Pure Global AI
Albania AKBPM registration 12976

Endurant Stent Graft System

AlbaniaMedtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USAIIIModel Endurant™ Stent Graft System; Endurant™ II Stent Graft System; Endurant™ IIs Stent Graft System; (sipas listes bashkengjitur) (BUDI-DI 0763000B00001977URegistered October 28, 2022
VerifiedAKBPM · official registry
Device classification
Risk Class
III
Product Model
Endurant™ Stent Graft System; Endurant™ II Stent Graft System; Endurant™ IIs Stent Graft System; (sipas listes bashkengjitur) (BUDI-DI 0763000B00001977U
Product Name
Endurant Stent Graft System
Registration information
Registration Date
October 28, 2022
Analysis ID
12976
Manufacturer
Name
Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA
Product information

Sistem stentash graft aortik Endurant per trajtimin e aneurizmave te aortes abdominale

About this record

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.