medtronic tavr mri safety

Patients who do not are more likely to have a stroke. If you need an MRI, tell your doctor that you have a Medtronic TAVR heart valve. GeneralImplantation of the CoreValve Evolut R, Evolut PRO+, and Evolut FX Systems should be performed only by physicians who have received Medtronic CoreValve Evolut R, Evolut PRO+, or Evolut FX training. Data backs durability of Medtronic CoreValve Evolut TAVR; . AMEND Mitral Annuloplasty Ring, All Sizes Valcare Medical LTD., www.valcaremedical.com. Complications at the area where the doctor cutthe skin or related to cutting the skin, includingbut not limited to: Hematoma blood collecting under the skin, Pseudoaneurysm blood collecting on theoutside of a vessel wall causing a balloon-likewidening, Irreversible nerve damage permanentdamage to nerves, Compartment syndrome squeezing ofnerves and muscles in a closed space thatcould cause muscle or nerve damage, Stenosis narrowing of a blood vessel(artery), Mitral valve regurgitation blood leakingbackward through the valve between the leftlower chamber of the heart to the left upperchamber of the heart, Hypotension or hypertension low or highblood pressure, Bowel ischemia decreased blood supply tothe intestines. Background: The two most common organisms found in infective endocarditis following transcatheter aortic valve implantation (TAVI-IE) are enterococci (EC-IE) and staphylococci (SC-IE). Prevent kinking of the catheter when removing it from the packaging. The Evolut FX transcatheter aortic valve system sets new expectations for precision, control, and predictability in TAVR procedures. Typically, patients begin walking the same day as their Medtronic TAVR procedure and are discharged within a day or two. The doctor willguide a thin, flexible tube with the heart valve into your artery and to your diseased valve. 1.5, 3. For direct aortic access, ensure the access site and trajectory are free of patent RIMA or a preexisting patent RIMA graft. Cerebrospinal Fluid (CSF) Shunt Valves and Accessories More. Please talk to your doctor to decide whether this therapy is right for you. Implantation of the bioprosthesis should be avoided in patients with aortic root angulation (angle between plane of aortic valve annulus and horizontal plane/vertebrae) of >30 for right subclavian/axillary access or >70 for femoral and left subclavian/axillary access. 1 The mechanism of cerebral embolism may differ according to the early time period (procedure related within 48 hours of TAVR), or later (nondirectly procedure related, eg, atrial fibrillation [AF] or valve leaflet thrombosis). After the procedure, administer anticoagulation and/or antiplatelet therapy per physician/clinical judgment. CORFLO Ultra Non-weighted Feeding Tube Stylet Removed Polyurethange Viasys Healthcard Systems Wheeling, IL Limited clinical data are available for transcatheter aortic valve replacement in patients with a congenital bicuspid aortic valve who are deemed to be at low surgical risk. MRI exams are safe for some devices MRI (magnetic resonance imaging) uses a large, circular magnet and radio waves to produce clear computer images of the body. Treat more TAVR patients The Evolut PRO+ system is indicated to treat annulus ranges up to 30 mm in diameter and has the ability to treat the broadest annulus range* of any commercially available TAVR system. During the procedure, monitor contrast media usage. Access instructions for use and other technical manuals in the Medtronic Manual Library. . Can you have MRI with aortic valve replacement? Safety Info ID# Safety Topic / Subject Article Text 179: Heart Valves and Annuloplasty Rings: . Failure to comply with the . If you have any questions about your TAVR device, reach out to our CardioVascular LifeLine Technical Support by phone or email. See the Confida Brecker Guidewire References Data on file (>20 clinical trials with over 20000 patients enrolled). Discuss this with your doctor. Patients assigned to this group will be implanted with commercially available balloon-expandable SAPIEN 3 Transcatheter Heart Valve or future iteration (SAPIEN 3; Edwards Lifesciences LLC, Irvine, CA, USA) or a commercially available self-expanding CoreValve Transcatheter Aortic Valve Replacement System, CoreValve Evolut . Published literature suggests a higher cumulative incidence . On the basis of available evidence to date, all patients with prosthetic heart valves or coronary stents can safely undergo MRI at 1.5 T and the vast majority at 3 T. What is a Tavr valve made of? Potential risks associated