Abstract: A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

Abstract: A system and method to configure a rule set used in connection with a medical monitoring system for monitoring patients and patient care equipment, especially medication delivery pumps, based on a variety of conditions and parameters associated with monitored biometric information and equipment information and for providing user-defined responses to those conditions and parameters.

Abstract: This invention relates to a more effective and comfortable method of treatment for problems such as hemorrhoids, vulvo-vaginitis, or post op, which the problems are commonly both internal and external and using the medication internally may not be effective for the external problems. Thus the applicant has introduced new methods of the application of the medicine to these areas in his previous applications and now he adds some more models and methods for reaching these goals easier. The new means consists of a pad means with use of a medication providing units such as a suppository, in which the pad means, prevents contamination of the underwear. Also he introduces suppository units made from a polymer and a method which allows the application of medications to the suppository and pads easy.

Abstract: System and components for inducing pleurodesis or other sclerosis or desired adhesion conditions to treat a patient, while minimizing likelihood of tissue damage from direct application of sclerosis-enhancing materials. A tube device is provided that is configured to elute sclerosis-enhancing material and/or other medicaments including autologous or otherwise patient compatible blood and/or blood component(s) via an assembly including fenestrated drainage tube which may be a multi-lumen assembly allowing simultaneous infusion/elution and drainage. The assembly of tube device with outer (typically drainage) tube may include one or more features configured to enhance delivery of medicament and/or drainage through the same assembly.

Abstract: An adaptive dosing system having a control module, a flow sensor unidirectionally connected to the control module for reporting a volume of a fluid passed through the system, a pump for dosing a required volume of the fluid and being uni-directionally connected to and controlled by the control module and a communication module bi-directionally connected with the control module, the communication module being configured to connect via Internet with an application server and a database server.

Abstract: An injection device includes a housing containing a cartridge containing a medicament and a movable bung. The housing includes an inner thread. The injection device includes a piston rod for moving the bung during dose dispensing. The piston rod includes an outer thread engaging the inner thread of the housing a bearing at its end facing the bung. The injection device further includes a driver coupled to the piston rod for driving the piston rod during dose dispensing. In the unused delivery state of the device, the bearing abuts the bung. The invention further refers to an assembly method for such an injection device.

Abstract: An inflatable balloon includes a base balloon having a cylindrical section and a conical section and at least one circumferential fiber extending circumferentially around the conical section. The inflatable balloon includes a plurality of reinforcing strips in the conical section over the at least one circumferential fiber. Each reinforcing strip includes a plurality of fibers extending at an angle relative to the at least one fiber. Each reinforcing strip is positioned a set circumferential distance away from a neighboring reinforcing strip.

Abstract: A medical device includes an elongate body having a proximal end and a deflectable distal region, a handle coupled to the proximal end, an actuator movable relative to the handle, and a resistance assembly adjacent the actuator. The resistance assembly exerts a force on the actuator that varies according to a direction in which the actuator is moving relative to the handle. For example, the resistance assembly can exert a lower (or zero) force when the actuator is moving relative to the handle in a direction that effects deflection of the distal region of the elongate body from neutral and higher when the actuator is moving relative to the handle in a direction that effects return of the distal region of the elongate body towards neutral. The resistance assembly can also include materials that exhibit anisotropic frictional properties and/or have surface finishes or treatments that yield directionally-dependent frictional forces.

Abstract: The dressing has a pad for adhesive securement to a patient that includes a bubble for covering over a housing of a Huber needle assembly embedded in the patient. A slit is formed in the pad to allow passage of the tubing of the Huber needle assembly. In one embodiment, an insert of foam material is provided in the bubble to rigidify the bubble. A second section may also be provided for folding over the pad to encase the tubing, catheter and clamp of the Huber needle assembly.

Abstract: The disclosed device, systems and methods relate to a novel catheter, system and methods. The various catheter implementations are for use in cardiopulmonary resuscitation and other medical or surgical conditions that require emergency restoration of cerebral and cardiac blood supply. The catheter or catheters have one or more lumens and balloons. Two catheters connected to a control unit can be disposed within the body to occlude and perfuse a region of the circulatory system.

Abstract: The present disclosure provides a plasma catheter including a tubular member; a conductive cylindrical member; a first electrode; and a second electrode. The tubular member defines a longitudinal lumen therethrough and has a proximal portion and a distal portion. The conductive cylindrical member is disposed at the distal portion of the tubular member. The first electrode is embedded in a first side of the tubular member and coupled to the conductive cylindrical member. The second electrode is embedded in a second side of the tubular member diametrically opposed to the first side. The second electrode is offset from the tubular member and aligned with a center axis defined by the conductive cylindrical member.

Abstract: A sub-epidermal electric warning device has electrodes penetrating through the patient's epidermis and bipolar electric warning signals are transmitted to the sub-epidermal tissue by these electrodes. A device for surveillance of vital signs, analyte levels, or treatment parameters is using a sub-epidermal electric warning device for notifying the patient in situations requiring intervention.

