Abstract: A deflectable catheter shaft section is disclosed comprising an elongated body extending along a longitudinal axis and comprising a distal end and a proximal end; and a plurality of lumens extending along the longitudinal axis of the elongated body, wherein at least one of the lumens is abutting at least another one of the lumens. A catheter comprising the deflectable catheter shaft section and a method of manufacturing the deflectable catheter shaft section are also disclosed. A catheter incorporating a deflectable catheter shaft section can further comprise first and second compression coils disposed over pull wires located within the catheter, wherein the compression coils are unattached to the catheter or components thereof, but can be constrained by a shaft coupler at a distal end of each of the compression coils and by at least a portion of a handle assembly at a proximal end of each of the compression coils.

Abstract: A medical connector includes a body having a distal end, a proximal end, and a sidewall extending between the distal end and the proximal end, a helical thread extending radially outward from a surface of the sidewall and comprising a crest portion, flank portions, and a root portion with the flank portions connecting the crest portion to the root portion, and at least one deformable protrusion extending radially outward from the root portion of the helical thread.

Abstract: A pump cassette includes fluid lumen adapted for passage of an infusion fluid toward a patient. A rotary valve assembly can be actuated to regulate fluid flow through the fluid lumen and a frame is coupled to the fluid lumen and the valve assembly. The frame is adapted to be inserted into a seat of a pump device, wherein the frame provides a platen relative to the fluid lumen. The frame is configured to be inserted into the seat only when aligned in a predetermined orientation relative to the seat.

Abstract: Occlusions in a delivery line of an infusion pump can be detected by measuring pressure differentials in the pump over short periods of time in order to minimize the effects of long term systematic sensor changes. In a delivery mode such as basal insulin delivery where a small portion of a volume of fluid is delivered, pressure readings can be obtained before and after the motor move to deliver each portion and compared. The differentials after one or more motor moves can be compared to determine whether an occlusion is present. In a delivery mode such as bolus insulin delivery in which an entire volume of fluid is delivered, pressure differentials can be obtained for consecutive deliveries at a common point in the delivery cycle of each delivery. Comparison of these pressure values can be used to determine whether an occlusion is present.

Abstract: An object is to provide a syringe that is capable of preventing a cap from being mounted to a syringe body at an oblique angle. The cap includes an elastic cylindrical body for receiving an injection needle therein and sealing a holding part, and an external cylindrical body for covering the circumference of the elastic cylindrical body and holding the elastic cylindrical body in such a manner as to prevent movement of the elastic cylindrical body. The external cylindrical body includes an opening part having a dimension configured to be larger than the holding part of the syringe body, and a guide part that guides the injection needle toward a certain direction by coming into contact with a part of the syringe body when the injection needle is received inside the elastic cylindrical body.

Abstract: Disclosed is a nozzle device and a minimally invasive injection device, and the nozzle device for a minimally invasive injection device according to an exemplary embodiment includes an outlet to generate a microjet of a liquid, and an injection part of a micro-scale size connected to the outlet and adapted to be inserted into a skin tissue to a preset depth.

Abstract: An implantable medical system that comprises a gas unit for supplying gas that is essentially oxygen and at least one functional cells unit configured to receive oxygen from the gas unit so as to maintain the cells in a viable condition. The cells unit is flexible. Several embodiments are disclosed.

Abstract: A retractable self-destructing safety syringe with pre-attached needle including a barrel, an inner needle base disposed in a barrel neck at an end of the barrel body, and an elastic engagement mechanism formed between the barrel neck and the inner needle base is provided. An asymmetric elastic locking member having an elastic function is disposed at the end of the plunger, with which a sleeve-type retractable locking member on the needle base can be interlocked by the elastic function. After being retracted into the barrel body, the needle base together with the needle will be forced to deflect to one side under an asymmetric force, and the needle therefore will be forced to incline in a direction nearly a 45 degree angle toward to one side of the inner wall of the barrel and is blocked by the barrel neck, so that the needle and the needle base could not be pushed out the barrel neck again and self-destruction of the syringe is truly achieved.

Abstract: A system for injecting a fluid medicament into a patient includes a drive mechanism, and a cassette loaded with a pre-filled hypodermic syringe. When the cassette is loaded, the syringe is held firmly inside and the cassette can be selectively engaged with the drive mechanism. The drive mechanism has two motors. A first motor initially moves the hypodermic syringe from a position inside the cassette where its needle is concealed, to a position where the needle extends from the cassette for insertion into a patient for an injection. With the needle inserted, a second motor pushes the syringe stopper to expel a fluid medicament from the syringe. After an injection, the first motor withdraws the syringe back into concealment inside the cassette, to again firmly hold the syringe on the cassette. The cassette and syringe, in combination, can then be removed from the drive mechanism and discarded.

