Abstract: An example injector includes a rotary knob for selecting a function and setting a dosing quantity for an injection, a button located on an end of the rotary knob for initiating the injection, an electric motor, an encoder for evaluating output rotary motion of the motor, and a processor that converts the dosing quantity into a number of encoder pulses and controls operation of the motor based on the number of encoder pulses when dosage is triggered. The injector also includes a transmission coupled to the electric motor to convert a speed of the motor, a threaded spindle coupled to the transmission that moves linearly based on the output rotary motion of the motor at the speed as converted by the transmission, and a punch connected to an end of the threaded spindle. The linear movement of the spindle causes the punch to release medicament.

Abstract: A drug injection system includes a cartridge adapter and a drug injection device. The cartridge adapter includes: a main body case; an attachment portion provided on the main body case used for attachment to the drug injection device; an accommodating portion that accommodates therein a drug cartridge; a piston; a piston gear that allows the piston to slide therethrough; a stopper that stops movement of the piston gear; and a release lever that releases a locked state of the piston gear. The drug injection device includes: a casing that accommodates therein a portion of the cartridge adapter; an engagement portion that engages with the cartridge adapter; a drive gear to which the piston gear of the cartridge adapter is connected; a motor connected to the drive gear; and a release bar that drives the release lever of the cartridge adapter.

Abstract: A mixing vial having a hollow interior chamber with a tubular portion having distal and proximal open ends and a stopper positioned in sealing relationship in the tubular portion, the stopper having a hollow interior chamber with an open end and a dislodgeable plug positioned in and sealing the open end.

Abstract: The disclosed technology relates to medicinal fluid injection devices. In one aspect, a medicinal fluid injection device includes a housing having an opening in a side surface thereof, a storage container arranged inside the housing and configured to store a medicinal fluid, an injection needle connected to the storage container and configured to inject the medicinal fluid when stored in the storage container through the opening, and a cover body covering the opening, wherein the cover body includes a cover part configured such that the shape of the cover part changes according to air pressure caused by the injection needle.

Abstract: Sensing systems are disclosed for determining the relative rotational movements of members of a medication delivery device which are proportional to the amount of a dose set and delivered by the medication delivery device. The sensing system comprises a first sensor component secured to a first member and a second sensor component secured to a second member. During dose setting, the second member is coupled to a third member which rotates relative to the first member in proportion to the dose set. During dose delivery, the second member is coupled to a fourth member which rotates relative to the first member in proportion to the dose delivered. The sensing system separately detects the relative rotational positions of the first and second sensor components during dose setting and dose delivery, and provides outputs used to determine the amounts of the set and delivered doses. The sensing system outputs this information to a controller which determines the amount of the dose set and delivered.

Abstract: An example injector includes a rotary knob for selecting a function and setting a dosing quantity for an injection, a button located on an end of the rotary knob for initiating the injection, an electric motor, an encoder for evaluating output rotary motion of the motor, and a processor that converts the dosing quantity into a number of encoder pulses and controls operation of the motor based on the number of encoder pulses when dosage is triggered. The injector also includes a transmission coupled to the electric motor to convert a speed of the motor, a threaded spindle coupled to the transmission that moves linearly based on the output rotary motion of the motor at the speed as converted by the transmission, and a punch connected to an end of the threaded spindle. The linear movement of the spindle causes the punch to release medicament.

Abstract: A determination device for determining a value representing a dose of a dose metering device includes an eddy-current-based rotational angle sensor. The rotational angle sensor can be coupled to a rotatable dosing knob of the dose metering device and can image a rotational angle of the dosing knob representing the dose in a rotational angle signal. The determination device further includes an analysis device that can establish the value of the dose using the rotational angle signal.

Abstract: An example injector includes a rotary knob for selecting a function and setting a dosing quantity for an injection, a button located on an end of the rotary knob for initiating the injection, an electric motor, an encoder for evaluating output rotary motion of the motor, and a processor that converts the dosing quantity into a number of encoder pulses and controls operation of the motor based on the number of encoder pulses when dosage is triggered. The injector also includes a transmission coupled to the electric motor to convert a speed of the motor, a threaded spindle coupled to the transmission that moves linearly based on the output rotary motion of the motor at the speed as converted by the transmission, and a punch connected to an end of the threaded spindle. The linear movement of the spindle causes the punch to release medicament.

