Abstract: A pocket sized diabetic kit carrying supplies that a diabetic patient will need for 24 hours includes but not limited to Lancet pen, lancets, small test strip bottle filled with test strips, blood test meter, one or more insulin types stored in a plurality of pre-filled syringes, one syringe splint or just one hard plunger, a plurality of alcohol pads, one blood plotter pad, Velcro straps and a syringe clipper. The pocket diabetic kit is compact, small and thin and can fit into a pocket so that a diabetic patient can be easily carried in the pants' pocket or other pockets without causing inconvenience or uncomfortable. The present invention also discloses ways to modify supplies including tools, medication syringes, etc.

Abstract: An infusion system fully compliant with international standard ISO 80639-1, Small-bore Connectors for Liquids and Gases in Healthcare Applications, yet compatible with a multipurpose infusion pump to enable operational redeployment of the pump. An attachment set, removably couplable to the pump inlet and outlet, includes a coded attachment set outlet connector detachably coupling the attachment set to an infusion set, and a coded attachment set pump fitting coupling the attachment set to the infusion pump, thereby identifying to the pump a particular infusion route.

Abstract: A patient care system includes a control unit capable of coupling with multiple modular medical devices. A modular medical device can be coupled with the control unit, wherein the behavior of the modular medical device automatically adjusts based on the status of being coupled or un-coupled with the control unit.

Abstract: An assembly of a drug delivery system, comprising: a first component; a second component which is configured to move linearly with respect to the first component; and, a resistance element configured to resist linear movement during transport of the first component with respect to the second component in a closed transport configuration but which is adapted to be overcome during nominal operation of the drug delivery system.

Abstract: An apparatus and method for syringe plunger positioning employing an actuator for linear advancement and retraction of the support member along a predetermined axis, and a plurality of arm members each interconnected to the support for movement therewith, and each moveable relative to the support member in corresponding different directions towards and away from the predetermined axis. The actuator may be operable to advance the support member to an advanced position for movement of the arm members from an open position in the different corresponding directions towards the predetermined axis to a closed position, and to retract the support member from the advanced position so that distal end portions of the arm members engage an inside surface of a plunger button of syringe having a barrel located in a fixed, axially aligned position on the predetermined axis. The apparatus and method may be employed in conjunction with syringe plunger positioning (e.g.

Abstract: A wearable infusion device for delivering medication into body of a user, the infusion device comprising a medication container containing a volume of medication to be dispensed; an infusion needle that is fully enclosed in a sterile environment until the infusion needle is inserted into underlying tissue; an infusion needle insertion mechanism associated with the infusion needle, powered by one or more mechanical springs, that when activated, inserts the infusion needle through the skin into underlying tissue; means for delivering medication out of the medication container and into underlying tissue via the infusion needle; and a housing associated with the medication container, the infusion needle, the infusion needle insertion mechanism and the means for delivering medication.

Abstract: Fluid delivery and measurement systems and methods are disclosed.

Abstract: A device for inserting an infusion cannula, or sensor, into a patient is presented. The device comprises an insertion needle removable within the infusion cannula, a handle connected to the insertion needle, and a needle cover. The needle cover pivotably mounted on the handle is rotatably movable between a first position, i.e., the front of the insertion needle is in the needle cover, and a second position, i.e., the front is exposed. An infusion site interface comprises a body mounted on a pad attached to the patient; an infusion cannula for inserting into the patient that is connected to the body; a cavity within the body fluidly connected to the cannula; and a septum that seals closed the cavity. The septum is penetrable by an insertion needle in the infusion cannula and by a hollow needle of an infusion tubing connector coupled to the infusion site interface.

Abstract: A method of operating an infusion pump includes transmitting light through or around a drop of fluid suspended from an end of a drip tube for the infusion pump, the end of the drip tube located in a drip chamber for the infusion pump, wherein the drip tube is configured for connection to a source of the fluid; receiving, using an optical system for the pump, light transmitted through or around the drop; transmitting, to a specially programmed microprocessor and using the optical system, data regarding the received light; and, using the microprocessor to calculate a volume of the drop using the data.

