Home Ovulation Test - FDA Registration 97cb430ce1b27aecb263cba1cbf57ba1

Access comprehensive regulatory information for Home Ovulation Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 97cb430ce1b27aecb263cba1cbf57ba1 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.