Profile: Cenogenics Corp. specializes in the manufacturing, distribution and contract manufacturing of in-vitro diagnostic tests. We manufacture and distribute immunodiagnostic test systems for syphilis, c-reactive protein, rheumatoid factor, infectious mononucleosis, febrile antigens, and rapid one-step tests for pregnancy & ovulation. Our SB-19 Tri-Slide™ patient envelope kit contains 50 patient envelope kits. Each patient Kit contains one Tri-Slide with controls and 3 applicator sticks. The envelopes are printed with patient instructions. It also has 3 X 10ml developing solution. Our SB-24 stool blood tape test kit contains 100 inches tape in dispenser and a 10ml developing solution.
The company was founded in 1981, has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001:2008, ISO 13485:2003 certified.
FDA Registration Number: 2250030
27 Products/Services (Click for related suppliers)
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• Antisera, Control for Non-Treponemal Test (FDA Code: GMP / 866.3820) |
• Antistreptolysin-Titer/Streptolysin O Reagent (FDA Code: GTQ / 866.3720) |
• Brucella Spp Agglutination Antigen (FDA Code: GSO / 866.3085) |
• C-Reactive Protein (CRP) |
• C-Reactive Protein Test System (FDA Code: DCN / 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. |
• Colorectal Cancer Test |
• Diagnostic Kits |
• Diagnostic Reagents |
• Diagnostic Test Kits For Pregnancy |
• Febrile Antigen (FDA Code: GSZ / 866.3410) |
• Febrile Antigens Slide/Tube Test (FDA Code: GNC / 866.3550) |
• Fecal Occult Blood Test |
• Fecal Occult Blood Test Kits |
• 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) |
• 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. |
• Lyme Disease Test |
• Non-Treponemal Antigen (FDA Code: GMQ / 866.3820) |
• Occult Blood Reagent (FDA Code: KHE / 864.6550) An occult blood test is a device used to detect occult blood in urine or feces. (Occult blood is blood present in such small quantities that it can be detected only by chemical tests of suspected material, or by microscopic or spectroscopic examination.) |
• Positive and Negative Febrile Antigen Control Serum (FDA Code: GSN / 866.3085) |
• Rheumatoid Factor (RF) |
• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775) A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis. |
• Rose Bengal Brucella Antigen |
• Streptolysin O (FDA Code: IBA / 864.4400) Enzyme preparations are products that are used in the histopathology laboratory for the following purposes: |
• Syphilis Serology Reagents |
• Urinalysis Test Strips |
• Urinary Enzymatic Method (FDA Code: JIL / 862.1340) A urinary glucose (nonquantitative) test system is a device intended to measure glucosuria (glucose in urine). Urinary glucose (nonquantitative) measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, hypoglycemia, and hyperglycemia. |