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Pamira
Pamira® continues BIOTRONIK's legacy of reliability and performance by adding a proximal polyurethane overlay to the proven Plexa design. Pamira® is FDA approved for use with all ICDs and CRT-Ds with DF4 headers. It is available in single coil or dual coil variants as well as BIOTRONIK’s clinically proven DX platform – still the only system capable of providing true atrial sensing with a single lead.
Product Highlights
Long-Term Reliability
Ease of Implant
Proven Design
Product Details
- Built on the proven Plexa platform with an additional polyurethane (PU) overlay on the proximal section of the lead to further enhance durability
- Compatible with 8.5 F lead introducer
- Helical cabling designed to reduce stress and promote durability of the lead body within the intracardiac region
- Proprietary shock-coil design for reduced tissue ingrowth and efficient energy delivery
- Advanced screw mechanism with maximum flexibility for atraumatic fixation
- Fractal coating and steroid elution for low thresholds and optimal sensing
- Bipolar sensing and pacing with 11 mm tip-to-ring distance
- BIOTRONIK ProMRI1 allows patients to undergo MR scanning under specific conditions
- Full-body MRI conditional labeling for 1.5T and 3.0T scans combined with an Acticor/Rivacor ICD or CRT-D. Additionally, Pamira S DX maintains MRI conditionality when a BK-IS cap is added to the IS-1 connector for the atrial branch.
- Refer to the ProMRI System Technical Manual (https://manuals.biotronik.com/) for a complete list of MRI conditional device/lead configurations and scanning conditions
Downloads & Related Links
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References
1. For combination of MR conditional devices, please see the "ProMRI System Technical Manual"