Abstract: The disclosure provides a dose controlled multi-shot injection device comprising a housing and a dose setting mechanism, wherein the dose setting mechanism includes a drive spring, a rotatable dose setting handle adapted to set a dose of medicament, thereby biasing the drive spring, and a ratchet mechanism for maintaining the drive spring in a biased state against a spring force at a set dose.

Abstract: A needle guard device mountable to a pre-filled syringe in its ready-to-fill state. The device includes a device shield interconnected to a lock collar with flexible member and biased to move relative to the lock collar. The lock collar interfaces with the syringe neck to attach the device to the syringe. As the device shield moves proximally, rotation arms of the lock collar interact with angled cutouts in the device shield, causing the device shield to rotate relative to the lock collar and disengaging one or more keys on the device shield from one or more keyways in the lock collar triggering the device shield to move from a first configuration in which the device shield is retractable to expose a syringe sharp to a second configuration in which the device shield is fixedly positioned to cover the syringe sharp.

Abstract: A medical puncture needle comprising includes: a rod-shaped body portion; and a blade surface formed at a distal end portion of the rod-shaped body portion. The blade surface includes: a first blade surface portion that is inclined with respect to a central axis of the body portion and extends to a tip, and a second blade surface portion that is formed on a back side of the first blade surface portion. A blade edge extending to the tip is formed by a ridgeline at which the first blade surface portion intersects the second blade surface portion. The second blade surface portion comprises a first plane and a second plane having different angles with respect to a virtual plane including the central axis passing through the tip at an orthogonal cross-section that is orthogonal to the central axis.

Abstract: A wearable drug delivery device that can deliver a liquid drug stored in a container to a patient is provided. The container can be a prefilled cartridge that can be loaded into the drug delivery device by the patient or that can be preloaded within the drug delivery device when provided to the patient. A sealed end of the container is pierced to couple the stored liquid drug to a needle conduit that is coupled to a needle insertion component that provides access to the patient. A drive system of the drug delivery device can expel the liquid drug from the cartridge to the patient through the needle conduit. The drive system can include a spring coupled to a plurality of force transfer elements. The force transfer elements can have a variety of shapes and configurations.

Abstract: A needle mechanism module for automatically inserting a fluid path into a patient for drug delivery is provided. The needle mechanism module can be a component of a wearable drug delivery device. The needle mechanism module can insert a needle and cannula into the patient responsive to activation of the drug delivery device by a user. After insertion, the needle can be automatically retracted, leaving only the cannula in the patient. As a result, discomfort of the user is reduced.

Abstract: A pen needle assembly having a hub with an increased surface area that contacts a patient's skin is provided. The increased contact area of the hub with the patient's skin during injection of a cannula decreases the pressure exerted against the patient's skin, thereby increasing the comfort of the patient. A bonding adhesive is disposed on an outer surface of the hub, thereby decreasing the required curing time of the adhesive. Additionally, the increased contact area, between the cannula adhesive and hub increases the strength of the bond therebetween.

Abstract: An injection device includes a cylinder having a cavity for receiving liquid. A passage is connected to the cavity for inflow and/or outflow of liquid. The passage can be connected to an injection component. A shut-off valve has a valve body and flexible sealing ring with an opening. The valve body, proceeding from a release position in which the passage is freed, is at least partially movable through the opening of the sealing ring to a blocking position in which the valve body engages behind the opening so that movement of the valve body to the release position is blocked and the passage is sealed off against proximally directed flow. An adapter body is connected to the hollow cylinder. The shut-off valve is arranged at the proximal end of the adapter body and at the distal end of the hollow cylinder. The device can be used in a syringe.

Abstract: Described herein are compositions, methods and an apparatus relating to the pulmonary delivery of an inhalable composition comprising caffeine, or a salt thereof, and a solvent selected from the group consisting of propylene glycol, glycerol, ethanol and a combination thereof.

