Abstract: A system for detecting needle dislodgement includes a first sensor element and a second sensor element. The first sensor element is attached to a first associated dialysis tubing having a needle connected at one end offset from the needle and a sterile field, which is an area on a leg or arm adjacent to where the needle is inserted, such that movement of the first associated dialysis tubing results in movement of the first sensor element. The second sensor element attaches to a second associated dialysis tubing having a needle connected at one end and detects movement of the first sensor element with respect to the second sensor element. An alarm is in communication with the first or second sensor element and generates a signal when the movement of the first sensor element with respect to the second sensor element is outside a predetermined threshold.

Abstract: An assembly structured for concurrent irrigation and aspiration of a nasal cavity including a housing having a supply container disposed therein for the removable retention of irrigating fluid. A nasal applicator comprises first and second passages respectfully structured to deliver irrigating fluid to the nasal cavity and concurrently remove waste fluid therefrom. An activating assembly includes a plunger biased into a continuous pressure applying, dispensing relation to the irrigating fluid and a valve assembly is selectively disposable into an open position facilitating fluid communication between the supply container and the applicator for the delivery of the irrigating fluid therethrough into the nasal cavity. The activating assembly is further structured to create a negative pressure within the chamber which communicates with the second passage of the applicator to facilitate delivery of the waste fluid therefrom along a path of travel to an interior of the chamber.

Abstract: An infusion set (1) includes: a first flow path (10a) having a first connector (11a) and a downstream connector (19); a first open/close valve (12a), a first liquid surface sensor (13a), a second liquid surface sensor (13b), a drip chamber (14), and a variable valve (17) that are provided in this order on the first flow path from the first connector side toward the downstream connector side; a droplet sensor (15) with which the drip chamber is provided; a second flow path (10b) having a second connector (11b); and a second open/close valve (12b) provided on the second flow path. The second flow path is in communication with a portion of the first flow path between the first liquid surface sensor and the second liquid surface sensor. The controller is configured to control the first and second open/close valves and the variable valves based on signals from the first and second liquid surface sensors and the droplet sensor.

Abstract: A catheter includes: a first port; a second port; a first lumen communicating with the first port; a second lumen configured to selectively communicate with the first port and/or the second port; and a switching mechanism part selectively switchable between a first switching state in which the first port and the second lumen communicate with each other and a second switching state in which communication between the first port and the second lumen is blocked.

Abstract: The present disclosure provides a medical instrument, including a tubular main body; a plurality of operating lines; an operating part main body provided on the base end portion of the tubular main body; a bending operating part which is configured to bend a distal portion of the tubular main body; a path defining part which is configured to define a path of the operating line in the bending operating part; and a deviation preventive member which is configured to prevent the operating line from deviating from a path defined by the path defining part; wherein the operating line becomes in a relaxed state when the bending operating part is in a fixation position, while the operating line becomes in a strained state when the bending operating part is in an operation position.

Abstract: An injection device assembly including a housing, a syringe, a drive mechanism and one or more sensing systems are described. The drive mechanism advances the syringe from a storage position to an injection position, and a plunger advances the syringe piston from an initial position to a final position. The status sensing system may include one or more main PCB(s) disposed in an end portion of the injection device assembly's housing. The system may determine various parameters related to an operational status of the injection device, including the location of the devices components, an amount of medication remaining in the device, a temperature of the medication, and whether or not the device is properly contacting the users skin before injection. The system may communicate such determined parameters to an external device via a wireless communication link.

Abstract: Devices, agents, and associated methods for selective modulation of renal nerves by localized delivery of neural ablative substances are disclosed herein. One aspect of the present technology is directed to a method for delivering a neuromodulatory agent (e.g., capsaicin) via a catheter to a kidney of the patient. The neuromodulatory agent selectively neuromodulates afferent renal nerves in a patient compared efferent renal nerves of the patient. The method can also include removing the catheter from the patient after delivering the neuromodulatory agent to conclude the procedure.

