An apparatus for coupling a blood pump to a patients heart is provided. The apparatus includes a sewing ring designed to be sutured to the patients heart, wherein the sewing ring has an opening sized and shaped to receive an inflow cannula of the blood pump. The apparatus further includes a locking element coupled to a housing of the blood pump and transitionable between a closed state and an open state. The locking element is structured to receive the sewing ring in the open state and engage the sewing ring in the closed state to prevent translational and rotational movement of the locking element relative to the sewing ring. In addition, the apparatus includes a biased structure designed to bias the locking element in the closed state.

Systems and related methods for supplying power to an implantable blood pump are provided. A system includes a base module and a plurality of energy storage devices. A first energy storage device is operatively coupled to the base module. A second energy storage device is operatively coupled to the first modular energy storage device. The energy storage devices are mechanically coupled in series, electrically coupled in parallel, and configured to provide redundant sources of power to drive an implantable blood pump.

An implantable blood pump system is disclosed herein. The implantable blood pump system includes an implantable blood pump and a controller coupled to the blood pump. The controller includes a partially sealed housing defining an internal volume. The controller includes an energy storage component contained within the internal volume and a processor. The processor can generate one or several signals affecting operation of the implantable blood pump. The controller includes a connector receptacle including a plurality of contacts selectively coupled via a circuitry to the energy storage component. The circuitry can electrically couple the plurality of contacts to the energy storage component when a connector insert is received within the connector receptacle and deactivate the plurality of contacts from the energy storage component when the connector insert is not within the connector receptacle.

A medical devices and methods related thereto are disclosed. In an embodiment, the medical device including a pump configured to be inserted within an atrium of a heart, said pump comprising an inlet and an outlet. In addition, the pump includes a flexible outflow conduit coupled to the outlet and configured to carry blood. The outflow conduit includes a radially inner surface defining a throughbore, and a radially outer surface. Further, the pump comprises a driveline configured to conduct control and power signals between the pump and an external device. The driveline extends through the outflow conduit between the radially inner surface and the radially outer surface.

A catheter pump is disclosed herein. The catheter pump can include a catheter assembly that comprises a drive shaft and an impeller coupled to a distal end of the drive shaft. A driven assembly can be coupled to a proximal end of the drive shaft within a driven assembly housing. The catheter pump can also include a drive system that comprises a motor and a drive magnet coupled to an output shaft of the motor. The drive system can include a drive assembly housing having at least one magnet therein. Further, a securement device can be configured to prevent disengagement of the driven assembly housing from the drive assembly housing during operation of the pump.

The invention relates to a blood pump. The blood pump comprises a flexible drive shaft (3) guided in a catheter, a conveying element (6) connected to the drive shaft (3) in a distal region of the drive shaft (3), and a motor (7), wherein the motor (7) has a stator (36) and a rotor (30) mounted such that it can move in the stator (36). The stator (36) comprises a winding (37) and the rotor (30) comprises a rotor magnet (31). In addition, the drive shaft (3) is connected to the rotor (30) at a proximal end of the drive shaft (3). The stator (36) and the rotor (30) are nondetachably connected to one another, and form a gap (40) with a ring-shaped cross-section, which is delimited by the rotor (30) and the stator (36).

The invention relates to a fluid pump or rotary cutter having at least one first element (9″″, 10′″) which can be brought from a transport state into an operating state by changing at least one mechanical property. Such a pump can, for example, be a blood pump for the medical, microinvasive area. The object of achieving a transition between the transport state and the operating state which is as comfortable as possible and in so doing leaving a freedom in the design of the corresponding apparatus, in particular of a pump, which is as large as possible, is achieved using the means of the invention in that the first element at least partly comprises a material (24, 25, 26, 27) or can be filled with a material or material mixture which passes through a chemical reaction, in particular cross-linking, or a crystallization for transition into the operating state.

A blood oxygenator is disclosed comprising a housing, a blood inlet, a blood outlet, a spiral volute, a gas inlet, an oxygenator fiber bundle, and a gas outlet. The housing encloses the fiber bundle and provides the structure for the blood flow path and connectors. The fiber bundle comprises gas-exchange membranes which transfer oxygen to the blood and remove carbon dioxide when the blood flows across the membranes. The spiral volute guides the blood to flow through the fiber bundle. A gas flow chamber receives sweep gas containing oxygen and distributes the sweep gas into the fiber membranes, which gas is then exchanged with the blood being oxygenated.

The present invention provides an intravascular blood pump comprising a housing region that may be expandable and collapsible, wherein the expandable housing region includes the inlet to the pump and wherein the distal diameter of the expandable housing region, including the inlet, is larger than a proximal diameter of the expandable housing region. A non-expandable region may be provided and disposed between the expandable housing region and the pump assembly of the intravascular blood pump.

The invention relates to a method for determining a total fluid volume flow (1) in the region of an implanted vascular support system (2), comprising the following steps: a) determining a reference temperature (3) of the fluid, b) determining a motor temperature (4) of an electric motor (5) of the support system (2), c) determining the thermal dissipation loss (6) of the electric motor (5), d) ascertaining the total fluid volume flow (1) using the reference temperature (3), the motor temperature (4), and the thermal dissipation loss (6) of the electric motor (5).