Abstract: A pumping device that can be used with currently-available pressure bag infusers is disclosed. The pumping device is hand-held and lightweight. The device is controlled by a microprocessor. Thus constant pressure to the bag is maintained through automatic adjustment of pumping and venting functions. In addition, a novel, new pressure bag infuser and a modified Luer Lock fitting for use with the pumping device are described.

Abstract: Fluid communication to an end of a catheter is afforded through a connection hub selectively attachable thereto. The connection hub includes a catheter receiving element and a fluid coupling element that are relatively rotatable coaxially between a catheter receiving condition and a catheter capture condition of the connection hub. The catheter capture condition, a compressible sealing sleeve disposed interior of the connection hub between a pair of clamping jaws projecting from the catheter receiving element is urged into sealing engagement with the exterior of the catheter, catheter is gripped mechanically through the sealing sleeve by the clamping jaws. The exteriors of each of the catheter receiving element and the fluid coupling element are formed into planar actuation handles that facilitate relative rotation of the catheter receiving element and the fluid coupling element into coplanar alignment in the catheter capture condition of the connection hub.

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: The invention concerns a telescopic device (1) comprising a first tubular element (3) and an extension member (2) displaceably arranged in an axial direction within the first tubular element (3), wherein a coupling member (16) is provided relatively displaceable to the extension member (2), between at least,—a first axial position wherein the extension member is displaceable within the first tubular element, and—a second axial position wherein the coupling member (16) engages between the extension member (2) and the first tubular element (3) limiting displacement in at least one longitudinal direction, where the coupling member (16) engages the interior of the first tubular element (3).

Abstract: A catheter proximal section is preferably formed from a relatively soft part and a relatively rigid part, and includes a proximal terminal end that defines a perimeter of an opening into a lumen of the catheter. The proximal section may further include a feature for interlocking engagement with an accessory tool. An inner surface of each of the relatively soft and rigid parts may be located opposite one another, on either side of the catheter lumen. The relatively soft and rigid parts may be included in a sealing assembly that further includes an attachment feature for removable connection of the assembly to the proximal section catheter.

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: An infusion medium delivery system, device and method for delivering an infusion medium to a patient-user, includes a needle inserter device and method for inserting a needle and/or cannula into a patient-user to convey the infusion medium to the patient-user. The needle inserter device and method operate to insert a needle and cannula into a patient-user's skin and automatically withdraw the needle from the patient-user, leaving the cannula in place and in fluid flow communication with a reservoir. The delivery device may include a base portion and a durable portion connectable to the base portion, and wherein the base portion can be separated from the durable portion and disposed of after one or more specified number of uses. The base portion supports the reservoir and the needle inserter device, while the durable portion supports a drive device for selectively driving the infusion medium out of the reservoir and into the needle and/or cannula.

Abstract: A method and device for delivering medicament such as for ameliorating pain in a patient from an injector superiorly and/or laterally and/or anteriorly towards the sphenopalatine ganglion (SPG). A device for delivering a medicament to a patient in need thereof includes (a) an injector containing a first end configured to remain outside a nasal passage of the patient and a second end configured for entry into the nasal passage of the patient; and (b) an introducer configured for engagement with a nostril of the patient and containing a passageway configured for slidably receiving the injector. The injector is moveable between a storage position preceding the engagement and an engaging position pursuant to the engagement. The device may further include a locking connection assembly that is useful in other devices.

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 vascular guidewire system includes a tubular member which at least partially encloses a core wire. A first or distal gripper is connected with a handle to grip a proximal end portion of the tubular member. A second or proximal gripper is disposed in the handle and grips a proximal end portion of the core wire. A first or distal motor is disposed in the handle and is operable to rotate the core wire relative to the outer tubular member. A second or proximal motor is disposed in the handle and is operable to move the first or distal motor longitudinally relative to the handle to thereby move the core wire longitudinally relative to the outer tubular member. The second or proximal motor is disposed in a coaxial relationship with the first or distal motor. Rotational and/or longitudinally directed forces may be manually applied to the handle to move the tubular member and core wire relative to a patient's body.

Abstract: Fluid infusion systems and fluid couplings are described herein. The infusion systems may include one or more fluid couplings used to make fluidic connection between a supply line and delivery tubing. The fluid couplings separate the functions of providing a seal around a delivery tube and retaining the delivery tube within the fluid coupling. The seal provided around the delivery tube prevents leakage around an exterior surface of a delivery tube such that fluid passing through the coupling must pass through the delivery tube rather than leak around the delivery tube. The structure used to retain the delivery tube in the fluid coupling prevents ejection of the delivery tube from the coupling due to the fluid pressures present in the coupling. The separate functions are performed by different structures within the fluid couplings.

