IBL International GmbH

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Contact: G. Neubert - National Sales Manager
Web: http://www.ibl-international.com
E-Mail:
Address: Flughafenstr. 52a, Hamburg D-22335, Germany
Phone: +49-(40)-532891-0 | Fax: +49-(40)-532891-11 | Map/Directions >>

Profile: IBL International GmbH is engaged in the development, production and distribution of in-vitro diagnostic test systems for routine & research use. Our product range covers diagnostic fields like endocrinology, neuroscience, tumor markers, cytokines, auto immunity and infectious diseases. Our comprehensive infectious disease line allows determination of almost all infectious parameters by enzyme immunoassay, including toxoplasmosis, rubella, chlamydia and cytomegalovirus. The Neopterin ELISA screens blood donations to determine early stages of various viral infections. The test for the determination of autoantibodies directed to acetylcholine receptors is used for the diagnosis and follow-up of myasthenia gravis.

The company was founded in 1983, has revenues of USD 5-10 Million, has ~50 employees and is ISO 9001, ISO 13485 certified.

FDA Registration Number: 9710337
US Agent: Laura Nea / Tecan U.s.
Phone: +1-(919)-361-5200 Fax: +1-(919)-361-5201 E-Mail:

23 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.

• Acetylcholine Blocking And Non-Blocking Acetylcholine Receptor Autoantibodies (FDA Code: NST / 866.5660)

A multiple autoantibodies immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoantibodies (antibodies produced against the body's own tissues) in serum and other body fluids. Measurement of multiple autoantibodies aids in the diagnosis of autoimmune disorders (disease produced when the body's own tissues are injured by autoantibodies).

• Allergy Syringe

• Allergy Syringe Organizer

• Allergy Syringes/Trays

• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 862.1660)

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• C. Diphtheriae Fluorescent Antiserum (FDA Code: GOS / 866.3140)

• Catecholamines Chromatographic/Fluorometric Method Test (FDA Code: CHQ / 862.1165)

A catecholamines (total) test system is a device intended to determine whether a group of similar compounds (epinephrine, norepinephrine, and dopamine) are present in urine and plasma. Catecholamine determinations are used in the diagnosis and treatment of adrenal medulla and hypertensive disorders, and for catecholamine-secreting tumors (pheochromo-cytoma, neuroblastoma, ganglioneuroma, and retinoblastoma).

• Catecholamines Electrophoretic Method Test (FDA Code: CHT / 862.1165)

• Chrome Alum Hematoxylin (FDA Code: ICI / 864.1850)

Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

• 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 Labeled Anti-DNA Antibody (FDA Code: LRM / 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).

• 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.

• Haemophilus Influenza Antiserum (FDA Code: GRP / 866.3300)

• Inhibin-A Enzyme Immunoassay (FDA Code: NDR / 862.1260)

• Insulin Injector

• Lipoprotein(A) Test System (FDA Code: MSM / 862.1475)

A lipoprotein test system is a device intended to measure lipoprotein in serum and plasma. Lipoprotein measurements are used in the diagnosis and treatment of lipid disorders (such as diabetes mellitus), atherosclerosis, and various liver and renal diseases.

• Metabolism Analyzer

• Nitrosonaphthol Test for 5-Hydroxyindole Acetic Acid Nitrous Acid (FDA Code: CDA / 862.1390)

A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic acid/serotonin in urine. Measurements of 5-hydroxyindole acetic acid/serotonin are used in the diagnosis and treatment of carcinoid tumors of endocrine tissue.

• 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.

• 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.

• Secondary Calibrator (FDA Code: JIT / 862.1150)

A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also 862.2 in this part.)

• Testosterones and Dihydrotestosterone Radioimmunoassay (FDA Code: CDZ / 862.1680)

A testosterone test system is a device intended to measure testosterone (a male sex hormone) in serum, plasma, and urine. Measurement of testosterone are used in the diagnosis and treatment of disorders involving the male sex hormones (androgens), including primary and secondary hypogonadism, delayed or precocious puberty, impotence in males and, in females hirsutism (excessive hair) and virilization (masculinization) due to tumors, polycystic ovaries, and adrenogenital syndromes.