Abstract: A catheter (1) comprising an elongate tubular body (2) having a proximal end (3), a distal end (4), and an inner lumen (5) extending through the elongate tubular body (2), wherein the elongate tubular body (2) comprises a proximal section (6) and a distal section (7), wherein at least the proximal section (6) comprises at least two layers, wherein the proximal end (3) is connected with a catheter hub (8) being an adapter of greater radial outside dimension than the elongate tubular body (2), wherein the catheter hub (8) has an inner lumen (9) of larger inside diameter than the elongate tubular body (2), and wherein the innermost layer (10) of the proximal section (6) extends into the catheter hub (8) and flares from the proximal section (6) to the catheter hub (8). The catheter ensures a smooth transition of a medical device, e.g. a stent to be transferred from a storage device like a sheath into the tubular body of the catheter.

Abstract: A syringe assembly for administration of a neurotoxin, the syringe assembly comprising: a syringe comprising: a clear syringe barrel with dosage markings completely encircling the clear syringe barrel; and a plunger having a plunger body and a clear inverted plunger tip; and a needle assembly comprising a needle and a sealing hub for removably attaching the needle assembly to the syringe, wherein the needle is approximately 0.15 inches to approximately 0.3 inches in length and has a gauge of approximately 27 gauge to approximately 35 gauge.

Abstract: A method for controlling gas composition in a surgical cavity during an endoscopic surgical procedure includes monitoring for a plurality of gas species in a gas flow from a surgical cavity of a patient. The method includes measuring the plurality of gas species in the gas flow from the surgical cavity and determining if the gas species measured in the gas flow from the surgical cavity are each present and/or within a respective desired range. The method includes adding gas into the surgical cavity if one or more gas species in the plurality of gas species is outside of the respective desired range so as to bring a composition of gas species in the surgical cavity within the respective desired range.

Abstract: Modular fluid path assemblies are provided that include conduit, coupling, and needle portions of a fluid path fluidly coupled to an outlet of a container. The modular fluid path assemblies further include a needle shield having a tip of the needle embedded therein. So configured, in embodiments, the modular fluid path assemblies can be sterilized, a medicament can be filled in the container, and a stopper inserted in the container so that the pre-sterilized and pre-filled modular fluid path assemblies can have a closed container integrity (CCI) seal.

Abstract: The present disclosure relates to a bandage wherein the bandage comprise of a first layer of protective covering, wherein the first layer is removable; a second layer of covering, wherein the second layer of covering is made of a cloth material; a third layer of covering, wherein the third layer is the top most layer of the bandage and together with the second layer forms a support pad; an injector, wherein the injector is present on the second layer of covering; a cylinder, wherein the cylinder is present in the support pad, wherein the bandage is used for delivering a medication to a localized area on a patient's body. The bandage is further used for delivering localized, painless ozone gas treatment to a patient suffering from infectious disease. The bandage is easy to carry and comes in various shapes and sizes.

Abstract: An injection device comprises a housing (12) having a longitudinal axis. The injection device further comprises a dose selector (16) capable of setting a dose to be ejected from the injection device and a dose indicator comprising a units wheel (18) operatively connectable to the dose selector so that rotation of the dose selector about the longitudinal axis also rotates the units wheel, and a tens wheel (19) selectively engageable with the units wheel so that rotation of the units wheel also rotates the tens wheel. A biasing means biases the dose indicator axially-rearwardly in the housing. An internal surface of the housing is provided with a tens housing feature selectively engageable with the tens wheel to prevent rotation thereof.

Abstract: An endoscopic tool for facilitating injection of fluid into a submucosal layer of tissue includes a first cannula, a suction source, a fluid lumen, and a second cannula. The first cannula has a suction surface disposed at a distal end, and defines a suction lumen. The suction source is coupled to the first cannula and creates a negative pressure within the suction lumen. The second cannula is disposed in a fluid lumen separate from the suction lumen, is adapted to be coupled to a source of fluid, and carries a needle at a distal end thereof. The tool draws the mucosal layer via the suction, which enlarges the submucosal layer, and injects a fluid into the enlarged portion of the submucosal layer via the needle, thereby creating a raised portion of tissue around the injection site.