Abstract: A method of operating an infusion pump includes transmitting light through or around a drop of fluid suspended from an end of a drip tube for the infusion pump, the end of the drip tube located in a drip chamber for the infusion pump, wherein the drip tube is configured for connection to a source of the fluid; receiving, using an optical system for the pump, light transmitted through or around the drop; transmitting, to a specially programmed microprocessor and using the optical system, data regarding the received light; and, using the microprocessor to calculate a volume of the drop using the data.

Abstract: Some embodiments a multi-modal medicine delivery system can be configured to control dispensation of medicine according to any of a plurality of delivery modes, such as closed-loop delivery modes and open-loop delivery modes, and according to a secondary feedback loop to determine user-specific settings related to dosage delivery.

Abstract: Some embodiments a glucagon administration system can provide a suggested glucagon dosage based on one or more particular parameters (e.g., the user's recent blood glucose characteristics, a glucagon sensitivity value of the user, and other parameters). In some circumstances, the glucagon administration system can receive information indicative of the user's blood glucose level and suggest a glucagon dosage that is at least partially dependent upon a previously stored glucagon sensitivity for the user.

Abstract: A system for optimizing a patient's basal insulin dosage regimen over time, adapted to determine from blood glucose values whether and by how much to vary a patient's present recommended amount of the insulin-containing drug in order to maintain the patient's future blood glucose level measurements within a predefined range, and wherein a given blood glucose value is disregarded if no patient-actuated operation being indicative of the administration of a dose of an insulin containing drug has been detected in a pre-defined amount of time prior to the determination of the given blood glucose value.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of operating an infusion device to deliver fluid to a user in accordance with an operating mode involves obtaining operational information pertaining to one or more prior instances of the operating mode, obtaining status information pertaining to the infusion device, and determining a diagnosis time based at least in part on the operational information. The diagnosis time is prior to a subsequent instance of the operating mode. At the diagnosis time, the method automatically determines the viability of the subsequent instance of the operating mode based at least in part on the status information and automatically generates a notification indicative of a recommended action for the user based at least in part on the viability.

Abstract: A syringe tip cap is provided for use with an automatic syringe loading apparatus. The cap includes a body having an exterior surface and an interior surface, and having a first end and an opposite second end. The first end is defined by at least one generally “V”-shaped ramp on each of two sides of the exterior surface.

Abstract: The present invention relates to a mixing and injector device which can include: a housing having a plurality of separate and distinct chambers disposed therein; one or more displacement mechanisms corresponding to each of the plurality of chambers disposed within the housing; a needle assembly being provided about one of the plurality of chambers, the needle assembly including the following: a septum; a needle being separated from the plurality of chambers by the septum, the needle having a proximal end configured to pierce the septum in an actuated state; and a needle carrier, the needle carrier being configured to translate axially with respect to and toward the septum and pierce the septum and provide fluid communication from the plurality of chambers through the needle in the actuated state.

Abstract: A syringe includes a barrel, a plunger, and a sealing member creating a seal between the plunger and the barrel. The barrel includes a first portion with a first inner diameter and a second portion with a second inner diameter that is larger than the first inner diameter. The sealing member engages the first portion of the barrel to give rise to a first contact pressure when the barrel is filled with product. The first contact pressure is sufficient to maintain a gas-tight seal over the expected temperature ranges ?25° C. to 40° C. A first force is applied to the plunger to overcome the first contact pressure and move the plunger out of the first portion and into the second portion to dispense product. The sealing member engages the second portion of the barrel to give rise to a second contact pressure that is lower than the first contact pressure.

Abstract: A device for monitoring a manually operated syringe that according to one embodiment includes a basis which is adapted to be connected to a medication administration point of a patient and comprises a syringe insertion port to receive the syringe dispensing tip, the basis being configured such that when the syringe is inserted in the insertion port the syringe barrel is not in direct contact with the basis, and at least part of the syringe barrel projects from the basis in the direction of the barrel axis, and further comprising an image acquisition system arranged on the basis and adapted to capture an image of at least part of the syringe plunger when the syringe is inserted in the insertion port.

