An automatic washer for continuous positive airway pressure equipment has a housing defining a wash chamber having an open face providing access to the wash chamber, a door selectively closing the open face, a dual eccentric nozzle protruding into the wash chamber, a rack slidingly receivable within the wash chamber, and a spray nozzle in the bottom surface of the wash chamber. The rack has a hose clamp oriented to secure an end of a CPAP hose when seated in the rack with an open end of the CPAP hose facing the dual eccentric nozzle. The dual eccentric nozzle has an air conduit that introduces air during a drying cycle and a water conduit that introduces water during a rinse cycle, and when the rack is fully inserted in the wash chamber, the dual eccentric nozzle is received inside the hose clamp, thereby, inside the CPAP hose when present.

A syringe pump to deliver heparin to into the blood circuit of a hemodialysis system. The syringe pump is configured to receive a syringe having a plunger movable within a lumen of an elongate tubular member. The syringe pump may include a housing having a recess configured to receive at least a portion of the syringe, a drive mechanism for moving the plunger within the lumen, the drive mechanism comprising a motor and a lead screw; and a grabber mechanism. The grabber mechanism includes a control arm, back panel, and upper and lower control fingers, the control fingers each have first and second ends, and a curved portion therebetween having a width, an interior edge, and an exterior edge, wherein the first ends of the upper and lower control fingers are coupled to the control arm via first and second spring hinges.

An information collection method for an injection pen includes several steps as follows. The action of the pressing knob is sensed to determine whether the rotation information of the pressing knob is obtained. The traveling movement of the injection pen is sensed to determine whether the movement information of the injection pen is obtained. A determination is made that the traveling movement of the injection pen is conformed as an intending injection action according to the rotation information of the pressing knob and the movement information of the injection pen. When the traveling movement of the injection pen is conformed as the intending injection action, an actual injection dose that the injection content is pushed outwards from the injection pen is calculated according to the rotation information of the pressing knob. The actual injection dose is recorded.

Percutaneous access sheaths used to provide access to the vasculature and heart for the introduction of percutaneous ventricular assist devices (pVADs), and to remain in place for the duration of pVAD use. The sheaths include actively closeable seals engageable to seal against the drive lines of the pVADs to minimize blood loss during pVAD use.

The present invention discloses a sterile PRP separation kit that has compartmentalized container having a cover that allows for a stage-specific exposure of sterile components of the sterile PRP separation kit housed within stage-specific compartments to a non-sterile environment commensurate with a specific stage of operation of a separation process of PRP. The sterile PRP separation kit includes a PRP tube with segregated portals for injection of blood into the PRP tube, aspiration of PRP from the PRP tube, and for maintaining an interior pressure of the PRP tube at equilibrium with ambient pressure during both injection and aspiration.

A system and method for extracting a pVAD device that is implanted with a distal portion in an aorta of the heart and a drive line extending across an inter-atrial septum and out of the body via a superior vessel of the venous vasculature, include a first device that is introduced into a femoral artery and through the descending aorta used to engage a distal part of the pVAD device in the aorta of a patient using an instrument. A second, cutter, device is introduced into the venous vasculature superior to heart, advanced to a position adjacent the inter-atrial septum, and used to cut the pVAD drive line adjacent to the inter-atrial septum. After cutting, a first portion of the pVAD is withdrawn from the body via the venous vasculature, and a second portion is withdrawn from the body via the femoral artery.

This disclosure relates to a system and method for disinfecting a conduit, such as a conduit for use in a continuous positive airway pressure (CPAP) system. An example system according to this disclosure includes a sheath a probe magnetically suspended within the sheath. The probe includes an ultraviolet light source configured to emit ultraviolet light. Further, the probe is spaced-apart from an inner dimension of the sheath to allow a conduit to pass between the probe and the sheath.

A dispenser actuator assembly (100) for actuating a dispenser (10) is disclosed. The dispenser (10) is in the form of a glass ampoule assembly (10) having a rupturable glass ampoule (12) containing a flowable material (M). The glass ampoule (12) is contained within an outer container (14) wherein the outer container (14) has a first open end (22) and a second closed end (24). The glass ampoule assembly (10) has an applicator (16) positioned in the first open end (22). The dispenser actuator assembly (100) has a base member (102) configured to mount on the outer container (14). The dispenser actuator assembly (100) also has an actuator assembly (104) operably connected to the base member (102) wherein the actuator assembly (104) has a first actuator arm (132a) and a second actuator arm (132b) each pivotally connected to the base member (102). The first actuator arm (132a) and the second actuator arm (132b) extend from the base member (102) in generally opposed relation defining a first position, or neutral position. The first actuator arm (132a) has a first protrusion (150a) depending therefrom and the second actuator arm (132b) has a second protrusion (150b) depending therefrom. The first actuator arm (132a) and the second actuator arm (132b) are pivotable from the first position towards one another to a second position, or actuating position, that is configured such that the first protrusion (150a) engages the outer container (14) and the second protrusion (150b) engages the outer container (14) to crush the glass ampoule (12) wherein the flowable material (M) is configured to be dispensed from the glass ampoule assembly (10).

Some embodiments relate to a method for providing, during a single inhalation from an inhaler, a controllable ratio between at least a first active substance and a second active substance provided from the same source material, comprising: defining a ratio between the first and second active substances to be delivered to a user; setting operation parameters in accordance with the ratio, the operation parameters including at least one of a heating profile of the source material and an airflow profile through the source material; and operating the inhaler according to the operation parameters to deliver to the user, during a single inhalation, at least the first and second active substances at the defined ratio.

A method for using a universal electronic toolset for indicating and adjusting of an implantable programmable bodily fluid drainage valve regardless of whether the valve includes a fixed reference magnet used to determine an angle of orientation of the implantable programmable bodily fluid drainage valve or not. A magnetic field detection sensor array in an indicator tool of the electronic toolset determines whether the fixed reference magnet is present in the implantable programmable bodily fluid drainage valve. If the presence of the fixed reference magnet is detected then the center and direction of flow of the adjustable valve unit is ascertained via electronic feedback from the electronic toolset; otherwise, the center and direction flow is ascertained via exclusively by manual physical palpation of the valve.