5068Steerable Electrode Catheter for Intracardiac Ablation
Albania medical device registration · Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA · III · Model Steerable Electrode Catheter for Intracardiac Ablation (sipas listes) · Registered March 26, 2019
- Risk Class
- III
- Product Model
- Steerable Electrode Catheter for Intracardiac Ablation (sipas listes)
- Product Name
- Steerable Electrode Catheter for Intracardiac Ablation
- Registration Date
- March 26, 2019
- Analysis ID
- 5068
Kateterë Elektroda të kthyeshme për ablacionin intrakardiak
Access comprehensive regulatory information for Steerable Electrode Catheter for Intracardiac Ablation 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 March 26, 2019.
This page provides complete registration details including product model (Steerable Electrode Catheter for Intracardiac Ablation (sipas listes)), 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.