Medion Diagnostics Ag

Contact: Peter Schwind
Web: http://www.medion-diagnostics.ch
Address: Bonnstrasse 9, Duedingen CH-3186, Switzerland
Phone: +41-(26)-4928511 | Fax: +41-(26)-4928656 | Map/Directions >>

Profile: Medion Diagnostics Ag deals with reagents for grouping bloods. We provide blood grouping, rhesus sera, blood typing antisera, reagent red cells, anti-human globulins, quality controls, centrifuges, auxiliary materials and gram stain. Our monoclonal ABO antisera are produced using in-vitro cell culture of mouse hybridoma cell lines. We supply IgM Anti- Mono-Type®, which contains a human monoclonal IgM antibody that allows detection of all D variants with the exception of category DVI. Our reagent red cells include the cells for reverse typing, antibody screening, and antibody identification. Our Reverse-Cyte®, is a combination of A1 and A2 for detecting irregular anti-A1. Our Bromelase® 30 removes glycoproteins from the surface of erythrocytes. Anti-Human Globulins are prepared from serum of immunized rabbits and from serum of a mouse hybridoma cell line and are used for the detection of in-vivo or in-vitro coating of red cells with immunoglobulin or complement. Our Screen-Cyte® is a three cell panel with an optimal antigen configuration ideal for antibody screening. This is used to find out the clinically relevant antigens present in homozygous form. We offer Sero-Cyte®, with two cell panels for antibody screening with Rh antigens always present in homozygous form and its each lot contains Cw. Our Data-Cyte® plus is a panel consisting of eleven cells in 3° suspension with the ideal antigen configuration for antibody identification.

The company is ISO 9001:2000, ISO 13485:2003 certified.

FDA Registration Number: 3002806769
US Agent: Diane Day
Phone: +1-(510)-923-4579 E-Mail:

10 Products/Services (Click for related suppliers)

• Automated Combs Test System (FDA Code: KSM / 864.9300)

An automated Coombs test system is a device used to detect and identify antibodies in patient sera or antibodies bound to red cells. The Coombs test is used for the diagnosis of hemolytic disease of the newborn, and autoimmune hemolytic anemia. The test is also used in crossmatching and in investigating transfusion reactions and drug-induced red cell sensitization.

• Blood Antibody Potentiator

• Blood Grouping Reagents

• Centrifuges

• FTA-ABS Test Anti-Human Globulin (FDA Code: GMS / 866.3830)

• Hematology Stain (FDA Code: KQC / 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.

• Hemoglobin Control (FDA Code: GGM / 864.8625)

A hematology quality control mixture is a device used to ascertain the accuracy and precision of manual, semiautomated, and automated determinations of cell parameters such as white cell count (WBC), red cell count (RBC), platelet count (PLT), hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC).

• Mono - Rapid Infectious Mononucleosis Heterophile Antibody (IgM) Test Kit

• Quality Control Kit for Blood Banking Reagents (FDA Code: KSF / 864.9650)

A quality control kit for blood banking reagents is a device that consists of sera, cells, buffers, and antibodies used to determine the specificity, potency, and reactivity of the cells and reagents used for blood banking.

• Sickle Cell Test (FDA Code: GHM / 864.7825)

A sickle cell test is a device used to determine the sickle cell hemoglobin content of human blood to detect sickle cell trait or sickle cell diseases.