CARDIAC SURGERY SOLUTIONS

ADVANCING MINIMALLY
INVASIVE CARDIAC SURGERY

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Perceval®

Aortic
Pericardial
Heart Valve

Memo 4D®

Mitral Valve
Annuloplasty
Ring

DESIGNED SPECIFICALLY TO ADVANCE
MINIMALLY INVASIVE CARDIAC SURGERY

PERCEVAL®

Aortic Pericardial Heart Valve

• Truly Sutureless

  • Self-expanding sutureless design reduces operative time, trauma and manipulation of aortic structures1

• Minimized Incision

  • Reduced incision size and less surgical trauma during implantation due to collapsible profile2,3

• Maximized Visibility

  • Reproducible technique and collapsible profile allows the surgeon full visibility of the annulus3

• Shorter Procedure

  • Shorter procedure minimizes blood transfusion and complications regardless of surgical approach4,5
Perceval Product Information Download Perceval Brochure
Indication for Use

The Perceval bioprosthesis is indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic aortic valves.

Summary of Risks

The risks or potential adverse events associated with cardiac valve replacement with a bioprosthesis include, but may not be limited to: cardiac arrhythmias, death, endocarditis, heart failure, hemorrhage, intravalvular and/or paravalvular leak, stroke or any related neurologic disorders, structural valve deterioration, reoperation and explant. Beyond the previously mentioned adverse events, specific events related to the implant of the Perceval prosthesis may include, but not be limited to dislodgement and/or migration of the prosthesis. Please refer to the product Instructions for Use (IFU) for detailed information on warnings, precautions, and potential adverse events. For a copy of the IFU, please contact: [email protected]

RESHAPING MITRAL REPAIR

MEMO 4D®

Mitral Valve Annuloplasty Ring

• ReChord System

  • “According to our experience, the temporary chordal guide system allows a correct implantation of PTFE neochordae without the need for chordal measurement, short operative times and doesn’t require a long learning process. In our opinion, its use might standardize the 'respect rather than resect' mitral valve repair technique, further facilitating a MIMV surgical approach.”6

• Increase of the Anteroposterior Diameter

  • Helps accommodate excess leaflet tissue and
    avoids the risk of Systolic Anterior Motion (SAM)

• Accessories Designed to Facilitate MICS

  • Extended Uni handle and unique
    low-profile holder template

• Gradual Saddle Shape

  • Designed to optimize the physiological
    geometry in enlarged annuli

• Unique Range of Sizes

  • Up to size 42 mm to
    treat large annuli
Memo 4D Product Information
Download Memo 4D Brochure
Indication for Use

Memo 4D device is intended for correction of mitral insufficiencies or steno-insufficiencies. The use of the Memo 4D device is indicated for correction of congenital or acquired mitral insufficiencies with dilatation and deformation of the mitral annulus.

Summary of Risks

The use of prosthetic annuloplasty rings is associated with serious potential complications, which indlude: death; reopertation; explant; residual or recurrent regurgitation; partial/total ring dehiscence; systolic anterior motion (SAM) and left ventricular outflow tract obstruction (LVOTO). Please refer to the product Instruction for Use (IFU) for detailed information on warnings, precautions, and potential adverse events. For a copy of the IFU, please contact: [email protected]