Abstract: It is an object of the present invention to provide an attachment mechanism capable of being attached to a variety of solution sources. The attachment mechanism is uniquely configured to provide at least two different seals with a solution source. The attachment mechanism may also be used in a variety of applications.

Abstract: An infusion pump includes a housing. The housing includes a tube port adapted to receive an intravenous (“IV”) tube. The tube port includes a tube channel and a rib. The tube channel has an inlet and an outlet end. The rib is positioned along the channel adjacent the outlet end. The rib is formed to extend towards the tube when the tube is passed through the tube port thereby indenting the tube and tending to prevent full occlusion of the tube. The tube port may also include a plurality of ribs positioned around a perimeter of the tube port on the exterior side of the housing. The plurality of ribs are configured to prevent an occlusion in the tube when the tube is bent on the exterior side of the housing.

Abstract: The present disclosure is directed towards dosing unit for use in an ambulatory infusion system, the dosing unit including: a dosing cylinder and a piston arranged inside the dosing cylinder and in a sliding displaceable manner along a displacement axis. The piston is convertible form a storing configuration into an operational configuration, wherein a circumferential sealing member of the piston is mechanically relieved in the storing configuration and is in sealing and sliding engagement with a circumferential inner surface of the dosing cylinder in the operational configuration. The dosing unit includes a configuration switch member in operative mechanical coupling with the piston, the configuration switch member being movable relative to the piston from a storing position into an operational position, thereby switching the piston configuration from the storing configuration to the operational configuration.

Abstract: A sterile fluid pathway connector includes a piercing member, a connector hub, and a pierceable seal; wherein at least a portion of the pierceable seal is configured to move from a first position in which the piercing member is retained within a sterile cavity between the pierceable seal and the connector hub, to a second position in which the pierceable seal has been penetrated by the piercing member. A filter may be utilized to enclose the sterile cavity from the outside environment. Such fluid pathway connections may be integrated into a fluid container having a barrel and a plunger seal. The components of the fluid pathway connector may further be capable of transmitting a signal to the user upon completion of fluid delivery, for example, upon contact between the plunger seal and the pierceable seal. A fluid delivery pump includes such integrated fluid pathway connectors and fluid containers.

Abstract: Ambulatory infusion pumps, pump assemblies, and disposable assemblies, including cartridges, baseplates, cannulas, inserters, and related components therefor, as well as component combinations and related methods.

Abstract: Disclosed is a valve clutch that has a central member extending along a central axis and includes a drive coupler that receives a driving torque. A coupling member is provided that includes coupling pins extending parallel to the central axis. A valve is rotatably disposed around the central axis between inlet and outlet positions. A sleeve is configured to rotationally engage the valve, the sleeve including at least one clamping member. The valve clutch is reversibly changeable between (1) an unengaged configuration wherein a driving torque received by the central member is not transmitted to the sleeve member, and (2) an engaged configuration wherein the at least one coupling pin is clamped between the central member and the at least one clamping member, thereby transmitting the driving torque that is received by the central member via the sleeve member to the valve member.

Abstract: A method for performing a continuous infusion process using at least two infusion devices (1A, 1B) comprises the steps of: delivering a first fluid (M1) from a first medication container (100A) through a first delivery line (11A) at a first flow rate (F1) using a first infusion device (1A) in a first phase; and delivering a second fluid (M2) from a second medication container (100B) through a second delivery line (11B) at a second flow rate (F2) using a second infusion device (1B) in a second phase following the first phase.

Abstract: A device for administering fluid to a patient comprising: a fluid source for providing fluid, a patient end which is designed to connect to a patient, a continuous throughflow path connecting the fluid source and the patient end for continuously supplying fluid from the fluid source to the patient end, a bolus flow path connected to the fluid source and to the patient end and arranged in parallel to the continuous throughflow path for supplying the bolus dose of fluid, wherein the bolus flow path is provided with a bolus reservoir for storing the bolus dose and a manually adjustable throughflow contro, adjustable by an operating person, which is designed for manual adjustment of a flow rate, wherein the manually adjustable throughflow control is arranged in the bolus flow path parallel to the bolus reservoir.

Abstract: A system for modulating delivery of a fluid medium to a selected site within a patient's body includes a syringe for injecting the fluid medium, a delivery catheter including a conduit for delivering the fluid medium from outside of the body to the selected site within the body, and a flow diverter assembly disposed in a fluid medium flow path between the syringe and the delivery catheter. The syringe includes a chamber for receiving the fluid medium therein. The flow diverter assembly is configured to simultaneously divert at least some of the fluid medium within the chamber of the syringe away from the delivery of the medium through the delivery catheter conduit during injecting with the syringe, and wherein the flow diverter assembly creates increasing medium fluid flow resistance with increasing pressure level of the fluid medium within the flow diverter assembly. A method for modulating fluid delivery to a selected site within a patient's body is also disclosed.

