Inverness Medical Innovations Australia Pty Ltd.

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Web: http://www.panbio.com.au
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Address: 532 Seventeen Mile Rocks Rd, Sinnamon Park, Queensland 4073, Australia
Phone: +61-(7)-3363-7100 | Fax: +61-(7)-3363-7199 | Map/Directions >>

Profile: Inverness Medical Innovations Australia Pty Ltd. focuses on development, manufacturing and marketing of consumer & professional medical diagnostic products. Our focal areas include infectious diseases, cardiology, womens' health, drugs of abuse and oncology. Our brand names are Clearview®, Testpack®, Binax®, Determine® and Biosite®. Our Panbio® dengue IgM Capture ELISA, detects IgM antibodies to dengue antigen in serum, as an aid in the clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever.

The company has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001:2000, ISO 13485:2003 certified.

14 Products/Services (Click for related suppliers)

• Anti-acetylcholine Receptor Alpha Monoclonal Antibody

• Antinuclear Antibody, Indirect Immunofluorescen (FDA Code: DHN / 866.5100)

An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjogren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).

• B.Pertussis Antigen (FDA Code: GOX / 866.3065)

• Cytomegalovirus Virus IF Antibody Igm Test (FDA Code: LKQ / 866.3175)

Cytomegalovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to cytomegalovirus in serum. The identification aids in the diagnosis of diseases caused by cytomegaloviruses (principally cytomegalic inclusion disease) and provides epidemiological information on these diseases. Cytomegalic inclusion disease is a generalized infection of infants and is caused by intrauterine or early postnatal infection with the virus. The disease may cause severe congenital abnormalities, such as microcephaly (abnormal smallness of the head), motor disability, and mental retardation. Cytomegalovirus infection has also been associated with acquired hemolytic anemia, acute and chronic hepatitis, and an infectious mononucleosis-like syndrome.

• Enzyme Immunoassay

• Epstein-Barr Virus IF Antibody IGM (FDA Code: LJN / 866.3235)

Epstein-Barr virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to Epstein-Barr virus in serum. The identification aids in the diagnosis of Epstein-Barr virus infections and provides epidemiological information on diseases caused by these viruses. Epstein-Barr viruses are thought to cause infectious mononucleosis and have been associated with Burkitt's lymphoma (a tumor of the jaw in African children and young adults) and postnasal carcinoma (cancer).

• Human and Animal Sera (FDA Code: KIS / 864.2800)

Animal and human sera are biological products, obtained from the blood of humans or other animals, that provide the necessary growth-promoting nutrients in a cell culture system.

• Monoclonal Antibody Test

• Polyclonal Antibody

• Polyclonal Antibody Goat Anti-HbsAg IgG

• Polyclonal Antibody Goat Anti-human IgG

• Polyclonal Antibody Goat Anti-mouse IgG

• Polyclonal Antibody Goat Anti-rabbit IgG

• Polyclonal Antibody Goat Anti-whole hCG