DLP FLEXIBLE ARCH ARTERIAL CANNULA - FDA Registration a2ab4c8838609d265645d3a18169c24f

Access comprehensive regulatory information for DLP FLEXIBLE ARCH ARTERIAL CANNULA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a2ab4c8838609d265645d3a18169c24f 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.