Rapid Test COVID-19 Ag
This test is for the detection of the SARS-CoV-2 nucleocapsid protein antigen. The antigen is generally detectable in samples from the upper respiratory tract during the acute phase of infection. Rapid diagnosis of SARS-CoV-2 infection will help healthcare professionals to treat patients and manage the disease more efficiently and effectively.
This is a product classified as "In Vitro Diagnosis", it is not a "Self Diagnosis" product, therefore it cannot be sold to private persons, but to Hospitals, Health Centers, Clinics, Laboratories, Nursing Homes, Public Services , Mutuals for Risk Prevention or Companies, provided they have health personnel to carry them out.
The tests must be used following the criteria indicated by current legislation (RD 1162/2000 on medical devices for "in vitro" diagnosis).
In the purchase process, the number of the Registered Physician who will carry out the diagnosis and follow-up will be requested.