Abstract: A method comprises positioning a medical appliance having a primary pressure sensor at or within a patient incision site and supplying an insufflation fluid to the patient cavity. The method further comprises measuring a pressure in the patient cavity by the primary pressure sensor and controlling the supply of insufflation fluid by an insufflator to the patient cavity based at least on the measured pressure. The method further comprises determining, by a processor associated with the insufflator, that the measured pressure may be inaccurate and, in response to determining that the measured pressure may be inaccurate, controlling, by the insufflator, the supply of the insufflation fluid to the patient cavity based at least on a pressure measured by a backup pressure sensor.

Abstract: An inhaler is proposed, comprising an annular magazine having capsule chambers oriented radially and capsules provided in said chambers, which allows ease of use and reliable dispensing of a formulation to be inhaled which is held in the capsules.

Abstract: Sole purpose of this invention process is to discretely and freely gravity feed highly viscous and solid matter medical marijuana concentrate substances from within a portable, closed and compact vaporizer system, offering protection of the very costly chambered concentrates as well as allow the user to abide by or use discretion with the use of their medicinal concentrate substance.

Abstract: The present disclosure provides devices for delivery of powder formulations and methods of manufacture and use of such devices.

Abstract: In one embodiment, the present invention provides a system to deliver at least one therapeutic gas to a spontaneously breathing patient, wherein the rate of delivery of the at least one therapeutic gas exceeds the patient's inspiratory flow rate, and the amount of the at least one therapeutic gas that is wasted is minimized or eliminated.

Abstract: A method of detecting stroke in a patient receiving a pressure support therapy includes: receiving data from one or more sensors structured to gather data related to patient respiration while receiving pressure support therapy from an airflow generator via a patient circuit; analyzing the data from the one or more sensors while pressure support therapy is provided to the patient; determining that the analyzed data from the one or more sensors is indicative of a patient experiencing respiratory changes indicative of a stroke; and responsive to said determining, triggering at least one alarm.

Abstract: The present invention relates to a method and a respiration device having a respiration unit for generating an airflow for the respiration and having a monitoring unit. The monitoring unit is used to detect a respiration parameter and to classify events in the respiration on the basis of monitoring of the respiration parameter. In this case, the monitoring unit is configured to carry out an event analysis to recognize an occurrence, which is characteristic for Cheyne-Stokes respiration, of chronologically successive events and for this purpose to ascertain the period length thereof and to compare them to one another and to register the presence of Cheyne-Stokes respiration when the compared period lengths each deviate by less than 40% from one another.

Abstract: A cushion is for use in a pressure support system for delivering a flow of breathing gas to an airway of a patient. The cushion includes a body having a first end and a second end located opposite the first end. The body defines a space therein. The cushion further includes a sealing portion defining a single opening into the space. The single opening is adapted to surround both a first nostril and a second nostril of a patient. The sealing portion is located between the first end and the second end. The sealing portion includes a first protruding portion and a second protruding portion each extending outwardly from the body and being adapted to sealingly engage against an interior surface of a corresponding one of the first nostril and the second nostril.

Abstract: A mask system for use between a patient and device to deliver a breathable gas to the patient includes a mouth cushion, a pair of nasal prongs, an elbow, and a headgear assembly. The mouth cushion is structured to sealingly engage around an exterior of a patient's mouth in use, and the pair of nasal prongs are structured to sealingly communicate with nasal passages of a patient's nose in use. The elbow delivers breathable gas to the patient. The headgear assembly maintains the mouth cushion and the nasal prongs in a desired position on the patient's face. The headgear assembly provides a substantially round crown strap that cups the parietal bone and occipital bone of the patient's head in use.

Abstract: A patient interface structure for delivery of respiratory therapy to a patient includes a front plate configured to conform to the shape of the patient's face; a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; and a nasal cushion configured to seal the patient's nasal airways. The nasal cushion is supported by the mouth cushion, does not contact a bridge of the patient's nose in use, and extends at least partially into the breathing chamber. A patient interface system includes a patient interface structure and a patient interface structure positioning system configured to position, stabilize and secure the patient interface structure in sealing engagement with the patient's face.

