The present technology relates to vascular access devices, systems, and methods configured to monitor a patient's health. In some embodiments, the vascular access device may include a sensing element, and the system of the present technology may be configured to obtain physiological measurements of the patient via the sensing element, determine at least one physiological parameter based on the physiological measurement, compare the at least one physiological parameter to a predetermined threshold, and, based on the comparison, provide an indication of the patient's health.

A surgical port includes a first end, a second end opposite the first end, and a longitudinal axis extending through the first end and the second end. An outer sidewall extends between the first end and the second end. First and second channels extend through the port from the first end to the second end. A first electrically conductive portion extends from the first channel to the outer sidewall, and a second electrically conductive portion extends from the second channel to the outer sidewall. The first electrically conductive portion provides a first electrically conductive path between the first channel and the outer sidewall and the second electrically conductive portion provides a second electrically conductive path the second channel and the outer sidewall. The second electrically conductive path is separate from the first electrically conductive path. Devices and methods relate to surgical ports.

A mechanical circulatory support system includes an implantable blood pump, an implantable prosthetic rib assembly, and an implantable drive cable. The prosthetic rib assembly includes a prosthetic rib segment and a percutaneous electrical connector mounted to the prosthetic rib segment. The prosthetic rib segment is configured to be mounted to a patient's rib in place of a resected segment of the patient's rib. The electrical connector includes a skin interface portion configured to interface with an edge of a skin aperture through the patient's skin. The electrical connector is configured to expose a connection port of the electrical connector via the skin aperture. The implantable power cable is connected with or configured to be connected with each of the blood pump and the percutaneous electrical connector for transferring electric power received by the percutaneous electrical connector to the blood pump.

A percutaneous lead assembly for an active implantable device, the lead assembly comprising a sheath with a plurality of wires extending from a proximal end to a distal end. The wires being adapted to power the active implantable device; the distal end having at least one electrode fixed thereon. The electrodes being in communication with sensor electronics and wherein at least one electrode is on the outer layer of the lead assembly in which the electrode is used to detect at least one of acceleration and electrical signals of an organ.

The invention relates to a device A for monitoring a vessel opening for an extracorporeal blood treatment device B with an extracorporeal blood circulation (I), which has an arterial blood line (20) with an arterial cannula (19) and a venous blood line (21) with a venous cannula (22). Moreover, the invention relates to an arrangement with a device A for monitoring a vessel opening and an extracorporeal blood treatment device B, and a method for monitoring a vessel opening during an extracorporeal blood treatment. The monitoring device A comprises a sensor (1) for detecting at least one physical variable, which is characteristic for the state of the vessel opening, and an evaluation apparatus (7), connected to the sensor (1) by way of a connection cable (6), for producing signals characteristic for the state of the vessel opening. The evaluation apparatus (7) has a data transmission unit (38) for establishing a wireless connection between the evaluation apparatus (7) and the blood treatment device B. The evaluation apparatus (7) is distinguished by a control unit (39) configured in such a way that an interruption in the wireless connection between the evaluation apparatus (7) and the blood treatment device B is identified, for example if the patient were to lie on the evaluation apparatus (7). Moreover, the monitoring device A has a signal unit (40), which has a vibration transducer (40A) which causes the housing (8) of the evaluation apparatus (7) to vibrate when the wireless connection is interrupted.

A surgical port assembly for use with surgical instruments includes a body including an exterior surface and an interior space defined by an interior surface of the body. The surgical port assembly includes a control interface including a plurality of drive members coupled to the body and controllable to apply a force to a different portion of a shaft of an surgical instrument, when the shaft is disposed within the interior space, to move a distal portion of the surgical instrument to a desired position within a body cavity.

An electrical connector clamp for attaching to a distal end of a wire of a Central Venous Access Device (CVAD) including a first plate having a first side, a second side, a first edge, and a second edge. A second plate also is included having a third side, a fourth side, a third edge, and a fourth edge, wherein the first edge and the third edge are connected by a hinge that enables the first and second plates to pivot relative to each other, and the hinge enables the first side and the third side to come in contact. A latch holds the first side of the first plate against the third side of the second plate in a closed position. An electrically conductive material is on the first side of the first plate, and an electrical connector is on the second side of the first plate that is electrically connected to the electrically conductive material on the first side of the first plate. The first and third sides are to be pivoted together in the closed position around a wire to provide an electrical connection between the wire and the electrical connector.

A surgical port includes an end face comprising a channel extending through the end face, the channel having a cross section shaped to receive a surgical instrument cannula, and a lateral wall extending around a perimeter of the end face, the lateral wall and end face enclosing an open volume. An end portion of a wound retractor is received in the open volume of the surgical port and in engagement with an inner surface of the lateral wall, and the surgical port is configured to abut a body wall in an inserted position of the wound retractor through the body wall.

Implantable devices and associated devices, systems, and methods are disclosed herein. The devices and systems of the present technology may be equipped with electronic components that provide a platform for remote patient and/or device monitoring. Operation of an implantable devices and/or one or more components thereof can be modulated over time depending on certain conditions. This modulation can include limiting wireless data communication with external devices to certain time intervals, varying parameters of data collection by sensing elements, and/or controlling power supplied to electronic components, for example. In some examples, an implantable device may operate in a low-power standby state in which data is obtained via sensing elements and stored in local data storage, but the data is not wirelessly transmitted to an external device until a modulation signal is received by the implantable device, causing the implantable device to change to a more active power state.

A medicine delivery and tracking system includes a medicine injection pen and a delivery port. The pen includes a needle through which medicine is dispensed and an electronic unit configured to at least one of log dispensing of medicine from the pen, control dispensing of medicine from the pen, or communicate regarding dispensing of medicine from the pen. Alternatively, the electronic unit may be part of a separate computing device. The delivery port is configured for attachment to a user and to receive the needle of the pen such that medicine dispensed from the pen is dispensed into the delivery port and through the delivery port to the user. The delivery port includes a detector mechanism configured to detect a presence of the pen and, in response thereto, to communicate a signal to the electronic unit for use in the at least one of logging, controlling, or communicating.