Abstract: A piercing mechanism for piercing a cartridge (10) comprises a cartridge container (20) adapted to receive and hold a cartridge (10) and allow a movement of the cartridge (10) from a start position via a piercing state to an end position, the cartridge (10) comprising a septum (14) covering a dispensing port (15) and a piston (12) adapted to be moved from a proximal position along an axial direction of the cartridge (10) to a distal position, a hollow needle (30) having a distal end (31) and a proximal end (32), the hollow needle (30) being immovably fixed in the piercing mechanism and adapted to pierce the septum (14) with the proximal end (32) when the cartridge (10) is moved from the start position via the piercing state to the end position, a plunger (40) adapted to cause the movement of the piston (12) when the plunger (40) is moved from a first position to a second position, wherein the second position is closer to the hollow needle (30) than the first position, and a spring mechanism (50) adapted to be

Abstract: A low medicament sensor for a medicament delivery device having a reservoir, a pump, and a fluid path therebetween for medicament, the sensor including a switch and a snap dome. The snap dome is initially in contact with the switch, in fluid communication with the fluid path, and configured to snap out of contact with the switch when a pressure within the snap dome decreases below a predetermined pressure.

Abstract: An implantable perfusion device (2) comprises a tubular transmission line (4) with an inlet end (6), an outlet end (8) and a flow restriction element (10) located therebetween, whereby an inlet section (12) of the transmission line is defined between the inlet end and the flow restriction element and whereby an outlet section (14) of the transmission line is defined between the flow restriction element and the outlet end. Moreover, the device comprises a perfusion chamber (16) containing a load of biologically active cells and is provided with a fluid entrance (18), a fluid exit (20) and a chamber volume (22) formed therebetween. The fluid entrance comprises at least one first microchannel platelet (24) and the fluid exit comprises at least one second microchannel platelet (26), each one of the microchannel platelets comprising at least one array of microchannels (28) defining a fluid passage between respective external and internal platelet faces, the microchannels having an opening of 0.2 to 10 ?m.

Abstract: A drug delivery system having a drug delivery device and an associated sensor is provided. The sensor can be associated with a sensing site on user. The drug delivery device can be positioned over the sensor in any rotational position and can be associated with an infusion site on the user. The close positioning of the sensor and the drug delivery device allows data from the sensor to be relayed to the drug delivery device and then on to a remote control device. Further, the drug delivery device can be replaced at the end of its duration of use, which is shorter than the duration of use of the sensor, without disturbing the sensor. Subsequent drug delivery devices can then be used with the sensor while allowing each corresponding infusion site to be changed, thereby providing more efficient operation of the drug delivery system.

Abstract: A physiological parameter associated with tissue of a host may be monitored in the tissue to confirm subcutaneous delivery of medication to the host. More particularly, such may involve delivering medication subcutaneously to the host with a medical device which includes a sensor used to measure the physiological parameter, particularly within a predetermined time period after delivery of the medication. Such may also or otherwise involve forming a depot in the tissue with the medication, and using the sensor to measure the physiological parameter while the sensor is at least partially within the depot.

Abstract: Methods, systems, and apparatuses for integrating medical device data are disclosed. In an example embodiment, an integration engine receives infusion therapy progress data from an infusion pump and renal failure therapy progress data from a renal failure therapy machine. The integration engine determines a plurality of different types of infusion parameters, determines a plurality of different types of renal failure therapy parameters, and causes a combination user interface to display the plurality of infusion parameters, the plurality of renal failure therapy parameters, and mathematical operations for selection by an operator. The integration engine enables the operator to create derivative data by receiving a selection of an infusion parameter, a renal failure therapy parameter, and a mathematical operation. The integration engine then causes the combination user interface to display the derivative data in conjunction with the infusion therapy progress data and the renal failure therapy progress data.

