A bearingless and sealless rotary blood pump is disclosed which provides multidirectional flow intended to provide low-pressure, high-volume right-sided partial assist circulatory support in a univentricular Fontan circulation on a permanent basis. The pump includes a housing and an impeller suspended in the center of the housing. The housing incorporates flow optimization features between inlet and outlet ends, as well as with the impeller surface. Large fluid gaps maintained between impeller and housing eliminate any potential for blood flow obstruction. The impeller contains some motor components. It includes a central stator and surrounding rotor. The motor includes a brushless DC outrunner electrical motor design. An electromagnetic stator core is surrounded by a circumferential passive magnetic ring. The rotor is further levitated about the stator spindle by a plurality of axially and radially located passive magnetic and hydrodynamic journal bearings on both ends of the spindle. The rotor is bearingless and sealless. During impeller rotation, blood entering the space between the rotor and stator is induced to flow by centrifugal pumping action and the fluid film separates the stator hydrodynamic bearings from the rotor so that there is no direct mechanical contact between the rotor and stator.

Mechanical circulatory support systems and methods are disclosed herein. In some examples, the present technology comprises a system for providing cardiac support to a patient where the system comprises a first elongated shaft configured to receive a delivery catheter therethrough, a second elongated shaft, and a pressure source coupled to the first and second elongated shafts. The first elongated shaft may have a distal end portion configured to be intravascularly positioned at a first cardiovascular location, and the second elongated shaft may have a distal end portion configured to be intravascularly positioned at a second cardiovascular location downstream of the first location. Pressure generated by the pressure source pulls blood from the first location proximally through the first shaft to the pressure source, then pushes the blood distally through the second shaft and into circulatory flow at the second cardiovascular location, thereby providing mechanical circulatory support to the patient.

Mechanical circulatory support systems and methods are disclosed herein. In some examples, the present technology comprises a system for providing cardiac support to a patient where the system comprises a first elongated shaft configured to receive a delivery catheter therethrough, a second elongated shaft, and a pressure source coupled to the first and second elongated shafts. The first elongated shaft may have a distal end portion configured to be intravascularly positioned at a first cardiovascular location, and the second elongated shaft may have a distal end portion configured to be intravascularly positioned at a second cardiovascular location downstream of the first location. Pressure generated by the pressure source pulls blood from the first location proximally through the first shaft to the pressure source, then pushes the blood distally through the second shaft and into circulatory flow at the second cardiovascular location, thereby providing mechanical circulatory support to the patient.

Some embodiments disclosed herein relate to devices and methods for controlling placement of intraocular implants within a patient's eye including but not limited to placement within or near the collector ducts of Schlemm's canal located behind the trabecular meshwork. In some embodiments, a handheld peristaltic rotor device having a compression element can be positioned on a corneal surface of the eye and rotated to create a peristaltic movement of blood in one or more episcleral veins to generate blood reflux within Schlemm's canal such that one or more collector ducts, or channels, of Schlemm's canal can be located. In some embodiments, an implant can be implanted near the identified location of the one or more collector ducts, or channels.

Some embodiments disclosed herein relate to devices and methods for controlling placement of intraocular implants within a patient's eye including but not limited to placement within or near the collector ducts of Schlemm's canal located behind the trabecular meshwork. In some embodiments, a handheld peristaltic rotor device having a compression element can be positioned on a corneal surface of the eye and rotated to create a peristaltic movement of blood in one or more episcleral veins to generate blood reflux within Schlemm's canal such that one or more collector ducts, or channels, of Schlemm's canal can be located. In some embodiments, an implant can be implanted near the identified location of the one or more collector ducts, or channels.

The present disclosure relates to a saccular cavopulmonary assist device, including a shell, an inflow tube (6) and an outflow tube (4), wherein a blood storage cavity (A) and a power cavity (B) are arranged in the shell, and the power cavity (B) is used for providing contraction and relaxation power for the blood storage cavity (A); the inflow tube (6) is arranged at a position corresponding to the power cavity (B) on the shell, an outer end is used for communicating with the vena cava, and an inner end communicates with the blood storage cavity (A) after passing through the power cavity (B); the outflow tube (4) is arranged at a position corresponding to the blood storage cavity (A) on the shell, an outer end is used for communicating with the pulmonary artery, and an inner end communicates with the blood storage cavity (A). This device can assist the cavopulmonary circulation of the single ventricle, realize repeated blood drawing and pumping actions, provide the required power for the pulmonary circulation of the patient, and restore the biventricular blood flow in the human body; and because the arrangement of the inflow tube in the power cavity, the internal structure of this device is more compact, the overall shape is smaller, and the energy of the power cavity can be fully utilized.

The present disclosure describes a surgical system for a valve in an aorta. The surgical system is configured to serve as a temporary valve and/or filter to facilitate maintenance of proper blood flow while also capturing debris of an excised leaflet as needed.

The present disclosure describes a surgical system for a valve in an aorta. The surgical system is configured to serve as a temporary valve and/or filter to facilitate maintenance of proper blood flow while also capturing debris of an excised leaflet as needed.

Apparatus and methods for driving a circulatory assist device with motive power from a fluid motor. In one example a parallel plate Tesla-type of motor extracts power from the circulatory system of a biological unit to drive a non-positive displacement pump and increase blood pressure in the biological unit.

An autologous perfusion fluid collection reservoir basin includes a basin body configured to receive an extracorporeal organ and blood and includes a sloped bottom. The sloped bottom is configured to channel fluid toward an outlet port. The autologous perfusion fluid collection reservoir basin also includes a connector that extends from the outlet port. The connector is configured to connect to tubing of a cardiopulmonary bypass system or to enable direct connection to a cardiopulmonary bypass system.