Profile: Accumed International Ltd. manufactures and markets a line of proprietary, instruments and integrated automated cytopathology systems. We produce bacterial identifications and antimicrobic susceptibility testing systems for use in clinical and veterinary microbioway labs.
The company has revenues of USD 1-5 Million, has ~40 employees and is CE certified. NASDAQ:ACMI (SEC Filings)
FDA Registration Number: 8021914
US Agent: Rob Norris
Phone: +1-(913)-888-0939 E-Mail:
13 Products/Services (Click for related suppliers)
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• Antifungal Susceptibility Test Plate (FDA Code: NGZ / 866.1640) An antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases. |
• Antimycobacterial Susceptibility Test Powders (FDA Code: MJA / 866.1640) |
• Auto reader & Interpretation of Overnight Susceptiblity Systems (FDA Code: LRG / 866.1640) |
• Auto Reader of Overnight Microorganism Identification System (FDA Code: LRH / 866.2660) A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease. |
• Blood Culturing System (FDA Code: MDB / 866.2560) A microbial growth monitor is a device intended for medical purposes that measures the concentration of bacteria suspended in a liquid medium by measuring changes in light scattering properties, optical density, electrical impedance, or by making direct bacterial counts. The device aids in the diagnosis of disease caused by pathogenic microorganisms. |
• Clinical Nephelometer (FDA Code: JQX / 862.2700) A nephelometer for clinical use is a device intended to estimate the concentration of particles in a suspension by measuring their light scattering properties (the deflection of light rays by opaque particles in their path). The device is used in conjunction with certain materials to measure the concentration of a variety of analytes. |
• Diagnostics Contract Research & Development |
• Gram Negative Identification Panel (FDA Code: LQM / 866.2660) |
• Gram Positive Identification Panel (FDA Code: LQL / 866.2660) |
• Lead Atomic Absorption Test (FDA Code: DOF / 862.3550) A lead test system is a device intended to measure lead, a heavy metal, in blood and urine. Measurements obtained by this device are used in the diagnosis and treatment of lead poisoning. |
• Manual Antimicrobial Susceptibility Test System (FDA Code: JWY / 866.1640) |
• Mueller Hinton Agar Broth Culture Media (FDA Code: JTZ / 866.1700) A culture medium for antimicrobial susceptibility tests is a device intended for medical purposes that consists of any medium capable of supporting the growth of many of the bacterial pathogens that are subject to antimicrobial susceptibility tests. The medium should be free of components known to be antagonistic to the common agents for which susceptibility tests are performed in the treatment of disease. |
• Non-Selective and Non-Differential Culture Media (FDA Code: JSG / 866.2300) A multipurpose culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes for the cultivation and identification of several types of pathogenic microorganisms without the need of additional nutritional supplements. Test results aid in the diagnosis of disease and also provide epidemiological information on diseases caused by these microorganisms. |