Abstract: An assembly for an autoinjector device, the assembly including a syringe support for supporting a syringe by limiting forward axial movement of the syringe relative to the syringe support, and a guard element attachable to the syringe support by an attachment so that the guard element is axially restrained both axially forwardly and axially rearwardly relative to the syringe support by the attachment. Forwardly directed axial loads received by the guard element are transmitted to the syringe support via the attachment.

Abstract: A cannula comprising a hollow tube made of a biocompatible, thermoplastic polymer, memory shape material, tipped with an injection needle at it distal end, assumes desired shapes as it distally emerges from a lumen or channel of an instrument such as an introducer or endoscope. The desires shape includes a curvature conforming to an inverse tangent function. The cannula may be supplied alone, with or without an injection needle, and in a sterile pouch, for use with a device of an user's choice that has a suitable lumen or channel to guide the cannula, of the cannula may be used without such an instrument.

Abstract: A sealed medication dispensing and administering device has a syringe, a plunger, a connecting holder, an elastic valve, and a liquid stopper. The syringe has an outer barrel having an air inlet tube and an inner barrel inserted inside the outer barrel and having a medication inlet tube. The plunger is inserted within the outer and inner barrels. The connecting holder is connected to the syringe and has a connecting cover with at least one outer connecting hole and two piercing needles respectively piercing inside the air inlet tube and the medication inlet tube. Inner spaces of the two piercing needles communicate with the at least one outer connecting hole. The elastic valve selectively covers the two piercing needles. The fluid stopper is disposed within the connecting cover and blocks one of the at least one outer connecting hole and the inner space of the air inlet tube.

Abstract: An incremental syringe useful for multiple injections of medications like botulinum toxin is provided. The syringe includes detents on the syringe plunger which provide a tactile feeling, a discrete audible sound or “click,” or preferably both, for every unit of medication aspirated or injected to or from an individual syringe. Hence, there is no need to look at the syringe, or bring it to the eye level, during use thereof. In some embodiments, a second set of detents is included, and in some embodiments a third set of detents is included. Syringe plungers useful for combining with a syringe body to produce such an incremental syringe are also described.

Abstract: A dose recording device adapted to be detachably sleeved on an injection pen having a wheel, a dial gauge and a press button both linked with the wheel is provided. The dose recording device includes a casing, a circuit board module, at least one optical sensor, a motion sensor and an adjustable fixing assembly. The casing includes a through hole for the injection pen passing through. The optical sensor is electrically connected to the circuit board module for detecting at least one of a value on the dial gauge and a position of the press button. The motion sensor is electrically connected to the circuit board module for detecting rotating vibration of the wheel and inversion state of the injection pen. The adjustable fixing assembly is for fixing the casing to the injection pen. A dose recording method is further provided.

Abstract: A system for delivering an injection of a fluid into a void within a subject is disclosed. A barrel extends from a first end to a second end and forms a lumen extending from the first end to the second end. A plug and a floating seal are arranged within the lumen. A hollow needle includes a distal end with an opening for fluid to flow from the lumen. The plug, the barrel and the floating seal include material and dimensions selected based on a threshold flowrate for a fluid arranged within the lumen to: overcome a force opposed to a force being applied to the fluid in the lumen to move the floating seal and the hollow needle into a tissue of the subject, and succumb to the opposing force to displace the fluid through the opening into the void.

Abstract: An automatic injection device including a housing, a chamber with a first compartment and a second compartment, and a seal structure between the compartments. The seal structure is initially in a sealing condition that seals the first compartment from the second compartment, where the seal includes a plug and an outer sealing member. The plug is slidably movable within the outer sealing member to convert the seal structure from the sealing condition to a mixing condition by opening a path between the first compartment and the second compartment. The automatic injection device also includes a needle assembly and an activation assembly. Activation of the activation assembly causes (1) pressurization of the first compartment, (2) the seal structure to convert from the sealing condition to the mixing condition, and (3) the first and second medicament components to be mixed and forced through the needle assembly.