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: A proximal terminal end of a proximal section of a catheter, preferably tapered, defines a perimeter of an opening into a lumen of the catheter and includes an exposed sealing area. A sealing assembly, that may be removed from the catheter, includes a relatively soft part and a relatively rigid part, wherein the exposed sealing area is formed by the soft part, and the relatively rigid part may include an attachment feature for removable connection of the assembly to the catheter. The lumen of the catheter, within the proximal section, may include a seal zone portion, which preferably includes a slit segment intersecting a funnel-like segment of a bore. The catheter proximal section may further include a feature for interlocking engagement with an accessory tool.

Abstract: Disclosed herein are disinfecting caps that can be used to cover and disinfect a male luer post of a medical connector when not in use or when disconnected from its female connector counterpart. The caps are configured to engage threads of the connector. The caps contain a disinfecting agent disposed in a chamber of the cap.

Abstract: Enteral safety system (ESS) may include oral dispenser having visual indicator such as barrel with measurement marks of a color. Barrel may allow content viewing. ESS may include hub for connecting oral dispenser to enteral set. Hub may have a visual indicator such as being same color as barrel's marks. Enteral tubing or set may have a visual indicator such as a lengthwise stripe same color as barrel's marks. Enteral tubing may allow content viewing. ESS may include an enteral tubing-feeding tube hub for connecting enteral tubing to a feeding tube. This hub may have visual indicator such as same color as barrel's marks. Feeding tube may have visual indicator such as a lengthwise stripe same color as barrel's marks. Feeding tube may allow content viewing. The oral dispenser, oral dispenser-enteral tubing hub, enteral tubing, enteral tubing-feeding tube hub, and feeding tubing are properly connectable by reference to visual indicators such as color matching.

Abstract: A system for transferring medical fluid includes a male Luer connector and a female Luer connector, the male Luer connector including a collar surrounding at least part of a male conical portion whose outer surface is supported against the female conical connection surface of the female Luer connector during the assembly of the connectors. The maximum inside diameter at the entrance to the collar of the male Luer connector is strictly less than the smallest outside diameter of a standard female Luer connector or one according to ISO 594-2. The female Luer connector includes a collar surrounding at least part of the female conical connection, this collar having an inside diameter greater than or equal to the outside diameter of the collar of the male Luer connector, to engage and at least partially cover the collar of this male Luer connector during the assembly of the connectors.

Abstract: A luer connector assembly is provided for enhancing the frictional engagement between medical devices such as syringes and needle assemblies. The assembly needle includes a female luer fitting having a passageway and a relatively soft, resilient member bounding the passageway. The passageway is also bounded by the body of the fitting, which is harder than the soft, resilient member. A male luer fitting inserted into the passageway engages both the soft, resilient member and the body of the female luer fitting. A method of manufacturing such a connector assembly is further provided. A first material is injected into a mold to form the body of a female luer fitting, the fitting including a passageway and a recess extending into the body. A second material is then injected such that it extends into the recess and bounds the passageway. The second material, when cool, is softer than the first material.

Abstract: A cannula connector adapted for a resealable septum component and assemblies comprising a combination of connectors are provided. The connectors are reversibly engageable and lockable to provide a fluid path between the components. Assemblies comprising the connector and various septum components are provided.

Abstract: A connection system is disclosed herein in accordance with an embodiment. The connection system includes a male component and a female component. At least one of the male component and the female component may define a tapered surface. The connection system also includes a keyed interface disposed on either the male component or the female component. The keyed interface is configured to prevent the male component and the female component from unintentionally being coupled with a non-conforming connection system component.

Abstract: Catheter (1) for vascular access comprising a cannula (2) having at least one first lumen (21), at least one first connection tube (3), and a connection molded simultaneously on an end of the cannula (2) and on at least one part of the first connection tube (3) and manufacturing process comprising the following stages: taking a cannula (2) having at least one first lumen (21), taking one first connection tube (3), placing in a mould one end of the cannula (2) and one end of the first connection tube (3), injecting into the mould a molding material to obtain the connection (4) between the end of the first connection tube (3) and the end of the cannula placing the first lumen (21) and at least the first tube (3) in fluid communication and device for implementing the manufacturing process.

