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Flexible Cryoprobe - FDA Registration f309cd42764c8390b13db98029f89199

Access comprehensive regulatory information for Flexible Cryoprobe in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f309cd42764c8390b13db98029f89199 and manufactured by Erbe Elektromedizin GmbH. The device was registered on April 27, 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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f309cd42764c8390b13db98029f89199
Flexible Cryoprobe
FDA ID: f309cd42764c8390b13db98029f89199
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Device Classification
Brand Name
Heir
Registration Information
Analysis ID
f309cd42764c8390b13db98029f89199
Registration Date
April 27, 2022
Manufacturer
Authorized Representative