10510results about "Couplings" patented technology

A plug-type connection arrangement for a hose and a pipe, the connection arrangement comprising a sleeve having an outer wall and an inner wall, wherein the hose is insertable from an end of the sleeve and is clampable in the sleeve, wherein the sleeve has at another end thereof a first annular groove with an open resilient connecting ring which extends over more than 180° and is lockable to the sleeve and the pipe, and a sealing ring for sealing the sleeve relative to the pipe in a connected state of the pipe and the hose, the connecting ring being comprised of a plate spring ring with inwardly directed flanges at both circumferential edges thereof, wherein the flanges of one circumferential edge are engageble in the first annular groove and the flanges of the other circumferential edge are engageable behind a holding rib on the pipe, wherein the sealing ring is mounted in a second annular groove formed by the inner wall of the sleeve and the axially inner wall of the first annular groove, and wherein an end portion of the pipe is insertable into the sleeve.

A coupling part for a fluid coupling device, especially a hose coupling, which has a looking device switchable between two positions. The locking device has locking elements mounted on a base body, and a socket-shaped actuating element that interacts with the locking elements. The coupling part is switchable between a retaining and releasing positions by an axial releasing movement of the actuating element. In the retaining position, the locking elements hold the counterpart of the coupling, e.g. a hose stem, to prevents it from being pulled out and, in the releasing position, the locking elements release the same in order to disengage the coupling. The actuating element can be moved from the retaining position into a locking position, prohibiting a releasing movement, by rotating the actuating element in a limited manner around the longitudinal axis of the coupling. As a result, the coupling is prevented from being unintentionally disengaged.

A seal assembly adapted for use in conjunction with a trocar assembly includes a plurality of seal segments, each seal segment including a peripheral edge and a seam edge. Each seal segment further includes a first section and a second section with a vertical wall connecting the first section and the second section in such a way that the first section is displaced relative to the second section such that the first section of a first seal segment may be placed upon the second section of a second seal segment with the first sections of the first and second seal segments lying in the same plane and the second sections of the first and second seal segments lying in the same plane. The seal segments are assembled in an overlapping woven arrangement to provide a complete seal body without the need for a secondary seal.

Embodiments of a manifold assembly are provided herein. In some embodiments, a manifold assembly includes a first manifold having a first inlet, for coupling to a high temperature fluid source, and a first outlet; a second manifold having a second inlet and a second outlet; and a connector portion coupling the first outlet of the first manifold to the second inlet of the second manifold, the connector portion includes a polymer block; and a thermal isolator disposed between the polymer block and the first manifold.

The present invention relates to the connections between respiratory humidifiers and / or other such devices and heated breathing conduits used to couple a patient to the humidifier. In particular, the invention is a connector to couple a gases supply means and a conduit, such that the connector causes there to be an electrical and pneumatic, that is, sealed connection between a conduit including an electrical wire extending within, throughout or about it and a gases supply device, such as a humidifier, blower or the like. The connector may be of a single port type or a dual port type. The dual port type connector is suitable for ventilator apparatus that have a dry line (dry breathing conduit) extending from a ventilator or blower that carries dry gas to a humidifier and an inspiratory limb that extends from the humidifier to the patient and carries humidified gases to the patient.

A shut-off valve or connecting valve capable of connecting a fuel supply to a fuel cell is disclosed. The valve comprises a first valve component and a second valve component. Each valve component has an outer housing and a biased slidable member disposed inside the housing forming an internal seal. During the connection process, the two valve components establish an inter-component seal. Afterward, in one suitable embodiment the slidable member moves inward and opens the internal seal in the valve component to establish a flow path. In another embodiment, the slidable member moves inward and exposes a first filler and the first filler abuts a second filler in the other valve component to establish a flow path. In other embodiments, at least one valve component is sized and dimensioned to limit access to the internal seal.

