Abstract: A therapy delivery device stores a plurality of time-dependent therapy settings. The therapy delivery device is configured to administer time-dependent therapies according to the time-dependent therapy settings based on a universal conception of time that is independent of a local time zone. A mobile device includes a display adapted to depict information about therapy or therapy-related data as compared to a local time that is stored on the mobile device based on a local time zone setting found in the mobile device. The therapy delivery device and a mobile application executing on the mobile device are configured to keep separate clocks, with each clock being based on a universal concept of time that is independent of a local time zone.

Abstract: A system for adjusting blood glucose level including an insulin delivery device configured to release insulin into the body of a person, and an EEG monitor having an EEG sensing part including EEG electrodes. The EEG monitor can be arranged in the ear region of the person with the EEG sensing part arranged subcutaneously at the scalp or arranged in the ear canal. The EEG monitor includes an EEG signal processor arranged at the ear and adapted for identifying onset of hypoglycemia. The system further includes a wireless link between the EEG monitor and the insulin delivery device. The EEG monitor is configured to submit a warning signal to the insulin delivery device if an upcoming onset of hypoglycemia is identified. The warning message will cause the insulin delivery device to restrict insulin delivery for a predetermined time, and a warning is provided to the person or to a caregiver.

Abstract: Several embodiments of a catheter are described, having a balloon configured to slowly inflate and then quickly deflate to create an area of low pressure in the vessels. The balloon can be cycled near the vessels of the kidneys, thereby helping to draw out blood from the kidneys and enhance fluid processing to the bladder.

Abstract: A medicine container for medicine substances which can be mixed with one another includes a container body, a stopper and a mixing element. The container body has a first end with a stopper opening and a second end with a base having an outlet. The stopper is displaceable between the ends. A mixing chamber for receiving the medicine substances is delimited by a portion of an inner casing surface of the container body, a side of the stopper and the base. The mixing element can be disposed in the mixing chamber. The medicine container is adapted to discharge the medicine substances from the medicine container by displacement of the stopper in the direction of the outlet. The stopper is adapted to receive the mixing element at least partially by a recess. The invention further relates to a method for operating such a medicine container.

Abstract: An after-use safety system for a syringe, including a barrel which defines a central axis along which it can move in translation and which includes a radial opening forming a guidance path for a pin, an immobiliser, which is arranged inside the barrel and which includes the pin interacting with the barrel, and a return spring configured to elastically load the barrel forwards with respect to the immobiliser, the immobiliser including a radial stopping means for immobilising the barrel along one axis radial to the central axis when the barrel is forced towards the rear after use of the syringe.

Abstract: A fluid delivery Y-site is described that is configured to receive and control delivery of two or more fluid flows. Fluid flow is controlled within a chamber by a valve and float. Flow of a primary fluid into the chamber is reduced or halted by the movement of a valve. The valve may occlude a first flow port into the chamber in response fluid flowing from a second flow port into the chamber. A float is moveably disposed within the chamber and configured to engage the valve in response a fluid flow into the chamber from the second flow port. As fluid flow from the second flow port into the chamber is reduced or ceases, the valve and float allow the flow from the primary flow port to once again enter the chamber and exit from an outlet port.

Abstract: Medical devices including vascular access kits and methods of using the kit are disclosed. In some embodiments, a conduit is measured using an outside diameter measurement apparatus to determine if the conduit is compatible with a connector such that there is a continual lumen between the conduit and the connector. In some embodiments, various outside diameter measurement devices and the methods of their use are disclosed. In some embodiments, the methods of connecting a conduit, and in some embodiments a strain relief structure, to a connector are described.

Abstract: A steerable sheath includes an elongate shaft, a handle, an actuator element on the handle, and a plurality of control wires operably coupled to the elongate shaft and the actuator element. Actuation of the actuator element adjusts a shape of a proximal curve and a distal curve on the elongate shaft.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of operating an infusion device capable of delivering fluid to a user involves determining a current amount of active fluid in the body of the user, determining a threshold amount of active fluid in the body of the user, and automatically altering operation of the infusion device to modify delivery of the fluid to the user based on a relationship between the current amount and the threshold amount.

Abstract: A needleless injector assembly can have a spring injector and an ampule. The spring injector can include a housing having a first housing portion and a second housing portion defining a bore and having a casing located in the bore and fixed relative to the first housing portion but the second housing portion can be rotatable relative to the casing. The casing can have a threaded receiving end at an end to threadedly receive a threaded end of an ampule. A pin having an end can project from the second housing portion and into an opening of the first housing portion and wherein the pin is retractable away from the first portion before the second housing portion is rotatable relative to the casing.

Abstract: The present invention relates to an intravenous infusion set providing delivery of intravenous fluid to patients. An intravenous infusion set (10) to administer continuous air free delivery of intravenous fluid to a patient, said intravenous infusion set (10) comprising: a drip chamber (12), a flexible infusion line (22) of sufficient length connecting a lower end (20) of the drip chamber (12) to a standard connector (24) at the patient end so that a needle or a catheter could be connected to the patient; a roller clamp (26) arranged between the drip chamber (12) and the standard connector (24) being movable along the length of the flexible infusion line (22), said drip chamber (12) provided with a spike (14) on the upper end (16) and a flow regulating and stopping member (18) at its lower end (20) configured to administer continuous air free delivery of intravenous fluid to patients.

