SenSight Burr Hole Device B31000
Albania medical device registration · Medtronic Inc. 710 Medtronic Parkway Minneapolis,MN 55432 USA · Teimplantueshmeaktive · Model SenSight Burr Hole Device B31000
- Risk Class
- Teimplantueshmeaktive
- Product Model
- SenSight Burr Hole Device B31000
- Product Name
- SenSight Burr Hole Device B31000
- Analysis ID
- 13918.0
Pajisje ndihmese per neurostimulatorin
Access comprehensive regulatory information for SenSight Burr Hole Device B31000 in the Albania medical device market through Pure Global AI's free database. This Teimplantueshmeaktive medical device is manufactured by Medtronic Inc. 710 Medtronic Parkway Minneapolis,MN 55432 USA.
This page provides complete registration details including product model (SenSight Burr Hole Device B31000), 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.