Abstract: A loader and method for loading a transcatheter heart valve into a delivery sheath or catheter is described that is also configured to facilitate retrieval of the heart valve back through the delivery sheath while protecting the delivery sheath from damage. Another loader provides for easier crimping and loading of a THV into a delivery sheath or catheter from a storage jar or container. A method for crimping a THV facilitates easier end user preparation of the valve for implantation and reduces the likelihood of tissue deformation in the valve during storage. These devices and methods for deploying THVs simplify the valve replacement procedure.

Abstract: A medical device can include a housing, a first seal structure, and a seal expander. The first seal structure can have a proximal end and a distal end, and a side wall surrounding and defining an interior chamber. A seal wall can be connected to the side wall and include an expandable opening. A seal expander can be coupled to the housing, and can be at least partially in the interior chamber of the first seal structure. The seal expander can include an expandable neck portion and a seal interface portion, the seal interface portion being near an intersection of the side wall and the seal wall.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator is positioned to extend proximally in the interior cavity and support a seal member positioned thereon in the interior cavity. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator is positioned to extend proximally in the interior cavity and support a seal member positioned thereon in the interior cavity. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: A medical device can include a housing, a first seal structure, and a seal expander. The first seal structure can have a proximal end and a distal end, and a side wall surrounding and defining an interior chamber. A seal wall can be connected to the side wall and include an expandable opening. A seal expander can be coupled to the housing, and can be at least partially in the interior chamber of the first seal structure. The seal expander can include an expandable neck portion and a seal interface portion, the seal interface portion being near an intersection of the side wall and the seal wall.

Abstract: A valve is provided for a sheath, catheter, or other tubular device that includes a first face, a second face opposite the first face and an axis extending between the first and second faces. A first slit extends substantially parallel to the axis from the first face towards the second face to a first intermediate location within the valve body, a second slit extends substantially parallel to the axis from the second face towards the first face to a second intermediate location within the valve body, and a bore extends along the axis between the first intermediate location and the second intermediate location.

Abstract: A cannula cap is disclosed. A cannula cap according to some embodiments of the invention includes an instrument guide attachment; a cannula attachment; and a seal captured between the instrument guide attachment and the cannula attachment. In some embodiments, a cannula cap can include a lid; a locking ring; a base; and a cannula seal captured between the lid and the base.

Abstract: A first connector part (110) for establishing a fluid connection with a second connector part comprises a valve (111) with a valve seat (112), the valve seat comprising a valve chamber (116) and a circular opening with a circumferential sealing lip (114); a valve member (113), the valve member being provided in the valve chamber, and being able to sealingly close the circular opening of the valve seat when being pushed against the circular opening; and a resilient element (115) that subjects the valve member to a bias force pushing the valve member against the circular opening of the valve seat. The valve member further comprises a circumferential wall around the circular opening, located on a side of the circular opening opposite to the valve chamber.

Abstract: A disclosed antimicrobial medical device includes a fluid transfer device configured to couple between a patient and a fluid reservoir, a fluid pathway extending through the fluid transfer device, a first electrode coupled to the fluid transfer device, and a second electrode coupled to the fluid transfer device and spaced apart from the first electrode. The first electrode includes a first conductive material and the second electrode includes a second conductive material different from the first conductive material. The second electrode is configured to form a galvanic cell with the first electrode.

Abstract: A sealing ring protection sheet for a trocar of the present invention includes a positioning skirt, a support piece and a curved protection sheet. An upper end of the support piece is connected to an inner side of the positioning skirt, and a lower end of the support piece is connected to an upper end of the curved protection sheet. The curved protection sheet is of a curved and asymmetrical sheet-like structure, forming an easily deformable region and a protection region along two sides of a center line and its extension line of the positioning skirt separately. A left side and a right side of the curved protection sheet have different curvatures. The design of different curvatures of the left and right sides reduces resistance forces when various special-shaped instruments are inserted and removed.

Abstract: Certain aspects of the present disclosure provide a low friction trocar valve comprising a set of sheets arranged circularly and defining an entry point for the insertion of an instrument. In certain aspects, each sheet of the trocar valve's set of sheets comprises areas that overlap with two adjacent sheets. The trocar valve is formed in an opening of a valve housing coupled to or formed as part of a trocar cannula to provide a sealing mechanism for preventing the escape of pressurized fluids from the trocar cannula.

