Abstract: An assembly is configured to position a peristaltic tube with respect to a linear peristaltic pump drive of an infusion pump. The assembly can include a peristaltic tube, first and second tube couplers, a frame, first and second securement plates, a free-flow prevention arm, and a biasing mechanism. The frame can include a snap-fit tab configured to releasably secure the assembly to an assembly receptacle of the infusion pump. The free-flow prevention arm can be selectively movable between a free-flow preventing position and a free-flow allowing position. A latching mechanism can be ergonomically manipulable to latch the free-flow prevention arm in a free-flow allowing position, and to unlatch the free-flow prevention arm such that the biasing mechanism is able to bias the free-flow prevention arm to the free-flow preventing position.

Abstract: A dispersive return pad for a radiofrequency ablation procedure includes a skin material adapted to be worn on a patient's skin, a conductive material positioned adjacent to the skin material, a non-conductive material surrounding the conductive material, and a phase-change material surrounding at least a portion of a side edge of the conductive material. Further, the phase-change material is configured to undergo a phase transition at a target temperature range corresponding to a non-damaging hyperthermic temperature range for the patient's skin. As such, the phase-change material is configured to absorb excess heating from the RF ablation procedure and to prevent burns to the patient's skin.

Abstract: A trial stimulation system includes a disposable trial electrical stimulator that, in some examples, is sterilized for a single use in a stimulation trial of one patient. Additionally, systems for securing a disposable trial stimulator to the body of a patient are described, which may function to improve the durability of the system during the trial period and reduce the risk of damage or malfunction to the system due to lead/electrode dislocation and/or off-label uses like showering or bathing with the trial stimulator still secured to the body.

Abstract: An electrode assembly that includes an electrically conductive layer, a first impedance reduction system, and a second impedance reduction system. The electrically conductive layer forms an electrode portion of the electrode assembly and a first surface to be placed adjacent a person's skin. The first impedance reduction system is configured to dispense a first amount of an electrically conductive gel onto the first surface of the electrically conductive layer in response to a first activation signal. The second impedance reduction system is configured to dispense a second amount of the electrically conductive gel onto the first surface of the electrically conductive layer in response to a second activation signal.

Abstract: An electrode structure for use with a monitoring system. A thin flexible body of an electrode material comprising conductive rubber is provided with projections extending externally to a working surface. According to this construction of the working surface of the electrode only the projections make a contact to the recipient's skin. When the projections are provided with a small cross-section, the constant electrode-skin contact is ensured due to the resiliency of the electrode material.

Abstract: An electrode apparatus may be configured to provide electro-stimulation. The apparatus may include a current spreader and a spongeless volume disposed adjacent to the current spreader. The current spreader may be configured to spatially distribute electrical current across a stimulation area of a subject's skin. The spongeless volume may be configured to carry liquid gel or other fluent conductive substance that is configured to conduct electrical current between the current spreader and the stimulation area of the subject's skin to provide electro-stimulation.

Abstract: A medical electrode demonstrates a superior adhesiveness to a patient's skin during medical data acquisition or treatment procedure yet attaining painless electrode removal from the skin when needed. The subject medical electrode is designed with adhesive neutralizer (or remover) solvent fully enveloped in one or several compartments embedded in an adhesive layer of the medical electrode unit. The compartments have a contact with the patient's skin when the electrode is attached thereto. When compressed by a medical personnel, the compartment releases the adhesive remover solvent directly to the skin-adhesive interface, thereby neutralizing (or removing) the adhesive material, thereby easing the electrode removal. The adhesive layer is made from PEO, sodium chloride, and water. The adhesive remover solvent contains isopropyl alcohol. A method of manufacturing the medical electrode is presented.

Abstract: Provided is a bio-signal detection electrode including: an electrode section made of a gel including an electrolytic solution; and a support section configured to support the electrode section with respect to an accessory, the electrode section adhering to the support section.