Abstract: A fluid therapy method for an ADHF patient includes setting a urine output rate desired threshold, setting one or more desired negative net gain rates, and optionally setting a total fluid loss goal. The urine output of the patient is monitored and fluid is automatically administered to the patient at increasing rates to equal to or approximately match the patient's increasing urine output rates until the patient's urine output rate reaches the set urine output rate desired threshold. Thereafter, fluid is administered to the patient at rates to achieve the set desired negative net gain rate until the fluid loss goal is reached. Thereafter, until the end of therapy, fluid is administered to the patient at rates equal to or approximately equal to the monitored urine output rates.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary method involves operating an infusion device to deliver fluid to a user in accordance with a first operating mode of a plurality of operating modes, obtaining operational information pertaining to the first operating mode, and obtaining clinical information pertaining to the user. A destination operating mode of the plurality of operating modes is determined based at least in part on the operational information and the clinical information, and the infusion device is operated to deliver the fluid in accordance with the destination operating mode in a manner that is influenced by at least a portion of the operational information pertaining to the first operating mode.

Abstract: A treatment system configured to treat a condition using a first fluid, the treatment system including a first reservoir configured to store a first fluid, a cannula insertion mechanism configured to insert a cannula into a user, the cannula in fluid communication with the first reservoir, a first rotatable shaft member configured to pull a first plunger disposed within the first reservoir and coupled to the first rotatable shaft member by a first flexible member, and a drive mechanism having a first expandable member configured to move from a first position to a second position to rotate the first rotatable shaft member to deliver the first fluid to the user through the cannula.

Abstract: The present disclosure relates to the smart wear field. The smart wearable device comprises: a main body comprising a control unit and a biological feature parameter acquisition module, the biological feature parameter acquisition module is configured to acquire a monitored biological feature parameter of a user, and the control unit is configured to compare the monitored biological feature parameter and a pre-stored biological feature reference parameter so as to determine whether the user is in need of first aid according to the comparative result; a connecting part for putting on the smart wearable device on the body of the user; a power supply module for supplying power to the smart wearable device; and a first-aid processing module configured to give first aid to the user when it is determined according to the comparative result that the user is in need of first aid.

Abstract: An autoinjector having a body (1, 2), a reservoir (S) with piston, and a piston rod (5) movable between rest and injection positions. An actuator spring (6) urges the piston rod (5) towards its injection position. The autoinjector has a force-adjustment system (7, 8) exerting a force (F2) on the piston rod (5), adding to the force exerted by the spring (6) at the beginning of injection. Two pivot members (7) co-operate with the piston rod (5) and are connected together by two resilient elements (8). The body (1, 2) includes a sleeve (3), the pivot members (7) being pivotally mounted on the sleeve (3) to pivot about stationary pins (79). The autoinjector includes an end-of-injection indicator formed by and/or fastened to said sleeve (3) and includes an indication portion movable and/or deformable relative to the body (1, 2) to co-operate with a viewing window.

Abstract: An injector is provided for performing an injection operation comprising a housing (104), a needle extendable from a front end of the housing, a rear end of the housing and a longitudinal axis extending between the front end and the rear end, a safety pin (116) in an actuation locked position coupled to the housing and moveable to a safety released position coupled to the housing. The injector is locked against actuation when the safety pin is in the actuation locked position and the injector is ready for actuation of the injection operation when the safety pin is in the safety released position.

Abstract: The present invention relates to a medicament delivery device comprising a housing (16, 18), arranged to accommodate a medicament container(26); a power unit (64) arranged inside said housing, said power unit comprising a plunger rod (112), a drive spring (114) operably arranged to act on the plunger rod (112) and, which is, upon activation, operably arranged to act on said medicament container (26), an actuator (90) comprising holding elements (94, 100), capable of releasibly holding said plunger rod (1112) with said drive spring (114) in a tensioned state, and an actuator sleeve (76) operably connected to said actuator (90) for releasibly locking said holding elements (94, 100) in a holding state; said medicament delivery device further comprising a medicament delivery member guard (34) slidably movable in said housing (16, 18) and arranged to act on said actuator sleeve (76) for setting said holding elements (94, 100) with said actuator sleeve (76) in a first activation state; an activator unit (124) arran

