Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer - FDA Registration 35d8d2a14c1bf1d4f6d2dabf77a85c30

Access comprehensive regulatory information for Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 35d8d2a14c1bf1d4f6d2dabf77a85c30 and manufactured by AEHEALTH LIMITED. The device was registered on January 21, 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.