Abstract: A method for facilitating milk extraction from a female breast may involve applying a breast contacting portion of a breast pump system to a breast, activating the breast pump system to administer multiple breast pumping cycles, and applying vibrations to the breast during at least a portion of each of the breast pumping cycles, using a vibration device. A vibration generating device may be a component of a breast pump system, an added attachment on a breast pump system or a separate component that works in conjunction with a breast pump system.

Abstract: A chest valve including: a housing including an inlet configured to connect to a chest tube, an outlet and a fluid passage from the inlet to the outlet; and a one-way valve within the housing and included in the flow passage, wherein the one-way valve includes: (i) a first tubular strip wherein having an internal air passage and a first layer defining the air passage, wherein the first layer has a first thickness and the internal air passage of the first tubular strip is included in fluid passage of the housing; and (ii) a second tubular strip wherein having a second layer with a second thickness with a second thickness greater than the first thickness, wherein an outer surface of the second tubular strip is adjacent and overlaps an outer surface of the first tubular strip.

Abstract: The technical problem of the present invention to provide a medical device, which exhibits an increased safety of the device and facilitates a safe use is solved by medical device for delivering at least one drug agent, comprising a sensor, a control unit and an attachable dispense assembly, wherein the sensor is configured to detect attachment of the dispense assembly to the medical device, wherein the control unit is configured to determine at least based on a signal from the sensor whether the end of life of the dispense assembly is reached and wherein the medical device is configured to indicate the end of life of the dispense assembly. The technical problem is further solved by a method according to the invention.

Abstract: A disclosed drip chamber for an intravenous (IV) therapy system includes a container configured to hold an IV fluid, a drop former suspended over the container, and an inlet port disposed above the drop former and configured to receive the IV fluid from a reservoir. The drop former has an upper end, a lower tip, and an outer surface extending between the upper end and the lower tip. The inlet port is coupled to the outer surface to permit the IV fluid to descend down the outer surface.

Abstract: The present invention relates to a catheter valve for use with a catheter. The catheter valve comprises an inlet nozzle at a front end of the valve and an outlet nozzle at a rear end of the valve. The valve comprises a longitudinal stem encapsulated within a middle section of the valve which extends in between the front end and the rear end of the valve.

Abstract: A fluid delivery system (1) includes a reservoir (7) for storing a fluid, a pumping chamber (8) and an actuator (20). The pumping chamber (8) has a volume, an inlet valve (48) providing selective fluid communication between the pumping chamber volume and the reservoir, an outlet valve (49), and a membrane (47) the displacement of which changes the pumping chamber volume. The actuator (20) moves a drive member (21) in reciprocating motion. The actuator (20) is disposed in a housing (9) having an aperture (36) from which the drive member projects. The reservoir (7) and the pumping chamber (8) are arranged in a cartridge (3) removably attachable to the housing. When the cartridge (3) is attached to the housing (9) the drive member (20) is operatively coupled to the pumping chamber membrane (47). The fluid delivery system may be applied to an infusion system for the infusion of a liquid therapeutic product, such as insulin.

Abstract: A balloon catheter which allows for faster preparation and effective purging of air. The catheter includes an elongated, flexible catheter having a tubular outer member and a tubular inner member each having a respective lumen. The inner member is at least partially disposed in the outer member lumen such that an outer surface of the inner member and an inner surface of the outer member together define an annular inflation lumen. The outer member has micropores or micro-holes configured such that when a contrast agent is injected into the inflation lumen, the micropores or micro-holes allow air to pass therethrough and thereafter become clogged by the contrast agent. The catheter also has a balloon member having its ends secured to and circumferentially around the outer member such that an inner surface of the balloon member and the outer surface of the outer member define an inflatable balloon interior.

Abstract: For treatment of a patient who has a lesion in each of left lower limb artery and right lower limb artery, lesions at both sides can be rather easily and completely treated. A catheter is introduced from an artery of an arm of the patient, and an atherectomy catheter is used for a lesion at one side and continuously used for a lesion at the other side without being extracted to the outside of a human body, and thus damage of an excision portion of the atherectomy catheter and an unexpected situation such as no passage through twisted blood vessels are avoided so that a burden on the patient can be reduced, the treatment can be completed within a short time, and cost reduction can be achieved by reducing the number of catheter to be used.

Abstract: A needleless connector includes a body having a fluid path, a vent path, and a male fitting. The needleless connector also includes a valve disposed within the male fitting. The valve is configured to move between a first configuration, in which the fluid path is blocked, and a second configuration, in which the fluid path is open. The needleless connector further includes a seal disposed around the valve. The seal is configured to separate the fluid path from the vent path in the first and second configurations. Moving the valve from the first configuration to the second configuration also opens the vent path. The seal maintains the separation between the fluid path and the vent path when the valve moves from the first configuration to the second configuration.