Coronary Stent System - FDA Registration 869da3554650146ca0130dcaa0c92852

Access comprehensive regulatory information for Coronary Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 869da3554650146ca0130dcaa0c92852 and manufactured by Biosensors Interventional Technologies Pte Ltd. The device was registered on December 02, 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.