Abstract: Systems, methods, and apparatus are provided for containing and measuring a fluid in a reservoir. A sensing reservoir comprises a reservoir comprising an opening and a wall, the opening configured to allow passage of the fluid in and out of the reservoir, and the wall defining a chamber configured to contain the fluid. The sensing reservoir further comprises a fluid sensing unit coupled to the sensing reservoir, the fluid sensing unit configured to generate measurement data indicative of a volume of the fluid contained in the reservoir.

Abstract: A method for facilitating milk extraction from a female breast may involve applying a breast contacting portion of a breast pump system to a breast, activating the breast pump system to administer multiple breast pumping cycles, and applying vibrations to the breast during at least a portion of each of the breast pumping cycles, using a vibration device. A vibration generating device may be a component of a breast pump system, an added attachment on a breast pump system or a separate component that works in conjunction with a breast pump system.

Abstract: The invention relates to a rotary piston pump, in particular for pumping blood, comprising a piston rotor (1) which has particularly two or three faces when seen in cross-section, which is mounted in a piston chamber (2) and eccentrically rotates, the piston rotor (1) having in its interior a plurality of magnetically interacting elements (4, 4a, 4b), in particular permanent magnets and/or coils, and being driven by the magnetic interaction of these elements (4, 4a, 4b) with at least one moving magnetic field.

Abstract: An apparatus is disclosed including: an intracardiac pump device having a path for a guidewire extending through the pump device from a first opening to a second opening; and a lumen which extends from a first end located outside of the pump device, into the pump device through the first opening in the pump device, along the path for the guidewire, out of the pump device through the second opening, and to a second end located outside of the pump device. The lumen is configured to receive the guidewire such that when the guidewire passes through the lumen from the first end to the second end, the guidewire is positioned along the path.

Abstract: An electrical sensor for sensing electromagnetic properties of process fluids in a dialysis machine or a similar medical device can include a probe for interfacing with the fluids that is made from electronic fabric materials. The electronic fabric probe can include one or more conductors embedded in a non-conductive fabric layer. The electronic fabric probe is accommodated an enclosure which establishes a flow path with respect to the probe to establish fluid contact between the process fluids and the conductors. The conductors can apply or sense current and/or voltage with respect to the fluid. A portion of the electronic fabric probe can be disposed externally of the enclosure to provide electronic communication externally of the enclosure.

Abstract: A light shield is arranged in a light shielding position with respect to a sensor or a blood leakage detector installed in a medical apparatus and monitoring for changes of transmittance in a translucent fluid carried in a tubing connected to the medical apparatus. The light shield has a non-transparent configuration and is configured to prevent environmental light from being incident on a relevant detection active sensor area. Further, a disposable kit for a medical apparatus which is arranged to be mounted to the medical apparatus and to carry pre-installed disposables to be used during a medical treatment comprises a hard-shell subassembly arranged to be positioned in a region of the medical apparatus in the vicinity of a detection active sensor area of a sensor which is sensitive to light and installed in the medical apparatus.

Abstract: A peristaltic pump for an apparatus for extracorporeal blood treatment, especially for a dialysis machine, for conveying fluid in the apparatus is disclosed. The peristaltic pump includes a rotor driven by a drive shaft, the rotor interacting with an elastically deformable fluid line so as to form a cross-sectional constriction which is displaced along the fluid line for conveying fluid by rotation of the rotor, wherein the rotor is coupled to the drive shaft by a coupling structure so as to transmit a torque, wherein the coupling structure couples the rotor and the drive shaft with a play in the direction of rotation relative to each other.

Abstract: A system for obtaining plasma enriched in platelets is disclosed which is closed to the atmosphere. The system includes: a collection tube containing an anticoagulant portion and a separation gel; a first collection syringe adapted to collect a portion of fluid relatively depleted in platelets from said collection tube after centrifugation; and a second collection syringe adapted to collect plasma enriched in platelets from said collection tube after centrifugation, said second collection syringe further comprising a filter unit adapted to filter cells included in said plasma enriched in platelets.

