Abstract: Disclosed is a flow control device for a bronchial passageway. The device can includes a valve member that regulates fluid flow through the flow control device, a frame coupled to the valve member, and a membrane attached to the frame. At least a portion of the flow control device forms a seal with the interior wall of the bronchial passageway when the flow control device is implanted in the bronchial passageway. The membrane forms a fluid pathway from the seal into the valve member to direct fluid flowing through the bronchial passageway into the valve member.

Abstract: A check valve in particular for medical applications has a first hose connecting casing and a second hose connecting casing and a membrane disk configured between the two hose connecting casings. The membrane disk is made of a resilient material and cooperates with an annular valve seat. The membrane disk is fitted radially outside the valve's seat with apertures leading to a discharge space. The wall of the second hose connecting casing is opposite the apertures and fitted with a surface curved away from the membrane toward the discharge channel. The discharge channel is fitted with an intake mouth in the wall, and conically tapers within a transition segment toward the intake mouth. Recesses communicating with the discharge space are fitted into the transition segment and are dimensioned in a way to substantially compensate the different flow cross-sections between the intake mouth and the discharge channel.

Abstract: A device for suctioning material out of an instrument channel during an endoscopic procedure. The device includes a biopsy valve having a first end, a second end, and an outer circumferential surface. The biopsy valve defines an internal passage leading from the first end to the second end, wherein the first end is adapted for connection to an endoscope instrument channel inlet port. Tubing connects the biopsy valve second end to a suction source connector disposed remote from the biopsy valve. A flow controller is fixed to the tubing and disposed between the biopsy valve second end and the suction source connector. The device may include an irrigation port and an instrument entry port.

Abstract: A delivery device and a method for administering a fluid from a fluid reservoir, wherein an unintended free flow of the fluid from the reservoir to a recipient is reliably prevented, are disclosed. The delivery device has a tank for the fluid; a fluid delivery device which delivers the fluid from the tank; a valve body providing an input hole and an output hole; and an infusion set in order to guide the fluid from the tank to a distal end of the delivery device. The delivery device further provides a shutter assembly which is or can be mounted to the valve body and prevents the fluid from flowing inside the infusion set when the fluid exhibits a pressure which is lower than a predefined pressure.

Abstract: Disclosed herein is a fluid infusion device of the type that delivers medication fluid to the body of a patient. The device includes or cooperates with a fluid reservoir, and the device has a sealing assembly to receive and form a fluid seal with the fluid reservoir. A retractable sealing element surrounding a hollow fluid delivery needle may be used to seal a port of the fluid reservoir. The port may include a pressure vent that is sealed by the retractable sealing element. In one variation, the reservoir includes a moving valve sleeve that holds a septum. The septum moves to allow the reservoir to vent, and to form a seal with the port when the needle pierces the septum. In another variation, the device includes a needleless sealing assembly. In yet other variations, the device uses a needled fluid reservoir.

Abstract: Disclosed herein is a fluid infusion device of the type that delivers medication fluid to the body of a patient. The device includes or cooperates with a fluid reservoir, and the device has a sealing assembly to receive and form a fluid seal with the fluid reservoir. A retractable sealing element surrounding a hollow fluid delivery needle may be used to seal a port of the fluid reservoir. The port may include a pressure vent that is sealed by the retractable sealing element. In one variation, the reservoir includes a moving valve sleeve that holds a septum. The septum moves to allow the reservoir to vent, and to form a seal with the port when the needle pierces the septum. In another variation, the device includes a needleless sealing assembly. In yet other variations, the device uses a needled fluid reservoir.

Abstract: There is disclosed a tri-leaflet valve (100) in which the leaflets (102) extend for substantially the entire length of the valve (100). The valve (100) is provide with a waist (106). An element (16) inserted in the tri-leaflet valve (100) can be sealed by closure of the valve (100), for example by pressurization or twisting. The seat is more effective then prior art seals.

Abstract: A disposable set (5) for establishing a fluid connection between a fluid dispensing unit (17) and a dosing device adapted to dispense a fluid into a patient's vein. The disposable set comprises a length of tubing (15) having a first (1) and a second (10) tubing part. The first tubing part (1) having a one-way valve (3) which permits a fluid flow from the dispensing unit (17) towards the dosing device and to prevent a backward fluid flow from the dosing device towards the dispensing unit. The first and second tubing part are in fluid connection with each other by means of a releasable connection device (11, 12), which is adapted to permit a back flow from a patient in a released position of the releasable connection device and to prevent a back flow from the patient in a closed position.