Abstract: The safety syringe assembly is for inserting a needle into a patient and comprises a needle hub assembly and a safety cover. The needle hub assembly includes a needle, needle hub, and hub flex unit. The needle is mounted on the front side of the needle hub while the rear side is for receiving a syringe. The safety cover houses the needle hub assembly in a first position during shipping, a second position during insertion of the needle into the patient, and in a third position after the needle has been inserted into the patient while awaiting disposal. A portion of the safety cover includes magnification enabling a user to view a dosage calibration scale, needle bevel and air bubbles. The hub flex unit assumes a first enlarged position during shipping, is compressed during insertion into the patient, and slides into a third position after usage while awaiting disposal.

Abstract: A needle end and a safety syringe are provided, belonging to technical field of medical instruments. The safety syringe includes an injection end, a liquid storage device, and a base. The injection end includes a needle base, an injection needle, and a needle guard assembly. The injection needle is fixed to the needle base. The needle guard assembly is connected to the needle base. The needle guard assembly includes a protective casing and a spring, wherein a first terminal of the spring is connected to the needle base and a second terminal of the spring is connected to the protective casing. The liquid storage device includes a liquid storage container and a liquid storage sleeve. The liquid storage is sleeved on an outer surface the liquid storage container, wherein the liquid storage container is detachably connected to the injection end. The base is detachably connected to the liquid storage device.

Abstract: An attachment band for a fluid delivery apparatus includes an annular body having a wall defining a hollow inner space, an adjacent pair of attachment apertures extending through the wall, and an indicator aperture extending through the wall opposite the pair of attachment apertures. The indicator aperture includes an indicator portion that is configured to present an indication to a user of the fluid delivery apparatus of a tightness of the attachment band. A first strap extends radially outward from the annular body of the attachment band and is substantially aligned with the attachment apertures. A second strap extends radially outward from the annular body and is substantially aligned with the indicator aperture.

Abstract: An infusion device includes an infusion pump and an infusion tube assembly. The infusion tube assembly includes a first tube body connected to the infusion pump, a tube joint structure having first, second and third tube joints, a second tube body, and a clamping device on the second tube body. The clamping device is to clamp the second tube body. An infusion method includes instructing the infusion pump to perform an infusion operation. When bubbles are detected in a liquid in the infusion tube assembly, the infusion pump is instructed to stop the infusion operation and a bubble alarm is generated. After the infusion pump stops the infusion operation, it is determined whether a pressure of the liquid first drops to a first pressure value and then rises to a second pressure value. If yes, a rinsing operation is performed.

Abstract: A device for positioning a needle tip to a desired location by signaling pressure change is provided. The device includes a barrel, a piston, a biasing element, and a plunger. The barrel defines a reservoir, and it includes a distal end connectable to a puncturing apparatus. The plunger is slidably engaged with the piston, and both are movable within the reservoir. The biasing element connects the plunger and the piston, and its change in length corresponds to the relative position of the plunger and piston. In operation, the piston is at a first position relative to the plunger when the biasing element is at a first length. The piston later moves to a second relative position in response to the biasing element's change of the length resulting from a pressure change inside the reservoir when the puncturing apparatus reaches a location of a mass. The position's change of the piston is visually detectable.

Abstract: Microelectromechanical systems (MEMS) mesh-membrane nebulizers are described. The MEMS mesh-membrane nebulizers may include a piezoelectric MEMS mesh membrane. The piezoelectric MEMS mesh membrane may include a piezoelectric active layer patterned with openings for making droplets. One electrode of the piezoelectric MEMS mesh membrane may serve as an electrode for electroplating. Activation of the piezoelectric MEMS mesh membrane may generate droplets suitable for delivery of medicines or other uses.

