Abstract: A cap for a medical connector, the cap including a body having a closed proximal end and an open distal end, an interior volume within the body, an elongate member comprising an antimicrobial extending from the proximal end of body axially through at least a portion of the interior volume, the elongate member, threads for securing the cap to a medical connector, and a radially inwardly facing sealing surface on the cap, the inwardly facing sealing surface located distal to the threads and providing a liquid-tight seal between the cap and the medical connector when the cap is installed on the medical connector.

Abstract: A cap for disinfecting a needleless connector is described herein. The cap includes a housing having a cavity and an insert disposed within. The insert includes one or more cantilevered prongs disposed on a distal wall of the insert. The one or more cantilevered prongs are configured to bend upon insertion of the needleless connector. On an outer sidewall of the one or more cantilevered prongs are one or more ledges extending at essentially a right angle to the one or more cantilevered prongs, the one or more ledges being configured to push against the sidewall of the housing to resist further bending of the one or more cantilevered prongs upon advancement of the needleless connector.

Abstract: Implantable ports used for intravenous administration and methods of using the same.

Abstract: Needleless connectors are described. An example needleless connector includes a housing and a compressible valve. The housing may define an internal cavity and may include a body section having a first port and one or more internal contact tabs and a base section having a valve mount and a second port. The compressible valve may be disposed within at least a portion of the internal cavity and be movably retained within the housing. The compressible valve may include a flange portion for securing the compressible valve within the housing. A central longitudinal axis of the housing may be defined by a coaxial arrangement of the first and second port. The one or more internal contact tabs may be arranged to contact an outer side surface of the flange portion such that a radial force substantially orthogonal to the central longitudinal axis is provided for securement.

Abstract: The invention relates to a blood line (108) comprising an infusion site (145) intended to inject into the line a solution comprising: —a first main channel (200) having a first passage section, —a second main channel (220) having a second passage section, —means for the formation (210) of a turbulence area located downstream from the first main channel, located upstream from the second main channel, these formation means comprising a first fluid passage means (224) defining a reduction (225) in the passage section and whose smallest passage section is smaller than the first passage section and smaller than the second fluid passage section, —a secondary channel (230) comprising an inlet (231) for letting in the solution and an outlet (232) in fluid communication with the first main channel or the means for the formation of a turbulence area or the second main channel.

Abstract: An object is to provide a co-injection member which can smoothly collect a liquid of an internal flow route, which can smoothly inject a liquid into the internal flow route, and which can reliably prevent congestion of the liquid in the internal flow route. A co-injection member includes a main body that can be connected to a blood circuit through which blood is circulated, an internal flow route that is formed inside the main body, and that can circulate the liquid of the blood circuit, an inlet flow route that is formed inside the main body, and that introduces the blood into the internal flow route, an outlet flow route that is formed inside the main body, and that can discharge the blood of the internal flow route, and a rubber member that is attached to an opening formed in the main body, and that separates the inside and the outside of the internal flow route from each other.

Abstract: A disinfecting and pre-opening device is disclosed for use with a female needleless connector. The disinfecting and pre-opening device includes a housing comprising a chamber having a distal opening and configured to fit over the female needleless connector, and an elongated finger attached to the housing and disposed within the chamber such that the elongated finger opens the fluid path through the female needleless connector when the distal opening of the disinfecting and pre-opening device is placed proximally adjacent to the septum and the disinfecting and pre-opening device is advanced in the distal direction.

Abstract: A fluid infusion device is provided. The fluid infusion device includes a housing that includes a lock and a set connector assembly removably coupled to the housing to define a fluid flow path from the fluid infusion device. The set connector assembly includes a connector having a body that defines a graspable portion and a coupling portion. The coupling portion is receivable within the housing, and the graspable portion has at least one wing that defines a locking tab for engaging the lock. The at least one wing is movable relative to the body to disengage the locking tab with the lock.

Abstract: A set connector assembly for a fluid infusion device is provided. The set connector assembly includes a connector having a body. The body defines a graspable portion and a coupling portion, and the coupling portion is to be received within a portion of the fluid infusion device. The graspable portion has at least one wing that defines at least one locking tab for locking the connector to the fluid infusion device. The graspable portion is movable relative to the body to move the connector between a first, locked position and a second, unlocked position relative to the fluid infusion device.