Abstract: A “Smart Micro-catheter” (SMC) system comprising a device for controlled particle release and drug delivery into a blood vessel, hepatic artery or any patho-physiological target is disclosed. Methods of using the micro-catheter system for optimal targeted delivery of therapeutic microspheres comprising using subject-specific computer simulations of particle-hemodynamics are further provided.

Abstract: A catheter for connecting an administering device to an administering needle, the catheter including a catheter wall, a flow region limited by the catheter wall, and at least one catheter portion at which at least one partial piece of the catheter wall abuts at least one other partial piece of the catheter wall to releaseably block or obstruct the flow of a medium through the catheter, wherein the flow is unblocked or opened when the medium exhibits a pressure above a predetermined blocking pressure.

Abstract: A variable hydraulic resistor for use with implantable pumps is disclosed. The variable hydraulic resistor according to the present invention is particularly useful in varying the flow rate of a medication fluid from an otherwise constant flow implantable pump. An implantable pump is also disclosed, which does not require a complicated clinching system or the like, and which may include an undulating membrane and chamber design to reduce the height of the pump.

Abstract: A system for controlling administration of medical fluid includes a fluid passageway to which is attached a first flow regulator, a second flow regulator, and a flow detector. The system also includes a controller for controlling the first and second flow regulators in response to a measurement taken by the flow detector of fluid movement in the fluid passageway. The first flow regulator, such as a pump, is configured to maintain fluid movement at flow values greater than an unrestricted flow value. The second flow regulator, such as a variable adjustable valve, is configured to maintain fluid movement at a flow value less than the unrestricted flow value. A method of controlling administration of medical fluid includes obtaining a target flow value, moving fluid through the disposable assembly, taking a measurement of fluid movement in the disposable assembly, and actuating a flow regulating apparatus.

Abstract: A sanitary apparatus for intestinal cleansing to be attached to a water faucet (R), includes a faucet filter (2), a quick coupling (3) connectable to the faucet filter (2) and containing a pressure-relief device. A spiral hose (4) connects the pressure-relief device to a series of devices situated in a rectilinear tube section (16), the series of devices including a temperature control device (5), a flow regulator (6), a metering device (7), a check valve (13) and a rectal nozzle (14) in an end section of the sanitary apparatus. The end section includes a semirigid tube (9, 12) sustained by a fixing removable support (10) including a base plate (19) provided with at least a sucker (21) in its lower part, and with U bolt-shaped members (24) clamping the semirigid tube (9, 12) in its upper part.

Abstract: Equipment for use in changing a catheter, preferably of the type used for drainage of the urinary tract. The urinary catheter is used as an aid in emptying the urinary bladder in conditions where this cannot be done in the normal manner. The equipment of the present invention includes a sleeve mounting unit which is mounted to an indwelling catheter, and which has a branch member formed in one piece therewith and extending at an acute angle therefrom, for reception of an elongated sleeve having a longitudinal slit. The sleeve is positioned on the branch member and then progressively advanced onto the catheter, causing the slit to become enlarged as the sleeve surrounds the upstream portion of the catheter in a yielding manner. The catheter may then be quickly removed through the sleeve and a new catheter inserted in its place.

Abstract: A pressure activated valve comprises a valve housing defining a lumen for receiving bodily fluids therein and a flexible membrane disposed in the valve housing. The flexible membrane includes a slit extending therethrough so that the flexible membrane may be moved between an open and a closed configuration based on fluid pressure within the lumen. A nonthrombogenic coating may be formed on fluid contacting surfaces of the flexible membrane.

Abstract: A flow control apparatus 1 including a tubular outside member 4, a tubular inside member 10 placed in the outside member 4, and a valve member 20 is used. The inside member 10 includes a through-hole 14 passing through a side wall in a thickness direction and a contact portion 11 that is in contact with the outside member 4, which are arranged in that order in a direction from one opening 16 to the other opening 17. The valve member 20 is placed in the opening 17 of the inside member 10. The valve member 20 passes only a fluid supplied at a set pressure or higher in a direction from the one opening 16 to the other opening 17. The outside member 4 is formed so as to form a gap communicating with the through hole 14 between the outside member 4 and the contact portion 11 due to elastic deformation caused by an external force. The gap forms a flow path of a fluid in combination with the through-hole 14.