Abstract: A portable inhalation device includes a medication storage component, a flow controller, an atomizer, a medication delivery component, and a pressure sensor. The medication storage component is configured to store medication. The flow controller is configured to cause a force to be applied to the medication stored by the medication storage component to transport the medication to the atomizer. The atomizer is configured to generate droplets from the medication. The medication delivery component includes a delivery channel extending from the atomizer to an outlet opening. The medication delivery component is configured to receive the medication in the delivery channel from the atomizer and dispense the medication via the opening. The pressure sensor is configured to detect a pressure corresponding to a flow rate of air in the delivery channel and output an indication of the detected pressure.

Abstract: A medication delivery apparatus and system for the application of a medical agent to a treatment site, such as an airway, and method for use of same are disclosed. In one embodiment of the medication delivery apparatus and system, a reservoir supplies a medical agent to a lower chamber of a housing wherein an ultrasonic transducer applies ultrasonic energy thereto, thereby nebulizing the medical agent. A control valve is interposed between a source of positive pressure air and an upper chamber of the housing to selectively apply positive air pressure to the upper chamber. Upon the application of positive air pressure, the airflow delivers the nebulized medical agent to a target location, such as the airway.

Abstract: A breath actuated nebulizer for administration of an inhaled medication to a patient is provided with a generally cylindrical body in a horizontal orientation to the patient. Within the body is a Venturi configured to nebulizer a liquid medication in a reservoir. Within the body is a shaft integrated with a baffle and diaphragm that slides horizontally in response to the breathing of a patient. During inhalation by the patient, the diaphragm flexes shifting the baffle over the Venturi, allowing nebulization to occur. When the patient exhales, the diaphragm flexes to a default position in which the baffle is distal to the Venturi, thereby stopping the nebulization. The diaphragm is biased to rest in this default position until the patient inhales again.

Abstract: A liquid storage assembly includes a liquid storage tube having a liquid storage chamber, a sealing member, an adjusting member, and a lower cover. The sealing member is received in the liquid storage tube and defines a second liquid intake hole fluidly communicating with the liquid storage chamber. The adjusting member is received in the liquid storage tube and is rotatable relative to the sealing member, the adjusting defines a communicating portion corresponding to the second liquid intake hole.

Abstract: Formulations containing pharmaceutical active agent, propellant, and water at least partially adsorbed on or absorbed within one or more nylon pellets or nylon components of, for example, an inhaler such as a metered dose inhaler. Canisters, typically sealed canisters, containing such formulations. Inhalers, such as metered dose inhalers, containing such canisters. Methods of making and using the same.

Abstract: The present disclosure relates to systems and methods for producing a consistent and effective herbal vapor. A sealed container pod may include a chamber wall defining an internal volume within which a pre-processed herbal composition (e.g., cannabis) is located. The container pod may include filters for the vapor produced from the herbal composition. The container pod may also include a support member for holding and evenly distributing the herbal composition within the internal volume during vaporization. A vaporizer may be configured to obtain information regarding the contents of the herbal composition. The vaporizer may expose the herbal composition to an automated series of timed temperature adjustments specifically tailored for producing a desirable herbal vapor. The herbal vapor may be collected into a bag and/or canister for subsequent consumption.

Abstract: An inhaler (60) has a breath actuated trigger mechanism (100) reactive to an inhalation flow to trigger the release of a substance to be inhaled. The inhaler (60) has an inspiration flow which is subject to a higher degree of flow governing post-triggering than pre-triggering. This allows the triggering flow rate to be closer to, or even higher than, the governing flow rate of the inhaler.

Abstract: A lung isolation tube assembly comprising a control valve that is adapted to be moved between a left lumen position, a right lumen position, and a both lumens position, a connector that is in fluid communication with the control valve, and a tube that is in fluid communication with the connector. The tube comprises a left lumen that is in fluid communication with the connector and a right lumen that is in fluid communication with the connector. The assembly also comprises a first cuff that is disposed around a portion of the right lumen and the left lumen and a second cuff that is disposed around the left lumen. The assembly is adapted to convey airflow or oxygen to a human lung via at least one of the left lumen and the right lumen. A method for isolating a human lung.