Abstract: Apparatus and techniques are provided for interfacing a device with a surface. The apparatus and techniques provide gel encapsulation and isolation mechanisms to extend the shelf-life of the preparation devices, allow for the use of more effective materials, and improve the quality of the contact between a device and an application surface. Particular embodiments of these apparatus and techniques suitable for use in medical contexts are also provided.

Abstract: The present invention provides systems, apparatus and methods for applying electric current to neurons in the brain to treat disorders and to improve motor and/or memory functions in a patient. In a method according to the invention, an electrode is positioned adjacent to and spaced from the skin surface of the patient's head and an electric current is applied through the electrode to a target region in the brain to modulate one or more neurons in the target region. The electrode is housed within an enclosure and spaced from the skin surface so that the electrode does not directly contact the patient's tissue, which reduces the potential for collateral tissue damage or necrosis and shields the electrode from the patient's tissue which substantially inhibits Faradic products (e.g., H+, OH?, H2O2) of the electrode from reaching the target site.

Abstract: An electrode apparatus may be configured Electrode to provide electro-stimulation. The apparatus may include assembly a current spreader and a spongeless volume disposed adjacent to the current spreader. The current spreader may be configured to spatially distribute electrical current across a stimulation area of a subject's skin. The spongeless volume may be configured to carry liquid gel or other fluent conductive substance that is configured to conduct electrical current between the current spreader and the stimulation area of the subject's skin to provide electro-stimulation.

Abstract: A flexible biomedical surface electrode comprises an insulating substrate (10), a conductive electrode layer (12) screen-printed on the substrate, and an insulating masking layer (14) on the electrode layer. The masking layer is configured to expose selected regions (16) of the electrode layer. An electrically conductive adhesive gel layer (18) on the masking layer makes electrical contact with the exposed regions of the electrode layer.

Abstract: An electrode assembly that includes an electrically conductive layer, a first impedance reduction system, and a second impedance reduction system. The electrically conductive layer forms an electrode portion of the electrode assembly and a first surface to be placed adjacent a person's skin. The first impedance reduction system is configured to dispense a first amount of an electrically conductive gel onto the first surface of the electrically conductive layer in response to a first activation signal. The second impedance reduction system is configured to dispense a second amount of the electrically conductive gel onto the first surface of the electrically conductive layer in response to a second activation signal.

Abstract: The present disclosure provides electrodes that possess components capable of indicating to an end-user when the electrode is in need of replacement. In embodiments, the electrodes include a hydrogel in combination with a pH indicator which changes its color or opacity upon repeated use of the electrode, thereby indicating an appropriate time for changing or replacing the electrode.

Abstract: The present disclosure provides electrodes that possess components capable of indicating to an end-user when the electrode is in need of replacement. The electrode includes a substrate and a conductive composition on at least a portion of a surface of the substrate. The conductive composition includes at least one hydrogel and at least one component that precipitates from the hydrogel after repeated use of the electrode, thereby providing an indication to replace the electrode.

Abstract: A medical electrode is provided for detecting and transmitting electric pulses from the body surface of a patient to an electric pulse processor. The medical electrode includes an outer carrier and at least one inner carrier (3, 3?, 3?). The outer carrier and the inner carrier are connected at a defined number of geometrically distributed points (2). The points (2) form an outer edge (4) of the inner carrier and are perforated, so that the outer carrier and the inner carrier can be separated at these points (2). An adhesion area (5) is formed on the underside of the outer carrier (1) and of the inner carrier for adhering the medical electrode to the patient body surface. A contact element (7) is provided with a conductive area arranged concentrically to the contact element (7) for establishing contact with the body surface of the patient. The contact element (7) and the conductive area (8) are arranged within the inner carrier.

Abstract: A medical electrode for bonding to the skin of a patient comprises a support which adheres to the skin and a holding element for at least one electrically conducting connection piece, wherein the skin side of the connection piece is covered with an electrically conducting gel, in particular in a sponge, wherein the gap on the skin side between the holding element and the electrically conducting connection piece is closed by a sealing element which is preferably ring-like.