Abstract: A cartridge (100) for packaging a medicament and being suitable for use with multiple different types of dosing device is described, together with dosing devices and adaptors for dosing devices. The cartridge includes a generally tubular body (102) having an interior cavity (104), a closure member (106) disposed at a distal end of the body and comprising a sealing element (128), a piston member (108) disposed in the cavity to contain the medicament between the piston member and the sealing element (128), a coupling element (114) disposed at the distal end of the body for coupling the cartridge to a dosing device (200) or to an adaptor for a dosing device, and a seal arrangement (126, 129) for receiving a sealing element release member (214) of the dosing device or adaptor.

Abstract: The disclosure relates to a drug delivery device, comprising: an outer needle sleeve; a cartridge containing a dosage of a medicament and sealed with a sealing element that is arranged across an open distal end of the cartridge; a cartridge carrier adapted to hold the cartridge; a needle hub adapted to hold a double ended hollow needle; an inner needle sleeve arranged between the needle hub and the cartridge carrier; a removable cap coupled to the inner needle sleeve and adapted to cover and seal the needle; and a first locking mechanism adapted to lock the inner needle sleeve against axial movement in the proximal direction with respect to the cartridge carrier in an initial state, wherein in the initial state, the needle is spaced from the cartridge in the distal direction, and wherein the first locking mechanism is releasable by a rotational movement of the cap with respect to the outer needle sleeve.

Abstract: The described technology relates to a needleless syringe for injecting an injection objective substance into an injection target area. The needleless syringe includes a protruding member which is provided movably from a first position to a second position at which 1) a protruding length of a forward end of the protruding member from an end surface of a housing is shorter than a protruding length of the forward end at the first position and 2) the forward end and a discharge port can be brought in contact with the injection target area. The needleless syringe also includes a maintaining mechanism which maintains the protruding member at the first position and a power source circuit which applies a voltage to a driving unit when the protruding member having been maintained at the first position is moved to the second position. Accordingly, the unintended discharge from the syringe is appropriately avoided.

Abstract: Systems and methods for integrating a continuous glucose sensor, including a receiver, a medicament delivery device, and optionally a single point glucose monitor are provided. Manual integrations provide for a physical association between the devices wherein a user (for example, patient or doctor) manually selects the amount, type, and/or time of delivery. Semi-automated integration of the devices includes integrations wherein an operable connection between the integrated components aids the user (for example, patient or doctor) in selecting, inputting, calculating, or validating the amount, type, or time of medicament delivery of glucose values, for example, by transmitting data to another component and thereby reducing the amount of user input required. Automated integration between the devices includes integrations wherein an operable connection between the integrated components provides for full control of the system without required user interaction.

Abstract: In one aspect, a safety pen needle assembly includes a hub having an open proximal end, a needle fixed to said hub, said needle having a distal end for insertion into a patient, and a proximal end extending into said open proximal end of said hub, a shield having a distal opening and an internal thread that is engaged to said hub so as to be manually movable relative to said hub to selectively expose said distal end of said needle via proximal movement of said shield and cover said distal end of said needle via distal movement of said shield, said shield having an open distal end, and a cap that seals the distal opening of the shield.

Abstract: The disclosure refers to a cap assembly for covering a needle shield of an injection device, the cap assembly comprising: a collar, and a cap with a sheath and a bottom, wherein the collar is movable along a longitudinal direction relative to the sheath from an unlocked position not engaging the sheath towards a locked position, force-lockingly engaging the sheath, thereby locking the sheath to the needle shield.

Abstract: A needle guard for protecting a human or animal from accidental contact with a needle connected to said needle guard is disclosed. The needle guard comprises a mounting base for the needle, a hinge structure connecting the mounting base to a needle shield, and a needle shield hinge adjacent to the hinge structure and needle shield. The hinge structure is adapted to pivot the needle shield relative to the mounting base from an open position in which the needle shield is separated from the needle, to a closed position in which the needle shield encloses the needle. The needle shield hinge is adapted to pivot the needle shield relative to the hinge structure. A method of manufacturing the needle guard is also disclosed.

Abstract: An optically induced injection device is provided. The optically induced injection device includes: an injection needle, a light generator providing light to an affected area, a first optical cable which is disposed in the injection needle and through which the light passes, and an injection unit disposed in the injection needle and providing an injection solution to the affected area while the light is provided to the affected area.

