Abstract: A puncture needle connector (1) includes an outer cylinder (11), an inner cavity (1a) formed within the outer cylinder (11), an arm (15) provided at the outer cylinder (11), the arm (15) being elastically deformable by bending, and a claw (16) provided on the arm (15). The inner cavity (1a) is in communication with the outside via a first opening (21) and a second opening (22). When a puncture needle (210) is inserted into the inner cavity (1a) via a first opening (21), the claw (16) engages with an engagement structure (217) provided integrally with the puncture needle (210), a liquid-tight seal (25) is formed between an outer circumferential surface of the puncture needle (210) and an inner circumferential surface of the inner cavity (1a), and the puncture needle (210) and the second opening (22) are in communication with the each other.

Abstract: A male luer connector includes a body having a first end configured to be connected to a fluid line, a second end opposed to the first end, and a body longitudinal axis. The second end is configured to be inserted into and form a luer slip connection with a female luer connector. The male luer connector also includes a locking collar that is connected to the body in a manner such that the locking collar rotates about the longitudinal axis. In some cases, the body second end does not protrude beyond a plane that is transverse to the longitudinal axis and that includes an end face of the locking collar, and/or when male and female connectors are engaged, the locking collar engages an outer surface of the female fluid line connector and is deformed by the engagement.

Abstract: The present invention relates to a device for identifying the connection status between a patient catheter and a cassette system having flexible tubing assembly, which is intended to be used in a dialysis machine, wherein the device comprises the cassette system having flexible tubing assembly and an electrical circuit, which is disposed on the cassette system having flexible tubing assembly as well as on the patient catheter, and wherein the device furthermore comprises a measuring device for measuring at least one electrical property of the electrical circuit, which depends on said connection status.

Abstract: Devices and methods are described for occluding the left atrial appendage (LAA). The device excludes the LAA from blood flow to prevent blood from clotting within the LAA and subsequently embolizing, particularly in patients with atrial fibrillation. The implantable device is delivered via transcatheter delivery into the LAA and secured within the LAA. The implant comprises an expandable and compliant frame and an expandable and conformable tubular foam body. The device may have a thromboresistant cover at a proximal end. The frame may have recapture struts inclining radially outwardly from a central hub. The frame may have axially extending side wall struts, with adjacent pairs of side wall struts joined at one or more apexes. Anchors extend from the frame and into the foam to engage tissue.

Abstract: An assembly comprises a manifold configured to couple to a medical fluid cassette and a multi-lumen tube comprising a plurality of lumens within an outer wall of the multi-lumen tube. The manifold has a plurality of fluid connection ports and can be connected to the multi-lumen tube (e.g., via an adapter).

Abstract: A delivery member is provided for delivering and deploying an intravascular medical device. The delivery member includes a flexible distal portion including a wound wire coil surrounded by a flexible sleeve and inhibited from extending lengthwise by a stretch resistant member positioned through the lumen of the coil. The delivery member can include hypotubes positioned on either side (distally and proximally) from the wound wire coil to which the stretch resistant member and the wound wire coil can be attached.

Abstract: Disclosed herein are sealing devices and methods configured for improving sealing functionality with an engaged extension member of an apparatus. More specifically, disclosed herein are methods configured for improving insufflation gas containment in relation to trocars (and/or other related type of devices) that are used for enabling a surgical instrument such, for example, a laparoscope, to gain access to an abdominal cavity (or other body cavity). By providing for such improved insufflation gas containment, sealing devices as disclosed herein are particularly advantageous, desirable and useful in view of long-standing reasons for limiting insufflation gas leakage and in view of newly recognized reasons stemming from outbreak of COVID-19 disease for limiting insufflation gas leakage.

