DLP Single Stage Venous Cannula - FDA Registration 4bd4b548c12fb09ace44f4a73cb08361

Access comprehensive regulatory information for DLP Single Stage Venous Cannula in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4bd4b548c12fb09ace44f4a73cb08361 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.