Profile: Biomedical Technologies, Inc. manufactures growth factor and attachment factor products. Our extensive product line includes receptor-grade, aseptically packaged GFs and AFs. These are highly purified proteins that have been membrane filtered, aseptically filled and lyophilized. Our growth factors are tested in cell culture, receptor binding studies and in immunoassays. Our epidermal growth factor is isolated from mouse sub maxillary glands and is purified to electrophoretic homogeneity. Our endothelial mitogen is a partially purified preparation from bovine hypothalamus. It is originally prepared to facilitate the growth and survival of human (or mammalian) vascular endothelial cells in vitro. Our lipoproteins are isolated from fresh blood-bank produced human plasma. Each product is prepared via ultracentrifugation and is analyzed by agarose gel electrophoresis.
The company was founded in 1981, has revenues of USD 1-5 Million, has ~10 employees.
39 Products/Services (Click for related suppliers)
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| • Bone Wax (FDA Code: MTJ) |
| • Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045) A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure. |
| • Cell Growth Factors & Attachment Factors |
| • Cyclic AMP Radioimmunoassay Test (FDA Code: CHO / 862.1230) A cyclic AMP test system is a device intended to measure the level of adenosine 3', 5'-monophosphate (cyclic AMP) in plasma, urine, and other body fluids. Cyclic AMP measurements are used in the diagnosis and treatment of endocrine disorders, including hyperparathyroidism (overactivity of the parathyroid gland). Cyclic AMP measurements may also be used in the diagnosis and treatment of Graves' disease (a disorder of the thyroid) and in the differentiation of causes of hypercalcemia (elevated levels of serum calcium.) |
| • Cyclic GMP EIA Kits |
| • Cyclic GMP Radioimmunoassay Test (FDA Code: CGT / 862.1230) |
| • Diagnostics Contract Research & Development |
| • Disposable Pipette Tips, Non-sterile Disposable Tips |
| • ENT Synthetic Polyamide Polymer (FDA Code: KHJ / 874.3620) Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene. |
| • Enzyme Immunoassay |
| • Enzyme Immunoassay Test |
| • Filter Pipette Tips |
| • Human EGF EIA Kits |
| • Human Fibronectin Elisa Kits |
| • Human Fibronectins |
| • Human Involucrin Elisa Assays |
| • Human Lysozyme EIA Kits |
| • Human Osteocalcin RIA Kits |
| • Human TGF-alpha RIA Kits |
| • Immunochemical, Lysozyme (FDA Code: JMR / 862.1490) A lysozyme (muramidase) test system is a device intended to measure the activity of the bacteriolytic enzyme lysozyme (muramidase) in serum, plasma, leukocytes, and urine. Lysozyme measurements are used in the diagnosis and treatment of monocytic leukemia and kidney disease. |
| • Indirect Immunofluorescent Anti-Smooth Muscle Antibody Test (FDA Code: DBE / 866.5120) An antismooth muscle antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the antismooth muscle antibodies (antibodies to nonstriated, involuntary muscle) in serum. The measurements aid in the diagnosis of chronic hepatitis (inflammation of the liver) and autoimmune connective tissue diseases (diseases resulting from antibodies produced against the body's own tissues). |
| • Intact Human Osteocalcin EIA Kits |
| • Involucrin ELISA Kits |
| • Labware, Pipette Tip |
| • Low Density Lipoprotein (FDA Code: DFC / 866.5600) A low-density lipoprotein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the low-density lipoprotein in serum and other body fluids. Measurement of low-density lipoprotein in serum may aid in the diagnosis of disorders of lipid (fat) metabolism and help to identify young persons at risk from cardiovascular diseases. |
| • Lysozyme |
| • Micro Pipette Tips and Tip Racks |
| • Mid-Tact Human Osteocalcin EIA Kits |
| • Neuroleptic Drugs Radioreceptor Assay (FDA Code: LPX / 862.3645) A neuroleptic drugs radioceptor assay test system is a device intended to measure in serum or plasma the dopamine receptor blocking activity of neuroleptic drugs and their active metabolites. A neuroleptic drug has anti-psychotic action affecting principally psychomotor activity, is generally without hypnotic effects, and is a tranquilizer. Measurements obtained by this device are used to aid in determining whether a patient is taking the prescribed dosage level of such drugs. |
| • Non-Alterable Preformed Skull Bone Plate (FDA Code: GXN / 882.5330) A preformed nonalterable cranioplasty plate is a device that is implanted in a patient to repair a skull defect and is constructed of a material, e.g., stainless steel or vitallium, that cannot be altered or reshaped at the time of surgery without changing the chemical behavior of the material. |
| • Non-Barrier Pipette Tip, Racked |
| • Non-Sterile Barrier Pipette Tips |
| • Pipette Tip Disposal Box |
| • Racked Non-Sterile Non-Barrier Multi-Channel Pipette Tips |
| • Racked Non-Sterile Non-Barrier Pipette Tips |
| • Radioimmunoassay Test |
| • Radioreceptor Test |
| • Sterile Barrier Pipette Tips |
| • Sterile Non-Barrier Pipette Tips |