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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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19-04-2012 дата публикации

Sample and Hold Circuitry for Monitoring Voltages in an Implantable Neurostimulator

Номер: US20120092031A1
Принадлежит: Boston Scientific Neuromodulation Corp

Sample and hold circuitry for monitoring electrodes and other voltages in an implantable neurostimulator is disclosed. The sample and hold circuitry in one embodiment contains multiplexers to selected appropriate voltages and to pass them to two storage capacitors during two different measurement phases. The capacitors are in a later stage serially connected to add the two voltages stored on the capacitors, and voltages present at the top and bottom of the serial connection are then input to a differential amplifier to compute their difference. The sample and hold circuitry is particularly useful in calculating the resistance between two electrodes, and is further particularly useful when resistance is measured using a biphasic pulse. The sample and hold circuitry is flexible, and can be used to measure other voltages of interest during biphasic or monophasic pulsing.

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03-05-2012 дата публикации

Protecting an implantable medical device from effects caused by an interfering radiation field

Номер: US20120109261A1
Принадлежит: MEDTRONIC INC

Techniques are described for protecting an implantable medical device (IMD) from effects caused by interfering radiated fields. An IMD incorporating these techniques may include a telemetry conduction path that includes a first end electrically coupled to a telemetry antenna and a second end electrically coupled to a telemetry circuit disposed within a housing of the IMD. The IMD may further include a stub filter electrically coupled to the telemetry conduction path and configured to attenuate an interfering signal induced in the telemetry conduction path. The stub filter may include a dielectric and a conductor disposed within the dielectric. The conductor may include a first end electrically coupled to the telemetry conduction path and a second end configured in an open circuit configuration. The conductor may have an electrical length approximately equal to one-quarter wavelength of the interfering signal when propagating through the stub filter.

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21-06-2012 дата публикации

Direct memory access (dma) controlled stimulation

Номер: US20120158096A1
Автор: Neil S. Sherman
Принадлежит: Spinal Modulation LLC

An implantable stimulation system (e.g., an implantable neurostimulation system (INS)) comprises memory including a first table and a second table. The first table stores blocks of stimulation event data corresponding to stimulation events that are to be performed during a period of time (e.g., a 0.5 sec. or 1 sec. period of time). The second table stores blocks of next stimulation event time data corresponding to the period of time. The implantable stimulation system also includes a direct memory access (DMA) controller including a first DMA channel and a second DMA channel. The first DMA channel selectively transfers one of the blocks stimulation event data from the first table to one or more registers that are used to control stimulation events. The second DMA channel selectively transfers one of the blocks of next stimulation event time data from the second table to a timer that is used to control timing associated with the stimulation events. In this manner, the DMA controller is able to control stimulation.

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21-03-2013 дата публикации

IMPLANTABLE AND RECHARGEABLE NEURAL STIMULATOR

Номер: US20130073000A1
Принадлежит:

One aspect of the present subject matter relates to an implantable medical device. An embodiment of the device comprises a rechargeable power supply adapted to be recharged through an ultrasound signal, a neural stimulator connected to the rechargeable power supply, and a controller connected to the rechargeable power supply. The neural stimulator is adapted to generate a neural stimulation signal for delivery to a neural stimulation target through an electrode. The controller is further connected to the neural stimulator to control the neural stimulator according to a neural stimulation protocol. Other aspects are provided herein. 1. A system for therapeutically stimulating a neural stimulation target of a human , comprising:an implantable medical device, wherein the implantable medical device includes a neural stimulator configured to deliver neural stimulation for use in stimulating the neural stimulation target, the implantable device including an ultrasound transducer configured to convert an ultrasound energy into an electrical energy,wherein the implantable medical device is configured to power the neural stimulator using the electrical energy converted from the ultrasound energy.2. The system of claim 1 , wherein the implantable medical device is remotely powered through the ultrasound energy.3. The system of claim 1 , wherein the ultrasound power signal includes data encoded within the ultrasound power signal claim 1 , wherein the implantable device is further configured to receive and process the data encoded in the ultrasound power signal.4. The system of claim 1 , further comprising an external device configured to send the ultrasound energy.5. The system of claim 1 , further comprising another implantable device configured to send the ultrasound energy.6. The system of claim 1 , wherein the implantable medical device further comprises:a blood pressure sensor configured to sense blood pressure; anda controller configured to control the neural stimulator ...

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21-03-2013 дата публикации

METHOD AND APPARATUS FOR A SMALL POWER SOURCE FOR AN IMPLANTABLE DEVICE

Номер: US20130073004A1
Принадлежит:

One example includes a battery that includes a stack of at least one substantially planar anode and at least one substantially planar cathode, wherein the stack defines a contoured exterior, and a battery housing enclosing the stack, the battery housing defining a battery housing exterior, wherein the contoured exterior of the stack is shaped to conform to a contoured interior of the battery housing that approximately conforms to the battery housing exterior, the battery produced by the process of modeling, using fluid dynamics, an exterior of a biocompatible housing and shaping the battery housing to conform to at least some of the exterior of the biocompatible housing. 1. An apparatus , comprising:an implantable electronics shell;electronics disposed in the implantable electronics shell;an implantable power source shell defining an implantable power source shell interior, the implantable power source shell being hermetically sealed to the implantable electronics shell with a first seal, with the electronics disposed outside the implantable power source shell; an annular anode connected to a first terminal; and', 'a cathode connected to a second terminal and disposed around the anode,', 'wherein the anode and the cathode are arranged in a bobbin configuration,, 'a power source disposed in the implantable power source shell interior, the power source being sealed in the implantable power source shell with a second seal, the power source comprisingwherein an exterior of the apparatus includes an exterior of the implantable electronics shell and an exterior of the implantable power source shell.2. The apparatus of claim 1 , wherein the electronics shell and the power source shell are cylindrical.3. The apparatus of claim 2 , wherein the electronics shell and the power source shell are arranged in a column.4. The apparatus of claim 1 , wherein the implantable power source shell defines an implantable power source shell exterior shaped using modeled fluid dynamics and ...

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18-04-2013 дата публикации

Battery Ventilation for a Medical Device

Номер: US20130096646A1
Принадлежит: MED-EL Elektromedizinische Geraete GmbH

A medical device is presented that includes an external portion adapted for placement external to the skin of a user. The external portion includes a battery pack for interfacing with at least one battery cell. The battery pack includes a housing, the housing defining air inlet and/or outlet holes such that fluid flow is enabled through at least a part of the housing. A micro-ventilation mechanism moves air through at least a part of the housing. 1. A medical device comprising: a housing, the housing defining air inlet and/or outlet holes such that fluid flow is enabled through at least a part of the housing; and', 'a micro-ventilation mechanism for moving air through at least a part of the housing., 'a battery pack for interfacing with at least one battery cell, the battery pack including, 'an external portion adapted for placement external to the skin of a user, the external portion including2. The medical device according to claim 1 , further comprising an implantable portion that receives a signal from the external portion.3. The medical device according to claim 2 , wherein the external portion includes a first coil claim 2 , and wherein the implantable portion includes a second coil claim 2 , the first coil and the second coil for transcutaneous transmission of the signal via electromagnetic coupling.4. The medical device according to claim 3 , wherein the battery pack supplies a power signal to the first coil claim 3 , for transcutaneous transmission to the second coil.5. The medical device according to claim 2 , wherein the implantable portion includes a stimulator module for producing for the auditory system of a user a stimulation representative of an acoustic signal.6. The medical device according to claim 5 , wherein the stimulation is an electrical stimulation and/or a mechanical stimulation.7. The medical device according to claim 2 , wherein the implantable portion includes one of a laryngeal pacemaker claim 2 , a middle-ear implant and a cochlear ...

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09-05-2013 дата публикации

METHOD FOR SAFEGUARDING IMPLANTED MEDICAL DEVICES IN A DIAGNOSTIC DEVICE EMITTING ELECTROMAGNETIC RADIATION

Номер: US20130116750A1
Принадлежит:

A method for safeguarding an implanted medical device from the electromagnetic radiation from a diagnostic device is provided. The method includes detecting the implanted medical device by a bidirectional communication with the diagnostic device, determining a device type of the medical device with the diagnostic device, checking whether the device type of the medical device may be operated without errors under the electromagnetic radiation of the diagnostic device and initiating a protective measure if the device type of the medical device cannot be operated without errors under the electromagnetic radiation. 1. A method for safeguarding an implanted medical device against electromagnetic radiation from a diagnostic device , comprising:detecting the medical device by bidirectional communication with the diagnostic device;determining a device type of the medical device with the diagnostic device;checking whether the device type of the medical device may be operated without errors under the electromagnetic radiation of the diagnostic device; andinitiating a protective measure when the device type of the medical device cannot be operated without errors under the electromagnetic radiation.2. The method as claimed in claim 1 , wherein the protective measure comprises a reconfiguration of the medical device such that the medical device is operated without errors under the electromagnetic radiation of the diagnostic device.3. The method as claimed in claim 2 , further comprising putting the diagnostic device into operation after the reconfiguration of the medical device and subsequently returning the medical device to its original program.4. The method as claimed in claim 1 , wherein the device type of the medical device is able to be determined on the basis of an identifier stored in the medical device.5. The method as claimed in claim 4 , further comprising interrogating the identifier from the medical device and undertaking the determination of the device type of ...

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23-05-2013 дата публикации

ELECTROCHEMICAL CELL WITH ADJACENT CATHODES

Номер: US20130131745A1
Автор: Viavattine Joseph J.
Принадлежит: Medtronic, Inc.

The disclosure includes an electrochemical cell comprising a first cathode and a second cathodes are adjacent one another in a stacked arrangement to form a cathode stack in the electrochemical cell. The first cathode includes a first current collector and a first cathode form of active material covering the first current collector, and the second cathode includes a second current collector and a second cathode form of active material covering the second current collector. The second current collector is in electrical contact with the first current collector. The electrochemical cell further comprises an anode adjacent to the cathode stack, and a separator located between the cathode stack and the anode. 1. An electrochemical cell comprising:a first cathode, wherein the first cathode includes a first current collector and a first cathode form of active material covering the first current collector;a second cathode, wherein the second cathode includes a second current collector and a second cathode form of active material covering the second current collector,wherein the second current collector is in electrical contact with the first current collector,wherein the first and second cathodes are adjacent one another in a stacked arrangement to form a cathode stack in the electrochemical cell;an anode adjacent to the cathode stack; anda separator located between the cathode stack and the anode.2. The electrochemical cell of claim 1 , wherein the anode is a first anode and the separator is a first separator claim 1 , the electrochemical cell further comprising:a second anode adjacent to the cathode stack and opposite the first anode relative to the cathode stack; anda second separator between the cathode stack and the second anode.3. The electrochemical cell of claim 2 , further comprising a third separator between the first and the second cathode.4. The electrochemical cell of claim 2 ,wherein the cathode stack further includes a third cathode such that the third ...

