Humidifier Chamber - FDA Registration c312bcfb0dc01eef67aea0db19e97ee9

Access comprehensive regulatory information for Humidifier Chamber in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c312bcfb0dc01eef67aea0db19e97ee9 and manufactured by VADI Medical Technology Co., Ltd. Yangmei. The device was registered on August 22, 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.