Abstract: A medical injector includes an injector housing defining a reservoir, a plunger rod, and a stopper engaged with a portion of the plunger rod, the stopper being slidably disposed within the reservoir and sized relative to an interior of the injector housing to provide sealing engagement with a sidewall of the injector housing. The medical injector further includes a needle having a sharpened first end and a second end in communication with the reservoir, a first cap covering the sharpened first end of the needle, and a second cap covering at least a part of the first cap. The second cap includes a body having a proximal end, a distal end, and a hemispherical member including a gripping component. The second cap is engaged with the first cap such that removal of the second cap simultaneously removes the first cap from the first end of the needle.

Abstract: A safety syringe structure includes a combined structure of a syringe barrel, a needle retreater, a needle, and a plunger. The needle retreater and the plunger are slidably received in the syringe barrel. The needle retreater is arranged adjacent to the front end of the syringe barrel. The needle is coupled to the needle retreater. The plunger has an end extended to form a sharp tip and is provided with a plug facing the needle retreater. The sharp tip extends outside the plug in a direction toward the needle retreater. The sharp tip is movable with the plunger toward the front end of the syringe barrel to pierce into and couple with the through hole of the needle retreater; and the sharp tip is movable with the plunger toward the rear end of the syringe barrel to drive, through the needle retreater, the needle into the channel.

Abstract: An injection device has a housing which includes a first housing part and a second housing part. The injection device has a receptacle for an injection needle. The receptacle is connected to a drive unit which moves the receptacle between proximal and distal end positions relative to the second housing part. The first housing part has a set piece for placing on the skin before triggering an injection. The first housing part is permanently fastened with respect to the second housing part. In a method for making the injection device, the first housing part is positioned on the second housing part so that the receptacle has a specified position relative to the set piece in the proximal end position thereof, and that the first housing part is permanently fastened in this position opposite the second housing part. A defined insertion depth can thus be ensured.

Abstract: A nebulizer assembly includes a nebulizer host and an auxiliary flow-guiding element. The auxiliary flow-guiding element is disposed on the nebulizer host. The auxiliary flow-guiding element has an auxiliary flow-guiding channel and at least one auxiliary bottom flow-guiding opening communicating with the auxiliary flow-guiding channel, and the auxiliary bottom flow-guiding opening penetrates through a bottom portion of the auxiliary flow-guiding element. A nebulized fluid generated by the nebulizer host can be sent to the auxiliary flow-guiding channel of the auxiliary flow-guiding element, and an outside air can pass through the auxiliary bottom flow-guiding opening and flow into the auxiliary flow-guiding channel. Therefore, the nebulized fluid in the auxiliary flow-guiding channel can be propelled towards a direction away from the auxiliary bottom flow-guiding opening by the outside air flowing into the auxiliary flow-guiding channel through the auxiliary bottom flow-guiding opening.

Abstract: At least one aspect is directed to a system and method for modifying the operational settings of vaporizer devices. An application executed on a client device may render a graphical user interface on a display of the client device for inputting operational settings of a vaporizer device. Once inputted via the user interface of the application, the client device may transmit the operational settings via a network to the vaporizer device. In response to the receipt, the vaporizer device may store and save the operational settings and may adjust the operations of one or more components of the vaporizer device to satisfy the operational settings.

Abstract: Systems and methods are described for monitoring usage of a medicament dispenser—particularly an inhaled medicament dispenser. While operating in a low-power mode, a first sensor is monitored for a signal indicative of handling of the medicament dispenser by a user. In response to detecting such handling, the device exits the low-power mode and begins to monitor a second sensor for a signal indicative of dispensing of the medicament. The usage monitoring device can be embodied as an attachment configured to be selectively coupled to one of a variety of different inhalers including, for example, a Diskus-type inhaler and a Respimat-type inhaler.

Abstract: A spacer chamber having a body with a base end; a tip end; a popoid section located between the base end and the tip end; a first aerosol port located on a first side of the body and near the tip end; a second aerosol port located on a second side of the body and near the tip end, the first side is opposite to the second side. Several therapeutic spray agents are simultaneously applied to a patient by the spacer chamber via the each one of the first aerosol port and the second aerosol port.

