Pericardial/Intracardiac Sumps - FDA Registration 49aed323822154a7142baf6e0b78db0f
Access comprehensive regulatory information for Pericardial/Intracardiac Sumps in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 49aed323822154a7142baf6e0b78db0f and manufactured by Viant Medical, Inc. The device was registered on July 01, 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
49aed323822154a7142baf6e0b78db0f
Pericardial/Intracardiac Sumps
FDA ID: 49aed323822154a7142baf6e0b78db0f
Device Classification
Brand Name
Medtronic
Registration Information
Analysis ID
49aed323822154a7142baf6e0b78db0f
Registration Date
July 01, 2022
Manufacturer
Authorized Representative

