DiaSys - FDA Registration 7a016837b570aa4cd7c5932639f583a8
Access comprehensive regulatory information for DiaSys in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7a016837b570aa4cd7c5932639f583a8 and manufactured by DiaSys Diagnostic Systems GmbH. The device was registered on March 18, 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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FDA Official Data
7a016837b570aa4cd7c5932639f583a8
DiaSys
FDA ID: 7a016837b570aa4cd7c5932639f583a8
Device Classification
Brand Name
DiaSys
Registration Information
Analysis ID
7a016837b570aa4cd7c5932639f583a8
Registration Date
March 18, 2022
Manufacturer
Authorized Representative