Abstract: A catheter mount is configured to be attached to a respiratory apparatus. The catheter mount includes a plurality of ports in fluid communication with each other. The plurality of ports include an interface port configured to connect to an interface tube, a conduit port configured to connect to a conduit tube, and at least one suction port configured to allow insertion of a suction catheter. The at least one suction port can be positioned to allow the suction catheter, when inserted, access to both the interface port and conduit port.

Abstract: The present invention provides an improved percutaneous dilation tracheostomy device. The device is configured to include all of the required components to perform a percutaneous tracheotomy. The device includes a retractable needle and an extendable j-wire rather than having separate components as in typical percutaneous tracheostomy devices. The device includes a dilator section to expand the diameter of a patient's stoma. The device is further configured to allow an operator to perform a bubble test to alert the user that the tube is in the trachea. In addition, the device is generally more compact than typical emergency tracheostomy devices.

Abstract: A sealing pad (100) for sealing a respiratory mask. The mask is configured to create a sealing interface. The sealing interface encircles the nostrils and includes portions crossing the nasal ridge and the concave portions. The pad has a face-contacting side to sealingly engage the face, and a mask contacting side to sealingly engage the mask. The pad (100) includes a portion for crossing the nasal ridge and portions (113) for crossing concave portions on either side of the nose such that the mask contacting side is engageable with the mask to define the portions of the sealing interface crossing the nasal ridge and the concave portions. The pad carries, or has one or more defined apertures (107) for carrying, one or more tube portions for conveying fluid across the sealing interface.

Abstract: A patient interface is configured to deliver a flow of pressurized breathable gas to a patient's airways. The patient interface includes a central portion with an opening configured to deliver the pressurized breathable gas to the patient's nares. A first stabilizing portion extends from the central portion and is structured to engage an outer side of a respective one of the patient's nostrils. A second stabilizing portion is opposite the first stabilizing portion and extends from the central portion. In addition, the second stabilizing surface is structured to engage an outer side of a respective one of the patient's nostrils. The central portion, the first stabilizing portion and the second stabilizing portion cooperate to form a U-shape configured to cradle the patient's nose so that the tip of the patient's nose remains exposed when the patient interface is mounted on the patient's face.

Abstract: Lightweight, portable oxygen concentrators that operate using an ultra rapid, sub one second, adsorption cycle based on advanced molecular sieve materials are disclosed. The amount of sieve material utilized is a fraction of that used in conventional portable devices. This dramatically reduces the volume, weight, and cost of the device. Innovations in valve configuration, moisture control, case and battery design, and replaceable sieve module are described. Patients with breathing disorders and others requiring medical oxygen are provided with a long lasting, low cost alternative to existing portable oxygen supply devices.

Abstract: The invention relates to a non-heated humidification device comprising a wick; a chamber for holding water in contact with the wick; and a gas inlet to the chamber, wherein the chamber and wick are configured to humidify gas passing through or over the wick at ambient conditions. The device may be modular and attachable to a flow generator. The device may comprise dual gas circuits and a control system for controlling the gas flow through the gas circuits in order to control the humidity of the gas output.

Abstract: The present disclosure pertains to manipulating electrical activity in the brain of a subject to facilitate wakefulness. The system comprises: a sensory stimulator; a sensor configured to generate output signals conveying information related to brain activity, activity of the central nervous system, and/or activity of the peripheral nervous system of the subject; and a processor configured to: receive a target wake-up moment for the subject; determine one or more activity parameters of the subject during the sleep session; determine whether the one or more activity parameters indicate the subject is in deep sleep a predetermined amount of time before the target wake-up moment; and, responsive to the one or more activity parameters indicating the subject is in deep sleep, cause the one or more sensory stimulators to guide the activity parameters and facilitate/accelerate a transition from deep sleep to light sleep before the target wake-up moment.

