Female Home Fertility Test - FDA Registration 93d3db29451c5d1e3a1412e8b61848b4

Access comprehensive regulatory information for Female Home Fertility Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 93d3db29451c5d1e3a1412e8b61848b4 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.,. The device was registered on October 29, 2021.

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.