Abstract: A medical connector including a first rigid body capable of being connected to a medical infusion line and having an elongated tubular element in which there is a conduit opening out at opposite extremities, a first extremity of the tubular element being capable of being directly connected to the medical infusion line, the elongated tubular element being capable of being closed off at one of its first open extremities by a second body associated with the first body. The second body is of yielding material and at least partly covers the elongated element and extends beyond the second extremity of that element in such a way as to close off the opening thereof, such second body being overmoulded onto the first body and forming a single piece therewith.

Abstract: Hemostasis valves and methods for making and using hemostasis valves are disclosed. An example hemostasis valve may include a main body having a proximal end region. A cartridge may be at least partially disposed within the proximal end region. The cartridge including a seal member. The cartridge may have a proximal member, a distal member, and may define a seal holding region. The seal member may have an axial thickness of about 0.04 to about 0.2 inches. The seal member may be secured within the seal holding region by a mechanical bond.

Abstract: A cannula sleeve for a surgical trocar assembly. The cannula sleeve includes a hollow shaft, at least a portion of which is made of a rigid material, and a seal at the distal end of the hollow shaft, the seal being movable between a first open position and a second closed position. The shaft defines a proximal end, a distal end, a periphery, and a longitudinal axis. The shaft further includes a channel at the periphery substantially parallel to the longitudinal axis, the channel being in communication with the hollow shaft.

Abstract: A connection assembly for conducting a medical liquid, comprising a connection piece, an attachment part attached to the connection piece; an opening into which the connection piece engages; and a seal element for sealing a passage between the connection piece and the attachment part. The seal element is held between the attachment part and the connection piece and has a sealing head, which closes the opening of the attachment part against the passage of liquid when the attachment part is attached to the connection piece, and a body, which adjoins the sealing head and which can be arranged in the opening at a radial distance to the attachment part.

Abstract: A needleless connector includes a body having a fluid path, a vent path, and a male fitting. The needleless connector also includes a valve disposed within the male fitting. The valve is configured to move between a first configuration, in which the fluid path is blocked, and a second configuration, in which the fluid path is open. The needleless connector further includes a seal disposed around the valve. The seal is configured to separate the fluid path from the vent path in the first and second configurations. Moving the valve from the first configuration to the second configuration also opens the vent path. The seal maintains the separation between the fluid path and the vent path when the valve moves from the first configuration to the second configuration.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator is positioned to extend proximally in the interior cavity and support a seal member positioned thereon in the interior cavity. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: A system for providing vascular access in a patient's body may comprise at least one hemostatic valve (610) and at least one clamp (210) to be used with a vascular graft (110). The vascular graft (110) comprises a tubular body having a proximal end (110A) and a distal end (110B), the proximal end (110A) being configured to be attached to a vessel in a patient's body. The at least one valve (610) is configured to be attached to the distal end (110B) of the graft's tubular body and comprises a housing (616) including a flexible membrane (611) that allows a medical device (810) to be inserted through the membrane (611) into said vascular graft (110). The valve (610) further comprises an introducer sheath (615) configured to be inserted into the distal end (110B) of the graft's tubular body.

Abstract: The invention relates to an intravenous catheter apparatus comprising: a catheter hub (12) arranged at a proximal end of a catheter tube (10), the catheter hub (12) having an inner surface (14) defining a chamber (16); a needle (20) defining an axial direction and having a needle tip (24), the needle (20) extending through the chamber (16) and the catheter tube (10) when in a ready position; a needle guard (32) slidably arranged on the needle (20) and at least partially received in the chamber (16) when the needle (20) is in the ready position, the needle guard (32) including a base portion (34) and first and second arms (36, 38) extending from the base portion (34), wherein the first arm (36) is deflected radially outwards by the needle (20) against a restoring force when the needle (20) is in the ready position whereby the needle guard (32) is brought into retaining contact with the catheter hub (12); and wherein the catheter apparatus includes a valve which separates a distal space arranged in distal direc

Abstract: A valve for a needleless valve system. The valve includes a body configured to be disposed in the needleless valve system and controlling fluid flow through the needleless valve system and wherein the body is tail-less. The body includes a continuous top surface, and a compression feature configured to control how the body is compressed to allow fluid flow through the needleless valve system.

Abstract: A medical device can include a housing, a first seal structure, and a seal expander. The first seal structure can have a proximal end and a distal end, and a side wall surrounding and defining an interior chamber. A seal wall can be connected to the side wall and include an expandable opening. A seal expander can be coupled to the housing, and can be at least partially in the interior chamber of the first seal structure. The seal expander can include an expandable neck portion and a seal interface portion, the seal interface portion being near an intersection of the side wall and the seal wall.