Abstract: A branch blood vessel insertion catheter has a catheter body having a lumen penetrating therethrough from a distal end of the catheter body to a proximal end thereof to allow a guide wire to be inserted therethrough. The catheter body has an inner layer, a wire-wound reinforcing member provided on an outer surface of the inner layer, and an outer layer covering both the inner layer and the reinforcing member. The catheter body has a first physical property change point located at a position apart from a distal end of the catheter at a distance of 3.0 to 7.0 mm and a rigidity of a portion of the catheter body located proximally from the first physical property change point is set higher than that of a portion of the catheter body located distally from the first physical property change point.

Abstract: A catheter and a manufacturing method thereof are disclosed, which can restrain a guide wire lumen and a dilation lumen from communicating with each other during thermal fusion-bonding while suppressing an increase in an outer diameter of a catheter shaft. A catheter has a catheter shaft in which a distal side shaft, an inner tube shaft, and a proximal side shaft are integrated with each other in a fusion region. The inner tube shaft has an opening portion which, opens outward and an arc-shaped portion which extends from the opening portion to a proximal side and which has only a portion of an entire circumference in a circumferential direction of the inner tube shaft. The fusion region includes the opening portion located on a distal side of a proximal end of the distal side shaft.

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 dialysis machine includes an ultrafiltration pump that pumps fluid from a pump inlet to a pump outlet, and a calibration fluid container. The container including a bottom, an upstanding sidewall, a container inlet and a container outlet, the bottom and the upstanding sidewall defining a container interior. The container may be to the atmosphere. At least the container outlet being disposed in the sidewall proximate to the bottom. The first end of a first hose is fluidly coupled to the pump inlet, and the second end of the first hose is removably, fluidly coupleable to the container outlet. The first end of a second hose is fluidly coupled to the pump outlet, and the second end of the second hose is removably, fluidly coupleable to the container inlet. In this way, a calibration process may be performed when the second ends of the first and second hoses are fluidly coupled to the container outlet and the container inlet, respectively.

Abstract: An adaptor for an endoscopic device includes (a) a cylindrical core extending from a first end to a second end along a central axis and (b) a collar slidably received over the core. The second end includes first and second slots defining first and second arms which radially expandable toward the axis and away from the axis. The second end is sized and dimensioned to engage an end of a first conduit of a biopsy device. The collar extends from a first end to a second end and being movable from a first position in which the second end of the collar is axially separated from the arms and a second position in which a portion of the collar is positioned over the arms radially compressing the arms to lockingly grasp a free end of a first conduit positioned therebetween to create a fluid-tight seal about the first conduit.

Abstract: The present invention provides a connector (1, 2) for use in fluid driving applications such as enteral feeding sets, catheters, and other medical devices, comprising a body (3) having a cylindrical coupling portion (7) with a substantially circular coupling surface (8) and having an outer surface (9) extending from the coupling surface (8) to form an internal cavity (11), a tube mating portion (13) extending outward from the body (3) for connecting to a tube, at least one thread sector (15) provided at the coupling portion (7), and at least one locking means (17) on the coupling portion (7), and at least one locking means (17) on the coupling surface (8).

Abstract: In a microcatheter, a shaft tube thereof is sectioned into a proximal zone, an intermediate zone, and a distal zone from a connector to the forward end thereof, each being formed of a multilayered tube, including three types of multilayered tubes different in hardness, an inner layer extending along all the zones from the proximal zone to the distal zone of the shaft tube, and a reinforcing material being fitted to the outer circumference of the inner layer, a first outer layer extending along all the zones from the proximal zone to the distal zone of the shaft tube so as to coat, and adhere to, the inner layer and the reinforcing material, to form a base layer structure of the inner layer/reinforcing material/first outer layer, a third outer layer coating the first outer layer of the base layer structure in the proximal zone, a second outer layer coating the first outer layer of the base layer structure in the intermediate zone.

