Respiratory Humidifer and Chamber - FDA Registration ee3dd2e8a5f3a4cc4b4157034d7a57d1

Access comprehensive regulatory information for Respiratory Humidifer and Chamber in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ee3dd2e8a5f3a4cc4b4157034d7a57d1 and manufactured by VADI Medical Technology Co.,Ltd. The device was registered on March 15, 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.