Abstract: A valve actuator that moves in a catheter assembly between a first position where a valve is closed and a second position where the valve is open, the valve actuator including a shaft portion at a distal end of the valve actuator that is configured to pierce the valve, a mating portion at a proximal end of the valve actuator that is configured to engage a Luer device, a diameter reduction region that connects the shaft portion and the mating portion, and a plurality of windows that extend through the valve actuator for flushing fluid, the plurality of windows being disposed in the diameter reduction region, wherein each of the plurality of windows does not extend a full length of the diameter reduction region.

Abstract: An apparatus for creating a sealed conduit between separate volumes includes a first unit and a second unit. The first unit includes a housing defining a first volume, a conduit, and at least one first penetrable interface. The at least one first penetrable interface is reconfigurable from a closed, sealed, condition when not penetrated by the conduit to a sealed condition with the conduit passing therethrough when penetrated by the conduit. The second unit includes a housing defining a second volume and at least one second penetrable interface.

Abstract: Hemostasis valves and methods for making and using hemostasis valves are disclosed. An example hemostasis valve may include a main body having a distal end region and a proximal end region. A first seal member may be disposed within the proximal end region of the main body. A cartridge may be at least partially disposed within the proximal end region of the main body. The cartridge may include a second seal member. The cartridge may have one or more projections formed thereon. The proximal end region of the main body may have one or more recesses formed therein. The one or more recesses may be designed to engage the one or more projections. A plunger may be coupled to the proximal end region of the main body.

Abstract: Some fluid coupling devices described herein are configured for use in fluid systems for purposes of providing a repeatable, aseptic fluid coupling system. Such repeatable, aseptic fluid coupling systems are configured to facilitate multiple connection and disconnection cycles while repeatably establishing a sterile fluid pathway through the coupling system. The repeatable, aseptic fluid coupling systems can repeatably establish a sterile fluid pathway through the coupling system even though the coupling system may be used in a non-sterile environment.

Abstract: A vacuum probe comprises a sharpened body that is displaceable downward and toward a vacuum bag during vacuum hose quick connection. The sharpened body and a valve element inside the vacuum probe move in tandem until the sharpened body projects outside the vacuum probe. A vacuum pressure applied via the vacuum hose pulls the vacuum bag upwards and towards the projecting sharpened body, which then punctures the vacuum bag, thereby enabling air under the vacuum bag to be evacuated via the vacuum probe as vacuum pressure continues to be applied.

Abstract: An injection port assembly including a body having first and second mating structures configured to mate with a first connector for a first fluid pathway and a second connector on a device, respectively. A resilient barrier substantially contained within the body and compressible from a first position in which fluid flow between the first and second connectors is blocked to a more compressed second position in which fluid flow between the first and second connectors is permitted. A hollow cannula can be coupled with the first mating structure and disposed within the resilient barrier, the hollow cannula having a distal end configured to extend through the resilient barrier when the resilient barrier is in the second position, the distal end having lateral slots. The resilient barrier can have first and second annular sealing rings positioned above and below the lateral slots respectively.

Abstract: A valve body, e.g. a valve body adapted to be disposed in a connector to be connected to a catheter, has an opening/closing part which opens upon inserting a member into the opening/closing part and which closes upon withdrawing the member from the opening/closing part. The valve body includes a main body part made of a silicone rubber and a surface layer disposed on a surface of the main body part. This surface layer serves as a sliding surface which, when a guide wire has been inserted into the opening/closing part, slides on the guide wire. The surface layer is constituted mainly of silicon oxide and hence improves the sliding properties of the guide wire. Thus, the valve body is reduced in the resistance of sliding on the guide wire.

Abstract: Presented herein are embodiments of septum holders for use in syringe connectors that are used to connect syringes to other elements of liquid transfer apparatuses. The septum holders comprise a septum holder body, at least one resilient elongated arm that terminates with a distal enlarged element attached to the sides of the body, and a septum. The septum holders of the invention are characterized in that they comprise at least one bore that is created in the septum or in an insert fixed in either the body of the septum holder or in the septum that functions as the seat of a needle valve and in that the septum is attached to the bottom of the body of the septum holder projecting downwards parallel to the at least one elongated arm.

Abstract: A multi-port connector such as a closed intravenous (IV) access device with a y-port needle-free connector may be provided. The multi-port connector may include a main housing with a longitudinal axis, a needle free connector disposed along the longitudinal axis, and a y-port extending from a sidewall of the main housing at an angle that is non-parallel with the longitudinal axis. The needle-free connector may include a compressible sealing member that, when compressed opens a first fluid pathway from a first port, through a chamber within the housing, and to an output port. The y-port may be fluidly coupled to the chamber and the output port.

