LH Rapid Quantitative Test - FDA Registration bad1abde79f59ec4ddea06c372701386

Access comprehensive regulatory information for LH Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bad1abde79f59ec4ddea06c372701386 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on September 09, 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.