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 catheter 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, thin 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: A valved connector for controlling the flow of fluid having a valve assembly positioned within a connector housing having a first position wherein the valve assembly prevents fluid flow through the connector housing, and a second position wherein the valve assembly permits fluid flow through the connector housing. The valve assembly may be movable from the first position to the second position by a male luer fitting. The valve assembly is configured for multiple and repeated access and also for minimizing fluid flow restrictions. The valved connector may be designed for use with a catheter to provide for “over the guidewire” placement or replacement techniques with little or no bleed-back or air embolism.

Abstract: A leak preventing AV needle assembly including an AV needle, a catheter having a first end engaged with the AV needle and a second end, and a one-way valve assembly including a housing having a first end portion engaged with the second end of the catheter, and a second end portion having an opening for receiving a fluid transmission conduit, is disclosed. The valve assembly further includes an axially displaceable closure element for closing the opening in the second end portion when the second end portion is not engaged with the conduit. The needle assembly further includes an elongated housing within which is disposed a biasing element for urging the closure element away from the first end and into sealing engagement with an opening in the second end of the valve assembly housing into which a fluid transmission conduit can be inserted for fluid communication with a catheter inserted into the first end of the valve housing.

Abstract: An auto-occlusion safety device is provided for use in preventing rupture of infusion components during rapid infusion procedures. An occlusion valve is disclosed having a threshold pressure that is less than a rupture tolerance of the infusion system components. As the fluid pressure of the infusion system increases beyond the threshold pressure of the occlusion valve, the occlusion valve is automatically activated thereby occluding fluid flow upstream from a vulnerable infusion component. An accumulator is further disclosed for use in combination with the safety device to compensate for time delays in full activation of the occlusion valve.

Abstract: A check valve for medical infusion lines and the like, includes a diaphragm made of elastic material set between a first tubular connector and a second tubular connector. The diaphragm includes an end wall of a cup-shaped element, having an outer peripheral edge of which is normally pressed in seal contact against an annular valve seat with a conical surface of the first tubular connector under an axial thrust exerted by a side wall of the cup-shaped element. A free edge of the side wall of the cup-shaped element is set resting against a transverse surface of the second tubular connector only in regions corresponding to angular portions of the latter separated by non-resting angular portions.

Abstract: An endovascular valve device for use in a vessel during a therapy procedure includes a catheter having at its distal end a valve. The valve is constructed of a braid of elongate first filaments coupled together at their proximal ends in a manner that the first filaments are movable relative to each other along their lengths. The first filaments have a spring bias that radially expands the valve. A filter is provided to the braid formed by electrostatically depositing or spinning polymeric second filaments onto the braided first filaments. The lumen of the catheter is in communication with the center of the valve.

Abstract: One embodiment of the invention provides a method to purge air or liquid from a powered injection system. In this embodiment, the method includes driving a first pumping device in a first operational mode to inject an amount of a first liquid medium through disposable tubing and a disposable valve, driving the first pumping device in a second operational mode to deform the disposable valve, and driving a second pumping device to inject an amount of a second liquid medium through the disposable tubing and the deformed valve. In one embodiment, the first pumping device comprises a first syringe, the second pumping device comprises a second syringe, and the disposable valve comprises an elastomeric valve.

Abstract: Described is drug infusion device with one or more check valves for inhibiting the unintentional discharge of medication from a cartridge. The device includes a chamber capable of receiving a cartridge of medication in a fluid form and one or more novel check valves for ensuring the drug is not unintentionally released due to pressure differentials between the cartridge and the ambient pressure outside of the drug infusion device.

Abstract: An in-line connector for use in an enteral feeding system includes a first component connectable to a first feeding device of the feeding system, and a second component connectable to a second feeding device of the feeding system. A releasable coupling is configured between the first and second components, wherein in a connected state the first and second components define a fluid passage between the different feeding devices. Each of the first and second components includes a one-way automatic shutoff valve configured therein such that in a disconnected state of the components, the shutoff valve in the first component prevents flow out of the first component in a first direction and the shutoff valve in the second component prevents flow out of the second component in a second direction that is opposite from the first direction.

