HIV Rapid tests - FDA Registration 676be83570c26f708f313876213f3a8e

Access comprehensive regulatory information for HIV Rapid tests in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 676be83570c26f708f313876213f3a8e 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.