The COVID-19 Antigen Rapid Test (latex) offers a quick and reliable response for both symptomatic and asymptomatic patients with regard to a SARS-CoV-2 infection. For example, a precise screening of people with known contact with SARS-CoV-2 infected people can be carried out and the infection status can be determined. The COVID-19 Antigen Rapid Test (latex) test kit contains all the necessary materials and can be used by healthcare professionals from any location.
 Saliva and stool samples
 The test is intended for professional use.
 In addition to the existing corona test strategy.
 Reliable, fast, qualitative detection of a specific SARS-CoV-2 antigen in human saliva or stool samples
 Information on Selling COVID-19 Rapid Antigen Tests to Private Individuals What a COVID-19 Rapid Antigen Test? A rapid COVID-19 antigen test detects an acute COVID-19 infection by detecting protein components of the virus. Viral antigens can be detected within a short time (usually 15 to 20 minutes), the sample taken does not have to be evaluated in a laboratory. How reliable is a COVID-19 rapid antigen test? COVID-19 antigen rapid tests always provide snapshots of the infection process. No medical test can guarantee 100% security. When using COVID-19 antigen rapid tests, the information on sensitivity and specificity must be observed. Since the concentration of the viral nucleoprotein antigens fluctuates over the course of the disease, it can fall below the detection limit of the test. A possible infection with the coronavirus cannot be ruled out due to a negative test result. A COVID-19 antigen rapid test is therefore not a substitute for a PCR test! Who can perform a rapid COVID-19 antigen test? A COVID-19 rapid antigen test is only intended for use by healthcare professionals. According to the information provided by the Federal Ministry for Social Affairs, Health, Care and Consumer Protection (as of November 25, 2020), COVID-19 antigen tests may currently be carried out by the following people or professional groups: • Doctors in accordance with the Medical Act 1998, • People who have successfully completed a degree in natural science or veterinary medicine according to the Physicians Act 1998 or the MTD Act, in particular also pharmacists • Biomedical analysts according to the MTD Act, • Higher service for health and nursing according to a doctor's order according to GuKG, • Nursing assistant according to a doctor's order according to GuKG, • nursing assistance according to a doctor's order and under the supervision of a doctor or a qualified nurse according to GuKG, • paramedics according to SanG, • laboratory assistance according to a doctor's order and under the supervision of a doctor a doctor or a biomedical analyst / a biomedical sc hen analyst according to MABG, • doctor's assistant as directed by a doctor and under the supervision of a doctor or a qualified health care professional according to MABG. Can a COVID-19 antigen rapid test also be carried out by medical laypersons in self-application? No. A COVID-19 rapid antigen test is not suitable for self-application by medical laypersons. Incorrect implementation or incorrect interpretation of the test result can result in false security. A positive COVID-19 antigen rapid test must also be reported to the responsible health authority as a suspected COVID-19 case by the persons or professional groups addressed in accordance with the Epidemics Act. A positive antigen test result must always be verified by a subsequent PCR test (exception: Category I contacts with COVID-19 symptoms).
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