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27-06-2013 дата публикации

Pressure-Sensitive External Charger for an Implantable Medical Device

Номер: US20130165997A1
Автор: Aghassian Daniel

An improved external charger for an implantable medical device is disclosed in which charging is at least partially controlled based on a sensed pressure impingent on its case, which pressure is indicative of the pressure between the external charger and a patient's tissue. The improved external charger includes pressure detection circuitry coupled to one or more pressure sensors for controlling the external device in accordance with the sensed impingent pressure. The sensed pressure can be used to control charging, for example, by suspending charging, by adjusting a maximum set point temperature for the external charger based on the measured pressure, or by issuing an alert via a suitable user interface. By so controlling the external charger on the basis of the measured pressure, the external charger is less likely to create potentially problematic or uncomfortable conditions for the user. 1. An external charger for an implantable medical device , comprising:a coil configured to transmit energy to the implanted medical device during a charging session;pressure detection circuitry configured to sense a pressure on the external charger; andcontrol circuitry coupled to the pressure detection circuitry and configured to suspend the transmission of energy during the charging session when the pressure exceeds a set critical pressure value.2. The charger of claim 1 , wherein the critical pressure value is set by a reference voltage.3. The charger of claim 1 , wherein the critical pressure value is programmed.4. The charger of claim 1 , wherein the critical pressure value is adjustable via a user interface of the external charger.5. The charger of claim 1 , further comprising a case claim 1 , wherein the pressure sensed on the external charger comprises a pressure on the case.6. The charger of claim 1 , wherein the transmission of energy is suspended when the pressure exceeds the critical pressure value for a first amount of time.7. The charger of claim 6 , further ...

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11-07-2013 дата публикации

HIGH POWER ULTRASOUND WIRELESS TRANSCUTANEOUS ENERGY TRANSFER (US-TET) SOURCE

Номер: US20130178915A1
Принадлежит: PIEZO ENERGY TECHNOLOGIES, LLC

A bio-implantable energy capture and storage assembly is provided. The assembly includes an acoustic energy transmitter and an acoustic energy receiver. The acoustic energy receiver also functions as an energy converter for converting acoustic energy to electrical energy. An electrical energy storage device is connected to the energy converter, and is contained within a bio-compatible implant for implantation into tissue. The acoustic energy transmitter is separate from the implant, and comprises a substantially 2-dimensional array of transmitters. 1. A bio-implantable energy capture and storage assembly , comprising:i. an acoustic energy transmitter and an acoustic energy receiver, said acoustic energy receiver also functioning as an energy converter for converting acoustic energy to electrical energy; andii. an electrical energy storage device connected to said energy converter, wherein said acoustic energy receiver-converter is contained within a biocompatible implant for implantation in tissue, wherein said acoustic energy transmitter is separate from said implant.2. The bio-implantable energy capture and storage assembly of claim 1 , wherein the transmitter is comprised of a 2-dimensional array of elements arranged on a support.3. The bio-implantable energy capture and storage assembly of claim 1 , wherein said substantially 2-dimensional array of elements is arranged in a circle.4. The bio-implantable energy capture and storage assembly of claim 1 , wherein said substantially 2-dimensional array of elements is arranged in a substantially regular 2-dimensional geometric shape.5. The bio-implantable energy capture and storage assembly of claim 4 , wherein said substantially regular 2-dimensional geometric shape is selected from the group consisting of a square claim 4 , a pentagon claim 4 , a hexagon and an octagon.6. The bio-implantable energy capture and storage assembly of claim 1 , further including a wireless feedback loop between said implant and ...

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18-07-2013 дата публикации

Automatic On-Off Charger for an Implantable Medical Device

Номер: US20130184785A1
Автор: Aghassian Daniel

An external charger for an implantable medical device is disclosed which can automatically detect an implant and generate a charging field. The technique uses circuitry typically present in an external charger, such as control circuitry, a Load Shift Keying (LSK) demodulator, and a coupling detector. An algorithm in the control circuitry periodically issues charging fields of short duration in a standby mode. If the coupling detector detects the presence of a conductive material, the algorithm issues a listening window during which a charging field is generated. If an LSK reply signal is received at the LSK demodulator, the external charger can charge the implant in a normal fashion. If a movement signature is detected at the LSK demodulator indicative of a predetermined user movement of the external charger, a charging field is issued for a set timing period, to at least partially charge the IPG battery to restore LSK communications. 1. A method for charging a battery in an implantable medical device using an external charger , comprising:(a) automatically determining at the external charger that the implantable medical device is possibly proximate the external charger;(b) upon determining that the external charger is possibly proximate the implantable medical device, automatically generating a second magnetic field from a first coil in the external charger;(c) receiving at the external charger and during the second magnetic field at least one indication from the implantable medical device; and(d) upon receiving the at least one indication, automatically generating a third magnetic field from the first coil in the external charger to wirelessly charge the battery in the implantable medical device.2. The method of claim 1 , wherein step (a) comprises:periodically generating a first magnetic field from the first coil in the external charger; andautomatically determining during one or more of the first magnetic fields that the implantable medical device is possibly ...

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01-08-2013 дата публикации

IMPLANTABLE WIRELESS ACCOUSTIC STIMULATORS WITH HIGH ENERGY CONVERSION EFFICIENCIES

Номер: US20130197609A1
Принадлежит: EBR Systems, Inc.

Receiver-stimulator with folded or rolled up assembly of piezoelectric components, causing the receiver-stimulator to operate with a high degree of isotropy are disclosed. The receiver-stimulator comprises piezoelectric components, rectifier circuitry, and at least two stimulation electrodes. Isotropy allows the receiver-stimulator to be implanted with less concern regarding the orientation relative the transmitted acoustic field from an acoustic energy source. 1. An implantable receiver-stimulator for harvesting acoustic power from an acoustic field and generating electrical power , comprising:a hermetically sealed enclosure with an inner and outer surface;a first plurality of acoustic piezoelectric components which converts the acoustic field to electrical power, each piezoelectric component defined by a thickness and a base with a width and configured with the base mounted to the inner surface;a plurality of individual rectifiers, where each rectifier is electrically connected to a corresponding piezoelectric component of the first plurality of piezoelectric components such that the electrical power from the piezoelectric components is converted by the rectifiers arranged in a circuit assembly to a biologically stimulating electrical output; and at least two stimulation electrodes which receive the stimulating electrical output and deliver said output to tissue at sufficient electrical energy levels to stimulate the tissue;wherein the acoustic piezoelectric components are distributed about the inner surface along three axes such that acoustic energy is harvested efficiently from any direction of the propagating acoustic energy field.2. The device of claim 1 , wherein at least part of the inner surface is configured as a circuit claim 1 , optionally wherein the acoustic piezoelectric components and the rectifier circuitry are disposed on the circuit.3. The device of claim 2 , wherein the acoustic piezoelectric components are composed of a piezoelectric material ...

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15-08-2013 дата публикации

Alignment Indication for Transcutaneous Energy Transfer

Номер: US20130211479A1
Принадлежит: Medtronic, Inc.

System for transcutaneous energy transfer. An implantable medical device, adapted to be implanted in a patient, has componentry for providing a therapeutic output. The implantable medical device has an internal power source and a secondary coil operatively coupled to the internal power source. An external power source, having a primary coil, provides energy to the implantable medical device when the primary coil of the external power source is placed in proximity of the secondary coil of the implantable medical device and thereby generates a current in the internal power source. An alignment indicator reports the alignment as a function of the current generated in the internal power source with a predetermined value associated with an expected alignment between the primary coil and secondary coil. 1. A system for transcutaneous energy transfer , comprising:an implantable medical device having componentry for providing a therapeutic output, said implantable medical device having an internal battery and a secondary coil operatively coupled to said internal battery, said implantable medical device adapted to be implanted in a patient; andan external power source having a primary coil, said external power source providing energy to said implantable medical device when said primary coil of said external power source is placed in proximity of said secondary coil of said implantable medical device and thereby generating a current, having a value, passing through said internal battery;wherein said external power source automatically varies its power output based on a value associated with said current passing through said internal battery.2. The system as in wherein said external power source automatically varies its power output based on a signal proportional to said current passing through said internal battery.3. The system as in wherein said external power source automatically varies its power output based on a current proportional to said current passing through said ...

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19-09-2013 дата публикации

External Controller/Charger System for an Implantable Medical Device Capable of Automatically Providing Data Telemetry Through a Charging Coil During a Charging Session

Номер: US20130245721A1
Автор: Aghassian Daniel

An external controller/charger system for an implantable medical device is disclosed, in which the external controller/charger system provides automatic switching between telemetry and charging without any manual intervention by the patient. The external controller/charger system includes an external controller which houses a telemetry coil and an external charging coil coupled to the external controller. Normally, a charging session is carried out using the external charging coil, and a telemetry session is carried out using the telemetry coil. However, when a patient requests to carry out telemetry during a charging session, the external charging coil is used instead of the internal telemetry coil. 1. A method for communicating with an implantable medical device using an external system , comprising:receiving a data telemetry request at the external system, wherein the data telemetry request involves data to be transmitted to the implantable medical device; and if the external system is not engaged in a charging session to provide power to the implantable medical device, transmitting the data from a telemetry coil in the external system;', 'if the external system is engaged in a charging session to provide power to the implantable medical device though a charging coil in the external system, transmitting the data from the charging coil in the external system., 'in response to the data telemetry request2. The method of claim 1 , wherein the data telemetry request is generated automatically at the external system.3. The method of claim 1 , wherein the data telemetry request results from a patient's interaction with the external system.4. The method of claim 1 , wherein data is transmitted from the telemetry coil and the charging coil at the same frequency.5. The method of claim 1 , wherein data is transmitted from the telemetry coil and the charging coil using the same communication protocol.6. The method of claim 1 , wherein data is transmitted from the telemetry ...

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26-09-2013 дата публикации

CIRCUIT, SYSTEM AND METHOD FOR FAR-FIELD RADIATIVE POWERING OF AN IMPLANTABLE MEDICAL DEVICE

Номер: US20130253612A1
Автор: Chow Eric Y.
Принадлежит: CYBERONICS, INC.

