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Bactus AB

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Contact: Hakan Randahl
Web: http://www.bactus.com
E-Mail:
Address: Lunastigen 3, Huddinge SE 141 44, Sweden
Phone: +46-(8)-6088630 | Fax: +46-(8)-7468496 | Map/Directions >>
 
 

Profile: Bactus AB is a biotech company dedicated to clinical and industrial microbiology. We offer a range of products based on the co-agglutination technology. We have a large production of microbiological substrates. We offer a product range of solid and liquid media for transport or cultivation of bacteria, encompassing more than 400 items. We produce plates for surveillance of clean rooms, and radiation sterilized agar plates. We are engaged in the contract development that takes the prototypes through the production process to a customer ready product. We develop, manufacture and market a range of products for rapid & simple microbiological tests. Our product range is very broad and includes the well-known Phadebact Tests for bacterial determination based on co-agglutination technology as well as the PhP technology product portfolio used for bacterial phenotyping. We also produce a wide range of microbiological substrates. The Phadebact®/Phadirect® co-agglutination product ranges are indented for the clinical microbiology laboratories. The co-agglutination technology offers a simple and easy way for identification of pathogenic bacteria after cultivation on agar plates or direct detection of antigen in clinical specimens. Reagents for all Phadebact kits are slotted, in the order in which they are used, into a compact workstation. Phadebact kits contain a choice and volume of reagents designed to reflect a typical lab's workload.

8 Products/Services (Click for related suppliers)  
• Escherichia Coli Antisera (FDA Code: GNA / 866.3255)
• Haemophilus Influenza Antiserum (FDA Code: GRP / 866.3300)
• N. Meningitidis Antisera (FDA Code: GTJ / 866.3390)
• Neisseria Controls (FDA Code: LSC / 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.
• Neisseria Gonorrhoeae Antiserum (FDA Code: LIC / 866.3390)
• Streptococcus Pneumoniae Antisera (FDA Code: GWC / 866.3740)
• Streptococcus Spp Antigen (FDA Code: GTY / 866.3740)
• Streptococcus Spp Antiserum (FDA Code: GTZ / 866.3740)

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