MaxLINE HIV 1 & 2 Tri-Line Rapid Test Serum/Plasma - FDA Registration d6bf3112444fb0d6e8421d95422982e7

Access comprehensive regulatory information for MaxLINE HIV 1 & 2 Tri-Line Rapid Test Serum/Plasma in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d6bf3112444fb0d6e8421d95422982e7 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.