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DRG International, Inc.

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Contact: S. Dawson - Marketing Assistant
Web: http://www.drg-international.com
E-Mail:
Address: 1167 US Highway 22 East, Mountainside, New Jersey 07092, USA
Phone: +1-(908)-233-2075 | Fax: +1-(908)-233-0758 | Map/Directions >>
 
 

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Profile: DRG International, Inc. is a multinational specialty medical equipment and diagnostics manufacturer & distributor. We offer products for enzyme immunoassays, rapid saliva & tumor tests, radio immunoassays & lab equipments. Our enzyme immunoassays include adrenocorticotropic hormone, alpha fetoprotein, anti-nuclear antibodies, atrial natriuretic polypeptide, acylation-stimulating protein, adiponectin rat elisa, neopterin elisa, norepinephrine and vanyl mandelic acid. We offer laboratory equipments such as check strips, microplate reader, incubator, photometer check set, rack tubes, sperm quality analyzer and strip reader.

The company was founded in 1970, has revenues of USD 10-25 Million, has ~100 employees and is ISO 9000, ISO 9001, CE certified.

FDA Registration Number: 2245285

51 to 100 of 196 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 [2] 3 4 >> Next 50 Results
• Chloride Coulometric Test (FDA Code: JFS / 862.1170)
A chloride test system is a device intended to measure the level of chloride in plasma, serum, sweat, and urine. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.
• Chromatographic Barbiturate Identification Test (FDA Code: DKX / 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.
• Clinical Colorimeter (FDA Code: JJQ / 862.2300)
A colorimeter, a photometer, or a spectrophotometer for clinical use is an instrument intended to measure radiant energy emitted, transmitted, absorbed, or reflected under controlled conditions. The device may include a monochromator to produce light of a specific wavelength.
• Clinical Lab Equipment
• Clostridium Difficile Toxin Reagent (FDA Code: LLH / 866.2660)
A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.
• Coated Tube Sep. Rabbit Antibody Digoxin (125-I) Radioimmunoassay (FDA Code: DPO / 862.3320)
A digoxin test system is a device intended to measure digoxin, a cardiovascular drug, in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of digoxin overdose and in monitoring levels of digoxin to ensure appropriate therapy.
• Cocaine (COC) Rapid Home Kit
• 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 Thin Layer Chromatography Test (FDA Code: DMN / 862.3250)
• Complement C3 (FDA Code: CZW / 866.5240)
A complement components immunological test system is a device that consists of the reagents used to measure by immunochemical techniques complement components C1q, C1r, C1s, C2, C3, C4, C5, C6, C7, C8, and C9, in serum, other body fluids, and tissues. Complement is a group of serum proteins which destroy infectious agents. Measurements of these proteins aids in the diagnosis of immunologic disorders, especially those associated with deficiencies of complement components.
• Compound S (11-Deoxycortisol) Radioimmunoassay (FDA Code: JKB / 862.1185)
A compound S (11-dioxycortisol) test system is a device intended to measure the level of compound S (11-dioxycortisol) in plasma. Compound S is a steroid intermediate in the biosynthesis of the adrenal hormone cortisol. Measurements of compound S are used in the diagnosis and treatment of certain adrenal and pituitary gland disorders resulting in clinical symptoms of masculinization and hypertension.
• Computer Softwares
• Control Antiserum Antigen Fitc Sperm (FDA Code: DFX / 866.5800)
A seminal fluid (sperm) immunological test system is a device that consists of the reagents used for legal purposes to identify and differentiate animal and human semen. The test results may be used as court evidence in alleged instances of rape and other sex-related crimes.
• Copper Diethyldithiocarbamate (Colorimetric) (FDA Code: JKZ / 862.1190)
A copper test system is a device intended to measure copper levels in plasma, serum, and urine. Measurements of copper are used in the diagnosis and treatment of anemia, infections, inflammations, and Wilson's disease (a hereditary disease primarily of the liver and nervous system). Test results are also used in monitoring patients with Hodgkin's disease (a disease primarily of the lymph system).
• Coronary Stent (FDA Code: MAF)
• Corticosterone Radioimmunoassay (FDA Code: CHA / 862.1200)
A corticosterone test system is a device intended to measure corticosterone (a steroid secreted by the adrenal gland) levels in plasma. Measurements of corticosterone are used in the diagnosis and treatment of adrenal disorders such as adrenal cortex disorders and blocks in cortisol synthesis.
• Cortisol Radioimmunoassay Test (FDA Code: CGR / 862.1205)
A cortisol (hydrocortisone and hydroxycorticosterone) test system is a device intended to measure the cortisol hormones secreted by the adrenal gland in plasma and urine. Measurements of cortisol are used in the diagnosis and treatment of disorders of the adrenal gland.
• Cryptosporidium Spp. (FDA Code: MHJ / 866.3220)
• Culture Media Supplements (FDA Code: JSK / 866.2450)
