Abstract: A computerized electro-mechanical drug delivery device configured to deliver at least one dose of two or more medicaments. The device comprises a control unit. An electro-mechanical drive unit is operably coupled to the control unit and a primary reservoir for a first medicament and a secondary reservoir for a fluid agent, e.g. a second medicament. An operator interface is in communication with the control unit. A single dispense assembly is configured for fluid communication with the primary and the secondary reservoir. Activation of the operator panel sets a first dose from the primary reservoir and based on the first dose and a therapeutic dose profile, the control unit is configured to determine a dose or range of the fluid agent. Alternatively, the control unit determines or calculates a dose or range of a third medicament. Further, a dispense interface for use with a drug delivery device is disclosed.

Abstract: A medicament injection device including a needle, a first stage that controls positioning of the needle at a depth into an animal when the device is pressed against the animal, and a second stage that injects the medicament through the needle into the animal after the needle is positioned at the depth and the device is further pressed against the animal. The device preferably includes a mechanism that permits the second stage to inject the medicament only after the needle is positioned at the depth. The depth of the needle preferably is adjustable, as is the amount of the medicament injected. In preferred aspects, these two features are independently adjustable. One or more springs, pneumatics elements, or other elements may automatically reset the first stage, the second stage, or both after the device is withdrawn from the animal. Also, associated methods.

Abstract: The present invention relates to a medicament delivery device comprising a housing (60), which housing is arranged to accommodate a medicament container (62); a drive unit (86) operably arranged to act on said medicament container (62) for expelling a dose of medicament; an activation unit (74) operably connected to said drive unit for activating said drive unit (86); said drive unit (86) comprising an actuation element (84) arranged movable inside the housing (60) from an initial position prior to activation, to a displaced position after activation; at least a first NFC-chip (170, 172) comprising specific information arranged on said actuation element; at least one shielding element (174) arranged to said housing, such as to shield said at least first NFC-chip (170, 172) from being read by an NFC-chip reader when said actuation element (84) is either in the initial position or in the displaced position.

Abstract: A jet injector that includes a prefilled syringe. The syringe includes a fluid chamber that contains a medicament. The syringe also has an injection-assisting needle, and a plunger is movable within the fluid chamber. A housing is configured for allowing insertion of the needle to a penetration depth. The housing includes a retractable guard and an interference component, e.g., a lock ring, adjacent to the retractable guard that interferes with the movement of the retractable guard. An energy source is configured for biasing the plunger to produce an injecting pressure to jet inject the medicament from the fluid chamber through the needle to an injection site.

Abstract: Processes and devices are disclosed for parenteral delivery of therapeutic fluids, in particular high-viscosity therapeutic fluids (e.g., protein therapeutics), by a chemical reaction that generates a gas. The device may include a first actuation chamber containing a first reagent, a second reaction chamber containing a second reagent, and a third therapeutic fluid chamber containing the therapeutic fluid. In a loaded configuration, a plunger separates the first chamber from the second chamber. In a delivery configuration, the plunger allows the first reagent from the first chamber to communicate and react with the second reagent from the second chamber. The generated gas acts upon a plunger to deliver the therapeutic fluid from the third chamber.

Abstract: A medicament delivery device and a controller is disclosed. The medicament delivery device includes a medicament container, plunger rod and a resilient member. The plunger rod is in contact with a slidable stopper within the medicament container for expelling a medicament. The resilient member is used for applying a force to the plunger rod upon a delivery of the medicament. In addition, the controller is configured to detect a completion of a delivery stroke of the plunger rod according to an inductive property of the resilient member.

Abstract: An injection device (1) for the delivery of medicament has an indicator (50) for providing an end of dose indication. The device comprises a housing (10), an extendable plunger (40), an actuation mechanism (30), a trigger arrangement (15), and an indicator (50). The extendable plunger (40) comprises a leading portion (42) and a trailing portion (48) configured to allow the plunger (40) to extend from an initial length to a maximum extended length, the plunger portions ((42),48) being slidably mounted within the housing (10). The actuation mechanism (30) is configured to move the leading portion (42) of the plunger (40) forwardly relative to a syringe (20) so as to express medicament from the syringe (20). The trigger arrangement (15) is moveable in use to release the actuation mechanism (30).

