Profile: Diagnostic Systems Laboratories, Inc. develops and markets in vitro diagnostics. We are an ISO 9001, CE MARK & ISO 13485 certified company. Our DSL active cortisol (saliva) EIA is optimized specifically to measure cortisol in human saliva. Our ferritin kit consists of specific two-site IRMA, with antibodies prepared against human spleen-derived ferritin. By continually exploring new technologies and applications, we stay at the forefront of the in vitro diagnostic industry in terms of innovation and responsiveness to evolving laboratory procedures
The company was founded in 1981, has revenues of USD 10-25 Million, has ~110 employees and is ISO 9001, CE certified.
• 11-keto Testosterone EIA Kit |
• 17- Dehydroxy Progesterone Testing Set |
• 17-Hydroxyprogesterone Radioimmunoassay Test (FDA Code: JLX / 862.1395) A 17-hydroxyprogesterone test system is a device intended to measure 17-hydroxyprogesterone (a steroid) in plasma and serum. Measurements of 17-hydroxyprogesterone are used in the diagnosis and treatment of various disorders of the adrenal glands or the ovaries. |
• 17-OH Progesterone Kit |
• ACTH Radioimmunoassay Test (FDA Code: CKG / 862.1025) An adrenocorticotropic hormone (ACTH) test system is a device intended to measure adrenocorticotropic hormone in plasma and serum. ACTH measurements are used in the differential diagnosis and treatment of certain disorders of the adrenal glands such as Cushing's syndrome, adrenocortical insufficiency, and the ectopic ACTH syndrome. |
• Aldosterone Radioimmunoassay Test (FDA Code: CJM / 862.1045) An aldosterone test system is a device intended to measure the hormone aldosterone in serum and urine. Aldosterone measurements are used in the diagnosis and treatment of primary aldosteronism (a disorder caused by the excessive secretion of aldosterone by the adrenal gland), hypertension caused by primary aldosteronism, selective hypoaldosteronism, edematous states, and other conditions of electrolyte imbalance. |
• Alpha-Fetoprotein for Testicular Cancer Test Kit (FDA Code: LOJ / 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. |
• Androstenedione Radioimmunoassay Test (FDA Code: CIZ / 862.1075) An androstenedione test system is a device intended to measure androstenedione (a substance secreted by the testes, ovary, and adrenal glands) in serum. Adrostenedione measurements are used in the diagnosis and treatment of females with excessive levels of androgen (male sex hormone) production. |
• Angiotensin I and Renin Radioimmunoassay Test (FDA Code: CIB / 862.1085) An angiotensin I and renin test system is a device intended to measure the level of angiotensin I generated by renin in plasma. Angiotensin I measurements are used in the diagnosis and treatment of certain types of hypertension. |
• Blood Bank Test Kits |
• C Peptides of Proinsulin Radioimmunoassay Test (FDA Code: JKD / 862.1135) A C-peptides of proinsulin test system is a device intended to measure C-peptides of proinsulin levels in serum, plasma, and urine. Measurements of C-peptides of proinsulin are used in the diagnosis and treatment of patients with abnormal insulin secretion, including diabetes mellitus. |
• Calcitonin |
• Calcitonin Assay Immunoradiometric (IRMA) Assay |
• Calcitonin ELISA Kit |
• Calcitonin Immunoassay |
• calcitonin nasal Spray |
• Calcitonin Radioimmunoassay |
• Calcitonin Radioimmunoassay Test (FDA Code: JKR / 862.1140) A calcitonin test system is a device intended to measure the thyroid hormone calcitonin (thyrocalcitonin) levels in plasma and serum. Calcitonin measurements are used in the diagnosis and treatment of diseases involving the thyroid and parathyroid glands, including carcinoma and hyperparathyroidism (excessive activity of the parathyroid gland). |
• Calcitonin RIA Kit |
• Cancer Test Kits |
• Carcinoembryonic antigen (CEA) |
• Cardiac Markers kits |
• 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. |
• Enzyme Immunoassay Chemistry Analyzer |
• 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. |
• Estradiol |
• Estradiol ELISA Kit |
• Estradiol Kits |
• 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 |
• Estrone E1 ELISA Kit |
• Estrone ELISA Kits |
• 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. |
• Estrone-3 Glucuronide, Fertility Monitor |
• Estrone-3-Glucuronide (E1G) EIA Test Kit |
• 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. |
• FerritiN EliSA Test Kit |
• Ferritin Enzyme Immunoassay Test Kit |
• Ferritin Radioimmunoassay Test (FDA Code: JMG / 866.5340) |
• Ferritin Testing Kit |
• 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 Estriol (E3) |
• Free Or Complexed Prostate Specific Antigen (PSA) |
• Free Prostate Specific Antigen (PSA) |
• Gamma Dab Ferritin Kit |
• Guinea Pig Anti-Insulin Detection Kit |
• Hormone Reagents & Test Kits |
• Hormone Test Kit, Estrone |
• Hormone Test Kits |