Abstract: A method comprising obtaining a bodily fluid from a subject; contacting the bodily fluid with an adsorbent material comprising a synthetic carbon particle (SCP) to produce a first filtrate having a level of disease mediators (y); contacting the first filtrate with an adsorbent material comprising the SCP and an anion exchange resin where the ratio of SCP to anion exchange resin is from about 0.1:100 to 100:0.1 to produce a second filtrate; contacting the second filtrate with an adsorbent material comprising the SCP and a cation exchange resin where the ratio of SCP to cation exchange resin is from about 1:100 to produce a third filtrate; and administering the third filtrate to the subject.

Abstract: An infusion pouch set with a built-in injection medicine bottle having a vial function including: a discharge port 20 provided at an outlet 12 of a pouch container 10; and an injection port 30 provided at an inlet 14 of the pouch container 10; wherein the injection port 30 comprises, an injection needle part 40 configured to have an injection needle 44 provided vertically on an upper part of an injection needle holder 42 which is welded to the inlet 14 of the pouch container 10; an inner cap 50 having a sealing membrane 52 which is coupled to the injection needle holder 42 of the injection needle part 40, accommodates the injection needle 44 therein, and is punctured by the injection needle 44 when lowered; an outer cap 60 which is vertically moveable along the same axis as the inner cap 50 and accommodates an injection medicine bottle 70 in an upside down state therein; and a packing holder 90 which is vertically movably coupled at an upper part of the sealing membrane 52 of the inner cap 50, and a lower par

Abstract: A patient care system is disclosed that includes a medical device such as an infusion pump. The medical device generates a data message containing information such as the status of the therapy being delivered, operating data or both. An alarm generating system assesses the data message from the pump and generates an alarm message if certain conditions established by a first set of rules are met. The alarm message is assessed according to a second set of rules as to whether to suppress the alarm message. The data message contains a required input for both the first and second algorithms. A dispatching system is adapted to forward the alarm message to an alarm destination according to a third set of rules. The alarm destination expresses an alarm upon receipt of the alarm message.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary infusion device includes a motor operable to deliver fluid to a body of a user, a first control module to enable input power for the motor and provide a dosage command for operating the motor, and a second control module coupled to the first control module to receive the dosage command and operate the motor using at least a portion of the input power based at least in part on the dosage command. One of the first control module and the second control module detects an anomalous condition, and in response, disables the input power to the motor, stores diagnostic information for the anomalous condition in its internal memory, and automatically resets thereafter.

Abstract: Improvements in an adhesive patch for an infusion set include the addition of an antiperspirant, wound healing and/or antimicrobial agent to the adhesive surface, and the layering of different backing materials to improve performance characteristics of the patch. Patches may be offered as part of a product line, in which differently shaped patches are provided for attachment to different parts of the body, and different pressure sensitive adhesives provide different peel strength according to different use patterns of the end user.

Abstract: Disclosed is a medical intervention apparatus. The medical intervention apparatus includes a needle rotation unit configured to include a first needle rotation member, a second needle rotation member that is disposed to be separated from the first needle rotation member, and a first driver that drives the first and second needle rotation members to rectilinearly move in opposite directions and a needle insertion unit configured to insert a needle, which is inserted between the first needle rotation member and the second needle rotation member, into a target.

Abstract: A method is disclosed for state sensing and controlling of a multi-state drug delivery device. In some embodiments a power switch is reused as a state sensor. Optionally the state sensor may be toggled by user actions and/or the movements of parts of the device, for example needle and/or a protective element. Optionally, drug discharge and/or status indication is controlled in accordance with sensor output. In some embodiments control is by means of a processor. Alternatively or additionally, control is by means of simple physical circuits.

Abstract: A replaceable fluid restriction mechanism includes: an aperture residing adjacent to a fluid pathway connection and configured to permit flow of a drug fluid through the aperture when the fluid pathway connection is open; an entry point of a fluid channel configured such that the flow of drug fluid can travel through aperture to the entry point and through the fluid channel to an exit point; and an outlet aperture of a port through which the flow of drug fluid may travel after exiting the exit point, wherein a fluid conduit is connected to the fluid restriction mechanism at the outlet aperture. A configurable fluid restriction mechanism includes a plurality of fluid channels, selectable to align with the entry point and an exit point of the fluid restriction mechanism.

