Abstract: A dialysis system includes a dialysis instrument including at least one pump actuator; a disposable cassette operable with the at least one pump actuator; a plurality of supply containers connected fluidly to the disposable cassette; and a cart which includes a rotatable bearing plate onto which the instrument and supply containers are loaded, the bearing plate allowing a patient to turn the instrument and supply containers relative to the cart for selective access to the instrument or the supply containers.

Abstract: A system and method for creating a medicated atmosphere in an organ, or body cavity is disclosed. The system includes a flexible aerosolization catheter that can be manipulated during use, a device for the introduction of the aerosolization catheter, a medication delivery apparatus configured to control delivery of a medication to the catheter, a gas delivery apparatus in communication with the catheter, a gas pressure relief apparatus configured to relieve pressure in the organ or body cavity, and a central controller. The method includes providing insufflation gas and an aerosol of medication to an organ or body cavity while controlling overall pressure in the organ or cavity. The method may also include re-entering a patient through at least one port to apply gas and an aerosolized medicament, in either a post-operative procedure or in a chemotherapy context.

Abstract: A system and process for providing safety limits on the delivery of an infusion formulation by an infusion pump system in response to a sensed biological state. The safety limits may comprise user-initiated event signals corresponding to events that may significantly affect the biological state. The safety limits may further comprise user-initiated event ranking signals for respective events which specify a degree, quantity, or measure for the respective event. The user-initiated event and event ranking signals may be communicated to a computing element associated with the infusion pump by an associated communication device having a user interface which comprises a plurality of user-selectable operators for entering information about the events and event rankings.

Abstract: An infusion pump uses sensors and a computer program to detect tubing in a tube-loading section of the pump. The pump and the computer program also measures one or more of the tubing outer diameter, outer circumference, inner diameter, inner circumference, and tubing wall thickness. The infusion pump utilizes proximity sensors, such as an ultrasonic sensor, a capacitive sensor, or even an air-in-line sensor to detect proximity between two infusion pump surfaces, such as the surfaces that clamp the tubing in the pump, to determine thickness. At least one of the clamping surfaces is equipped with sensors to indicate contact length of the tubing with the surface. Using these measurements, the tubing wall thickness and inner diameter can be determined. Knowing the actual tubing inner diameter, increased volumetric accuracy is possible, up to a three or four percent improvement over present measurements.

Abstract: A medical device includes a sensor that is configured to measure a property of an outer layer of an anatomical body surface. The sensor includes a source probe configured to stimulate a local surface of the outer layer of an anatomical body surface. The sensor also includes a detector configured to measure a response of the outer layer resulting from the source probe stimulation. A controller coupled to the source probe and the sensor drives the source probe using a tailored stochastic sequence and determines the property of the outer layer using the measured response received from the detector. The sensor can be used with medical devices, such as drug delivery devices including microneedle transport devices and needleless injection devices.

Abstract: A housing of the injector is made from a thin-walled sheet-metal part. The sheet-metal part has at least two branches or legs. Each branch has, at the free end thereof, an angled retaining element or a recess as a means of receiving the cylinder of a cylinder/piston unit. The branches are elastic flexural beams which, in the middle area, are each bent in a Z-shape or S-shape to form a supporting portion for the piston-actuating ram. The contact zone situated between an individual supporting portion and the piston-actuating ram represents a wedge gear pairing that forces the respective branch outwards. The trigger unit comprises at least a trigger element which is slidably supported on the metal sheet, wherein the support section or, respectively the contact sections extend outwardly into longitudinal grooves. The branches may be provided with a locking tongue to engage corresponding openings in the trigger element to lock the housing in position as desired.

Abstract: Needle-free hypodermic jet injection devices having an actuation system to effect an injection from a drug delivery system. The actuation system includes an injection force assembly adapted to transmit a driving force to the drug delivery system. The actuation system further includes a trigger assembly adapted to alter the actuation system between a plurality of configurations including a fired configuration in which the injection force assembly transmits a driving force to the drug delivery system. In some embodiments, the device has a recoil restriction system including a restriction member adapted to couple the recoil restriction system to the trigger assembly and a recoil member coupled to the injection force assembly and movable relative to the restriction member. The restriction member limits movement of the recoil member once the recoil member moves a predetermined distance relative to the restriction member.

