Syphillis Rapid tests - FDA Registration ec6611c5012dbee26dfca58b90c7845d

Access comprehensive regulatory information for Syphillis Rapid tests in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ec6611c5012dbee26dfca58b90c7845d and manufactured by Zhejiang Orient Gene Biotech Co.,ltd. The device was registered on September 08, 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.