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: Methods, devices, algorithms, and systems controlling insulin delivery employ velocity-weighting. Predicted glucose outcomes are penalized with a cost modulated by a factor that is a function of the glucose velocity, wherein glucose outcomes are penalized increasingly less for increasingly negative glucose velocities, when glucose level is high, and/or wherein a hyperglycemic glucose value that is already converging to the euglycemic zone results in less corrective action by the controller than were the hyperglycemic state steady.

Abstract: Methods and system for providing diabetes management including automatic time acquisition protocol and expiration date detection are provided.

Abstract: A medicament delivery device includes a generally elongated tubular housing having opposite proximal and distal parts; a needle shield sleeve slidably and coaxially arranged inside the housing with a proximal part of the sleeve protruding a distance outside the proximal part of the housing; a syringe carrier mechanism having a syringe carrier slidably and coaxially arranged within the needle shield sleeve, a syringe having a stopper, a medicament, and a needle, the syringe being coaxially arranged within the syringe carrier; and a holding member connected to the syringe carrier; a first activator member an a second activator member; a drive mechanism adapted to accumulate a drive force for moving the syringe carrier mechanism in a first step and a second step. The second activator member is arranged within an information device for producing audible, visual, and/or tactile feedback to a user about a completed injection.

Abstract: A drug delivery device (1) is provided comprising a housing (2), a cartridge holder (3) which is adapted and arranged for receiving a cartridge (4) for holding a plurality of doses of a drug (5), wherein the cartridge holder (3) is removable from the housing (2) to enable an exchange of the cartridge (4), a piston rod (9) adapted and arranged to be moved from an initial position towards an end position for dispensing a dose of drug (5) from the device (1) and to be moved from the end position back towards the initial position to perform a reset operation of the device (1), and at least one resilient member (20, 25). The at least one resilient member (20, 25) is in direct mechanical contact with the piston rod (9) and the resilient member (20, 25) is adapted and arranged to prevent an unintentional movement of the piston rod (9) towards the initial position due to mechanical cooperation with the piston rod (9).

Abstract: An assembly for a drug delivery device is provided comprising a housing, and a lead screw having a longitudinal axis, a distal end and a proximal end, the lead screw being rotatably fixed during dose setting and dose delivery and axially movable in a distal direction relative to the housing, the lead screw further including a thread. The assembly further comprises a drive nut threadedly engaged with and screwable along the lead screw thread and a dial link connected with the drive nut and axially movable and rotatably fixed relative to the drive nut, where the dial link comprises a first portion of a feedback ratchet. The assembly is configured such that, during dose delivery, the assembly generates a feedback signal.

Abstract: The present disclosure relates to a medicament delivery device comprising: a housing (3), a plunger rod received by the housing (3), which plunger rod is rotatable in a first direction relative to the housing (3) and linearly displaceable, an activation button arrangement linearly displaceable from a first position to a second position to thereby rotate the plunger rod in the first direction, a second direction rotation preventer having an annular outer member that is rotationally fixed relative to the housing (3) and an annular inner member partially received by the outer member, wherein the outer member and the inner member are arranged to receive the plunger rod and wherein the inner member is rotationally interlocked with the plunger rod, wherein the outer member and the inner member are structured to allow the inner member to rotate in the first direction relative to the outer member and to prevent the inner member from rotating in a second direction opposite to the first direction, and a recording unit

Abstract: A medical injection device, comprising: a housing having a first end cover and a second end cover provided at two ends thereof, respectively; a dial threaded rod, which is in threaded connected to the first end cover; and, a piston rod, which is used for expelling a dose, an upper end of the piston rod being connected to the dial threaded rod through a driving mechanism while a lower end thereof is in threaded connected to the second end cover. It further comprises a dosage adjustment mechanism, which is arranged between the dial threaded rod and the housing and used for driving the dial threaded rod to move in an axial direction of the housing.

Abstract: A cap assembly (200) for a drug delivery device is presented. The cap assembly (200) comprises a fixing element (134) with a connection feature (154), an outer part (130) with an opening (164), and an inner part (131) being located inside of the outer part (130), the inner part (131) further comprising a corresponding connection feature (170), wherein a section of the fixing element (134) extends through the opening (164) of the outer part (130), such that the fixing element (134) is connected to the inner part (131) by an interaction of the connection feature (154) and the corresponding connection feature (170).