Abstract: A bowel management system includes a waste collection catheter having at least two distinct sections. The first section is patient proximal when disposed in the patient's rectum and has durometer hardness in the range of about 50 A to about 90 A. The second catheter section is connected to the first section and has durometer hardness in the range of about 5 A to about 49 A. A selectively collapsible, substantially spherical retention balloon is attached coaxially and exterior of the first catheter section such that the proximal-most end of the retention balloon is coincident to the proximal-most end of the first section of the waste collection catheter, the substantially spherical retention balloon having an inflated size so as to be sufficiently large enough to retain the patient proximal end of the catheter in the patient's rectum without being so large as to trigger a defecatory response in the patient.

Abstract: The present invention is directed to, in one aspect, a medical apparatus having a nasogastric tube with hypopharyngeal suctioning capability. In one embodiment, the medical apparatus has a flexible nasogastric tube for insertion through a patient's nose. The nasogastric tube has a first end defining a first opening, a distal, second end that defines a second opening, and a length sufficient to allow the second opening to be positioned in a patient's stomach. The medical apparatus also has a flexible oropharyngeal tube for insertion through a patient's mouth. The oropharyngeal tube has a first end and a distal, second end that defines a suction intake. The oropharyngeal tube has a length that is less than the length of the nasogastric tube and which allows the suction intake to be positioned in a patient's hypopharynx region. In another embodiment of the invention, the medical apparatus has a laryngeal mask with hypopharyngeal suctioning capability.

Abstract: A gland member within a medical valve is configured to have a substantially consistent or enlarging internal volume as the valve transitions from a closed mode to an open mode. To that end, the valve has a housing forming an interior containing a flow path, and a stationary post member within the interior. The post member has a lumen that is a part of the flow path. The lumen has an opening to the interior of the housing. The valve further includes a gland member circumscribing the post member to produce a variable volume region formed at least in part between the gland member itself and the post member. In addition, the variable volume region is a part of the flow path, while the gland member occludes the post lumen opening when in the closed mode. The variable volume region has an open volume (i.e., when the valve is in the open mode) that is no less than its closed volume (i.e., when the valve is in the closed mode).

Abstract: A nasal passage washing device includes a pliable body including an open top; and an applicator cap removably attached to the pliable body to cover and uncover the open top. The applicator cap includes an applicator tip having a substantially frustoconical configuration sized and shaped for receipt at least partially within a nostril of a user for sealing engagement therewith, the applicator tip including a hole to transfer washing solution there through, a washing solution transfer tube in communication with the hole of the applicator tip and a bottom of an inside of the pliable body to transfer washing solution from the bottom of the inside of the pliable body to the hole of the applicator tip, and a one-way air valve that only allows air flow into the pliable body through the one-way air valve and does not allow air flow and washing solution flow out of the pliable body through the one-way air valve.

Abstract: Novel outdwelling normally closed bulbous medical bidirectional slit valves and outdwelling slit valve assemblies for influent and effluent fluid flow into and from a medical patient are disclosed, as well as related methods.

Abstract: A one-way check valve in an IV system set is provided with structural features to capture contaminant particles and inhibit the particles from adversely impacting the performance of the check valve. A screen can be provided upstream of the valve seat and the valve may be provided with flow channels for accumulating the particles. Modifications of the valve seat provide open volumes for accumulating contaminants.

Abstract: Certain embodiments disclosed herein include, but are not limited to, at least one of compositions, methods, devices, systems, kits, or products regarding rejuvenation or preservation of germ cells or gametes. Certain embodiments disclosed herein include, but are not limited to, methods of modifying germ cells or gametes, or methods of administering modified germ cells or gametes to at least one biological tissue.

Abstract: A pressure actuated valve for controlling the flow of fluid through a medical device, the valve comprises a housing including a lumen extending therethrough and a flow control membrane extending across the lumen to control the flow of fluid through the lumen. The membrane includes a plurality of slits extending therethrough so that, when the membrane is acted upon by a pressure of at least a threshold magnitude, the slits open to permit flow through the lumen and, when not acted upon by a pressure of at least the predetermined magnitude, the slits are maintained closed by a biasing force applied thereto by the membrane to prevent flow through the lumen. Each of the slits extends between end portions thereof along a curve wherein a distance between a first end portion of a first one of the slits and a first end portion of a second one of the slits is a minimum distance between the first and second slits.

