VC2 Venous Cannula - FDA Registration f03e1feca477acb71f17bcd51fe8243a

Access comprehensive regulatory information for VC2 Venous Cannula in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f03e1feca477acb71f17bcd51fe8243a 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.