Abstract: A laparoscopic surgical device is provided, including a removable tool-comprising shaft having an outer shaft and an inner actuation rod that may be removably or permanently connected together. A handle of the device includes a two-button mechanism for engaging and releasing the removable tool-comprising shaft. The two-button mechanism is configured to engage overlapping corresponding apertures of the outer shaft and the inner rod that extends through the outer shaft, and the handle may include a variety of configurations that can readily interchangeably be used with different tool bodies.

Abstract: A medical device including an operation determiner for determining operations to be performed by the medical device in response to a gesture of the device with respect to the medical device, and an operation data accessor for accessing operation data for the operation performed by the medical device.

Abstract: An IV set is configured for coupling with a pump device. The IV set comprises a fluid lumen adapted for passage of an infusion fluid toward a patient. A frame is coupled to the fluid lumen and is adapted to be inserted into a seat of a pump device, wherein the frame provides a platen relative to the fluid lumen, wherein the frame is sized and shaped such that the frame can only be inserted into the pump device when aligned in a predetermined orientation relative to the pump device. An information device is adapted to store information associated with the IV set, wherein the information device is accessed in response to proper placement of the IV set in the pump device.

Abstract: A resuscitator has a patient airway interface device, a bag, a flow passage coupled between the bag and patient airway interface device, and a sensor assembly. The patient airway interface device may be a mask or an endotracheal tube. The sensor assembly has a display, at least one sensor coupled to the flow passage and configured to provide a measurement of at least one parameter, and a processor coupled to the display and the at least one sensor. The processor is configured to receive the measurement from the sensor and provide information on the display based on the received measurement. The information may include a current breath rate, a pressure-vs-time curve, and guidance to the user to assist in achieving a target breath rate.

Abstract: A patient warming device with patient access for maintaining normothermia and/or treating hypothermia is provided. The device includes a first compliant layer and a second compliant layer sealed together around an outer border to contain a liquid between the two layers and to form a wrap that surrounds and conforms to a body portion of a patient. A plurality of flaps extends from opposite sides of a generally longitudinal central portion of the wrap, such that one or more flaps from the opposite sides fasten to each other to surround the body portion. The flaps are openable during functional use to provide access to an underlying patient body surface. A continuous fluid flow path extends between the first compliant layer and the second compliant layer between a fluid inlet and a fluid outlet to carry liquid and deliver heat through the wrap.

Abstract: A compressive patient warming device is provided. The device includes an elastic inner layer that conforms snugly to a shape of an appendage of a patient so that the inner layer wraps around and substantially contacts most of an underlying surface area of the appendage. An outer layer is attached to and covers the inner layer to form a space that holds a heat transfer medium between the inner layer and the outer layer while the inner layer is wrapped around the appendage. The outer layer may be a rigid layer, and a predetermined compressive load may be applied to the outer layer to encourage blood flow in the appendage. A source of heat may be applied to the device to maintain normothermia and/or treat hypothermia.

Abstract: Provided is a high frequency oscillating ventilator comprising a housing assembly, a linear actuator, a linear coil, a piston mounted on a pushrod, a diaphragm dividing a housing into a first and second side and having an opening formed on the second side that is fluidly connected to the patient's airway for delivering gas thereto. The linear actuator is fixedly mounted to the housing assembly and has a linear coil coaxially disposed therewithin. A pushrod supports the linear coil on the linear actuator to allow relative axially sliding therebetween. The piston is directly mounted to the diaphragm such that reciprocation thereof as effectuated by the linear coil cooperating with the linear actuator alternately produces positive and negative pressure waves in the gas in the patient's airway.

Abstract: A medical device controller operating in conjunction with a medical device determines one or more current versions of executable code associated with one or more processors in a medical device. Medical devices may include infusion pumps, other patient treatment devices as well as vital signs monitors. The medical device controller determines one or more current versions of executable code and configuration information associated with the one or more processors in the medical device. The medical device controller further determines which of the processors in the medical device require updated executable code, and which of the processors in the medical device require updated configuration information. The medical device controller distributes to the medical device as required at least one of the updated executable code and the updated configuration information. The medical device deploys the distributed updates, and activates the updates at a clinically appropriate time.

