A sutureless securing device for securing on an opening in a ventricular wall, includes: a hollow main body with an outer surface; a ring received at a first end of the hollow body, this ring being mobile along part of the outer surface of the hollow body; a tubular membrane covering the outer surface, whilst extending between the ring and the second end of the hollow body; a distal end of this tubular membrane, placed on the side of this second end, being self-expandable between a first configuration in which it has a tubular form, and a second configuration in which it defines a first flange extending radially, starting from the hollow body; the other end of this tubular membrane being able to be deformed by the displacement of the ring, such as to form a retention flange, the position of which can vary relative to the first flange.

A cannula supporting a percutaneous pump can include a proximal section with a first flexural modulus. The cannula can include one or more distal sections with a flexural modulus that is different than the first flexural modulus. The material and its arrangement along the length of the cannula can be selected so as to influence bending properties. This can, for example, allow efficient positioning of the cannula in a desired location without displacing the guidewire.

A delivery sheath can comprise an elongate tubular member and an anchor on a distal portion of the elongate tubular member, the anchor being configured to engage with the coronary sinus ostium, or both the coronary sinus ostium and a portion of the coronary sinus adjacent to the ostium, so as to provide stable transcatheter access into the coronary sinus. The anchor can be configured to permit blood flow through the ostium while in engagement with the ostium.

Disclosed herein is a system and method directed to placing a first medical instrument in a patient body, where the system includes the first medical instrument being an implantable medical instrument, a second medical instrument comprising an optical fiber having one or more of core fibers, and a console having stored thereon logic that, when executed, causes operations including providing an incident light signal to the optical fiber, receiving reflected light signals, processing the reflected light signals, and determining (i) a shape of the second medical instrument within the patient body, and (ii) a shape of the first medical instrument within the patient body based on the shape of the second medical instrument.

A cannula system and method for accessing a blood mass in the brain. The system comprises a cannula with a camera mounted on the proximal end of the cannula with a view into the cannula lumen and the surgical field below the lumen. A prism, reflector or other suitable optical element is oriented between the camera and the lumen of the cannula to afford the camera a view into the cannula while minimizing obstruction of the lumen. The system may also include an obturator with a small diameter shaft and a large diameter tip which is optically transmissive, so that a surgeon inserting or manipulating the assembly can easily see that the obturator tip is near brain tissue (which is white) or blood (which is red).

An apparatus for occluding the inflow conduit of a ventricular assist device comprising a plug body, a plug surface, and a plug cap. The plug cap is configured to extend around an external surface of the cylindrical body of the plug body. The plug cap may be removeably connected to the plug body.

The exoskeleton (10) for assisting surgical positioning is made of biocompatible material and formed to be substantially form-preserving. The exoskeleton (10) comprises a shell (11) having a coupling surface (15b) fitting to at least a part of a surface of an organ to be operated, and a guiding channel (13) is formed in the shell (11) at a predetermined position, said guiding channel having a predetermined orientation with respect to said shell and a predetermined cross-sectional area for directing a surgical tool to the organ to be operated.

A surgical access assembly includes an instrument valve housing defining a cavity, and a seal assembly disposed within the cavity of the instrument valve housing. The seal assembly includes a flange seal member and a centering mechanism. The flange seal member includes an annular member, a flange portion extending from the annular member, and a seal portion supported by the annular member and defining an opening dimensioned to receive a surgical instrument in a sealing relation. The flange portion includes first and second arcuate portions adjustably engaging the instrument valve housing in a sealing relation. The first and second arcuate portions have a parabolic profile. The centering mechanism maintains the seal assembly centered within the cavity of the instrument valve housing.

A method for carrying out a cardiac procedure includes: a. via an inferior artery, advancing a perforating tip of a perforation device towards an aorta; b. positioning the perforating tip adjacent a wall of the aorta, proximate a left pulmonary artery; and c. advancing the perforating tip to perforate through the wall of the aorta and then through a wall of the left pulmonary artery, to create a pathway between the aorta and the left pulmonary artery.

A cannula assembly includes an elongate shaft assembly that is adjustable by a clinician to vary the length of the cannula assembly. In particular, the elongate shaft assembly may be transitioned to provide various lengths of the cannula assembly by selectively positioning a plurality of segments of the elongate shaft assembly. In this manner, a single cannula assembly may be tailored to each patient or a surgical procedure being performed.