UCP Biosciences, Inc.

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Web: http://www.ucpbiosciences.com
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Address: 1445 Koll Circle, Ste. 111, San Jose, California 95112, USA
Phone: +1-(408)-392-0064 | Fax: +1-(408)-392-0163 | Map/Directions >>

Profile: UCP Biosciences, Inc. specializes in lateral flow rapid tests by utilizing thin-layer chromatography to detect the presence of specific antigens, antibodies in urine, feces, serum, plasma or whole blood. Our rapid diagnostic tests are simple, easy to use and provide a preliminary diagnosis in minutes instead of days. We currently have several medical device formats available including Dipstick, Cassette, Dip card, Midstream and Cup. Our main product lines contain four major categories namely; drugs of abuse, fertility, infectious diseases and tumor markers. Our luteinizing hormone (LH) ovulation urine test is designed to detect LH surge in urine and is an ideal test for predicting ovulation. Our human follicle stimulating hormone (FSH) menopause urine test is designed to detect FSH in urine. It is helpful in predicting menopause or identifying gonadal dysfunction.

FDA Registration Number: 3004987297

41 Products/Services (Click for related suppliers)

• Alphafetoprotein Tests

• 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 Test Strip

• Amphetamine Urine Dip Strip Test

• 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.

• Barbiturate Urine Cassette Test

• 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.

• Benzodiazepine Urine Cassette Test

• Benzodiazepines Test Strip

• 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.

• Carcinoembryonic Antigen Test System (FDA Code: DHX / 866.6010)

A tumor-associated antigen immunological test system is a device that consists of reagents used to qualitatively or quantitatively measure, by immunochemical techniques, tumor-associated antigens in serum, plasma, urine, or other body fluids. This device is intended as an aid in monitoring patients for disease progress or response to therapy or for the detection of recurrent or residual disease.

• 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

• Cocaine Urine Dip Strip Test

• Cocaine Urine Drug Test

• Drugs Of Abuse Test Kits

• Fertility Tests

• H. Pylori Test Kits

• H.Pylori Testing kits

• Hcg Pregnancy Test Strip

• HIV and H.Pylori testing kits

• HIV Detection Test (FDA Code: MZF)

• Infectious Disease Test Kits

• Menopause Test kits

• Menopause Test strip (Urine)

• Metamphetamine Thin Layer Chromatography Test (FDA Code: DJC / 862.3610)

A methamphetamine test system is a device intended to measure methamphetamine, a central nervous system stimulating drug, in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of methamphetamine use or overdose.

• Methadone Enzyme Immunoassay Test (FDA Code: DJR / 862.3620)

A methadone test system is a device intended to measure methadone, an addictive narcotic pain-relieving drug, in serum and urine. Measurements obtained by this device are used in the diagnosis and treatment of methadone use or overdose and to determine compliance with regulations in methadone maintenance treatment.

• Methadone Gas Chromatography Test (FDA Code: DMB / 862.3620)

• Methadone Test Strip

• Opiates Enzyme Immunoassay Test (FDA Code: DJG / 862.3650)

An opiate test system is a device intended to measure any of the addictive narcotic pain-relieving opiate drugs in blood, serum, urine, gastric contents, and saliva. An opiate is any natural or synthetic drug that has morphine-like pharmocological actions. The opiates include drugs such as morphine, morphine glucoronide, heroin, codeine, nalorphine, and meperedine. Measurements obtained by this device are used in the diagnosis and treatment of opiate use or overdose and in monitoring the levels of opiate administration to ensure appropriate therapy.

• Ovulation Test

• Ovulation Test Strip (Urine)

• Phencyclidine Enzyme Immunoassay (FDA Code: LCM)

• Propoxyphene Enzyme Immunoassay (FDA Code: JXN / 862.3700)

A propoxyphene test system is a device intended to measure propoxyphene, a pain-relieving drug, in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of propoxyphene use or overdose or in monitoring levels of propoxyphene to ensure appropriate therapy.

• Prostate-Specific Antigen Tests

• Testing Devices

• Tricyclic Antidepressant Drugs Radioimmunoassay Test (FDA Code: LFG / 862.3910)

A tricyclic antidepressant drugs test system is a device intended to measure any of the tricyclic antidepressant drugs in serum. The tricyclic antidepressant drugs include imipramine, desipramine, amitriptyline, nortriptyline, protriptyline, and doxepin. Measurements obtained by this device are used in the diagnosis and treatment of chronic depression to ensure appropriate therapy.

• Tricyclic Antidepressants

• Tumor Marker Test Kits

• Tumor Markers