Abstract: A device detracts fluid from a flow line into a repository for temporary storage and later use. Before an infusion set is changed, medication from the infusion set is detracted into the repository, where it is temporarily stored. Once the new infusion set is connected, medication is dispensed from the repository into the flow line of the new infusion set. The device thus reduces or eliminates waste of medication that was in the flow line of the infusion set, by saving the medication in the repository while the infusion set is being changed.

Abstract: The system has a male tubing fitting extending along a longitudinal axis. The male tubing fitting has a first internal bore and an end portion including a male plug. The system also has a female tubing fitting that has a second internal bore configured to receive the male plug. Also, the system has a collar disposed about the male tubing fitting and positioned to slide freely along the longitudinal axis from a first position to a second position. In the first position the male and female tubing fittings are unlocked with respect to each other such that the male plug is removably insertable into the second internal bore of the female tubing fitting. In the second position the male and female fittings are locked with respect to each other such that the male plug is prevented from being removed from the second internal bore of the female tubing fitting.

Abstract: An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled.

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.

Abstract: An adapter bridging 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. Once the medication providing device is coupled to the core, additional rotational movement, in either direction, of the medication providing device would only cause the core to rotate freely relative to the housing shroud, thereby preventing the medication providing device from being removed from the adapter. The inner shroud has a catch mechanism that enables it to mate readily with a connector when rotated in one direction.

Abstract: An adapter for a medical receptacle having a skirt with an outside diameter and a threaded inside diameter, and a tapered post within the skirt, the adapter includes a proximal end portion having a threaded surface including at least one thread configured to threadingly engage the threaded inside diameter of the skirt, a distal end portion having a surface portion and a cylindrical recess, a conduit positioned between the tapered recess and the cylindrical recess such that the conduit is in fluid communication with both the tapered recess and the cylindrical recess; and a longitudinal axis. The proximal end portion includes a tapered recess defined by a wall, a chamfer, and a seat and the surface portion includes a means for gripping, which in one embodiment may be at least two wings.

Abstract: A male luer connector is disclosed, the male luer connector being attached to a first tube and connectable to a female luer connector for providing a flow channel from said first tube to said female luer connector. The male luer connector includes a male luer part, which includes a tapered outer peripheral wall, a side wall, and an outlet opening. A tube member is also provided, the tube member having a flow channel therein. The tube member has openings at first and second ends thereof, the first end being movably inserted into an inner space of the side wall and the second end being connected to the first tube. The tube member further includes a male luer part sealing arrangement for sealing the outlet opening.

Abstract: Body pressing surfaces of A and B members at which a body of the packing is to be pressed come into contact with the body of the packing, and the body starts to be pressed. Then, projections of the packing are pressed with a delay from the pressing of the body because of gaps provided between the projections of the packing and projection-pressing surfaces at which the projections of the packing are to be pressed.

Abstract: A device and method for preventing an occlusion of a catheter including a catheter adapter and a catheter where a flexured portion of the catheter is supported by a bending surface of the catheter adapter. The flexured portion of the catheter may also include a maximum insertion length mark and/or a flexible support member to support and strengthen the flexured portion of the catheter against occlusions. A bending surface is provided over which a flexured portion of the catheter may gently bend to accommodate the transition of the catheter from the catheter adapter to the insertion site without occluding the catheter.

Abstract: A connecting system for components through which fluid flows for medicine and medical technology, in particular infusion or transfusion tubes, selector valves, multi-way distributors, injection equipment such as needles, accesses or the like, and combinations thereof, comprising a female tubular receptacle, which comprises an inner receiving section and an outer first fixing section, and/or a male tubular plug element for reception in the female receiving section and an outer second fixing section, which cooperates with the first fixing section for fixing the connecting system. The surfaces of the connecting system that come in contact with the fluid are produced at least in some sections from amorphous copolyester. Use of amorphous copolyester for producing a corresponding connecting system.

Abstract: In an apparatus having at least one first hollow element for conducting a fluid having a connection element, to enable and facilitate a simple and reliable connection to a second hollow element, a snap-in element of the connection element having a latching surface which contacts an abutment surface in a connection state with the second hollow element is made as a radially widenable snap-in ring.

