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Amplatz Dilation Set Mini - FDA Registration 503b7d816cfda3fa2e795e78b46a15a6

Access comprehensive regulatory information for Amplatz Dilation Set Mini in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 503b7d816cfda3fa2e795e78b46a15a6 and manufactured by Marflow AG. The device was registered on December 02, 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
503b7d816cfda3fa2e795e78b46a15a6
Amplatz Dilation Set Mini
FDA ID: 503b7d816cfda3fa2e795e78b46a15a6
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Device Classification
Brand Name
Marflow
Registration Information
Analysis ID
503b7d816cfda3fa2e795e78b46a15a6
Registration Date
December 02, 2022
Manufacturer
Authorized Representative