Profile: Biomerica manufactures and distributes medical diagnostic products for the laboratory, doctor's office & pharmacy use. Our products are used for the detection & monitoring of chronic diseases & certain medical conditions. Our allerquant 14G elisa kit is intended for in vitro quantitative analysis of IgG antibodies to 14 specific food allergens in human serum. Our EZ-HCG(tm) is a one-step immunoassay for the rapid, qualitative determination of human chorionic gonadotropin (hCG) in urine, for the early detection of pregnancy.

The company was founded in 1971, has revenues of USD 5-10 Million, has ~30 employees and is ISO, CE certified. OTC:BMRA (SEC Filings)

FDA Registration Number: 2025099

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• ACTH Radioimmunoassay Test (FDA Code: CKG / 862.1025) An adrenocorticotropic hormone (ACTH) test system is a device intended to measure adrenocorticotropic hormone in plasma and serum. ACTH measurements are used in the differential diagnosis and treatment of certain disorders of the adrenal glands such as Cushing's syndrome, adrenocortical insufficiency, and the ectopic ACTH syndrome.

• Allergy Test

• Allergy Testing

• Amphetamine Enzyme Immunoassay Test (FDA Code: DKZ / 862.3100) An amphetamine test system is a device intended to measure amphetamine, a central nervous system stimulating drug, in plasma and urine. Measurements obtained by this device are used in the diagnosis and treatment of amphetamine use or overdose and in monitoring levels of amphetamine to ensure appropriate therapy.

• Amphetamine Urine Dip Strip Test

• Antigen (PSA) - Detection Kit

• Barbiturate Enzyme Immunoassay Test (FDA Code: DIS / 862.3150) A barbiturate test system is a device intended to measure barbiturates, a class of hypnotic and sedative drugs, in serum, urine, and gastric contents. Measurements obtained by this device are used in the diagnosis and treatment of barbiturate use or overdose and in monitoring levels of barbiturate to ensure appropriate therapy.

• Barbiturates Test Device

• Benzodiazepine Enzyme Immunoassay Test (FDA Code: JXM / 862.3170) A benzodiazepine test system is a device intended to measure any of the benzodiazepine compounds, sedative and hypnotic drugs, in blood, plasma, and urine. The benzodiazepine compounds include chlordiazepoxide, diazepam, oxazepam, chlorzepate, flurazepam, and nitrazepam. Measurements obtained by this device are used in the diagnosis and treatment of benzodiazepine use or overdose and in monitoring levels of benzodiazepines to ensure appropriate therapy.

• Benzodiazepines Test Strip

• Bio-Intact PTH Testing Kit

• Biopotential Amplifier and Signal Conditioner (FDA Code: DRR / 870.2050) A biopotential amplifier and signal conditioner is a device used to amplify or condition an electrical signal of biologic origin.

• C-Peptide ELISA Kit

• C-Reactive Protein (CRP), FITC Conjugate (FDA Code: DCK / 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.

• Calcitonin

• Calcitonin Assay Immunoradiometric (IRMA) Assay

• Calcitonin ELISA Kit

• Calcitonin Immunoassay

• calcitonin nasal Spray

• Calcitonin Radioimmunoassay

• Calcitonin Radioimmunoassay Test (FDA Code: JKR / 862.1140) A calcitonin test system is a device intended to measure the thyroid hormone calcitonin (thyrocalcitonin) levels in plasma and serum. Calcitonin measurements are used in the diagnosis and treatment of diseases involving the thyroid and parathyroid glands, including carcinoma and hyperparathyroidism (excessive activity of the parathyroid gland).

• Calcitonin RIA Kit

• Campylobacter Pylori (FDA Code: LYR / 866.3110)

• Cancer Detection Test

• Candida Albicans ID Antigen (FDA Code: LHK / 866.3165)

• Cannabinoids Enzyme Immunoassay Test (FDA Code: LDJ / 862.3870) A cannabinoid test system is a device intended to measure any of the cannabinoids, hallucinogenic compounds endogenous to marihuana, in serum, plasma, saliva, and urine. Cannabinoid compounds includedelta -9-tetrahydrocannabinol, cannabidiol, cannabinol, and cannabichromene. Measurements obtained by this device are used in the diagnosis and treatment of cannabinoid use or abuse and in monitoring levels of cannabinoids during clinical investigational use.

• Cocaine and Cocaine Metabolites Enzyme Immunoassay Test (FDA Code: DIO / 862.3250) A cocaine and cocaine metabolite test system is a device intended to measure cocaine and a cocaine metabolite (benzoylecgonine) in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of cocaine use or overdose.

• Cocaine Test Strip

• Diabetes Test

• Diagnostic Products

• Drugs Of Abuse Test Kits

• Elisa Allergy test Kit

• Enzyme Immunoassay

• Enzyme Immunoassay Test

• Erythropoietin (Epo)

• Erythropoietin Assay (FDA Code: GGT / 864.7250) A erythropoietin assay is a device that measures the concentration of erythropoietin (an enzyme that regulates the production of red blood cells) in serum or urine. This assay provides diagnostic information for the evaluation of erythrocytosis (increased total red cell mass) and anemia.

• Fecal Occcult Blood Enzymatic Method

• Fertility Monitors, Pregnancy Test Kits

• Glutamic Acid Decarboxylase (GAD) Autoantibody

• HCG Over The Counter Pregnancy Test Kit (FDA Code: LCX / 862.1155) A human chorionic gonadotropin (HCG) test system is a device intended for the early detection of pregnancy is intended to measure HCG, a placental hormone, in plasma or urine.

• Home Allergy Test Kit

• Home pregnancy test kits, Hcg

• Human Chorionic Gonadotropin (hCG)

• Human Chorionic Gonadotropin Radioimmunoassay (FDA Code: JHI / 862.1155)

• Human Erythropoietin ELISA Kits

• Human Myoglobin ELISA Kits

• Indirect Immunofluorescent Anti-Thyroid Antibody

• Insulin Autoantibody (IAA)

• Intact PTH

• Latex Allergy Test Kit