Abstract: This single unit, known as a self flushing duel compartment container, can be used with or without an electrical feeding pump. It will perform a dual, fluid composition administration process, which would usually require two separate units to perform. Thus eliminating the need for the use of a secondary unit needed to follow the administrations seen in the existing products used primary/secondary fluid delivery technique. Two separate compartments are capable of retaining their own fluid composition within the boundary of it's own separate compartment separated by an air tight, sealed section of the single unit that divides this single unit into two separate compartments. Each compartment leads into a section of thermoplastic tubing, which eventually forms a pre-attached junction tubing similar to the “Y”, shaped tubing that becomes a single much longer section of thermoplastic tubing.

Abstract: A catheter is disclosed providing a balloon catheter having a distal tip that is flexible while additionally incorporating high column strength. The present invention additionally provides a distal tip region that accommodates for various sized guidewires. In preferred embodiments, the distal tip region is initially configured for accommodating the passage of 0.12-inch guidewires only. Through specific manufacturing processes, however, the distal tip is modified so that it also may be expanded to accommodate the passage of 0.14-inch guidewires. In additional preferred embodiments, an elastomeric sleeve is disposed over the modified distal tip to allow the tip to return to the initial 0.12 -inch accommodating profile when the larger 0.14-inch guidewire is withdrawn from the catheter.

Abstract: A non-compliant medical balloon may be changed from a deflated state to an inflated state by increasing pressure within the balloon. The non-compliant medical balloon is composed of a matted fabric layer composed of at least two matted fabric fibers forming an angle. The angle remains substantially unchanged when the balloon changes from a deflated state to an inflated state.

Abstract: A disposable safety injection apparatus includes a liquid medication tube, a syringe needle, a push rod, and a tube ring. The syringe needle is connected to an insert tenon at a front end of the liquid medication tube. The insert tenon includes a connecting portion having concentric C-shape lacerable slot and circular lacerable slot respectively disposed at a connecting position of a top wall at the front end of the liquid medication tube and the connecting position of the top wall and an external side of the tube ring. A rod column having a latch portion is extended axially from the front end of the body of the push rod, passed through and fixed to the tube ring, such that the rod column can be slidably contained in liquid medication tube. The push rod is pushed forward to press the tube ring against top wall and latch the latch portion to a connecting portion in the insert tenon.

Abstract: The present invention relates to a device for creating a vascular access for extracorporeal blood treatment including an electrically conductive puncture needle with a proximal endpiece, a distal endpiece, and a base body made of electrically non-conductive material into which the distal endpiece is inserted. In a properly arranged vascular access, the base body, including an electrically conductive contact element, lies on the skin of the patient, when the puncture needle is located within the vessel of the patient. A disconnection or dislocation is detected by the impedance between the electrically conductive puncture needle and the electrically conductive contact element being measured and compared to a limit value. If the impedance measured is within predetermined limits, this indicates a properly arranged vascular access. A disconnection or dislocation of the puncture needle leads to a strong variation in the impedance.

Abstract: Some embodiments of a medical infusion pump system include a pump device having a flexible pushrod that can adjust from a curved configuration to a generally straight configuration. The flexible pushrod is part of a drive system of the pump device so that the flexible pushrod can be controllably and incrementally advanced toward a medicine reservoir to incrementally dispense the medicine therein. In particular embodiments, the flexible pushrod may comprise an anti-rotation mechanism, an anti-torsion mechanism, or a combination thereof.