Abstract: A flow component for medical infusion/transfusion lines includes a tubular body having a side inlet connector, housed in a fluid-tight way in which is an elastic sealing element that can be traversed by a fluid introducer. The elastic sealing element has at least one axial cavity, which defines, for traversal by the fluid introducer, a diaphragm of small thickness.

Abstract: A syringe adapter tool facilitates inline connection of a syringe with a catheter lumen, as well as torque transfer between the syringe and catheter. The adapter tool may further facilitate passage of an instrument through a seal zone portion of the catheter lumen, which seal zone portion is located in a proximal section of the catheter.

Abstract: A medical connector, of a female luer type, comprises an external tubular body (4) which contains an internal tubular body (2) free to rotate about an axis thereof. The external tubular body exhibits a screw-coupling surface. The internal tubular body exhibits a conical luer seal surface. An insert (5), which has a pawl (9) snap-fitted in a window (8) afforded on the external tubular body, constrains the two tubular bodies solidly to one another, in an axial displacement direction. The connector is used to connect a blood line to a blood port of a dialyser, preventing the blood line from twisting on itself and kinking.

Abstract: Cannula and handle systems and cannulas having substantially continuous interior pathways or channels are provided. The interior pathway may extend from the inlet to the cannula to the outlet, such that tissue collected at the inlet is carried to the outlet without contacting other components. Moreover, the substantially continuous nature of the interior pathway, with an absence of drop-offs, blind pockets or other discontinuities, facilitates cleaning. In addition, inlet holes are sized to promote the transfer of tissue through the channel to the outlet, and to the avoidance of damaging collected tissue.

Abstract: A connector apparatus includes first and second mating connectors that can be joined to make a fluid connection. The connectors are constructed to discriminate improper connectors so that no fluid tight connection can be formed with improper connectors. The connector apparatus can be used with a system for compression therapy to prevent deep vein thrombosis.

Abstract: The invention relates to a secure connector set for a liquid circuit, including: a male connector and a female connector, each including a proximal coupler and a distal coupler, the distal coupler of each connector defining a passage and including a tubular part, in which a connection member fixedly mounted on the proximal coupler extends coaxially, and an elastically deformable membrane which is substantially tubular, closed at a distal end by a membrane body, and movable between a downstream plugging position, in which the membrane sealingly covers a free end of the connection member, and an upstream connection position, in which the connection member passes through the membrane, in which the tubular part of the distal coupler of the male connector is designed to be inserted, upon connection, into the tubular part of the distal coupler of the female connector, and wherein, in a downstream plugging position, for the male and the female connectors, the membrane sealingly blocks the passage in the distal coupl

Abstract: A medical catheter assembly including a multi-piece connector. In one embodiment, the medical catheter assembly is a PEG implanting assembly comprising a tubular dilator and a silicone feeding tube having an internal bolster at its rear end. The assembly also comprises a multi-piece connector comprising an inner ring, a fitting and an outer ring. The inner ring has an outer diameter greater than the inner diameter of the feeding tube and is coaxially disposed within the feeding tube by a friction-fit. The fitting comprises a front portion, an intermediate portion and a rear portion, the intermediate portion including a shoulder having an outer diameter greater than the inner diameter of the feeding tube. The front portion of the fitting is inserted through the rear end of the dilator and is secured to the dilator by a plurality of barbs.

Abstract: A connecting structure for a connector in which a male-side connector and a merging pipe are connected by screwing together a female screw having protrusions formed on the inner peripheral surface of a lock ring and a male screw comprising protrusions formed on the outer peripheral surface of the merging pipe is provided with engaging recess parts on the female screw and engaging projections on the outer peripheral surface of the merging pipe which are able to engage with the engaging recess parts whereby when the male screw and the female screw are screwed together to reach an appropriate screwed state, the engaging protrusions engage with the engaging recess parts.

Abstract: A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula.

Abstract: Devices having male connectors for preventing connection to non-compatible female connectors are described. An exemplary male connector includes an elongate tip and a collar disposed coaxially around the elongate tip including a plurality of ribs disposed on either an inside surface or an outside surface of the collar for preventing entry of a non-compatible female connector into a channel formed between the elongate tip and the collar. One or more embodiments pertain to a device with a male connector and a compatible female connector including a threaded portion for engaging a corresponding threaded portion of the male connector.

Abstract: Apparatuses and methods for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump are provided. A base is provided which is adapted to receive a reservoir and engage a cap. 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 is in a first detent position, and the needle pierces a reservoir septum when the base is in a second detent position. When the reservoir, the base and the cap are connected to form an integrated unit, this unit is then capable of being inserted and secured in the infusion pump housing. In some embodiments, an integral connector couples directly to the reservoir.

