Abstract: A liquid transport device is attachable to a living body and transports a liquid to the living body. The liquid transport device includes a pump unit that includes a storage portion for storing the liquid and a pumping portion for transporting the liquid in the storage portion to the living body, and a seal portion that attaches the pump unit to the living body. A portion of a surface of the living body side of the pump unit is separated from an upper surface of the seal portion. In the liquid transport device, the pump unit is easily fixed to a flexible surface of the living body and a load on the living body is reduced while securing areas for the lower surface of the pump unit and the sealing surface of the seal portion.

Abstract: An apparatus (110) includes an activation mechanism (20) and a safety latch (122). The activation mechanism is operative to deploy a needle (116) to protrude out of a housing (112), the needle (116) having a longitudinal axis. The safety latch (122) is movably mounted on the housing (112) and formed with a needle opening (129) to allow the needle (116) to pass therethrough. The safety latch (122) has a first position wherein the needle (116) is aligned to pass through the needle opening (129) and a second position wherein the safety latch (122) is moved with respect to the housing (112) such that the needle (116) is blocked from movement in a direction parallel to the longitudinal axis thereof by a portion of the safety latch (122) distanced from the needle opening (129).

Abstract: An infusion pump assembly is disclosed. The infusion pump assembly includes a locking tab and a pump barrel inside a pump barrel housing, where the pump barrel accommodates a reservoir assembly. The reservoir assembly includes a reservoir and a plunger rod. The infusion pump assembly also includes a locking disc at a terminus of the pump barrel. The locking disc includes a clearance hole for the plunger rod. The locking disc also includes at least one locking tab notch in close proximity with the locking tab. The locking tab is in moveable engagement with the locking tab notch, and the reservoir moves the locking tab from a locked position to an unlocked position when the plunger rod is inserted through clearance hole. The locking disc rotates upon torque being applied to the reservoir assembly, the locking disc rotating from a non-loaded position to a loaded position with respect to the plunger rod and a drive screw.

Abstract: A patch-sized fluid delivery device may include a reusable portion and a disposable portion. The disposable portion may include components that come into contact with the fluid, while the reusable portion may include only components that do not come into contact with the fluid. Redundant systems, such as redundant controllers, power sources, motor actuators, and alarms, may be provided. Alternatively or additionally, certain components can be multi-functional, such a microphones and loudspeakers that may be used for both acoustic volume sensing and for other functions and a coil that may be used as both an inductive coupler for a battery recharger and an antenna for a wireless transceiver. Various types of network interfaces may be provided in order to allow for remote control and monitoring of the device.

Abstract: A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

Abstract: A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

Abstract: Clips or straps may be used to position a patient-controlled-analgesia (PCA) pump control in a position where a patient can easily operate a PCA pump. A strap that allows a PCA pump control to always be in hand or very close at hand is preferable to a strap or clip that merely keeps a PCA pump control nearby.

Abstract: A medicament delivery device is shown for the administration of one or more drug agents. The device comprises a medicament cartridge retainer for holding a medicament cartridge. A dispense interface can be attached to an attachment of the device for facilitating fluidic communication from the device. Further, an interface sensor is configured to provide an output indicative of whether the dispense interface is attached to the attachment. The device also comprises a piston rod for driving a bung of the medicament cartridge, and a drive train for advancing the piston rod to the bung. A controller is configured to control the drive train to advance the piston rod towards the bung when the output of the interface sensor indicates that the dispense interface is not on the attachment. The controller is further configured to disable advancement of the piston rod when the output of the interface sensor indicates that the dispense interface is at least partially on the attachment.

Abstract: A drug delivery device is provided with a cartridge holder having at least one guide track, and a body having at least one interaction member adapted and arranged to mechanically cooperate with the at least one guide track. The guide track has a first section and a second section, wherein the path which is defined by the first section encloses an angle with the longitudinal axis of the device, wherein the angle which is enclosed by the path defined by the first section with the longitudinal axis is smaller than the angle which is enclosed by the path defined by the second section with the longitudinal axis.

