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Aurora EV-ICD™ offers the advantages of an extravascular system while also providing ATP and Pause Prevention pacing in a device the same size as transvenous ICDs.
The Aurora EV-ICD system is also approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model number: DVEA3E4
Cobalt™ XT ICDs and CRT-Ds with BlueSync™ technology enable tablet-based programming and app-based remote monitoring. These devices include an automated anti-tachycardia pacing (ATP) algorithm and are compatible with a simplified heart failure risk stratification tool.
The Cobalt XT system is also approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model numbers: DDPA2D4, DDPA2D1, DVPA2D1, DVPA2D4
Cobalt™ ICDs and CRT-Ds with BlueSync technology enable tablet-based programming and app-based remote monitoring, and offer exclusive algorithms to manage atrial fibrillation (AF) patients.
The Cobalt system is also approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model numbers: DDPB3D1, DVPB3D1, DVPB3D4, DDPB3D4
Crome™ ICDs and CRT-Ds with BlueSync technology enable tablet-based programming and app-based remote monitoring, and provide proven exclusive shock reduction algorithms.
The Crome system is also approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model numbers: DVPC3D4, DVPC3D1, DDPC3D4, DDPC3D1
Using the TruAF™ Detection Algorithm, Visia AF MRI™ and Visia AF™ are single chamber ICDs that can detect atrial fibrillation (AF) using a traditional lead.
The Visia AF MRI ICD system is also approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model numbers: DVAB1D4, DVAB1D1, DVFC3D4, DVFC3D1, DVFB1D4, DVFB1D1
Evera MRI™ ICDs are the first portfolio of ICDs to be approved for full body scanning in the MR environment, when MR conditions for use are met. Evera MRI is approved for 1.5 and 3T MR Conditional use.
Model numbers: DVMB1D4, DDMB1D4, DDMB1D1, DDMC3D1, DDMC3D4
The Primo MRI™ ICD system includes SmartShock™ 2.0 Technology, the PhysioCurve™ design, and is approved for 1.5T and 3T MR Conditional use, when MR conditions for use are met.
Model numbers: DVMD3D4, DVMD3D1, DDMD3D4, DDMD3D1
Evera™ ICD introduced the PhysioCurve™ design.
Model numbers: DDBB1D1, DDBB1D4, DDBC3D1, DDBC3D4, DVBB1D1, DVBB1D4, DVBC3D1, DVBC3D4
This is not a complete list of our previously marketed implantable cardioverter defibrillators (ICD).
If you cannot find the ICD you are looking for, please search our manual library.
View a listing of pacing leads approved for use with Medtronic ICDs.
Sprint Quattro™ defibrillator leads are designed for reliability, proven by active monitoring.
The Medtronic Subcutaneous lead model 6996SQ is implanted subcutaneously and can be used to offer low DFTs and high success in complex cases.
No spec sheet available.
The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s).
Please note that the intended use of a product may vary depending on geographical approvals.
See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.
For an MRI compatible device(s), consult the MRI information in the device manual(s) before performing an MRI.
If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.
Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.
Medtronic products placed on European markets comply with EU and UK legislation (if applicable) on medical devices.
For any further information, contact your local Medtronic representative and/or consult the Medtronic website at eurasia.medtronic.com.