Dengue Ag and Ab Combo Rapid Test Cassette (Whole Blood/ Serum/ Plasma) - FDA Registration 56106681ab297152d7ef44582ee41caf

Access comprehensive regulatory information for Dengue Ag and Ab Combo Rapid Test Cassette (Whole Blood/ Serum/ Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 56106681ab297152d7ef44582ee41caf and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on July 01, 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.