Abstract: An auto-injector for receiving a primed syringe includes: a plunger driver for coupling to a plunger head of the syringe when the syringe is fitted within the auto-injector, and configured to drive a plunger into a barrel of the syringe, wherein the plunger driver positioned on the auto-injector such that it is below the plunger head when the syringe is primed and fitted within the auto-injector.

Abstract: The present invention relates to an injection device comprising a torsion spring operatively connected to a dose setting member being adapted to set a dose to be ejected from the injection device. A rotatably mounted display member adapted to display the dose to be ejected in accordance with a setting of the dose setting member is also provided. The rotatably mounted display member is adapted to be rotated over an angle corresponding to at least one revolution of the display member. The display member may be implemented as a dose indicator barrel having numerals arranged along a helical path on an outer surface thereof, or alternatively, as a counting device having two or more display wheels having numerals arranged on an outer surface thereof.

Abstract: The present invention provides a drug injection device (1) for delivering multiple doses of drug, comprising: a housing (2) extending along a main axis, a dose expelling mechanism comprising a piston rod (60) configured to move relative to the housing (2) from a first position to a second position to cause ejection of a dose of drug, the piston rod (60) extending between a proximal piston rod end and a distal piston rod end and comprising a dosing track (63), the piston rod (60) further being movable relative to the housing (2) from an initial pre-use position to a final end stop position to cause accumulated ejection of a predefined total dose, a dosing track follower (17) fixed with respect to the housing (2) and adapted to travel the dosing track (63) during dose ejection, a dose setting mechanism operable to set the dose to be ejected by the dose expelling mechanism, electronic means (82, 90, 91, 92, 95) for registering a dose setting operation and for registering a dose size of an ejected dose, and a dis

Abstract: A rotary encoder includes an electret unit, an electrostatic field sensor, and a controller. The electret unit generates an electrostatic field. The electrostatic field sensor is disposed proximate to the electret unit to sense a modulation of the electrostatic field that varies with rotation of one or more rotary components of the rotary encoder about a rotation axis of the rotary encoder. The controller is electrically coupled to the electrostatic field sensor to track activations of the electrostatic field sensor as the one or more rotary components rotate. The controller is configured to digitally encode a rotational position of the one or more rotary components based upon the activations.

Abstract: An injection system, including an injector having a dispensing mechanism configured to dispense a medicament, and a ready-to-use indicator. The ready-to-use indicator includes a controller configured to interact with the ready-to-use indicator and an audio and/or visual indicator, a temperature sensor, and a temperature analog having similar thermodynamic properties of the medicament. The temperature sensor is configured to detect a temperature of the temperature analog which represents the dynamic temperature of medicament as the medicament is heated or cooled. The temperature sensor is configured to communicate the detected temperature to the controller and to alert the controller when a preset temperature is reached. The ready-to-use indicator is configured to alert a user when the preset temperature is reached, signifying the medicament is thermally ready to be delivered by the dispensing mechanism. The audio and/or visual indicator is configured to display indicate one or more notifications to the user.

Abstract: A drug pellet delivery system includes a housing having a cavity. A cartridge is positioned within the cavity and includes a body having a channel. The body includes a first pair of rails and a second pair of rails. A plunger is slidably disposed in the housing and the cartridge. The plunger is configured to move a drug depot through the channel and out of the housing. Kits and methods of use are disclosed.

Abstract: The present disclosure relates to a monitoring device arranged to be operably connected to a medicament delivery device, said medicament delivery device has a manually operated movable dose activating element, said monitoring device having an electronic circuit, said electronic circuit having a light emitting element and a light sensor, wherein said light emitting element and said light sensor are positioned in relation to said dose activating element so as to detect a manual operation of said dose activating element from an initial position.

