12879Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent System
Albania medical device registration · Medtronic, Inc. 710 Medtronic Parkway Minneapolis, MN 55432,USA · III · Model Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent System (BUDI-DI 0763000B00000156T) (sipas listes bashkengjitur) · Registered October 06, 2022
- Risk Class
- III
- Product Model
- Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent System (BUDI-DI 0763000B00000156T) (sipas listes bashkengjitur)
- Product Name
- Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent System
- Registration Date
- October 06, 2022
- Analysis ID
- 12879
Sistem stentash koronare te implantueshme, te veshur me bar per perdorim ne kardiologji
Access comprehensive regulatory information for Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent 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 Minneapolis, MN 55432,USA. The device was registered on October 06, 2022.
This page provides complete registration details including product model (Resolute Onyx Zotarolimus-Eluting Coronary Stent System; Onyx Trucor Zotarolimus-Eluting Coronary Stent System (BUDI-DI 0763000B00000156T) (sipas listes bashkengjitur)), 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.