Tools
Sales sheet
FAQs
Fact sheet for healthcare providers
Fact sheet for patients

  • COV-ID; the Diagnostic Kit (Colloidal Gold) for IgG/IgM Antibody to SARS-CoV-2 is available in specific global markets in compliance with country requirements.
  • COV-ID; the Diagnostic Kit (Colloidal Gold) for IgG/IgM Antibody to SARS-CoV-2 is CE marked and MHRA registered. This test has also been submitted for Health Canada Interim Order (IO) review as well as for review by ANVISA in Brazil.
  • COV-ID; the Diagnostic Kit (Colloidal Gold) for IgG/IgM Antibody to SARS-CoV-2 has been U.S. Food and Drug Administration (FDA) notified and submitted for FDA Emergency Use Authorization (EUA) review. For professional use only in qualified CLIA certified high complexity settings. Please contact Lumos for specific product details that align with U.S. FDA notification procedures.

Contact us to order or learn more about the COV-ID antibody (IgG/IgM) test.