Statens Serum Institut

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Contact: Jens Hummeluhr - Director of Marketing
Web: http://www.serum.dk
E-Mail:
Address: 5, Artillerivej, Copenhagen S DK-2300, Denmark
Phone: +45-(0)-3268 3268 | Fax: +45-(0)-3268 3868 | Map/Directions >>

Profile: Statens Serum Institut prevents and controls infectious diseases, biological threats and congenital disorders. Our expertise includes monitoring, advising and teaching on the incidence, prevention and treatment of infectious diseases and congenital disorders. We specialize in the diagnosis of infectious, autoimmune, congenital and genetic diseases. We supply vaccines, other biological products and diagnostic services through production & procurement. We can also supply growth media additives specially designed for hybridoma development. We develop the growth media additive which is convenient and practical to use in the hybridoma laboratory when developing monoclonal antibodies. We offer polyclonal antibodies for botulinum toxins.

The company has revenues of USD 5-10 Million, has ~1050 employees.

32 Products/Services (Click for related suppliers)

• Allergen and Vaccine Delivery System (FDA Code: LDH)

• Anti-acetylcholine Receptor Alpha Monoclonal Antibody

• Antimicrobial Susceptibility Test Powder (FDA Code: JTT / 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.

• Bacterial Diagnostic Test

• Biological Monitor

• Biological Sterilization Process Indicator (FDA Code: FRC / 880.2800)

A biological sterilization process indicator is a device intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor adequacy of sterilization. The device consists of a known number of microorganisms, of known resistance to the mode of sterilization, in or on a carrier and enclosed in a protective package. Subsequent growth or failure of the microorganisms to grow under suitable conditions indicates the adequacy of sterilization.

• Cell Culture Suspension System (FDA Code: KJF / 864.2240)

Cell and tissue culture supplies and equipment are devices that are used to examine, propagate, nourish, or grow cells and tissue cultures. These include such articles as slide culture chambers, perfusion and roller apparatus, cell culture suspension systems, and tissue culture flasks, disks, tubes, and roller bottles.

• E. Coli DNA Probes

• Enterobacteriaceae Identification Kit (FDA Code: JSS / 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.

• Escherichia Coli Antigens (FDA Code: GMZ / 866.3255)

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

• Gene Kits

• General Virus Reagent

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

• Immunological Kits

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

• Moist Heat and Dry Heat Sterilization Equipments

• Monoclonal Antibody Test

• Mycobacteria Identification Kit (FDA Code: JSY / 866.2660)

• Mycobacterium Tuberculosis Fluorescent Antiserum Test (FDA Code: GRT / 866.3370)

• Neisseria Gonorrhoeae Identification Kit (FDA Code: JSX / 866.2660)

• Pathogenic Neisseria Culture Media (FDA Code: JTY / 866.2410)

A culture medium for pathogenicNeisseria spp. is a device that consists primarily of liquid or solid biological materials used to cultivate and identify pathogenicNeisseria spp. The identification aids in the diagnosis of disease caused by bacteria belonging to the genusNeisseria, such as epidemic cerebrospinal meningitis, other meningococcal disease, and gonorrhea, and also provides epidemiological information on these microorganisms.

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

• Salmonella Spp Antigen (FDA Code: GRL / 866.3550)

• 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.

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

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

• Strain Detector

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

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

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