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Amplatz Sheath - FDA Registration e58a70e6f9531c78b9c0d56e81634ed4

Access comprehensive regulatory information for Amplatz Sheath in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e58a70e6f9531c78b9c0d56e81634ed4 and manufactured by Marflow AG. The device was registered on November 14, 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
e58a70e6f9531c78b9c0d56e81634ed4
Amplatz Sheath
FDA ID: e58a70e6f9531c78b9c0d56e81634ed4
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Device Classification
Brand Name
Marflow
Registration Information
Analysis ID
e58a70e6f9531c78b9c0d56e81634ed4
Registration Date
November 14, 2022
Manufacturer
Authorized Representative