Abstract: Peritoneal dialysis systems and methods are provided by the present disclosure. In a general embodiment, a peritoneal dialysis system includes a peritoneal dialysis fluid supply, a supply line in fluid communication with the peritoneal dialysis fluid supply, the supply line terminating at a supply connector, a patient connector in fluid communication with a patient's indwelling catheter, and a device configured to be placed around at least one of the supply connector and the patient connector during a connection of the supply connector and the patient connector, the device including an ultraviolet (“UV”) transmissive material to allow UV energy to be directed inwardly through the device towards a mating surface of the at least one of the supply connector and the patient connector during the connection of the supply connector and the patient connector.

Abstract: A universal introducer adapter which can be inserted into a pre-placed introducer of arbitrary dimensions eliminates the need to replace or remove the introducer. The adapter includes a distal portion with a retainer in the form of a soft elastic material.

Abstract: A medical infusion fluid handling system, such as an automated peritoneal dialysis system, may be arranged to de-cap and connect one or more lines (such as solution lines) with one or more spikes or other connection ports on a fluid handling cassette. This feature may reduce a likelihood of contamination since no human interaction is required to de-cap and connect the one or more lines and the one or more spikes. For example, the automated peritoneal dialysis system may include a carriage arranged to receive the one or more lines each having a connector end and a cap. The carriage may move along a first direction so as to move the connector ends of the one or more lines along the first direction, and a cap stripper may be arranged to engage with the caps on the one or more lines on the carriage. The cap stripper may move in a second direction transverse to the first direction, as well as to move with the carriage along the first direction.

Abstract: The invention inter alia relates to a dispense interface for an ejection device. The dispense interface comprises at least two inlets, at least one outlet and a part having a body portion and a cover portion; wherein the body portion and the cover portion are connected by a living hinge such that the body portion and the cover portion are foldable towards each other; wherein the body portion and the cover portion are configured to form a fluid channel arrangement between surfaces of the body portion and the cover portion facing each other when the body portion and the cover portion are folded towards each other; wherein the living hinge is arranged next to the facing surfaces; and wherein the fluid channel arrangement is configured to provide fluid communication between the at least two inlets and the at least one outlet.

Abstract: A connector for medical infusion lines, transfusion lines, and the like, includes a tubular body having at one end a male connector including an inner tubular element and an outer hollow element, which is internally threaded and can be coupled by screwing to a complementary female connector. The line connector further includes an outer maneuvering sleeve coupled in unidirectional rotation to the body in the direction corresponding to screwing of the male connector with respect to the complementary female connector and free to turn in the opposite direction, formed by two parts coupled together on the body of the connector.

Abstract: A surgical introducer including a body portion, a shaft and a sensor is disclosed. The body portion includes a reference indicator. The shaft defines a longitudinal axis and is positionable adjacent the body portion. The shaft is rotatable with respect to the body portion and includes a longitudinal indicator and a circumferential indicator. The sensor is disposed in mechanical cooperation with a distal portion of the shaft and is adapted to provide physiological data pertaining to a surgical worksite. At least a portion of the sensor is substantially aligned with the circumferential indicator. Rotation of the shaft with respect to the body portion causes displacement between the circumferential indicator and the reference indicator. Longitudinal movement of the shaft with respect to the body portion causes displacement between the longitudinal indicator and the reference indicator.

Abstract: A catheter includes a pressure actuated seal within a manifold. A catheter body is coupled with the manifold, and a manifold lumen and a 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 fluids in the manifold press 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 a pressure of the pressurized fluids. In the open configuration, the pressure actuated seal element relaxes in an absence of the pressurized fluids, and the seal element lumen is open and configured to allow passage of an instrument.

Abstract: An access port for the introduction of a needle cannula tip into an IV tube set includes a rigid tubular housing and a resilient member disposed adjacent an inlet of the housing. The resilient member includes an axial perforation extending through the resilient member, and is normally closed by a resilient character of the resilient member. A depression is defined in a proximal face of the resilient member, and includes sidewalls extending between the proximal face and the axial perforation to guide the needle cannula tip toward the axial perforation as a needle cannula associated with the needle cannula tip is introduced into the access port.

