The Contour 3D™ ring is indicated for the reconstruction and/or remodeling of pathological tricuspid valves.
Contraindictions include heavily calcified valves, valvular retraction with severely reduced mobility, and active bacterial endocarditis.
Only physicians who have received proper training in valve repair should use this device. Adverse events can include thromboembolic events, dehiscence, hemolysis, stenosis, residual incompetence, heart block, endocarditis, right ventricular outflow tract obstruction, anticoagulant-related bleeding, or hemorrhage.
Caution: Federal law (United States) restricts these devices to sale by or on the order of a physician.
For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the instructions for use. For countries that use eIFUs, consult instructions for use at this website: medtronic.com/manuals.
UC202409165 EN
Find more information, including other available configurations, for Contour 3D™ annuloplasty ring.
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