Abstract: Embodiments of the shield assemblies include a shield that is pivotably secured to a needle hub. A ball-and-socket hinge secures the shield and the hub to one another. The assembly includes a reversible shield lock to hold the shield in the needle-protected position. The assembly further includes at least one stop piece to stop the shield from over-rotating.

Abstract: A frontal attachment for a conventional aspirating dental syringe comprising a barrel connector housing releasably attachable to the front end of the barrel of an aspirating dental syringe, an injection needle guide attached to the barrel connector housing, an injection needle attached to and supported by a needle holder assembly reciprocatably disposed in a needle guide slot between the injection needle guide and the barrel connector housing in oblique relation to the longitudinal axis of the aspirating dental syringe, and a second needle projecting rearwardly from the barrel connector housing to establish fluid communication with a carpule disposed in the conventional aspirating dental syringe.

Abstract: An adapter for delivering an atomized spray from a syringe. The adapter includes an adapter guide including a side wall, an interior surface of the side wall defining a through-bore and a shoulder in the through-bore. A pin guide is located in the through-bore. The pin guide includes a seat and a sleeve extending from the seat. A spring positioned around the pin guide sleeve and between the pin guide seat and the shoulder, wherein the spring and the sleeve provide a passageway there between. A pin extends from the pin guide seat and through the passageway. Affixing the adapter onto a syringe provides an atomizing delivery device. A method of dispensing an atomized spray from a syringe is provided by affixing the adapter to the syringe.

Abstract: According to one non-limiting example of the disclosure, a system, a method, a device and a computer program are provided for the automated manufacture of electronic cigarettes. The apparatus comprises an electronic smoking device for delivering a vaporized liquid comprising a frame (200), an air flow path (122), an air inlet, a container (140) for storing a smoking liquid, and a circuit. At least a part of the circuit comprising traces printed on the frame (1306). The method comprises a frame, that can include slots configured for mating with and containing various components of the electronic smoking device. The computer readable medium comprises sections or segments of code that, when executed on a computer, cause the processes described herein to be carried, such as, for example, the process of assembling the electronic smoking device.

Abstract: An apparatus for vaporizing a concentrate and/or a non-concentrate material is provided. The apparatus can include a housing, a reservoir, a vessel, and a heating element. The reservoir can be coupled to a lid of the apparatus and configured to hold the concentrate. The vessel can be disposed at least partially inside of the housing and can be configured to receive the reservoir when the lid of the apparatus is in a closed position with respect to the housing. The heating element can be configured to generate heat for heating the vessel, thereby vaporizing the concentrate in the reservoir to form an aerosol. Coupling the reservoir to the lid of the apparatus can enable the apparatus to be used for vaporizing the concentrate while decoupling the reservoir from the lid of the apparatus can enable the apparatus to be used for vaporizing the non-concentrate material. Related methods are also provided.

Abstract: A breathing gas-carrying patient connection (2) for the artificial respiration of a patient (1) by an anesthesia apparatus or respirator (3) with one or more sensors (9, 10, 11) for detecting patient-relevant measured variables and with a telemetric transmission of the sensor data from the patient connection (2) to a machine-side connection element (13) for the patient connection (2), wherein the telemetric transmission of the sensor data is designed for wireless bidirectional communication between the patient connection (2) and the connection element (13), makes possible the reliable transmission of data into the machine-side connection element (13).

Abstract: A respiratory device for supplying breathing air to a patient, including an oxygen inlet to be connected to an oxygen supply, and a compressed air inlet to be connected to a compressed air supply. The respiratory device also includes a turbine for sucking in ambient air. Switching between the individual operating modes can be done automatically or manually.

Abstract: A patient interface face contact (14) element comprises a surface for contacting the face of a patient, and a connection face for coupling the patient interface face contact element to a support (15) using a magnetic coupling (30). The support is also provided as well as the complete patient interface. Headgear strap clips can also be retained magnetically.