Abstract: A Transcutaneous Electrical Nerve Stimulator (TENS) and electrode pad that is capable simultaneously of delivering hot or cold thermal therapy for the relief of pain.

Abstract: An electrode assembly for neuro-cranial stimulation includes an electrode, a conductive gel, and an adapter including an interior compartment for positioning the electrode relative to the adapter and for receiving and retaining the conductive gel. The conductive gel contacts the electrode along an electrode-gel interface. An orifice at one end of the interior compartment and adjacent to a positioning surface of the adapter for positioning the electrode assembly against a skin surface of a user enables the conductive gel is able to contact the skin surface of the user to define a gel-skin interface, such that a minimum distance between the electrode-gel interface and the gel-skin interface is maintained between 0.25 cm and 1.3 cm. An electrode assembly mounting apparatus is provided for adjustably positioning a plurality of electrode assemblies against target positions on the cranium.

Abstract: An apparatus including a wettable structure and a plurality of conductive fibers carried by the wettable structure.

Abstract: Composite electrode pads/plugs are configured to be utilized in an electrical stimulator device, particularly one designed to provide surface-applied electrical twitch obtaining intramuscular stimulation (eToims®). The composite pads/plugs include a porous liquid absorbent (e.g., felt) plug sized to be placed in a receptacle of the stimulator device, and a composite pad of porous liquid absorbent (e.g., cotton) material that covers the plug. In an embodiment, the composite pad is formed of cotton stuffing material encased between two sheets of cotton mesh/pad material. The composite pads/plugs can serve to increase, and improve wetting of, the surface area which contacts the patient and delivers the electrical stimulation. In addition to convenience of application, the disclosed structures have been found to help reduce sharp pain felt by the patient during stimulation, without interfering with the ability of the electricity to penetrate deeply in order to provide effective eToims®.

Abstract: An electrode for measuring an electrocardiogram. The electrode comprises a signal detector operable to detect an electrocardiogram signal. An electrolytic gel is coated onto a first surface of the signal detector. The gel is electrically conductive and operable to adhere to a skin. A connector is electrically connected to the signal detector.

Abstract: The invention provides an electrode device that prevents disconnection of an electrode layer effectively by reducing stress at the time when a recess is formed. An electrode device (10) has a protrusion (70), which projects upward, in the part of an outward flange section (110f), other than a recess (60) formed by molding. The protrusion (70) is arranged so as to surround an outer periphery of the recess (60). When the recess (60) is cold-pressed, the protrusion (70) prevents warp (warp waving along a peripheral direction) in the outward flange section (110f) from occurring. Consequently, the protrusion (70) also eases warp of an electrode layer (30) extending on the outward flange section (110f) and prevents disconnection of the electrode layer (30).

Abstract: An electrode assembly arranged to carry out a bioelectrical interaction with an individual, said electrode assembly comprising a conductive material having a contact surface arranged to be brought into contact with a receiving area of the individual's skin, said conductive material being electrically connectable to a suitable electronic device to enable said interaction, the electrode assembly having an impedance control means arranged to measure and control the impedance of the receiving area of the individual's skin prior to an event of the bioelectrical interaction.

Abstract: A medical electrode for conducting an electrical current to or from the skin of a patient. The electrode comprises a thin, flexible metallic conductor, a layer of electrolyte in electrical contact with the conductor and positioned to be in electrical contact with the skin when the electrode is applied to a patient, and an insulating layer overlying the conductor, wherein a peripheral edge of the metallic conductor is sealed with an insulating material so that the peripheral edge of the conductor is substantially out of electrical contact with the electrolyte. This tends to increase the shelf life of the electrode because the more highly worked (e.g., from being die cut during manufacture), and thus higher energy state, peripheral edge is electrically isolated.

Abstract: Medical electrodes are provided for use in applications that require long shelf life and/or shelf life at high temperatures. Some electrodes include high temperature adhesives and/or foams and an encapsulated electrolyte.