Abstract: A breakaway coupling assembly includes a male coupling and a female coupling. The male coupling includes ribs that flex portions of the female coupling as an insert of the male coupling is positioned within the female coupling. Once the insert of male coupling is positioned into the female coupling a predefined distance, the ribs snap into a circumferential retention groove of the female coupling to secure the male coupling to the female coupling and form a fluid seal. The male coupling is decoupled from the female coupling by pinching the female coupling to release the ribs from the retention groove.

Abstract: A handle for a medical instrument having a handle housing that can be closed by a cover and having at least one drainage or irrigation hose in the handle housing that can be connected to a hose connection support. To create a handle that is of a simple construction and ensures a reliable fluid-proof insulated connection of the at least one hose and the hose connection support while protecting a material of the at least one hose, it is proposed that each drainage or irrigation hose should be connectable by an adaptor to the hose connection support and that the adaptor upon closing the handle housing can be pressed against the hose connection support by a stop positioned on the cover or on a base portion of the handle housing.

Abstract: A steerable delivery catheter includes an outer sheath with a housing disposed at a distal end thereof to define a chamber for a medical device, the chamber having an open distal end and a proximal inner shelf. An inner shaft is slidably disposed within the sheath and has an abutment attached to the distal end of the shaft, the abutment being slidably contained within the chamber. During navigation of the catheter, when the inner shaft is tensioned the abutment engages the shelf to apply a compressive force to the sheath to selectively deflect a distal region of the catheter. When the catheter has been navigated to the deployment site the sheath is withdrawn while the abutment maintains the medical device in place as it is deployed. A delivery method also is disclosed.

Abstract: A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. A base is provided which is adapted to receive a reservoir. The base has a base engagement member, such as a detent, projecting therefrom. A cap is provided which is adapted to receive the base. The cap includes a first cap engagement member, such as a detent opening, which is adapted to removably engage the base detent. The cap further includes a second cap detent opening which is adapted to removably engage the base detent. A piercing member, such as a needle, is disposed in the interior of the cap in such a manner that the needle is separated from the reservoir septum when the base detent is in the first cap detent opening, and the needle pierces the reservoir septum when the base detent is in the second cap detent opening.

Abstract: A fluid conduit connector assembly includes a connector having a body with an inner surface defining a fluid channel. The connector also includes an inlet region for flow of fluid into the fluid channel, and an outlet region for flow of fluid from the fluid channel. The connector further includes an axial alignment member outward of the body, and a pair of flexible tabs arranged generally circumferentially of the alignment member and outward of the body. The connector can be configured as a day-side connector, transfer member with check valve, and/or patient-side connector. An implementation includes a day-side connector, a patient-side connector, and a transfer member, each of which has a pair of flexible tabs. The pairs of tabs are configured such that the transfer member releasably couples the day-side and patient-side connectors. A method for aseptically connecting a fluid conduit is also disclosed.

Abstract: A clam shell shaped adapter for retaining a catheter to establish a fluid path between the catheter and a fluid device or line has first and second shells integrally connected by a living hinge. The first shell has a luer end and a catheter end. A flexible tubing at an inner surface of the first shell connects the luer end to the catheter end. The catheter is inserted through the catheter end to extend along the flexible tubing. A retainer structure is provided at an inner surface of the second shell so that when the first and second shells close upon each other, the retainer structure presses against the flexible tubing to fixedly retain the catheter in a fluidly sealing manner. Respective latch mechanisms provided at the shells lockingly couple the first and second shells to each other.

Abstract: A medical connector includes a body defining a lumen for fluid flow through the medical connector. The medical connector includes a luer member and an annular member disposed about the luer member. The annular member includes internal and/or external engagement structures. The medical connector may be provided on the outlet of a syringe or on a catheter. A fluid path is disclosed including a first section and a second section. The first and second sections may each include a medical connector to provide a removable connection with a syringe and a catheter, respectively. The medical connector may provide a removable connection between the first and second sections. A fluid delivery system is disclosed including an injector, a syringe operatively associated with the injector, and a fluid path connecting the syringe and a source of injection. The medical connector may provide a removable connection between the syringe and fluid path.