Abstract: Embodiments of the invention are directed to methods and systems associated with a disposable dispenser (100, 200) of therapeutic fluid. Preferred embodiments having a small size of less than about 75 mm in length, less than 50 mm in width and less than about 10 mm in thickness and may be releasably attached to the body (B). In one embodiments, the dispenser draws fluid from a flexible volume-conformable reservoir (4) and operates a dosing and metering pump (6, 61, 62, 63) incorporating a motor to deliver fluid through a fluid delivery tool (8, 81, 82). Disposed on the housing bottom (2B) is a peel-off tape (22) that when removed, electrically connects a power supply (18) to power the operative components (3) of the dispenser into operation, exposes an adhesive (28) and a window (21) in the housing (2), and allows the fluid delivery tool (8) to extend for insertion into the skin (S).

Abstract: An apparatus includes a housing, a medicament container, an actuator, and a biasing member. The actuator is configured to move the medicament container within the housing when the actuator is moved from a first configuration to a second configuration. The actuator includes a gas container and a puncturer. When the actuator is in the first configuration, a portion of the puncturer is disposed apart from the gas container. When the actuator is in the second configuration, the portion of the puncturer is disposed within the gas container. The gas container has a longitudinal axis offset from a longitudinal axis of the medicament container. The biasing member is configured to bias the actuator toward the second configuration.

Abstract: It may desirable to monitor or control a pump remotely. For example, the pump may be positioned near the patient, with remote control or monitoring of the pump occurring in a control room. In one exemplary embodiment, the pump is used in an MRI environment. In another exemplary embodiment, the pump is used in a hyperbaric chamber. The pump may monitor one or more physiological parameters and transmit them to the remote. The pump may also transmit information relating to the pump's operation. The pump may send the device and/or physiological data using one or more packets. The packets may consist of low priority sequential packets and high-priority asynchronous packets. The high-priority packets may enable the real-time monitoring of a patient's heart beat or other physiological parameter.

Abstract: The miniaturized injection device (1) for medical use comprises a tube (2) extending along a certain axis (A-A) and in which there is disposed at least one reservoir (12) for receiving a medicinal substance, the reservoir being connected to at least one needle (14). The needle is movable in the tube (2) along said axis (A-A) and the injection device (1) further includes a pump (13) interposed between the needle and the reservoir. The pump is controlled by a switch (21) that operates in response to the needle (14) moving in the tube along said axis (A-A).

Abstract: An assembly and method for percutaneous placement of a catheter comprising an elongated hollow catheter having a distal end and a reduced cross-section portion at a proximal end thereof. An introducer needle is slidably mounted over said catheter. The introducer needle has an elongated slit adapted to slide over the reduced cross-section portion to separate the needle from the catheter. A syringe may be attached to the proximal end of the catheter. Also, a valve may be attached to the catheter to permit easy collection of fluid.

Abstract: A laparoscopic insufflation device is provided in the configuration of a coil with a blunt tip. The device is capable of passing through the abdominal wall without cutting tissue, and exiting the abdominal wall substantially parallel to the inner surface. While rotation of the coiled device results in forward movement through the abdominal wall, a counter force can be applied to the device to create a safety space between the wall and the interior organs. With the blunt distal tip, parallel exit angle, and safety space, there is substantially no threat to the interior organs during placement of the device. Further space can be generated with the use of pressured gas to produce an abdominal cavity for the subsequent placement of trocars. By rotatably attaching the coiled insufflation device to a trocar, the advantage of a counter force can be used not only to establish the safety space but also to pull the trocar into the abdominal wall with a counterforce which resists tenting.

Abstract: An access device places a medical article within a body space of a patient. The device has a needle that includes an elongated body and a needle hub. The device further includes a dilator disposed on and slideable along the elongated body of the needle and a medical article. The medical article is disposed on and slideable along the dilator. A track extends in a proximal direction from the dilator. The needle hub slides along at least a portion of the track between a first position and a second position. The device further includes a locking mechanism operably disposed between the track and the needle hub so as to inhibit further axial movement of the needle in the proximal direction when the needle hub is in the second position.

