For decades, Epic™ has been the surgical valve platform that cardiac surgeons and patients have relied on for more. We continue to drive for more with our recently added Epic Max. More flexibility. More possibilities.
Epic™ Max delivers everything you’ve come to expect — excellent hemodynamics, and implantability to enable implantation for even challenging patient anatomy. The Epic™ Max is built as part of the Epic™ Platform which has proven long-term durability, and features designed for future intervention.
With Epic™ Max you and your patients can continue to depend on Epic valves for more — both now and in the future. Reliable therapy for today, tomorrow, and the road ahead.
Learn about the features of the Epic Max valve.
| Model Number | Valve Size (mm) | Tissue Annulus Diameter (mm) | Internal Diameter1 (Stent ID mm) | Aortic Protrusion (mm) | Total Height (mm) | Cuff Diameter (mm) |
|---|---|---|---|---|---|---|
| EMAX-19 | 19 | 19 | 20.8 | 11 | 15 | 27.5 |
| EMAX-21 | 21 | 21 | 22.6 | 13 | 16 | 29.0 |
| EMAX-23 | 23 | 23 | 24.5 | 13 | 17 | 31.0 |
| EMAX-25 | 25 | 25 | 26.3 | 14 | 19 | 33.0 |
| EMAX-27* | 27 | 27 | 28.4 | 15 | 20 | 35.5 |
1 Stent Internal Diameter does not account for the tissue/fabric covering the stent which may vary in thickness between approximately 1 to 2 mm.
*This size may not be available in your region
| Model Number | Description |
|---|---|
| EMAX-1000 | Epic™ Max Heart Valve Sizer Set One (1) click -in aortic series holder handle Five (5) double ended aortic sizers (19, 21, 23, 25, 27 mm) |
Indications for Use
The Epic™ Max valve is indicated for patients requiring replacement of a diseased, damaged, or malfunctioning native aortic heart valve. It may also be used as a replacement for a previously implanted aortic prosthetic heart valve.
Contraindications
None known.
Potential Adverse Events
Adverse events potentially associated with the use of bioprosthetic heart valves (in alphabetical order) include: angina; cardiac arrhythmias; endocarditis; heart failure; hemolysis; hemolytic anemia; hemorrhage, anticoagulant/antiplatelet-related; leak, transvalvular or paravalvular; myocardial infarction; nonstructural dysfunction (entrapment by pannus or suture, inappropriate sizing or positioning, or other); prosthesis regurgitation; stroke; structural deterioration (calcification, leaflet tear, or other); thromboembolism; valve thrombosis. It is possible that these complications could lead to: reoperation; explantation; permanent disability; death.
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