Abstract: A needle shield assembly for enclosing a needle cannula includes a needle cannula having a needle hub at a proximal end thereof and a sharp distal end. A needle shield adapter is mounted to the needle hub and a needle shield is connected to the adapter. The needle shield is moveable between a first position enclosing the needle cannula and a second position exposing the needle cannula for use.

Abstract: A needle-exchangeable and self-destruction insulin syringe comprises a barrel (1), a push rod (2), a rubber piston (3) and a needle seat (4). The barrel (1) is provided with a connection needle seat (7) matched with a needle hub (5). The connection needle seat (7) is supported and fastened at the front end of the barrel by a support seat (8). The needle hub (5) is extended downwards to form a fixing ring (9). A snap ring (10) is formed at an upper end of the connection needle seat (7). The snap ring (10) is protruded into the bore of the fixing ring (9) and locked with the fixing ring (9). A large groove (13) is provided in the wall of the bore of the connection needle seat (7). The upper end of the support seat (8) is protruded into the bore of the connection needle seat (7). First elastic detents (14) are formed at the upper end of the support seat (8) and come together towards the center.

Abstract: To securely position a needle tip and a blade face of a needle tube inserted into the skin in a predetermined site of a living body, such as the upper layer of skin, an injection needle assembly includes a needle tube having a needle tip capable of puncturing a living body, a hub holding the needle tube, a stabilizer, and a guide portion. The stabilizer is formed in a tubular shape surrounding the circumference of the needle tube, and an end face is pressed against the skin, and thereby a raised portion of the skin is formed in a tube hole. The guide portion is arranged on the stabilizer, and is adapted to recognize a press-in distance y of the stabilizer to the skin.

Abstract: A drive mechanism of a drug delivery device is presented having, a piston rod to operably engage with a piston of a cartridge containing a medicament, a first functional component and a second functional component whose position or orientation relative to each other is unambiguously correlated to a predefined axial position of the piston rod, wherein the first and/or the second functional component comprise at least one engaging portion to inseparably and to adhesively engage the first and the second functional component with each other for rendering the drive mechanism inoperable when the predefined axial position of the piston rod has been reached.

Abstract: Various exemplary embodiments relate to an electronic device for dispensing a medicament. The electronic device may include a medicament storage case or an electronic medicament device. The medicament storage case includes: a door moveable between an open position and a closed position; a lock moveable between a locked position where the lock maintains the door in the closed position and an unlocked position where the lock allows the door to move to the open position; a medicament dispensing device containing medication; an input device located on an external surface of the storage case activatable by a user; a communication unit configured to initiate a two-way communication between the user and a remote access control center upon activation of the input device and configured to receive an access signal from the remote access control center; and an actuator responsive to the access signal to move the lock to the open position upon receipt of the communication from the remote access control center.

Abstract: A medical hand and arm protection apparatus and method of protection including a protective shell which is capable of receiving a patient's hand and arm. A sheet is attached to the protective shell, which is tucked under the patient to anchor the hand and arm protector in place. The protective shell also has one or more perforations that allow the medical professional access to the interior of the surgical arm protector to view the patient's IV sites and other medical equipment attached to the patient's hand or arm.

Abstract: The invention relates to a small-volume nebulizer with a valve system to provide lung physiotherapy during airway therapy with small-volume nebulizers. The valve system may be incorporated into a small-volume nebulizer. The small-volume nebulizer may be pre-filled with at least one unit-dose of medicine and hermetically sealed until use. The nebulizer may be sealed at the top with a removable cap that may be detached at the time of use and replaced with a patient connector. Likewise, the nebulizer may be sealed at the bottom with a bottom cap that is replaced with a gas source at the beginning of a therapeutic aerosol treatment.

Abstract: A method of manufacturing an atomizing body for an atomizing device includes the steps of providing a support element having a first layer on a first surface of the support element and a second layer on a second surface of the support element, the first layer including a first perforated membrane and the second layer including a process orifice, etching a cavity through the support element, the cavity forming a fluid connection from the process orifice to the perforated membrane, by providing etching substance to the process orifice. The atomizing body as obtained may advantageously be applied in an atomizing device or an inhaler.