Abstract: A warming device for an IV fluid line according to the present invention includes a warmer unit and a wye type fitting with an injection site. The warmer unit includes a tube for intravenous fluid and channels containing a warming fluid to heat the IV tube. One fitting branch is connected to an intravenous fluid source, while the remaining branch houses the injection site. The injection site branch includes an injection safety member that ensures a syringe needle or other instrument is contained within the fitting to prevent rupture of the IV tube. The warming device may include an additional wye type fitting coupled to the initial fitting and including another injection site, where the fittings typically exclude the safety member. A syringe needle is inserted into the additional injection site to prevent rupture of the IV tube. In addition, the warming device may be configured for needleless injections.

Abstract: An implantable percutaneous fluid delivery device is described that includes a subcutaneous base portion having one or more ports for supplying fluid to one or more implanted catheter devices and a percutaneous portion including an extracorporeal surface. The one or more ports of the subcutaneous base portion are accessible from the extracorporeal surface of the percutaneous portion. The subcutaneous base portion is at least partially insertable into a complementary recess formed in a bone, the subcutaneous base portion including one or more features for gripping the internal surface of such a complementary recess thereby directly anchoring the subcutaneous base portion to the bone. The device may be used to route fluid to neurosurgical catheters optionally via a router unit.

Abstract: An intravascular valve assembly having a valve case and a flexible pressure-actuated flow control valve. The valve case includes attached proximal and distal case portions that present respective spaced apart fluid ports and a fluid passageway extending between the ports. The flexible pressure-actuated flow control valve is disposed within the fluid passageway and includes a slitted central valve wall. The proximal case portion includes an axially-extending boss that projects distally, with a portion of a distal end of the boss contacting the flow control valve. The valve permits fluid flowing in a distal direction to pass through the slit. Fluid flowing in a proximal direction, however, causes the valve to compresses against the boss and the slit to close, thus restricting fluid flow in a proximal direction.

Abstract: A tracheostomy tube is provided. The tracheostomy tube includes an outer cannula that comprises an outer cannula connector comprising a first keying feature. The tracheostomy tube further comprises an inner cannula comprising an inner cannula connector including a second keying feature configured to complement the first keying feature when the inner cannula is inserted into the outer cannula. Further, a method is provided, whereby the method comprises inserting an outer cannula into a patient's trachea, and inserting an inner cannula into the outer cannula such that a keying feature on an inner cannula connector of the inner cannula engages a second keying feature on an outer cannula connector of the outer cannula.

Abstract: A catheter set includes a catheter and a fixing device. The fixing device includes a tubular member which is formed in such a way as to increase or decrease in diameter under axial extension or compression. A first projection and a second projection are provided at both ends of the tubular member. A movable tubular body is disposed around the tubular member between the first projection and the second projection. A distal part is coupled to the tubular member by a support member. The distal part is disposed distally of the tubular member and is configured to at least contact a proximal portion of a tubular device for medical use through which the catheter runs.

Abstract: Catheter connectors, systems, and methods of use in which a catheter is attached to a connector such that the catheter is retained on the connector by inward radial compression between an outer surface of a hollow pin located within the catheter and a collet fitted over the portion of the catheter containing the pin. The collet may be moved from an unlocked position to a locked position by axial displacement of the collet along a longitudinal axis of the connector.

Abstract: A needle-free connector includes a hollow connector, an elastic block, and a switch assembly. The inner perimeter of the hollow connector forms a first annular wall and a second annular wall. The elastic block is disposed in the hollow connector. The switch assembly has a stop member and a guide tube connected to the stop member, the stop member being pressed between the annular block and the elastic block, the guide tube being disposed in the hollow connector, the external perimeter of the stop member forming a first annular portion against the first annular wall and a second annular portion against the second annular wall, a groove being disposed between the first annular portion and the second annular portion of the stop member, the groove being connected to the guide tube. Thus, the structure stability and closing performance are achieved such that the outside air cannot leak into the connector.