Abstract: The present disclosure relates to a cap assembly for a medicament delivery device, having a cap containing a tubular body provided with a distal opening, the cap being configured to be mounted to a proximal end of a medicament delivery device, a tubular remover configured to be received in the distal opening of the cap, the remover having flexible radially inwards extending grippers configured to engage with a delivery member shield, and a tubular remover insert configured to be received by the remover and configured to be fixedly attached to the cap to prevent axial displacement of the remover insert relative to the cap, wherein the remover is axially displaceable relative to the cap and relative to the remover insert, from a first position in which the grippers are pressed radially outwards by an outer surface of the remover insert, to a second position located distally relative to the first position, in which second position the grippers are arranged distally beyond the outer surface of the remover insert,

Abstract: In one aspect, a safety pen needle assembly is provided herein which includes a hub with a needle fixed to the hub, the needle having a distal end, formed for insertion into a patient, and a proximal end. The assembly further includes a shield and a biasing member disposed between the hub and the shield configured to urge the shield distally. A protrusion extends from at least one of the hub and the shield with a channel being formed in at least the other of the hub and the shield. The channel is formed to accommodate the protrusion. The shield is movable from a first position to a second position. In the first position, the shield is spaced from the distal end of the needle such that the distal end of the needle is exposed. In the second position, the shield covers the distal end of the needle. The channel guides the protrusion as the shield moves from the first position to the second position. With this arrangement, a shield may be directed to move in a desired path with stability.

Abstract: In one aspect, a safety pen needle assembly is provided herein which includes a hub with a needle fixed to the hub, the needle having a distal end, formed for insertion into a patient, and a proximal end. The assembly further includes a shield and a biasing member disposed between the hub and the shield configured to urge the shield distally. A protrusion extends from at least one of the hub and the shield with a channel being formed in at least the other of the hub and the shield. The channel is formed to accommodate the protrusion. The shield is movable from a first position to a second position. In the first position, the shield is spaced from the distal end of the needle such that the distal end of the needle is exposed. In the second position, the shield covers the distal end of the needle. The channel guides the protrusion as the shield moves from the first position to the second position. With this arrangement, a shield may be directed to move in a desired path with stability.

Abstract: A drug delivery device is provided herein, the device including a reservoir for containing a medicament. The medicament includes a suspension of solids in a liquid carrier. The device also includes a needle having a distal end for injection into a patient, a proximal end in communication with the reservoir, and a lumen extending between the distal and proximal ends. A path is defined from the reservoir to the distal end of the needle through the lumen, the path having an inner diameter that decreases in a proximal to distal direction along at least a portion thereof. Advantageously, with the subject invention, a flow path may be defined which provides a more gradual transition in diameter from the reservoir to a distal tip of the needle. In this manner, changes in velocity of the suspension may be less abrupt than in the prior art, thus better maintaining solid particles in the suspension.

Abstract: The present invention relates to a position determination device (100) (and system) for determining and registering an injection location of a liquid drug administered on a body part of a user, wherein the position determination device (100) (and system) comprises a position determination element (110) configured to provide a position signal representing a current location of the position determination device (100), and one or more processing units (150) configured to derive data representing an actual injection location based on the user in response to a current location being determined by the position determination unit (110). The position determination device may be further configured for determining a dosage activity performed by a liquid drug administration device (200) based on obtaining at least one vibration signal from a vibration determination element (110).

Abstract: A syringe type ejection device capable of reducing an amount of residual liquid is provided. A syringe type ejection device includes: a barrel; a nozzle disposed to face the barrel; and a core inserted in the nozzle, the barrel having a large-diameter portion provided with a discharge space for discharging liquid, the nozzle being provided with a holding space for holding the core, the holding space being in communication with the discharge space, and the core being inserted in the discharge space.

Abstract: An inhalation device for delivering medication to a user may include a mouthpiece, a dosing chamber, and a flow channel connecting the mouthpiece to the dosing chamber. The dosing chamber may be configured to deliver the medication to the user via the mouthpiece. The inhalation device may include an electronically driven vibratory element, a sensor system configured to generate a pressure signal indicative of air flow through the flow channel, and a controller. The controller may be configured to receive the pressure signal from the sensor system (e.g., a micro-electrical mechanical (MEMS) pressure sensor). The controller may be configured to perform an inhalation detection procedure to determine a plurality of successful inhalations. For example, the controller may be configured to generate a trigger signal to control timing of operation of the electronically driven vibratory element to release medication into the dosing chamber based on the plurality of successful inhalations.

