

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