COVID (hereinafter referred to as UD-Bio) was founded in June 2016 and is headquartered in Shenzhen. It is a Shenzhen and National high-tech company engaged in the research, development, production, sales and services of IVD instruments and reagents.Wholesale COVID-19 ANTIGEN RAPID TEST Cassett (Saliva ...Test Procedure 1) Use the ...
Overview Key Attributes Applications Register Interest Other Tests EuGeni Rapid Diagnostic Platform CE Certification- April 2021 SARS-CoV-2 Ag RDT 15-minute COVID-19 antigen rapid test has been approved for the platform, with a saliva-based test currently in validation. Overview EuGeni is a fast, accurate and compact solution for rapid point-of-care testing.Clungene saliva antigen rapid self test kit - Arcpeaks MedicalClungene saliva antigen rapid self test kit. Hangzhou Clongene Biotech Co.. ISO13485 passed. Output:0.5million pcs pur day. This test kit is with CE certificate confirmed by chinese government department CHINA CHAMBER OF COMMERCEFOR IMPORT&EXPORT OF
Made in Canada Health Canada approved CE Mark and ISO certified The product has proven to have 100% Specificity and 96% Sensitivety Stock availabity 2 Million tests/kit in Canada Production up to 5 Million tests/kit weekly The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral Diagnos Swab Covid-19 Rapid Antigen & Flu A+B Combo Diagnos Swab Covid-19 Rapid Antigen & Flu A+B Combo Test Kit Box of 25 Tests (CE-IVD Certified) 150.00 The COVID-19 & Influenza A+B Rapid Antigen Combo Test Kit (Colloidal Gold) is a rapid visual immunoassay for the qualitative detection of COVID-19 antigen and influenza A+B viral antigen (nucleoprotein) in human throat swab and CE Certificate Antigen Rapid Test Kit Influenza a B Antigen ComboInfluenza B IgM ELISA kit - Rapid TestThe Diagnostic Automation Inc. Influenza B IgM antibody test kit is based on the principle of the enzyme immunoassay (EIA). Influenza B antigen is bound on the surface of the microtiter strips. Diluted patient serum or ready-to-use standards are pipetted into the wells of the microtiter plate. A binding between the IgM antibodies of the serum CE Certificate Antigen Rapid Test Kit Influenza a B Antigen Combo
The SARS-CoV-2 IgM/IgG Ab Rapid Test is used to detect the IgM and IgG antibodies to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in human serum, plasma or whole blood sample qualitatively. It it to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by SARS-CoV-2.Resilient Rápido Direct Read SARSCoV-2 Antigen Paper-Strip CE Certificate Antigen Rapid Test Kit Influenza a B Antigen ComboThe proposed test setting is non-lab point of care, CLIA waved lab, and/or over the counter or home use without prescription. The manufacturer of the Resilient & Rápido Direct Read SARSCoV-2 Antigen Paper-Strip Test has CE certification. This test can be sold commercially to any country that accepts CE.Sofia 2 Flu + SARS Antigen FIA QuidelThe Sofia 2 Flu + SARS Antigen FIA with the Sofia 2 analyzer provides automated and objective results in 15 minutes, allowing for testing of patients suspected of influenza A, influenza B, and COVID-19/2019-nCoV at the Point of Care. Healthcare professionals can purchase the Sofia 2 Flu + SARS Antigen FIA through select authorized distributors.
Test Procedure 1) Use the disposable paper cup to collect saliva. 2) Cough deeply. Make the noise of Kruuua from the throat to clear the saliva from deep throat. Once the saliva is in your mouth , release it into the container.then spit saliva (about 2 ml) 3Unscrew the diluent bottle, Unscrew the cap of the extraction tube, Add all of CE Certificate Antigen Rapid Test Kit Influenza a B Antigen Combocobas&Influenza A/B Assay - diagnostics.rocheInfluenza affects 5-10% of adults and 20-30% of children each year. 1 Whether its a typical flu season, or a worst-case pandemic, testing and screening for influenza A and B can help protect patients by enabling appropriate antiviral prescribing or patient isolation. 2,3. The cobas &Influenza A/B assay, a multiplex real-time polymerase chain reaction (PCR) test, running on the innovative CE Certificate Antigen Rapid Test Kit Influenza a B Antigen Combo
Influenza Virus (IFV) (a) & (b) are the most common respiratory viruses in the winter and spring. With the tough situation that the COVID-19 pandemic has brought into the many countries around the world, a test kit for On-Site Rapid Diagnosis & Screening of the Coronavirus 2 (SARS-CoV-2) pneumonia & Influenza virus (IFV) A/B should be very useful to identify the infected cases in coming cold CE Certificate Antigen Rapid Test Kit Influenza a B Antigen Combo