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DiaSys - FDA Registration fdb32226814d066f18b2c70f6edbd7a1

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 fdb32226814d066f18b2c70f6edbd7a1 and manufactured by DiaSys Diagnostic Systems GmbH. The device was registered on March 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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fdb32226814d066f18b2c70f6edbd7a1
DiaSys
FDA ID: fdb32226814d066f18b2c70f6edbd7a1
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Device Classification
Brand Name
DiaSys
Registration Information
Analysis ID
fdb32226814d066f18b2c70f6edbd7a1
Registration Date
March 22, 2022
Authorized Representative