with the implantation of the CoreValve Evolut R, Evolut PRO+, or Evolut FX transcatheter aortic valve may include, but are not limited to, the following: Please reference the CoreValve Evolut R, Evolut PRO+, and Evolut FX Instructions for Use for more information regarding indications, warnings, precautions, and potential adverse events. Please talk to your doctor to decide whether this therapy is right for you. 3: . AorTechAorticModel 3800TitaniumHeart ValveAortech Ltd.Strathclyde, U.K. AorTechMitralModel 4800titaniumheart valveAortech Ltd.Strathclyde, U.K. Aortic Mitroflow Synergy PCAortic Pericardial Heart ValveSize 19 mmSulzer Carbomedics, Inc., www.sorin.com, Aortic Mitroflow Synergy PCAortic Pericardial Heart ValveSize 29 mmSulzer Carbomedics, Inc., www.sorin.com, Aortic SJM Regent ValveMechanical Heart ValveSize 27 mm27AGN-751Rotatable AorticStandard Cuff-Polyester, AGNSt. Each patient is different, and the potential risks and benefits are based on individual treatment and health conditions. Built with RESILIA tissue , the INSPIRIS valve is designed to oer enhanced tissue anti-calcication technology that will potentially allow the valve to last longer. Find more detailed TAVRinformation, educationalresources, and tools. It also: Improves overall visualization. Share this card with your family members and all members of your healthcare team, including your dentist. There are significant risks associated with TAVR procedures. The Evolut PRO+ system is indicated to treat annulus ranges up to 30 mm in diameter and hasthe ability to treat the broadest annulus range* of any commercially available TAVR system. Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices, Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification. +1-763-505-4626, 9850 NW 41st Street, Suite 450, Doral, FL 33178 The EDWARDS INTUITY Elite valve system represents our commitment to continued innovation for surgeons and patients in heart valve therapy.. If the product name you seek is not listed, try looking for information by device type. Unlike open-heart surgery, TAVR does not require stopping the heart. TAVR is less invasive than open-heart surgery,and the procedure typically takes less than one hour. For some patients, the Medtronic TAVR procedure risks may outweigh the benefits. The study retrospectively analyzed 1,128 TAVR and 971 surgery patients from the CoreValve U.S. High Risk and SURTAVI randomized trials. Your dentist and all doctors need to know about your Medtronic TAVR valve. You will be asked to return to the valve clinic to have your heart valve checked at 30 days and one year after your procedure, and as recommended by your physician. During Use After the procedure, administer appropriate antibiotic prophylaxis as needed for patients at risk for prosthetic valve infection and endocarditis. Search by the product name (e.g., Evolut) or model number. In addition, you may experience otherproblems that have notbeen previouslyobservedwith this procedure. Evolut FX TAVR/TAVI Deployment Video A VCC is usually your first point of contact at a TAVR hospital. Does my heart need to be stopped for TAVR? Home Catheter ablation is a well-accepted rhythm control strategy for patients with symptomatic atrial fibrillation (AF). With an updated browser, you will have a better Medtronic website experience. Conduct the procedure under fluoroscopy. This procedure should only be performed where emergency aortic valve surgery can be performed promptly. If 2 of these factors are present, consider an alternative access route to prevent vascular complications. Prior to the procedure, measure the patients creatinine level. Once the Portico valve has been implanted, patients may experience immediate improvement in quality of life or may feel better gradually. With an updated browser, you will have a better Medtronic website experience. Your doctor can help you decide which Medtronic TAVR heart valve is right for you. Download Citation | Prevalence and significance of relative apical sparing in aortic stenosis: insights from an echo and cardiovascular magnetic resonance study of patients referred for surgical . You should start feeling better right away. Webb, John. At the start of the procedure,your doctor will make a small cut in one of three typically used access routes: a small cut in the groin (1), the neck (2), or a space between your ribs (3). 