An isolated circuit including a RF input configured to receive a far field radiative powering signal and a rectified voltage output configured to provide a rectified voltage based on the received far field radiative powering signal. The isolated circuit also includes a first power assembly comprising a first impedance coupled to the RF input where the first impedance is provided, at least in part, by activating a first switch in response to the rectified voltage satisfying a first voltage threshold. The isolated circuit also includes a second power assembly comprising a second impedance coupled to the RF input where the second impedance is provided, at least in part, by activating the first switch and a second switch in response to the rectified voltage satisfying the first voltage threshold and a second voltage threshold, respectively. 1. An isolated circuit comprising:a RF input configured to receive a far field radiative powering signal;a rectified voltage output configured to provide a rectified voltage based on the received far field radiative powering signal;a first power assembly comprising a first impedance coupled to the RF input, the first impedance provided, at least in part, by activating a first switch in response to the rectified voltage satisfying a first voltage threshold; anda second power assembly comprising a second impedance coupled to the RF input, the second impedance provided, at least in part, by activating the first switch and a second switch in response to the rectified voltage satisfying the first voltage threshold and a second voltage threshold, respectively.2. The isolated circuit of claim 1 , further comprising:a first threshold detector coupled to the second switch, the first threshold detector configured to receive the rectified voltage and to activate the second switch when the rectified voltage increases to the second voltage threshold.3. The isolated circuit of claim 2 , wherein the first switch is a first transistor and the second ...

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03-10-2013 дата публикации

POWERING MULTIPLE IMPLANTABLE MEDICAL THERAPY DELIVERY DEVICES USING FAR FIELD RADIATIVE POWERING AT MULTIPLE FREQUENCIES

Номер: US20130261703A1
Принадлежит: CYBERONICS, INC.

A system includes a first implantable medical device configured to receive a first far field radiative signal at a first frequency from an external transmitter to charge a first charge storage device. The first implantable medical device includes a first therapy delivery unit powered by the first charge storage device. The first therapy delivery unit delivers a first therapy to a first target tissue of a patient. The system also includes a second implantable medical device configured to receive a second far field radiative signal at a second frequency from the external transmitter to charge a second charge storage device. The second implantable medical device includes a second therapy delivery unit powered by the second charge storage device. The second therapy delivery unit delivers a second therapy to a second target tissue of the patient. 1. A system comprising:a first implantable medical device configured to receive a first far field radiative signal at a first frequency from an external transmitter and to charge a first charge storage device using the first far field radiative signal, the first implantable medical device further comprising a first therapy delivery unit powered by the first charge storage device and configured to deliver a first therapy to a first target tissue of a patient, wherein the first therapy includes delivery of a first electrical stimulation signal to the first target tissue; anda second implantable medical device configured to receive a second far field radiative signal at a second frequency from the external transmitter and to charge a second charge storage device using the second far field radiative signal, the second implantable medical device further comprising a second therapy delivery unit powered by the second charge storage device and configured to deliver a second therapy to a second target tissue of the patient, wherein the second therapy includes delivery of a second electrical stimulation signal to the second target tissue ...

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17-10-2013 дата публикации

OPERATION AND ESTIMATION OF OUTPUT VOLTAGE OF WIRELESS STIMULATORS

Номер: US20130274828A1
Автор: WILLIS N. PARKER
Принадлежит: EBR Systems, Inc.

A controller-transmitter transmits acoustic energy through the body to an implanted acoustic receiver-stimulator. The receiver-stimulator converts the acoustic energy into electrical energy and delivers the electrical energy to tissue using an electrode assembly. The receiver-stimulator limits the output voltage delivered to the tissue to a predetermined maximum output voltage. In the presence of interfering acoustic energy sources output voltages are thereby limited prior to being delivered to the tissue. Furthermore, the controller-transmitter estimates the output voltage that is delivered to the tissue by the implanted receiver-stimulator. The controller-transmitter measures a query spike voltage resulting from the electrical energy delivered to the tissue by the receiver-stimulator, and computes a ratio of the predetermined maximum output voltage and a maximum query spike voltage. The maximum query spike voltage is computed by detecting a query spike voltage plateau. Based on this ratio, the controller-transmitter uses a measured query spike voltage to estimate the output voltage delivered by the receiver-stimulator to tissue. 1. An acoustic controller-transmitter device for transmitting acoustic energy into a body , comprising:an output transducer assembly configured to transmit acoustic energy into the body, wherein the acoustic energy is received by an implantable acoustic receiver-stimulator configured to convert the acoustic energy into electrical energy and deliver the electrical energy to tissue;a control circuitry configured to estimate an output voltage delivered to the tissue by the receiver-stimulator; anda sensing electrode assembly, wherein the sensing electrode assembly is in contact with the body and is configured to detect and measure a query spike voltage as a result of the electrical energy delivered to the tissue by the receiver-stimulator.2. The device of claim 1 , wherein the controller-transmitter is configured to determine a maximum query ...

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21-11-2013 дата публикации

Methods and devices for modulating excitable tissue of the exiting spinal nerves

Номер: US20130310901A1
Принадлежит: Neural Diabetes LLC

A method for modulating nerve tissue in a body of a patient includes implanting a wireless stimulation device in proximity to a dorsal root ganglion or an exiting nerve root such that an electrode, circuitry and a receiving antenna are positioned completely within the body of the patient. An input signal containing electrical energy and waveform parameters is transmitted to the receiving antenna(s) from a control device located outside of the patient's body via radiative coupling. The circuitry within the stimulation device generates one or more electrical impulses and applies the electrical impulses to the dorsal root ganglion or the exiting nerve roots through the electrode.

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12-12-2013 дата публикации

Power Architecture for an Implantable Medical Device Having a Non-Rechargeable Battery

Номер: US20130331910A1

An improved architecture for an implantable medical device using a primary battery is disclosed which reduces the need for boosting the voltage of the primary battery, and hence reduces the power draw in the implant. The architecture includes a boost converter for boosting the voltage of the primary battery and for supplying that boosted voltage to certain of the circuit blocks, which is particularly useful if the battery voltage is necessarily lower than the minimal input power supply voltage necessary for the circuit blocks to operate. However, circuitry capable of operation even at low battery voltages—including the telemetry tank circuitry and the compliance voltage generator—receives the battery voltage directly without boosting, thus saving power. 1. Circuitry for an implantable medical device , comprising:an electrode configured to pass a therapeutic current through a patient's tissue;a non-rechargeable battery outputting a battery voltage;boosting circuitry configured to boost the battery voltage to a boosted voltage;first circuitry powered by boosted voltage; and a DC-DC converter configured to produce a compliance voltage for powering a digital-to-analog converter configured to produce the therapeutic current; and', 'tank circuitry coupled to a telemetry coil configured to communicate data wirelessly with an external device., 'second circuitry powered by and directly connected to the battery voltage, wherein the second circuitry comprises2. The circuitry of claim 1 , wherein the first circuitry comprises one or more regulators.3. The circuitry of claim 2 , wherein each of the one or more regulators supplies a power supply voltage to power at least one circuit element of the implantable medical device.4. The circuitry of claim 3 , wherein one of the circuit elements is an analog circuit.5. The circuitry of claim 3 , wherein one of the circuit elements is a digital circuit.6. The circuitry of claim 3 , wherein one of the circuit elements is a memory.7. The ...

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09-01-2014 дата публикации

External Charger for a Medical Implantable Device Using Field Inducing Coils to Improve Coupling

Номер: US20140012352A1
Автор: Aghassian Daniel

By incorporating magnetic field-inducing position determination coils (PDCs) in an external charger, it is possible to determine the position of an implantable device by actively inducing magnetic fields using the PDCs and sensing the reflected magnetic field from the implant. In one embodiment, the PDCs are driven by an AC power source with a frequency equal to the charging coil. In another embodiment, the PDCs are driven by an AC power source at a frequency different from that of the charging coil. By comparing the relative reflected magnetic field strengths at each of the PDCs, the position of the implant relative to the external charger can be determined. Audio and/or visual feedback can then be communicated to the patient to allow the patient to improve the alignment of the charger. 1. An external charger for providing power to an implantable medical device , comprising:one or more current or voltage sources configured to provide a plurality of currents that produce a plurality of magnetic fields at different locations in the external charger; andan alignment sensing circuit configured to determine an alignment of the external charger relative to the implantable medical device, wherein the determination is based on electrical measurements for each of the plurality of currents taken from the one or more current or voltage sources.2. The external charger of claim 1 , further comprising a position indication circuit configured to receive the determination and to indicate a misalignment of the external charger relative to the implantable medical device.3. The external charger of claim 2 , wherein the position indication circuit is further configured to indicate how to improve the alignment of the external charger relative to the implantable medical device.4. The external charger of claim 2 , wherein the position indication circuit is configured to activate visual indicators on the external charger.5. The external charger of claim 4 , wherein the visual indicators ...

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23-01-2014 дата публикации

Self-Affixing External Charging System for an Implantable Medical Device

Номер: US20140025140A1

An external charging system for charging or powering an implantable medical device is disclosed which is self-affixing to the patient without the need for a holding device. The charging system can comprise two modules attached to opposite ends of a flexible member. The flexible member is bendable, and when bent will firmly hold its position on the patient. The two modules can comprise a coil module containing a charging coil, and an electronics module including a user interface and the necessary electronics for activating the charging coil to produce a magnetic charging field. Wires can couple the charging coil in the coil module to the electronics in the electronics modules. The entire assembly can be encased in a water proof sleeve having a high-friction surface, which protects the charging system and helps the charging system to adhere to the patient. 1. A charging system for implantable medical devices , comprising:a flexible support;a first module coupled to a first end of the flexible support, wherein the first module comprises a coil; anda second module coupled to a second end of the flexible support, where the second module comprises circuitry configured to activate the coil to produce a charging field to charge or power an implantable medical device,wherein the flexible support is bendable to a position and holds the position after being bent.2. The system of claim 1 , wherein the flexible support comprises a metal tube.3. The system of claim 2 , wherein the metal tube comprises a gooseneck tube.4. The system of claim 1 , wherein the flexible support is non-conductive.5. The system of claim 1 , further comprising wires to couple the coil to the circuitry.6. The system of claim 5 , wherein the wires pass through the flexible support.7. The system of claim 5 , wherein the wires pass along side the flexible support.8. The system of claim 1 , further comprising a sleeve for enclosing the flexible support and the first and second modules.9. The system of claim 1 ...

