Myanmar FDA registration c312bcfb0dc01eef67aea0db19e97ee9
Humidifier Chamber
Myanmar·VADI Brand·VADI Medical Technology Co., Ltd. Yangmei·Registered August 22, 2022Device classification
- Brand Name
- VADI Brand
Registration information
- Analysis ID
- c312bcfb0dc01eef67aea0db19e97ee9
- Registration Date
- August 22, 2022
Manufacturer
Authorized Representative
- Name
- AMTT CO., LTD
About this record
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.
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