Abstract: A medicament delivery device for the administration of one or more drug agents is described. The device has a priming mode and a drug delivery mode for administering delivery of the drug agents. The device includes a controller operative for controlling the device to perform a priming operation, and a user interface for activation of the priming operation. The controller is operative to perform the priming operation by way of a plurality of intermittent doses of medicament, the number of intermittent doses being dependent on the activation of the user interface.

Abstract: An assembly for a drug delivery device comprises a housing, at least one stop feature and at least one blocking member. For setting a dose of a drug, the stop feature is configured to be rotated in a dose setting direction with respect to the blocking member and with respect to the housing. For delivering the set dose of the drug, the blocking member is configured to be axially displaced with respect to the stop feature away from an axial starting position and towards an axial interaction position. When the blocking member is in the axial starting position, the blocking member is axially offset from the stop feature and, when the blocking member is in the axial interaction position, the blocking member is configured to mechanically cooperate with the stop feature such that rotation of the stop feature in the dose setting direction with respect to the housing is prevented.

Abstract: A drug delivery device is provided comprising a container, a first product and a second product. The device is configured to mix the first product and the second product with each other within the container for forming a drug mixture. The device is further configured for dispensing the drug mixture. The device comprises a mixing member. The device is switchable from a first state, in which the first product and the second product are separated, into a second state, in which the first product and the second product are mixed. The mixing member is configured to exert a force onto the container in order to move the container to mix the first product and the second product with each other. Furthermore, a method for maintaining a predetermined property of a drug mixture to be dispensed from a drug delivery device is provided.

Abstract: Described is a needle safety device comprising a needle hub including an axial stem having one or more grooves, a needle having a distal tip, a needle shield telescopically coupled to the needle hub and including a first aperture for allowing the needle to pass through, and an inner sleeve rotatably coupled to the needle shield and including a second aperture for allowing the needle to pass through. The inner sleeve includes one or more resilient arms adapted to engage the groove. In a first axial position and a first angular position, the needle shield covers the distal tip of the needle and the first aperture is aligned with the second aperture. In a second axial position, the distal tip of the needle is through the first aperture and the second aperture and extends distally beyond the needle shield. In a third axial position and a second angular position, the needle shield covers the distal tip of the needle and the first aperture is not aligned with the second aperture.

Abstract: The invention refers to a needle safety arrangement for protecting a hollow injection needle of a syringe after an injection, the needle safety arrangement comprising: a needle sheath having essentially the shape of a hollow cylinder arranged to surround the needle, the needle sheath slidable in longitudinal direction with respect to the syringe and biased in proximal direction (P), a sheath linkage, slidable in longitudinal direction, a syringe carrier for holding the syringe, the syringe and syringe carrier arranged for joint axial translation and rotation relative to the needle sheath, wherein the sheath linkage comprises means for restricting translation in proximal direction (P) with respect to the syringe by abutting against the syringe carrier, wherein in an initial state the sheath linkage is abutted against the syringe carrier and latched to the needle sheath for joint axial translation, wherein the syringe carrier exhibits at least one cam on its circumference, wherein the cam is arranged to de-l

Abstract: An apparatus for targeting a desired target site on a body tissue comprising a wall of a first body cavity of a patient includes a target catheter. A framing member has a collapsed condition and an expanded condition. The framing member has a framing member body which includes a bulbous portion defining a maximum body footprint having proximal and distal body ends which are both longitudinally spaced from the maximum body footprint. The framing member is comprised of a plurality of framing member beams. At least three framing member beam arrays of framing member beams are arranged in non-overlapping longitudinal sequence to form at least a portion of the framing member. The framing member beams that make up the framing member substantially each have a width-to-thickness fractional ratio in the range of 0.6-3.0.