A supplement for culture media is a device, such as a vitamin or sugar mixture, that is added to a solid or liquid basal culture medium to produce a desired formulation and that is intended for medical purposes to enhance the growth of fastidious microorganisms (those having complex nutritional requirements). This device aids in the diagnosis of diseases caused by pathogenic microorganisms.
• Cysticercosis Reagent (FDA Code: MDJ / 866.3200)
• Desoxycorticosterone Radioimmunoassay Test (FDA Code: JLE / 862.1250)
A desoxycorticosterone test system is a device intended to measure desoxycorticosterone (DOC) in plasma and urine. DOC measurements are used in the diagnosis and treatment of patients with hypermineralocorticoidism (excess retention of sodium and loss of potassium) and other disorders of the adrenal gland.
• Digoxin (125-I) Radioimmunoassay (FDA Code: LCS / 862.3320)
• Drug Mixture Control Materials (FDA Code: DIF / 862.3280)
A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials.
• Drugs of Abuse Test Systems (FDA Code: MGX)
• ECG Analyzer
• Echinococcus SPP Agglutinating Antigen (FDA Code: GPF / 866.3200)
• ELISA Chemistry Analyzer
• ENT Computer Software
• Entamoeba Histolytica Antigen (FDA Code: KHW / 866.3220)
• Enzyme Immunoassay (EIA) Kits
• Enzyme Immunoassay Test
• Enzyme Labeled Antinuclear Antibody (FDA Code: LJM / 866.5100)
An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjogren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).
• Epstein-Barr Virus (FDA Code: LSE / 866.3235)
Epstein-Barr virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to Epstein-Barr virus in serum. The identification aids in the diagnosis of Epstein-Barr virus infections and provides epidemiological information on diseases caused by these viruses. Epstein-Barr viruses are thought to cause infectious mononucleosis and have been associated with Burkitt's lymphoma (a tumor of the jaw in African children and young adults) and postnasal carcinoma (cancer).
• Epstein-Barr Virus Nuclear Antigen Test (FDA Code: LLM / 866.3235)
• 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.
• Escherichia Coli Antigens (FDA Code: GMZ / 866.3255)
• Estradiol Radioimmunoassay Test (FDA Code: CHP / 862.1260)
An estradiol test system is a device intended to measure estradiol, an estrogenic steroid, in plasma. Estradiol measurements are used in the diagnosis and treatment of various hormonal sexual disorders and in assessing placental function in complicated pregnancy.
• Estriol Radioimmunoassay Test (FDA Code: CGI / 862.1265)
An estriol test system is a device intended to measure estriol, an estrogenic steroid, in plasma, serum, and urine of pregnant females. Estriol measurements are used in the diagnosis and treatment of fetoplacental distress in certain cases of high-risk pregnancy.
• Estrone Radioimmunoassay Test (FDA Code: CGF / 862.1280)
An estrone test system is a device intended to measure estrone, an estrogenic steroid, in plasma. Estrone measurements are used in the diagnosis and treatment of numerous disorders, including infertility, amenorrhea, differentiation of primary and secondary ovarian malfunction, estrogen secreting testicular and ovarian tumors, and precocious puberty in females.
• Febrile Antigens Slide/Tube Test (FDA Code: GNC / 866.3550)
• Ferritin (FDA Code: DBF / 866.5340)
A ferritin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the ferritin (an iron-storing protein) in serum and other body fluids. Measurements of ferritin aid in the diagnosis of diseases affecting iron metabolism, such as hemochromatosis (iron overload) and iron deficiency amemia.
• Fertility Monitoring Test
• Fertility Monitors, Pregnancy Test Kits
• Follicle Stimulating Hormone Radioimmunoassay (FDA Code: CGJ / 862.1300)
A follicle-stimulating hormone test system is a device intended to measure follicle-stimulating hormone (FSH) in plasma, serum, and urine. FSH measurements are used in the diagnosis and treatment of pituitary gland and gonadal disorders.
• Free Thyroxine Radioimmunoassay (FDA Code: CEC / 862.1695)
A free thyroxine test system is a device intended to measure free (not protein bound) thyroxine (thyroid hormone) in serum or plasma. Levels of free thyroxine in plasma are thought to reflect the amount of thyroxine hormone available to the cells and may therefore determine the clinical metabolic status of thyroxine. Measurements obtained by this device are used in the diagnosis and treatment of thyroid diseases.
• Galactose Enzymatic Method Test (FDA Code: JIA / 862.1310)
A galactose test system is a device intended to measure galactose in blood and urine. Galactose measurements are used in the diagnosis and treatment of the hereditary disease galactosemia (a disorder of galactose metabolism) in infants.
• Gardnerella Vaginalis DNA-Probe (FDA Code: MJM / 866.2660)
• Gastrin Radioimmunoassay Test (FDA Code: CGC / 862.1325)
A gastrin test system is a device intended to measure the hormone gastrin in plasma and serum. Measurements of gastrin are used in the diagnosis and treatment of patients with ulcers, pernicious anemia, and the Zollinger-Ellison syndrome (peptic ulcer due to a gastrin-secreting tumor of the pancreas).
• General Medical Equipment

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