XIENCE XPEDITION® LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM - FDA Registration MDR-07156

Access comprehensive regulatory information for XIENCE XPEDITION® LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07156 and manufactured by Abbott Vascular Netherlands B.V. in USA. The device was registered on June 28, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. Philippines, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.