Abstract: A patient interface device includes a cushion member, a frame member, and nasal pillows. A first side of the cushion member forms a seal with a patient's mouth. The nasal pillows are structured to form a seal with the patient's nares. The nasal pillows are attached to the frame member. The frame is attached to a second side of the cushion member. The frame member includes a connecting portion, a first aperture, and a second aperture. The nasal pillows include a first nasal pillow element and a second nasal pillow element. The first nasal pillow element is at least partially removably disposed in the first aperture. The second nasal pillow element is at least partially removably disposed in the second aperture. The connection portion is connected to the second side of the cushion member.

Abstract: This disclosure relates to a portable oxygen concentrator system. The system includes a case containing a portable oxygen concentrator, a mask, and a button. The case is configured to be worn on a user's back. The mask is configured to deliver oxygen from the portable oxygen concentrator to the user. The button, when activated, is configured to cause the portable oxygen concentrator to deliver an increased flow of oxygen to the user for a period of time.

Abstract: A high flow nasal therapy system (1) has a gas supply (2), a nebulizer (12), and a nasal interface (7). There are two branches (11, 10) and a valve (6) linked with the controller, the branches including a first branch (11) for delivery of aerosol and a second branch (10) for delivery of non-aerosolized gas. The controller controls delivery into the branches (11, 10), in which flow is unidirectional in the first and second branches, from the gas supply towards the nasal interface. The first branch (11) includes the nebulizer (12) and a line configured to store a bolus of aerosol during flow through the second branch (10). The valve (6) comprises a Y-junction between the gas inlet on one side and the branches on the other side.

Abstract: A vaporizer arrangement for a breathing apparatus serves the double purpose of vaporizer and pressurized supply of vapor-containing gas for direct delivery to a patient. The vaporizer arrangement has at least a first gas inlet channel for conveying a flow of a carrier gas into a vaporization chamber, a vaporizer for vaporizing a liquid into the carrier gas in the vaporization chamber, and a gas outlet channel for conveying a flow of vapor-containing carrier gas out of the vaporization chamber and toward the patient. The vaporizer arrangement further has a gas flow regulator that maintains the carrier gas within the vaporization chamber at an overpressure, and that controls the flow of vapor-containing carrier gas out of the vaporization chamber in a variable manner.

Abstract: An ear-worn electronic device includes a right ear device comprising a first processor and a left ear device comprising a second processor communicatively coupled to the first processor. A physiologic sensor module comprises one or more physiologic sensors configured to sense at least one physiologic parameter from a wearer. A motion sensor module comprises one or more sensors configured to sense movement of the wearer. The first and second processors are coupled to the physiologic and motion sensor modules. The first and second processors are configured to produce a three-dimensional virtual sound environment comprising relaxing sounds, generate verbal instructions within the three-dimensional virtual sound environment that guide the wearer through a predetermined mental exercise that promotes wearer relaxation, and generate verbal commentary that assesses wearer compliance with the predetermined mental exercise in response to one or both of the sensed movement and the at least one physiologic parameter.

Abstract: An arrangement adapted for enhanced continuous flow of urine in a catheterized patient, the arrangement comprising a catheter tube having an inner diameter of less than six millimeters, said tube having an inner surface which is hydrophobic at least along a first segment thereof and being adapted to provide a continuously negative fluid pressure therein.

Abstract: In some examples, a medical device package may include a tray and a lip. The tray defines a recess configured to receive an elongated medical device in a coiled state. The lip is configured to cover at least a portion of the recess. The lip and tray define a mouth to the recess. The tray and lip define an opening configured to expose the elongated medical device when the elongated medical device is received in the recess. The mouth is configured to facilitate removal of the elongated medical device from the recess through the opening while the elongated medical device is in the coiled state.

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

Abstract: The guidewire advancing device and method according to the present invention is used with a tubular catheter body configured to receive a hollow needle for receiving the guidewire. The guidewire advancing device includes the guidewire, guidewire housing, and means for advancing and retracting the guidewire. The means for advancing the guidewire includes a spool assembly or a slide tab and may also include a rack and pinion assembly for translation of forces to advance the guidewire.

