Aptima SARS-CoV-2 Assay & Controls Kit - FDA Registration 3a9c1fa750c0b209d9b44a8ec878b00a

Access comprehensive regulatory information for Aptima SARS-CoV-2 Assay & Controls Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3a9c1fa750c0b209d9b44a8ec878b00a and manufactured by Hologic, Inc.. The device was registered on January 19, 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.