Abstract: A tearaway introducer sheath assembly (100,200) having an integrated valve (300). The valve is seated within a valve housing (222) defined by the hub portion (200) of the sheath (200). The valve (300) includes a pair of distally extending opposed side walls or flaps (324) extending to converge at a distal tip (328) having a virtual opening (334) therethrough. The valve further includes a pair of tensioners (340) along outer surfaces of the opposed side walls (324) that extend radially outwardly to engage and bear against the interior valve housing surface (230) to press the opposed side walls (324) together at the distal tip (328) for sealing, both when a dilator extends through the valve and sheath and afterward upon removal of the dilator.

Abstract: This invention provides devices and methods for insertion of a catheter into a vessel. The devices include coaxial slidably mounted needle, dilator and catheter components. The methods include piercing a vessel with the needle component, dilating the pierced hole with the dilator component, retraction of the needle component, insertion of the catheter and withdrawal of the dilator.

Abstract: An anchoring system for securing a dialysis catheter to a patient comprises an anchor pad and a retainer. The anchor pad is attached to the skin of the patient by an adhesive layer on one side of the pad. The retainer is disposed upon the surface of the anchor pad opposite the adhesive layer and includes a base and a cover and a adhesive spot. A groove upon the base is arranged to receive a Y-site portion of a dialysis catheter where the lumens merge distal to the insertion site. A post also protrudes from the base to the cover at a position which will be disposed between the two distal branches of the dialysis catheter. The cover closes over the base, securing the Y-site between the groove and the post. Closing the cover also places at least a portion of the catheter in contact with the adhesive spot. This contact between the retainer, adhesive spot and catheter thereby inhibits inadvertent motion of the catheter upon the patient.

Abstract: A universal device for securing a catheter on a patient includes a base which optionally has one or more locating elements for positioning or securing a catheter or catheter fitting of various shapes or sizes. The base optionally includes a recessed or flat receiving area defined by locating elements arranged in any configuration suitable to hold or receive a catheter or catheter fitting, e.g., in a tapering or V shaped formation. Additional locating elements may be positioned elsewhere on the base for receiving or holding a flange or wing of a catheter fitting and preventing its movement in various directions. The base optionally has an angled surface to maintain the desired angle for catheters or catheter fittings in a patient. A cover is removably or permanently connected to the base and may optionally have one or more top openings for receiving tabs or extensions of a catheter fitting.

Abstract: A device for storing and administering active substances, including a plurality of reservoirs for respectively accommodating at least one active substance. The reservoirs are disposed in a radial manner with an end face facing the direction of the center of the device. A mechanism is mounted in the device to open and close the reservoirs. A needle-free injection device delivers at least one active substance to a user.

Abstract: The present disclosure describes a needle guard device or system that can be used with drugs requiring reconstitution. The needle guard is preferably a passive needle guard that can be used during reconstitution without activating the safety mechanism. Following administration of the medication, the needle guard shields a user from inadvertent needle sticks by extending a protective shield over the needle.

Abstract: The syringe is intended for one-off use and has a syringe barrel (1), a barrel stopper (12) which can be displaced in the syringe barrel (1) by means of a plunger rod (11) and a needle unit (25) accommodated in the syringe barrel (1). The plunger rod (11) and the needle unit (25) are connected to one another by coupling means (20, 40) in order to retract the needle unit (25) into the syringe barrel (1) after the injection. As proposed by the invention, the needle unit (25) comprises a needle holder (26) made from plastic surrounding an injection needle (27) made from stainless steel along part of its length, which is closed off from an interior of the syringe barrel (1) containing an injection solution (50) by means of a seal insert (36) made from pharmaceutical rubber through the injection needle (27) extends from the rear end. As a result of this feature, an injection solution (50) contained in the syringe is in contact exclusively with permitted materials and the syringe can therefore be stored pre-filled.

Abstract: To provide a syringe barrel and a syringe capable of allowing an operator to feel the amount of injected medical solution or the inserting distance of a piston by a difference in sliding resistance when an injection operation is performed. A syringe 1 includes a syringe barrel 11 which has an inner surface provided with a structure in which a sliding resistance F is changed step by step upon sliding a piston 32. The syringe barrel 11 includes steps which are formed at one or two or more positions of the inner surface in the axial direction so as to face from the rear end to the front end or from the front end to the rear end, and which include edges formed along the circumferential direction.