Abstract: An IV line temperature controlled warming device includes a housing and a fluid cassette or cartridge that receives fluid from an IV line and includes intravenous line tubing arranged in a preformed configuration. The configuration includes tubing sections arranged in generally circular and concentric portions and a central serpentine tubing section that basically reverses fluid flow and facilitates flow in opposing directions within adjacent tubing sections. The fluid cassette is retained within the device on a base plate partially disposed within a device housing interior, while a housing cover is selectively opened and closed to permit access to the base plate. The base plate includes a heater plate disposed thereon, while the cover and heater plate each include heating elements to apply heat to opposing surfaces of the tubing cassette. The heating elements are controlled by a controller in response to measured temperatures of the heater plate and fluid.

Abstract: A dry powder inhaler including a housing defining a chamber for receiving a dose of powdered medicament, an inhalation port in fluid communication with the chamber, at least one airflow inlet providing fluid communication between the chamber and an exterior of the housing, and a flutter element in the chamber and associated with a dose of powdered medicament. The flutter element has a tensioned distal end proximate the at least one airflow inlet and a free proximal end opposite to the distal end and downstream of the inlet. The flutter element is configured to vibrate in response to airflow through the chamber and aerosolize the dose of powdered medicament.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one valve element (3) for controlling the passage of gas from the second compartment (2) to the first compartment (1). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly (10) in fluid communication with said source of NO gas.

Abstract: A headgear assembly for attachment to a patient interface that delivers breathable gas to a patient, includes a pair of side portions and a rear portion that interconnects the pair of side portions, each of the side portions including an upper side strap and a lower side strap, the rear portion including an upper strap, a lower strap, and intermediate connecting straps extending between the upper strap and the lower strap. The headgear assembly is designed and configured so as to be used with a plurality of different mask systems, and to accommodate for variations in the anthropometrics across a wide variety of patients.

Abstract: A system for collecting an anaesthetic agent, having at least one anaesthetic gas scavenging system (AGSS) for receiving exhaust gas from a plurality of sources, the exhaust gas including the anaesthetic agent to be collected, each AGSS comprising at least one power source for providing suction of the exhaust gas from the plurality of sources under negative pressure, and a central collection system for receiving the exhaust gas. The central collection system comprises a disinfection module for disinfecting the exhaust gases and outputting a disinfected exhaust gas and at least one collector for receiving the disinfected exhaust gas, wherein the at least one collector is configured to adsorb the anaesthetic agent from the exhaust gas. The central collection system may be configured to received the exhaust gases from the at least one AGSS, with the central collection system being located downstream of the at least one AGSS.

Abstract: This disclosure describes systems and methods for providing novel back-up ventilation. Further, this disclosure describes systems and methods for delivering ventilation when exhalation pressure and/or exhalation flow are unknown or unreliable by the ventilator.

Abstract: There are disclosed a wearable computing device and a method for a user interface. The wearable computing device includes a drowsiness detection unit configured to detect a user's drowsiness; a controller configured to determine whether a current situation corresponds to a first mode not allowing the user's drowsiness or a second mode allowing the user's drowsiness when the user's drowsiness is detected; and a feedback output unit configured to provide the user with at least one feedback comprising a message of the first mode or the second mode according to the mode determined by the controller, wherein the message of the first mode is to fight off the drowsiness and wherein the message of the second mode is to help the user's sleep.

Abstract: A catheter assembly includes a urinary catheter and a package provided to contain the catheter. The catheter has a mid-section connected between a proximal end and a distal end. The proximal end of the catheter is adapted for insertion into a urinary canal and the distal end of the catheter is connected to a seal. The package includes a proximal compartment section that is removable from a distal section of the package to provide an outlet in the distal section of the package. The catheter is adapted to move relative to the distal section of the package such that (a) the seal at the distal end of the catheter slides relative to the distal section of the package and (b) at least the mid-section of the catheter is movable through the outlet in the distal section of the package.

Abstract: Packaging for a catheter includes coiled tubing for receiving the catheter and a mounting card coupled to the coiled tubing. The windings of the coiled tubing are welded together to maintain the coiled configuration. The mounting card includes an integral support flap for reducing the risk of damage during catheter insertion and removal, an integral luer retainer for securing a catheter luer, and one or more integral tabs for attaching catheter accessories to the packaging. The integral support flap creates a contact zone which discourages grasping the packaging at a location that can potentially damage an object passing through the packaging, such as a balloon and/or stent. The integral luer retainer is configured to selectively alternate between a configuration which secures the catheter luer and configuration which allows releases the luer for easy insertion and removal of the catheter.