Abstract: An inhalation delivery device for dry powder with adjusting resistance through detachable heads, which combines four different detachable heads and uses a single base. The desired resistance and the medicament delivery/allocation to the lungs, are set, offering a practical, low cost solution while, at the same time, a high performance personalized treatment. The detachable head (1) comprises a mouthpiece (2) for the mouth of the patient, a medicament intake orifice (3) sized to fit into the mouth of a patient and a protrusion (4) for a sliding connection between the detachable head (1) and the base (5), via notches (6) carried by the base (5). Each detachable head (1) possesses a corresponding protrusion (4) which may be fitted onto the base (5). The device comprises typically four different heads (1), covering the entire spectrum of patients accordingly to their inhalation capacity, the medicament type/dose and the targeted point of treatment.

Abstract: The present invention provides for an enhanced eductor element that significantly increases the amount of pressure generated at the siphon tube without significantly increasing the flow resistance through the eductor. The invention further provides for breath-actuated inhalation devices including the enhanced eductor element as an actuation mechanism.

Abstract: An interface for positive pressure therapy includes a mask assembly, a headgear assembly and a connection port assembly. The mask assembly comprises a seal member that has an upper portion movably connected to an integrated lower portion, wherein the upper portion rolls during hinging movement of the upper portion relative to the lower portion. The headgear assembly allows connection to the mask assembly in a direction substantially normal to a direction of strap tension. The connection port assembly includes a swivel elbow with a valve member that controls flow through a port that opens toward the user.

Abstract: An endobronchial tube is provided that includes a medical tube comprising an endotracheal portion and a bronchial portion having a common single lumen extending between a proximal end and a distal end of the tube, a first endotracheal inflatable cuff for sealing against a trachea of a patient, a second endotracheal inflatable cuff positioned distal to the first endotracheal inflatable cuff for sealing against the trachea of the patient; a bronchial inflatable cuff positioned near a distal end of the medical tube after the first endotracheal inflatable cuff and the second endotracheal inflatable cuff, for sealing the left main stem bronchi of the patient, an intraluminal balloon blocker positioned along an inner surface of the bronchial portion for sealing the common single lumen at the distal end of the bronchial portion, and an aperture positioned between the endotracheal portion and the bronchial portion.

Abstract: An intubation system includes: a base configured to be secured relative to a subject; a guide movably coupled to the base to allow the guide to move relative to the base; and a connector configured to be connected to a distal end of the guide and to detachably connect to an endotracheal tube such that as the guide is moved relative to the base toward the subject, the endotracheal tube is inserted into the subject.

Abstract: An expandable endotracheal device includes: an elongated body configured to change from smaller-size state to a larger-size state; where in the smaller-size state, a perimeter, and thus a cross-sectional area, of the elongated body is restricted to facilitate insertion of the elongated body within a passageway of an in-use endotracheal tube; and where the elongated body is configured to: have at least a portion of the perimeter of the elongated body seal to a trachea of a subject; or provide an inner passageway extending through the elongated body along a length of the elongated body and with a boundary defining the inner passageway being configured to slidably receive a ventilation mechanism; or a combination thereof.

Abstract: An endotracheal intubation device has a flexible main tube having an outer end and a patient end for permitting passage of air from an environment outside a patient into a trachea of the patient when the patient is intubated with the device. An inflatable and deflatable balloon is attached to the main tube at a position closer to the patient end than the outer end of the main tube. The balloon is inflatable in the trachea to immobilize the main tube in the trachea. The balloon has a wall and the wall has a recess in a top surface thereof for collecting fluid secretions of the patient intubated with the device to prevent the fluid secretions from passing down the trachea into lungs when the balloon is deflated in the trachea. Preventing fluid from reaching the lungs when the device is removed reduces risk of ventilator associated pneumonia (VAP).

