DILUENT - FDA Registration 2456129d7f5e901ac28459e8b5b7768a
Access comprehensive regulatory information for DILUENT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2456129d7f5e901ac28459e8b5b7768a and manufactured by URIT Medical Electronic Co., Ltd.,. The device was registered on December 21, 2021.
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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FDA Official Data
2456129d7f5e901ac28459e8b5b7768a
DILUENT
FDA ID: 2456129d7f5e901ac28459e8b5b7768a
Device Classification
Brand Name
URIT Brand
Registration Information
Analysis ID
2456129d7f5e901ac28459e8b5b7768a
Registration Date
December 21, 2021
Manufacturer
Authorized Representative
Name
AMTT CO., LTD