Abstract: A mask system for delivery of respiratory therapy to a patient includes a nares portion and a mouth portion and an inlet conduit connected to at least one of the nares portion and the mouth portion to deliver the pressurized, breathable gas. The mask system is adapted to selectively utilize the nares portion and/or the mouth portion in a first mode utilizing both the nares portion and the mouth portion, and in a second mode utilizing the nares portion and not utilizing the mouth portion.

Abstract: A patient interface structure for delivery of respiratory therapy to a patient includes a front plate configured to conform to the shape of the patient's face; a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; and a nasal cushion configured to seal the patient's nasal airways. The nasal cushion is supported by the mouth cushion, does not contact a bridge of the patient's nose in use, and extends at least partially into the breathing chamber. A patient interface system includes a patient interface structure and a patient interface structure positioning system configured to position, stabilize and secure the patient interface structure in sealing engagement with the patient's face.

Abstract: A patient interface structure for delivery of respiratory therapy to a patient includes a front plate configured to conform to the shape of the patient's face; a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; and a nasal cushion configured to seal the patient's nasal airways. The nasal cushion is supported by the mouth cushion, does not contact a bridge of the patient's nose in use, and extends at least partially into the breathing chamber. A patient interface system includes a patient interface structure and a patient interface structure positioning system configured to position, stabilize and secure the patient interface structure in sealing engagement with the patient's face.

Abstract: A positive pressure ventilation (PPV) appliance module includes an adapter that couples to a port on an NIV mask and an appliance for performing a respiratory care procedure. The adapter is configured to form a PPV seal with the port of the PPV mask and also form a PPV seal with the appliance. The PPV appliance module allows clinicians to perform procedures through the NIV mask without disrupting the therapeutic pressure.

Abstract: A conduit for conveying a flow of a gas therethrough includes an inner wall having a first end and an opposite second end. The inner wall is disposed around, and defines a central passage extending between the first end and the second end. The central passage is structured to convey the flow of the gas therethrough between the first end and the second end. The conduit also includes an outer wall disposed about the inner wall and a sealed compartment defined between the inner wall and the outer wall, the sealed compartment being structured to house a fixed quantity of a gas therein.

Abstract: Embodiments relate to systems and methods for therapeutic gas delivery for personal medical consumption. A hydrogen delivery system herein can include one or more electrolytic cores which use source water to carry out electrolysis-based reactions, and obtain free hydrogen (H2) gas which can be separated using a proton exchange membrane (PEM) or other filter for collection and delivery to a user. In aspects, the electrolytic core or cores can be constructed or scaled to produce a sufficient amount of hydrogen (H2) gas so that the user can ingest that gas directly, immediately, and/or in real-time or near real-time, without a need for storage of the gas. In aspects, the system can be portable, and configured with a vent port to eliminate oxygen (O2) gas that may accumulate during electrolytic reactions, and also a coalescer unit to reduce or eliminate water or water vapor from the output hydrogen (H2) gas.

Abstract: A breathing circuit for delivering heated, humidified gases to a patient for medical purposes is described, comprising a humidifier chamber holding a quantity of water, a blower unit that delivers a pressurized gases stream to the chamber inlet, and a control system that adjusts output parameters of the breathing circuit, the circuit including a heater plate which heats the water in the chamber so that gases flowing through the chamber become heated and humidified, the circuit also including a gases transportation pathway and patient interface to convey heated humidified gases to a patient, the gases transportation pathway including an RFID tag located at the patient end which senses a parameter of the gases passing through the pathway, the control system including an RFID interrogator interrogating and receiving data relating to the sensed parameter from the RFID tag in real time, and adjusting the output parameters of the breathing circuit accordingly.

Abstract: A catheter with a lumen and comprising side port(s) through the elongate body of the catheter at predetermined locations. The side port(s) may be positioned at anatomical locations of interest and a fluid, e.g., a medicament, infused down the catheter's lumen, the fluid flowing out of the side port(s) to treat the anatomical location. Alternative embodiments may include a translatable inner sheath that may cover some of the side port(s) and may also include an aperture that may align with at least one of the side port(s). The side ports may be opened and closed by means of an acuator such as a push/pull wire or an electrically response shape memory material. A selective filter may be used to cover the side ports, whereby only fluids of certain viscosities and/or molecular size may pass through the filter and side port.

