Systems, methods, and devices for securing a driveline to a portion of skin are disclosed herein. The driveline can connect an external controller to an implantable blood pump. The skin anchor can include a driveline capture portion. The driveline capture portion can receive the driveline and fix a position of the driveline with respect to the driveline capture portion. The driveline capture portion includes: a driveline receiver that can receive the driveline; and a driveline anchor that can engage the driveline to fix the position of the driveline with respect to the driveline receiver. The skin anchor can include a force distribution portion. The force distribution portion can engage a portion of skin and fix a position of the portion of skin with respect to the force distribution portion.

The present invention generally relates to heart treatment systems. In some aspects, methods and systems are provided for facilitating communication between implanted devices. For example, an implantable cardiac rhythm management device may be configured to communicate with an implantable blood pump. The implantable cardiac rhythm management device may deliver heart stimulation rate information in addition to information associated with any detected abnormalities in heart function. In response, the pump may be configured to adjust pumping by the pump to better accommodate a patient's particular needs.

Systems and methods for controlling an implantable pump are provided. For example, the exemplary controller for controlling the implantable pump may only rely on the actuator's current measurement. The controller is robust to pressure and flow changes inside the pump head, and allows fast change of pump's operation point. For example, the controller includes, a two stage, nonlinear position observer module based on a reduced order model of the electromagnetic actuator. The controller includes an algorithm that estimates the position of the moving component of the implantable pump based on the actuator's current measurement and adjusts operation of the pump accordingly. Alternatively, the controller may rely on position measurements and/or velocity estimations.

Systems, assemblies, and related modules for connecting components of medical devices employ connector cables with electrical conductors and optical fibers. A connector assembly for coupling a battery module with a medical system including an implanted or worn medical device includes an input connector and an output connector. The input connector includes metal contact plates, has no moving parts, and is sealed to prevent water or dust ingression into the housing. The output connector includes metal pins to electrically couple to the metal plates of the input connector, a connector cable including electrical conductors coupled to the metal pins configured to transmit electrical power and an optical fiber configured to transmit data, and a latching mechanism disposed at an end of the output connector configured to physically attach the output connector to the housing. The cable body has a substantially flat cross-section.

HeartWare medical device bag cover kit comprises: (a) a three dimensional, generally rectangular-shape cover with a closing flap; a cover means a thing which lies around something, especially in order to protect or conceal it; right and left side opening/slit for driveline accessibility; (b) at least 3 magnetic fasteners; (c) a detachable cover for the carrying strap, which will be adjustable in length, therefore coincided with the existing medical grade strap, that is provided for the device; (d) a separate shoulder pad will also be included with a thicker padding and coordinating fabric(s).

All covering will be sold as a kit for the Lvad/Rvad device bag, including the adjustable strap cover that will give patients the freedom to determine the cosmetic appearance, without altering the function and safety of the device, as provided by the manufacturer.

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.

A patient adapter for connecting a driveline cable between an implantable blood pump and a controller. The patient adapter provides a sufficiently large form factor to make connecting ends of a driveline cable easy for patients who lack dexterity or have unclear vision. The patient adapter includes an adapter body that defines a central lumen that extends through an entire length of the adapter body. The central lumen is configured to receive an end of a percutaneous end connector of the driveline cable and an end of a controller end connector of the driveline cable. The patient adapter includes a first mating feature configured to engage a corresponding feature of the percutaneous end connector and a second mating feature configured to engage a corresponding feature of the controller end connector. A thickness of the adapter body is greatest at a position proximate the controller end connector.

A medical prosthesis includes a tube having a length between a first end and a second end. The tube includes a polymer and at least one drug. The tube is configured to be manipulated to selectively increase and decrease the length of the tube. Kits, systems and methods are disclosed.

An apparatus for starting operation of a motor of an implantable blood pump including a memory storing one or more default parameters for at least one of controlling and monitoring the startup operation. A processor operatively coupled to the motor is included, the processor is configured to: commence the startup operation based on the one or more default parameters; detect an error during the startup operation; adjust at least one of the one or more default parameters in response to the detected error; store the at least one adjusted parameter in the memory; and commence subsequent startup operations based at least in part on the at least one adjusted parameter.

A heart failure recovery device includes a fluid pump having an inlet and an outlet in fluid communication with a pump reservoir, and a pumping element disposed within the pump reservoir, the pumping element including a protrusion that in an active state is configured to rotate and move fluid away from the inlet and towards the outlet. A receiver coil can be electrically coupled to the fluid pump and is configured to subcutaneously absorb electromagnetic energy for powering the fluid pump. In certain embodiments, an implantable port provides fluid access to the pump reservoir for cleaning and maintaining the fluid pump. In other embodiments, a valve closes fluid access to at least one of the inlet and the outlet during periods when the device is not being used for treatment.