Abstract: Systems and methods are described herein for guided injection, which include: one or more controllable light-emitting elements configured to emit non-destructive light and a computing device operably connected to the one or more controllable light-emitting elements configured to emit non-destructive light, the computing device including a processor operable to receive at least one digital representation of a body region of an individual, the body region of the individual including one or more physical registration landmarks, the at least one digital representation including one or more digitally registered injection sites and one or more digital registration landmarks corresponding to the one or more physical registration landmarks on the body region; and control the one or more controllable light-emitting elements to illuminate a location of a surface of the body region of the individual corresponding in location to at least one of the one or more digitally registered injection sites.

Abstract: The invention relates to a liquid storage and delivery system including a reusable housing (8) comprising a control and drive unit, a container (2), a pump module (4) fluidically connected to the container (2), and a coupling system (6) configured for removably coupling the pump module (4) to the control and drive unit (6). The pump module comprises a pump engine (20), a pump outlet (22), and a transmission input coupling (18) coupled to the pump engine (20). The housing comprising the control and drive unit also comprises a pump drive (34) configured to engage the transmission input coupling (18) of the pump module (4) when the pump module (4) is coupled to the housing comprising the control and drive unit. The container (2) is in the form of a flexible pouch and the pump module (4) is permanently integrated with the flexible pouch and forms therewith a disposable unit.

Abstract: Drug delivery device adapted to receive a cartridge, comprising a drive tube with an inner thread, a motor assembly comprising a drive shaft and being adapted to be received inside the drive tube, a drive member attached to the drive shaft and with an outer thread in engagement with the drive tube inner thread. The drive tube is arranged axially displaceable but non-rotational relative to the motor assembly, whereby rotation of the drive member results in axial, non-rotational displacement of the drive tube. To provide flexibility the drive shaft is connected to the drive member via a first flexible joint, and the motor assembly proximal portion is connected to a support structure via a second flexible joint.

Abstract: A flush syringe assembly comprises a barrel including a cylindrical side wall having an inside surface defining a chamber for retaining fluid, an open proximal end and a distal end having a passageway therethrough in fluid communication with the chamber. A plunger including an elongate body portion having a stopper at its distal end is provided. The stopper is slidably positioned in fluid-tight engagement with the inside surface of the barrel for driving fluid out of the chamber through the passageway. The stopper includes a distal portion and a proximal portion separated by a spring element and configured to compress when fluid is being driven through the passageway by motion of the plunger and to continue to drive fluid through the passageway after motion of the plunger has stopped.

Abstract: Provided is a flexible and conformal wearable, self-contained medical device. The medical device comprises an integral housing formed by a flexible upper portion and a flexible lower portion joined along their perimeters. The medical device is also provided in a plurality of shapes and configurations for increasing the flexibility and conformability of the housing. The components contained within the housing, such as a drug reservoir, printed circuit board, and power supply are preferably constructed from flexible materials and are formed, connected and positioned according to the configuration of the housing in a manner for enhancing flexibility of the housing. A thermal bubble micropump is provided for controlling flow of a drug from the flexible reservoir, that utilizes a thermal resistor provided locally to a thermal expansion fluid that causes a surrounding membrane to expand and displace a volume of drug to be provided to the user.

Abstract: Methods and devices are provided for inhibiting nerves when activating brown adipose tissue (BAT). In general, a first nerve type (e.g., sympathetic nerves) innervating BAT can be activated while at least one other nerve type (e.g., parasympathetic nerves and/or sensory nerves) innervating BAT is being suppressed. A first neuromodulator (e.g., an electrical signal, a chemical, a light, cooling, etc.) can be applied to activate the first nerve type, and a second neuromodulator can be applied to inhibit the at least one other nerve type. In this way, parasympathetic nerves and/or sensory nerves innervating BAT can be inhibited when activating sympathetic nerves innervating BAT.

Abstract: A pump and pump controller which uses an algorithm to quickly achieve and maintain a set pressure in a surgical site when high resistance hardware is being used is provided. The algorithm uses a gravity control type loop and uses pressure loss calculations to quickly respond to changing joint conditions. A method of using such a pump and pump controller is also provided.

Abstract: Apparatus and methods for performing cryogenic ablation of tissue and adjusting the size and/or location of a cryogenic cooling region. A cooling assembly may include tubes for dispensing and exhausting a coolant or refrigerant. One or both of the tubes may be moved, e.g., slidably adjusted, in order to adjust the location or size of a cryogenic ablation region. The cooling assembly may be integrated into cryogenic ablation devices including a cryogenic balloon device that includes an inner inflatable balloon and another balloon that is at least partially wrapped around the inner balloon and carries refrigerant for performing cryo-ablation. Electrodes permit electrical mapping of tissue before or after cryo-ablation to verify success of the procedure.