Abstract: A patch-sized fluid delivery device may include a reusable portion and a disposable portion. The disposable portion may include components that come into contact with the fluid, while the reusable portion may include only components that do not come into contact with the fluid. Redundant systems, such as redundant controllers, power sources, motor actuators, and alarms, may be provided. Alternatively or additionally, certain components can be multi-functional, such a microphones and loudspeakers that may be used for both acoustic volume sensing and for other functions and a coil that may be used as both an inductive coupler for a battery recharger and an antenna for a wireless transceiver. Various types of network interfaces may be provided in order to allow for remote control and monitoring of the device.

Abstract: A nasal administration device is disclosed which enables delivery of a well collimated stream of medication through the nasal orifice of a human being to the pharyngeal orifice of the eustachian tube. The device utilizes alignment tabs to properly position the collimated stream utilizing facial landmarks and an alignment arrow to confirm such alignment. Certain preferred embodiments of the disclosed device include adjustable alignment tabs enabling more precise alignment for a range of facial profiles.

Abstract: A brushless DC motor including a rotor, a magnet provided to the rotor, a pair of bearings to rotatably support the rotor, a stator assembly that at least partly surrounds the rotor and magnet thereof and adapted to control movement of the rotor, and a bearing tube having an exterior surface and an interior surface that defines a tube interior. The stator assembly is provided along the exterior surface of the tube and the bearings are provided along the interior surface of the tube to support the rotor and magnet within the tube interior. The motor has sample application for use in PAP devices for delivery of positive airway pressure therapy for users or patients.

Abstract: A therapeutic device for treating one or more conditions associated with a user's nasal cavities, sinuses, and/or ear canals. The therapeutic device includes a vibration generator that includes an acoustic device configured to provide a sound. The therapeutic device further includes a seal that may be applied to a nasal interface of the user, the nasal interface being located around the nose and/or mouth of the user. The therapeutic device further includes a housing that the user may hold and that is connected to the vibration generator and the seal. The sound may be applied to the nasal interface of the user when the seal is applied to the nasal interface of the user.

Abstract: A pressure support system includes a pressure generating system structured to generate a flow of breathing gas, a patient circuit including a patient interface device, the patient circuit being coupled to the pressure generating system and structured to carry the flow of breathing gas, a barometric pressure sensor coupled to the patient circuit within a gas flow path of the patient circuit, wherein the barometric pressure sensor is structured to generate a barometric pressure signal indicative of a barometric pressure within the gas flow path proximate the patient, and a control system. The control system is structured to control an outlet pressure of the pressure generating system based on at least the barometric pressure signal in a manner that compensates for a pressure drop across the patient circuit due to a pneumatic resistance of the patient circuit.

Abstract: A sleep mask valve structure for treating a patient suffering from obstructive sleep apnea is provided. The valve structure includes a rigid valve housing comprising an inspiratory valve and an adjustable expiratory valve. The housing defines an outside mask side and an intra-mask side, and further defines an expiratory airflow conduit accommodating airflow from the intra-mask side to the outside mask side and an inspiratory airflow conduit accommodating airflow from the outside mask side to the intra-mask side. The expiratory airflow conduit includes at least two changes of direction, with each direction change greater than or equal to 75 degrees and the inspiratory airflow conduit includes comprising at least one change of direction greater than or equal to 75 degrees. The two paths share at least one change of direction.

Abstract: A respiratory mask for providing positive pressure therapy and a bias-flow venting system configured to reduce discernable draft generated by exhausted air are disclosed herein. The respiratory mask has a ball jointed elbow, one or more detachable forehead pieces and a headgear with a spacer fabric region. The elbow is configured to be removable when oriented to a predetermined position. The forehead pieces are provided in one or more sizes. The spacer fabric region having two or more layers wherein the raw edges are turned to the inside of the layers. The seal having improved seal performance and accommodating a wider variety of facial geometries. The bias-flow system having a tube and exhaust holes radially aligned on a bead of the tube. The bias-flow system also having an annular component exhaust holes and a shroud having a plenum chamber around the exhaust holes.

Abstract: The ventilation interface for sleep apnea therapy interfaces a ventilation device to the patient's airways. The ventilation interface includes a pair of nasal inserts made from flexible, resilient silicone which are oval shaped in cross-section and slightly tapered from a base proximal the ventilation supply to the distal tip end. A bead flange is disposed about the exterior of each insert at the distal end of the insert. A bleed port for release of exhaled air is defined through a conical vent projecting normally to the path of the incoming air flow, and continues through a nipple extending to the exterior of the air conduit. In one embodiment, a pair of nasal inserts are integral with a nasal cannula body, with bleed ports axially aligned with each insert. In another embodiment, each insert is independently connected to a separate, thin-walled, flexible supply line.

