Endurant Stent Graft System - Albania Medical Device Registration

Access comprehensive regulatory information for Endurant Stent Graft System in the Albania medical device market through Pure Global AI's free database. This III medical device is manufactured by Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA. The device was registered on October 28, 2022.

This page provides complete registration details including product model (Endurant™ Stent Graft System; Endurant™ II Stent Graft System; Endurant™ IIs Stent Graft System; (sipas listes bashkengjitur) (BUDI-DI 0763000B00001977U), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.