AVEIR™ VR Leadless Pacemaker’s
helical fixation is designed for
chronic retrieval, expanding
Battery is projected to offer up to
twice the longevity of current VR
leadless pacemakers based on ISO
AVEIR™ VR Leadless Pacemaker mapping capability is designed to help reduce the number of
The software for AVEIR VR Leadless Pacemaker was designed for expandability to a dual chamber system to be introduced to the AVEIR VR system via software updates in the future, upon regulatory approval.1***
AVEIR VR LP is MR Conditional for full body scans using a 1.5T or 3T field strength MRI scanner.****
* Limited data is available for Aveir Leadless Pacemaker. The Aveir Leadless Pacemaker’s predicate device has chronic retrieval success rate >80% with helix fixation through 7 years regardless of implant duration
** ISO standard settings: VVIR, 60bpm, 2.5V @0.4 ms, 600 Ω, 100% pacing
***CAUTION: Dual Chamber configuration is currently investigational and is limited to investigational use only in accordance with Canadian Law. Contact your local sales representative for the regulatory status of the device(s) in Canada
**** Stability of pacing capture thresholds is required prior to MRI scan. For additional information about specific MR Conditional, including warnings, precautions, adverse conditions to MRI scanning and potential adverse events, please refer to the MRI-Ready Leadless Systems Manual at medical.abbott/manuals or check our MRI Ready resources at cardiovascular.abbott/mriready
MAT-2210336 v1.0 | Item approved for Canada use only.
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