Dentium Advanced Sinus Kit - FDA Registration 8c06449e0b1b722309eaf046b253ed8e

Access comprehensive regulatory information for Dentium Advanced Sinus Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8c06449e0b1b722309eaf046b253ed8e and manufactured by Dentium Co., Ltd. The device was registered on October 04, 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.