Abstract: The present invention relates to a novel snow globe having an aroma diffuser function, which can obtain indoor air freshening effects without installation of a separate aroma diffuser in the room, the snow globe comprising: a glass globe in which a miniature, a transparent liquid, and white flakes or powder are stored; and a support on which the glass globe is placed, wherein all or a part of the support is formed of an absorbent material, and the portion formed of the absorbent material is impregnated with a fragrance oil.

Abstract: A conditioning apparatus is provided with a control and command unit which can be activated remotely using an electronic device. A method to activate and control the conditioning apparatus includes regulating the functioning parameters of the conditioning apparatus at least as a function of a state of wakefulness or sleep of a user.

Abstract: A pineal gland vibration unit which may be designed to fit in the roof of the mouth of a user. The system may be designed to vibrate at a frequency which is pleasing to the senses. The system may be wirelessly operated. The system may induce spiritual awareness while meditating with the system installed. The device may further allow a user to meditate and become more aware of oneself during self-healing processes.

Abstract: A catheter for an extracorporeal blood circulator disperses a flow of blood flowing out from a blood feeding hole to reduce the impact of blood collision on a living organ. The catheter 60 includes a blood feeding lumen 61 extending in an axial direction and a blood feeding hole 63 communicating with a distal end of the blood feeding lumen, and a side portion 63a of the blood feeding hole on the proximal side facing the blood feeding lumen is cut out to a bottom portion 63b of the blood feeding hole.

Abstract: A gastric diverter and an antibacterial digestive tract catheter thereof are provided. The catheter comprises a membrane tube (31). One end of the membrane tube (31) is connected to a stent (32). The membrane tube (31) is made of an antibacterial material. The membrane tube (31) has an outer diameter of 10-35 mm, and a wall thickness of 0.001-0.3 mm. The membrane tube (31) is fixedly connected to the stent (32) by means of stitching, hot pressing, ultrasonic welding, or laser welding. The antibacterial digestive tract catheter is made of an antibacterial material to minimize occurrences of intestinal inflammation, and to ameliorate metabolic diseases, while also avoiding complications such as liver abscess and pancreatitis. Thus, the invention provides a safer and more effective medical instrument for the treatment of metabolic diseases such as diabetes.

Abstract: Disclosed is a catheter device including a proximal tube having a first part of a first lumen; a distal tube having a second part of the first lumen; a second lumen connecting the proximal tube and the distal tube; wherein the connection comprise an area of discontinuity between the first part and second part; wherein the area of discontinuity comprises a support element configured to resist axial movement of the distal tube relative to the proximal tube and vice versa; and wherein the second lumen is arranged to activate or cause at least one obstruction element to restrict the flow of urine from the proximal tube to the area of discontinuity and to restrict the flow of urine from the area of discontinuity to the distal tube.

Abstract: As a clot retrieval device, a dual-layer expandable aspiration catheter having a catheter with a distal slit and a flexible sheath surrounding the slit. The dual-layer expandable aspiration catheter maintains column strength (along the axis of the catheter) while the distal slit provide radial flexibility only to circumferential direction. This structure prevents the distal expandable segment from crumpling, thereby the stent retriever can be pulled into the expandable catheter smoothly.

Abstract: A fluid directing device may include a catheter and a skirt. The catheter may define a lumen and may have a distal end and a proximal end. The skirt may be attached to a distal region of the catheter and may encircle the catheter. The skirt may have a proximal end attached to the catheter, and a free distal end, the skirt having a sidewall extending between the proximal and distal ends thereof, the skirt configured to move between a collapsed state and an expanded state in which the sidewall extends radially away from the catheter, the sidewall defining an interior chamber in the expanded state, wherein the skirt is configured to prevent contrast media that exits the catheter lumen from passing through the sidewall.

