Abstract: An assembly structured for concurrent irrigation and aspiration of a nasal cavity including a housing having a supply container disposed therein for the removable retention of irrigating fluid. A nasal applicator comprises first and second passages respectfully structured to deliver irrigating fluid to the nasal cavity and concurrently remove waste fluid therefrom. An activating assembly includes a plunger biased into a continuous pressure applying, dispensing relation to the irrigating fluid and a valve assembly is selectively disposable into an open position facilitating fluid communication between the supply container and the applicator for the delivery of the irrigating fluid therethrough into the nasal cavity. The activating assembly is further structured to create a negative pressure within the chamber which communicates with the second passage of the applicator to facilitate delivery of the waste fluid therefrom along a path of travel to an interior of the chamber.

Abstract: A laparoscopic port assembly includes a cannula unit including three cannulas each extending at an acute angle relative to a base. The cannulas are flexible for receiving respective angulated laparoscopic instruments. The cannula unit is rotatingly received in a port holder for rotation about a longitudinal axis of the holder, the holder being disposable in an opening in a patient's skin.

Abstract: A device for applying medical fluid to an area and for cutting within the area is provided. The device includes an inlet port, a fluid flow channel, an outlet and a blade. The inlet port is configured for receiving the medical fluid into the device. The fluid flow channel is configured for the fluid to flow through the device. A first end of the fluid flow channel is connected to the inlet port. An outlet is configured for the fluid to come out of the device. The outlet is positioned at a second end of the fluid flow channel. The blade is configured for cutting within the area.

Abstract: In an elongated casing, an active agent container connected to an injection needle can be shifted axially by a spring force. Auto-injectors which are sold or distributed filled and with the springs tensed have to be provided with a needle protecting cap to ensure the sterility of the injection needle. When such a needle protecting cap is removed as preparation for using the auto-injector, a tensile force can be exerted on the active agent container. Therefore, the active agent container comprising the injection needle must be prevented from being undesirably pulled forwards. At least one latching tongue prevents the active agent container from being prematurely shifted with respect to the casing, by abutting a flange arranged on a sliding sleeve which accommodates the active agent container. When the auto-injector is placed onto a person's skin, a needle protecting tube is shifted into the casing, forcing the latching tongue away from the flange and, thus, freeing the travel path for needle movement.

Abstract: An apparatus, method and program product detects an occlusion in a fluid line by determining if a relationship between force measurements departs from an expected relationship.

Abstract: Injection devices for delivering pharmaceutical compositions into the eye are described. Some devices include a resistance component for controllably deploying an injection needle through the eye wall. The resistance component may be disposed on a removable injector attachment or on a portion of the injection device housing. Other devices may include a filter for the removal of air, infectious agents, and/or other particulate matter from the composition before the composition is injected into the eye. Related methods and systems comprising the devices are also described.

Abstract: Devices for delivering pharmaceutical formulations into the eye are described. The devices may be integrated to include features that allow safe and atraumatic manipulation of the devices with one hand. For example, accurate placement, including proper angulation, of the device on the eye and injection of a pharmaceutical formulation into the eye can be performed using one hand. The devices may also include improved safety features. For example, the devices may include an actuation mechanism that controls the rate and depth of injection into the eye. Some devices include a dynamic resistance component capable of adjusting the amount of pressure applied to the eye surface. Related methods and systems comprising the devices are also described.

Abstract: A balloon catheter comprises a shaft having a proximal end and a distal end. An inflatable member is disposed adjacent the distal end of the shaft. The inflatable member has an inner inflatable member and an outer inflatable member disposed around the inner inflatable member. The inflatable members have different compliant properties.

Abstract: The present invention inter-alia relates to an apparatus comprising a diaphragm valve, wherein a diaphragm of said diaphragm valve is made from a substantially rigid material, having at least partially an flexible cross-sectional shape.

Abstract: An electrosurgical instrument that reduces the amount of fatigue experienced by a physician performing electrosurgery includes a hand piece with a utility conduit connected to the hand piece. The utility conduit can include an electrical cable and a smoke/fluid evacuation hose. The location at which the utility conduit exits the hand piece is selectively adjustable to reduce the resistance to the movement of the electrosurgical instrument created by the weight of the utility conduit. An electrosurgical instrument may also include an extendable shaft that allows for selective adjustment of the reach of the operational capabilities of the instrument.

Abstract: A tissue removal device includes a cannula that can aspirate tissue, and a thermal element located at a tip of the cannula that can apply localized heat to the tissue to be aspirated. The tissue removal device may also include a device for applying a vacuum in the cannula, which may be configured for applying vacuum pulses according to a controlled pulse rate and vacuum level. The tissue removal device may also include a device for applying the heat at the tip according to a controllable pulse rate and power level.

