Mast Group Ltd.

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Contact: David Hogben
Web: http://www.mastgrp.com
E-Mail:
Address: Mast House, Derby Rd., Bootle, Merseyside L20 1EA, United Kingdom
Phone: +44-(151)-9337277 | Fax: +44-(151)-9441332 | Map/Directions >>

Profile: Mast Group Ltd. offers microbiology and immunology products. We also manufacture and supply diagnostic products for clinical, industrial & veterinary testing. We offer clinical diagnostic products for in vitro detection and identification of bacterial, fungal, viral & protozoan agents of human infectious diseases. Our products incorporate a variety of applications encompassing both traditional microbiology methods and modern molecular biology techniques for nucleic acid amplification & detection. Our Mast Adatab™ is a lyophilised tablet used for antibiotic susceptibility testing of clinical bacteria by breakpoint or Minimum Inhibitory Concentration (MIC). Each tablet contains a measured dose of antibiotic designed to effect a specific antibiotic breakpoint concentration in 100 ml medium. Our Adatab™ system isolates bacteria from clinical samples and can be simultaneously inoculated onto test plates using our multipoint inoculators. We offer products for investigation of immune system through identification and detection of immunological markers using flow cytometry, ELISA, ELISPOT & agglutination techniques. Our MHC multimers are reagents that identify antigen specific T cells by flow cytometry. Our MHC monomers are used in clinical and experimental applications for the isolation & detection of T cells directed against viral, tumor & transplantation antigens.

FDA Registration Number: 8020667
US Agent: Jay Hardy / Hardy Diagnostics
Phone: +1-(805)-346-2766 Fax: +1-(805)-614-9274 E-Mail:

29 Products/Services (Click for related suppliers)

• Antibiotic Assay Culture Media (FDA Code: JSA / 866.2350)

A microbiological assay culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes to cultivate selected test microorganisms in order to measure by microbiological procedures the concentration in a patient's serum of certain substances, such as amino acids, antimicrobial agents, and vitamins. The concentration of these substances is measured by their ability to promote or inhibit the growth of the test organism in the innoculated medium. Test results aid in the diagnosis of disease resulting from either deficient or excessive amounts of these substances in a patient's serum. Tests results may also be used to monitor the effects of the administration of certain antimicrobial drugs.

• B. Pertussis Agglutinating Antisera (FDA Code: GOY / 866.3065)

• Culture Media Supplements (FDA Code: JSK / 866.2450)

A supplement for culture media is a device, such as a vitamin or sugar mixture, that is added to a solid or liquid basal culture medium to produce a desired formulation and that is intended for medical purposes to enhance the growth of fastidious microorganisms (those having complex nutritional requirements). This device aids in the diagnosis of diseases caused by pathogenic microorganisms.

• Enriched Culture Media (FDA Code: KZI / 866.2330)

An enriched culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes to cultivate and identify fastidious microorganisms (those having complex nutritional requirements). The device consists of a relatively simple basal medium enriched by the addition of such nutritional components as blood, blood serum, vitamins, and extracts of plant or animal tissues. The device is used in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.

• Escherichia Coli Antisera (FDA Code: GNA / 866.3255)

• General Nutrient Broth Culture Media (FDA Code: JSC / 866.2350)

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

• Klebsiella Spp Antiserum (FDA Code: GTC / 866.3340)

• Legionella Direct & Indirect Fluorescent Antibody Regents (FDA Code: LHL / 866.3300)

• Listeria Monocytogenes Antisera (FDA Code: GSH / 866.3355)

• Microorganism Differentiation Strip and Reagent Disc (FDA Code: JTO / 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.

• Multiple Biochemical Test Culture Media (FDA Code: JSE / 866.2320)

A differential culture medium is a device that consists primarily of liquid biological materials intended for medical purposes to cultivate and identify different types of pathogenic microorganisms. The identification of these microorganisms is accomplished by the addition of a specific biochemical component(s) to the medium. Microorganisms are identified by a visible change (e.g., a color change) in a specific biochemical component(s) which indicates that specific metabolic reactions have occurred. Test results aid in the diagnosis of disease and also provide epidemiological information on diseases caused by these microorganisms.

• Non-Selective and Differential Culture Media (FDA Code: JSH / 866.2320)

• 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.

• Pseudomonas Aeruginosa Fluorescent Antisera Test (FDA Code: GSS / 866.3415)

• Salmonella Spp Antiserum (FDA Code: GRM / 866.3550)

• Selective and Differential Culture Media (FDA Code: JSI / 866.2360)

A selective culture medium is a device that consists primarily of liquid or solid biological materials intended for medical purposes to cultivate and identify certain pathogenic microorganisms. The device contains one or more components that suppress the growth of certain microorganisms while either promoting or not affecting the growth of other microorganisms. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.

• Selective and Non-Differential Culture Media (FDA Code: JSJ / 866.2360)

• Selective Broth Culture Media (FDA Code: JSD / 866.2360)

• Serratia Marcescens Antisera (FDA Code: GTA / 866.3630)

• Shigella Spp Antiserum (FDA Code: GNB / 866.3660)

• Single Biochemical Test Culture Media (FDA Code: JSF / 866.2320)

• Staphylococcus Aureus Screening Kit (FDA Code: JWX / 866.2660)

• Staphylococcus Colonies Resistant Markers, Genotypic Detection Test System (FDA Code: MYI / 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.

• Streptococcus Pneumoniae Antisera (FDA Code: GWC / 866.3740)

• Streptococcus Spp Antigen (FDA Code: GTY / 866.3740)

• Streptococcus Spp Antiserum (FDA Code: GTZ / 866.3740)

• Urine Screening Kit (FDA Code: JXA / 866.2660)

• Vibrio Cholerae Antiserum (FDA Code: GSQ / 866.3930)