Abstract: A pressure responsive slit valve assembly is designed to be used in a variety of configurations of medical devices to manage contemporaneous and pressure responsive fluid communications between such devices and a plurality of fluid sources. The pressure responsive slit valve assembly of the present invention includes a valve housing adapted to receive fluids from at least two sources and a pressure responsive slit valve means corresponding to each fluid sources.

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 catheter 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, thin 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: A fill and purge system for a drug reservoir is disclosed. The fill and purge system comprises a positive pressure source, a negative pressure source, a first valve, a second valve, and a delivery channel. The positive pressure source is fluidly connected to the first valve. The negative pressure source is fluidly connected to the second valve. The first and second valves are fluidly connected to the delivery channel. A method of filling and purging a drug reservoir is also disclosed.

Abstract: The haemostatic valve assembly (10) includes a housing (14) with a chamber (16) therewithin. A flexible valve element (26) is located in the chamber (16) and supported by the housing (14). A resilient element (21), for example of foam, is located in the chamber (16) and applies a constant closing force on the valve element (26). The valve (10) can be opened by aspirating fluid held within the chamber (16), for example by means of a pump or syringe, thereby to create a vacuum therein which compresses the resilient element (21). Removal of the vacuum allows the resilient element (21) to expand again and to close the valve (10).

Abstract: A medical connector for use in a fluid pathway includes a substantially transparent housing having a proximal end with a proximal opening and a distal end with a distal opening, and a cavity extending therebetween. The connector provides a substantially visible fluid flow path extending through a substantial portion of the connector.

Abstract: Two-way, three-position and one-way, two-position slit valves in cardiovascular access catheters with closed distal ends have slit geometries configured to overcome adhesion between opposed abutting slit faces, when pressure differentials are applied between the interior and the exterior of the catheter. Portions of the slit are oriented at a non-zero angle relative to the longitudinal axis of the catheter causing shear forces to be generated in abutting slit faces. Shear forces arise from tangential, radial, or longitudinal stresses generated in the catheter body. Slit geometries are planar or curved or include multiple end-to-end connected slit subsections. If a slit partially circumscribes a portion of the adjacent outer wall of the catheter body, restraint to outward and inward movement on that portion is reduced. Slit valves are configured to open inwardly to aspirate fluids, to open outwardly to infuse fluids, or both.

Abstract: A pressure actuated flow control valve for an infusion catheter permits gravity flow of a liquid through the catheter and into a patient while resisting back flow of blood from the patient and into the catheter. The valve has a hemispherical body with an outstanding circumferential flange and a normally closed, diametric slit. The slit is longer on the convex outer surface than on the concave inner surface. Dome thickness diminishes in the area adjacent the slit, reducing total apical deflection upon collapse of the slit toward the concave surface. An inner orthogonal rib biases the slit closed. Upon application of a predetermined pressure, the slit opens toward the concave surface to permit forward fluid flow. At lower pressures, the slit closes to check fluid flow. Greater reverse pressure is required to collapse the slit toward the concave surface to permit reverse fluid flow.

Abstract: A catheter device has an elongate body and a chamber positioned within the elongate body. The chamber has a chamber opening, and a barrier, such as a gate, moves over the chamber opening. The barrier moves between an uncovered position uncovering the chamber opening and a covered position covering the chamber opening. The catheter has at least one cutting edge by the chamber opening. In particular, the at least one cutting edge may be on the barrier, where the at least one cutting edge is guided over the chamber opening with movement of the barrier between the uncovered position and the covered position. The cutting edge cuts away a fibrin sheath blocking the chamber opening. The catheter may have multiple chambers connected by channels that allow the chambers to be flushed to prevent microbial colonization.

Abstract: A one-way valve comprises a seat and a membrane having an inner portion that is stretched over the seat, wherein, in use, the inner membrane portion is selectively deflected from the seat such that a fluid path is created from one side of the membrane to the other so as to open the valve, and wherein an outer peripheral portion of the membrane is stiffer than the inner portion such that the membrane deflection is substantially restricted to only the inner portion. The one-way valve may be used in a pump for an infusion system.

Abstract: A flow control device for medical liquid including a housing having an inlet and an outlet, and a channel formed in an inner surface of the housing, the channel extending at least partly in axial direction; a rotatable member rotatable in relation to the housing without being axially displaced, the rotatable member having at least two apertures; and a core member arranged inside the rotatable member, fixedly connected to the rotatable member. A helical flow path is formed between the lateral surface of the core member and the inner surface of the rotatable member, the at least two apertures of the rotatable member being in communication with said helical flow path, and wherein each of the apertures debouches into the channel in at least one rotational position of the rotatable member.

