MaxLINE HCV Rapid Test Device Serum/Plasma - FDA Registration 335bf711161de5e8747702675c5c966a

Access comprehensive regulatory information for MaxLINE HCV Rapid Test Device Serum/Plasma in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 335bf711161de5e8747702675c5c966a and manufactured by Avecon Healthcare Pvt. Ltd.. The device was registered on July 27, 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.