Abstract: A hydrogel and scrim assembly adapted for use with an electro-acupuncture device to enhance electrical conduction between the device and the skin and to provide an impedance matching layer between the device and the skin. The assembly includes a scrim with conductive hydrogel masses disposed on the surface of the scrim. The hydrogel masses are sized and dimensioned so that when the pad is adapted to the device, the hydrogel masses do not bridge the electrodes to cause a short between the electrodes.

Abstract: Surfactants useful for enhancing the electrical conduction of electrodes attached to the surface of a patient. The surfactants are also useful in transport of materials in and out of the body of a patient (animal or human) and in the measurement of disease states. Typical surfactants particularly useful in the invention are broadly represented by protein/fatty acid based compounds. The protein/fatty acid compounds may be lipopolypeptides. In some embodiments the lipopolypeptides may be acyl peptides. Typical acyl peptides are Lamepon S™, MayTein C™ and MayTein CT™.

Abstract: An electrode for establishing electrical contact with the skin is disclosed, said electrode having a low impedance and comprising an electrically conductive metallic layer (4) and an electrically conductive gel (12) attached to said metallic layer, wherein the pH of the electrically conductive gel (12) is chosen so as to provide a corrosion of the metallic layer (4).

Abstract: An electrical stimulation device method provides for exact repeatable positioning of stimulation pads onto a body part. The device includes a flexible member for contacting a body part and hook/loop members for tightly supporting the flexible member against the body part. At least one electrical bus is provided which may include a connector for enabling connection of the bus to an electrical lead wire and an electrical contact disposed on the inside of the flexible member. A conductive pad is provided which has dimensions substantially smaller than the dimensions of the flexible member and includes a cover adhesive layer for removably adhering the conductive pad to the flexible member inside with a first side of the cover layer covering the bus contact and an electrical communication therewith. A current controlling media is adhered to a second side of the cover layer and a base layer disposed on the current controlling media is provided for removably adhering the conductive pad to the body part.

Abstract: The present invention involves an electrode sensor attachable to a substrate for sensing electrical activity of a patient. The electrode sensor comprises an elongated conductive body having first and second ends, wherein the first end is adapted to contact the patient for sensing electrical activity of the patient. The second end is configured to conductively attach to the substrate. The elongated conductive body is greater than about 2 millimeters in length and is configured to extend from the substrate.

Abstract: A non-polarizable, silver/silver chloride biomedical electrode that is protected against corrosion during its shelf life by an organic corrosion retarding agent, preferably selected from the group consisting of mercaptans and azoles.

Abstract: A unitary electrode mounting and packaging system for roughening the skin of a patient and applying an electrocardiogram (ECG) monitoring electrode to the skin in a single step. A sheet of a thin plastic material is folded over itself to form a U-shaped carrier having an upper panel connected to a lower panel by the fold. The upper panel supports an electrode and an amount of an electrically conductive gel in a pocket that is covered by the electrode. The lower panel includes an abrasive or roughened material on the bottom surface of the lower panel opposite the electrode. To place the electrode on the skin, the carrier is positioned against the skin of a patient such that the roughened material contacts the skin and pressure is applied downwardly on the electrode. A tab connected to the lower panel then is grasped and pulled by an individual such that the roughened material abrades the skin beneath the carrier to clear the portion of the skin located beneath the electrode.

Abstract: An array of electrodes is constructed to allow the user to easily adjust to the correct size of the patient's head. The array is self-adhesive, pre-gelled and disposable. The array fits easily over the temple and forehead areas where EEG signals can be acquired by specially designed monitors for purposes of monitoring a number of bodily phenomena, including but not limited to, depth of anesthesia, and/or ischemia, and burst suppression. The array is connected to the monitor via a tab connector that is integral to the disposable device. The tab connector is insertible into a reusable connector that is part of a monitoring system.

Abstract: A biological electrode includes an electrode element having electroconductivity with respect to a living body, the biological electrode used by disposing said electrode element at a predetermined position, and the electrode element being made of biodegradable material.