4,45 The incidence of new-onset . Implantable Cardiac Devices - MR Conditional Status, Find MRI technical support phone numbers and supplemental MRI resources. Transcatheter aortic valve replacement with a balloon-expandable valve in low-risk patients. This could make you feel sick or cause death. The study objectives are to assess the safety and efficacy of the CoreValve Evolut 34R transcatheter aortic valve replacement (TAVR) system in . Find important safety information about the Medtronic transcatheter aortic valve and TAVR procedure. Is it safe to have an MRI with a Medtronic TAVR heart valve? Medtronic plc (NYSE:MDT), a global leader in healthcare technology, today announced it will participate in the 41st annual J.P. Morgan healthcare conference. The Medtronic CoreValve Evolut R, CoreValve Evolut PRO, and Evolut PRO+ systems are indicated for use in patients with symptomatic heart disease due to failure (stenosed, insufficient, or combined) of a surgical bioprosthetic aortic valve who are judged by a heart team, including a cardiac surgeon, to be at high or greater risk for open surgical therapy (e.g., STS predicted risk of operative mortality score 8% or at a 15% risk of mortality at 30 days). The Interject Sclerotherapy Needle features a unique star-shaped inner catheter design to help promote reliable needle actuation in tortuous anatomy (even after kinking). Learn how the Evolut platform isdesigned to go beyond proceduraloutcomes to benefit your patients. Jude Medical St. Paul, M, Aortic ValveSize 16 mmA419529D 16ASulzer Carbomedics, Inc., www.sorin.com, Apical ConnectorModel 174Aheart valveMedtronic Heart Valve DivisionMinneapolis, M. Shellock R & D Services, Inc. email: Frank.ShellockREMOVE@MRIsafety.com. Transcatheter aortic valve (bioprosthesis) Accelerated deterioration due to calcific degeneration of the bioprostheses may occur in: children, adolescents, or young adults; patients with altered calcium metabolism (e.g., chronic renal failure or hyperthyroidism). TAVR began at Medtronic in 2009 when the business acquired the CoreValve self-expanding TAVR system following its launch in Europe in 2007. Any and all information provided is intended for general overview. Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA, Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices, Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification. The Medtronic TAVR heart valveis designedto work like your own heart valve. Copyright 2023 by Shellock R & D Services, Inc. and Frank G. Shellock, Ph.D. All rights reserved. You just clicked a link to go to another website. Treatments & Therapies These data are summarized in the Instructions for Use and support the findings of the primary analysis. Raynham, MA. Elekta (Stockholm:EKTA-B) says an FDA 510 (k) clearance represents a new era in precision radiation therapy to treat cancer in the U.S. The Sweden-based cancer and brain treatment tech company . With an updated browser, you will have a better Medtronic website experience. Update my browser now. Dysfunctions of a Medtronic TAVR valve,including but not limited to: Valve frame does not open (expand) allthe way, Pannus the formation of scar tissuethat may cover or block the valve fromfunctioning normally, Wear, tear, or movement forward (prolapse)or backward (retraction) from the normalposition of the valve leaflets, A break in the stitches (sutures) of the valveframe or leaflets, Leakage through or around the valve orvalve frame, Incorrect position of the valve, either toohigh or too low, Regurgitation backward flow of bloodthrough the valve, Stenosis narrowing of the opening ofthe valve, Valve migration upward or downwardmovement of the device from where itwasoriginally placed, Embolism an abnormal particle (air, bloodclots) floating in the blood stream or attachedto an object, including the valve or deliverysystem component, Infection of the heart, blood, or other areas, Thrombosis (including valve thrombosis) blood clot, including a blood clot on the valve, Individual or multi-organ insufficiency or failure. Before Use Exposure to glutaraldehyde may cause irritation of the skin, eyes, nose, and throat. Products The CoreValve and Evolut transcatheter aortic valve replacement (TAVR) devices have been evaluated in more than a dozen clinical trials. Implanting a CoreValve Evolut R, Evolut PRO, or Evolut PRO+ bioprosthesis in a degenerated surgical bioprosthetic valve (transcatheter aortic valve in surgical aortic valve [TAV-in-SAV]) should be avoided in the following conditions: The degenerated surgical bioprosthetic valve presents with: a significant concomitant paravalvular leak (between the prosthesis and the native annulus), is not securely fixed in the native annulus, or is not structurally intact (e.g., wire form frame fracture); partially detached leaflet that in the aortic position may obstruct a coronary ostium; stent frame with a manufacturer-labeled inner diameter < 17 mm. Mechanical failure of the delivery catheter system and/or accessories may result in patient complications. February 28, 2023 By Danielle Kirsh. Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices. Products Transcatheter aortic valve (bioprosthesis) Accelerated deterioration due to calcific degeneration of the bioprostheses may occur in: children, adolescents, or young adults; patients with altered calcium metabolism (e.g., chronic renal failure or hyperthyroidism). The Medtronic CoreValve Evolut R, Evolut PRO+, and Evolut FX Systems are indicated for relief of aortic stenosis in patients with symptomatic heart disease due to severe native calcific aortic stenosis who are judged by a heart team, including a cardiac surgeon, to be appropriate for the transcatheter heart valve replacement therapy. That brings expected full-year . At some point, the Medtronic TAVR valve may need tobe replaced. Prior to the procedure, measure the patients creatinine level. You may also call 800-961-9055 for a copy of a manual. The safety and effectiveness of the bioprostheses for aortic valve replacement have not been evaluated in the following patient populations: Patients who do not meet the criteria for symptomatic severe native aortic stenosis as defined: (1) symptomatic severe high-gradient aortic stenosis aortic valve area 1.0cm2 or aortic valve area index 0.6cm2/m2, a mean aortic valve gradient 40mmHg, or a peak aortic-jet velocity 4.0m/s; (2) symptomatic severe low-flow, low-gradient aortic stenosis aortic valve area 1.0cm2 or aortic valve area index 0.6cm2/m2, a mean aortic valve gradient <40mmHg, and a peak aortic-jet velocity <4.0m/s; with untreated, clinically significant coronary artery disease requiring revascularization; with a preexisting prosthetic heart valve with a rigid support structure in either the mitral or pulmonic position if either the preexisting prosthetic heart valve could affect the implantation or function of the bioprosthesis or the implantation of the bioprosthesis could affect the function of the preexisting prosthetic heart valve; patients with liver failure (Child-Pugh Class C); with cardiogenic shock manifested by low cardiac output, vasopressor dependence, or mechanical hemodynamic support; patients who are pregnant or breastfeeding. Find more detailed TAVRinformation, educationalresources, and tools. Less information (see less). Source: Medtronic Medtronic's Evolut PRO transcatheter aortic valve. TAVI with the Portico valve can offer several key benefits. Medtronic does not review or control the content on the other website, and we are not responsible for any business dealings or transactions you have there. After total correction for tetrolgy of fallot (TOF), right ventricle behaves in an unpredictable manner depending on type of right ventricular outflow tract (RVOT) reconstruction and surgical expertise of infundibular muscle resection. If you are on a computer, that is maintained by an admin and you cannot install a new browser, ask your admin about it. The bioprosthesis size must be appropriate to fit the patients anatomy. Cardiovascular Medtronic, Inc., www.medtronic.com. The Evolut PRO+ system offers the lowest delivery profile for 2329 mm valves, excellent hemodynamics, the broadest annulus range,* and advanced sealingwith an external tissue wrap on all valve sizes. This is the first comprehensive analysis to support clinical criteria for valve performance and durability using all four components of BVD and its association with clinical outcomes. Safety Topic / Subject ActiFlo Indwelling Bowel Catheter System also known as Zassi Bowel Management System Hollister Incorporated Libertyville, IL. Update my browser now. How long it lasts varies from patient to patient. The CoreValve Evolut R, CoreValve Evolut PRO, and Evolut PRO+ systems are contraindicated in patients who cannot tolerate Nitinol (Titanium or Nickel), an anticoagulation/antiplatelet regimen, or who have active bacterial endocarditis or other active infections. The Medtronic CoreValve Evolut R, Evolut PRO+, and Evolut FX Systems are indicated for relief of aortic stenosis in patients with symptomatic heart disease due to severe native calcific aortic stenosis who are judged by a heart team, including a cardiac surgeon, to be appropriate for the transcatheter heart valve replacement therapy. TAVR may be