Abstract: An aerosol inhalation device assembly for diagnostic and therapeutic use for deep lung alveolar aerosol targeted drug delivery includes a nebulizer for generating an aerosol containing droplets of a liquid. The nebulizer has a pressurized gas inlet and a nebulizer outlet. An inhalation chamber is in fluid communication with the nebulizer outlet. The inhalation chamber is defined by at least one sidewall. An inhalation mouthpiece assembly is in fluid communication with the inhalation chamber and extends outwardly from the at least one sidewall of the inhalation chamber. A filter assembly is in fluid communication with the inhalation chamber. The filter assembly includes a filter medium. An exit port is in direct fluid communication with the filter assembly. A method of using the nebulizer is also provided.

Abstract: A nebulizer with a negative pressure structure includes a nebulization body, a carrying cavity, a nebulizing element and a negative pressure generating element. The carrying cavity is provided for carrying a nebulized liquid and has a through hole. The nebulizing element is installed at the through hole and includes a piezoelectric driving unit and a nebulizing plate disposed on a side of the piezoelectric driving unit. The negative pressure generating element is formed on the carrying cavity and provided for changing the volume of the carrying cavity or removing air from the carrying cavity to reduce the air pressure in the carrying cavity, so as to nebulize a liquid of low surface tension or high viscosity effectively.

Abstract: A trocar sleeve that isolates the surgical device or movement thereof to inhibit or prevent an established non-jet streaming condition from becoming a jet streaming condition and a method of inhibiting or preventing a jet streaming condition from occurring due to instrument obstruction.

Abstract: A delivery device for and method of delivering substance, in particular a vaccine, to a mucosal surface within the oral cavity of a subject, the device comprising: a mouthpiece unit to be gripped in the mouth of a subject, wherein the mouthpiece unit is configured such that, on exhalation or attempted exhalation by the subject, a pressure is developed in the oral cavity which is such as to close the oropharyngeal velum of the subject; and an oral outlet unit including at least one outlet from which substance is in use delivered to a mucosal surface within the oral cavity of the subject.

Abstract: A Positive Airway Pressure (PAP) device includes a flow generator that generates a supply of pressurized air. The flow generator includes a programmable controller. The programmable controller is adapted to allow continuous access to at least one active operating mode and selective access to at least one dormant operating mode. The programmable controller includes a mode control system adapted to receive a data signal to control the selective access to the at least one dormant operating mode.

Abstract: A medical vaporizer includes a liquid drug reservoir configured to receive and hold a liquid drug. A low power graphical display is configured to intermittently receive power. The low power graphical display is operable to visually present information and maintain the visual presentation of information in the absence of power. A controller is configured to intermittently receive power and upon receiving power the controller operates to determine a status of a medical vaporizer. The controller operates the low power graphical display to present the status of the medical vaporizer as visually presented information.

Abstract: A mask for delivery of respiratory therapy to a patient may include one or more of the following improvements: rigidizer provided to headgear strap, locking clip/clip receptacle headgear connection, keyed headgear buckles, lotion dispenser on frame, rotatable prongs to adjust orientation, alignment indicators provided to prong, cushion and/or frame, chin flap with bellows arrangement, vent holes positioned away from gas entry port, and vent holes to direct washout gas at an angle.

Abstract: A mask assembly includes a mask with an inflatable bladder. The internal pressure of the inflatable bladder can be set to be higher than the delivered therapeutic pressure. The pressure offset may be constant, or it may vary over the range of therapeutic pressures. Thus, the force necessary to maintain a contact seal between the mask and the patient can be reduced, thereby providing a system that is more comfortable to the patient, which increases patient compliance.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: An air delivery conduit for conveying breathable gas from a positive airway pressure device to a patient interface includes a tubular wall structure constructed from a textile material. A reinforcing structure may be provided to the wall structure that is structured to prevent kinking or collapsing of the wall structure. The wall structure may include a warp having a plurality of lengthwise textile warp threads arranged in a circle and a weft having a textile weft thread that is woven through the warp threads.

Abstract: A device and a process for the heating and humidification of gas, especially respiratory gas. Fluid from a fluid reservoir is supplied to a sprinkling type chamber where, for the purpose of humidification, it is moved through the gas. The point is that the fluid is heated by a temperature controlled heater to a preset temperature. In addition to the description of the device, a description of the process underlying the operation of the device is described.