Abstract: A patient interface device is includes a cushion and a frame assembly coupled to the cushion, the frame assembly including a main frame member and a stiffening structure coupled to the main frame member, the stiffening structure having a main arm, a first Y-portion coupled to a first end of the main arm having first and second front branches extending at upward and downward angles, respectively, from the first end of the main arm, and a second Y-portion coupled to a second end of the main arm having first and second rear branches extending at upward and downward angles, respectively, from the second end of the main arm.

Abstract: A sensor adaptor couples a face mask to a gas sampling tube connected to a device detecting end-tidal carbon dioxide. The sensor adaptor includes a shaft and connector. The shaft includes a channel providing a pathway for the carbon dioxide to travel toward the gas sampling tube. One end of the shaft includes an adaptor tip which extends through an exit port of the face mask. A connector is attached to the other end of the shaft and couples the sensor adaptor to the gas sampling line. A gripper may surround the shaft and prevent improper advancement of the shaft into the face mask. The sensor adaptor can be designed for use with any gas sampling tube and any face mask including exit ports.

Abstract: A wearable oxygen concentrator can be used in both an ambulatory mode and a stationary mode. The wearable oxygen concentrator is physically connected to a docking station in the stationary mode such that it can draw power from the docking station and remain energy efficient in both modes. The disclosed oxygen generation system incorporates effective gas flow by means compressor configurations for use in lower flow ambulatory modes and higher flow stationary modes.

Abstract: Supplemental oxygen is used by millions of people each year in hospitals and at home. The device and methods described allow people on supplemental oxygen through a feedback loop to optimize their blood oxygen level by measuring oxygen and/or carbon dioxide and/or other related gases in the blood. Because the device and methods optimize the level of supplemental oxygen and/or carbon dioxide and/or other related gases, complications (from too much or too little oxygen and/or carbon dioxide) including death can be prevented. In addition, users can reduce their costs by reducing the amount of oxygen needed as well as labor costs. Additionally, helicopters, ambulance, and mobile surgical sites can reduce weight in critical situations. In addition, the device and methods described also allow patients on ventilators through a feedback loop to optimize ventilation by measuring carbon dioxide in the blood; which can reduce complications, and reduce labor costs.

Abstract: An aerosol delivery system is disclosed, the system comprising: an aerosol delivery unit, the aerosol delivery unit comprising: a cartridge receiver, which is configured to receive a cartridge assembly; and an inductor configured to receive the cartridge assembly and heat a liquid formulation within a capillary tube to produce an aerosol by induction heating. The cartridge assembly including an active part of the cartridge assembly including a capillary tube; a susceptor, the susceptor configured to partially surround the capillary tube; and a pair of displaceable covers, which surround at least the capillary tube and the susceptor.

Abstract: Disclosed are methods of treatment that permit a reduction of risk of mortality in infants who are candidates for treatment with inhaled nitric oxide, by identifying a subset of such infants who are at an increased risk of mortality upon treatment with inhaled nitric oxide; also disclosed are related systems for use in administering inhaled nitric oxide and methods of distributing a pharmaceutical product.

Abstract: An apparatus for delivering a flow of gas, has a housing 3202? with a recess, and an outlet port 3210? for a flow of gas. The recess is defined by at least one wall 3256, 3262 that is substantially continuous, gas impermeable, and unbroken, other than a gasflow passage from the recess to the outlet port of the housing.

Abstract: A flow regulating valve for a respiratory treatment system is disclosed, as well as a vent arrangement comprising the flow regulating valve. The flow regulating valve may include an inlet, an outlet, and a variable conduit in fluid communication with the inlet and the outlet. The variable conduit may include a movable portion that may move to vary an impedance of the variable conduit, thereby regulating a flow rate of the air travelling through the variable conduit. Advantageously, the flow regulating valve may thus reduce wastage of air (e.g. humidified air) that is exhausted from a respiratory treatment system, while maintaining sufficient washout of air.

Abstract: Disclosed herein are portable gas delivery systems and therapeutic methods of use. More specifically, the portable gas delivery systems herein include a regulator having an inhalation device, such as a mouthpiece, and is configured to operably couple with removable sealed gas cartridges that comprise a therapeutic gas mixture of either one or more noble gases or nitrous oxide.

