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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

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.

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