Syphilis Rapid Test Cassette (Whole Blood/ Serum/ Plasma) - FDA Registration 92e1a5f3a52f215da6521801bc931dc3

Access comprehensive regulatory information for Syphilis 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 92e1a5f3a52f215da6521801bc931dc3 and manufactured by ACRO BIOTECH INC.. The device was registered on August 24, 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.