Abstract: The present adjustable-length dual-lumen hemodialysis catheter can eliminate the need to stock various lengths of hemodialysis catheters and can provide a hemodialysis catheter, which can be trimmed to various lengths in order to precisely accommodate patients of various shapes and sizes. Specifically, the present adjustable-length dual-lumen hemodialysis catheter can comprise a cuff ring assembly, which can be secured at selected locations along the trailing limbs of the catheter allowing the cuff ring assembly to be installed in a location chosen to precisely fit a particular patient.

Abstract: A docking station for maintaining sterilization of temporarily disconnected male medical line connectors. The docking station has a plurality of docking bays, each of which retain an ampule therein containing a sterilization fluid and has an access mouth exteriorly exposed when the ampule is secured in its respective bay. The mouth of the ampule is provided with a female medical line connection for temporarily receiving and securing one of the male medical line connector temporarily disconnected from a patient. A tubular tip and a concentric connection collar of the one of the male medical line connector is thereby immersed in the sterilization fluid for sterilization while docked. Each of the ampules is secured against rotation in a clockwise direction in their respective docking bay to facilitate threadable connection of one of the male medical line connector.

Abstract: An adapter that bridges the connecting ends of a medication providing device and a fluid connector includes a housing shroud that is fitted at one end with a core and at its other end with an inner shroud. Once fitted to the housing shroud, the core and the inner shroud each are not removable from the housing shroud. A catch hub is provided within the housing shroud for non-removably maintaining the core to the housing shroud. The core is rotatable relative to the housing shroud.

Abstract: A luer connector assembly (100) including a luer connector body (102), a luer cap (110) and a protective flexible sleeve (120). The protective sleeve is assembled to the distal end (116) of the luer cap (110) to define a cap/sleeve subassembly (130), and the luer cap proximal end (112) is removably affixable to the distal end (106) of the luer connector (102). A prepared end (202) of a proximal catheter lumen (200) of a patient-implanted catheter assembly is inserted through the protective sleeve (120) and through and beyond the luer cap (110) to be affixed to the luer connector distal end (106). The luer cap/sleeve subassembly (130) is then slid proximally to be removably affixed to the luer connector distal end (106), whereafter the clamp (204) on the catheter lumen (200) is positionable onto and around the protective sleeve (120), to protect the catheter lumen (200) during clamping.

Abstract: A medical tubing connector pair includes a female tubing connector, and a male tubing connector. The female tubing connector has an external thread and the male tubing connector has an internal thread, the external and internal threads threadingly engaged to secure the female and male tubing connectors together. The internal thread is made from a flexible material to permit the female and male tubing connectors to be connected to or disconnected from each other without rotation of the tubing connectors relative to each other.

Abstract: A neonatal feeding tube (10) includes electronics and instrumentation for monitoring a neonate and for provides nourishment to the neonate. The tube (10) includes electrodes (20) for sensing ECG signals of the neonate. Thermistors (22, 24, 28, 30) are placed at various points along the tube (10) to measure the neonate's temperature at those points. Breathing effort is measured by calculating a pressure differential at two pressure ports (32, 34). Pulse and SpO2 are measured at a fiber optic window (35). The electrodes (20), a distal electrode (64) and a light source (66) aid in helping a caregiver position the tip (12) of the tube (10) correctly in the stomach of the neonate.

Abstract: The male connector of the present disclosure allows for the flow of fluids therethrough and includes a movable blunt needle having a shoulder projecting radially outwards from the movable blunt needle. The male connector also includes an outer cylinder body formed around the movable blunt needle and disposed in coaxial alignment to the movable blunt needle, a blunt needle retainer which retains the movable blunt needle so that the movable blunt needle can move in an axial direction, and a valve which opens as a result of the movable blunt needle moving in the axial direction when the posterior end presses against the valve. This occurs when the movable blunt needle is inserted into a corresponding connection site, such as a female connector, and the shoulder presses against the connection site to force the movable blunt needle in the axial direction.

