DLP PEDIATRIC ONE-PIECE ARTERIAL CANNULA - FDA Registration ce787c1fa1c89702204c455ebe9e9c17

Access comprehensive regulatory information for DLP PEDIATRIC ONE-PIECE ARTERIAL CANNULA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ce787c1fa1c89702204c455ebe9e9c17 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.