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Bit Analytical Instruments

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Contact: Ruediger Gerd Foerster
Web: http://www.bit-instruments.com
E-Mail:
Address: Am Kronberger Hang 3, Schwalbach/taunus DE-65824, Germany
Phone: +49-(6196)-806 100 | Fax: +49-(6196)-806 111 | Map/Directions >>
 
 

Profile: Bit Analytical Instruments is a contract service provider for a wide range of analytical and medical instrument applications. We merge customer's application know-how with our medical instrumentation & provide reliable tailor-made system solutions. We also provide module development including electronics & embedded software, instrument development including embedded, user- and GUI-software, and product life time support.

The company is ISO13485, 9001, FDA certified.

FDA Registration Number: 3003601075
US Agent: Sandeep Lad / Sandeep Lad
Phone: +1-(858)-613-1200  E-Mail:

9 Products/Services (Click for related suppliers)  
• Antistreptolysin-Titer/Streptolysin O Reagent (FDA Code: GTQ / 866.3720)
• IGA Control (FDA Code: CZP / 866.5510)
An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.
• IgG Control (FDA Code: DEW / 866.5510)
• Multipurpose System for Invitro Coagulation Studies (FDA Code: JPA / 864.5425)
A multipurpose system for in vitro coagulation studies is a device consisting of one automated or semiautomated instrument and its associated reagents and controls. The system is used to perform a series of coagulation studies and coagulation factor assays.
• Nephelometer (FDA Code: JZW / 866.4540)
Immunonephelometer equipment for clinical use with its electrical power supply is a device that measures light scattering from antigen-antibody complexes. The concentration of these complexes may be measured by means of reflected light. A beam of light passed through a solution is scattered by the particles in suspension. The amount of light is detected by a photodetector, which converts light energy into electrical energy. The amount of electrical energy registers on a readout system such as a digital voltmeter or a recording chart. This electrical readout is called the light-scattering value and is used to measure the concentration of antigen-antibody complexes. This generic type of device includes devices with various kinds of light sources, such as laser equipment.
• Qualitative and Quantitative Factor Deficiency Test (FDA Code: GGP / 864.7290)
A factor deficiency test is a device used to diagnose specific coagulation defects, to monitor certain types of therapy, to detect coagulation inhibitors, and to detect a carrier state (a person carrying both a recessive gene for a coagulation factor deficiency such as hemophilia and the corresponding normal gene).
• Radioimmunoassay for Immunoglobulin G, A, M (FDA Code: CFQ / 866.5510)
• Rhodamine C-Reactive Protein Test System (FDA Code: DCH / 866.5270)
A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.
• Russel Viper Venom Reagent (FDA Code: GIR / 864.8950)
Russell viper venom reagent is a device used to determine the cause of an increase in the prothrombin time.

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