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 vital-signs patch in a patient monitoring system is disclosed. The patch includes a housing configured to be attached to the skin of a patient, the housing containing a radio that can selectably transmit and receive on more than one frequency and a processor. The processor configures the radio to transmit and receive on a determined frequency based at least in part on the level of noise detected on the frequencies.

Abstract: A double cylinder system is disclosed, comprising at least one controller being adapted to transmit hydraulic control signals; at least one slave being in fluid communication with the controller and being configured to respond to the hydraulic control signals transmitted by the controller; and at least one control line providing hydraulic communication between the controller and the slave. Also disclosed is a surgical device, comprising at least one controller located at a proximal end of the device, the controller being adapted to transmit hydraulic control signals; at least one manipulator, the manipulator being configured to be controlled by a human hand and to actuate the controller; at least one slave located at a distal end of the device, the slave being in fluid communication with the controller and being configured to respond to the hydraulic control signals transmitted by the controller; and at least one control line providing hydraulic communication between the controller and the slave.

Abstract: A disinfecting and pre-opening device is disclosed for use with a female needleless connector. The disinfecting and pre-opening device includes a housing comprising a chamber having a distal opening and configured to fit over the female needleless connector, and an elongated finger attached to the housing and disposed within the chamber such that the elongated finger opens the fluid path through the female needleless connector when the distal opening of the disinfecting and pre-opening device is placed proximally adjacent to the septum and the disinfecting and pre-opening device is advanced in the distal direction.

Abstract: A matrix infusion cassette for use with an intravenous (IV) pump is disclosed. The matrix infusion cassette includes a body configured to attach to the IV pump, the body having one or more inlet ports, an outlet port, and a plurality of pumping chambers, and a plurality of fluid conduits connecting the inlet ports to at least one pumping chamber, interconnecting the pumping chambers, and connecting at least one pumping chamber to the outlet port.

Abstract: The invention relates to a method for determining the temporal position of a wave packet (31) in a flow measuring apparatus, and to a flow measuring apparatus. The method includes the sampling of the wave packet at a plurality of points in time, wherein a measured value is created at each point in time. Subsequently, a sum of products (43, 54, 55, 63, 64) is calculated, wherein each product is calculated for a determined point in time from a plurality of points in time and each product is the product of a value of a compare function (44, 53, 56, 61, 62) at the determined point in time and the measured value at the determined point in time. Finally, the temporal position of the wave packet is calculated from the sum of products.

Abstract: Provided is a universal interface adapted for providing continuous positive airway pressure to a patient when the interface is used with a standard ventilator. The interface is configured to operate at a supply pressure no greater than about 120 centimeters of H2O in order to deliver pressure to the patient of up to about 15 cm of H2O at a flow rate of up to about 12 liters/minute. The universal interface may comprise an interface body having a space pair of breathing passageways intersecting a corresponding of supply passageways. Each one of the breathing passageways is comprised of a patient passageway and an exhalation passageway. Each one of the supply passageways includes a jet venturi having a taper portion. Each one of the exhalation passageways includes a taper portion which tapers outwardly along a direction from the patient passageway toward the exhalation passageway.

Abstract: A respiratory therapy device including a housing and an interrupter valve assembly. The housing is sized for handling by a patient and defines a patient breathing passage extending from a patient end and through which a patient inhales and exhales air. The interrupter valve assembly is carried by the housing and includes a control port, a valve body, and a drive mechanism. Expiratory airflow is released from the patient breathing passage through the control port. The valve body is sized to at least partially obstruct fluid flow through the control port. The drive mechanism moves the valve body relative to the control port in response to the expiratory airflow such that the valve body repeatedly transitions between a position of maximum obstruction and a position of minimum obstruction relative to the control port to create an oscillatory positive expiratory pressure effect.

Abstract: A latching mechanism is particularly suited for use in latching a slide mechanism, such as used to slidably mount a drawer. The latching mechanism includes a latch assembly comprising a latch lever mounted for movement between a first, second and third positions, a latch tab for selective engagement with a second end of the latch lever, and a piezo electric controller. The controller has a plunger configured to selectively control the movement of the latch lever between the first and second positions, the plunger movable between an extended position corresponding to a first, locked position of the latch lever and a retracted position corresponding to the second, unlocked position of the latch lever, the controller when unpowered preventing the plunger from moving from the extended to the retracted position and the controller when powered permitting the plunger to move from the extended to the retracted position.

Abstract: Systems and methods of measuring pressure of fluid in a disposable IV set connected to a fluid supply pump is disclosed. At least one sensing arrangement coupled to the fluid supply pump is provided. A chamber having a movable element is provided, the movable element configured to move in response to changes in fluid pressure within the disposable IV set and thereby cause a change in a sensed measurement variable associated with the sensing arrangement without contacting the sensing arrangement. A measuring signal indicative of the sensed measurement variable is generated. The fluid pressure within the disposable IV set is determined based on the measuring signal.