Abstract: A catheter assembly for insertion into the brain. The assembly comprises a first length of tubing made of a first material. A second material surrounds the first length of tubing, the second material being more flexible than the first material and having a hardness of less than 50 Rockwell E. The second material provides damping to the first length of tubing.

Abstract: An electrically nonconductive occludent constructed and arranged to forcefully infill a tissue opening so as to effectively prevent transport of electrical current, fluid and bacteria through the tissue opening. A cochlear implant comprising: an elongate electrode carrier member having at least one electrode disposed thereon, wherein the carrier member is configured to traverse a cochleostomy to position the electrodes in the cochlea; and an electrically nonconductive occludent constructed and arranged to circumferentially surround a portion of the carrier member traversing the cochleostomy, and to forcefully infill cochleostomy thereby segregating perilymphatic canals of the cochlea from extracochlear regions.

Abstract: The application relates to a drip chamber for an infusion device, to an infusion device with a drip chamber, and to an arrangement composed of an infusion container and of such an infusion device. The drip chamber has a securing part for securing the drip chamber releasably to the infusion container. The securing part of the drip chamber has securing elements which are arranged along the circumference of a circle and which, on the inner sides facing each other, have grooves extending along the circumference of a circle. The securing elements can be spread from a position in which they engage firmly around the connector part of the infusion container to a position in which they release the connector part of the infusion device. The securing elements secure the piercing spike of the drip chamber against slipping out of the piercing part of the connector part of the infusion container.

Abstract: A catheter guiding device includes a bolt including a shaft configured to be inserted within a hole drilled in a bone and a passageway extending longitudinally therethrough along a bolt axis and a guide member received within the passageway of the bolt and extending longitudinally along a guide axis. The guide member includes a guide channel extending therethrough along the guide axis, wherein, in a first configuration, the guide member is arrangeable to a desired position relative to the bolt to align the guide axis with a target area and, in a second configuration, the guide member is fixed in the desired position relative to the bolt such that the guide axis is at a desired angle relative to the bolt axis within a permitted range of angulations.

Abstract: A venous access device is generally discussed herein with particular discussions extended to port access device having a protective clip. The port access device includes a needle hub having a needle extending therefrom and a catheter hub having a catheter tube extending therefrom with the needle positioned inside the tube in a ready to use position. A tip protector is positioned inside a clip housing, which is positioned in between the catheter hub and the needle hub.

Abstract: An attachment arrangement has a housing and a needle located within the housing. The arrangement allows administration ports of different sizes to be inserted into and secured within the housing. In certain embodiments, compliant retainers secure the administration port within the housing. In certain other embodiments, the administration port is secured within the housing when the housing is compressed against the administration port by a housing compression element. Once the administration port is secured within the housing, a fluid-tight seal is formed between the attachment device and the administration port.

Abstract: A retention feature configured to provide interference between a threaded connection of a Luer access device and a separate device, wherein the Luer access device further comprises a septum that provides a soft interfaced between the two threadedly connected devices. The retention features of the instant invention are designed to provide the user with a tactile sensation of a tightening threaded connection, despite a soft interface between the interconnected devices. The retention features of the instant invention further prevent “spring back” and unintentional disengagement of the interconnected devices.

Abstract: Methods and apparatus are disclosed for making and using adjustable epidermal tissue ingrowth cuff and catheter assemblies for transcutaneous placement to provide periodic or continuous external access for medical purposes to an interior body region of a patent who requires such medical treatment over an extended period of time.

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 transcutaneous implantable access port for removal and/or return of fluids of a patient comprises a fixation unit adapted to be fixed to a bone of the patient; a valve unit comprising a sealing membrane at its distal end and one or more chambers; an internal conduit fluidly connectable to vascular structure of the patient and releasably connectable to the valve unit to establish fluidic communication between the internal conduit and said one or more chambers; and an extracorporeal connecting member having an end portion. The extracorporeal connecting member is connectable to the distal end of the valve unit, opening and closing a fluidic passage between the connecting member and said one or several chambers when the connecting member is respectively connected to the access port and withdrawn therefrom. The access port can be used for high volume removal and/or return of blood or other fluids from the patient.