Abstract: The present disclosure provides for a method of performing a percutaneous dilational tracheostomy (“PDT”) that includes inserting a tracheal tube including an inflatable cuff through a mouth and into a trachea of a patient; inserting a bronchoscope into the tracheal tube; inserting a puncturing wire through a channel of the bronchoscope. The puncturing wire includes a sharp cutting end and a dull gripping end. The method also includes puncturing the trachea of the patient with the sharp cutting end of the puncturing wire from within the trachea at a selected location to create a stoma; passing at least one dilator over the sharp cutting end of the puncturing wire for dilating the stoma; inserting a tracheostomy tube into the trachea through the stoma; and removing the puncturing wire from the patient.

Abstract: A facemask configured to be used by multiple sized/shaped heads can include a primary, a secondary and a tertiary seal. In some embodiments, the primary seal is contact with the nose and cheek regions; the secondary seal is in contact with the chin region; and the tertiary seal is in contact with the cheek and chin regions. In some embodiments, the tertiary seal extends inwardly and outwardly when applied to the face. In some embodiments, the mask includes test scissors.

Abstract: A full-face mask assembly includes a frame and a cushion provided to the frame. The cushion is adapted to form a seal around the patient's nose and mouth. A flexible lip is provided to an interior wall of the cushion. The flexible lip is adapted to engage the frame to provide a seal in use.

Abstract: A nasal assembly for delivering breathable gas to a patient includes a frame having an integrally formed first connector portion. A nozzle assembly includes a gusset or base portion and a pair of nozzles. At least one inlet conduit is structured to deliver breathable gas into the frame and nozzle assembly for breathing by the patient. A pair of second connector portions are removably and rotatably connected to respective first connector portions of the frame and are in communication with respective inlet conduits, e.g., directly or via angle connectors. A headgear assembly is removably connected to the pair of second connector portions and/or the angle connectors so as to maintain the frame and the nozzle assembly in a desired adjusted position on the patient's face.

Abstract: New medical circuit components and methods for forming such components are disclosed. These components include microstructures for humidification and/or condensate management. The disclosed microstructures can be incorporated into a variety of components, including tubes (e.g., inspiratory breathing tubes and expiratory breathing tubes and other tubing between various elements of a breathing circuit, such as ventilators, humidifiers, filters, water traps, sample lines, connectors, gas analyzers, and the like), Y-connectors, catheter mounts, humidifiers, and patient interfaces (e.g., masks for covering the nose and face, nasal masks, cannulas, nasal pillows, etc.), floats, probes, and sensors in a variety of medical circuits.

Abstract: Filter made entirely with natural and biodegradable materials, for the protection of the respiratory tract of patients in the medical-surgical field and process for making it. The filter has a porosity or 80-98% and pore diameters of 100-350 micrometers and the pores have a shape of channels open at the ends, which are parallel to each other. The filter is obtained by preparing an aqueous solution of chitosan and an aqueous solution of gelatin, mixing them, pouring it into a container, keeping the container closed until obtaining a hydrogel and freeze-drying. A cross-linking step takes place by (a) adding a chemical cross-linker to the mixture of the chitosan and gelatine solutions and cross-linking before freeze-drying, or (b) subjecting the freeze-drying product to a thermal dehydration treatment.

Abstract: A system for generating nitric oxide can include an apparatus positioned in a trachea of a mammal, the apparatus in-eluding a respiration sensor for collecting information related to one or more triggering events associated with the trachea, an oxygen sensor for collecting information related to a concentration of oxygen in a gas, and one or more pairs of electrodes for initiating a series of electric arcs to generate nitric oxide, and the system for generating nitric oxide can also include a controller for determining one or more control parameters based on the information collected by the respiration sensor and the oxygen sensor, wherein the series of electric arcs is initiated based on the control parameters determined by the controller.