Abstract: A closed loop catheter useable for heat exchange is manufactured by forming a plurality of generally transverse bore holes though a flexible, multilumen catheter body, lacing a tube trough the bore holes so that loops of the tube protrude from the catheter body, connecting one end of the tube to an inflow lumen of the catheter and connecting the other end of the tube to an outflow lumen of the catheter. A heated or cooled heat exchange medium may then be circulated through the tube while the catheter is inserted in the vasculature of a subject, thereby resulting in heat exchange between the subject's flowing blood and the heat exchange medium being circulated through the tube.

Abstract: A catheter, with one or more lumens, having a first portion and a second portion and an arcuate transition region extending between the first portion and the second portion. The first portion is nonparallel to the second portion.

Abstract: A neuromodulation catheter includes an elongate shaft and a neuromodulation element. The shaft includes two or more first cut shapes and two or more second cut shapes along a helical path extending around a longitudinal axis of the shaft. The first cut shapes are configured to at least partially resist deformation in response to longitudinal compression and tension on the shaft and torsion on the shaft in a first circumferential direction. The second cut shapes are configured to at least partially resist deformation in response to longitudinal compression on the shaft and torsion on the shaft in both first and second opposite circumferential directions.

Abstract: The instant invention relates generally to catheters and to introducer catheters used to help deliver catheters or other medical devices to locations within the human body. In particular, the instant invention relates to large diameter catheters and introducer catheters having a torque transfer layer that includes at least two flat wires braided into a wire mesh. The flat wires have a width of at least about 0.007 inches and a depth of at least about 0.003 inches. The lumen diameter of the catheter is at least about 6 French. The torque transfer layer provides increased strength, flexibility, and kink resistance.

Abstract: An interventional catheter for treating an artery includes an elongated body sized and shaped to be transcervically introduced into a common carotid artery at an access location in the neck. The elongated body has an overall length such that the distal most section can be positioned in an intracranial artery and at least a portion of the proximal most section is positioned in the common carotid artery during use.

Abstract: Attachable implements, systems, and methods for identifying the migration of a medical device extending through a percutaneous insertion site of a patient's skin are disclosed. In one embodiment, an attachable implement for identifying migration comprises a attachable implement body having a coupling surface and a skin contacting surface, the coupling surface arranged to couple to a surface of the medical device, and the skin contacting surface arranged to contact the skin of the patient; wherein the attachable implement body is arranged to be side mountable on the medical device and wherein the attachable implement is configured to move from a first position adjacent to the patient's skin to a second position remote from the patient's skin. Systems, methods, and other embodiments are disclosed.

Abstract: A catheter is responsive to external and internal magnetic field generators for generating signals representing position and pressure data, with a reduced number of sensing coil leads for minimizing lead breakage and failure. The catheter includes a flexible joint with pressure sensing and position coils, at least pair of a pressure sensing coil and a position coil are serially connected. Methods of calibrating a catheter for position and pressure sensing, and detecting magnetic field interference with one catheter by another catheter or other metal or ferrous object advantageously use signals between two sets of sensors as a “back up” or “error check”.

Abstract: A catheter securement device includes a body having a generally curved channel configured to receive a central venous catheter and reposition it in a different direction than the direction of the catheter as it exits the skin of the patient. The securement device includes a cover that slidably connects to the securement device body to prevent the catheter from being pulled out of the curved channel.

Abstract: A guidewire includes a core shaft including a distal end portion and a proximal end portion, an outer coil disposed so as to cover the distal end portion, and an inner coil disposed inside of the outer coil. The outer coil includes a first bent portion that is bent at a first angle in a first direction. The inner coil includes a second bent portion that is bent at a second angle in the first direction. The second angle is larger than the first angle.

