Albania AKBPM registration 13918.0SenSight Burr Hole Device B31000
AlbaniaMedtronic Inc. 710 Medtronic Parkway Minneapolis,MN 55432 USATeimplantueshmeaktiveModel SenSight Burr Hole Device B31000
VerifiedAKBPM · official registry
Device classification
- Risk Class
- Teimplantueshmeaktive
- Product Model
- SenSight Burr Hole Device B31000
- Product Name
- SenSight Burr Hole Device B31000
Registration information
- Analysis ID
- 13918.0
Manufacturer
Product information
Pajisje ndihmese per neurostimulatorin
About this record
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.