Abstract: A valve may include (a) a housing defining a valve lumen adapted for fluid connection with a lumen of a catheter; (b) a substantially conical valve member coupled to the housing and extending across the valve lumen to control flow therethrough; (c) a plurality of slits extending through the valve member and separated from one another circumferentially around the valve member; and (d) a ramp formed within a distal end of the valve lumen extending proximally from a distal tip of the valve member toward a ramp vertex separated from the distal tip by a predetermined distance.

Abstract: Fluid communication to an end of a catheter is afforded through a connection hub selectively attachable thereto. The connection hub includes a catheter-receiving element and a fluid-coupling element that are relatively rotatable coaxially between one of two states by way of a determinant assembly feature. The first state is an unlocked state and the second state is a locked state. The unlocked state is for determinately receiving a catheter and the locked state is for determinately securing the catheter. A method of making a connection hub is also provided.

Abstract: A pressure actuated valve for controlling the flow of fluid through a medical device, the valve comprises a housing including a lumen extending therethrough and a flow control membrane extending across the lumen to control the flow of fluid through the lumen. The membrane includes a plurality of slits extending therethrough so that, when the membrane is acted upon by a pressure of at least a threshold magnitude, the slits open to permit flow through the lumen and, when not acted upon by a pressure of at least the predetermined magnitude, the slits are maintained closed by a biasing force applied thereto by the membrane to prevent flow through the lumen. Each of the slits extends between end portions thereof along a curve wherein a distance between a first end portion of a first one of the slits and a first end portion of a second one of the slits is a minimum distance between the first and second slits.

Abstract: An infusion status indicator disposed in the medical infusion line includes a housing with an opening through which the status of the infusion may be determined. A flexible membrane is located at the opening to indicate the status of fluid in the cavity. A recessed flexible membrane indicates insufficient flow of medical fluid into the cavity from the fluid supply, a level flexible membrane indicates correct flow of fluid through the indicator, and a concave flexible membrane indicates an insufficient flow of medical fluid out of the cavity, possibly indicating an occlusion of the fluid line downstream of the indicator. Check valves may be included upstream and downstream of the cavity so that a bolus of fluid may be forced out of the cavity to the patient by pressing the flexible membrane into the cavity.

Abstract: Drug delivery connectors are provided for permitting and blocking fluid flow between a container and a catheter connector or other drug delivery site. Embodiments of the drug delivery connectors include a ball valve for forming a releasable seal within the drug delivery connectors. In one or more embodiments, the ball valve prevents fluid flow between an open proximal end and an open distal end of the drug delivery connector and is movable in a proximal direction to release the releasable seal to permit fluid flow from the open proximal direction to the open distal direction.

Abstract: A catheter includes a pressure actuated seal within a manifold. A catheter body is coupled with the manifold, and a manifold lumen and catheter lumen are configured to receive pressurized fluids. The pressure actuated seal includes a pressure actuated seal element having a seal element lumen. The seal element lumen is in communication with the manifold and catheter lumens. The pressure actuated seal element is deformable between an open configuration and a sealed configuration. In the sealed configuration, the pressurized fluid in the manifold presses on the pressure actuated seal element along a first seal face. The pressure actuated seal element compresses inwardly around the seal element lumen according to the pressure of the pressurized fluid. In the open configuration, the pressure actuated seal element relaxes in the absence of the pressurized fluid, and the seal element lumen is open and configured to allow passage of an instrument.

Abstract: A catheter with a balloon anchor may be sized to fit through an inner needle and introduced into the patient through the needle. The inner needle may comprise an atraumatic needle with a side port and/or a blunt tip. The catheter may include a radiopaque coil disposed over the distal portion of the catheter body to assist with catheter placement when viewed with fluoroscopy and/or x-ray. The distal portion of the catheter can be very flexible. A balloon inflation tube may terminate proximal to a proximal end of the expandable balloon anchor such that the distal portion of catheter can be flexible. This termination of the inflation tube may also position the inflation tube away from the annulus and nerve roots, so as to avoid irritation of the annulus and rubbing of the nerve roots that may potentially obscure FAD test results.