Abstract: A prosthetic heart valve for replacing a native valve includes a collapsible and expandable stent having a proximal end and a distal end, the stent being formed of a plurality of struts forming cells. A valve assembly is disposed within the stent, the valve assembly including a plurality of leaflets and a cuff. At least one runner is coupled to a cell and configured to transition from a first configuration to a second configuration when the stent moves from the collapsed condition to the expanded condition.

Abstract: A prosthetic heart valve for replacing a native valve includes a collapsible and expandable stent having a proximal end and a distal end, the stent being formed of a plurality of struts forming cells. A valve assembly is disposed within the stent, the valve assembly including a plurality of leaflets and a cuff. At least one runner is coupled to a cell and configured to transition from a first configuration to a second configuration when the stent moves from the collapsed condition to the expanded condition.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A method of implanting a stented device in a cardiovascular system of a mammalian subject includes guiding a delivery device that has an anchoring device connected to a distal end thereof within the cardiovascular system to a target location. The anchoring device has a body and a mooring feature extending from the body. The anchoring device is anchored at the target location by penetrating tissue at the target location with the mooring feature. The mooring feature is configured to anchor the body to the tissue when penetrated therein. The stented device is then guided through the cardiovascular system to the target location and deployed such that a stent of the stented device engages the anchoring device so as to restrict movement of the stented device within the cardiovascular system.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A method of implanting a stented device in a cardiovascular system of a mammalian subject includes guiding a delivery device that has an anchoring device connected to a distal end thereof within the cardiovascular system to a target location. The anchoring device has a body and a mooring feature extending from the body. The anchoring device is anchored at the target location by penetrating tissue at the target location with the mooring feature. The mooring feature is configured to anchor the body to the tissue when penetrated therein. The stented device is then guided through the cardiovascular system to the target location and deployed such that a stent of the stented device engages the anchoring device so as to restrict movement of the stented device within the cardiovascular system.

Abstract: An anchoring device for use within a cardiovascular structure includes an expandable ring having a central axis extending in a longitudinal direction. At least one leg extends from the ring in the longitudinal direction. The leg includes a first end connected to the ring and a free end, with at least one anchor connected to the leg. The anchoring device may be used to anchor a transcatheter heart valve within the cardiovascular structure.

Abstract: A prosthetic heart valve for replacing a native valve includes a collapsible and expandable stent having a proximal end and a distal end, the stent being formed of a plurality of struts forming cells. A valve assembly is disposed within the stent, the valve assembly including a plurality of leaflets and a cuff. At least one runner is coupled to a cell and configured to transition from a first configuration to a second configuration when the stent moves from the collapsed condition to the expanded condition.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: An anchoring device for use within a cardiovascular structure includes an expandable ring having a central axis extending in a longitudinal direction. At least one leg extends from the ring in the longitudinal direction. The leg includes a first end connected to the ring and a free end, with at least one anchor connected to the leg. The anchoring device may be used to anchor a transcatheter heart valve within the cardiovascular structure.

Abstract: An implant tool for use with an endocardial or other implantable lead having an extendable/retractable active fixation tip includes a housing, a shaft rotatably supported by the housing, and a shaft rotation mechanism for rotating the shaft through a predetermined angular travel. The shaft includes a lead attachment portion for selectively coupling a lead to the shaft such that the lead is rotatable with the shaft. The implant tool may include a control tab slidably supported by the housing, wherein longitudinal movement of the control tab actuates the shaft rotation mechanism. The shaft rotation mechanism may include a gear train, an electric motor, a double acting spring mechanism, or a retractable tape wound around the shaft. The gear train includes an input member coupled to the control tab and an output gear coupled to the shaft. The input member meshes with an input gear supported by the housing.

Abstract: An implant tool for use with an endocardial or other implantable lead having an extendable/retractable active fixation tip includes a housing, a shaft rotatably supported by the housing, and a shaft rotation mechanism for rotating the shaft through a predetermined angular travel. The shaft includes a lead attachment portion for selectively coupling a lead to the shaft such that the lead is rotatable with the shaft. The implant tool may include a control tab slidably supported by the housing, wherein longitudinal movement of the control tab actuates the shaft rotation mechanism. The shaft rotation mechanism may include a gear train, an electric motor, a double acting spring mechanism, or a retractable tape wound around the shaft. The gear train includes an input member coupled to the control tab and an output gear coupled to the shaft. The input member meshes with an input gear supported by the housing.

Abstract: This document discusses, among other things, a ureteroscope having a notch or other structure at a distal end configured to engage a guide wire and facilitate cannulation.

Abstract: This patent document discusses assemblies and methods for transferring a subject from a first surface to a second surface. In varying examples, an assembly includes a first roller and a second roller. An assembly frame rotatably supports the rollers and, in some examples, longitudinally extends from a frame first end to a frame second end. A belt is coupled to the first and second rollers in such a matter that the assembly frame is positioned, at least in part, between the rollers and surrounded by the belt. A motor, powered by a power source, is coupled to the belt via the first or second roller. In one such example, the motor is coupled with a portion of a first roller inner surface. In another example, an outer surface of one or both of the rollers include belt driving projections matable with projection receiving portions disposed on a belt underside surface.

Abstract: This document discusses, among other things, a ureteroscope having a notch or other structure at a distal end configured to engage a guide wire and facilitate cannulation.

Abstract: This patent document discusses assemblies and methods for transferring a subject from a first surface to a second surface. In varying examples, an assembly includes a first roller and a second roller. An assembly frame rotatably supports the rollers and, in some examples, longitudinally extends from a frame first end to a frame second end. A belt is coupled to the first and second rollers in such a matter that the assembly frame is positioned, at least in part, between the rollers and surrounded by the belt. A motor, powered by a power source, is coupled to the belt via the first or second roller. In one such example, the motor is coupled with a portion of a first roller inner surface. In another example, an outer surface of one or both of the rollers include belt driving projections matable with projection receiving portions disposed on a belt underside surface.