Abstract: The present disclosure relates to a urinary catheter comprising a catheter tube having a proximal end and a distal inlet end portion comprising a rounded catheter tip. The distal inlet end portion further comprises a lateral urine inlet opening and the catheter tube comprises a drainage channel in fluid communication with the urine inlet opening. The catheter furthermore comprises an inflatable retention member at the distal inlet end portion, wherein the inflatable retention member is in fluid communication with an inflation channel. The distal inlet end portion is provided with a curved internal cavity. The curved internal cavity furthermore extends in a longitudinal direction along the distal inlet end portion, over the rounded catheter tip and extends further along the opposing side of the distal inlet end portion in a longitudinal direction. The inflatable retention member is formed by said curved internal cavity.

Abstract: The invention relates to urinary catheters having a catheter tube with a first connection on the distal end and at least one catheter eye to be positioned in the urinary bladder. The urinary catheters are distinguished in particular in that they may be used problem-free as indwelling catheters. To this end, disposed in the urinary bladder is a reservoir container that is connected via a channel running parallel to the catheter tube to a second connection as distal end of the channel. In addition, the channel is connected to the urethra via at least one opening of the channel wall.

Abstract: A combination flush catheter and selective catheter as one convertible catheter and methods of using the same. The selective catheter may be a reverse curve or guide catheter. The additional steps of removal of the flush catheter and re-insertion of the selective catheter may be eliminated, reducing the possibility of errors and making the procedure smoother and shorter.

Abstract: A coated urinary catheter or urinary stent device includes a urinary catheter or stent which, in a deployed position, includes or defines a protective surface area and a protected surface area and a coating upon at least a portion of the protective surface area. The coating includes a lubricant and an antimicrobial and/or pH buffering material. The device is configured such that, upon application of negative pressure to the catheter or stent, tissue of a urinary tract of a patient conforms or collapses onto the protective surface area and is thereby prevented or inhibited from occluding one or more protected drainage holes, ports or perforations of the catheter or stent.

Abstract: A deflection catheter is disclosed for aiding in bending of a catheter or other elongate medical device transseptally delivered within a left atrium of a heart. The deflection catheter includes a deflection aid assembly having an outer component, an inner component and a connecting band. The connecting band connects a first inner branch segment and a second inner branch segment of the inner component, and also extends between a first outer branch segment and a second outer branch segment of the outer component whereby a catheter receiving opening is defined between the connecting band and the first and second outer branch segments. Proximal/distal movement of the inner component relative to the outer component increases/decreases an area of the catheter receiving opening in order to secure the catheter or other elongate medical device to the deflection aid assembly for subsequent bending by proximally tugging or pulling on the deflection aid assembly.

Abstract: A steerable catheter having a hub with a control feature includes a semi-rigid catheter with the hub attached at the proximal end. The distal end of the catheter includes a distal tip and a flexible portion adjacent the distal tip. The catheter includes a working channel, and further includes a channel through which a tension member or wire extends to the distal tip. Tension in the wire causes the distal tip to deflect and be steered. The hub includes a fixed member attached to the catheter, an inner member that moves axially relative to the fixed member, and an outer member that rotates relative to the inner member and the fixed member. Rotation of the outer member results in translation of the inner member, which is attached to the tension member and provides for controlled steering of the distal tip.

Abstract: The present teachings provide a delivery catheter with a deflectable tip and the deflection angle of the deflectable tip can be accurately controlled. Specifically, the delivery catheter includes a deflectable distal tip operably coupled to a pull wire, an elongated catheter portion, and a control mechanism. The control mechanism is configured to activate a rapid transformation of the deflectable tip from its linear profile to its curved profile. The control mechanism further includes a linear actuation mechanism. Such linear actuation mechanism converts a rotation motion of the control mechanism to a precise linear motion, which in turn accurately controls the bend angle of the deflectable tip of the delivery catheter. Such control mechanism can be used in applications that require the control of the distal deflection of the catheter, such as EP catheter, trans-septal device, and other devices.