Abstract: A dressing (2) and an apparatus (1) comprising the dressing, for cleansing the wounds (5) in which an irrigant fluid from a reservoir (12) connected to a conformable would dressing and would exudate from the dressing are moved by a device (18) (which may be a single pump or two pumps) for moving fluid through a flow Path (6, 7, 9, 10) which passes through the dressing with a means for providing simultaneous aspiration and irrigation of the wound, to provide a desired balance of fluid at a controlled nominal flow rate that removes materials deleterious to wound healing, while distributing materials that are beneficial in promoting would healing over the would bed.

Abstract: A surgical sponge detection system includes a plurality of surgical sponges (2) having radio frequency identification tags (1) securely attached thereto and a non-optical hand-held reader (40) for detecting the sponges by detecting the tags (1). Also disclosed is a device (30) for automatically counting, weighing, and calculating blood loss contained within, soiled surgical sponges (2) which includes a cabinet with an opening (3) at the top through which sponges (2) are deposited, a reader (6) which scans each sponge (2) entered and determines sponge type from a tag (1) affixed to each sponge (2), and a disposable bag (8) into which the sponges (2) are deposited.

Abstract: Drainage belongs to medical equipment, particularly to medical tools and is specified for drainage of cavities. Drainage comprises a first tube, an additional tube, which is fixed upon it, a unit of the clot's splitter and the splitter's fixing element. The additional tube has a smaller diameter with an opening, inside which the conductor is mounted, a unit of clots splitter is installed on the working end of the drainage, it comprises a cylinder, a tube with an opening, placed on it, which is the continuation of the additional tube of the drainage and a spring with a cutter inside the cylinder. A cutter is located diametrically inside the working head, while in the end of the wall of the first tube and the splitter's unit comprises a channel, inside which splitter's fixing element was led, its working end is inside the unit's cylinder and fixes the splitter.

Abstract: A disposable inner bag liner for an ostomy appliance, the inner bag liner being adhered to a release liner prior to attachment to an outer receiving member. The release liner includes an alignment element and a gripping element. An ostomy appliance including the aforementioned inner bag liner with the gripping element and/or the alignment element is also provided, along with a method of application of the inner bag liner.

Abstract: A mounting structure for installation at a corporeal port opening. The mounting structure includes mounting structure for installation at a corporeal port opening, such mounting structure including a blowmolded article comprising enlarged cylindrical sections interconnected by tube segments, adapted to engage the corporeal port opening at a tube segment intermediate the enlarged cylindrical sections and with the enlarged cylindrical sections being in abutting contact with internal and external corporeal surfaces surrounding said port opening. The mounting structure is useful employed for anchoring of a therapeutic device such as an ostomy bag at a corresponding port of the body, with the enlarged sections of the device providing effective anchoring of the mounting structure and permitting the mounting structure to be comfortably worn by a patient during therapeutic intervention.

Abstract: The absorbent article provides a signal viewable from the top surface of the absorbent article which gives a perception of depth within the absorbent article. This creation of depth perception is accomplished by the use of at least two tones within a color and/or by the use of multiple tones and multiple colors operating together to create a perception of depth within the absorbent article.

Abstract: Disclosed is a unitary absorbent structure including a fluid acquisition stratum; a fluid distribution stratum; and a fluid storage stratum between the acquisition stratum and the distribution stratum. Each of the acquisition, distribution, and storage strata are in fluid communication with each other.

Abstract: A single adjustable sanitary napkin or panty liner includes both folding panels and tear-away panels to adjust the width and/or the length to a particular woman or outfit. The panels may be folded and/or torn away to adjust the shape and the size of the sanitary napkin or panty liner. Adhesive strips may be provided to retain folded panels. Thus a single sanitary napkin or panty liner fits the needs of a variety of women and outfits.

