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Implatable Cardioverter/ Defibrillators - Albania Medical Device Registration

Access comprehensive regulatory information for Implatable Cardioverter/ Defibrillators in the Albania medical device market through Pure Global AI's free database. This TëimplantueshmeAktIve medical device is manufactured by Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA. The device was registered on October 26, 2022.

This page provides complete registration details including product model (Implatable Cardioverter/ Defibrillators: PROTECTA™ XT CRT-D : D354TRG; PROTECTA™ CRT-D: D364TRG; PROTECTA™ XT DR: D354DRG; PROTECTA™ DR: D364DRG; PROTECTA™ XT VR D354VRG; PROTECTA™ VR: D364VRG), 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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TëimplantueshmeAktIve
Implatable Cardioverter/ Defibrillators
Albania Medical Device Registration
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Product Information

Elektroda te implantueshme aktive per rregullimin e eritmit endokardial per perdorim ne kardiologji dhe hemodinamike

Device Classification
Risk Class
TëimplantueshmeAktIve
Product Model
Implatable Cardioverter/ Defibrillators: PROTECTA™ XT CRT-D : D354TRG; PROTECTA™ CRT-D: D364TRG; PROTECTA™ XT DR: D354DRG; PROTECTA™ DR: D364DRG; PROTECTA™ XT VR D354VRG; PROTECTA™ VR: D364VRG
Product Name
Implatable Cardioverter/ Defibrillators
Registration Information
Registration Date
October 26, 2022
Analysis ID
12968