Abstract: The EEG electrode and EEG electrode locator assembly may be used in combination with an EEG electrode locator headgear including a plurality of locator straps connectable to one or more of the EEG electrode locators that form an electrode locator assembly with the EEG electrode, for accurately positioning one or more of the EEG electrodes relative to the user's scalp, and for biasing the plurality of electrodes toward the user's scalp. The EEG electrode is adapted to be received in and cooperate with an EEG electrode locator ring, to form the electrode locator assembly. The EEG electrode includes a dispenser assembly adapted to dispense an electrically conductive gel onto the user's scalp to prepare the user's scalp.

Abstract: There is provided a skin engageable, electrode assembly for making selectable contact with the skin. The electrode facilitates the selective collection of electrical data and/or provides selective electrical stimulation. The electrode includes a conductive element, preferably of fabric construction, a semi-fluid conductive layer surrounding the conductive element, a cover preferably made of a perforated fabric or other porous material cell, and one or more temperature sensitive wires embedded in the cover that constrict when heated to cause the semi-liquid conductive layer to permeate the cover via the pores to engage the skin for electrical communication. When the wires cool, they loosen causing the semi-fluid conductive layer to be reabsorbed within the cover to prevent electrical communication with the skin.

Abstract: There is provided a skin engageable, electrode assembly for making selectable contact with the skin. The electrode facilitates the selective collection of electrical data and/or provides selective electrical stimulation. The electrode includes a conductive element, preferably of fabric construction, a semi-fluid conductive layer surrounding the conductive element, a cover preferably made of a perforated fabric or other porous material cell, and one or more temperature sensitive wires embedded in the cover that constrict when heated to cause the semi-liquid conductive layer to permeate the cover via the pores to engage the skin for electrical communication. When the wires cool, they loosen causing the semi-fluid conductive layer to be reabsorbed within the cover to prevent electrical communication with the skin.

Abstract: Bioadhesive Compositions which comprise a hydrophobic polymer wherein the concentration of the polymer at the surface of the adhesive is greater than its concentration in the bulk of the adhesive are described; and biomedical electrodes, fixation products and wound dressings containing them.

Abstract: A method is disclosed which provides for a reduced corrosion of an electrically conductive metallic layer during storage of an electrode comprising said electrically conductive metallic layer in intimate contact with an electrically conductive gel, said electrode being adapted for establishing electrical contact with the skin, wherein the access to oxygen is reduced or eliminated.

Abstract: An electric therapeutic device having easy operability and improved therapy effects for treating the affected part of a user with electric current flowing from a conductor (3) attached to the affected part, including a hot water or cold water circulator (4) for circulating hot or cold water in the conductor (3).

Abstract: The invention provides an electrode kit for muscle stimulation to be used in conjunction with a splint, the kit including an electrode carrier attachable to an interior surface of the splint and consisting of a relatively thin, flexible, tray-like member; a thin, flexible electrode member fixedly attached to the electrode carrier, and a skin-contacting pad member consisting of a piece of medium-absorptive material fixedly mounted on a rigidifying frame attachable to, and removable from, the electrode carrier.

Abstract: The present disclosure relates to a defibrillation/pacing electrode that comprises an electrode body, a conductor element, and an adhesive layer. When the electrode is in use, electrically conductive gel can be placed between the electrode and the patient's skin to form low impedance contact therebetween. In one embodiment, the electrically conductive gel is contained within a reservoir provided on the body, wherein the electrically conductive gel can be delivered from the reservoir to a patient's skin. In another embodiment, the electrically conductive gel is delivered to the skin through a valve mounted on the top surface of the body. In a further embodiment, the electrically conductive gel is supplied by a plurality of rupturable capsules that are impregnated within the adhesive layer.

