Myanmar FDA registration d6adf2d511f1f2da6b9fe9ff7d63cb4f
Water Pump
Device classification
- Brand Name
- FUJIFILM
Registration information
- Analysis ID
- d6adf2d511f1f2da6b9fe9ff7d63cb4f
- Registration Date
- September 23, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Water Pump in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d6adf2d511f1f2da6b9fe9ff7d63cb4f and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Hanamaki Office. The device was registered on September 23, 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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