Abstract: A rotatable connector for medical use is provided, applicable to connecting infusion tubings or serving as part of infusion tubing, including a first tube, a second tube, a casing cover, and an elastic sealing member; the first tube having a coupling end, the coupling end having an outer wall disposed with a stopper; the second tube having a docking member; the casing cover having one end sheathing outside of stopper and the other end fixed to docking member; a housing space being formed by inner wall of casing cover and outer wall of coupling end; the elastic sealing member being disposed inside housing space, tightly adhered to outer wall of coupling end as well as diving housing space into two disconnected spaces. As such, when applied to infusion tubings, the first tube of the connector of the present invention can rotate to resolve a blockage and free of leakage.

Abstract: A medical connector for minimizing leakage of fluids during connection and disconnection is described. The medical connector includes a body having an inlet port, at least one outlet port adjacent to a male luer portion of the body, and a fluid path between the inlet port and the at least one outlet ports. A retractable seal adjacent to the male luer portion of the body and blocks the outlet ports of the body when the male luer portion of the medical connect is in a disconnected state. The retractable seal is positioned on the body such that it is moved away from the outlet ports upon insertion of the male luer portion of the medical connector into a medical access device thereby unblocking the outlet ports and creating a fluid path through the medical connector.

Abstract: The invention generally relates to an intravascular catheter that includes a proximal hub and a distal elongated tubular member. In one embodiment, the hub is designed to mitigate the introduction of air into a patient's vasculature during the delivery of a second device through the catheter into the patient's body.

Abstract: A valve for selectively permitting a fluid flow between first and second medical implements is disclosed. The valve has a housing with an interface suitable for receiving a connector portion of a first medical device such as a catheter, and a seal made of a flexible material. The seal has a first end in fluid communication with the interface, a second end suitable for receiving the second medical device, and at least one slit in fluid communication with the first end and the second end. The slit defines a restricted fluid flow path and a relatively small interior volume when in an undisturbed state, defines an expanded fluid flow path and a larger interior volume upon the introduction of the second medical instrument into the slit, and retracts to define a restricted flow path and a small interior volume upon the withdrawal of the second medical device from the seal.

Abstract: A system is provided for use and handling a medical liquid (e.g. hazardous drugs) that includes a transfer adapter having a port rotatably interconnectable to a male luer fitting of a needleless syringe or infusion tubing line port, and a patient connector having a port rotatable interconnectable to a female luer fitting of an intravascular catheter access port. Ports of the transfer adapter and patient connector are interconnectable to automatically define a closed fluid passageway. A vial adapter and/or a reservoir adapter may be provided for selective interconnection to the transfer adapter wherein a second closed fluid passageway and/or a third closed fluid passageway are automatically defined upon interconnection with the transfer adapter.

Abstract: A low profile adaptor is disclosed to reduce the length of a gastrostomy tube that has been inserted by means of conventional endoscopic procedures or with a replacement feeding tube inserted into the patient's stomach. The gastrostomy tube is cut to the appropriate length by the physician. The adaptor comprises a stem which is inserted into the open end of the gastrostomy tube. The valve assembly contains a seal that functions as a one-way valve to prevent reflux of gastric contents but permits the introduction of feeding solution into the feeding tube. A lock and key mechanism is incorporated into the hub of the gastrostomy tube to prevent disconnection of the feeding tube. A cover is placed over the opening of the adapter to prevent contamination of the lumen of the gastrostomy tube.

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: A removable, resilient atraumatic sheath for arthroscopic instruments. The sheath covers sharp edges on the arthroscopic instrument, particularly the distal tip of the rigid cannula, and thereby protects tissue and objects near a surgical site from accidental trauma. The sheath may be provided in the form of an inflow/outflow sheath that allows a surgeon to irrigate and drain a surgical field without the use of a separate irrigation instrument. The sheath is provided with a cylindrical grip on the proximal end to resiliently squeeze the proximal end of the arthroscopic instrument. A lever is provided to move the grip radially outwardly to release the grip from the arthroscopic instrument.