Abstract: A sleep aid system and an operation method thereof are disclosed. The sleep aid system includes a sleep aid device including a retrieving module, a processing module, and a transmitting module, and a server. The retrieving module retrieves a brainwave signal including specific frequency band signals. The processing module analyzes the brainwave signal to obtain an index in each of the specific frequency band signals and calculates a sleepless degree parameter representing one of at least five brainwave states regarding sleep accordingly. The transmitting module transmits a parameter signal corresponding to the sleepless degree parameter. The server receives the parameter signal from the transmitting module. The server stores comparison data, compares the parameter signal to the comparison data, and generates a first feedback signal according to a comparison result. The first feedback signal includes a command to switch an audio file or stream which is currently being played.

Abstract: Computer implemented method and system for achieving a preferred state of mind of a user are disclosed. In a first aspect, the method comprises detecting a biological marker (biomarker) of a user utilizing one or more sensors; and inferring a state of mind of the user based upon data received from the one or more sensors that are provided to computational hardware. Finally the method includes providing an antidote to the user if the inferred state of mind is different than the preferred state of mind utilizing an actuator. In a second aspect, the system comprises one or more sensors for detecting a biological marker (biomarker) of the user and computational hardware for inferring a state of mind of the user based upon data received from the one or more sensors. Finally the system includes an actuator for providing an antidote to the user if the inferred state of mind is different than a preferred state of mind.

Abstract: A method of making a platform of medical devices from a single tube of a memory metal is described. The single tube, which may be generally cylindrical, is cut to form perforations that function as scoring lines and are located adjacent to the proximal and distal ends. The perforations allow the manufacturer to cleanly tear proximal memory metal strips from each other and to cleanly tear distal memory metal strips from each other so that the freed proximal memory metal strips may be re-attached to each other and the freed distal memory metal strips may be re-attached to each other to form a medical device that may be positioned inside a catheter that has an inner diameter (ID) that is less than the outer diameter of the single tube. The formed medical device may be in the form of an expandable, shape-set basket with x-ray markers that may be used to remove an intracranial blood clot.

Abstract: The present technology is directed to a dilator centering device and assemblies and methods using same. In particular, a dilator centering device in accordance with the disclosed technology can be used with a sheath hub assembly. In one embodiment, a dilator centering device includes a lumen capable of receiving a dilator shaft and centering a dilator shaft with respect to the sheath hub as the dilator shaft enters the sheath hub. In one embodiment, the dilator centering device can be attached to the sheath hub during manufacturing or it can be attached at the use site. In one embodiment, the dilator centering device can be integrated with and non-removable from the sheath hub. The embodiments disclosed herein are illustrative and do not limit the scope and spirit of the disclosed technology.

Abstract: A device may operate a guide wire and be operable by a single operator digit. The device may include an insertion control device for advancing the guide wire in a forward and in a reverse direction and along a longitudinal axis of the guide wire; and a rotary device for rolling a guide wire about the longitudinal axis. A robotic instrument driver may be operatively coupled to the device and configured to control axial movement of the guide wire along the longitudinal axis according to input received from the insertion control device and to control rotational movement of the guide wire according to input received from the rotary device.

Abstract: Some embodiments relate to an apparatus comprising an elongate flexible tube sized to be received within a tract and having a proximal end and a distal end; a drive mechanism coupled to the proximal end of the tube; and a liquid column extending from the proximal end to the distal end; wherein the drive mechanism is configured to cause movement of the liquid column within the tube to impart forward momentum to the tube and thereby promote advancement of at least the distal end of the tube within the tract when at least the distal end is received within a part of the tract.

Abstract: A catheter for use in a patient's heart, especially for mapping a tubular region of the heart, has a catheter body, a deflectable intermediate section and a distal a mapping assembly that has a generally circular portion adapted to sit on or in a tubular region of the heart. A control handle of the catheter allows for single-handed manipulation of various control mechanisms that can deflect the intermediate section and contract the mapping assembly by means of a deflection control assembly and a linear control assembly. The deflection control assembly has a deflection arm and a rocker member. The linear control assembly has a linear control member, an inner rotational member and a cam. A pair of puller members are responsive to the deflection control assembly to bi-directionally deflect the intermediate section. A third puller member is responsive to the linear control assembly to contract the generally circular portion of the mapping assembly.

