Dexall Biomedical Labs, Inc.

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Contact: Glen M. Ford - Director of Product Development
Web: http://www.dexall.com
E-Mail:
Address: 18904 Bonanza Way, Gaithersburg, Maryland 20879, USA
Phone: +1-(301)-840-1884 | Fax: +1-(301)-330-0883 | Map/Directions >>

Profile: Dexall Biomedical Labs, Inc. is a manufacturer of diagnostic devices. Our robotic automated enzyme immuno assay system, 7074 plus is a computer controlled, acti-tip enzyme immuno assay system. It is operated under the control of MaestroDex software, and can process an unlimited number of enzyme immuno assay test protocols, based on our patented Acti.Tip technology. It is a flexible system, composed of individual units linked together by a computer. It has the capacity of analyzing 288 Acti·Tip samples at a time. Our robotic solid phase Acti·Tip sample processor and washer, RoboDex-312 carries Acti·Tip samples through all phases of incubation and washings, without operator intervention.

The company was founded in 1978, has revenues of USD 1-5 Million and is CE certified.

18 Products/Services (Click for related suppliers)

• Allergy Test

• Allergy Testing

• C-Reactive Protein Test System (FDA Code: DCN / 866.5270)

A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.

• Campylobacter Pylori (FDA Code: LYR / 866.3110)

• Chlamydia Group Enzyme Linked Immunoabsorbent Assay (FDA Code: LJC / 866.3120)

Chlamydia serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to chlamydia in serum. Additionally, some of these reagents consist of chlamydia antisera conjugated with a fluorescent dye used to identify chlamydia directly from clinical specimens or cultured isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusChlamydia and provides epidemiological information on these diseases. Chlamydia are the causative agents of psittacosis (a form of pneumonia), lymphogranuloma venereum (a venereal disease), and trachoma (a chronic disease of the eye and eyelid).

• 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.

• Elisa Allergy test Kit

• Home Allergy Test Kit

• Hypersensitivity Pneumonitis Test System (FDA Code: DGW / 866.5500)

A hypersensitivity pneumonitis immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulin antibodies in serum which react specifically with organic dust derived from fungal or animal protein sources. When these antibodies react with such dusts in the lung, immune complexes precipitate and trigger an inflammatory reaction (hypersensitivity pneumonitis). Measurement of these immunoglobulin G antibodies aids in the diagnosis of hypersensitivity pneumonitis and other allergic respiratory disorders.

• Latex Allergy Test Kit

• microplate reader

• Peroxidase-conjugated Anti-IgE (FDA Code: DGO / 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.

• Product Development, Allergy Test Strips

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

• Robotic Automated Enzyme Immuno Assay Systems

• Robotic Sample Processor/Washers

• Strip Readers

• Urea Nitrogen Photometric Urease Test (FDA Code: CDN / 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.