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30-01-2014 дата публикации

ELECTRICAL CONTACTS ON A MEDICAL DEVICE PATCH

Номер: US20140031890A1
Автор: Mashiach Adi, Ruytjens Tim
Принадлежит:

A device for conveying power from a location external to a subject to a location within the subject may include a flexible carrier and an adhesive on a first side of the carrier. A coil of electrically conductive material may be associated with the flexible carrier. A mechanical connector may be associated with the carrier opposite the adhesive, wherein the mechanical connector is configured to retain a housing and permit the housing to rotate relative to the flexible carrier. At least one electrical portion may be associated with the carrier in a manner permitting electrical connection to be maintained between the flexible carrier and the housing as the housing is rotated. 1. A device for treating sleep apnea by conveying power from a location external to a subject to a location within the subject , the device comprising:a flexible carrier configured for location between a neck and a chin of the subject;an adhesive on a first side of the carrier;a coil of electrically conductive material associated with the flexible carrier, the coil configured to facilitate power transfer to an implant proximate a genioglossus muscle of a subject;a mechanical connector associated with the carrier opposite the adhesive, wherein the mechanical connector is configured to retain a housing and permit the housing to rotate relative to the flexible carrier, andat least one electrical portion associated with the carrier in a manner permitting electrical connection to be maintained between the flexible carrier and the housing as the housing is rotated.2. The device of claim 1 , wherein the mechanical connector is configured to permit more than about 360-degree rotation of the housing relative to the flexible carrier.3. The device of claim 1 , wherein the mechanical connector is configured to permit rotation of less than about 360-degree rotation of the housing relative to the flexible carrier.4. The device of claim 1 , wherein the at least one electrical portion includes conductive ...

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13-02-2014 дата публикации

External Charger Usable with an Implantable Medical Device Having a Programmable or Time-Varying Temperature Set Point

Номер: US20140046403A1
Автор: Aghassian Daniel

An improved external charger for charging the battery within or providing power to an implantable medical device is disclosed. The improved external charger includes circuitry for detecting the temperature of the external charger and for controlling charging to prevent exceeding a maximum temperature. The external charger in some embodiments includes a user interface for allowing a patient to set the external charger's maximum temperature. The user interface can be used to select either constant maximum temperatures, or can allow the user to choose from a number of stored charging programs, which programs can control the maximum temperature to vary over time. Alternatively, a charging program in the external charger can vary the maximum temperature set point automatically. By controlling the maximum temperature of the external charger during charging in these manners, the time needed to charge can be minimized while still ensuring a temperature that is comfortable for that patient. 1. An external charger for producing energy to power or charge an implantable medical device during a charging session , comprising:temperature sensing circuitry configured to determine a temperature of the external charger during the charging session;a user interface configured to provide a plurality of options selectable by a user, wherein each selection provides at least one temperature set point; andcontrol circuitry configured to control the energy produced to power or charge the implantable medical device in accordance with the provided at least one temperature set point and the determined temperature.2. The external charger of claim 1 , further comprising a coil claim 1 , wherein the coil is configured to produce the energy.3. The external charger of claim 2 , wherein the energy comprises a magnetic field.4. The external charger of claim 2 , wherein the control circuitry is configured to control the energy produced by adjusting a current through the coil.5. The external charger of ...

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13-02-2014 дата публикации

IMPLANTABLE MEDICAL DEVICE CHARGING

Номер: US20140046404A1
Автор: JOSHI HIMANSHU
Принадлежит: CYBERONICS, INC.

A particular method of providing power to an implantable medical device includes providing a first signal to a primary coil that is inductively coupled to a secondary coil of an implantable medical device. The method also include determining a first alignment difference between a voltage corresponding to the first signal and at least one of a current corresponding to the first signal and a component voltage at a component of a primary coil circuit. The method further includes determining a frequency sweep range based on the first alignment difference. The method also includes performing a frequency sweep over the frequency sweep range. 1. An implantable medical device comprising:a secondary coil coupled to a circuit and operable to inductively couple to a primary coil to receive energy from the primary coil;a battery charging system coupled to the secondary coil and operable to receive a current from the secondary coil and to apply a charging voltage to a battery responsive to the current; anda measurement system coupled to the circuit and operable to measure an electrical property of the circuit and to output information indicative of a value of the electrical property;wherein the secondary coil receives a charging signal from the primary coil, and wherein a frequency of the charging signal is determined based on the information indicative of the value of the electrical property and based on a detected alignment relationship between a voltage corresponding to a signal applied to the primary coil and at least one of a current corresponding to the signal and a component voltage at a component associated with the primary coil.2. The implantable medical device of claim 1 , wherein the measurement system measures the charging voltage.3. The implantable medical device of claim 1 , further comprising a conductive housing enclosing at least the secondary coil and the battery.4. The implantable medical device of claim 1 , further comprising a controller operable to generate ...

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13-02-2014 дата публикации

Pressure-Sensitive External Charger for an Implantable Medical Device

Номер: US20140046405A1
Автор: Aghassian Daniel

An improved external charger for an implantable medical device is disclosed in which charging is at least partially controlled based on a sensed pressure impingent on its case, which pressure is indicative of the pressure between the external charger and a patient's tissue. The improved external charger includes pressure detection circuitry coupled to one or more pressure sensors for controlling the external device in accordance with the sensed impingent pressure. The sensed pressure can be used to control charging, for example, by suspending charging, by adjusting a maximum set point temperature for the external charger based on the measured pressure, or by issuing an alert via a suitable user interface. By so controlling the external charger on the basis of the measured pressure, the external charger is less likely to create potentially problematic or uncomfortable conditions for the user. 1. An external charger for an implantable medical device , comprising:pressure detection circuitry configured to sense a pressure on the external charger;temperature detection circuitry configured to sense a temperature; andcontrol circuitry configured to transmit energy to the implantable medical device, wherein the control circuitry is further configured to maintain the sensed temperature in accordance with a temperature set point,wherein the sensed pressure is used to set the temperature set point.2. The charger of claim 1 , wherein the pressure detection circuitry compares the sensed pressure to a critical pressure value.3. The charger of claim 2 , wherein the critical pressure value is programmable.4. The charger of claim 2 , wherein the critical pressure value is set by a reference voltage in the pressure detection circuitry.5. The charger of claim 2 , wherein if the sensed pressure is below the critical pressure value claim 2 , the temperature set point is set to a first temperature set point claim 2 , and wherein if the sensed pressure exceeds the critical pressure value ...

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13-02-2014 дата публикации

IMPLANTABLE WIRELESS ACCOUSTIC STIMULATORS WITH HIGH ENERGY CONVERSION EFFICIENCIES

Номер: US20140046420A1
Принадлежит: EBR Systems, Inc.

Receiver-stimulator with folded or rolled up assembly of piezoelectric components, causing the receiver-stimulator to operate with a high degree of isotropy are disclosed. The receiver-stimulator comprises piezoelectric components, rectifier circuitry, and at least two stimulation electrodes. Isotropy allows the receiver-stimulator to be implanted with less concern regarding the orientation relative the transmitted acoustic field from an acoustic energy source. 1. A method for manufacturing an implantable receiver-stimulator for converting an acoustic field to electrical power comprising the steps of:forming an insulating layer on an electrically conductive sheet;forming a circuit pattern on the insulating layer; electrically connecting a first plurality of acoustic piezoelectric components to the circuit pattern on the sheet;electrically connecting a plurality of individual rectifier circuits to the circuit pattern on the sheet, the rectifier circuits configured to convert electrical power output from the piezoelectric components to a biologically stimulating electrical output;electrically connecting the biologically stimulating electrical output to a pair of stimulation electrodes; and folding the sheet into an octagonal or otherwise substantially cylindrical can structure, thereby arranging the acoustic piezoelectric components such that acoustic energy is harvested efficiently from any direction of the propagating acoustic field.2. The method of claim 1 , wherein the acoustic piezoelectric components are composed of a piezoelectric material claim 1 , optionally wherein the piezoelectric material is one of a poly crystalline ceramic piezoelectric material or a single crystal piezoelectric material.3. The method of claim 2 , wherein the piezoelectric components are in the shape of a cuboid claim 2 , wherein one of the faces of the cuboid is mounted to the circuit pattern on the sheet.4. The method of claim 1 , wherein the rectifier circuitry comprises one or more ...

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20-02-2014 дата публикации

Transcutaneous Power Conveyance Device

Номер: US20140052219A1
Принадлежит:

Some embodiments of the present disclosure may include a device for conveying power from a location external to a subject to a location within the subject The device may include a flexible carrier, an adhesive on a first side of the carrier, a coil of electrically conductive material associated with the flexible carrier, and a mechanical connector extending from a second side of the carrier opposite the adhesive. The mechanical connector may be configured to be received by and retained by a receiver associated with a housing configured for mounting on the carrier. 1. A device for treating sleep apnea by conveying power from a location external to a subject to a location within the subject , the device comprising:a flexible carrier configured for location between a chin and a neck of the subject;an adhesive on a first side of the carrier;a coil of electrically conductive material associated with the flexible carrier, the coil being configured for use in transmitting power to an implant associated with a genioglossus muscle of the subject; anda mechanical connector extending from a second side of the carrier opposite the adhesive, wherein the mechanical connector is configured to be received by and retained by a receiver associated with a housing configured for mounting on the carrier.2. The device of claim 1 , further comprising an electrical connector associated with the carrier establishing an electrical connection between housing and coil.3. The device of claim 1 , wherein the housing is retained in a manner in which at least a portion of a sidewall and a top of the housing is exposed when mounted to the carrier4. The device of claim 1 , wherein the mechanical connector is a rodlike element.5. The device of claim 1 , receiver includes an opening into which the mechanical connector extends.6. The device of claim 1 , wherein the mechanical connector includes a detent portion.7. The device of claim 1 , wherein the mechanical connector includes a bayonet connection ...

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27-02-2014 дата публикации

IMPLANTABLE MEDICAL DEVICE WITH CONTROL OF NEURAL STIMULATION BASED ON BATTERY STATUS

Номер: US20140058467A1
Принадлежит: Cardiac Pacemakers, Inc.

An implantable medical device is powered by a battery to deliver one or more therapies including at least one non-life-sustaining therapy such as neural stimulation for enhancing quality of life of a patient. When the battery approaches its end of life, the implantable medical device reduces power consumption of the neural stimulation (e.g., intensity of the neural stimulation) for extending the remaining battery life while maintaining a certain amount of therapeutic benefits for the patient. In one embodiment, the intensity of the neural stimulation is reduced in a tiered manner. In one embodiment in which the implantable medical device also delivers at least one life-sustaining cardiac stimulation therapy, the neural stimulation is disabled or adjusted to reduce its power consumption (e.g., intensity) while the intensity of the cardiac stimulation therapy is maintained when the battery is near its end of life. 1. An implantable medical device for use in a body , comprising:a battery;a battery monitoring circuit coupled to the battery, the battery monitoring circuit configured to monitor an energy level of the battery and produce a battery status parameter indicative of the energy level;a neural stimulation circuit configured to deliver neural stimulation for modulating neural activities; a power controller configured to set a current power mode of the implantable medical device to a first reduced-power operation mode of a plurality of power modes in response to the battery status parameter indicating that the energy level has fallen below a first energy level threshold of a plurality of energy level thresholds; and', 'a neural stimulation controller configured to control the delivery of the neural stimulation using neural stimulation parameters and to adjust one or more parameters of the neural stimulation parameters within the first reduced-power operation mode such that an intensity of the neural stimulation is reduced within the first reduced-power operation ...

