HBV Combo Rapid Test Cassette (Serum/Plasma) - FDA Registration 5877a48eff1649fbf6fe75b4d2b9e153

Access comprehensive regulatory information for HBV Combo Rapid Test Cassette (Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5877a48eff1649fbf6fe75b4d2b9e153 and manufactured by Hangzhou AllTest Biotech Co., Ltd. The device was registered on September 08, 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.