DLP Straight Tip Arterial Cannula - FDA Registration f576be75498d385c2a340be2934b8210

Access comprehensive regulatory information for DLP Straight Tip Arterial Cannula in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f576be75498d385c2a340be2934b8210 and manufactured by Viant Medical, Inc. The device was registered on August 08, 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.