Abstract: A trocar assembly includes a trocar housing that defines a working chamber, and a cannula coupled to the trocar housing at a proximal end to facilitate communication between the cannula and the working chamber. A tool stabilizing device is coupled to at least one of the trocar housing and the cannula and is actuatable to stabilize and center a surgical tool within the cannula.

Abstract: Methods and devices for treatment of damaged tissue are disclosed, including treatment of wounds by employing non-electrically powered, reduced pressure therapy devices. Maintenance and control of the sub atmospheric pressure exerted may be provided by such devices while minimizing discomfort to the user. The devices may be configured to be worn inconspicuously underneath clothing.

Abstract: A medical connector includes: a housing including a male connector connection portion comprising a male connector connection port having a cylindrical shape, a medical instrument connection portion, and a valve body housing portion; and a valve body configured to open and close the male connector connection port, the valve body including a head portion, and a barrel portion that connects to the head portion. When a male connector is inserted into the male connector connection port, the head portion moves from the male connector connection port into the valve body housing portion and a slit in the head portion opens, such that a flow passage from the male connector connection portion to the medical instrument connection portion is formed.

Abstract: A flow component particularly for hemodialysis medical lines includes a duct having a first and a second end tubular connector coaxial to each other and designed to be connected to the line, and an intermediate tubular connector of the female luer type arranged orthogonally to the duct. A hollow elastic element substantially extends along the entire intermediate tubular connector and the body is internally configured so that, in use, the flow along the duct is partly diverted towards the intermediate tubular connector and introduced with a swirling motion along the cavity of the hollow elastic element.

Abstract: Methods and devices for treatment of damaged tissue are disclosed, including treatment of wounds by employing non-electrically powered, reduced pressure therapy devices. Maintenance and control of the sub atmospheric pressure exerted may be provided by such devices while minimizing discomfort to the user. The devices may be configured to be worn inconspicuously underneath clothing.

Abstract: An introducer sheath is disclosed capable of reducing a physical burden on a patient by shortening a time necessary for hemostasis at an introduction part after removing the introducer sheath percutaneously introduced into a body lumen. The introducer sheath includes a catheter main body, which is percutaneously introduced into a body lumen, a hub, which is connected to a proximal side of the catheter main body, and a tube member which includes a thrombus inducing material M. The tube member is disposed at a proximal side of an outer surface of the catheter main body.

Abstract: An assembly for disinfecting a female port of a medical implement is provided. The assembly includes a receiving portion and a disinfecting member disposed substantially inside the receiving portion. The receiving portion includes an open proximal end, a side wall, and a syringe tip having an external surface. An internal surface has a plurality of protrusions disposed near the open proximal end. The syringe tip includes a passageway therethrough in a fluid communication with the chamber and an external surface extending towards the open proximal end so as to create a cavity between the internal surface of the side wall and the external surface of the syringe tip. The protrusions are shaped to engage helical threads of the female port of a medical implement. The second disinfecting member is disposed substantially inside the cavity created by the protrusions of the internal surface and the external surface of the syringe tip.

Abstract: A pneumatic screw driving device includes a body having a grip to be held by an operator and housing a pneumatic motor, a rotating terminal member for cooperating with a screw driving element and liable to be driven in rotation by the motor, and a coupling piece for an air feed tube for supplying air to the motor. The coupling piece includes a first element partly mounted inside the grip, and a second element external to the grip for being connected to the air feed tube. The second element is fixedly attached to the first element by a rotating link. The first element and the second element are mobile relative to each other.

Abstract: The Purpose of our devise “Peripheral Intravenous Catheter With an internal Bi-Valvular Secure System” is to Avoid Back-flow spilling of blood or any other biological substance during the insertion of a catheter. Not only the Bi-valvular secure system is adaptable for the use in intravenous or arterial catheters but it can also be adapted to any type of Medical system catheters available in Medical practice due to its unique design, and without the need of changing the complete physical structure of the catheter. The present invention is for Medical field use and it provides a much more sterile and secure approach in reducing the risk of exposure to biological substances while at the same time reducing the risk of contamination to both the patient and the health care provider.

Abstract: A filter cartridge for operatively coupling to an appliance interface for treating fluid to the appliance. The filter cartridge includes a cartridge housing and a filter media contained within the cartridge housing. An engagement fitting extends from the cartridge housing. The engagement fitting to be received by the interface. The engagement fitting includes a base portion and a sealing member. The base portion has an inlet aperture on a first side of the sealing member and an outlet aperture on a second side of the sealing member. An interference member actuator extends axially and distally from one of the first end of the cartridge housing and the first end cap. The interference member actuator is configured to actuate an interference member of the interface from an interference position in which the interface is prevented from being actuated from a bypass mode to a filtering mode to a non-interference position.

