ARCHITECT Folate Assay - FDA Registration 3b22a295fe795bb5828a30c129e36010

Access comprehensive regulatory information for ARCHITECT Folate Assay in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3b22a295fe795bb5828a30c129e36010 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on March 21, 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.