Abstract: A biopsy device is disclosed that includes a housing maintaining a stylet and a cannula. A control device is operably coupled to operate the stylet and the cannula. A handle operates to modify the device from a loading configuration with an expanded profile to a delivery configuration with a reduced profile.

Abstract: A drawer assembly that includes a cartridge, a drawer configured to receive the cartridge, and a docking connector attached to the drawer. The cartridge includes a body having a plurality of bins, a plurality of lids that are moveably attached to the body and releasably secured over the bins, and a connector attached to the body. The cartridge is configured such that the lids cannot be opened unless a signal is received through the connector. The docking connector is configured to mate with the connector of the cartridge when the cartridge is received in the drawer.

Abstract: A cartridge for use in a dispensing system is disclosed. The cartridge includes a body having an exterior and a plurality of bins. A plurality of lids are movably attached to the body and are configured to cover a bin. A release mechanism is movable along an axis. A plurality of latches are movably attached to the body. Each latch is configured to secure the respective lid when in a first position and to release the respective lid when in a second position. The release mechanism will not cause a latch to move to the second position when the release mechanism is moving along the axis in a first direction. The release mechanism will cause a single latch to move to the second position while leaving the remaining latches in the first position when the release mechanism is moving along the axis in a second direction.

Abstract: A device for holding an IV tube in a pumping apparatus and for selectively occluding the tube when the door of the pumping apparatus is opened, to prevent free flow of fluid in the tube. A flange provided on a sliding clamp is designed to prevent inadvertent finger slippage causing pushing of a tab positioned in the sliding direction from the flange, resulting in undesirable fluid leakage. The flange is made slip-resistant using a textured surface, having a concave shape, or having an angled top portion to prevent finger slippage or having a concave setback to guide a finger when pushing the sliding clamp.

Abstract: An intravenous fluid pump (IV) contains a disposable part including a fluid chamber having a resilient top membrane and a non-disposable part including a piston abutting a resilient membrane and a vacuum chamber fitted on top of the resilient top membrane. An external pump is used to create vacuum in the vacuum chamber, resulting in the resilient top membrane being held taut. The flow rate through the pump is relatively independent of changes in the pressure of IV fluid on the upstream and the downstream due to changes in the relative elevation of the fluid reservoir and the patient with respect to the fluid pump.

Abstract: A pump having a disposable fluid contacting portion which defines a fluid inlet and outlet and a fluid path there between. The pump includes a drive portion configured to engage the disposable portion to cause fluid to be moved from the fluid inlet to the fluid outlet. The disposable portion is configured to be selectively coupled to the drive portion. The disposable portion includes a driven membrane which forms a portion of the fluid path, and the drive portion includes a drive membrane. The two membranes are vacuum coupled to each other, whereby movement of the drive membrane causes the driven membrane to move, causing fluid to be pumped through the disposable portion. The pump has particular utility in the medical field for moving fluid from a source to a patient. The pump may include features such as an air-trap, bubble detection, fluid flow controls, and pressure detection.

Abstract: Described herein are embodiments of systems and methods for providing an automated medication handling system that can, among other things, single-dose package medications, store and dispense medications in a pharmacy, transport medications to a nursing unit or other remote location, store them at that remote location, and load them into a portable unit carried by a nurse, who may dispense the medication at a bedside.

Abstract: The concentration of air or other agents in a fluid delivery line is determined by monitoring agent signals and processing those agent signals along with information regarding the age of each agent signal. The processor determines a primary agent concentration value based on the received agent signal values, with the primary agent concentration value determined by giving greater weight to more recent agent signal values. Where the primary agent concentration value exceeds a primary threshold value, an alarm signal may be activated. The processor also may determine a secondary agent concentration value, which may be determined from the actual agent signal values instead of the weighted agent signal values. Where the secondary agent concentration value exceeds a secondary threshold value, an alarm signal may be activated.

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.

Abstract: A gas blender with auxiliary mixed gas outlet for mixing a primary gas, generally air, and a secondary gas, generally oxygen, to obtain a mixed gas having several controlled characteristics. The gas blender may be incorporated into a Continuous Positive Airway Pressure (CPAP) device. The gas blender controls the mixing to produce the mixed gas having a predetermined mixture setpoint, generally an oxygen percentage, and a predetermined control setpoint, generally a pressure setpoint or flow rate setpoint. The gas blender provides an auxiliary mixed gas source for use by an auxiliary piece of equipment such as a nebulizer or resuscitation bag. The gas blender includes a primary gas inlet passageway, a secondary gas inlet passageway, a gas mixing apparatus, a mixed gas distribution passageway with an auxiliary mixed gas outlet, a gas sensor, a delivery sensor, a mixed gas delivery control valve, a mixed gas controlled passageway, and a controller.