Abstract: A sensor for biopotential measurements is designed to detect low voltage electrical signals on a subject's skin surface. A plurality of soft elastomeric bristles are arranged about the surface of the skin. Various bristles contain a wick, made of polyolefin, polyester or nylon, extending along its center axis with one end protruding from the bristle and another end in contact with a fluid reservoir. The wick is saturated with an electrically conductive liquid, such as a salt solution. The solution may contain a surfactant. The rheological properties of the electrically conductive liquid are optimized for predictable flow through the wick onto the skin surface. An electrode is positioned in the vicinity of the wick and the reservoir. Alternatively, a sensor comprises a plurality of hollow, soft elastomeric bristles filled with a hydrogel. An electrically conductive cap provides the electrical contact between the hydrogel and the electrical circuit.

Abstract: Improved electrodes for transmission of electrical current through living tissue for various therapeutic, analgesic, muscle training, and recreational uses. These user manipulate-able electrodes permit the use of low voltage alternating current (AC) instead of direct current (DC). The electrodes are manufactured by overlaying a conductive material with nonconductive semi-porous material which, when wetted, becomes conductive and serves as a skin moistening vehicle. Electrical resistance is controlled by adding layers of semi-porous material as desired. A potentiometer is available to the user for major adjustments to the current flow. These electrodes are supplied power by means of less complex and cheaper Alternating Current power supplies. In addition to the handheld version, there are other configurations intended for various uses.

Abstract: A sensor for biopotential measurements is designed to detect low voltage electrical signals on a subject's skin surface. A plurality of soft elastomeric bristles are arranged about the surface of the skin. Various bristles contain a wick, made of polyolefin, polyester or nylon, extending along its center axis with one end protruding from the bristle and another end in contact with a fluid reservoir. The wick is saturated with an electrically conductive liquid, such as a salt solution. The solution may contain a surfactant. The rheological properties of the electrically conductive liquid are optimized for predictable flow through the wick onto the skin surface. An electrode is positioned in the vicinity of the wick and the reservoir. Alternatively, a sensor comprises a plurality of hollow, soft elastomeric bristles filled with a hydrogel. An electrically conductive cap provides the electrical contact between the hydrogel and the electrical circuit.

Abstract: A hydratable bioelectrode for use in an iontophoretic delivery device comprising a hydrating component and a bioelectrode component. The hydrating component includes a cradle having a chamber containing one or more fluid containing ampule(s) and ampule breaking means associated with the cradle for rapidly breaking the one or more fluid containing ampule(s).

Abstract: A medical electrode assembly includes a conductive electrode, an electrically insulative backing layer on one side of the electrode, an electrically conductive coupling agent in contact with another side of the electrode, an attachment mechanism rigidly connected to a center portion of the electrode, and an electrical conductor connected to the attachment mechanism. The combination of the electrode with the attachment mechanism is constructed with substantial circumferential uniformity such that electrical current provided to the center portion of the electrode through the low-profile attachment mechanism is distributed radially through the electrode in a substantially circumferentially uniform distribution. The electrode is constructed to perform defibrillation or cardioversion. The attachment mechanism is substantially flat and has a low profile. The electrical conductor has a substantially flat, strap-like configuration.

Abstract: The present invention provides a housing structure of a bioelectrode capable of maintaining moisture of the bioelectrode in equilibrium condition quickly without incurring decrease in adhesive strength due to over-dryness and damage. In a housing 10 for housing a bioelectrode which is used by coming into contact with an organism, the housing 10 including the bioelectrode-attaching portion 11 attaching a bioelectrode 1 is made of a water absorption material.

Abstract: A catheter assembly comprising a elongated, flexible support structure having an axis. The assembly also includes an elongated porous electrode assembly carried by the support structure along the axis for contact with tissue. The elongated porous electrode assembly comprises a wall having an exterior peripherally surrounding an interior area, a lumen to convey a medium containing ions into the interior area, and an element coupling the medium within the interior area to a source of electrical energy. At least a portion of the wall comprising a porous material is sized to allow passage of ions contained in the medium to thereby enable ionic transport of electrical energy through the porous material to the exterior of the wall to form a continuous elongated lesion pattern in tissue contacted by the wall. The support structure can have a curvilinear geometry, e.g., a loop shape, and the elongated porous electrode assembly conforms to the curvilinear geometry.