Abstract: A catheter that comprises a hub, an elongated conduit, and at least one lumen therein. The lumen includes a proximal lumen section, a distal lumen section, and an intermediate lumen section extending between the proximal and distal lumen sections. The cross-sectional dimension of the intermediate lumen section is less than the cross-sectional dimension of the distal lumen section. In one embodiment, the cross-sectional dimension of the intermediate lumen section is less than the cross-sectional dimension of the proximal lumen section. In certain embodiments, the lumen tapers from the distal and/or proximal lumen sections to the intermediate lumen section.

Abstract: A dialysis system is disclosed including an autoconnection mechanism. The autoconnection mechanism in an embodiment is configured such that (i) a tip protector remover is translated in a first direction towards a plurality of supply line connectors, (ii) the tip protector remover is locked to each of a plurality of supply line tip protectors connected to the plurality of supply line connectors, (iii) the tip protector remover is translated in a second direction away from the plurality of supply line connectors to remove the plurality of supply line tip protectors from the supply line connectors, the tip protector remover is translated in a third direction different from the first and second directions, and (v) solution line connectors are translated towards the supply line connectors to connect each of the solution line connectors to one of the supply line connectors.

Abstract: Ureteral access sheaths can have a nonuniform axial-stiffness. A nonuniform axial-stiffness ureteral access sheath can have an inner liner defining a longitudinally extending and generally uniform bore. A non-uniform axial-stiffness outer jacket can define a longitudinally tapered outer surface, and a reinforcement layer can be encapsulated between the inner liner and the non-uniform axial-stiffness outer jacket. The reinforcement layer can have a non-uniform axial-stiffness. For example, a proximal portion of the reinforcement layer can be thicker than a distal portion of the reinforcement layer. A coil of wire can be included in the reinforcement layer, and a diameter of the wire in a proximal portion of the reinforcement layer can be larger than a diameter of the wire in a distal portion of the reinforcement layer. In some instances, the diameter of the wire tapers from the proximal portion to the distal portion.

Abstract: The present invention relates to a connection piece for an enteral transfer system and to an enteral transfer system with such a connection piece, and also to an arrangement composed of such a transfer system and of an enteral feed probe. The connection piece according to the present invention comprises a distal attachment piece for attachment of a connection piece of a probe tube of an enteral feed probe, and a proximal attachment piece for attachment of the connection tube of a transfer system. The distal attachment piece of the connection piece is conical or is designed in stepped fashion with several portions of different diameter. The distal attachment piece can therefore be releasably connected to the funnel-shaped connection pieces of different diameter of the probe tubes of the known feed probes. The connection piece according to the present invention can be used universally in this respect.

Abstract: A catheter set includes a catheter and a fixing device. The fixing device includes a tubular member which is formed in such a way as to increase or decrease in diameter under axial extension or compression. A first projection and a second projection are provided at both ends of the tubular member. A movable tubular body is disposed around the tubular member between the first projection and the second projection. A distal part is coupled to the tubular member by a support member. The distal part is disposed distally of the tubular member and is configured to at least contact a proximal portion of a tubular device for medical use through which the catheter runs.

Abstract: Drainage catheters for use in a variety of medical procedures are presented herein. The drainage catheter features an improved tension member locking mechanism. In use, once the drainage catheter is placed as desired, a second connector piece is rotated relative to a first connector piece to wind the tension member around a spooling region and pull the distal end of the catheter tube into a locked configuration. Once the tension member is tensioned, the first and second connector pieces are pulled into a locking engagement thereby securing the catheter tube in the locked configuration.

Abstract: An activator attachment that can be attached to the proximal end of a catheter adapter and can activate a blood control valve within the catheter adapter.