Abstract: A catheter connector system, including a catheter hub and a coupling member. The catheter hub includes a cannula portion connected to a housing portion and a distal interface including a tapered seal post fixed to the housing portion, a deformable sealing element surrounding the tapered seal post, and a retention collar surrounding the sealing element. The coupling member includes an opening to receive the distal interface, an inwardly extending portion to engage the retention collar, and an actuating member to engage the deformable sealing element.

Abstract: A medical device including: a cannula, a first tube joined to the cannula; a second tube joined to the cannula; and a unitary fastener secured to the first tube, cannula and second tube, the fastener being subject to opposing forces from the first and second tubes.

Abstract: A catheter connection system is disclosed. In one embodiment, a catheter connection system may include at least two components and a deformable sealing element positioned between the at least two components configured to allow, upon deformation, fluid flow through the at least two components. In another embodiment, the catheter connection system may include a sealing element positioned between at least two components, wherein the components are coupled to one another by a locking member.

Abstract: The present invention relates to a lockable connection system for components in medicine and medical technology that have fluids passing through them with a female, tube- or cone-shaped receptacle (11, 21, 41, 51) having an interior receptacle section and an external first fixing section, and a male, tube- or cone-shaped insertion element (12, 62, 72, 82, 92, 112, 132, 152) to be accommodated in the female receptacle section (11, 21, 41, 51) and an external second fixing section (14, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150) interacting with the first fixing section for fixing the connection system. The invention is characterized in that the first or second fixing section has at least two radially outward-protruding lobes (13, 13?, 23, 23?, 33, 33?, 43, 43?, 53, 53?), the radial external edge of which lies on a diameter greater than 7.83 mm and/or whose axial thickness at the base is greater than 1.3 mm.

Abstract: A flared strain relief member for medical device delivery systems for stents, prosthetic valve devices, and other implantable articles inside a patient's body are provided. An elongate outer sheath has proximal and distal end portions defining a passageway, and the proximal end portion having an outer layer including melt bonding material. A strain relief member has a tubular first end portion of a first outer diameter and a flared second end portion of a greater second outer diameter. The strain relief member has an inner engaging surface that includes melt bonding material, at least a portion of which disposes concentrically about, and melt bonded to, the outer sheath proximal end portion melt bonding outer layer. The strain relief member second end portion is operatively coupled between a handle first connector and handle second connector. Methods of making a flared strain relief member for medical device delivery systems are also provided.

Abstract: An improved injection site (12) for infusion of parenteral fluids and the like is provided, having a pressure-actuated valve (20) and a novel split septum unit (24), which effectively prevent reflux of blood into the assembly (10). The septum unit (24) includes a resilient split septum body (64) which is precompressed so that the septum body (64) is caused to protrude proximally (78) upon insertion of a cannula (16). Consequently, upon removal of the cannula (16), there is essentially no “drumming” or creation of friction-induced negative pressures sufficient to generate blood reflux. The preloaded septum body (64) also has its proximal surface (74) essentially flush and coplanar with the adjacent proximal end (66b) of the tubular septum holder (66) to enhance the cleanliness of the unit (24).

Abstract: An apparatus comprising a torque wire connected to an imaging probe; and a torque limiter defining a bore, a first end of the torque limiter being in mechanical communication with a motor, a second end of the torque limiter being in mechanical communication with the torque wire, the torque wire being disposed through the bore of the torque limiter. The torque limiter comprises a member defining at least one cutout which causes the torque limiter to break when rotational force on the torque wire exceeds a predetermined amount, thereby decoupling the motor from the torque wire.

Abstract: A connector includes a male connector section having a cavity, a female connector section having a cavity to which another male connector section the same as the male connector section can be connected, a male lock section or a female lock section, disposed adjacent to the male connector section so that the connection direction thereof is parallel to that of the male connector section, a female lock section disposed adjacent to the female connector section so that the connection direction thereof is parallel to that of the female connector section, and to which another male lock section the same as the male lock section can be coupled, or a male lock section disposed adjacent to the female connector section so that the connection direction thereof is parallel to that of the female connector section, and to which another female lock section the same as the female lock section can be coupled, and a seal member formed from an elastic material, for maintaining liquid-tightness of the connection between the other