Abstract: A high-density region-containing sheet having a high-density region and a low-density region, a sheet member produced by joining the high-density region of the high-density region-containing sheet to an elastic member, and a disposable diaper using the sheet member as its chassis are provided. A sheet in a soft state by imparting preheat is pressed between a pair of opposed shaping rolls and having a toothed region and rotatable. Thus, a high-density region-containing sheet where high-density regions and low-density regions are formed is produced. Such two high-density region-containing sheets are joined through an extended elastic member to form a projection/recess pattern. In such a way, a high-density region-containing sheet can be produced. A sheet member in which at least one of two sheets is a high-density region-containing sheet, the high-density regions are joined through an extended elastic member, and a projection/recess pattern can be formed when the elastic member is contracted is produced.

Abstract: Folded disposable pants which include an outer wear sheet of pants shape and an absorbent main body adhered to a skin-contacting surface side in the outer wear sheet, wherein elastic members are added at least to circumferences of a waist opening and a leg opening. The folded disposable pants are formed by folding back a crotch part of the disposable pants over a center pants part on the upside of the crotch part, folding back a left lateral part and a right lateral part of the pants over the center pants part, and then folding back an upper pants part in which the left and the right lateral parts of the pants are overlapped with each other, over a downside part thereof.

Abstract: The present invention provides an absorbent article having a composite sheet with a plurality of gathers on an inner surface facing a wearer's body, which fits and adheres comfortably to the wearer's skin. The composite sheet is provided which includes a stretchable non-woven fabric which expands and contracts in at least one direction, a non-stretchable non-woven fabric, a junction which binds intermittently the stretchable non-woven fabric to the non-stretchable non-woven fabric in the stretching direction, and a plurality of gathers which is formed by loosening a unbounded area of the non-stretchable non-woven fabric in a contracted state, and is arranged along a direction intersecting the stretching direction, in which an apex of each gather does not reach the neighboring gather when the gathers lean to one side of the stretchable direction.

Abstract: Skin antiseptic composition dispensers and methods of use are disclosed. The skin antiseptic composition dispenser may include a container with one or more walls that are substantially impermeable to ethylene oxide gas during normal ethylene oxide sterilization processes. In some embodiments, the container may include flexible walls free of metallic foil barrier layers. The containers may also include one or more vents in addition to one or more openings used to dispense the skin antiseptic composition within the container. The dispenser may include an applicator with a hydrophilic foam.

Abstract: A device and method for determining at least one infusion and/or injection region for infusing and/or injecting a medical drug into a heterogeneous body structure in order to achieve a distribution of the medical drug in a desired target region of the heterogeneous body structure is provided. The device and method provide at least one property of the heterogeneous body structure that influences the spatial distribution of the medical drug in the heterogeneous body structure; and determine the at least one infusion and/or injection region from which the medical drug is to be transported through the heterogeneous body structure to the at least one target region as a function of the at least one property of the heterogeneous body structure and a position of the desired target region.

Abstract: An apparatus is provided. The apparatus includes a tube having a first end and a second end. The second end prevents access to an inner wall of the tube. Further, the apparatus includes a valve operably connected to the first end of the tube and configured to provide access to the inner wall of the tube to a guiding member inserted through the valve. The guiding member positions the tube in an umbilical vessel of an umbilical cord prior to occlusion of the umbilical vessel so that the tube remains within the umbilical vessel after occlusion of the umbilical vessel.

Abstract: Devices, systems, and methods for myocardial infarct border zone reinforcement. In at least one embodiment of a suction/infusion catheter for facilitating myocardial infarct border zone reinforcement, the catheter comprises one or more apertures defined along a portion of the catheter at or near a distal end of the catheter, a first configuration when the suction/infusion catheter is at least partially extended from a delivery catheter, and a second configuration when the at least one suction/infusion catheter is positioned within the delivery catheter, the second configuration different from the first configuration, wherein the suction/infusion catheter, when introduced into a pericardial space surrounding a heart at or near a myocardial infarct border zone, is operable to inject a glue-like substance through a lumen of the suction/infusion catheter and out from the one or more apertures to deliver the glue-like substance into the pericardial space at or near the myocardial infarct border zone.