Abstract: A dose setting mechanism for a drug delivery device includes a primary drug delivery assembly and a secondary drug delivery assembly. The dose setting mechanism includes a primary dose dial component for setting a dose in the primary drug delivery assembly and a secondary dose dial component for setting a dose in the secondary drug delivery assembly. The primary dose dial component and the secondary dose dial component are configured to rotate during dose setting. A gear mechanism is configured such that in a first phase of the dose setting, rotation of the primary dose dial component is transferred to the secondary dose dial component and such that in a second phase of the dose setting, the secondary dose dial component is decoupled from the primary dose dial component such that rotation of the primary dose dial component is prevented from being transferred to the secondary dose dial component.

Abstract: The present invention relates to a syringe and a syringe safety cap assembly and, specifically, to a syringe safety cap assembly capable of preventing a user from being injured when a syringe needle is inserted into a cap and completely preventing reuse of the syringe or the syringe needle to be discarded. In addition, the present invention relates to the syringe having a valve member capable of filtering foreign substances during the inflow of a drug and restraining the filtered foreign substances from being discharged during the discharge of the drug, when foreign substances such as glass dust are mixed with substances such as a syringe drug.

Abstract: The present invention is directed to a device which facilitates injection of a medicament using a hypodermic syringe. An exemplary embodiment of the device includes an injection application for a hypodermic syringe comprising a main body, a cover, an axial force structure, and a rate controller. The main body includes a perimeter bounding and defining an enclosure about a primary axis and operable to mechanically grip and enclose a major section of the hypodermic syringe. The cover is opaque, extends from the main body, and is continuous and unitary with the main body. The axial force structure is disposed in the main body and is operable to provide axial travel force to the hypodermic syringe along the primary axis. A rate controller is in cooperation with the axial force, and is operable to control the rate of travel of the hypodermic syringe from the unimpeded axial force.

Abstract: A smart monitoring device for automatically monitoring the injection of medicines such as insulin which can be retrofitted to a conventional insulin pen in which the device has an optical motion sensor for detecting actuation of the injection pen together with an optional accelerometer sensor, medicament temperature and mounting sensors, the monitoring device being communicable with external smart devices such as smartphones.

Abstract: Systems, methods, and devices can detect a dangerous or adverse condition or anticipated condition that indicates an undesirable amount of electric current in a patient-connected tube providing fluid to a patient. The fluid flow to the patient is stopped responsive to the detection. Stoppage of fluid flow to the patient can reduce or prevent electric current in the fluid from reaching a patient, flowing through the patient to ground, and/or continuing to flow through the patient.

Abstract: The present invention relates to a nebulizer, such as a spray can, for the topical application of a liquid and/or solid to a surface. The nebulizer is characterized by a valve comprising a mixing chamber designed for forming a colloidal mixture comprising a dispersed phase consisting of a liquid and/or a solid substance and a continuous phase consisting of a propellant gas before delivering the colloidal mixture to the nozzle. The invention also relates to a method for the topical cooling of the skin of a person or animal. In addition, the invention relates to various other uses of the device.

Abstract: The present disclosure generally relates to the field of nebulizers for aerosol generation and methods of using same for treating diseases and disorders.

Abstract: An atomizer includes a cartridge with a reservoir containing a fluid and a heating system configured to atomize the fluid into a vapor for inhalation. A respiratory indicator is configured to determine an inhalation period and an exhalation period of a patient using the atomizer. The atomizer then increases atomization of the vapor during the inhalation period and decreases atomization of the vapor during the exhalation period. An impedance sensor measures an amount of the fluid in the atomizer and deactivates atomization in response to an indication of a low fluid level.