Abstract: A breast pump system includes a vacuum break backflow preventer for preventing breast milk from accidentally backflowing into a suction tube leading to a vacuum pump. The backflow preventer is a vacuum passageway with two spaced apart suction openings. The two openings convey air to cyclically pressurize and depressurize a small milk charging chamber. If milk accidentally covers one of the openings, air at the other opening minimizes the pressure differential that might otherwise draw the milk deep into the suction tube and toward the vacuum pump. For ease of cleaning and sanitizing, the system avoids or minimizes the use of baffles, permanently enclosed passageways, moving parts, and tight inside corners. Some passageways can be split open for access during cleaning. To make the breast milk collection device less protruding under a brassier, the vacuum passageway curves around the side of a nipple receptacle rather than in front of it.

Abstract: A medical connector includes a body having a distal end, a proximal end, and a sidewall extending between the distal end and the proximal end. The medical connector further includes a helical thread extending radially outward from a surface of the sidewall and at least one protrusion extending radially outward from a surface of the sidewall. The at least one protrusion has a first side and a second side. A radial height of the at least one protrusion from the surface of the sidewall tapers circumferentially from the first side of the at least one protrusion to the second side of the at least one protrusion.

Abstract: A perfusion catheter system comprises a main line, a first branch line having a tip at a distal end thereof, and a second branch line having a tip at a distal end thereof. The tip of the first branch line is heavier than the tip of the second branch line. The tip of the first branch line may be weighted. There may be a self-inflating balloon at the tip of the first branch line. There may be a self-inflating balloon at the tip of the second branch line. There may be a clamp disposed along the second branch line. The clamp may include a base, a clamping arm hingedly connected to the base, and an aperture extending through the base. The second branch line may extend through the aperture in the base.

Abstract: A method of bariatric embolization includes deploying an intravascular pressure modulating device at a target location, operating the pressure modulating device to reduce pressure within the fundus, and infusing an embolizing agent into the fundus. Use of the pressure modulating device prevents delivery of the embolizing agent into proximal and distal non-target vessels. The method takes advantage of unique flow and pressure dynamics of the arterial vessels in the stomach.

Abstract: The invention relates to a dispense interface comprising a body comprising at least a first channel structure and a second channel structure, wherein each of the at least two channel structures comprises at least a first inlet channel comprising a first inlet opening and a second inlet channel comprising a second inlet opening, wherein each of the at least two inlet openings of one channel structure is configured for fluid communication with a respective reservoir of at least two reservoirs and wherein at least one connecting channel configured for a fluid communication between at least one outlet opening and one of the at least two channel structures is provided.

Abstract: A pre-assembled kit for administering ischemic postconditioning comprising a catheter and a handle having a fluid circuit to control and modulate flow of inflation fluid to and from a balloon wherein the catheter is free from additional assembly and preparation procedures such that it is ready-to-use within a variety of vessel sizes.

Abstract: A medical personal-services suction handle includes a hand-graspable housing and a primary suction pathway disposed through the hand-graspable housing and having a suction line port at one end and an intake port at an opposing end thereof. An on/off valve disposed at least partially within the primary suction pathway has a user-manipulable interface by which the on/off valve selectively opens the primary suction pathway and occludes the primary suction pathway. A user-engageable pneumatic pathway serves, when selectively engaged, to pneumatically couple the primary suction pathway to a secondary external port in the hand-graspable housing such that suction is applied via the primary suction pathway to both the intake port and the secondary external port. By one approach the secondary external port comprises a thumb-control port.

Abstract: A desiccation device for operation on a target tissue includes a handle, a shaft extending distally from the handle, and a head. The shaft defines a lumen therethrough, and the head has a loop configuration supported on a distal end of the shaft. The head is hollow and defines a lumen therethrough. The lumen is in fluid communication with the lumen of the shaft. At least a portion of the head is electrically connected to a source of electrosurgical energy. A fluid is circulatable through the lumen of the shaft and the head.

Abstract: Methods and apparatus provide a therapeutic fluid to devices implanted in the body, for example to containers of devices implanted in the eye of a patient. The methods and apparatus may comprise an injector to increase an amount of therapeutic agent injected into the device implanted in the eye, or a structure to receive the therapeutic fluid within the device implanted in the eye, or combinations thereof. The device implanted in the eye may comprise a reservoir chamber having a fluid with a density different than the therapeutic fluid, and the apparatus can be adapted to at least partially separate the implanted device fluid from therapeutic fluid within the reservoir chamber to increase and amount of therapeutic fluid placed in the reservoir chamber.

Abstract: A device for self-administration of fractional amounts of a total volume dose of liquid medicament supplied from a capsule over a period of time for delivery to the sublingual area of a patient. The device contains an inner chamber and a track within which confines a moveable ball. The space between the chamber wall and track permits liquid medication from the capsule to flow past the ball and be available for discharge through an exit port when the ball is not seated upon the exit port.

Abstract: A medical valve transitions between an open mode that permits fluid flow, and a closed mode that prevents fluid flow. To that end, the medical valve has a housing with an inlet and an outlet, a rigid member movably mounted within the housing, and a resilient member with a sealing portion. The housing also has at least one relief zone that is in fluid communication with the outlet when the valve is in the closed mode. The rigid member may have a proximal end, a distal end, and a flow channel. The relief zone may be radially outward from the sealing portion. The sealing portion may seal the valve and prevent fluid from passing through the valve when in the closed mode.