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: An injection site for tubular medical connectors, includes a perforable body inserted in a seat of a connector delimited by an annular wall having a retention edge turned in against the outer end of the perforable body. The outer end is formed with a peripheral annular step and with an exposed portion with reduced cross section projecting axially. The peripheral step is defined by an annular groove having a shape complementary to that of the turned-in retention edge of the connector, and the portion with reduced cross section of the perforable body connects up to the groove through an annular surface projecting radially above at least part of the turned-in retention edge and resting against it.

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: The present application provides a device and methods of making and using these devices. The devices comprise porous caps and porous vents made from sintered porous polymeric media comprising plastic particles, elastomeric particles or a combination thereof. These devices are used with medical devices or components thereof to provide ease of use, resistance to infection, sterilization and venting.

Abstract: A connector (900) for fluid conduit includes a connector body (901) having a lumen (902) passing along a longitudinal axis (903), and a luer access port (800) extending distally along a transverse axis (905). The luer access port (800) is made from a thermoplastic elastomer (500) having a domed interior portion (501) and a stair-stepped perimeter (502) that is coupled to a cylindrical wall (600). The thermoplastic elastomer (500) and cylindrical wall (600) can be integrally coupled in an insert molding process.

Abstract: An enteral feeding device includes a first tube having a first proximal end, a first distal end, a first inner tube wall surface and a first exterior wall surface and a rescue port having a second proximal end, a second distal end, a second inner tube wall and a second exterior wall surface.

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: The invention relates to a blood line (108) comprising an infusion site (145) intended to inject into the line a solution, comprising: —a first main channel (200) having a first passage section, —a second main channel (220) having a second passage section, —means for the formation (210) of a turbulence area located downstream from the first main channel, located upstream from the second main channel, these formation means comprising a first fluid passage means (224) defining a reduction (225) in the passage section and whose smallest passage section is smaller than the first passage section and smaller than the second fluid passage section, —a secondary channel (230) comprising an inlet (231) for letting in the solution and an outlet (232) in fluid communication with the first main channel or the means for the formation of a turbulence area or the second main channel.

Abstract: An irrigating cannula includes a hub having an inner passage and a side port extending through the hub and connecting to the inner passage. The inner passage is configured to receive an instrument, and a fluid passage is defined between the hub and the instrument. The fluid passage is configured to deliver a fluid through an incision in a body.

Abstract: Some embodiments disclosed herein relate to a medical connector having a selectively closable male end portion. Embodiments are configured to open upon connection with a female connector or female tipped medical implement. Some embodiments include an internal cavity configured to change size as the connector moves from the open to closed or closed to open positions. In some embodiments, the connector is configured to draw fluid from the male end toward the other end of the connector as the connector closes.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. 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. A punch tool is provided to form a tri-slit in the membrane 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 connector of improved configuration. Annular grooves are formed in both inner and outer surfaces of an outer peripheral portion of an elastic valve element to form an annular constricted section. An outer peripheral side from the constricted section is made to serve as an annular fixation section. A valve receiving seat is formed at an inner peripheral edge of an aperture portion in a housing, and an annular ring is fixed to the aperture portion to sandwich and support the annular fixation section between the valve receiving seat and the annular ring. Engaging projections formed on mutually facing surfaces of the valve receiving seat and the annular ring are engaged with the annular grooves, and either the engaging projection and/or the engaging projection is divided in a circumferential direction to have a plurality of projection-divisions.

Abstract: Systems, methods, and articles for delivering an antimicrobial composition into the lumen of a trans-dermal catheter and to proximal elements of the transdermal catheter are disclosed. In an embodiment, the system comprises an elongate member configured for insertion into a lumen of a catheter, the elongate member containing an antimicrobial. In an alternative embodiment, an antimicrobial composition placed on an interior surface a cap element, and transfers antimicrobial to the exterior of the proximal end of the transdermal catheter.

Abstract: Systems, methods, and articles for delivering an antimicrobial composition to the proximal elements of a trans-dermal catheter and into the lumen of the transdermal catheter are disclosed. In an embodiment, an antimicrobial composition placed on an interior surface a cap element, and transfers antimicrobial to the exterior of the proximal end of the transdermal catheter. The system comprises an elongate member configured for insertion into a lumen of a catheter, the elongate member containing an antimicrobial.