Abstract: The present invention provides an aerosol device for delivering a pharmaceutical formulation by inhalation via the mouth to the lungs or to the nostril in metered doses comprising: a pressurised aerosol canister including a vial containing a pharmaceutical formulation comprising an active ingredient, a propellant and, optionally, a co-solvent, the aerosol canister further comprising a metering valve having a valve stem; and an actuator for the aerosol canister, the actuator including a delivery outlet and a stem block, the stem block having a receptacle into which the valve stem of the metering valve of the aerosol canister is received and axially located and being displaceable relative to the vial of the aerosol canister to actuate the metering valve of the aerosol canister, a sump extending below the receptacle, the stem block further defining a discharge orifice arranged to direct the pharmaceutical formulation through the delivery outlet, a transfer tunnel having an input opening and an output opening thr

Abstract: A system for improving an artificial respirator is disclosed. In particular, the system may be utilized to improve the quality of life of a user that utilizes an artificial respirator and to improve the quality of life of a caregiver of the user. In order to do so, the system may include an apparatus that suspends or activates one or more functions of the artificial respirator based on various conditions. As an example, if the system detects a threshold change in tension associated with a band supporting a respiration mask positioned on the user, the system may suspend a function of the artificial respirator. Similarly, if the system detects a temperature reading outside a temperature range, detects a unique sequence of inputs, detects a threshold distance between the user and the respiration mask, or detects other conditions, the system may suspend a function of the artificial respirator.

Abstract: Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus.

Abstract: The invention provides a tracheal tube having at least two suction ports, located very closely to an inflatable cuff. The ports open out onto channels which together subtend an angle of almost 360° around the tube, providing efficient and thorough suctioning of fluids that may have accumulated in the subglottal region above the cuff.

Abstract: An airway assessment and intubation guidance system, device and method that is portable, simple to use, and effective in reliably locating the trachea within the neck of a wide variety of patients and independent of fluids that may be found within the trachea. The system permits an objective assessment of the likelihood of a difficult intubation, and further provides, depending upon the embodiment, both visual and audible feedback regarding the location of a compatible stylet relative to the trachea.

Abstract: An oxygen face mask and component system is provided, the mask is designed to cover a user's nose and at least partially cover a user's mouth, the mask having lateral sampling ports, an oxygen port, and a facial access opening superior to the oxygen port. The opening may be sufficiently large to allow a surgical or diagnostic procedure to be performed on part of a user's face or to allow a physician's hands or other caregiver hand's to manipulate a scope or other devices into a user's mouth. Additional components are further provided, including a colorimetric C02 detector, a sealing cap with or without a resilient sealing flap, a capnography gas analysis unit, a non-rebreather valve, a pulmonary function module, nebulizer, a gas scavenging system, a gas reservoir system, a gas filter, sample lines that are either straight or at an angle, and an aerosol mask platform; and methods of making and using a face mask are also provided.

Abstract: Headgear for a respiratory mask includes a strap arrangement including front strap portions adapted to be disposed over a patient's cheeks and having front ends adapted for attachment to an airway interfacing portion, top strap portions connected to respective front strap portions and adapted to be disposed over the top of a patient's head and to connect to each other, and a back strap extending rearwardly from and connecting respective junctions of the front strap portions and top strap portions or regions adjacent these junctions and adapted to locate underneath a patient's occiput. In use with a patient having long hair, the back strap is adapted to extend under the patient's hair and urge upwardly on the patient's hair and against the patient's head beneath the occiput. In use with a patient having short hair, the back strap is adapted to urge against the patient's head beneath the occiput. In an embodiment, front strap portions of the headgear may be provided with a sleeve or cover (e.g.

Abstract: This application is related to a head-mounted display system and related methods for entertainment, diagnostics, and treatment. The HMD includes various sensors and tools to take physical measurements, perform physical procedures, adjust physical conditions, or manipulate digital data. In some embodiments, the HMD produces different types of sensory stimuli, such as releasing or filtering certain compounds in liquid or aqueous forms in the space near the HMD, or adjusting different physical features of the space near the HMD, such as temperature and flow, to enhance the augmented or virtual reality environment being displayed. In some embodiments, the HMD performs regular monitoring, a specific examination, a surgical intervention, or other care procedures on the eyes automatically or in conjunction with a device of an eye care professional across a computer network to care for the user's eyes in real time or on an ongoing basis.

