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Victorch Meditek, Inc.

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Contact: Ashley Johnson
Web: http://www.victorch.com
E-Mail:
Address: 7313 Carroll Rd., Suite A-b, San Diego, California 92121, USA
Phone: +1-(858)-530-9191 | Fax: +1-(858)-530-9192 | Map/Directions >>
 
 

Profile: Victorch Meditek, Inc. is a manufacturer of in vitro medical diagnostic products. Our product line includes rapid gold assays & ELISA test kits for human hormones, drugs of abuse, cancer markers and infectious diseases. In our rapid tests, the colloidal gold provides a conjugate and color indicator for rapid lateral flow & flow through assays. It is used to react with the substance being detected in patients specimen to form an antigen/antibody complex or sandwich.

FDA Registration Number: 2032364

26 Products/Services (Click for related suppliers)  
• 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.
• 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.
• 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.
• 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.
• CEA Rapid Test
• 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.
• Drugs Of Abuse Test Kits
• ELISA Kits for Cancer
• ELISA Kits for Infectious Diseases& Parasitology
• ELISA Kits for Steroid
• ELISA Test Kits, Human Growth Hormone, (HGH)
• 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.
• Human Chorionic Gonadotropin Radioimmunoassay (FDA Code: JHI / 862.1155)
• In Vitro Diagnostics
• 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.
• Methamphetamine Gas Chromatography Test (FDA Code: LAF / 862.3610)
• Midstream Urine Test
• 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.
• Phencyclidine Enzyme Immunoassay (FDA Code: LCM)
• Pregnancy Urine Card Test
• Syphilis Rapid Test
• 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.
• Urine Dipstick/Analyzers
• Urine Reagent Strips, Glucose
• Urine Strips

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