An assembly for attachment to a gastrostomy feeding tube is provided. The assembly comprises a valve connector and an anchor. The valve connector comprises a housing, a conduit traversing the housing from an inlet to an outlet; and a retaining element extending outwardly from the housing. The anchor comprises an anchor housing configured to receive a portion of the valve connector. The anchor housing has a gastrostomy feeding tube attachment feature for attaching the anchor to the feeding tube, and a valve connector retaining feature that defines a retaining space, wherein the retaining space receives the retaining element of the valve connector and is sized to enable rotation of the retaining element and the valve connector relative to the anchor such that the conduit of the valve connector maintains fluid connection with the gastrostomy feeding tube during rotation. Additional assemblies and systems are also provided for other medical devices.

An assembly for attachment to a gastrostomy feeding tube is provided. The assembly comprises a valve connector and an anchor. The valve connector comprises a housing, a conduit traversing the housing from an inlet to an outlet; and a retaining element extending outwardly from the housing. The anchor comprises an anchor housing configured to receive a portion of the valve connector. The anchor housing has a gastrostomy feeding tube attachment feature for attaching the anchor to the feeding tube, and a valve connector retaining feature that defines a retaining space, wherein the retaining space receives the retaining element of the valve connector and is sized to enable rotation of the retaining element and the valve connector relative to the anchor such that the conduit of the valve connector maintains fluid connection with the gastrostomy feeding tube during rotation. Additional assemblies and systems are also provided for other medical devices.

Described are systems and methods for administration of nitric oxide (NO) with use of left ventricular assists devices (LVADs), as well as systems and methods for monitoring the NO delivery devices and/or the LVAD.

An attachment mechanism between a controller for an implantable blood pump and a battery housing. The attachment mechanism includes a latch moveably coupled to the controller. The latch includes a pawl configured to engage the battery housing. The latch is configured to only pivot when the battery housing is engaged to the pawl during attachment of the battery housing to the controller.

Methods and devices for tying management of an implantable medical device to the activities of a primary care physician are described, including access control, simplified parameter optimization, support for tuning a device in response to the effects of other treatments in parallel, and support for helping a primary physician and a patient work together to tune device configuration to the activity and performance needs of the patient. In some embodiments, a medical device is self-configuring in a device parameter domain, based on inputs provided in a patient performance domain. The self-configuring of the medical device is based, for example, on an automatically applied transformation of inputs derived from patient performance domain observations into changes in the configuration of the medical device which affect technical parameters of its operation.

A catheter apparatus can include a first magnet coupled to a catheter and a second magnet configured to couple to a patient's skin. When the catheter and the first magnet are positioned within a patient's body, the second magnet can exert a magnetic force on the first magnet that stabilizes the catheter relative to the second magnet. The second magnet can be directly attached to the patient's skin or secondary devices such as straps can be used to place the second magnet in a fixed position relative to the patient's body. In some implementations, a plurality of magnets can facilitate holding the catheter in a substantially fixed position within the patient.

Devices, systems and methods for controlling or preventing left and/or right ventricular overload with and without concurrent extracorporeal life support.

A multiple lumen device for percutaneous left ventricular unloading during venoarterial extracorporeal membrane oxygenation comprising: an expandable cage, an outer catheter, and an inner catheter, wherein a proximal end of the expandable cage is attached to the outer catheter and a distal end of the expandable cage is attached to the inner catheter, such that when the proximal end of the inner catheter is retracted, the cage moves from a compressed configuration to an expanded configuration is described. Also provided are methods for causing the blood of a subject to flow in a retrograde manner using a multiple lumen device.

Methods and devices for tying management of an implantable medical device to the activities of a primary care physician are described, including access control, simplified parameter optimization, support for tuning a device in response to the effects of other treatments in parallel, and support for helping a primary physician and a patient work together to tune device configuration to the activity and performance needs of the patient. In some embodiments, a medical device is self-configuring in a device parameter domain, based on inputs provided in a patient performance domain. The self-configuring of the medical device is based, for example, on an automatically applied transformation of inputs derived from patient performance domain observations into changes in the configuration of the medical device which affect technical parameters of its operation.

This document relates to materials and methods for circulatory bypass of a ventricle in the heart of a mammal. For example, materials and methods for bypassing a permanently or temporarily impaired left ventricle in the heart of a mammal (e.g., a human) are provided.