XIENCE Xpedition Everolimus Eluting Coronary Stent System - FDA Registration 8945d0b4e28068029aef3ab0e1521c21

Access comprehensive regulatory information for XIENCE Xpedition Everolimus Eluting Coronary Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8945d0b4e28068029aef3ab0e1521c21 and manufactured by Abbott Vascular. The device was registered on September 07, 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.