Salubris Inc.,

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Contact: Thomas Silier
Web: http://www.salubrisinc.com
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Address: Zumrutevler Mahallesi, Seher Sokak No: 41 Kat: 3 Aras Is Merkezi, Maltepe 34852, Turkey
Phone: +90-(216)-4421680 | Fax: +90-(216)-4421607 | Map/Directions >>

Profile: Salubris Inc., is a provider of laboratory products and services in the fields of human and veterinary health. We specialize in tuberculosis diagnostic products. Our products include devices for the diagnosis of tuberculosis, quantitative culture sample preparation kit for respiratory & other specimens, microbiological stains & sampling and transport devices. We offer Mycoprosafe®, TK media®, and Myco type®, all for the diagnosis of tuberculosis.

15 Products/Services (Click for related suppliers)

• Clinical Laboratory Tests

• Clinical Reference Laboratory

• Detergent (FDA Code: JCB / 864.4010)

• 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.

• Microbial Growth Monitor (FDA Code: JTA / 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.

• Microbiological Stain (FDA Code: JTS / 864.1850)

Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

• Microbiology Diagnostic Device (FDA Code: LIB / 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.

• Mycobacterium Tuberculosis Cell-Mediated Immunity Test (FDA Code: NCD)

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

• Respiratory Apparatus

• Respiratory Kit Disinfectants

• 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.

• Sterile Specimen Mailer and Storage Container (FDA Code: KDT / 864.3250)

A specimen transport and storage container, which may be empty or prefilled, is a device intended to contain biological specimens, body waste, or body exudate during storage and transport in order that the matter contained therein can be destroyed or used effectively for diagnostic examination. If prefilled, the device contains a fixative solution or other general purpose reagent to preserve the condition of a biological specimen added to the container. This section does not apply to specimen transport and storage containers that are intended for use as part of an over-the-counter test sample collection system for drugs of abuse testing.

• Tuberculosis Card Test