SARS-CoV-2 Rapid Antigen Test 2.0 Nasal - FDA Registration 5a45ff269257b949fc0029261f338f73

Access comprehensive regulatory information for SARS-CoV-2 Rapid Antigen Test 2.0 Nasal in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5a45ff269257b949fc0029261f338f73 and manufactured by SD Biosensor, Inc.. The device was registered on November 18, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.