Abstract: A humidifying device (nebulizer) includes a liquid receptor configured to temporarily store a liquid, a liquid transfer mechanism configured to transfer a liquid from a container to the liquid receptor, a receptor-side aerosol forming member configured to suck the liquid of the liquid receptor from a liquid suction port by a negative pressure produced by a gas jetted from a gas jetting part of a nozzle member, and form an aerosol of the liquid with a receptor-side aerosol generation nozzle, and a heating mechanism configured to heat at least part of the liquid of the liquid receptor or the liquid in the receptor-side aerosol forming member. A humidifying device that can perform efficient and hygienic heating by using a heater during humidification can thus be provided.

Abstract: In one embodiment, there is a computer-implemented method for delivering therapy to a user, comprising: providing data representative of an initial sensory stimulus to a sensory stimulus device and causing the sensory stimulus device to provide the initial sensory stimulus to the user; receiving alpha wave biometric data of the user from a brain electrical activity sensor while the sensory stimulus device provides the initial sensory stimulus; determining whether the alpha wave biometric data meets sensory stimulus adjustment criteria; if the alpha wave biometric data meets sensory stimulus adjustment criteria, adjusting the sensory stimulus provided to the user by providing data representative of an adjusted sensory stimulus to the sensory stimulus device and causing the sensory stimulus device to provide the adjusted sensory stimulus; and if the alpha wave biometric data fails to meet sensory stimulus adjustment criteria, continue causing the sensory stimulus device to provide the initial sensory stimulus t

Abstract: A lighting system includes a number of light sources with multiple light colors configured to affect circadian rhythms, and a power supply configured to power the light sources and to control an overall output color.

Abstract: Embodiments of a method and system for improving sleep characterization and/or a sleeping-related disorder for a user associated with a sleep session can include receiving a log of use dataset corresponding to user digital communication behavior at a mobile device, the log of use dataset associated with the sleep session; receiving a supplementary dataset characterizing activity of the user and/or mobile device, the supplementary dataset associated with the sleep session; characterizing a sleep-related parameter for the user based on at least one of the log of use dataset and the supplementary dataset; determining a sleep care plan for the user based on the sleep-related parameter, the sleep care plan including a therapeutic intervention; and promoting a therapeutic intervention to the user according to the sleep care plan.

Abstract: A catheter system configured for delivering a neuromodulation therapy, includes a first therapeutic element positionable in a first target vessel selected from the group of blood vessels consisting of the superior vena cava, left brachiocephalic vein, right brachiocephalic vein, azygos vein or azygos arch, and a second therapeutic element in a second target vessel selected from the group of blood vessels consisting of the superior vena cava, left brachiocephalic vein, right brachiocephalic vein, azygos vein or azygos arch. The system and associated method deliver therapeutic energy to at least one parasympathetic nerve fiber external to the first target vessel using the first therapeutic element, and deliver therapeutic energy to at least one sympathetic nerve fiber external to the second target vessel using the second therapeutic element.

Abstract: Micro-cutting machines for forming cuts in catheters, guidewires, and similar products, are disclosed, including a micro-cutting machine that can directly control the dimensions of the resultant beams being cut into products, and that can capture images of each cut for feedback control and accuracy verification.

Abstract: A device for introducing a material into a body cavity is shown. The device includes a catheter with a distal tip. A first lumen extends through the catheter. The catheter is configured to form a mist from liquid passed through the first lumen, for example including a misting nozzle in fluid communication with the first lumen and configured to provide a mist from a flow of liquid through the first lumen. An inflatable balloon may be included on the catheter to allow the user to isolate the portion of the body in which the material is introduced. Additional described features can provide for controlled deflection of a distal region of the catheter, guidewire or guide loop tool lumens, first and second misting nozzles on the catheter, and delivery apparatuses including the catheter devices coupled or that can be coupled to endoscopes such as bronchoscopes. Methods of use of the catheter devices and delivery apparatuses are also described.

Abstract: Apparatus and methods for an endovascular catheter that can be inserted within tortuous body anatomies and then selectively stiffened and fixed in place. In a particular embodiment, this stiffness is reversible. The stiffness or a comparable mechanical characteristic of the catheter assembly may be adjusted to a relatively low value during insertion (so that it easily navigates a guide wire or the like), and then subsequently adjusted to a relatively high value in situ to keep the catheter assembly substantially fixed in place (i.e., during delivery of an interventional device).

