Dengue (NSI Ag+ IgG/ IgM) DUO Rapid Test Kit - FDA Registration 521ab4850887757de1b127d16e2bc350

Access comprehensive regulatory information for Dengue (NSI Ag+ IgG/ IgM) DUO Rapid Test Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 521ab4850887757de1b127d16e2bc350 and manufactured by Jiangsu Bioperfectus Technologies Co., Ltd. The device was registered on October 31, 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.