DLP CURVED TIP ARTERIAL CANNULA - FDA Registration 68edcaeda1012871f9a81301d51b203a
Access comprehensive regulatory information for DLP CURVED TIP ARTERIAL CANNULA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 68edcaeda1012871f9a81301d51b203a and manufactured by Viant Medical, Inc. The device was registered on August 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
68edcaeda1012871f9a81301d51b203a
DLP CURVED TIP ARTERIAL CANNULA
FDA ID: 68edcaeda1012871f9a81301d51b203a
Device Classification
Brand Name
Medtronic
Registration Information
Analysis ID
68edcaeda1012871f9a81301d51b203a
Registration Date
August 01, 2022
Manufacturer
Authorized Representative