Abstract: The technical objective of the present disclosure is to provide a steerable catheter enabling a lumen tip to approach an affected area only with an endoscope inserted together, without the aid of a C-type gantry based tomography apparatus. To this end, the steerable catheter according to the present disclosure includes: a housing; a lumen shaft; upper left, lower left, upper right and lower right wire parts; upper left, lower left, upper right and lower right stoppers; and a steering part for upwardly steering the terminal end of the lumen shaft by pulling the upper left and upper right wire parts, downwardly steering the terminal end of the lumen shaft by pulling the lower left and lower right wire parts, leftwardly steering the terminal end of the lumen shaft by pulling the upper left or lower left wire part, and rightwardly steering the terminal end of the lumen shaft by pulling the upper right or lower right wire part.

Abstract: A guidewire including a thin elongated structure and an outer shell around at least a portion of the thin elongated structure. The outer shell includes a first portion and a second portion. The first portion and the second portion of the outer shell are each coupled to the thin elongated structure. The first portion is spaced from the second portion by a gap. The guidewire is configured to move between a flexible state and a rigid state. The gap has a first distance when the guidewire is in the flexible state and the gap has a second distance greater than the first distance when the guidewire is in the rigid state.

Abstract: A system a guidewire and a tensioning mechanism. The guidewire includes a thin elongated structure and an outer shell around a first portion of the thin elongated structure. A second portion of the thin elongated structure is exposed outside the thin elongated structure. The tensioning mechanism is configured to engage the second portion of the thin elongated structure to move the guidewire between a flexible state and a rigid state.

Abstract: Catheter-supported therapeutic and diagnostic tools can be introduced into a patient body with a sheath slidably disposed over the tool. Once the tool is aligned with a target tissue, a first fluid-driven actuator can move the sheath axially from over the tool, for example, to allow a stent, stent-graft, prosthetic valve, or other self-expanding tool, to expand radially within the cardiovascular system, without having to transmit large deployment forces along the catheter shaft and sheath from outside the patient. A second fluid-driven actuator can be arranged in opposition to the first actuator to control release of the expanding tool or to recapture the tool within the sheath. The first and/or second actuators may comprise a balloon having a diameter larger than the sheath to provide the desired deployment and recapture forces with moderate fluid pressure.

Abstract: A tubular body that includes a plurality of first wires distributed in an annular portion of the tubular body, and a plurality of deformed second wires alternately disposed between each of the plurality of first wires, the plurality of first wires and the plurality of deformed second wires being in an alternately twisted arrangement in a longitudinal direction of the tubular body, where each of the plurality of first wires has a substantially circular shape in a cross section view, and each of the plurality of deformed second wires has a non-circular shape in the cross section view, has an arcuate side portion that receive a part of a side surface of an adjacent wire of the plurality of first wires, and has an annular sector shape protruding in a radial direction in the cross section view of the tubular body.

Abstract: The present invention relates to methods of transvascular retrograde access placement and to devices that facilitate these methods. For purposes of the present invention, transvascular retrograde access placement generally comprises the insertion of a vascular catheter into a central blood vessel through the puncturing of the central blood vessel from the inside of the central blood vessel with a needle or other similarly configured device, or a needle-tipped guidewire of the present invention, and exiting that needle from the patient through the skin rather than the traditional approach of inserting a needle from the outside of the skin surface to the inside of a blood vessel.

Abstract: A method for treating back pain in a patient in need of such treatment is provided. The method includes positioning a balloon catheter in or adjacent to a treatment zone containing a basivertebral nerve. A chemical denervation agent is administered with the balloon catheter such that the chemical denervation agent chemically ablates at least a portion of the basivertebral nerve. Kits, systems and methods are disclosed.

Abstract: A device for occlusion removal from a bodily lumen is described. The device includes a multi-lumen catheter, a manifold that attaches to the catheter, and an aspiration device that inserts through a lumen of the catheter. A method of removing an occlusion from a bodily lumen is also described, as is a kit containing the device.