Abstract: A liquid-transfer adapter operatively interposable between an injector and a vial is provided. The adapter has an injector engaging portion configured for fluidly coupling to an injector and a vial coupling. The vial coupling includes a spike that has a spike axis and a tip portion configured for piercing a septum of a vial. The tip portion includes a plurality of facets that meet each other at one or more edges and at least one of the one or more edges is sloped with respect to the spike axis. The spike defines a channel extending therethrough in fluid communication with the injector engaging portion. A channel opening is defined in at least one of the facets and disposed without interrupting the edges.

Abstract: A seal to permit the passage of a device through the seal. The seal includes an elastic component having a proximal end, a distal end, and an elongated trough adjacent the distal end. The elastic component has a slit that intersects the elongated trough.

Abstract: A fluid connection system and a method of attaching the same are provided to create a sterile fluid-flow path. The connection system includes a fluid access device having a female connector with a female elastomeric member disposed at a proximal end thereof and is coupled to an internal surface of the fluid access device. A male connector is coupled to an external surface of the female elastomeric member. Additionally, a male elastomeric member is disposed within the distal end of the male connector and seals a distal opening thereof. At least one aperture is disposed through a sidewall of the distal end of the male connector. An internal cannula is exposed out of the female connector to open the female elastomeric member upon engagement with the male connector. The male connector is sealed to the female connector by the male elastomeric member.

Abstract: A guide catheter for use in treating sinuses, the catheter including a catheter shaft configured to provide suction about a balloon catheter and a distal portion shaped for navigating body anatomy. In one embodiment, the guide catheter includes a valve for sealing the balloon catheter and a vent for controlling suction.

Abstract: A quick water intake device comprises a tubular main body. The main body has a channel, and a first seal core, and an elastic piece. Under the action of the elastic piece, the first seal core can block the channel. A second seal core is also slidably arranged inside the main body. The second seal core is located between the first seal core and an outlet end of the main body, and when subjected to forces, the second seal core can move toward the first seal core and drives the first seal core to compress the elastic piece. A sealing structure arranged between an outer wall of the second seal core and an inner wall of the main body can form a seal between an outer wall of the second seal core and the main body to block the channel when the second seal core moves toward the outlet end.

Abstract: A medical connector including a first rigid body capable of being connected to a medical infusion line and having an elongated tubular element in which there is a conduit opening out at opposite extremities, a first extremity of the tubular element being capable of being directly connected to the medical infusion line, the elongated tubular element being capable of being closed off at one of its first open extremities by a second body associated with the first body. The second body is of yielding material and at least partly covers the elongated element and extends beyond the second extremity of that element in such a way as to close off the opening thereof, such second body being overmoulded onto the first body and forming a single piece therewith.

Abstract: A piston for a needleless valve system comprising a head portion configured to be disposed in the needleless valve system and controlling fluid flow through the needleless valve system. The head portion comprising a continuous top surface, and an opening disposed proximate the continuous top surface, wherein the continuous top surface is non-planar when the opening is in an open position.

Abstract: A valve core capable of suppressing manufacturing costs, including: a first core cylinder body, a second core cylinder body having a valve opening on an opposite side to the first, a movable member having a valve body which opens and closes the valve opening at the front end of a shaft section linearly movably extending through the insides of the core cylinder bodies, an elastic member in contact with the movable member and the first body and biasing to sandwich the second body between the first and valve body, and a pair of fitting sections including a first and a second fitting section on the core cylinder bodies and which are rotatably fitted and are separable from each other without interfering. The fitting sections have cylindrical shapes that are detachably fitted to each other, and the first section has a stepped surface with which the second section is in contact.

Abstract: A fluid-connecting element with a first receiving space with a first connecting element and a first displaceable valve element, and a second receiving space with a second connecting element and a second displaceable valve element. A fluid connection between the first receiving space and the first connecting element being interrupted by the first valve element in the first position, and a fluid connection between the first receiving space and the first connecting element being opened by the first valve element in the second position. The second valve element is displaceable between two positions, wherein a fluid connection between the second receiving space and the second connecting element is interrupted by the second valve element in the first position, and a fluid connection between the second receiving space and the second connecting element is opened by the second valve element in the second position.

Abstract: A needleless valve system includes a cannula comprising a cannula tip; a valve comprising a valve tip, wherein the valve is disposed around the cannula; and a housing comprising a housing tip, wherein the cannula tip, the valve tip, and the housing tip comprise a flat surface when the needleless valve system is in a sealed position.