A needless valve is described which avoids the suctioning problems of the prior needleless devices upon deactivation and which preferably provides a positive self-purging effect. The valve is self-purging at the end of an administration cycle, avoiding clogging of attached catheters or other devices, and ensures that substantially all of liquid received into the valve is delivered to the receiver. The valve is also extremely simple in design and easy to construct and assemble, since it consists of only three pieces. The valve has a base with a connector for fluid communication attachment to tubing or other device, a solid elongated fluid channeling rod, and an internal fluid flow conduit; a flexible hollow expandable and contractible plug fitting over and moveable along the rod; and a tubular housing fitting over the plug and attached to the base. When the valve is activated by insertion of a nozzle of a fluid source, the rod and plug wall cooperate so that as the plug retracts along the rod, it is stretched and its interior expanded. Upon deactivation, the plug contracts, the interior volume decreases, and the resiling plug wall forces residual fliud within the valve to be expelled through the outlet, purging the residual fluid from the valve. No negative pressure is formed, so no suctioning of blood or other fluid from a patient or receiver occurs.

A hemostatic valve couples to a sheath proximal hub having an inside and an outside surface. The hemostatic valve has a valve body having a proximal porting and end, and a distal portion and end. A passageway extends longitudinally through the valve body between the proximal and distal ends. A sealing element is positioned within the passageway. The distal portion of the valve body includes a pair of contact surfaces forming an annular gap receiving the sheath proximal hub of the sheath so that the contact surfaces sandwich the sheath proximal hub forming a seal on both the inside and outside surfaces of the hub. The valve body and the sheath proximal hub includes two oppositely placed longitudinal lines of fissure that allow the hub to be separated into two halves with the valve body.

A self-sealing male connector having a body, a resilient boot mounted over the body, and a male thread hub. The body is formed with an elongate post that extends to the distal end. The body includes a fluid flow lumen extending from its proximal end to its distal end. At its proximal end, the body may be formed as a female Luer connector, or may be directly connected to tubing, or other arrangements. The internal fluid flow lumen extends through the post to its distal end. The body includes a first groove in which is mounted the boot. In a second groove is mounted the thread cuff. The thread cuff is used to engage a female connector and through thread action, draw in into engagement with the post. As the female connector is further engaged with eh sealed male connector, the post protrudes through the boot and into fluid communication with the female fluid flow passage thus establishing a flow path through both connectors. The boot forms a seal with the female connector when engaged and returns to seal the male connector post and fluid flow passage within disconnected from the female connector.

A self-sealing male Luer connector for connection with a female Luer connector. The male Luer connector includes a housing having a distally-projecting tubular male body and a surrounding cuff interconnected by a proximal wall in which is formed at least one activation opening. A valve plug is slidably installed within the housing and formed with a distal end configured to sealingly engage the distal end of the male body's interior flow passage and with at least one activation arm at its proximal end configured to extend through the activation opening into the cavity formed between the male body and the cuff. An elastomeric device is sealingly configured within the activation opening about the activation arm to secure the valve plug in position and bias it distally. The proximal end of the male Luer connector may be configured as a conventional female connector, a blood collection device, or other such device.

A connector apparatus for controlling fluid dispensing / transmission that includes a control component for communication between couplers thereof. A first coupler has a transmitter, and is releasably connected with a mating reader coupler that has a transmitter and fluid control device to exchange information with the transmitter of the first coupler. The transmitters communicate and are operated by wireless means such as by RF devices. Upon confirming that the first coupler is properly coupled to the mating coupler and that the first coupler has a proper identification, the fluid control device controls fluid flow, using the transmitters of the first coupler and the mating reader coupler, under predetermined parameters, e.g., pressure, temperature, duration, and flow rate, as indicated in the first coupler.

A reconstitution device is disclosed and includes a first container receiver having a first component cannula disposed therein, the first component cannula having a withdrawal port and a first transfer port formed thereon, a second container receiver having a second component cannula disposed thereon, the second component cannula having a vent port and a second transfer port formed thereon, a device body coupling the first container receiver to the second container receiver and having a transfer lumen formed therein, the transfer lumen in fluid communication with the first and second transfer ports, a selectively sealing interface secured to the device body and in fluid communication with the withdrawal port, and a venting member in communication with the vent port through a vent lumen.