Abstract: A dressing includes a transparent film layer having a top side, an opposite bottom side, and an insertion site viewing portion. The bottom side has an adhesive portion and an adhesive-free portion. The adhesive-free portion is disposed within the viewing portion. An antimicrobial member having a top side and an opposite bottom side is disposed in the viewing portion. A portion of the antimicrobial member is adhered to the film layer adhesive portion, and a portion of the antimicrobial member is disposed in the adhesive-free portion. The antimicrobial member includes an outer edge and an opening disposed within the outer edge. The opening is disposed in the adhesive-free portion. A catheter extending from an insertion site is receivable through the opening in the antimicrobial member. The antimicrobial member surrounds the insertion site when the dressing is applied to a patient.

Abstract: A sensor guide wire for an intravascular measurement of a physiological variable in a living body includes a sensor region in a distal part of the sensor guide wire, a sensor element arranged in the sensor region, a male connector at a proximal part of the sensor guide wire, a least one electrical micro-cable connecting the male connector to the sensor element, and an elongated guide wire body arranged between the sensor region and the male connector. The at least one electrical micro-cable extends essentially helically around the guide wire body along the length of at least a part of the guide wire.

Abstract: An occlusion device is described and depicted for occluding a body lumen. The device can comprise an occluding body member and one or more protruding portions or members disposed on the body member such that the protruding portion is provided with spacing, or surface area, to allow for tissue in-growth. The device can also comprise an expandable plug. The expandable plug may be twisted or otherwise formed into a shape, e.g., helical, in its initial deployment configuration, and untwist upon deployment.

Abstract: A medical instrument for treating and/or diagnosing anorectal disorders which comprises a slender member that is sized and shaped for being placed in the anal canal of a patient, along at least a portion of the anal sphincter, so that an outer surface of the slender member is in contact with inner walls of the anal canal.

Abstract: The present invention provides a device, a system, and a method for application of fluids.

Abstract: A cream application assembly includes a handle that has a first end and a second end. The handle has a first portion slidably coupled to a second portion such that the handle has a telescopically adjustable length. An applicator is rotatably coupled to the handle and the applicator is infused with a cream. The applicator is used to apply the cream to a user.

Abstract: A low cost transdermal patch comprises water soluble microneedles and has good performance. A transdermal patch comprises a microneedle sheet, which comprises a plurality of water soluble microneedles, moisture permeable sheet, wherethrough water vapor passes, and a reinforcing film. The reinforcing film is adhered, by an adhesive layer having an adhesive strength less than that of an adhesive layer, onto an outer surface of the moisture permeable sheet, which is the side opposite the skin opposing surface. The reinforcing film includes a water vapor barrier sheet, which blocks the passage of water vapor through at least a first area, and a removable portion around the water vapor barrier sheet. The removable portion is configured such that it can be separated from and peeled off the water vapor barrier sheet.

Abstract: The device according to the invention includes a hollow body delimiting an inner passage. It further includes an assembly for maintaining the material in position in the inner passage. The maintaining assembly includes a radially compressible member delimiting, when idle, a through passage aperture of the material, and a radial compression member compressing the compressible member, radially movable relative to an axis of the passage aperture to outwardly compress the compressible member. It includes a member for actuating the or each compression member, radially movable relative to the body to cause the compression member to go from a radially retracted position, in which the section of the passage aperture is maximal, to a position radially deployed in the compressible member, in which the section of the passage aperture is minimal.

Abstract: A line, in particular to a line of a blood tubing system or of a blood bag system, having a closing member blocking the line passage, with the closing member being formed by a plastically deformable closing body which is arranged in the line and which closes the line in at least one state and with at least the portion of the line in which the closing body is located being made flexible.

