DLP Cardiac Suction Tubes - FDA Registration 94c3b9cbe9ec57c9e82ac84bff958ec5

Access comprehensive regulatory information for DLP Cardiac Suction Tubes in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 94c3b9cbe9ec57c9e82ac84bff958ec5 and manufactured by Viant Medical, Inc. The device was registered on June 29, 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.