Abstract: A guidewire suppresses an increase in operating resistance during pushing and pulling within a blood vessel that is extremely crooked and secures sufficient operability. The guidewire includes a core shaft and a coil body wound around the core shaft. The core shaft includes a first shaft portion positioned inside the coil body and a second shaft portion positioned proximally from the coil body. A twisted portion that is twisted along a longitudinal axis of the core shaft is provided in at least part of the second shaft portion.

Abstract: A lockable syringe having an actuating mechanism for rapidly and selectively placing a movable thread bearing plunger member and stationary internally threaded cylinder into or out of threaded engagement, particularly for using the syringe to pressurize therapeutic medical balloon catheters, or the like. The mechanism includes a plunger having both a piston at its end to engage a barrel portion of a unitary syringe body, selectively deployable and retractable threaded segment, and an internally threaded cylindrical structure disposed within a unitary syringe body having a barrel. The plunger is engageable with the threaded cylinder by means of a threaded segment, and an operator actuated desmodromic arrangement to controllably reciprocate the threaded segment in a positive manner in order to allow either rapid manual or thread controlled plunger and piston movement within the syringe's barrel for purposes of displacing or pressurizing working fluid contained therein.

Abstract: A stoma dilation device that includes a tubular support and an inflatable dilation portion located on the tubular support. The inflatable dilation portion includes a stiffening portion and inflation lumen. The device may have a retention portion configured to have a diameter upon full, unrestrained inflation that is greater than the diameter of the dilation portion. The device is designed to be placed in a patient to dilate the stoma for the installation of a catheter feeding tube. The device may be placed and withdrawn with the use of an endoscope which need be inserted into the patient only one time. The single insertion of the endoscope significantly reduces the trauma to the patient in comparison with multiple endoscope insertion methods.

Abstract: An electronic skin treatment device with an integrated specimen dispenser is disclosed, with which specimen dispense can be concurrently applied to target skin area while ultrasonic vibrations, mechanical massaging motions, galvanic stimulations, or light illuminations are used and as such a customizable, easier and better skin beautification can be achieved.

Abstract: An applicator and method for dispensing a stream of a particulate and a fluid from a cannula and a mixing tip. The mixing tip includes a housing having an inlet, an outlet, and a mixing channel extending therebetween. A fin is positioned within the housing and extends along at least a portion of the mixing channel. The fin spirals about the mixing channel from the inlet toward the outlet for mixing and distributing the particulate generally uniformly within the fluid. The stream is directed into the mixing channel of the mixing tip and spiraled along the fin within the mixing channel. The spiraling increases turbulence and mixes the stream into a mixed stream of particulate and fluid. The mixed stream is discharged from the mixing tip for being dispensed onto an anatomical site.

Abstract: A microneedle array applicator is configured to apply a microneedle array in cosmetic and medical applications. The microneedle array applicator has a holding apparatus configured to define detachable holding of a microneedle array comprising a planar substrate. The microneedle array applicator also has a drive mechanism for driving the microneedle array in a first direction perpendicular to the planar substrate and in a second direction parallel to the planar substrate. A method for applying a microneedle array includes the microneedle array applicator enabling safe breaking off of the microneedles, optionally laden with an active ingredient, in the skin.

Abstract: An apparatus is presented comprising a first part comprising a sealing structure, a membrane being attached to said first part and a second part being attached to said membrane, wherein said second part comprises a valve area with a first opening and a second opening, wherein said valve area is located in the area of said sealing structure, wherein said valve area is configured to allow for a fluidic communication between said first opening and said second opening and wherein said sealing structure is configured to allow for an interruption of said fluidic communication between said first opening and said second opening.

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: The present invention relates generally to iontophoretic drug delivery systems for transdermal delivery of therapeutic agents and, more particularly, to packaging such systems for long shelf life and easy assembly for use. The system package includes an iontophoretic skin worn patch component that accommodates a power source, electronics, electrodes and a drug pack component that carries a therapeutic agent which is contained as a separate sealed component. The packaged system further provides for ease of assembly at the time of use.