Abstract: Devices, systems and methods are disclosed for electrical stimulation of the vagus nerve to treat or prevent disorders in a patient. The devices comprise a handheld device having one or more electrode interfaces for contacting the outer skin surface of a patient, a power source and a signal generator coupled to the electrode/interfaces for applying one or more electrical impulses to a deep nerve within the patient, such as the vagus nerve. The device further comprises a filter situated in series between the signal generator and the electrode/interfaces for filtering out undesired high frequency components of the electrical impulses to create a cleaner, smoother signal. The filter may comprise an electrically conductive medium and/or a low-pass filter between the signal generator and the electrode/interface.

Abstract: A stimulation electrode arrangement for a device (10) for electrostimulation of the eye is described, the device (10) having a spectacles-like frame (11) with a nosepiece (12), an arrangement, connected to the nosepiece (12), for holding the frame (11) on the head of the patient, and at least one electrode holder (24, 25), arranged on the nosepiece (12) in adjustable fashion, for the wire-shaped stimulation electrode (26, 27). The stimulation electrode arrangement comprises an electrode carrier, which can be attached to the electrode holder (24, 25) in detachable fashion and on which the stimulation electrode (26, 27) is arranged.

Abstract: An artificial sensory epithelium (1) to be embedded in a cochlea (301) of a patient includes a piezoelectric film (2) and multitude microelectrodes (3), (3), . . . arranged on the cochlea. The piezoelectric film is arranged along a basilar membrane (306) in the cochlea. A portion of the piezoelectric film that corresponds to a portion of the basilar membrane that is induced to vibrate by sound waves coming from outside the cochlea vibrates. A microelectrode of the microelectrodes that is arranged on the portion of the piezoelectric film provides electric stimuli to spiral ganglion neurons (311). The artificial sensory epithelium preferably includes a support member (4) configured to support the piezoelectric film and be fixable in the cochlea.

Abstract: The present invention relates to an electromagnetically-countered display system including at least one wave source and at least one counter unit, where such a wave source irradiates harmful electromagnetic waves and the counter unit emits counter electromagnetic waves for countering the harmful waves therewith. More particularly, the present invention relates to various counter units for the electromagnetically-countered display system and to various mechanisms to counter the harmful waves with the counter units, e.g., by matching configurations of the counter units with those of the wave sources, by matching wavefronts of the harmful waves with those the counter waves, and so on. The present invention also relates to various methods of countering the harmful waves with such counter waves by source and/or wave matchings, various methods of providing the counter units for emitting the counter waves defining desired wave characteristics, and the like.

Abstract: The present invention relates to a topical or cosmetic system that includes a first element capable of acting as an electron donor and a second element capable of acting as an electron acceptor. Such first and second elements are spaced apart by a predetermined distance across a skin surface. The system also includes a third element extending over the predetermined distance across the skin surface, while the third element contains an electrically conductive medium for electrically connecting the first and second elements, thereby generating an electrical current that flows across the skin surface from the first element through the conductive medium to the second element in the absence of any power source. The present invention also relates to methods of using the above-described system for preventing or treating skin damage.

Abstract: A method of treating or preventing a hair-condition of a user comprising: subjecting the user's scalp to at least 200 distinct electrode-scalp contact events during a time-interval of at most one minute and dividable into 5 non-overlapping equal-duration sub-intervals covering the time-interval, method performed such that i. for at least a majority of the electrode-scalp contact events, no electrode of the event enters into the dermis; ii. a duration of each electrode contact event is at most 100 milliseconds; and iii. for each electrode contact event, an electrical current flows between the electrode and the scalp so as to deposit electrode-released ions of a first metal or of a second metal on the scalp, thereby forming a respective metal-ion-deposition island on the user's scalp.

Abstract: Embodiments of the invention provide a reusable intra-oral device for treating xerostomia. The device having a structure adaptable for oral cavities of multiple users. The hermitically sealed housing comprises of an electronic module having a signal generator configured to generate electrical signals based on one or more values of one or more predefined parameters. Further, the device comprises of electrodes connected to the electronic module. The electrodes are configured to apply the electric signals for stimulating lingual nerves in the oral cavities to induce salivation.

