Response Biomedical Corp.

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Web: http://www.responsebio.com
E-Mail:
Address: 8081 Lougheed Highway, Burnaby, British Columbia V5A 1W9, Canada
Phone: +1-(604)-681-4101 | Fax: +1-(604)-412-9830 | Map/Directions >>

Profile: Response Biomedical Corp. develops proprietary technology for the rapidly growing medical and industrial diagnostic markets. We offer products such as cardio vascular, biodefense, west nile virus, ramp demonstration & flu A+B. Our Ramp® system renders a quantitative measurement of cardiac markers in whole blood to assist in the diagnosis of a heart attack. Our Ramp® troponin I assay is a quantitative immunochromatographic test used with the ramp reader to measure cardiac troponin I levels in EDTA whole blood.

The company was founded in 1991, has revenues of USD 1-5 Million, has ~50 employees and is CE certified. TSE:RBM (SEC Filings)

FDA Registration Number: 3004205692
US Agent: Rene Van De Zande / Emergo Global Representation Llc
Phone: +1-(512)-327-9997 Fax: +1-(512)-327-9998 E-Mail:

10 Products/Services (Click for related suppliers)

• Enzyme Immunoassay Chemistry Analyzer

• Fluorometer for Clinical Use (FDA Code: KHO / 862.2560)

A fluorometer for clinical use is a device intended to measure by fluorescence certain analytes. Fluorescence is the property of certain substances of radiating, when illuminated, a light of a different wavelength. This device is used in conjunction with certain materials to measure a variety of analytes.

• Influenza Virus CF Antigen (FDA Code: GNX / 866.3330)

Influenza virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to influenza in serum. The identification aids in the diagnosis of influenza (flu) and provides epidemiological information on influenza. Influenza is an acute respiratory tract disease, which is often epidemic.

• Isoenzymes Fluorometric Method (FDA Code: JHX / 862.1215)

A creatine phosphokinase/creatine kinase or isoenzymes test system is a device intended to measure the activity of the enzyme creatine phosphokinase or its isoenzymes (a group of enzymes with similar biological activity) in plasma and serum. Measurements of creatine phosphokinase and its isoenzymes are used in the diagnosis and treatment of myocardial infarction and muscle diseases such as progressive, Duchenne-type muscular dystrophy.

• Myoglobin (FDA Code: DDR / 866.5680)

A myoglobin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the myoglobin (an oxygen storage protein found in muscle) in serum and other body fluids. Measurement of myoglobin aids in the rapid diagnosis of heart or renal disease.

• Natriuretic Peptide Test (FDA Code: NBC / 862.1117)

The B-type natriuretic peptide (BNP) test system is an in vitro diagnostic device intended to measure BNP in whole blood and plasma. Measurements of BNP are used as an aid in the diagnosis of patients with congestive heart failure.

• POC Cardiac Marker Analyzers

• POC Cardiac Marker Analyzers, RAMP System

• Respiratory Syncytial CF Antigen (FDA Code: GQG / 866.3480)

Respiratory syncytial virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to respiratory syncytial virus in serum. Additionally, some of these reagents consist of respiratory syncytial virus antisera conjugated with a fluorescent dye (immunofluorescent reagents) and used to identify respiratory syncytial viruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of respiratory syncytial virus infections and provides epidemiological information on diseases caused by these viruses. Respiratory syncytial viruses cause a number of respiratory tract infections, including the common cold, pharyngitis, and infantile bronchopneumonia.

• Troponin Subunit Enzymatic Method (FDA Code: MMI / 862.1215)