A needless valve is described which avoids the suctioning problems of the prior needleless devices upon deactivation and which preferably provides a positive self-purging effect. The valve is self-purging at the end of an administration cycle, avoiding clogging of attached catheters or other devices, and ensures that substantially all of liquid received into the valve is delivered to the receiver. The valve is also extremely simple in design and easy to construct and assemble, since it consists of only three pieces. The valve has a base with a connector for fluid communication attachment to tubing or other device, a solid elongated fluid channeling rod, and an internal fluid flow conduit; a flexible hollow expandable and contractible plug fitting over and moveable along the rod; and a tubular housing fitting over the plug and attached to the base. When the valve is activated by insertion of a nozzle of a fluid source, the rod and plug wall cooperate so that as the plug retracts along the rod, it is stretched and its interior expanded. Upon deactivation, the plug contracts, the interior volume decreases, and the resiling plug wall forces residual fluid within the valve to be expelled through the outlet, purging the residual fluid from the valve. No negative pressure is formed, so no suctioning of blood or other fluid from a patient or receiver occurs.

A hemostasis cannula unit including a valve housing, a cap, and a hemostasis valve, wherein the hemostasis valve includes a valve gasket and a valve membrane compressed against the valve gasket by the valve housing, wherein the valve gasket is thicker than the valve membrane.

An open end of a standard pipe fitting is enlarged in diameter to coaxially receive an O-ring and a retainer having a cylindrical surface. A plurality of locking teeth project from the cylindrical surface and are engageable with both the inner surface of the fitting and an outer surface of a pipe end inserted coaxially into the fitting open end. Each of the locking teeth have oppositely disposed edges facing obliquely inwardly and outwardly to engage both the pipe end and the fitting and resisting motion of the pipe end relatively to the fitting. In an alternate embodiment, a first plurality of teeth each have an edge facing obliquely inwardly of the fitting to engage the pipe end and resist motion tending to withdraw the pipe end from the fitting. A second plurality of teeth each have an edge facing obliquely outwardly of the fitting and resist motion tending to withdraw the retainer from the fitting.

Injection port valves are generally discussed herein and more particularly to port valves that have a valve housing with a nozzle having an inlet opening, a body section, a skirt section, an interior cavity, and a valve seat at an intersection of the first nozzle and the body section in the interior cavity. A piston may be positioned within the interior cavity of the valve housing having a body section having an exterior surface, an upper piston section, a seal surface, and a piston cavity, and wherein the body section includes a wall layer that emits lubricant from within the wall layer to the exterior surface. A nut, which may be a Luer nut, having a flow passage in communication with a discharge nozzle having a discharge lumen may be attached to an end of the skirt section of the valve housing to thereafter connect to an infusion line. A spring can be positioned within the piston cavity and abutting against the nut, wherein when used, the spring being in a first position when the seal surface of the piston is abutted against the valve seat of the valve housing, and the spring being in a second position when the seal surface of the piston is separated from the valve seat.

A needle-free medical connector includes a housing with a first port and a second port. The connector also includes a piston element defining a fluid passageway between the first and second ports. The piston element is movable between flow and non-flow positions. The piston element has an expandable section having a variable inner width and volume that forms a part of the flow path through the connector. As the piston is compressed to the flow position, the expandable section is expanded in width by movement over a flow post thereby maintaining or increasing the volume of the fluid passageway through the connector. The expandable section has a configuration permitting the continuous flow of fluid through its entirety.

An iris-type valve assembly for controlling a flow of fluid. The assembly comprises a base member, a rotatable member, and an elongated elastomeric valve sheath. The distal end of the valve sheath is secured to the base member and the proximal end of the valve sheath is secured to the rotatable member. At least one of the valve sheath ends includes a flange that is secured to a valve-receiving surface of the base member or the rotatable member. The base member and the rotatable member are aligned to define an elongated passageway therethrough for passage of an interventional device, and the elastomeric valve sheath is disposed along the passageway and has a longitudinal opening therethrough for passage of the interventional device. Upon rotation of the rotatable member relative to the base member the longitudinal opening of the valve sheath is selectively constrictable to comprise a seal around the interventional device. The assembly may be provided with ratcheting members to inhibit recoil of the rotatable member, and rib members along the inner surface of the valve sheath to enhance the seal provided by the assembly.