Abstract: Disclosed herein are systems and methods for treating memory impairment, and more specifically to customized visual presentation for treating memory-related disorders and diseases. The disclosed systems and methods can predict clinical status of patients based on platform user behavior, such as those of patients. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Abstract: The invention concerns a device for helping a user fall asleep, comprising a light source designed to emit a substantially monochromatic red or quasi-monochromatic light encouraging the user to fall asleep, characterized in that it comprises a control unit designed to automatically control said light source according to a predefined law according to which the light power emitted by said light source decreases gradually over time in such a way as to change automatically between a maximum power value and a minimum power value, the light power emitted by said light source at a given time always being greater than or equal to the light power emitted at a subsequent time.

Abstract: An electronic stress relieving device has a base with at least one light source attached to the base. The at least one light source produces a light that passes through a light diffuser which is at least partially translucent and is disposed over the at least one light source so that the light is diffused when viewed through the light diffuser. An energy source is provided and electrically connected to the at least one light source and an electronic controller. The electronic controller allows a user to operate the at least one light source in a selected mode of operation and the user then views the pattern of light as it is displayed on the light diffuser to help relieve stress.

Abstract: The present invention is a visual effect software that operates in a cyclical manner to guide breath meditation and promote mindfulness. The present invention works closely with a device operating system, allowing the user to run other applications in addition to the invention. This invention is differentiated in its ability to guide meditation and make the user more mindful alongside regular device use, without a user interface or information input. The invention is unique in its novel form of visual communication, communicating with users via overall pixel-quality time differentials, as opposed to absolute pixel states. The list of applicable devices is comprised of computers, smartphones, and tablets, and works with attached devices like projectors. After a user learns the breath meditation, the invention can make the user more mindful whenever the user perceives its presence. The effectiveness of the invention increases when the user completes complementary guided meditations.

Abstract: Disclosed herein are expandable introducer sheaths and methods of making and using the same. The sheaths minimize trauma to a patient's vasculature by allowing for temporary expansion of a portion of the sheath to accommodate passage of a delivery system for a cardiovascular device, then return to a non-expanded state after the passage of the device. The sheath includes an elongated annular member through which the cardiovascular device and its delivery system pass. In an embodiment, the annular inner member can be formed by coextruding a first and second material. The first material includes a fold, and the second material radially spaces the different parts of the fold from each other during fabrication and provides support for maintaining the tubular structure. The second material is removed once the coextrusion process is complete.

Abstract: A catheter includes a tubular inner layer, a reinforcing layer disposed at least partially within the inner layer or on an outer circumference of the inner layer, and an outer layer. The reinforcing member is made of wound wires, each adjacent pair of the wires having a gap therebetween. A bonding portion is disposed in the gap of the reinforcing layer and includes an inner layer protruding portion of the inner layer that extends into the outer layer and is engaged with an outer layer protruding portion of the outer layer that extends into the inner layer. This configuration enlarges the area across which the outer layer and the inner layer are bonded to each other within the gap of the reinforcing layer, leading to a strengthened bond between the outer layer and the inner layer.

Abstract: A multilumen curved split-tip catheter comprises a proximal end, a distal end and an elongated portion arranged between a proximal end and a distal end, defining a longitudinal axis. Elongated portion includes triple lumens for a blood flow therethrough, two arterial lumens and one venous lumen. The triple lumens are fixed to make a venous lumen is located between two arterial lumens along the length of the catheter to two dividing points. Also, the triple lumens are not at the same level with respect to each other inside a blood vessel after insertion. Each lumen extends between a distal end and a proximal end and includes a port at a distal end thereof in a communication with the lumen. Distal end has three curved distal segments that are splitted (separated) from each other with respect to a longitudinal axis.

Abstract: The following describes various applications and uses for a controllably rigidizable flexible device or sheath. Such rigidizing mechanisms can allow for a transition between a rigid state and a flexible state of a sheath. Rigidization can be applied along an entire length of a flexible sheath or along select portions of the sheath, and the rigidization can be of varying stiffness. Rigidization can be user controlled or automatically controlled using computer processes.