Abstract: A nebulizer assembly includes a nebulizer host and a main flow-guiding element. The main flow-guiding element is disposed on the nebulizer host. The main flow-guiding element has a main flow-guiding channel and at least one main bottom flow-guiding opening communicating with the main flow-guiding channel, and the main bottom flow-guiding opening penetrates a bottom portion of the main flow-guiding element. A nebulized fluid generated by the nebulizer host can be sent to the main flow-guiding channel of the main flow-guiding element, and an outside air can be introduced into the main flow-guiding channel by passing through the main bottom flow-guiding opening. Therefore, the nebulized fluid in the main flow-guiding channel can be propelled towards a direction away from the at least one main bottom flow-guiding opening by the outside air flowing into the main flow-guiding channel through the main bottom flow-guiding opening.

Abstract: The present invention relates to a handheld vibrating mesh nebuliser for delivery of a medicament to the respiratory system in therapy. The present invention also relates to a supply container for loading the nebuliser with liquid medicament. The present invention also relates to a kit for delivery of a medicament to a respiratory system and a method of loading a vibrating mesh nebuliser with liquid medicament from a supply container. The present invention also relates to compositions for use in a method of treatment of a respiratory disease in a patient by therapy.

Abstract: A cartridge for use with an aerosol-generating system has a housing defining a liquid containing volume. The housing includes a sidewall extending from a mouthpiece end to a power supply end. The housing includes a transparent region forming at least a portion of the sidewall. The housing includes a light source fixed to the sidewall. The light source is configured to transmit light into the liquid containing volume. The light source may be fixed to an inner surface of the sidewall, fixed to an outer surface of the sidewall, or form a portion or the sidewall.

Abstract: There is disclosed a device for nicotine delivery, comprising: a vapour outlet conduit for coupling to, and for fluid communication with, a vapour creation system, said vapour outlet conduit defining a fluid passage therethrough for delivery of vapour from a vapour creation system to a user, wherein said vapour outlet conduit comprises a nicotine carrier unit region configured to accept a nicotine carrier unit and retain said nicotine carrier unit in said fluid passage. Also disclosed is a system for nicotine delivery and kits-of-parts for assembling the device and system.

Abstract: A device may receive information that identifies a dosage associated with a vaporized substance. The device may determine that the dosage associated with the vaporized substance has been generated. The device may provide information that identifies that the dosage associated with the vaporized substance has been generated.

Abstract: Systems and methods may include a gas source, a gas delivery circuit, and a nasal interface allowing breathing ambient air through the nasal interface. A gas flow path through the nasal interface may have a distal gas flow path opening. A nozzle may be associated with a proximal end of the nasal interface a distance from the distal end gas flow path opening. At least a portion of an entrainment port may be between the nozzle and the distal end gas flow opening. The nozzle may deliver gas into the nasal interface to create a negative pressure area in the gas flow path at the entrainment port. The nasal interface and the nozzle may create a positive pressure area between the entrainment port and the distal end gas flow path opening. Gas from the gas delivery source and air entrained through the entrainment port may increase airway pressure or lung pressure or provide ventilatory support.

Abstract: A respiratory device includes a blower having an inlet and an outlet, a patient interface, and a valve including a valve member that is rotatable through a first angular displacement in a first direction from a first position to a second position. The outlet of the blower is coupled to the patient interface so that positive pressure is provided to a patient's airway via the patient interface when the valve member is in the first position. The inlet of the blower is coupled to the patient interface so that negative pressure is provided to the patient's airway via the patient interface when the valve member is in the second position. The valve member is rotatably oscillated back and forth when the valve member is in the first position and when the valve member is in the second position so that oscillations in the positive pressure and negative pressure, respectively, are provided to the patient's airway.

Abstract: CPAP treatment apparatus is disclosed having a controllable positive airway pressure device. A sensor generates a signal representative of patient respiratory flow that is provided to a controller. The controller is operable to determine the occurrence of an apnea from a reduction in respiratory airflow below a threshold determined from long term ventilation. When an apnea or hypopnea has occurred the calculation of the threshold is suspended until the end of that event.

Abstract: Disclosed herein is a gas delivery and monitoring apparatus that can be used, for example, to deliver oxygen and monitor exhaled carbon dioxide in a subject while under anesthesia. One advantage of the disclosed apparatus is the ability to deliver oxygen directly to the back of the mouth instead of in front of the face. Another advantage of the disclosed apparatus over existing nasal cannulas is the ability to capture carbon dioxide exhaled from both the nose and mouth.

Abstract: In one embodiment, a monitoring system includes a monitoring device configured to removably attach to a tracheotomy tube, the monitoring device including a skin sensor configured to detect contact with skin of a patient's neck.