Abstract: A medical stimulation device such as a cochlear implant configured to provide stimulation of one or more spatially-restricted contiguous portion(s) of the spiral array of auditory nerve fibers in the cochlear (“discrete stimulation regions”). Each discrete stimulation region is defined by the constructive and/or destructive interference of stimulating and limiting signals simultaneously applied to electrode channels of an implanted electrode array, the stimulating and limiting signals being determined based upon transimpedance measurements of intracochlear electrode channels of the implanted electrode array representing specific spread functions of an individual recipient. The stimulating signal is preferably applied through a targeted electrode channel; that is, one or more successive electrodes which is/are adjacent to the discrete stimulation region.

Abstract: A method of activating at least two electrodes in a multichannel electrode array using channel specific sampling sequences is presented. A channel specific sampling sequence is defined for each electrode, the sequence having a particular duration, pulse amplitude distribution, and number of pulses. A weighting factor is applied to the channel specific sampling sequence. Each electrode in the multichannel electrode array is then simultaneously activated using sign-correlated pulses, the sign-correlated pulses based on parameters of spatial channel interaction reflecting geometric overlapping of electrical fields from each electrode, non-linear compression, and each electrode's weighted channel specific sampling sequence.

Abstract: A method is described for adjusting hearing implant operating parameters for electrode contacts in an implantable electrode array to minimize tinnitus in an implanted patient. A channel tinnitus masking stimulation level is measured for each electrode contact at which maximum tinnitus masking occurs, Ytin,n. A channel threshold stimulation level also is measured for each electrode contact that represents a lowest detectable stimulation level, Tmeas,n. And a channel maximum stimulation level is measured for each electrode contact that represents a maximum comfortable stimulation level, MCLmeas,n. Channel threshold stimulation level Tn and channel maximum stimulation level MCLn are then adjusted for each electrode contact as a function of the channel tinnitus masking stimulation level Ytin,n and tinnitus masking stimulation levels for adjacent electrode contacts, Ytin,adj.

Abstract: Electrode structures for transvascular nerve stimulation combine electrodes with an electrically-insulating backing layer. The backing layer increases the electrical impedance of electrical paths through blood in a lumen of a blood vessel and consequently increases the flow of electrical current through surrounding tissues. The electrode structures may be applied to stimulate nerves such as the phrenic, vagus, trigeminal, obturator or other nerves.

Abstract: A method for heart treatment includes analyzing the cardiac rhythm. The method further includes utilizing a generator to produce discharges (Si) of N pulses (I) of VNS stimulation in succession. The discharge may be synchronized to a detected R ventricular depolarization wave of each cardiac cycle. The method further includes controlling a stochastic modulation of the discharges control of the delivery of each VNS pulse of each discharge by selective inhibition or not of the generation of these VNS pulses. The number of pulses of each discharge thus randomly varies, and thus varies the VNS stimulation energy of this discharge, which is artificially induced, cycle-to-cycle variability in the RR interval. This stochastic therapy is applied if the spontaneous heart rate variability falls below a minimum level.

Abstract: This device comprises a generator producing bursts (Si) of N pulses (I) of VNS stimulation generated in succession during respective periods of activity (TON) separated by intermediate periods of inactivity (TOFF) during which no stimulation is issued. Stochastic modulation circuitry controls the delivery of the bursts of each of the N pulses of each VNS burst by selective inhibition or not, of the generation of each of the VNS pulses depending on the result of a respective randomization. The number of VNS pulses of each burst is thus randomly varying, and thus the VNS stimulation energy of this burst and the interval between successive pulses, which counteract the appearance of a physiological compensation loop.

Abstract: The invention is a distributed implantable neuro-stimulation system, comprising an implant controller including control logic to transmit two time-varying power signals, varying between two levels and out of phase with the other, and a command signal modulated onto at least one of the power signals. One or more electrode cells, each having control logic to extract charge from the power signals and recover commands from the command signal. A two-wire bus interconnecting the implant controller and all the electrode cells, to carry one of the time varying signals in each of the two wires, and to carry the command signal.

Abstract: External pacemaker systems and methods deliver pacing waveforms that minimize hydrolysis of the electrode gel. Compensating pulses are interleaved with the pacing pulses, with a polarity and duration that balance the net charge at the electrode locations. The compensating pulses are preferably rectangular for continuous pacing, and decay individually for on-demand pacing.