Profile: Akers Biosciences, Inc. provides two rapid manual assays into the clinical laboratory, which include Pifa® Heparin/PF4 rapid assay and the lithium system. We offer products such as breathscanr, PIFAr Heparin/PF4 rapid assay, Heparin/PF4 antibody serum panels, tri cholesterol, healthtestr cytomegalovirus & healthtestr infectious mononucleosis. Our test formats help to reduce operator error and potentially eliminate the need to outsource laboratory services. Our drugs of abuse are a rapid one step test to detect drug substances in human urine. The test is quick and easy to perform & the results can be read in 5 minutes.

The company was founded in 1989, has revenues of USD 10-25 Million, has ~40 employees. LON:AKR (SEC Filings)

FDA Registration Number: 2247413

1 to 50 of 68 Products/Services (Click for related suppliers)  Page: [1] 2

• Acquired Immune Deficiency Syndrome (AIDS) Antibody Test

• Alcohol Analyzer

• Alcohol Breath Trapping Device (FDA Code: DJZ / 862.3050) A breath-alcohol test system is a device intened to measure alcohol in the human breath. Measurements obtained by this device are used in the diagnosis of alcohol intoxication.

• Alpha-Fetoprotein Rapid Test Strip

• Amphetamine Test Strip

• Anaerotestr Test Strips

• Benzodiazepines Test Strip

• Blood Glucose Test Strips

• Blood Leak Test Strips

• Breath Alcohol Detection System

• BreathScanr Alcohol Detector

• Carcinoembryonic Antigen Rapid Test Strip

• Chlamydia Trachomatis (FDA Code: MGM / 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).

• Chlamydia trachomatis IgA ELISA Kit

• Chlamydia trachomatis IgG ELISA Kit

• Chlamydia Trachomatis IgG Kit

• Chlamydia trachomatis IgM ELISA Kit

• Chlamydia Trachomatis Real Time PCR Kit

• Cholesterol Test Strips

• Cocaine Test Strip

• Creatinine Test Strips

• Cytomegalovirus Enzyme Linked Immunoabsorbent Assay (FDA Code: LFZ / 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.

• Diabetes Test Strips

• Diagnostics Contract Research & Development

• Drugs of Abuse Test Systems (FDA Code: MGX)

• Dry Reagent Test Strips

• 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.

• Fecal Occult Blood Test Strip

• General Virus Reagent

• Glutaraldehyde Test Strips

• Hcg Pregnancy Test Strip

• Hepatitis B Antigen Identification System (FDA Code: KSJ)

• Infectious Mononucleosis Test System (FDA Code: KTN / 866.5640) An infectious mononucleosis immunological test system is a device that consists of the reagents used to measure by immunochemical techniques heterophile antibodies frequently associated with infectious mononucleosis in serum, plasma, and other body fluids. Measurements of these antibodies aid in the diagnosis of infectious mononucleosis.

• Insulin Test Strip

• LDL & VLDL Precipitation, Cholesterol Via Esterase-Oxidase (FDA Code: LBS / 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.

• Leukocyte Typing Test (FDA Code: LGO / 864.7675) A leukocyte peroxidase test is a device used to distinguish certain myeloid cells derived from the bone marrow, i.e., neutrophils, eosinophils, and monocytes, from lymphoid cells of the lymphatic system and erythroid cells of the red blood cell series on the basis of their peroxidase activity as evidenced by staining. The results of this test are used in the differential diagnosis of the leukemias.

• 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).

• Lyme Disease Test

• Menopause Test strip (Urine)

• Methadone Test Strip

• Methamphetamine Test Strip

• Mouse Rheumatoid Factor (RF) ELISA Kit

• Over-The-Counter Blood Glucose Test System (FDA Code: NBW / 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.

• Ovulation Test Strip (Urine)

• Oxidase Test Device for Gonorrhea (FDA Code: LGA / 866.2420) An oxidase screening test for gonorrhea is an in vitro device that consists of the articles intended to identify by chemical reaction, cytochrome oxidase, an oxidizing enzyme that is associated with certain bacteria includingNeisseria gonorrhoeae. A sample of a male's urethral discharge is obtained on a swab which is placed into a wetting agent containing an ingredient that will react with cytochrome oxidase. When cytochrome oxidase is present, the swab turns a dark purple color within 3 minutes. Because it is unlikely that cytochrome oxidase-positive organisms other thanNeisseria gonorrhoeae are present in the urethral discharge of males, the identification of cytochrome oxidase with this device indicates presumptive infection of the patient with the causative agent of gonorrhea.

• Peracetic Acid Test Strips

• PeriScreen Test Strips

• pH Test Strips

• Phencyclidine Test Strip

• Plasma Coagulation Control (FDA Code: GGN / 864.5425) A multipurpose system for in vitro coagulation studies is a device consisting of one automated or semiautomated instrument and its associated reagents and controls. The system is used to perform a series of coagulation studies and coagulation factor assays.