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Infusion pump - FDA Registration c344987f3b986622e02cbdb12c17f027

Access comprehensive regulatory information for Infusion pump in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c344987f3b986622e02cbdb12c17f027 and manufactured by Daiwha Corp.,Ltd. The device was registered on June 07, 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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c344987f3b986622e02cbdb12c17f027
Infusion pump
FDA ID: c344987f3b986622e02cbdb12c17f027
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Device Classification
Brand Name
Daiwha
Registration Information
Analysis ID
c344987f3b986622e02cbdb12c17f027
Registration Date
June 07, 2022
Manufacturer
Authorized Representative