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27-02-2014 дата публикации

Minimizing Interference Between Charging and Telemetry Coils in an Implantable Medical Device

Номер: US20140058479A1

An improved implantable pulse generator (IPG) containing improved telemetry circuitry is disclosed. The IPG includes charging and telemetry coils within the IPG case, which increases their mutual inductance and potential to interfere with each other; particularly problematic is interference to the telemetry coil caused by the charging coil. To combat this, improved telemetry circuitry includes decoupling circuitry for decoupling the charging coil during periods of telemetry between the IPG and an external controller. Such decoupling circuitry can comprise use of pre-existing LSK circuitry during telemetry, or new discrete circuitry dedicated to decoupling. The decoupling circuitry is designed to prevent or at least reduce induced current flowing through the charging coil during data telemetry. The decoupling circuitry can be controlled by the microcontroller in the IPG, or can automatically decouple the charging coil at appropriate times to mitigate an induced current without instruction from the microcontroller. 1. An implantable medical device , comprising:a case;a charging coil within the case configured to wirelessly receive power, wherein the charging coil is wound in a first plane around a first area; anda telemetry coil within the case configured to wirelessly receive data, or wirelessly transmit data, or wirelessly receive and transmit data, wherein the telemetry coil is wound in a second plane around a second area,wherein the first and second planes are parallel, and wherein the second area of the telemetry coil at least overlaps the first area of the charging coil.2. The device of claim 1 , further comprising a circuit board claim 1 , wherein the charging coil is proximate to one side of the circuit board claim 1 , and the telemetry coil is proximate to the other side of the circuit board.3. The device of claim 1 , wherein the second area of the telemetry coil is entirely within the first area of the charging coil.4. The device of claim 1 , wherein the ...

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13-03-2014 дата публикации

METHOD OF MINIMIZING INTERRUPTIONS TO IMPLANTABLE MEDICAL DEVICE RECHARGING

Номер: US20140074185A1
Принадлежит: GREATBATCH, LTD.

A system and method of controlling the charging of the battery of a medical device using a remote inductive charger, with the method utilizing both a relatively fast closed-loop charging control based on a proxy for a target power transmission value in conjunction, and a slower closed-loop control based on an actual measured transmission value to control a charging power level for charging the medical device. 1. A method for charging a rechargeable battery in a medical device using an external charger , said method comprising the steps of:wirelessly transmitting a power signal from the external charger to the medical device, said power signal including power for charging the rechargeable battery;in the medical device, measuring a value of a first variable relating to the power signal received by the medical device from the external charger;in the external charger, measuring a value of a second variable relating to the power signal transmitted by the external charger to the medical device; andadjusting the power signal transmitted from the external charger to the medical device at least partly based on values of both said first variable and said second variable.2. The method of claim 1 , wherein the value of said first variable is wirelessly transmitted to said external charger by said medical device.3. The method of claim 2 , wherein said step of adjusting includes the steps of: said external charger calculating an updated power signal for transmitting to said medical device using said first variable and said second variable; and said external charger transmitting said updated power signal to said medical device.4. The method of claim 1 , wherein said step of adjusting includes the steps of: said external charger calculating an updated power signal for transmitting to said medical device using said first variable and said second variable; and said external charger transmitting said updated power signal to said medical device.5. The method of claim 1 , wherein said ...

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13-03-2014 дата публикации

NEURAL STIMULATION DEVICES AND SYSTEMS FOR TREATMENT OF CHRONIC INFLAMMATION

Номер: US20140074186A1
Принадлежит:

A system for treating chronic inflammation may include an implantable microstimulator, a wearable charger, and optionally an external controller. The implantable microstimulator may be implemented as a leadless neurostimulator implantable in communication with a cervical region of a vagus nerve. The microstimulator can address several types of stimulation including regular dose delivery. The wearable charger may be worn around the subject's neck to rapidly (<10 minutes per week) charge an implanted microstimulator. The external controller may be configured as a prescription pad that controls the dosing and activity of the microstimulator. 1. A system for treating chronic inflammation in a patient , the system comprising:an implantable microstimulator configured for implantation around a cervical portion of a vagus nerve to modulate inflammation by applying a low duty-cycle stimulation;a charger configured to be worn around the patient's neck and to charge the implantable microstimulator; andan external controller configured to set a dose amplitude and dose interval for the microstimulator.2. The system of claim 1 , further comprising a POD for securing the microstimulator within the patient.3. The system of claim 1 , wherein the system is configured to charge the implantable microstimulator for less than about 10 minutes per week.4. The system of claim 1 , wherein the charger comprises a belt-like loop that fastens around the patient's neck so that power may be transmitted by the loop to the implant.5. The system of claim 1 , wherein the external controller comprises an electronic prescription pad.6. The system of claim 1 , wherein the implantable microstimulator comprises a hermetically sealed capsule body having at least two conductive regions claim 1 , the capsule body surrounding a resonator claim 1 , battery and an electronic assembly sealed within the capsule body claim 1 , wherein the electronic assembly is connected to the capsule body by a suspension ...

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07-01-2016 дата публикации

NEUROSTIMULATOR SYSTEM, APPARATUS AND METHOD FOR CONDUCTING A CLINICAL TRIAL

Номер: US20160001079A1
Принадлежит:

The invention relates to a method () for conducting a clinical trial with a medical device. The method () includes the step () of providing a medical device to a trial subject, the medical device being capable of providing an adjustable level of therapy. The method also comprises the step () of using the medical device to apply therapy to the trial subject. The method further comprises the step () of controlling the application of therapy applied to the trial subject according to a clinical trial design. 149-. (canceled)50. A method for conducting a clinical trial with a medical device , the method comprising the steps of: a full therapy mode in which stimulation is applied at a level sufficient to both apply therapy to the trial subject and to allow the trial subject to perceive that the therapy is being applied,', 'a placebo therapy mode in which stimulation at a level sufficient to apply therapy is not applied, and', 'a sub-perception therapy mode in which stimulation is applied at a level sufficient to apply therapy to the trial subject, but insufficient to allow the trial subject to perceive that therapy is being applied, the sub-perception therapy mode blinding the trial subject as to whether full therapy or placebo therapy is being applied., 'implanting a neurostimulator in a trial subject, the neurostimulator configured to apply therapy according to a clinical trial design, the clinical trial design comprising a therapy mode from a group of available therapy modes, wherein the group of available therapy modes comprises51. The method recited in claim 50 , further comprising the step of providing a handheld controller to the subject claim 50 , wherein the handheld controller is configured to inductively power the implanted medical device and to communicate with the implanted medical device.52. The method recited in claim 50 , wherein:the full therapy mode comprises stimulation parameters for applying to the trial subject a predetermined level of stimulation ...

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07-01-2016 дата публикации

METHOD FOR MONITORING POWER SUPPLY TO IMPLANTABLE MEDICAL DEVICE

Номер: US20160001085A1
Принадлежит:

An external control device includes a human-computer interface, a first controller and a power transmitting unit. An implantable medical device includes a power receiving unit, a second controller and a second detector. A method for monitoring power supply comprises: producing a first magnetic field by the power transmitting unit; sensing the first magnetic field to produce a second magnetic field and converting it into a direct current by the power receiving unit; detecting a power value of the direct current by the second detector to output a detection signal to the second controller; outputting a status information to the external control device by the second controller according to the detection signal; and receiving the status information by the first controller. The first controller transmits an adjustment signal to the power transmitting unit if informed of the status information that the power value is not within a designate power range. 1. A method for monitoring power supply to an implantable medical device interacting with an external control device , wherein the external control device includes a human-computer interface , a first controller and a power transmitting unit , the implantable medical device includes a power receiving unit , a second controller and a second detector , the method comprising:producing a first magnetic field by the power transmitting unit;sensing the first magnetic field to produce a second magnetic field and converting the second magnetic field into a direct current by the power receiving unit;detecting a power value of the direct current by the second detector to output a first detection signal to the second controller;outputting a first status information to the external control device by the second controller according to the first detection signal; andreceiving the first status information by the first controller,wherein the first controller transmits an adjustment signal to the power transmitting unit if informed of the ...

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04-01-2018 дата публикации

FLEXIBLE SHEET FOR NEUROMUSCULAR STIMULATION

Номер: US20180001086A1
Принадлежит:

A flexible sheet for neurostimulation is described having a flexible non-conductive substrate matrix in which electrodes are embedded along a lower surface. Electrically conductive wires extend from the electrodes through the flexible substrate to another exterior surface of the substrate. Methods of making the flexible sheet and making a device using the flexible sheet are also disclosed. 1. A flexible sheet , comprising:a non-conductive, flexible substrate;a plurality of electrodes embedded within the flexible substrate; andelectrically-conductive wires running through the flexible substrate from a common exterior surface of the flexible substrate to each electrode.2. (canceled)3. (canceled)4. (canceled)5. The flexible sheet of claim 2 , wherein the flexible substrate comprises a top surface claim 2 , a bottom surface opposite the top surface claim 2 , and a plurality of side surfaces; wherein the plurality of electrodes is located on the bottom surface; and wherein the wires extend to one of the side surfaces.6. (canceled)7. (canceled)8. (canceled)9. The flexible sheet of claim 1 , further comprising a sensor embedded within the substrate.10. (canceled)11. (canceled)12. (canceled)13. The flexible sheet of claim 1 , further comprising a mechanical fastener embedded in the substrate claim 1 , for holding the flexible sheet in the form of a sleeve.14. (canceled)15. The flexible sheet of claim 1 , further comprising insulating ceramic dispersed throughout the flexible substrate.16. A system for muscular neurostimulation claim 1 , comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'an inner sleeve formed from the flexible sheet of ; and'}a compression sleeve surrounding the inner sleeve.17. A flexible sheet claim 1 , comprising:a fabric substrate;a plurality of conductive components on a bottom surface of the fabric substrate; anda plurality of non-conductive components on the bottom surface of the fabric substrate18. (canceled)19. The flexible sheet of ...

