Orion Diagnostica Oy

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Web: http://www.oriondiagnostica.com
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Address: P.O.Box 83, Espoo 02101, Finland
Phone: +358-(10)-4261 | Map/Directions >>

Profile: Orion Diagnostica Oy is a bio medical company. We specialize in rapid and easy-to-use clinical diagnostic & hygiene-monitoring products aimed at enhancing the quality & effectiveness of health-care services. Our products are used in large clinical laboratories, which perform high-volume analysis. Our on-site hygiene monitoring tests provide a tool for institutions, industries and authorities to detect microbial contaminants & monitor the effectiveness of cleaning & disinfection routines. Our QuikRead System consists of an easy-to-use small instrument and dedicated, ready-to-use reagent kits. The system is especially convenient for small laboratories and doctors offices but it is also a useful adjunct in large hospital departments. QuikRead CRP is indicated for quantitative determination of C-reactive protein (CRP) concentration in whole-blood, serum or plasma samples. QuikRead FOB is ideal for the immunological detection of faecal occult blood in human faeces.

The company has ~320 employees and is ISO 9001, CE certified.

FDA Registration Number: 9610102
US Agent: Kyung-ah Kim / Princeton Biomeditech Corporation
Phone: +1-(732)-274-1000 Fax: +1-(732)-274-1010 E-Mail:

21 Products/Services (Click for related suppliers)

• Adenovirus 1-33 CF Antisera (FDA Code: GOA / 866.3020)

Adenovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to adenovirus in serum. Additionally, some of these reagents consist of adenovirus antisera conjugated with a fluorescent dye and are used to identify adenoviruses directly from clinical specimens. The identification aids in the diagnosis of disease caused by adenoviruses and provides epidemiological information on these diseases. Adenovirus infections may cause pharyngitis (inflammation of the throat), acute respiratory diseases, and certain external diseases of the eye (e.g., conjunctivitis).

• Alkaline Phosphatase Isoenzymes Electrophoretic Separation Test (FDA Code: CIN / 862.1050)

An alkaline phosphatase or isoenzymes test system is a device intended to measure alkaline phosphatase or its isoenzymes (a group of enzymes with similar biological activity) in serum or plasma. Measurements of alkaline phosphatase or its isoenzymes are used in the diagnosis and treatment of liver, bone, parathyroid, and intestinal diseases.

• C-Reactive Protein (CRP), FITC Conjugate (FDA Code: DCK / 866.5270)

A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.

• Campylobacter Pylori (FDA Code: LYR / 866.3110)

• Clinical Beta/Gamma Counter (FDA Code: JJJ / 862.2320)

A beta or gamma counter for clinical use is a device intended to detect and count beta or gamma radiation emitted by clinical samples. Clinical samples are prepared by addition of a radioactive reagent to the sample. These measurements are useful in the diagnosis and treatment of various disorders.

• Clinical Laboratory Tests

• Estradiol Radioimmunoassay Test (FDA Code: CHP / 862.1260)

An estradiol test system is a device intended to measure estradiol, an estrogenic steroid, in plasma. Estradiol measurements are used in the diagnosis and treatment of various hormonal sexual disorders and in assessing placental function in complicated pregnancy.

• General Examination Supplies

• Iron Reagent (FDA Code: CFM / 862.1410)

An iron (non-heme) test system is a device intended to measure iron (non-heme) in serum and plasma. Iron (non-heme) measurements are used in the diagnosis and treatment of diseases such as iron deficiency anemia, hemochromatosis (a disease associated with widespread deposit in the tissues of two iron-containing pigments, hemosiderin and hemofuscin, and characterized by pigmentation of the skin), and chronic renal disease.

• Laboratory Testing Services

• Low Density Lipoprotein (FDA Code: DFC / 866.5600)

A low-density lipoprotein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the low-density lipoprotein in serum and other body fluids. Measurement of low-density lipoprotein in serum may aid in the diagnosis of disorders of lipid (fat) metabolism and help to identify young persons at risk from cardiovascular diseases.

• Microbiology Kit

• Multi Analyte Control (FDA Code: JJY / 862.1660)

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• 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.

• Reagent Contract Manufacturing

• Rotavirus Enzyme Linked Immunoabsorbent Assay (FDA Code: LIQ / 866.3405)

Poliovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to poliovirus in serum. Additionally, some of these reagents consist of poliovirus antisera conjugated with a fluorescent dye (immunofluorescent reagents) used to identify polioviruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of poliomyelitis (polio) and provides epidemiological information on this disease. Poliomyelitis is an acute infectious disease which in its serious form affects the central nervous system resulting in atrophy (wasting away) of groups of muscles, ending in contraction and permanent deformity.

• 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)

• Testosterones and Dihydrotestosterone Radioimmunoassay (FDA Code: CDZ / 862.1680)

A testosterone test system is a device intended to measure testosterone (a male sex hormone) in serum, plasma, and urine. Measurement of testosterone are used in the diagnosis and treatment of disorders involving the male sex hormones (androgens), including primary and secondary hypogonadism, delayed or precocious puberty, impotence in males and, in females hirsutism (excessive hair) and virilization (masculinization) due to tumors, polycystic ovaries, and adrenogenital syndromes.

• Water-microbiology kit