Abstract: A guide catheter extension, including a push member having a lumen, a proximal end and a distal end; a tube frame defining a lumen therein, a longitudinal axis, and a proximal segment and a distal segment, wherein the tube frame comprises a plurality of cut patterns therein; and a tongue element extending from the proximal segment of the tube frame, wherein the tongue element is coupled to the push member.

Abstract: Drive systems and methods of use are disclosed herein for performing medical procedures on a patient. The drive systems include various handle types and triggers for controlling catheters and end effectors. The various handle types include a flexible handle and ambidextrous handles that can alter the handedness of the handle for particularized use. The handles drive articulation sections of the catheter and end effectors with various degrees of freedom, and include locks for holding the catheter and/or end effector in place. The catheter systems include structures for allowing degrees of freedom, such as notches, mechanical interlocks, and articulation joints. In addition, the catheters articulate via cables or fluids.

Abstract: A medical balloon includes a generally cylindrical barrel wall having proximal and distal ends disposed between tapered cone walls and neck walls with a fiber layer comprised of circumferentially wrapped ribbon-shaped fiber embedded in a continuous matrix of polymer material defining the tapered cone walls and barrel wall, wherein the distance between the fiber wraps defines a fiber pitch or density that varies over the working length of the barrel wall in non-linear increments, for example in step-wise increments over the length of the barrel wall.

Abstract: Infusion balloon catheter with fortified proximal infusion outlet port, and manufacturing thereof. Infusion balloon catheter includes: inflatable balloon member; shaft having distal end attached to balloon member, and shaft wall enclosing: first lumen providing passage to balloon inflation fluid, and second lumen providing passage to infusion fluid and guidewire; and bending-resistant insert member housed in second lumen and located proximally to balloon member, insert member is affixed to, and conforms to shape of, shaft inner wall surface, and includes one or more openings(s). Shaft wall has infusion outlet port located along, and providing opening to, second lumen proximally to balloon member. Insert opening(s) is/are in direct fluid communication with infusion outlet port whose cross-sectional area is larger than that of infusion inlet opening. Bending-resistant insert member provides fortifying structural support to shaft wall portion surrounding infusion outlet port.

Abstract: In some examples, a catheter may include a catheter body, a first expandable member, and a second expandable member. The catheter body may define a first lumen, a second lumen, a delivery port, and a surface extending from the delivery port into the first lumen. The first lumen may define a first central longitudinal axis. The second lumen may define a second central longitudinal axis spaced from the first central longitudinal axis in a direction orthogonal to the second central longitudinal axis. The delivery port may be in fluid communication with the first lumen. The surface extending from the delivery port into the first surface may be oriented at an obtuse or acute angle relative to the first central longitudinal axis.

Abstract: A medical elongated body or a balloon catheter that include a catheter main body, a tubular body, and a distal member at a distal end of the tubular body. The distal member is more flexible than the tubular body. The distal end of the tubular body is joined to the distal member at a joint portion. The tubular body includes an outer layer and an inner layer disposed inside of the outer layer in the radial direction of the tubular body. The material of the inner layer possesses better fusing properties with respect to the distal member than the fusing properties of the outer layer material with respect to the distal member material. The inner layer is interposed between the distal member and the outer layer by extending between the distal member and the outer layer at the joint portion.

Abstract: The present disclosure is directed toward a semi-compliant to non-compliant, conformable balloon useful in medical applications. Conformable balloons of the present disclosure exhibit a low straightening force when in a curved configuration and at inflation pressures greater than 4 atm. Balloons of the present disclosure are constructed of material that can compress along an inner length when the balloon is in a curved configuration. In further embodiments, balloons of the present disclosure can be constructed of material that sufficiently elongates along an outer arc when the balloon is in a curved configuration. As a result, medical balloons, in accordance with the present disclosure, when inflated in a curved configuration, exhibit kink-free configurations and do not cause a significant degree of vessel straightening.

Abstract: Methods and devices for trans-jugular carotid access are disclosed. Methods within the scope of this disclosure include methods of trans-jugular carotid access originating in the leg of a patient or other location remote to the jugular vein and carotid artery and methods originating at the neck of a patient. Devices used in connection with the disclosed methods may comprise access catheters, lumens, and stylets.