Abstract: A connector for connecting a container with a fluid preparation device for preparing a fluid, in particular a container with a concentrate for the preparation of dialysis fluid, as well as the combination of the connector, the corresponding container and the fluid preparation device. In order to simplify the handling during both the manufacturing process of such containers and the connection of such containers to the fluid preparation devices, the connector connects a first and second fluid line of the container with a third and fourth fluid line of the fluid preparation device with two laterally spaced-apart mounting elements which each incorporate one of two orifices terminating the first and second fluid lines.

Abstract: A catheter includes a proximal end, a distal end, a tubular member, and an inner member extending through the tubular member. The inner member is movable axially relative to the tubular member. The catheter also includes a seal member including a first portion and a second portion. The seal member extends between the tubular member and the inner member. The first portion of the seal member remains stationary relative to the tubular member, and the second portion of the seal member remains stationary relative to the inner member during relative axial movement between the tubular member and the inner member.

Abstract: Aseptic connector which has a body, an axially extending opening in the body, a seat surrounding the opening for receiving the connecting flange of a fitting, and a clamp for pressing the flange into the seat. The seat has a radially extending sealing surface with an annular outer portion and a conically inclined inner lip that extends inwardly and upwardly from the annular portion toward the opening.

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 laparoscopic port assembly includes a cannula unit including three cannulas each extending at an acute angle relative to a base. The cannulas are flexible for receiving respective angulated laparoscopic instruments. The cannula unit is rotatingly received in a port holder for rotation about a longitudinal axis of the holder, the holder being disposable in an opening in a patient's skin.

Abstract: Some embodiments disclosed herein relate to a medical connector having a backflow resistance module configured to prevent fluid from being drawn into the connector when a backflow inducing event occurs. In some embodiments, the backflow resistance module can include a variable-volume chamber configured to change in volume in response to a backflow-inducing event and a check valve configured to resist backflow. In some embodiments, the medical connector can include a fluid diverter configured to direct fluid flowing through the medical connector into the variable volume chamber to prevent fluid stagnation therein. In some embodiments, the medical connector includes a body member, a base member, a seal member, a support member, and a valve member.

Abstract: A connector for coupling to a base of an indwelling device equipped with a circular hub having a radius, a top surface, a side surface, and a circumferential recess defined in the side surface. The connector has a resilient assembly including a plurality of release buttons extending from the resilient assembly and may include a conduit defining a fluid pathway through the connector. Each release button has a finger contact zone and a catch. The catch is configured to releasably engage the circumferential recess. The connector is coupled by positioning the connector on the circular hub and depressing the connector until the catches engage the circumferential recess such that the connector is configured to rotate completely about the circular hub. The connector is decoupled from the hub by pressing the release buttons to reversibly displace the respective catches radially to disengage from the circumferential recess.

Abstract: An infusion catheter assembly has the ability to infinitely titrate the length of a porous fluid distribution section in situ. The infusion catheter assembly thereby provides a length of infusion that can be infinitely varied over a prescribed range, to control the effective infusion length and the rate of infusion. Using the infusion catheter assembly, a physician has the capability to treat only the length of the vessel desired, thereby preventing excessive drug/patient exposures. The porous fluid distribution section can include an array of spaced apart apertures that vary in size and/or density along the length of the porous fluid distribution section, such that the flow rate remains essentially constant for a given inlet pressure independent of the effective infusion length.

Abstract: A cannula assembly having a hollow elongate cannula with a proximal end, a distal end, and a central axis. A coiled reinforcing member is disposed along a portion of the hollow elongate cannula and is adapted to provide structural support to the elongate cannula. An intermediate reinforcing band is disposed on the elongate cannula between the proximal end and the distal end to reinforce a perforated section in the wall of the cannula and includes a forward edge, a rearward edge, at least one rib and at least one protrusion extending orthogonally from the forward edge and at least one protrusion extending from the rearward edge. A distal reinforcing band is disposed at the distal end of the elongate cannula and has a plurality of fingers that taper slightly inwardly toward the central axis of the hollow elongate cannula.