Abstract: A respiratory therapy system is configured to supply breathing gases to a patient and comprises a controller configured to control the pressure of breathable gas delivered to the patient. The system can control the flow of breathable gas to the patient taking into account whether or not a breath is detected, and whether or not the patient is awake or asleep. The system is configured to: detect when the patient is inhaling and to control the flow generator to deliver breathable gas at an inspiration pressure (IPAP), detect when the patient is exhaling and to control the flow generator to deliver breathable gas at an expiration pressure (EPAP), the EPAP being lower than the IPAP, and detect when the patient is at least one of awake and/or asleep.

Abstract: The endotracheal tube system (10) includes an endotracheal tube (12), an auxiliary sterilizing tube (20), and a sterilizing agent source (28) for sterilization of the endotracheal tube (12) while it is in use. The endotracheal tube (12) is an elongated, hollow tube having a distal end (14) and a proximal end (16). An inflatable cuff (18) is disposed on the elongated hollow tube (12), adjacent the distal end (14). The sterilizing tube (20) has a closed distal end (24) and an open proximal end (22). The closed distal end (24) is secured to the elongated hollow tube (12) adjacent the inflatable cuff (18), and a plurality of pores (26) are formed through at least a portion of the sterilizing tube (20). The sterilizing agent source (28) injects chlorhexidine into the sterilizing tube (20), which is distributed to the elongated hollow tube (12) through pores (26).

Abstract: Disclosed herein is an endotracheal tube stylet that uses air flow to articulate the stylet and endotracheal tube during intubation. This has the dual advantage of providing oxygen to the patient during intubation while also replacing existing mechanical forms of articulation.

Abstract: The present invention relates to a multipurpose airway device adapted for insertion into the mouth of a patient. The airway device comprises an elongate, tubular airway body of substantially elliptical or substantially circular cross-section and has a substantially straight section, the proximal end of which is adapted to function as an integral bite block; a curved distal section with a distal tip; and a central channel for accepting an intubation device. The airway device further comprises a substantially oval-shaped detachable intraoral seal and a connector for facilitating attachment of breathing or anaesthesia equipment thereto. The invention also relates to an ETT locking device for attachment to the multipurpose airway device and a multipurpose airway pack comprising the multipurpose airway device and ETT locking device.

Abstract: This invention relates to a patient interface, a system and/or method for providing a dedicated or sole inspiratory line or conduit for provision of inspiratory gases to a patient, and a dedicated or sole expiratory line or conduit for provision of expiratory 5 gases to a downstream device, where the inspiratory line or conduit is sealing engageable with the first of a user's nares and the expiratory line or conduit is sealing engageable with the second of the user's nares.

Abstract: In one embodiment, a nasal cannula is shaped to fit within a user's nares, where the nasal cannula includes at least one prong allowing high flow delivery of humidified gases and creates positive airway pressure in the patient's airway. The prongs have angled ends such that, in use, gases flowing through the prongs are directed to the user's nasal passages. The nasal cannula body is partially swivelling and preferably has a ball joint connector. In another embodiment the nasal cannula may have at least one flared end prong that preferably seals within a patient's nare.

Abstract: A hose is described that includes a braided matrix with an interior lumen. The matrix also includes filaments that intersect each other creating a braid, a longitudinal axis that runs along the lumen and the filaments intersect the longitudinal axis at a braid angle. The braid angle can be varied by compressing or expanding the matrix along the direction of the longitudinal axis. A polymer coating is applied to the matrix such that the matrix is substantially impermeable to air. The hose has two states: (1) a relaxed state where the hose does not experience a force in the direction of the longitudinal axis; and (2) a stressed state where the hose experiences a force in the direction of the longitudinal axis. The braid angle is larger in the relaxed state as compared to the stressed state. A method of manufacture for the hose is also disclosed.

Abstract: Disclosed is a nasal ventilation mask having separate ports to monitor end-tidal CO2 expulsion integrated into the mask in order to monitor end-tidal CO2 expelled nasally or orally. Also disclosed is a CPR mask for nose-to-mouth and/or mouth-to-mouth resuscitation, having a body shaped to cover the nose and/or mouth of a victim, the mask including a CO2 absorber for eliminating at least in part rescuer's exhaled CO2 delivered to the victim.

Abstract: A method of manufacturing a patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways includes collecting anthropometric data of a patient's face. Anticipated considerations are identified from the collected anthropometric data during use of the patient interface. The collected anthropometric data is processed to provide a transformed data set based on the anticipated considerations, the transformed data set corresponding to at least one customised patient interface component. At least one patient interface component is modelled based on the transformed data set.