a good option for you if you are having symptoms and if tests performed by your heart team show that it may be helpful. If you have any questions about your TAVR device, reach out to our CardioVascular LifeLine Technical Support by phone or email. What is the optimal antithrombotic regimen after transcatheter aortic valve replacement? TAVR currentlyis approvedfor patients withheart diseasedue to symptomatic severe aortic stenosis of the native valve, and patients with a failingsurgical aortic valve who are at high risk or extreme riskdue to symptomatic, severe aortic stenosis for complications during surgery. Medtronic, www.medtronic.com. Safe More. Follow all care instructions to ensure the best possible results. Patients in both groups who developed BVD through 5 years were at about 1.5-fold greater risk of death or hospitalization for valve-related disease or heart failure as patients who did not develop BVD. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Update my browser now. Data, presented by Dr. Steven Yakubov, in a late-breaking clinical trial session at the 2023 annual meeting of Cardiovascular Research Technologies (CRT 2023), build upon the excellent results of the structural valve deterioration (SVD) analysis recently published in JAMA Cardiology. The 1-year mortality was the primary . Evaluate bioprosthesis performance as needed during patient follow-up. Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification, Patients with heart diseasedue to symptomatic, severe aortic stenosis of their native valve, Patients with a failing surgical aortic valve who are at high risk or extreme risk for complications during surgery, Serious bleeding (a bleeding event that requires a blood transfusion), Cannot take medications that reduce the risk of blood clots. A prospective multi center study of the SAPIEN 3 Ultra system in intermediate-risk patients with severe aortic stenosis. Abbott (NYSE:ABT) and the FDA are telling health providers that the company's Trifecta family of heart valves could deteriorate early. Actual results may differ materially from anticipated results. The operating model realignment program will include sourcing and demand management . Evolut FX Business & regional news, CRT 2023 Late-Breaking Data: CoreValve/Evolut platform demonstrates significantly lower bioprosthetic valve dysfunction compared to surgery at five years. Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. The Evolut FX valve frame also has gold markers beneath the outer wrap so your doctor can better see the valve during the procedure. MRI in Transcatheter Aortic Valve Replacement Patients (MRI in TAVR) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Some cookies are strictly necessary to allow this site to function. Speak to your doctor for more information about what you can expect. A number of factors determine a patients risk, including age and other medical conditionsthat make surgery more dangerous. Designed for dependable cardiac and vascular repair XenoLogiX* two-step processing treatment for dependable performance The same tissue with demonstrated long-term durability in Edwards' surgical heart valves** Ready to use after standard rinse duration Easy to suture with dependable suture retention Tissue thickness: 0.5 mm +/- 0.25 mm This procedure should only be performed where emergency aortic valve surgery can be performed promptly. +1-612-297-0501, Ryan Weispfenning Evolut EXPAND TAVR I will evaluate Evolut in patients with symptomatic moderate aortic stenosis or asymptomatic severe disease. A heart team is a specialized care team that includes interventional cardiologists, cardiac surgeons, imaging specialists, anesthesiologists, and other doctors as needed. After the procedure, most patients spend a few hours in the intensive care unit (ICU) before transferring to a patient room. How do I know if my Medtronic TAVR heart valve is working properly? Patients must present with transarterial access vessel diameters of 5 mm when using Model ENVEOR-US/ENVPRO-14-US/D-EVPROP2329US or 5.5 mm when using Model ENVEOR-N-US/ENVPRO-16-US or 6 mm when using Model D-EVPROP34US, or patients must present with an ascending aortic (direct aortic) access site 60 mm from the basal plane for both systems. If you need a replacement Medtronic TAVR valve information card, please call Patient Registration services at 763-514-7115. They help with testing, reviewing treatments, follow-up after the procedure, and can even help with insurance-related needs. (such as pacemaker, stent, otology implants, drug pump) Warning: Do not use magnetic resonance imaging (MRI) on a patient who has an implanted device until you review the following: All conditions for use for all implanted devices. Reach out to LifeLine CardioVascular Tech Support with questions. 