Abstract: A display control device and a display control method are provided. The display control method includes: acquiring current data of a user, the current data including identity information of the user and current time; matching the current data with feature parameters of video contents in a video database; and in case that the current data is matched with the feature parameters of the video contents successfully, setting the video contents as contents to be played, wherein the video contents include audio information and video information.

Abstract: A medical device, such as an electrophysiology catheter, has an elongate body including a wall. A reinforcing layer is encapsulated in the wall. The reinforcing layer includes one or more reinforcing fibers having glass cores and polymer cladding. In embodiments, the reinforcing fibers are non-magnetically-susceptible and non-electrically-conductive, facilitating the use of the medical device in connection with procedures such as magnetic resonance imaging (“MRI”).

Abstract: A urinary catheter may include a catheter shaft and a connector coupled with the proximal end of the catheter shaft. The connector may have a first arm ending in a fluid outlet configured to allow urine to flow out of the urinary catheter and a second arm with an aperture and ending in an inflation inlet used for introducing inflation fluid into the urinary catheter. The catheter may further include a primary lumen, an inflation lumen, a retention balloon mounted to the catheter shaft proximal to a fluid inlet and over a distal filling hole, and a pilot balloon mounted on the second arm of the connector over the aperture. The pilot balloon inflates at an inflation pressure that is higher than the inflation pressure of the retention balloon and lower than a predetermined pressure threshold.

Abstract: A urinary catheter may include a catheter shaft and a connector coupled with the proximal end of the catheter shaft. The connector may have a first arm ending in a fluid outlet configured to allow urine to flow out of the urinary catheter and a second arm with an aperture and ending in an inflation inlet used for introducing inflation fluid into the urinary catheter. The catheter may further include a primary lumen, an inflation lumen, a retention balloon mounted to the catheter shaft proximal to a fluid inlet and over a distal filling hole, and a pilot balloon mounted on the second arm of the connector over the aperture. The pilot balloon inflates at an inflation pressure that is higher than the inflation pressure of the retention balloon and lower than a predetermined pressure threshold.

Abstract: The present disclosure is directed to an expandable sleeve for a catheter assembly. The expandable sleeve includes a body configured to fit coaxially around an outer diameter of a catheter of the catheter assembly at a transition location between a hub and the catheter. Further, the body of the sleeve includes a length extending from a first end to a second end. As such, the sleeve is expandable between a compressed position and an expanded position so as to prevent the catheter from collapsing along the length of the sleeve. In addition, when in the expanded position, at least a portion of an interior surface of the sleeve contacts an outer diameter of the catheter.

Abstract: An interventional catheter for treating an artery includes an elongated body sized and shaped to be transcervically introduced into a common carotid artery at an access location in the neck. The elongated body has an overall length such that the distal most section can be positioned in an intracranial artery and at least a portion of the proximal most section is positioned in the common carotid artery during use.

Abstract: A pressure activated two-way slit valve assembly is designed to be used in combination with, but not limited to, a high flow rate catheter to prevent accidental ingestion of air or loss of blood if the closure cap comes off during non-use of the catheter. In addition, the potential for occlusion of the esthete due to blood clots in the catheter and catheter related infection is substantially reduced. The pressure activated two-way slit valve assembly includes a first end, a second end, a wall defining a dumbbell shaped channel, and a flexible, this disk having a slit and positioned within the pressure activated two-way slit valve assembly to reside within the dumbbell shaped channel. The slit and the dumbbell shaped channel are sized to enable the slit to deform in response to a predetermined pressure differential across the slit to allow fluid to pass therethrough.

Abstract: Disclosed is a robotic method for driving a catheter and a catheter guide, controlling a group of driving members and including: —a first operating mode in which the group of driving members moves the guide forward in translation; a second operating mode in which the group of driving members turns the guide about itself, the method also including a third operating mode in which the group of driving members simultaneously moves the guide forward in translation and turns the guide about itself, alternating between one direction and another.

Abstract: A sheath introducer system including a sheath introducer defining a lumen therethrough and having a proximal valve housing in fluid communication with a distal tubular sheath, wherein a proximal end of the valve housing defines a proximal opening of the lumen of the sheath introducer. A gasket seated within the valve housing has a first surface, a second surface and an outer periphery extending between the first and second surfaces. A first slit is formed into the first surface having an inner surface defining a first gap. A second slit formed into the second surface having an inner surface defining a second gap. A notch extends into the first gap of the first slit forming a bump on the inner surface of the first slit, wherein the second slit intersects the first slit at the notch such that the notch prevents the first and second slits from being in fluid communication.