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04-01-2018 дата публикации

EXTERNAL ENERGY TRANSFER SYSTEM FOR AN IMPLANTABLE MEDICAL DEVICE AND METHOD THEREFOR

Номер: US20180001095A1
Принадлежит:

User interface for external power source, recharger, for an implantable medical device. At least some of patient controls and display icons of an energy transfer unit are common with at least some of the patient controls and the display icons of a patient control unit. An energy transfer unit is operable by the patient with less than three operative controls to control energy transfer from the external energy transfer unit to the implantable medical device. An external antenna having a primary coil can inductively transfer energy to a secondary coil of the implantable medical device when the external antenna is externally placed in proximity of the secondary coil. An energy transfer unit has an external telemetry coil allowing the energy transfer unit to communicate with the implantable medical device through the internal telemetry coil in order to at least partially control the therapeutic output of the implantable medical device. 151.-. (canceled)52. An implantable medical device system , comprising:an implantable medical device having a secondary coil, said implantable medical device being configured to be transcutaneously controlled using telemetry; andan external unit comprising a primary coil configured to inductively transfer energy to said secondary coil of said implantable medical device when said primary coil is externally placed in proximity of said secondary coil and said external unit drives said primary coil;said external unit being configured to communicate with said implantable medical device by way of telemetry during the process of transferring, via said primary coil, energy to said implantable medical device;wherein said external unit is configured to time division multiplex between said telemetry and said process of transferring energy.53. The implantable medical device system as in wherein said external unit comprises circuitry and wherein said circuitry of said external unit drives said primary coil to inductively transfer energy to said ...

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04-01-2018 дата публикации

APPARATUS AND METHOD FOR REMINDING, PROMPTING, OR ALERTING A PATIENT WITH AN IMPLANTED STIMULATOR

Номер: US20180001096A1
Принадлежит: SETPOINT MEDICAL CORPORATION

An implanted stimulator can deliver a patient-detectable electrical stimulation to remind or prompt a patient to interact with an implanted therapeutic device (e.g., neurostimulator) when a prompting event occurs. For example, the apparatuses and methods described herein may be configured to apply a prompting patient-detectable electrical vagus nerve stimulation to remind a patient that it is time to administer a therapeutic dose. When the therapeutic device is operated in an automatic fashion, the apparatus can also deliver a patient-detectable warning stimulation prior to the therapeutic stimulation to let the patient know that a therapeutic stimulation will be delivered soon thereafter. 1. A method for prompting a patient to interact with a therapy device implanted in the patient , the method comprising:determining, in a processor, if the patient should interact with the therapy device; anddelivering a patient-detectable stimulation from the implanted therapy device when the processor determines that the patient should interact with the therapy device, wherein the patient-detectable prompting stimulation is different from a therapeutic dose for the implanted therapy device.2. A method for prompting a patient to interact with a therapy device implanted in the patient , the method comprising:determining, in a processor, if the patient should interact with the therapy device based on a prompting event selected from the group comprising: the implant requires charging, the implant requires maintenance, or it is time to prompt the patient to manually activate the implanted therapy device to deliver a therapeutic dose; anddelivering a patient-detectable prompting stimulation from the implanted therapy device when the processor determines that the patient should interact with the therapy device, wherein the patient-detectable stimulation is different from a therapeutic dose for the implanted therapy device.3. A method for prompting a patient to interact with a therapy ...

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02-01-2020 дата публикации

WIRELESS CARDIAC PACE MAKING

Номер: US20200001089A1
Автор: Chae Junseok
Принадлежит:

Systems, devices, and methods involving cardiac pace making are provided. Implantable wireless pace making systems, devices, and methods using electromagnetic waveforms to interact with subcutaneous implanted sensors or stimulators, or both, are described. Systems, devices, and methods can include wireless, miniaturized, battery-free, radiofrequency (RF) microwave activated, sensors or stimulators or integrated sensor/stimulators that are implanted in multiple thoracic cavity locations, and interact with a remote pace making control-module or multiple modules. 1. A cardiac pace making system comprising:a first biocompatible implant comprising sensor circuitry, stimulator circuitry, an antenna, and an exposed electrode; and wherein the sensor circuitry is configured to receive and reflect a radio-frequency (RF) signal from the control module,', 'wherein the sensor circuitry is further configured to sense a biometric cardiac signal and modulate the sensed biometric cardiac signal onto a radio frequency-signal received from the control module,', 'wherein the stimulator circuitry is configured to receive power via electromagnetic RF coupling from the control module,', 'wherein the antenna is electrically connected to the sensor circuitry and the stimulator circuitry, and', 'wherein the exposed electrode is electrically connected to the sensor circuitry and the stimulator circuitry., 'a control module comprising a remote pulse generator,'}2. The system of further comprising:a second biocompatible implant comprising sensor circuitry, stimulator circuitry, an antenna, and an exposed electrode; anda third biocompatible implant comprising sensor circuitry, stimulator circuitry, an antenna, and an exposed electrode.3. The system of wherein the first biocompatible implant the second biocompatible implant and the third biocompatible implant share an antenna and a time delay circuit claim 2 , the antenna and time delay circuit being composed of inductors claim 2 , capacitors ...

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03-01-2019 дата публикации

RECONFIGURABLE BIOSIGNAL PROCESSING ARCHITECTURE

Номер: US20190001121A1
Принадлежит:

Devices, systems, and methods herein relate to processing biosignal data. These systems and methods may obtain sensor data from a plurality of electrodes and may also be used to augment cortical function, treat neurological disease, and provide insight and analysis of biological processes and/or clinical therapeutic outcomes. An implantable biosignal processing system may comprise a lead having at least one biosignal sensor configured to transmit biosignal data based on electrophysiological activity of a subject. A first processing system may be coupled to the biosignal sensor and comprise a plurality of analog signal processing circuits configured to be selectively powered based on a selectable treatment mode. A second processing system in communication with the first processing system and may comprise a plurality of digital signal processing circuits configured to be selectively powered based on the treatment mode. A neurostimulator may stimulate tissue according to the set of biosignal characteristics. 1. An implantable biosignal processing system comprising:a first processing system comprising an analog signal processor having a plurality of analog signal processing circuits, wherein the first processing system is configured to connect to a lead comprising one or more biosignal sensors for acquiring and processing electrophysiological data of a brain region of a subject; anda second processing system in communication with the first processing system, the second processing system comprising a digital signal processor having a power management circuit and a plurality of digital signal processing circuits in communication with the power management circuit, wherein the power management circuit selectively activates and/or deactivates digital signal processing circuits according to a treatment mode of the second processing system to generate a set of electrophysiological data characteristics, andwherein each digital signal processing circuit has a data and clock ...

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03-01-2019 дата публикации

Multi-modal stimulation for treating tremor

Номер: US20190001129A1
Принадлежит: Cala Health Inc

A peripheral nerve stimulator to stimulate a peripheral nerve to treat essential tremor and other movement disorders, as well as overactive bladder, cardiac dysfunction and neurotransmitter dysfunction is provided. The peripheral nerve stimulator can be a noninvasive surface stimulator to provide multi-modal optimized therapy. Stimulation can be vibrational, electromechanical, thermal, radiant, electrical, magnetic, electromagnetic, light, mechanical, chemical, thermal, ultrasonic, radiofrequency (RF), acoustic, infrared, ultraviolet, x-ray, and/or microwave. Stimulation can be delivered using an open loop system and/or a closed loop system with feedback. Stimulation can be to one site or multiple sites.

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03-01-2019 дата публикации

SYSTEMS AND METHODS FOR PROVIDING PATIENT SIGNALING AND CONTINGENT STIMULATION

Номер: US20190001135A1
Принадлежит:

Systems and methods provide notification to a user about pending neurostimulation or ongoing neurostimulation using a variety of notification signals and obtaining a user response to the notification using a variety of methods by which the user response is provided. Systems using implanted neurostimulation devices, external neurostimulators which provide transcutaneous electrical nerve stimulation, or both provide responsive and scheduled therapy regimens that include ecosystem support for augmenting user compliance when treating symptoms, conditions, or disorders. The system is also to assist the user through assessment protocols for improved customization of stimulus regimen attributes such as stimulation protocol parameter values, electrode montages, user surveying, and compliance contingent operations. 1. A neurostimulation system for providing electrical stimulation and notification to a user comprising:a neurostimulator adapted to provide electrical stimulation to a target nerve of a user;a processor controlled control module mounted within said neurostimulator configured to operate in accordance with a predetermined stimulation protocol defining a current clock time, a next stimulation time for actuating the neurostimulator and an abort time interval between the current clock time and the next stimulation time; and,a processor controlled notification module within the neurostimulator and coupled to the control module, the processor controlled notification module configured to:(a) notify the user, using an electrical stimulation signal as a notification signal, that the neurostimulator will be actuated to provide stimulation at a predetermined clock time;(b) determine whether a user abort command signal is sent within the abort time interval prior to the next stimulation time;(c) actuate the neurostimulator at the next stimulation time if a user abort command signal is not sent within the abort time interval; or,(d) reschedule the next stimulation time if the ...

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12-01-2017 дата публикации

HYBRID COMMUNICATION CHANNEL FOR COMMUNICATING WITH AN IMPLANTABLE MEDICAL DEVICE

Номер: US20170007838A1
Автор: Ni Quan, Rondoni John
Принадлежит:

An apparatus comprises a communication channel comprising a plurality of disparate sequential communication links configured to facilitate bi-direction communication between an implantable medical device (IMD) and a programmer. A transceiver is configured to communicate with the programmer via a first communication link of the plurality of disparate communication links. A telemetry device is configured to communicate with the IMD via a second communication link of the plurality of disparate communication links. A third communication link communicatively couples the transceiver and the telemetry device. A power source is coupled to the transceiver and to the telemetry apparatus. An operational status of at least the first and second communication links can be individually determined in real-time. 1. An apparatus for effecting communication with an implantable medical device , the apparatus comprising:a wireless programmer configured to interrogate and program the implantable medical device; and a communication channel comprising a plurality of disparate sequential communication links configured to facilitate bi-direction communication between the wireless programmer and the implantable medical device;', 'a wireless transceiver configured to wirelessly communicate with the wireless programmer via a first communication link of the plurality of disparate communication links;', 'a telemetry device configured to wirelessly communicate with the implantable medical device via a second communication link of the plurality of disparate communication links;', 'a third communication link communicatively coupling the wireless transceiver and the telemetry device; and', 'a power source coupled to the wireless transceiver and the telemetry apparatus;, 'a telemetry apparatus, comprisingwherein the wireless programmer is configured to individually determine an operational status of at least the first and second communication links in real-time.2. The apparatus of claim 1 , wherein ...