Abstract: A needleless injector which can selectively induce the immune response and a method for introducing DNA including a region coding for an antigen to selectively produce an antibody in a living body of a mammal by using the needleless injector are provided. Disclosed is a needleless injector for injecting a DNA solution into an injection target area without using any injection needles. The needleless injector includes an accommodating unit which accommodates the DNA solution, a predetermined ignition device; and a predetermined nozzle unit. A temperature of the predetermined combustion product, which is provided during the pressurization, changes to a neighborhood of ordinary temperature within 20 msec after a pressure, which is applied to the DNA solution on account of the combustion of the igniter powder, reaches an initial peak discharge force during a pressurization process for discharging the DNA solution.

Abstract: A device for auricularly delivering and/or receiving medication which comprises an earcup, a drug cartridge or drug reservoir having active ingredients, and a fluid generator that generates a fluid having active ingredients and delivers the fluid to the earcup. A method for auricularly delivering medication which comprises the steps of receiving medication from a cartridge at a fluid generator, generating fluid comprising the medication, and passing the fluid to an earcup. A system for auricularly delivering medication comprising a headphone comprising at least one earcup, and a replaceable and consumable drug cartridge coupled to the headphone. A method for receiving medication which comprises the steps of placing an earcup on an ear, operating a headphone coupled to the earcup, and receiving fluid generated by a fluid generator, the fluid comprising active ingredients, wherein the fluid generator receives medication from a cartridge comprising active ingredients.

Abstract: A manual injection device having a lower body (1) for a reservoir (S), a piston (P) and a needle (A); a movable upper body (2) including a piston rod (TP); and an actuator sleeve (10) including a contact end (11) and movable relative to the lower body between projecting positions and an actuated position. The actuator sleeve (10) is in a first projecting position before the manual injection device is actuated, and in a second projecting position after it is actuated. The actuator sleeve co-operates with the lower body (1) or with any element secured to the lower body to define a pricking lock. The piston rod (TP) co-operates with the reservoir or with an element secured to the reservoir to define an injection lock. The force for actuating the pricking lock is less than the force for actuating the injection lock, such that the pricking lock is actuated first.

Abstract: A medical elongated body includes a tube shaped body provided with a spiral slit. The tube shaped body has a pair of opposing surfaces, on both sides of the slit, opposing surfaces have a first side and a second side, a first convex portion protrudes from the first side and a second convex portion protrudes from the second side, the first convex portion and the second convex portion are adjacent to each other in the circumferential direction of the tube shaped body, and base portions of the first convex portion and the second convex portion are located on a common first spiral.

Abstract: A system for detecting needle dislodgement includes a first sensor element, a second sensor element, and an alarm. The first sensor element attaches to an associated dialysis tubing having a needle connected at one end. The first sensor element also attaches to the associated dialysis tubing offset from the needle and a sterile field, which is an area on a leg or arm adjacent to where the needle is inserted, in a manner such that movement of the associated dialysis tubing results in movement of the first sensor element. The second sensor element secures to the arm or leg offset from the sterile field. The alarm is in communication with or includes at least one of the first sensor element and the second sensor element. The alarm generates a signal indicative of a position of the first sensor element with respect to the second sensor element.

Abstract: A device and method for aspirating bone barrow. The device includes a double syringe assembly having a distal syringe and a proximal syringe coupled to the distal syringe. A plunger includes a distal end disposed within a barrel of the distal syringe and a proximal end disposed within a barrel of the proximal syringe. A needle assembly is coupled to the double syringe assembly and includes a needle having an outer tube and an inner tube disposed within the outer tube. Upon actuation of the plunger, the distal syringe aspirates bone marrow through the outer tube of the needle and into a chamber of the distal syringe. At the same time, the proximal syringe injects fluid through the inner tube of the needle at the same rate in which the bone marrow is aspirated.