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Instrumentation Laboratory (Belgium) N.V./S.A

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Web: http://www.il-nl.com
E-Mail:
Address: Excelsiorlaan 48-50, Bus 8, Zaventem 1930, Belgium
Phone: +32-(2)-725-20-52 | Fax: +32-(2)-721-24-09 | Map/Directions >>
 
 

Profile: Instrumentation Laboratory (Belgium) N.V./S.A is a developer, manufacturer and distributor of in vitro diagnostic instruments, reagents, controls, consumables & services for use primarily in hospitals & clinical laboratories. Our products include critical care, hemostasis, clinical chemistry, automated urine microscopy and laboratory data management. Our ACL™ Top™ analyzer is a fully automated, user-friendly system that helps high volume labs maximize labor resources and improve patient care. This system provides clotting, chromogenic and immunoturbidimetric testing capabilities with a complete menu of routine & specialty assays. It is a powerful, intuitive system that offers 24-hour, 7-day continuous operation without interruption to workflow allowing the lab to increase testing efficiency and reduce turnaround time. The GEM Premier 4000 is a comprehensive whole blood analyzer offering a flexible analyte menu including pH, pO2, pCO2, electrolytes, metabolites and onboard CO-oximetry.

The company has revenues of < USD 1 Million, has ~20 employees and is ISO 9002, CE certified.

14 Products/Services (Click for related suppliers)  
• Automated Coagulation Analyzer (FDA Code: GKP / 864.5400)
A coagulation instrument is an automated or semiautomated device used to determine the onset of clot formation for in vitro coagulation studies.
• Blood Gas/pH analyzer
• Carbamazepine Enzyme Immunoassay Test (FDA Code: KLT / 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.
• Carcinoembryonic Antigen Test System (FDA Code: DHX / 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.
• Centrifugal Chemistry Analyzer (FDA Code: JJG / 862.2140)
A centrifugal chemistry analyzer for clinical use is an automatic device intended to centrifugally mix a sample and a reagent and spectrophotometrically measure concentrations of the sample constituents. This device is intended for use in conjunction with certain materials to measure a variety of analytes.
• Co-Oximeter
• Digoxin Enzyme Immunoassay Test (FDA Code: KXT / 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.
• Electrolyte Chemistry Analyzer
• Gentamicin Enzyme Immunoassay Test (FDA Code: LCD / 862.3450)
A gentamicin test system is a device intended to measure gentamicin, an antibiotic drug, in human specimens. Measurements obtained by this device are used in the diagnosis and treatment of gentamicin overdose and in monitoring levels of gentamicin to ensure appropriate therapy.
• Phenobarbital Enzyme Immunoassay Test (FDA Code: DLZ / 862.3660)
A phenobarbitol test system is a device intended to measure phenobarbital, an antiepileptic and sedative-hypnotic drug, in human specimens. Measurements obtained by this device are used in the diagnosis and treatment of phenobarbital use or overdose and in monitoring levels of phenobarbital to ensure appropriate therapy.
• Programmable Multi-Channel Chemistry Analyzer
• Theophylline Enzyme Immunoassay Test (FDA Code: KLS / 862.3880)
A theophylline test system is a device intended to measure theophylline (a drug used for stimulation of the muscles in the cardiovascular, respiratory, and central nervous systems) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of theophylline overdose or in monitoring levels of theophylline to ensure appropriate therapy.
• Therapeutic Drug Monitor Chemistry Analyzer
• Toxicology Lithium Flame Photometer

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