Euroimmun’s Antibody Test Earns Emergency Use Authorization

The FDA has issued an EUA for Euroimmun US’s COVID-19 antibody test.

The test kit detects IgG antibodies against SARS-CoV-2 in human serum and plasma. It is intended to be used as an aid in identifying individuals with antibodies to the coronavirus, indicating recent or prior infection.

Emergency use of the test is limited to authorized laboratories certified to perform high-complexity tests.