Respiratory Humidifier - FDA Registration cd0c7ec3a091b4159ec266897113c845

Access comprehensive regulatory information for Respiratory Humidifier in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cd0c7ec3a091b4159ec266897113c845 and manufactured by VADI Medical Technology Co., Ltd. Yangmei. The device was registered on September 21, 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.