Pure Global AI
Albania AKBPM registration 13921.0

SenSight Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M

AlbaniaMedtronic Inc. 710 Medtronic Parkway Minneapolis,MN 55432 USATeimplantueshmeaktiveModel SenSight Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M
VerifiedAKBPM · official registry
Device classification
Risk Class
Teimplantueshmeaktive
Product Model
SenSight Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M
Product Name
SenSight Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M
Registration information
Analysis ID
13921.0
Manufacturer
Product information

Kit zgjatues per Neurostimulatorin SenSight

About this record

Access comprehensive regulatory information for SenSight Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M 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 Extension Kit B34000 Variants: B3400040, B3400060, B3400095, B3400040M, B3400060M, B3400095M), 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.