This invention provides microfluidic devices that comprise a fluidics layer having microfluidic channels and one or more regulating layers that regulate the movement of fluid in the channels. The microfluidic devices can be used to mix one or more fluids. At least a portion of the fluidics layer can be isolated from the regulating layer, for example in the form of a shelf. Such isolated portions can be used as areas in which the temperature of liquids is controlled. Also provided are instruments including thermal control devices into which the microfluidic device is engaged so that the thermal control device controls temperature in the isolated portion, and a movable magnetic assembly including magnets with shields so that a focused magnetic field can be applied to or withdrawn from the isolated portion or any other portion of the microfluidic device. Also provided are methods of mixing fluids. The methods include stacking a plurality of alternating boluses of different liquids in a microfluidic channel, and moving the stacked boluses through the channel. In another method, the boluses are moved into a diaphragm valve having a volume able to accommodate several boluses, and then pumping the liquids out of the valve.

A spray gun and a detachable liquid reservoir releasably attached to the spray gun by engagement of mateable, non-threaded formations provided on the spray gun and the reservoir. The spray gun has an integral connector boss with a socket for reception of a connector tube of the reservoir. The boss has an external flange at the distal end and the reservoir has hook members separate from the connector tube. The hook members are co-operable with the flange when the connector tube is received in the socket to secure releasably the reservoir to the spray gun. In another arrangement, the connector tube is an interference friction-fit in the socket to secure releasably the reservoir to the spray gun. In yet another arrangement, the connector tube has bayonet lugs co-operable with bayonet grooves in the wall of the socket when the connector tube is received in the socket to secure releasably the reservoir to the spray gun. In a still further arrangement, the reservoir has an integral spout received in the socket integral with the spray gun and provided with a helical projection co-operable with the underside of a radial lug externally of the socket to secure the reservoir.

An iris-type valve assembly comprises a base, a rotatable member, and an elongated elastomeric valve sheath. The distal end of the valve sheath is secured to the base, and the proximal end of the valve sheath is secured to the rotatable member. At least one of the valve sheath ends includes a flange that is secured to a valve-receiving surface of the base or the rotatable member. The base and the rotatable member are aligned to define a passageway therethrough for passage of an interventional device. The valve sheath is disposed along the passageway and has a longitudinal opening therethrough for passage of the interventional device. Upon rotation of the rotatable member relative to the base, the longitudinal opening of the valve sheath is selectively constrictable to comprise a seal around the interventional device.

A needleless luer access connector is disclosed having a septum disposed in a housing. The septum has a proximal portion with a cross section, a medial portion with a cross section smaller than the cross section of the proximal portion, and a distal portion. A longitudinal slit extends through the septum from the proximal portion to the distal portion. The septum and housing are designed so that septum will not be rotated or removed from the housing when the connector is accessed by a male luer taper. In addition, the septum and housing are designed to bias the slit at the distal portion closed and so a male luer connector does not have to extend completely through the distal portion to open the slit at the distal portion. Finally, the septum and housing are designed to minimize the amount of dead space in the connector when accessed with a male luer taper.

A first fluid connector is provided for selective interconnection to and fluid transfer with a second fluid connector. The first connector comprises a fluid passageway, an internal member and an outer collar supportably disposed about the internal member for selective advancement and retraction relative thereto. At least a portion of the fluid passageway may extend through the internal member. The outer collar may be selectively retracted to facilitate cleaning of the internal member. In some embodiments, the outer collar and internal member may be disposed so that a distal portion of the internal member is substantially flush with or a distal portion of internal member projects beyond a distal end of the outer collar when the outer collar is in a retracted position relative thereto. To facilitate cleaning, a distal end or distal portion of the internal member may be substantially closed when the first and second connectors are disconnected. The second connector may be adapted to facilitate fluid interconnection with the first connector, and may also present a cleanable distal end when disconnected.

A medical connector adapted for placement between a catheter and a medical infusion or injection source includes a pair of interlocking half medical connector portions, one side of which attaches to the infusion source and the other side of which is coupled to the catheter connected to the patient and a locking mechanism for locking a medical connector portion to a medical fitting. The connection to the catheter and the infusion source can be via standard medical luer taper fittings, with or without specially designed locking mechanisms that prevent inadvertent disconnection. The medical connector itself is uniquely shaped and includes a raised surface feature and a recessed surface feature formed on the medical connector portions.