Demeditec Diagnostics

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Contact: Mark Kowal
Web: http://www.demeditec.com
E-Mail:
Address: Lise-Meitner-Str 2, Kiel-Wellsee D-24145, Germany
Phone: +49-(431)-71922-0 | Map/Directions >>

Profile: Demeditec Diagnostics deals with diagnostic test kits used in clinical laboratories. Our test kits are designed to be used for samples like blood, serum, plasma, and urine. We offer immunoassays ELISA technology & radioactive label tests that are used for the investigation of autoimmune diseases, thyroid disease, infertility and rheumatoid disease. Our Aspergillus fumigatus IgA antibody Elisa test kit is designed for the detection and quantitative determination of specific IgA antibodies against aspergillus fumigatus in serum and plasma.

The company is ISO 9001 , ISO 13485 certified.

FDA Registration Number: 3005542422
US Agent: Marka.kowal / Immuno-biological Laboratories, Inc.
Phone: +1-(763)-780-2955 Fax: +1-(763)-780-2988 E-Mail:

21 Products/Services (Click for related suppliers)

• 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.

• 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.

• 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.

• 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).

• 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.

• Diagnostic Kits

• Diagnostic Rapid Test 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 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.

• 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.

• 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).

• Glucagon Radioimmunoassay Test (FDA Code: JME / 862.1335)

A glucagon test system is a device intended to measure the pancreatic hormone glucagon in plasma and serum. Glucagon measurements are used in the diagnosis and treatment of patients with various disorders of carbohydrate metabolism, including diabetes mellitus, hypoglycemia, and hyperglycemia.

• Human Growth Hormone Radioimmunoassay (FDA Code: CFL / 862.1370)

A human growth hormone test system is a device intended to measure the levels of human growth hormone in plasma. Human growth hormone measurements are used in the diagnosis and treatment of disorders involving the anterior lobe of the pituitary gland.

• Immunoassays

• Infectious Disease Test Kits

• Progesterone Radioimmunoassay Test (FDA Code: JLS / 862.1620)

A progesterone test system is a device intended to measure progesterone (a female hormone) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of disorders of the ovaries or placenta.

• Prolactin Radioimmunoassay (FDA Code: CFT / 862.1625)

A prolactin (lactogen) test system is a device intended to measure the anterior pituitary polypeptide hormone prolactin in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of disorders of the anterior pituitary gland or of the hypothalamus portion of the brain.

• Radioimmunoassay for Dehydroepiandrosterone Sulfate (FDA Code: JKC / 862.1245)

A dehydroepiandrosterone (free and sulfate) test system is a device intended to measure dehydroepiandrosterone (DHEA) and its sulfate in urine, serum, plasma, and amniotic fluid. Dehydroepiandrosterone measurements are used in the diagnosis and treatment of DHEA-secreting adrenal carcinomas.

• Saliva Testing

• Tumor Markers