KONECT RESILIA aortic valved conduit
KONECT RESILIA aortic valved conduit
| Model | Valve size |
| 11060A† | 21 mm – 29 mm | 21, 23, 25, 27 & 29 mm |
| Model | Accessories |
| TRAY1190 | Accessory tray |
| 1190 | Individual sizers | 19 mm* – 29 mm |
| 1190SET | Sizer set | 19 mm* – 29 mm |
Electronic Instructions for Use (eIFU): eifu.edwards.com; + 1 888 570 4016
†For use only with the dedicated sizers that replicate the DualFit sewing ring (Model 1190 Sizers and Tray).
*KONECT RESILIA aortic valved conduit size 19mm not available.
Explore surgeons’ real-world experiences with the KONECT RESILIA aortic valved conduit
KONECT RESILIA aortic valved conduit brochure
Important Safety Information
KONECT RESILIA Aortic Valved Conduit
Indications: For use in replacement of native or prosthetic aortic heart valves and the associated repair or replacement of a damaged or diseased ascending aorta.
Contraindications: There are no known contraindications with the use of the KONECT RESILIA aortic valved conduit.
Complications and Side Effects: Thromboembolism, valve thrombosis, hemorrhage, hemolysis, regurgitation, endocarditis, structural valve deterioration, nonstructuraldysfunction, stenosis, arrhythmia, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, any of which could lead to reoperation, explantation,permanent disability, and death. Adverse events potentially associated with the use of polyester vascular grafts include hemorrhage, thrombosis, graft infection, embolism,aneurysm, pseudoaneurysm, seroma, occlusion (anastomotic intimal hyperplasia), immunological reaction to collagen (shown to be a weak immunogen; infrequent, mild,localized and self-limiting), intimal peel formation, and conduit dilatation, any of which could lead to re-operation, explantation, permanent disability, and death.
CAUTION: US law restricts this device to sale by or on the order of a physician. See instructions for use for full prescribing information.