Abstract: A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.

Abstract: A gas heater (1) and gas heater method heat a carrier gas flow. The gas heater includes a gas inlet (2) a gas outlet (3) and a connecting gas channel (4). A heating system (5), arranged in the gas channel, includes a heat exchanger (12) surface. The carrier gas at least partly flows over the surface to heat the carrier gas flow. The gas channel includes a first section (6), arranged upstream of the heat exchanger in a flow direction, and a second section (7) arranged downstream of the heat exchanger. A respective sensor (8a, 8b), for detecting a pressure value, is in the first and the second section or directly adjacent thereto. Pressure values are transmitted to a control and analysis unit (9) which ascertains a mass and/or volume flow of the carrier gas in the gas channel based on a pressure difference between the two pressure values.

Abstract: A resuscitation device is described that can include an electronic circuit board, a shaft that is operably coupled with the electronic circuit board and has a head, a gas-bag adjacent to the head and configured to store gas, and a valve operably coupled to the gas-bag. The electronic circuit board can actuate the shaft to move. The moving of the shaft can cause the head to compress the gas-bag. The compression of the gas-bag can cause the gas-bag to release gas. Related apparatuses, systems, methods, techniques and articles are also described.

Abstract: A method of preparing adipose tissue for transplantation, from lobular fat extracted, for instance, by liposuction, said fat consisting of a fluid component comprising an oily component, a blood component and/or sterile solutions and of a solid component comprising cell fragments, cells and one or more cell macroagglomerates of heterogeneous size, characterized in that it includes at least one step of forming an emulsion of the fluid component in the sterile washing solution by means of active and/or passive stirring means and discharging the emulsion from the outlet through a density gradient.

Abstract: An elongated medical device includes an elongated tubular element with a series of flexibility enhancing features along a length of the elongated tubular element. Each flexibility enhancing feature may include a circumferential series of cuts. The cuts of one flexibility enhancing feature may be offset relative to the cuts of a longitudinally adjacent flexibility enhancing feature. The flexibility enhancing features may be grouped into two or more interleaved sets, with each set of circumferential cuts being offset relative to the next set of circumferential cuts. Methods for manufacturing such elongated medical devices are also disclosed.

Abstract: In clinical practice, the procedure of urinary catheterization may cause severe irritation to urethra and bladder. In addition, physiological and pathological stricture and curvature of human urethra will increase the difficulty of urinary catheterization and aggravate the injury of lower urinary tract during insertion. The injury of lower urinary tract may induce or aggravate lower urinary tract infection and further affect the lower urinary tract or even the systemic organ function. At present, clinical solutions to urethral stricture comprise: The use of a stronger tip or metal probe or guide wire increases the external force to push forward, resulting in severe contusion of the urethra intima and susceptibility to infection; another method is to coat the outer surface of the urinary catheter with lubricating oil or lubricant coating, but using it alone is almost ineffective for urethral stricture.

Abstract: A catheter that is configured to achieve high velocity injections of contrast solution that will not readily wash out in retrograde blood flow. The distal end of the catheter can include a plurality of fluid outlet openings. The fluid outlet openings are spaced circumferentially around the circumference of the catheter and the fluid outlet openings have ejection axes that are angled in a direction toward the distal end so that a velocity component of the ejected contrast solution is against or opposite the retrograde blood flow.

Abstract: An electronic device is disclosed. The electronic device comprise an elongate electrical connector that is configured to connect to an integrated device package. The elongate electrical connector can comprise an elongate flexible substrate. The elongate flexible substrate has a proximal portion and a distal portion spaced from the proximal portion by a length along a longitudinal axis. The elongate flexible substrate has a width along an axis transverse to the longitudinal axis. The elongate flexible substrate defines an elongation ratio of the length to the width. The elongation ratio is at least 100:1. The elongate electrical connector can be connected to a bobbin. The elongate electrical connector can be configured to unspool from the bobbin.

Abstract: A medical device has a distal member with a configuration that can be changed by means of a control handle with a control assembly employing a rotational cam, a shaft, and a pulley, where the rotational cam is rotationally mounted on a portion of the control handle for rotation by a user. The rotational cam operates on the shaft to move it proximally or distally depending on the direction of rotation which in turn rotates the pulley to draw or release a puller wire to change the configuration of the distal member of the medical device. The shaft is oriented along a diameter of the control handle. The shaft has two ends which extends through two axial guide slots in the portion of the control handle to sit two opposing helical tracks formed on inner surface of the rotational cam. The guide slots are parallel with the longitudinal axis of the control handle and therefore maintain the shaft's diametrical orientation as the rotational cam is rotated to move the shaft proximally or distally.