1.5: Unsafe 2 More. CoreValve Evolut R Transcatheter Aortic Valve Heart Valve Prosthesis Medtronic, Inc., www.medtronic.com/MRI Ischemic stroke is an important complication in 2% to 6% of patients within 90 days following transcatheter aortic valve replacement (TAVR). The TAVR Procedure It is made up of a wire valve frame and bovine (cow) animal tissue leaflets. The safety and efficacy of a CoreValve Evolut R, Evolut PRO, or Evolut PRO+ bioprosthesis implanted within a transcatheter bioprosthesis have not been demonstrated. Caution:Federal Law (USA) restricts these devices to the sale by or on the order of a physician. Bitte whlen Sie Ihre Region. Transcatheter aortic valve replacement (TAVR) is a minimally invasive procedure to replace the aortic valve in patients with severe aortic stenosis. Home Subsequently, a supplemental analysis was performed, which included additional follow-up data on the same cohort. Indications, Safety, & Warnings. They will be with you throughout the TAVR journey to provide support and answer questions. We are Search by the product name (e.g., Evolut) or model number. Your doctor will remove the tube and close the cut. The Confida Brecker guidewire (CBG) is specifically designed for TAVI procedures. Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA, for transcatheter aortic valve replacement (TAVR). Products If you can't change your browser because of compatibility issues, think about installing a second browser for browsing and keep this old one for compatibility Your doctor will check your valve during your regular follow-up visits. Five-year rates of structural valve deterioration and non-structural valve dysfunction were significantly lower after TAVR compared to surgery [SVD-TAVR 2.2% vs SAVR 4.4%; p 0.004, NSVD-TAVR 4.3% vs SAVR 8.8%; p<0.001]. Cost-saving actions taken in the third quarter plus additional efforts last month should reduce Butterfly's cash outlay by around $60 million in 2023. Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA. For transfemoral access, use caution in patients who present with multiplanar curvature of the aorta, acute angulation of the aortic arch, an ascending aortic aneurysm, or severe calcification in the aorta and/or vasculature. The SURTAVI Trial was a prospective, randomized, multicenter, noninferiority study to assess the safety and efficacy of the Medtronic TAVR system to SAVR in patients with symptomatic severe aortic stenosis at intermediate surgical risk. With an updated browser, you will have a better Medtronic website experience. With valve durability becoming more critical as TAVR expands to younger, healthier patients, this analysis underscores the long-term promise of this minimally invasive approach and should be taken into consideration during initial valve selection.. The surgical heart valve market is evolving. Reach out to LifeLine CardioVascular Tech Support with questions. Treatments & Therapies Many heart valve prostheses and annuloplasty rings have been evaluated for MR issues, especially with regard to the presence of magnetic field interactions associated with exposure to MR systems opera, AAV-2 Heart Valve Aortic heart valve prosthesis Arbor Surgical Technologies, Inc. Irvine, CA, AccuFit Mitral Valve Replacement DeviceMarvel Medical Technologies, Irvine, CA, ACURATE TF (Transfemoral) Aortic Bioprosthesis Symetis SA, www.symetis.com, AHK 7700, Model 7700 heart valveMedtronic, www.medtronic.com, AMEND Mitral Annuloplasty Ring, All Sizes Valcare Medical LTD., www.valcaremedical.com, AMEND Mitral Annuloplasty Ring, All SizesValcare Medical LTD., www.valcaremedical.com, AnnuloflexAnnuloplasty RingSize 36 mmL004032A 36MSulzer Carbomedics, Inc., www.sorin.com, AnnuloflexSize 26 mmAnnuloplasty RingL001285A 26MModel AF800Sulzer Carbomedics, Inc., www.sorin.com, AnnuloFloMitral Annuloplasty DeviceSize 36Model AR-736TitaniumSulzer Carbomedics, Inc., www.sorin.com, AnnulofloSize 26 mmAnnuloplasty RingS011896A 26MSulzer Carbomedics, Inc., www.sorin.com, AnnulofloSize 36 mmAnnuloplasty RingS013460A 36MSulzer Carbomedics, Inc., www.sorin.com, Annuloplasty Ring, Models RNG5 and RNG7Dynamic Annuloplasty Ring SystemMiCardia, www.micardia.com, Annuloplasty ringtitaniumheartSulzer Medica and Sulzer Carbomedics, www.sorin.com.
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