Syphilis Test Cassette(Whole Blood/Serum/Plasma) - FDA Registration ffe0fedaee3933421e20bf5c9e3ff75e

Access comprehensive regulatory information for Syphilis 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 ffe0fedaee3933421e20bf5c9e3ff75e and manufactured by Nantong Egens Biotechnology Co., Ltd.. The device was registered on September 16, 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.