Abstract: Systems and methods of monitoring the axillary temperature of a person are disclosed. A portion of a temperature probe is provided within the axilla of the person. The temperature probe includes a wiring portion and a body connection portion and a sensing portion between the wiring and body connection portions. The sensing portion comprises a temperature sensing element. The wiring portion is coupled to a monitoring device and comprises a conductor having a first end and a second end, the first end coupled to the temperature sensing element, and the second end connected to the monitoring device. At least a portion of the body connection portion is attached to a second body portion of the person, such that the sensing portion is retained within the axilla.

Abstract: A patient care system is configured for infusing fluid to a patient. The system includes a plurality of fluid infusion pumps, each of which is connected to a respective fluid supply for pumping the contents of a fluid supply to a patient via fluid supply lines. The system includes a pressure sensor downstream of the fluid infusion pumps for determining if a particular fluid is connected to a designated infusion pump.

Abstract: A base portion for a needleless valve system comprising a body, and a valve coupling feature disposed on the body. The valve coupling feature is configured for coupling to a base coupling feature of a valve of a first type and a base coupling feature of a valve of a second type.

Abstract: Processing methods are described for improving the physical properties of elastomeric materials including elastomeric tubing. The methods include heating tubing in a post-cured step for a specified time and at a specified temperature. The methods also include irradiating the tubing with a desired dose of radiation. Embodiments can include treatment of silicon-based elastomers and/or non-silicon-based elastomers. The improved elastomers can be utilized in pumps.

Abstract: A connector for transferring fluid and method therefore. The connector may have a first port, a second port, and a third port which may be coupled together at a main channel with a first valve element therein controlling fluid flow through the first port. The first valve element is supported by a valve element support positioned between the first port and the third port, and the second port joins the main channel to provide a fluid path around the first valve element and through the third port.

Abstract: A cannula device for removing, including by aspirating, bodily material is disclosed. The device may include a cannula and a hub. The cannula includes an open proximal end and a deflectable distal segment, and one or a plurality of distal orifices fluidly connected to the lumen. When distally extended from an outer guide cannula, the deflectable segment assumes a curved shape, which includes temperature-dependent curvature subject to elevated temperature along a memory metal length of the cannula.

Abstract: A method of filtering a touch screen input is disclosed that includes the steps of detecting a position of a first touch on a touch screen, determining a validation area that includes the position of the first touch, detecting a position for each of one or more second touches on the touch screen, and providing a touch event signal if the positions of all of the second touches are within the validation area.

Abstract: An infusion management platform can determine, based on one or more infusion events, whether to group infusions or segments of infusions. Related apparatus, systems, techniques and articles are also described.

Abstract: An IV manifold includes a plurality of injection/aspiration ports including a needleless access port (NAC). A check valve included in the manifold is generally located between injection ports. A two-way aspiration can be provided by the NAC having a single elongate valve element including a plug at one end. The elongate valve element has properties for resiliently and sealingly biasing the plug into an aperture of the NAC. In use, the plug is mechanically displaced by insertion of a male Luer for injection or aspiration.

Abstract: A valve is disclosed that has a body with an inlet, an outlet, and a needleless access port coupled to the body. The access port has an interior space and is configured to be actuated by a needleless connector. The inlet is selectively coupled to the outlet through the interior space such that fluid entering the inlet entirely flows through the interior space to the outlet.

Abstract: A bi-directional flow sensor may be adapted for reducing pneumatic noise during pressure sensing with a flow passing through the flow sensor. The flow sensor may include a hollow, tubular member having a throat section disposed between a ventilator end and a patient end. A flow restrictor may be disposed in the throat section and may be adapted to measure differential pressure in the flow. A baffle may be mounted at the ventilator end and may be adapted to minimize non-axial flow at pressure taps located on opposing ends of the flow restrictor. The patient end may include a flow obstruction configured to promote uniform velocity across the flow at the pressure taps during exhalation flow from the patient end to the ventilator end. The flow sensor can minimize pneumatic noise to less than 0.1 LPM to allow accurate patient flow measurement and triggering of inhalation and exhalation phases at flow rates of 0.2 LPM.

Abstract: A ventilator including an inspiration flow control unit and an expiration flow control unit coupled to the inspiration flow control unit. The ventilator also includes a nasal intermittent mandatory ventilation (NIMV) control system coupled to the inspiration flow control unit and the expiration flow control unit. The NIMV control system is configured to automatically and simultaneously adjust an inspiration flow and an expiration flow. A pressure of the inspiration flow is increased from a baseline pressure to a control pressure. A pressure of the expiration flow is returned to the baseline pressure.