SARS-CoV-2 Rapid Antigen Test 2.0 - FDA Registration c8ade75f8869275e814eaeeeef086a54

Access comprehensive regulatory information for SARS-CoV-2 Rapid Antigen Test 2.0 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c8ade75f8869275e814eaeeeef086a54 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.