Abstract: RF/MRI compatible leads include at least one conductor that turns back on itself at least twice in a lengthwise direction, and can turn back on itself at least twice at multiple locations along its length. The at least one electrical lead can be configured so that the lead heats local tissue less than about 10 degrees Celsius (typically about 5 degrees Celsius or less) or does not heat local tissue when a patient is exposed to target RF frequencies at a peak input SAR of at least about 4 W/kg and/or a whole body average SAR of at least about 2W/kg. Related devices and methods of fabricating leads are also described.

Abstract: An internal medical device for implantation into a human or animal where the internal medical device has an electric field source that may be an active source of electromotive force such as a battery or capacitor, or may be an electric field generating material such as an electret, piezoelectric, or the like.

Abstract: Systems and methods for extraction of implanted articles are disclosed. According to aspects illustrated herein, there is provided a system for extraction of an implanted article that includes an elongated member, guide member disposed at a distal section of the elongated member and having a pathway in substantially parallel relationship to the elongated member, through which pathway an implanted article can be accommodated, and a cutting mechanism, situated between the distal section of the elongated member and the guide member, for severing a fibrous adhesion about the implanted article to allow the implanted article to be extracted.

Abstract: A cochlear lead includes a plurality of electrodes configured to stimulate an auditory nerve from within a cochlea and a flexible body supporting the plurality of electrodes along a length of the flexible body. A stiffening element is slidably encapsulated within the flexible body, the stiffening element extending past a most distal electrode at the tip of the cochlear lead, wherein a distal portion of the stiffening element plastically deforms upon insertion into a curved portion of the cochlea.

Abstract: An implantable lead includes an expandable paddle body and a plurality of electrodes disposed on the paddle body. The electrodes are configured and arranged to provide electrical stimulation to adjacent tissue when implanted and the lead is coupled to a control module. The paddle body is configured for percutaneous implantation through an introducer followed by expansion of a volume of the paddle body by at least 10%. Alternatively, the paddle body is configured for percutaneous implantation and when implanted the lead is configured and arranged so that a position or orientation of the plurality of electrodes relative to the paddle body can be altered.

Abstract: A particular implantable device may include an antenna configured to receive a far field radiative signal. The implantable device may also include a voltage rectifier configured to rectify the far field radiative signal received by the antenna to provide a rectified voltage signal. The implantable device may further include a charge storage element operative to receive the rectified voltage signal and to store charge responsive to the rectified voltage signal. The implantable device may also include a stimulation module powered by the charge storage element. The stimulation module may be operative to generate an electrical stimulation signal to stimulate a target nerve of a patient. The implantable medical device may further include a nerve wrap configured to house the voltage rectifier, the charge storage element, and the stimulation module. The nerve wrap may include one or more electrodes operative to deliver the electrical stimulation signal to the target nerve.

Abstract: A system comprises an implantable medical device and an actively deployable clip attached to the implantable medical device that restricts movement of the implantable medical device once the clip is deployed within a body of a patient. In one embodiment, the implantable medical device is a lead and a clip that includes electrically conductive portion is an electrode of the lead. The implantable medical device may be implanted proximate to any suitable tissue site within the patient, and in one embodiment, the implantable medical device is implanted proximate to an occipital nerve or a trigeminal nerve of the patient.

Abstract: Various embodiments concern a guide catheter for delivery of an implantable lead within the coronary vein. Such a guide catheter can comprise a tubular body having a main lumen and at least one preformed bend. The tubular body can comprise a liner defining an inner surface, braiding circumferentially surrounding the liner, a jacket covering the braiding and defining an exterior surface of the tubular body, and a plurality of inflation tubes embedded within the jacket. The guide catheter can include a balloon mounted on the tubular body, each of the plurality of inflation tubes in communication with the balloon. The guide catheter can further include a hub providing access to the main lumen, the hub comprising a first port for introduction of contrast media into the main lumen and a second port in communication with the plurality of inflation tubes.