Abstract: The present disclosure relates to a tube management device for an infusion set that includes a holding member attachable to the patient and which defines a holding chamber for the tube. The tube may be engaged and disengaged with the device while the lube is operably connected to convey medication. The device may also allow a) the length of flexible tube controlled by the device and b) the position of the final exit of the tube from the holding member relative to the initial entry of the tube into the holding member to both be selectively adjusted. In some embodiments, tire holding chamber is defined by a plurality of channels which may be either non-intersecting or intersecting channels.

Abstract: A catheter housing device for securing a catheter and needle assembly to a patient. The device can include a cover, an IV/catheter lock, a hub, and one or more fastening straps. The device can replace conventional devices and techniques for securing a catheter and needle to a patient that utilize adhesive materials and/or methods, which are ill-equipped to solve complications including infection/contamination of the insertion site, irritation/damage to the vein or insertion site due to inappropriate angling of the catheter/needle, etc. The devices and methods disclosed herein can provide catheter/needle securement and optimal inclination, a hermetically sealed chamber to resist infection and/or contamination, inert gas or soothing anesthetic vapor drugs in and around the device, and various skin-contacting layers and structures that promote ventilation and patient comfort in and around the insertion site.

Abstract: Vascular access system embodiments can be configured to remove gas and a piercing member from a catheter assembly. In some embodiments, vascular access systems can remove gas and at least a portion of a piercing member concurrently or simultaneously. In some embodiments, vascular access systems can remove gas before removing at least a portion of a piercing member. In several embodiments, a vascular access system can include a first barrel configured to remove gas and a second barrel configured to retract a piercing member.

Abstract: A wire for a medical device includes a wire body and a solid lubrication film. The wire body has an outer circumferential layer formed of a plurality of metal strands that are twisted with each other. The solid lubrication film is formed at least on outside exposed surfaces of the plurality of metal strands. When a virtual circle as a smallest circle enclosing the outer circumferential layer is assumed in a cross section perpendicular to a central axis of the wire body, a part of an outer edge of the solid lubrication film of the cross section is inside the virtual circle and a cross-sectional area of the solid lubrication film in the cross section satisfies A/B>0.7 where A is a size of a portion outside the virtual circle and B is a size of a portion inside the virtual circle.

Abstract: Methods and devices to quickly and accurately apply medication to a paranasal sinus are disclosed. Additionally, the methods and devices prevent the medication applied to a paranasal sinus from flowing down a patient's throat by expanding, using an inflation lumen of a device, an expandable member of the device adjacent to the patient's choana.

Abstract: A reduced pressure treatment system includes a liquid-collection canister for collecting liquid from a tissue site to which reduced pressure treatment is applied. The canister includes a first space configured to collect the liquid from the tissue site and a filter having a frame and a non-planar filter element. The filter defines a second space within the canister separated from the first space by the filter element. The filter element substantially prevents liquid from passing from the first space into the second space. The filter element substantially allows gaseous communication between the first space and the second space when the second space is exposed to a reduced pressure.

Abstract: A balloon catheter includes a catheter shaft, a balloon, a linear member, and a pressing member. The catheter shaft extends in an extension direction from a proximal end toward a distal end. The balloon is provided on the catheter shaft and inflatable in a radially outward direction centered on the catheter shaft. The linear member disposed on at least a portion of an outer circumferential surface of the balloon and extending in the extension direction. The pressing member presses the linear member against the balloon.

Abstract: A medical device for dilating urethral strictures comprises a urethral catheter disposed inside a slidable sheath. The device includes a localizing balloon and one or more dilating balloons capable of expanding radially outward to mechanically expand the urethral stricture. In certain embodiments, the device is adjustable in order to position the location of the one or more dilating balloons of the device relative to the urethral stricture of a patient.

Abstract: The present specification disclosed a noninvasive transdermal delivery device that relates generally to a handheld mechanical apparatus for noninvasive transdermal administration of gas, small to large water-soluble (hydrophilic) pharmaceutical agents, vitamins, and other therapeutic agents. Components of such delivery devices, methods of producing a substance comprising a supersaturated amount of a dissolved gas, as well as, methods of administering a therapeutic agent using such delivery devices and methods of treating a disease or condition using such delivery devices are also disclosed.