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14-01-2016 дата публикации

RELAY INTERFACE FOR CONNECTING AN IMPLANTED MEDICAL DEVICE TO AN EXTERNAL ELECTRONICS DEVICE

Номер: US20160008599A1
Принадлежит:

An interface relay system for use with a fully implantable medical devices that permits transcutaneous coupling of the implanted medical device to a consumer electronics device. In one embodiment, coupling the implanted medical device to the external electronics device provides a back-up source of power for operating the implanted medical device. In another embodiment, coupling the implanted medical device to the external electronics device allows for providing unidirectional and/or bidirectional data transfer between the devices. In one arrangement, the consumer electronics device may be connectable to a communications/data network to allow for network communication between the implantable medical device and a remote processing platform/server. 1. A system for use with an implantable medical device , comprising: a housing adapted for external mounting proximate to an implanted medical device;', 'a cable extending from the housing and terminating in a connector adapted for connection with a mating port;', 'a wireless transceiver for transcutaneously transmitting at least one of power or data received via the connector to an implanted medical device and transcutaneously receiving communications from the implanted medical device; and', a power source;', 'a processor;', 'a communications port, wherein the connector of the implant interface device is selectively connectable with the communications port; and', 'a wireless interface for interconnecting the consumer electronics device to a communications network, wherein the consumer electronics device is operative for at least one of transmitting data originating from the implantable medical device to the communications network and transmitting data originating from the communications network to the implantable medical device., 'a consumer electronics device including], 'an implant interface device comprising2. The system of claim 14 , wherein the consumer electronics device comprises a mobile phone.3. The system of claim ...

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14-01-2021 дата публикации

POWER EFFICIENT STIMULATORS

Номер: US20210008373A1
Автор: Laird James, SINGLE Peter
Принадлежит:

This disclosure relates to a device for applying a neural stimulus. A battery supplies electrical energy at a battery voltage and an electrode applies the electrical energy to neural tissue. A circuit measures the nervous response of the tissue and a voltage converter receives the electrical energy from the battery and controls a voltage applied to the electrode based on the measured nervous response of the tissue. This direct voltage control is energy efficient because losses across a typical current mirror are avoided. Further, the control based on the measured nervous response leads to automatic compensation of impedance variation due to in-growth or change in posture. As a result, the stimulation results in a desired neural response. 1. A device for applying a neural stimulus comprising:a battery to supply electrical energy at a battery voltage;an electrode to apply the electrical energy to neural tissue;a circuit to measure the nervous response of the tissue; anda voltage converter to receive the electrical energy from the battery and to control a voltage applied to the electrode based on the measured nervous response of the tissue.2. The device of claim 1 , wherein the converter comprises a processor programmed to calculate a voltage value based on the measured nervous response and to generate a control signal to the voltage converter indicative of the calculated voltage value.3. The device of wherein the converter circuit is a linear voltage-to-voltage converter.4. The device of wherein the converter is a switched-mode voltage to voltage converter.5. The device of claim 4 , wherein the converter comprises a pulse generator configured to generate a pulse signal to control switching of the switched-mode voltage to voltage converter.6. The device of claim 5 , wherein the pulse signal is based on the measured nervous response of the tissue.7. The device of wherein the pulse generator is a digital processor.8. The device of claim 7 , wherein the device comprises ...

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10-01-2019 дата публикации

METHOD AND APPARATUS FOR SELECTING STIMULATION CONFIGURATION AND TARGET FOR NEUROMODULATION

Номер: US20190009094A1
Принадлежит:

An example of a system for delivering neurostitnulation may include a programming control circuit, a storage device, and a user interface. The programming control circuit may be configured to program a stimulation device for delivering the neurostimulation according to a stimulation configuration specified by a waveform parameter set and an electrode parameter set. The storage device may be configured to store one or more neuromodulation relationships each relating one or more candidate stimulation configurations to one or more neural targets each specified by a target parameter set The user interface may include modulation control circuitry configured to determine the stimulation configuration for programming the stimulation device using a stored neuromodulation relationship. The modulation control circuitry may be configured to obtain two parameter sets of the waveform parameter set, the electrode parameter set, and the target parameter set and to determine the other parameter set. 1. A system for delivering neurostitnulation to tissue of a patient using a stimulation device and a plurality of electrodes and controlling the delivery of the neurostitnulation by a user , the system comprising:a programming control circuit configured to program the stimulation device for delivering the neurostimulation through one or more electrodes of the plurality of electrodes according to a stimulation configuration specified by a waveform parameter set defining a waveform of the neurostimulation and an electrode parameter set defining an electrode configuration of the neurostimulation;a storage device configured to store one or more neuromodulation relationships each relating one or more candidate stimulation configurations to one or more neural targets, the one or more candidate stimulation configurations each selectable to be the stimulation configuration for programming the stimulation device, the one or more neural targets each specified by a target parameter set; and obtain ...

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10-01-2019 дата публикации

DEVICES AND METHODS FOR POSITIONING EXTERNAL DEVICES IN RELATION TO IMPLANTED DEVICES

Номер: US20190009097A1
Принадлежит:

A stimulation system for a patient is provided. The system comprises: at least one implantable device comprising at least one implantable antenna; and an external device comprising at least one external antenna, wherein the at least one external antenna transfers power to the at least one implantable antenna. The at least one implantable device delivers therapy to the patient. A patient attachment device or body covering positions the at least one external antenna relative to the patient. 1. A stimulation system for a patient comprising:at least one implantable device comprising at least one implantable antenna; andan external device comprising at least one external antenna, wherein the at least one external antenna transfers power to the at least one implantable antenna;wherein the at least one implantable device delivers therapy to the patient.2. The system according to any claim herein , wherein the system is defined by a Z-parameter matrix including cross terms , wherein the at least one implantable antenna and the at least one external antenna each comprise an impedance , wherein the cross terms represent coupling between the antennas , and wherein the power transfer is optimized based on the antenna impedances and the cross terms.3. The system according to any claim herein , wherein the system is defined by a Z-parameter matrix , and wherein variation of the matrix is due to lateral displacement , rotational displacement , and/or depth displacement between the external device and at least one implantable device.4. The system according to any claim herein , wherein the at least one external antenna comprises a single-turn loop antenna with an impedance and the at least one implantable antenna comprises a single-turn loop antenna with an impedance , wherein the system is defined by a Z-parameter matrix including values representing the antenna impedances and the coupling between the at least one external antenna and at least one implantable antenna , and wherein ...

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09-01-2020 дата публикации

Modelling Relationships Between Stimulation Parameters and Use Thereof for Automatic Customization of Sub-Perception Therapy in a Spinal Cord Stimulation System

Номер: US20200009367A1
Принадлежит:

An algorithm for determining optimal sub-perception stimulation parameters for a Spinal Cord Stimulation patient is disclosed. The algorithm uses various modelling information, including a model determined based on empirical testing that relates optimal frequencies and pulse widths with perception thresholds reported by patients at those frequencies and pulse widths. A patient's perception threshold is then measured at different pulse widths, with the result compared to the model to determine a range or volume in the model that best relates frequency pulse width and perception threshold for that patient. Further modeling allows the perception thresholds to be related to an optimal amplitudes, thus resulting in optimal situation parameters (F, PW, and A) for the patient. The optimal stimulation parameters may be provided to a patient's external controller to allow the patient to adjust stimulation within a range of volume of these parameters. 1. A method for programming a stimulator device using an external device , the method comprising:receiving a model at the external device;providing from the external device a program for the stimulator device, the program specifying an amplitude, a pulse width, and a frequency of stimulation pulses to be provided at one of more of electrodes of the stimulator device; andreceiving at a Graphical User Interface (GUI) on the external device a user input that simultaneously adjusts the frequency and at least one of the pulse width or the amplitude of the stimulation pulses in accordance with the model.2. The method of claim 1 , wherein claim 1 , in accordance with the model claim 1 , the frequency and the at least one of the pulse width and the amplitude are not adjusted proportionately or inversely proportional with respect to each other.3. The method of claim 1 , wherein the model is specific to a particular patient having the stimulator device.4. The method of claim 3 , wherein the model comprises information indicative of a ...

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19-01-2017 дата публикации

DEVICES AND METHODS FOR CONTROLLING TREMOR

Номер: US20170014625A1
Принадлежит:

A peripheral nerve stimulator can be used to stimulate a peripheral nerve to treat essential tremor, Parkinson tremor, and other forms of tremor. The peripheral nerve stimulator can be either a noninvasive surface stimulator or an implanted stimulator. Stimulation can be electrical, mechanical, or chemical. Stimulation can be delivered using either an open loop system or a closed loop system with feedback. 1. A system for treating tremor in a patient , the device comprising: a decision unit,', 'a first peripheral nerve effector, comprising at least one stimulation electrode configured to be positioned to modulate an afferent nerve pathway, and', 'wherein the decision unit comprises a processor and a memory for storing instructions that, when executed by the processor, causes the device to:', "deliver an electrical stimulus to a first afferent nerve through the first peripheral nerve effector to reduce tremor in the patient's extremity;"], 'a wearable device, comprisinga communication device configured to communicate with and receive data from the wearable device, the communication device further configured to transmit the data to a cloud computing network or server for storage and/or data processing; anda computing device configured to be accessed by the patient's physician, the computing device in communication with the cloud computing network or server and further configured to retrieve and display the data from the cloud computing network or server.2. The system of claim 1 , wherein the first electrical stimulus has a frequency of at least 1000 Hz.3. The system of claim 1 , wherein the wearable device further comprises at least one biomechanical sensor configured to measure movement of the patient's extremity to characterize one or more features of the tremor claim 1 , the one or more features of the tremor selected from the group consisting of tremor frequency claim 1 , tremor period claim 1 , and tremor magnitude; ["measure the movement of the patient's ...

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19-01-2017 дата публикации

Spinal cord stimulator system

Номер: US20170014628A1
Принадлежит: Globus Medical Inc

Spinal cord stimulation (SCS) system having a recharging system with self-alignment, a system for mapping current fields using a completely wireless system, multiple independent electrode stimulation outsource, and IPG control through software on Smartphone/mobile device and tablet hardware during trial and permanent implants. SCS system can include multiple electrodes, multiple, independently programmable, stimulation channels within an implantable pulse generator (IPG) providing concurrent, but unique stimulation fields. SCS system can include a replenishable power source, rechargeable using transcutaneous power transmissions between antenna coil pairs. An external charger unit, having its own rechargeable battery, can charge the IPG replenishable power source. A real-time clock can provide an auto-run schedule for daily stimulation. A bi-directional telemetry link informs the patient or clinician the status of the system, including the state of charge of the IPG battery. Other processing circuitry in current IPG allows electrode impedance measurements to be made.

