Profile: IQ Products is a supplier of a range of products for perinatal diagnostics, transplantation related diagnostics and routine flow cytometry. We specialize in hematology, perinatal diagnosis, transplantation related diagnosis, sepsis and inflammation. The hematology products are single color reagents, dual color combinations, complete kits, Abbott hematology analyzer reagents, TGF-beta detection, HIT alert and triple color combinations. Our perinatal diagnosis includes sepsis, fetomaternal bleeding, erythrocytes and Fetal Cell Count™. The Fetal Cell Count kit assay is based on a combination of two antibodies; one is directed against HbF and the second is specific for carbonic anhydrase. The single color reagents are CD markers, leukocyte associated molecules, cell proliferation, cytokines, apoptosis and isotope controls.
The company has revenues of USD 1-5 Million, has ~20 employees and is NEN-EN-ISO 13485:2003. certified.
FDA Registration Number: 9681582
US Agent: Cindy Greer / Cedarlane
Phone: +1-(336)-513-5135 Fax: +1-(336)-513-5138 E-Mail:
3 Products/Services (Click for related suppliers)
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• Cytomegalovirus Conjugated Fluorescent Antisera Test (FDA Code: LIN / 866.3175) Cytomegalovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to cytomegalovirus in serum. The identification aids in the diagnosis of diseases caused by cytomegaloviruses (principally cytomegalic inclusion disease) and provides epidemiological information on these diseases. Cytomegalic inclusion disease is a generalized infection of infants and is caused by intrauterine or early postnatal infection with the virus. The disease may cause severe congenital abnormalities, such as microcephaly (abnormal smallness of the head), motor disability, and mental retardation. Cytomegalovirus infection has also been associated with acquired hemolytic anemia, acute and chronic hepatitis, and an infectious mononucleosis-like syndrome. |
• Cytomegalovirus IHA Antigen Test (FDA Code: LJO / 866.3175) |
• Differential Cell Counter (FDA Code: GKZ / 864.5220) An automated differential cell counter is a device used to identify one or more of the formed elements of the blood. The device may also have the capability to flag, count, or classify immature or abnormal hematopoietic cells of the blood, bone marrow, or other body fluids. These devices may combine an electronic particle counting method, optical method, or a flow cytometric method utilizing monoclonal CD (cluster designation) markers. The device includes accessory CD markers. |