Abstract: An instrument (203; 204) for endoscopic applications. The instrument is able to be guided through a curved shaped tube (201; 202) and has an intermediate cylindrical element (3) with a handling end portion with a flexible portion and actuating means located at an actuating end portion. The intermediate cylindrical element (3) has a first cylindrical part (31; 151) at the handling end portion, a second cylindrical part (35; 155) at the actuating end portion and a number of longitudinal elements (38; 60; 70; 80; 90; 100; 110; 130; 153) for transferring the movement of the actuating means to the handling end portion. The longitudinal elements are separated by longitudinal slits in the intermediate cylindrical element.

Abstract: A vascular catheter system is provided with a flexible main body and a flexible shaped tip. The tip is located at the distal end of the main body and has at least a portion configured to deviate from a longitudinal axis when in a relaxed state and towards alignment with the longitudinal axis when a guidewire is extended through a lumen of the shaped tip. The shaped tip is no longer than 1 cm and includes at least three sections. The second section is located distally from the first section, and the third section is located distally from the second section. The second section includes a first material having a first durometer and a second material having a second durometer lower than the first durometer. The first section includes the first material without the second material, and the third section includes the second material without the first material.

Abstract: A retainer includes a first arcuate wall and a second arcuate wall that together define a channel designed to receive a medical article. The retainer has an open configuration wherein a first end of the first arcuate wall is spaced away from a first end of the second arcuate wall, and a closed configuration wherein the first end of the first arcuate wall is adjacent the first end of the second arcuate wall. A second end of the first arcuate wall opposite the first end of the arcuate wall may be spaced away from the base in the open configuration and pressed against the base in the closed configuration. The retainer also may include a first support and a second support fixed to the base, and a first and second flexible coupling connecting the first and second supports to the first and second arcuate walls.

Abstract: A catheter apparatus may have a flexible shaft, guidewire lumens passing through the shaft, and a positioning device for positioning the guidewires relative to an external lumen. The positioning device may be an expansible scaffold covered with a retractable sheath. The positioning device may also be one or more balloons that are inflated through an inflation port in the shaft. The catheter apparatus may be operated by inserting a guide catheter into a vasculature with a chronic total occlusion, inserting the catheter apparatus into the guide catheter, and advancing the guidewires through the guidewire lumens and into contact with a chronic total occlusion. The positioning device may be activated before and/or between attempts to pass the guidewires through the chronic total occlusion to interrogate various parts of the chronic total occlusion.

Abstract: Some embodiments of a medical device anchor system include an anchor device that receives a catheter (or other medical instrument) and secures the catheter in place relative to a skin penetration point. In some embodiments, the anchor device can secure the catheter in an operative position relative to the skin without the use of sutures or skin tapes.

Abstract: A self-slitting open lumen cannula may be used with catheter adapters to reduce manufacturing complexity and costs, as well as improve the safety of the catheter adapters against fluid leakage. The open lumen cannula may also include one or more notches to facilitate flashback visualization. The catheter adapters may further include a catheter adapter body formed of a compliant material that houses one or more compression resistant septa with at least one lumen formed by the proximal end of the needle during a self-slitting process as the catheter adapter is assembled. The compression resistant septum may also be coupled to a compression cap that imparts a radial compression force on the one or more compression resistant septa such that the at least one lumen narrows and seals when the cannula is removed.

Abstract: The utility model discloses a urinary catheter for women and peristaltic pump, which comprises a body tube with an inner surface and an outer surface, and further comprises an external urethral orifice fixing part which can at least sleeve the catheter tip end inside when applied, a flexible urethral guide part, a urinary catheter driving part sleeved with the cylindrical body of the external urethral orifice fixing part, a hydrophobic part for leakage stop at the urinary outlet of the urinary catheter, a thin segment, a pump tube, a tube bed and other special structures for dilating the narrowed part of the urethra, which not only eliminate the defect of the traditional “non-guided suspended placement” in a safe mode of “US-guided adjacent placement” and completely avoid contamination of the urinary catheter by the periurethral tissue, but also avoid the injury of urethral intima caused by urethral stricture in the placement procedure to the greatest extent; avoid contamination of the urinary catheter outlet