Pharmacia Diagnostics AB

Web: http://www.phadia.us
Address: 4169 Commercial Avenue, Portage, Michigan 49002, USA
Phone: +1-(800)-346-4364 | Fax: +1-(269)-492-7540 | Map/Directions >>

Profile: Pharmacia Diagnostics AB concentrates in specific IgE blood testing to provide inspired, innovative allergy diagnostic solutions for laboratories. We developed and introduced vitro allergy testing to find diseases caused by allergies. Our product ImmunoCAP Specific IgE blood test is an objective tool for research use and routine diagnosis.

FDA Registration Number: 9610566
US Agent: Martin R. Mann / Phadia Us Inc.
Phone: +1-(269)-492-1957 Fax: +1-(269)-492-7541 E-Mail:

17 Products/Services (Click for related suppliers)

• Allergy Kits Instruments

• Allergy Reagents & Test Kits

• Amylase Starch-Dye Bound Polymer Test (FDA Code: CIW / 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).

• Amyloclastic, Amylase (FDA Code: CJA / 862.1070)

• 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.

• Beta-2-Microglobulin Immunological Test System (FDA Code: JZG / 866.5630)

Abeta -2-microglobulin immunological test system is a device that consists of the reagents used to measure by immunochemical techniquesbeta -2-microglobulin (a protein molecule) in serum, urine, and other body fluids. Measurement ofbeta -2-microglobulin aids in the diagnosis of active rheumatoid arthritis and kidney disease.

• Calibrators & Controls, Allergy

• CPK Isoenzymes Chromatographic Separation Test (FDA Code: JHT / 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.

• 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.

• Fluorometer for Clinical Use (FDA Code: KHO / 862.2560)

A fluorometer for clinical use is a device intended to measure by fluorescence certain analytes. Fluorescence is the property of certain substances of radiating, when illuminated, a light of a different wavelength. This device is used in conjunction with certain materials to measure a variety of analytes.

• Gliadin Antibodies (FDA Code: MST / 866.5750)

A radioallergosorbent immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the allergen antibodies (antibodies which cause an allergic reaction) specific for a given allergen. Measurement of specific allergen antibodies may aid in the diagnosis of asthma, allergies, and other pulmonary disorders.

• IgE Control (FDA Code: DGC / 866.5510)

An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.

• IgG Control (FDA Code: DEW / 866.5510)

• Immunoreactive Insulin Radioimmunoassay Test (FDA Code: CFP / 862.1405)

An immunoreactive insulin test system is a device intended to measure immunoreactive insulin in serum and plasma. Immunoreactive insulin measurements are used in the diagnosis and treatment of various carbohydrate metabolism disorders, including diabetes mellitus, and hypoglycemia.

• OSHA Compliance Training

• Pipetting and Diluting Station (FDA Code: JQW / 862.2750)

A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.

• Radio-Allergen Absorbent (RAST) Test (FDA Code: DHB / 866.5750)