Abstract: A system including method and device with attachments and elements as a means of enhancing vascular access or other medical procedures, such as wound care or diagnostics, or for general medical purposes by effectively stabilizing patients' upper or lower extremities in a safer, more reliable, less intrusive and less costly manner. One embodiment indicates a rigid device with attachments for securing and immobilizing the rigid device and a shape and inflatable pressure cuffs (211) or bands for stabilizing the extremity to the device by eliminating or reducing the number of involved medical personnel, reducing risk of injury or trauma such as medical adhesive related skin injuries or contusions and eliminating or reducing the need for sedation to accomplish the medical procedure especially in children, infants, neonates, and preemies. Other embodiments include multiple sizes, shapes, dimensions, materials and elements necessary to accomplish safe stabilization of an extremity.

Abstract: An apparatus includes a catheter having a balloon including at least one first radiopaque marking. A guidewire guides the balloon to the treatment area, and includes at least one second radiopaque marking adapted for corresponding to the at least one first radiopaque marking of the balloon when positioned at the treatment area. Related aspects and methods are disclosed.

Abstract: A guidewire for backloading and inserting a percutaneous pump affixed to a cannula includes a proximal section made of a first material, with a first diameter, a rounded proximal end, and a distal end. The guidewire also includes a distal section made of a second material, with a second diameter which is greater than the first diameter, a distal end, and a proximal end abutting the distal end of the proximal section. The first material of the proximal section is selected to be softer than a material of the percutaneous pump to reduce damage to the pump during backloading. The distal section of the guidewire is configured to be stiffer than the proximal section to insert the percutaneous pump in a desired location without damaging the guidewire.

Abstract: In various examples, an apparatus facilitates attachment of an extension wire to a guidewire. The apparatus includes a body portion including a lumen sized to accommodate a distal end of the extension wire therein. A cutout is defined within a portion of a sidewall of the body portion, the cutout allowing access to the lumen. A funnel portion is disposed within a distal end of the body portion and includes an opening in the distal end of the body portion. The funnel portion includes a tapered wall converging from the opening to the lumen, wherein, with the distal end of the extension wire disposed within the lumen, the funnel portion facilitates alignment and attachment of a proximal end of the guidewire with the distal end of the extension wire. In other examples, a system or a method facilitates attachment of an extension wire to a guidewire.

Abstract: A medical system includes an insertion device and an insertion device handle. The insertion device handle has a proximal portion and a distal portion, with a delivery shaft extending from the distal portion. The medical system also includes a medical device, including a spool and a medical device handle. The medical device handle has a central opening, and the spool and the medical device handle are rotatably movable to one another and form a channel. The medical system includes an adapter couplable to a portion of the insertion device handle, and the adaptor includes a post element to be received within the central opening of the medical device handle.

Abstract: A balloon-manipulating device for a balloon catheter includes, in some embodiments, a tubular body, a longitudinal hole through a least a portion of the tubular body, one or more balloon-compressing pieces of a sidewall of the tubular body, and one or more balloon-letting through holes through the sidewall. The longitudinal hole extends from an opened proximal end of the tubular body to at least a distal end portion of the tubular body. The longitudinal hole is configured for inserting a balloon-catheter shaft in the longitudinal hole. Each balloon-compressing piece is configured for compressing a different portion of an inflated balloon-catheter balloon when the balloon-manipulating device is disposed over the balloon. Each balloon-letting through hole is configured for allowing therethrough a different portion of an inflated balloon-catheter balloon when the balloon-manipulating device is disposed over the balloon. Also disclosed is a balloon catheter assembly and methods of the foregoing.

Abstract: A fluid management system for the treatment of ascites, pleural effusion or pericardial effusion is provided including an implantable device including a pump, control circuitry, battery and transceiver; a charging and communication system configured to periodically charge the battery and communicate with the implantable device to retrieve performance data; and monitoring and control software, suitable for use with conventional personal computers, for configuring and controlling operation of the implantable device and charging and communication system. The implantable device includes a number of features that provide automated movement of fluid to the bladder with reduced risk of clogging, with no patient involvement other than occasional recharging of the battery of the implantable device. The monitoring and control software is available only to the treating physician, such that the physician interacts with the implantable device via the charging and communication system.

