The correct detection and identification are the basic requirements for solutions. MEDsan therefore offers a broad product portfolio which is continuously expanded together with our research and development department. So our customers are always up to date and the decisive step ahead.
The novel virus SARS-CoV-2 and the resulting disease COVID-19 are currently of great importance. We are all more or less affected, both professionally and privately. In this situation regarding COVID-19 pandemic it is of great importance to detect active or recent infections with SARS-CoV-2 virus.
MEDsan Inc. provides different in vitro diagnostics (IVD) for the detection of SARS-CoV-2 nucleic acids as well as the specific IgM and IgG antibodies against SARS-CoV-2 infected cells.
The global pandemic caused by the virus known as SARS-CoV-2 affects us all. Human uncertainty is particularly great these days. This makes it all the more important to be able to offer a good, uncomplicated test method that can be used to get the right indication for makeing the right decisions.
MEDsan COVID-19 IgM/IgG Rapid Test is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgM and IgG antibodies against novel coronavirus SARS-CoV-2 infected cells in human whole blood, serum or plasma. The test kit is for professional use only and provides results within 10-15 minutes.
With this rapid test for the detection of antibodies in the blood of patients, you can now quickly and easily check what your status is for a COVID-19 disease. You will have feedback on the status within a very short time.
You will find more informaton after registration in our expert group.
MEDsan COVID-19 IgA/IgG Rapid Test
OMT (Oral Mucosal Transudate)
Sensitivity: 98.7% Specificity: >99.9%
You will find more informaton after registration in our expert group.
MEDsan Urine Test Marijuana (THC) is a competitive immunoassay utilizing highly specific reactions between antibodies and antigens for the qualitative determination of cannabinoids in human urine.
The test is the first step in a two-step process to provide consumers with information concerning the presence or absence of the above stated drug in a urine sample.
Information regarding confirmatory testing along with the materials for shipping a portion of the urine specimen to the laboratory for confirmation testing of a preliminary positive result is provided.
GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.
The package insert is currently available in 8 languages (German, English, Spanish, French, Italian, Portugues, Polish, Russian). Further languages are available upon request within 2 days.
Our leading expert team of chemists, biologists, pharmacists and medical doctors are available for our exclusive partners.
You will find more informaton after registration in our expert group.
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