Abstract: An infiltration cannula and method of using the infiltration cannula during a tumescent infiltration procedure are disclosed herein. The infiltration cannula may have an outwardly flaring hub which may be wedged into an adit of a patient to minimize leakage of fluid being infiltrated into the patient. Also, the infiltration cannula may be utilized to hydrate a dehydrated patient by a medically untrained person. The infiltration cannula may also be used to deliver an antibiotic/vasoconstrictive drug solution to minimize surgical site infections.

Abstract: A catheter is configured to prevent kinking of a catheter during handling or mounting of a pressure device. The catheter has a proximal end of its catheter shaft that is provided with a bending section having a flexibility greater than that of the section of the catheter shaft joining the proximal end.

Abstract: The present invention aims at offering: a syringe connectable to a port in a fixed manner as well as capable of demonstrating high operational performance even in the case of direct connection where a connector is not used; a connector used for the syringe; and a syringe able to attach the connector thereto. For the attainment of the above objectives, the medical syringe of the present invention is a medical syringe including a cyrindrical connection supporting member which enhances the holding force of a luer part inserted into a port when the medical syringe is connected to the port. The connection supporting member is set by sliding along the luer or a syringe body in a state of being movable between a first position near a tip of the luer and a second position away from the tip of the luer. The medical syringe is characterized in that, when the connection supporting member is moved to the second position, the tip of the luer part is exposed.

Abstract: An adapter assembly (120) for connecting a catheter assembly (50,52) to a tunneler (110) having a generally tubular body (122) having a first end (124), a second end (126) and a longitudinal axis (128) extending therethrough between the first end and the second end. The first end (124) of the adapter is constructed to engage the proximal end (114) of a trocar (110). The second end (126) of the adapter is constructed to releasably engage at least one catheter lumen (50,52). A slider (140) is disposed about the adapter (120) and is longitudinally slidable along the adapter. When the slider (140) is slid towards the second end (126) of the adapter, the slider engages a plurality of legs (134a-134d) on the adapter and biases the plurality of legs toward each other and the longitudinal axis of the adapter.

Abstract: A medical connector for use with one or more medical implements. In some embodiments, the connector minimizes or eliminates the retrograde flow of fluid into the connector from one end or port upon the disconnection of a medical implement from the other end or port. In some embodiments, the connector generates a positive flow of fluid out of the connector from one end or port when a medical implement is disconnected from the other end or port.

Abstract: A breakaway hemostasis hub for a catheter or introducer sheath includes a splittable or separable housing, a seal within the housing, an actuator partially slidably disposed within the housing, a pair of spring retainer members in the housing each adapted to receive at least one spring, and a pair of actuator retainer members adapted to retain the seal, the actuator, and the spring retainer members in the housing. The actuator is operable to assume a closed position and an open position and includes a dilator member configured to dilate the seal when the actuator is in the open position. The hub is splittable or separable into two generally symmetrical sub-assemblies to facilitate cutting the catheter for retraction from the patient's body without displacing its payload.

Abstract: The present invention is directed to, in one aspect, a medical apparatus having a nasogastric tube with hypopharyngeal suctioning capability. In one embodiment, the medical apparatus has a flexible nasogastric tube for insertion through a patient's nose. The nasogastric tube has a first end defining a first opening, a distal, second end that defines a second opening, and a length sufficient to allow the second opening to be positioned in a patient's stomach. The medical apparatus also has a flexible oropharyngeal tube for insertion through a patient's mouth. The oropharyngeal tube has a first end and a distal, second end that defines a suction intake. The oropharyngeal tube has a length that is less than the length of the nasogastric tube and which allows the suction intake to be positioned in a patient's hypopharynx region. In another embodiment of the invention, the medical apparatus has a laryngeal mask with hypopharyngeal suctioning capability.