Abstract: The present invention relates to a method for determining start timing of supply of drug to be given in which a peripheral circulatory function and an autonomic nervous function are activated through a stimulus applied to a stimulus application origin part of a body surface by an acupuncture needle or warm heating etc., and a drug conveyance system according to the method for determining start timing of supply of drug.

Abstract: A balloon cover is provided to enhance the performance of a medical balloon, the cover, in accordance with an embodiment, having overlapping portions and opposed apertures located at apexes of tapered ends of the balloon cover. A method of making balloon covers is also disclosed.

Abstract: Tools for determining and adjusting the setting of an adjustable valve are disclosed. These tools allow a medical professional to locate and non-invasively determine the setting of an implanted valve. After the valve has been located and the setting of the valve determined, the valve may be re-adjusted non-invasively. There are three tools: a locator tool, an indicator tool and an adjustment tool. The locator tool allows the physician to locate the adjustable valve of interest and align the locator tool with a specific orientation of the valve. The indicator tool indicates the current setting of the adjustable valve and confirms new settings of the valve after the new settings have been implemented. The adjustment tool interacts magnetically with the implanted adjustable valve to couple with a movable internal element to change the setting of the valve. The indicator tool and the adjustment tool physically cooperate with the locator tool to accomplish the respective functions of the tools.

Abstract: An injection device (100) including a body (108, 332) for containing and dispensing a medicament, the body (108, 332) having a plurality of dosage indicator windows (120, 124; 336, 340, 344) for indicating a desired dosage of medicament, and a dose set sleeve (192, 326, 352) rotatably connected with the body (108, 332) for setting the desired dosage, the dose set sleeve (192, 326, 352) having a plurality of dosage numbers (196, 348) disposed thereon. Upon rotating the dose set sleeve (192, 326, 352) to set the desired dosage, the dosage numbers (196, 348) are consecutively visible through alternating ones of the plurality of dosage indicator windows (120, 124; 336, 340, 344).

Abstract: An injection site for tubular medical connectors, includes a perforable body inserted in a seat of a connector delimited by an annular wall having a retention edge turned in against the outer end of the perforable body. The outer end is formed with a peripheral annular step and with an exposed portion with reduced cross section projecting axially. The peripheral step is defined by an annular groove having a shape complementary to that of the turned-in retention edge of the connector, and the portion with reduced cross section of the perforable body connects up to the groove through an annular surface projecting radially above at least part of the turned-in retention edge and resting against it.

Abstract: A system of catheter devices and methods for forming channels or passageways between a luminal anatomical structure (e.g., a blood vessel) and a target location (e.g., another blood vessel, an organ, a mass of tissue, etc.) for the purpose of rerouting blood flow or for delivering a substance or instrument, etc. to the target location.

Abstract: A catheter shaft including a metallic tubular member including a plurality of apertures formed in the tubular wall of the metallic tubular member to provide a desired degree of flexibility to the metallic tubular member. The metallic tubular member includes a tapered region intermediate a region and a second, reduced diameter region relative to the first region.

Abstract: Infusion systems and methods for infusing one or more drugs or other agents into the body of a human or animal subject. The system is programmed to take remedial action(s) upon sensing of a fault or error in connection with the infusion. In some embodiments, an agent may be infused through redundant flowpaths and, if a fault occurs in one flowpath, the system may respond by increasing flowrate through other non-faulting flowpath(s). In some embodiments, the fault may be a physiological reaction or symptom in the subject and the system may respond by adjusting or stopping flowrate(s) or one or more agents or changing the ratio of simultaneously infused agents.

Abstract: The present invention discloses an anti-free flow mechanism for a finger-type peristaltic infusion pump (DDS) and methods for avoiding anti-free-flow. The mechanism comprises: a passive mechanical interface (MS) which integrally accommodates a portion of the flexible infusion tube, and an anti-free flow valve (AFFV) which is a spring-activated latch, which is incorporated within said MS. The maneuverable latch is secured in the MS either in CLOSED or OPEN configurations: in its CLOSED configuration no flow is provided, and in its OPEN configuration, a free flow is facilitated. Said anti-free flow mechanism is configured in a manner such that when the MS is not properly mounted in the DDS, said AFFV is automatically actuated via one or more integrated springs, to its CLOSED configuration. When the MS is properly mounted in the DDS, said latch is adapted to be automatically switched to the OPEN configuration.