Abstract: A deflectable catheter including an outer member having a proximal portion and a distal portion, an elongated column member extending distally from the outer member and an inner member positioned coaxial with the outer member and attached to the column member. The inner member extends distally of the outer member and has a distal tip portion. A reinforcement member is positioned over the column member to restrict axial movement of the column member such that when one of the inner member or outer member is moved with respect to the other, axial compression of the column member is restricted by the reinforcement member causing the distal tip portion of the inner member to deflect laterally.

Abstract: A catheter stabilization device having a release liner and a catheter stabilization member with a permeable first layer and a bottom surface having an adhesive interposed between the release liner and the first layer. The catheter stabilization member includes an elongated continuous retention strip coupled to the first layer is of a deformably rigid material operably configured to have a first static state with a first shape, a dynamic state, generated by an external force, with a second shape different than the first shape, and a second static state, after removal of the external force, with the second shape in a fixed configuration.

Abstract: Various methods employing transvascular access devices are described, including a method of placing a central catheter in a peripheral vein in an arm of a patient; a method of providing percutaneous access to the heart of a patient; a method of clearing a clotted arteriovenous dialysis graft; a method of creating multiple access points into a single blood vessel; a method of creating an AV fistula in a patient; and a method of providing a bypass to a blockage in a popliteal artery in a patient.

Abstract: A post-cervical insemination catheter assembly including a cannula; a guide catheter slideably positioned about said cannula; and, a tip element securely connected to a distal end of said cannula. The tip element is configured to receive fluid from the cannula and dispense the fluid from a tip element outlet end. The tip element outlet end remains closed when loading the cannula through a vaginal canal and when traversing a cervix of the animal and then automatically opens when sufficient fluid pressure in the tip element is applied, thus enhancing injection of fluid to the utero-tubal junction, bio-secure delivery of fluids from any attached container, and a much safer less invasive experience for the recipient then prior post-cervical artificial insemination (PCAI) catheter assemblies.

Abstract: A transcatheter insertion system is provided for the insertion of an intracorporeal device using an insertion device. The system comprises an outer sheath arranged and configured to form a passageway for the intracorporeal device and/or the insertion device. The outer sheath guides the insertion device. A method of transcatheter insertion with the system is also provided.

Abstract: An introducer having a dilator positioned in a sheath is inserted into a first blood vessel and, thereafter, only the dilator tube is drawn out of the first blood vessel and the sheath while the sheath remains in the first blood vessel. A diagnostic instrument having an outer diameter smaller than a maximum outer diameter permitting insertion into the sheath tube is inserted into the second blood vessel, and a stenosis of the second blood vessel is diagnosed. While keeping the sheath indwelling in the first blood vessel, a therapeutic instrument or a catheter permitting the therapeutic instrument to be inserted therein, which therapeutic instrument or catheter has a maximum outer diameter permitting insertion into the sheath tube, is inserted into the second blood vessel, and the second blood vessel is treated.

Abstract: An elongate flexible steerable guidewire for facilitating placement of a medical implement is described having a proximal section, an intermediate section, and a distal steerable section. In embodiments the distal steerable section comprises a plurality of rotatable swivel members, and an elongate directional tip extending distally from the distalmost swivel member. At least one manipulation wire is secured to the swivel members and extends proximally to the proximal section. Axial movement of manipulation wires rotates the swivel members, thereby curving the guidewire and deflecting the directional tip. An actuator or handle may be incorporated with the guidewire. Methods include placing medical implements in target regions. Exemplary applications include guiding and placement of electrical leads in the spine, and placement of angioplasty devices in the vasculature.

Abstract: Inflatable medical devices and methods for making and using the same are disclosed. The devices can be medical invasive balloons, such as those used for transcutaneous heart valve implantation, such as balloons used for transcatheter aortic-valve implantation. The balloons can have high strength, fiber-reinforced walls.