Implatable Cardioverter/ Defibrillators

Albania medical device registration · Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA · TëimplantueshmeAktIve · 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 · Registered October 26, 2022

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

Manufacturer

Name: Medtronic Inc. 710 Medtronic Parkway N.E. Minneapolis MN 55432 USA

Product information

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

About this record

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.