Abstract: An apparatus for delivering a powdered agent into a subject's body may include a first passage for receiving a pressurized gas. The apparatus also may include a container housing a powdered agent. The container may be in fluid connection with the first passage. At least a portion of the pressurized gas is introduced into the powdered agent in the container to fluidize the powdered agent. The apparatus also may include a second passage for receiving the powdered agent from the container. In a first configuration of the apparatus, the second passage may not be in fluid connection with the container. In a second configuration of the apparatus, the second passage may be in fluid connection with the container. The apparatus may be configured to transition between the first configuration and the second configuration.

Abstract: A system and method for delivering a bathing liquid via a nostril of a face-down user maintains a column of the liquid in prolonged and predictable contact with the nasal and sinus mucosa, and creates turbulence in the column of liquid within the user's nasal cavity to enhance removal of debris from walls of the nasal cavity. A head orientation unit attaches to the user's head and includes an angle monitoring unit to provide an indication of the angular orientation of the user's head as it turns to optimize delivery of the liquid to target head structures. A liquid supply delivers the liquid through the user's nostrils to one or more head structures as a function of the angular orientation indication and at a pressure and flow rate that maintains a constant volume of liquid in the nasal and sinus cavities. Indicia on the angle monitoring unit permit the user to orient his/her head to predetermined angular positions.

Abstract: An applicator for providing localized relief and treatment to sensitive areas of the face, head, or body as a result of injury, trauma, operation, or cosmetic use. The applicator has an inner layer and an outer layer. The inner layer is saturated with a liquid to provide treatment or relief to the target area. The outer layer is at least semi-permeable so that when the applicator contacts the target area, the treatment liquid will seep out of the inner layer and pass through the outer layer onto to the skin or wound at the target area.

Abstract: A convenient and hygienic skin therapy system comprising an encaser, one or more therapeutic compositions, a sealing means and optional accessories is disclosed. A method of using such a skin therapy system is also provided. The skin therapy system and the use thereof provides an effective, efficient and safe therapeutic approach.

Abstract: A method of manufacturing a microneedle and a structure with an array of microneedles manufactured by using the method, in which a size, height, and shape of the microneedle formed on a base may be adjusted. The multiple microneedles may be uniform in size, height, and shape even though the multiple microneedles are simultaneously formed on the base. The method is economical because precise control is not required and an area of the structure with the array of microneedles may be increased only with a simple facility. The structure with an array of multiple fine microneedles formed on the base (or substrate), includes the microneedle having an upper end having a fine diameter that does not cause pain or trauma to the skin, and includes sufficient hardness required to penetrate a skin layer, and sufficient effective length and a stable shape delivering active ingredients to capillaries.

Abstract: A low-profile access port for subcutaneous implantation within a patient. The access port can include a set of receiving cups which can be placed in fluid communication with a catheter. The set of receiving cups can provide a greater skin surface with which to access the port to avoid repeated penetrations at a single locus, such as during consecutive dialysis treatments. The access port can alternatively include needle penetrable arms or elongate chambers that also have a slim, low profile. The access port can include a needle guide to direct subsequent needle access to different insertion points to permit healing at the previous insertion points. The access port can be formed of a modular construction with a first conduit, a second conduit, and an outer shell. The outer shell can include a proximal portion and a distal portion. The access port can include a stem assembly and a locking member.

Abstract: Disclosed herein are improved methods and apparatuses for providing hemostasis within a cavity defined by an internal surface of a bleeding tissue space. A catheter comprising a proximal end and a distal end may be advanced into the cavity through a proximal opening of the tissue space into the cavity. A distal balloon coupled to the catheter may be positioned adjacent a distal opening of the tissue space, and expanded to seal the distal opening. A hemostatic agent may be applied from the catheter to the internal surface of the tissue space to inhibit bleeding of the tissue space. The hemostatic agent may be applied without occluding the proximal opening, the distal opening, and a path extending therebetween with the hemostatic agent.

Abstract: Disclosed herein are improved methods and apparatuses for providing hemostasis within a cavity defined by an internal surface of a bleeding tissue space. A catheter comprising a proximal end and a distal end may be advanced into the cavity through a proximal opening of the tissue space into the cavity. A distal balloon coupled to the catheter may be positioned adjacent a distal opening of the tissue space, and expanded to seal the distal opening. A hemostatic agent may be applied from the catheter to the internal surface of the tissue space to inhibit bleeding of the tissue space. The hemostatic agent may be applied without occluding the proximal opening, the distal opening, and a path extending therebetween with the hemostatic agent.