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18-01-2018 дата публикации

CARDIAC PACEMAKER SYSTEM AND CONTROL METHOD THEREOF

Номер: US20180015279A1
Принадлежит:

A cardiac pacemaker system and control methods thereof are disclosed, wherein pacing logic and timing functions are enabled by a microprocessor and sensing and pulse delivery capabilities are accomplished by a peripheral IC. The microprocessor communicates with the peripheral IC via serial interfaces and electrical level signals. This allows for full use of internal resources of the modern ultra-low power microprocessor, lowering the dependence of the system on the peripheral IC and reducing the effort required for digital circuit design. 1. A cardiac pacemaker system , comprising:a microprocessor, comprising a main control unit, a first timer, a second timer, input/output ports and a microprocessor serial interface, wherein each of the first timer, the second timer, the input/output ports and the microprocessor serial interface is connected to the main control unit; anda peripheral IC, comprising a pacing and sensing control interface, a pacing control unit, a sensing control unit and a peripheral-IC serial interface, the pacing and sensing control interface being connected to each of the pacing control unit and the sensing control unit,wherein: the second timer and the input/output ports communicate with the pacing and sensing control interface by using a first electrical level signal and a second electrical level signal, respectively; the pacing and sensing control interface, upon sensing an atrial or ventricular event, notifies the second timer of the atrial or ventricular event by using the first electrical level signal; the input/output ports send a pacing request to the pacing and sensing control interface by using the second electrical level signal; the microprocessor serial interface is electrically connected to the peripheral-IC serial interface; and the microprocessor controls the peripheral IC to configure parameters by using data communicated between the serial interfaces.2. The cardiac pacemaker system of claim 1 , wherein when the main control unit is ...

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18-01-2018 дата публикации

SYSTEM AND METHOD FOR TREATING SLEEP APNEA

Номер: US20180015282A1
Принадлежит:

The present disclosure is directed to a system for the treatment of a sleep disorder through stimulation of the hypoglossal nerve or the geniohyoid muscle of a patient, e.g. a human patient. In general, the system comprises three components, namely a sensing component a stimulation component and a control system In some embodiments, the control system may be embedded within the sensing component or the control system may be embedded within the stimulation component 1. A system for the treatment of obstructive sleep apnea in a patient in need thereof , the system comprising a sensing component and a stimulation component , the sensing component comprising one or more wireless sensors for collecting one or more vital signs of the patient , the sensing component being in wireless communication with a control system , and wherein the stimulation component comprises (i) a surgically implantable body configured to deliver energy to one of a nerve or muscle; and (ii) a wearable appliance inductively coupled to the implanted body , the wearable portion configured to receive signals from the control system.2. The system of claim 2 , where the vital signs are selected form the group consisting of blood oxygen claim 2 , respiration rate claim 2 , and heart rate.3. The system of claim 1 , wherein the wearable portion is a dental appliance comprising a rechargeable battery claim 1 , a pulse generator claim 1 , and a means for inductively delivering energy to the surgically implantable body.4. The system of claim 3 , wherein the means for inductively delivering energy is a transmitter coil.5. The system of claim 4 , wherein the surgically implantable body comprises a receiver coil for receiving energy from the wearable portion.6. The system of claim 3 , wherein the surgically implantable body is configured to deliver energy to a hypoglossal nerve.7. The system of claim 1 , wherein the wearable portion is a dermal device for positioning on the patient's skin claim 1 , and wherein ...

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18-01-2018 дата публикации

IMPLANTABLE MEDICAL DEVICE WITH ANTENNA FOR WIRELESS COMMUNICATION

Номер: US20180015291A1
Принадлежит:

An implantable medical device having a hollow housing and a connector housing connected (e.g., rigidly) together, each containing electrical components. The components contained in the hollow housing include a receiver for wireless communication. The components contained in the connector housing include an antenna electrically connected to the receiver and configured to receive electromagnetic waves having a frequency greater than 100 MHz. The receiver/antenna allows the receipt of data in the MICS frequency band. The electrical components arranged in the connector housing additionally include a resonant circuit having a coil and a capacitor which is inductively coupled to the antenna. The resonant circuit is matched to magnetic alternating fields in a frequency range between 5 kHz and 50 MHz, preferably having a resonance frequency between 5 kHz and 50 MHz. The resonant circuit is suitable for data communication in the near field of the implantable medical device via magnetic alternating fields. 1. An implantable medical device comprising:a hollow housing and a connector housing, which is connected to the hollow housing, wherein both the hollow housing and the connector housing contain electrical components, of which the electrical components contained in the hollow housing comprise a receiver for wireless communication and the components contained in the connector housing comprise an antenna, which is configured to receive electromagnetic waves having a frequency of more than 100 MHz and which is electrically connected to the receiver, wherein the electrical components contained in the connector housing additionally comprise a resonant circuit, which has a coil and a capacitor and which is coupled inductively to the antenna, wherein the resonant circuit is configured to respond to magnetic alternating fields in a frequency range between 5 kHz and 50 MHz.2. The implantable medical device according to claim 1 , wherein the receiver in the hollow housing and the ...

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21-01-2016 дата публикации

IMPLANTABLE PULSE GENERATOR THAT GENERATES SPINAL CORD STIMULATION SIGNALS FOR A HUMAN BODY

Номер: US20160015977A1
Принадлежит:

An implantable pulse generator (IPG) that generates spinal cord stimulation signals for a human body has a programmable signal generator that can generate the signals based on stored signal parameters without any intervention from a processor that controls the overall operation of the IPG. While the signal generator is generating the signals the processor can be in a standby mode to substantially save battery power.

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21-01-2016 дата публикации

Implantable pulse generator that generates spinal cord stimulation signals for a human body

Номер: US20160015981A1
Принадлежит: Globus Medical Inc

An implantable pulse generator (IPG) that generates spinal cord stimulation signals for a human body includes a timing generator and high frequency generator. The timing generator generates timing signals that represent stimulation signals for multiple channels. The high frequency generator determines whether to modulate the timing signals and modulates them at a burst frequency according to stored burst parameters if the decision is yes. The high frequency generator can also independently control the pulse frequency of each channel according to the stored parameters. As such, the IPG provides the ability to generate both the low frequency and high frequency stimulation signals at different frequencies in different channels according to user programming in order to provide maximum flexibility in treatment.

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21-01-2016 дата публикации

ULTRA-THIN IMPLANTABLE ENERGY SOURCE

Номер: US20160015987A1
Принадлежит:

The invention relates to an implantable energy source comprising at least one energy storage sub-system () constructed in the form of a stack of thin layers () on a substrate (), characterised in that said energy storage sub-system has a plurality of through-openings () for allowing the development and the passage of blood vessels. Preferably, the energy source thereof has a thickness of less than, or equal to, 1 mm, over at least 80% of its surface. 1171175176174. An implantable power source comprising at least one energy storing subsystem () produced in the form of a thin-film stack () on a substrate () , characterized in that said energy storing subsystem has a plurality of through-apertures () in order to allow the development and passage of blood vessels.2. The implantable power source as claimed in claim 1 , in which each said aperture has an area comprised between 0.01 mmand 4 mm.3. The implantable power source as claimed in claim 1 , in which the spacing between said apertures is comprised between 1 mm and 1 cm.473182. The implantable power source as claimed in claim 1 , having a biocompatible coating ( claim 1 , ) covering at least one portion of its surface comprising the interior surface of said apertures.58182. The implantable power source as claimed in claim 4 , in which said biocompatible coating comprises an exterior film () made of a biocompatible organic material and an interior film () made of an inorganic material that is impermeable to moisture and oxygen.6. The implantable power source as claimed in claim 4 , in which said biocompatible coating is substantially transparent at least in a spectral range in the visible or near infrared.7. The implantable power source as claimed in claim 1 , in which said apertures are completely or partially filled with a gel promoting cellular growth.8172173. The implantable power source as claimed in claim 1 , in which said energy storing subsystem has a plurality of active regions () separated by interconnect ...

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21-01-2021 дата публикации

TRANSCUTANEOUS ELECTRICAL MUSCLE STIMULATION DEVICE FOR THE TREATMENT OF PREMATURE EJACULATION OR ERECTILE DYSFUNCTION, AND METHODS OF USE THEREOF

Номер: US20210016078A1
Автор: GOLLAN Tal
Принадлежит: Virility Medical Ltd.

In one embodiment, the present invention provides a device, wherein the device comprises a skin patch, configured to attach to the skin surface of the perineum of a subject suffering from premature ejaculation, wherein the skin patch contains electrodes configured to deliver electrical impulses transcutaneously to the bulbcavernosus muscle of the subject, wherein the transcutaneously delivered electrical impulses are configured to treat premature ejaculation. 1. A device , comprising:a skin patch having a first surface and a second surface, wherein said first surface is configured to attach said skin patch to a skin surface of a subject, wherein the skin patch contains at least two electrodes positioned at a distance between each other suitable to deliver electrical impulses transcutaneously to one or more of the bulbospongiosus muscle, the bulbocavernosus muscle, the ischiocavernosus muscle, and to the neuromuscular junction of the nerves innervating the ischiocavernosus and bulbospongiosus muscles of the subject; a battery connected to said at least two electrodes;', 'an electronic circuitry including a controller electrically connected to said battery;, 'an electronic circuit housing integrated with said second surface of said skin patch, and comprisingwherein said electronic circuitry is configured to receive a radio frequency signal, and to deliver said electrical impulses from said battery to said at least two electrodes in response to said radio frequency signal.2. The device of claim 1 , wherein all of said device including said skin patch which includes said at least two electrodes and said electronic circuit housing claim 1 , is shaped and sized to be attached to to said skin surface of said subject.3. The device of claim 2 , wherein all of said device is shaped and sized to be attached to the skin surface of the subject.4. The device of claim 1 , wherein said device is configured to fit between and conform to each of the thigh-groin crease of a subject.5. ...

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16-01-2020 дата публикации

IMPLANTABLE RELAY MODULE

Номер: US20200016417A1
Принадлежит:

A passive implantable relay module includes a first coupler arm configured to wirelessly receive electromagnetic energy radiated through electric radiative coupling from a transmitting antenna located outside a subject's body; a second coupler arm; and a connector portion comprising a first metal core and a first dielectric coating surrounding the first metal core, the connector portion configured to connect the first coupler arm to the second coupler arm such that when the passive implantable relay module is implanted inside the subject's body and the transmitting antenna initiates wireless energy transfer to the first coupler arm via non-inductive coupling, electromagnetic waves carrying the electromagnetic energy received at the first coupler arm propagate along the first metal core to arrive at the second coupler arm, where the electromagnetic energy arriving is wirelessly transferred, again via non-inductive coupling, to a receiving antenna on a passive wireless neural stimulator device. 1a first coupler arm configured to wirelessly receive electromagnetic energy radiated through non-inductive coupling from a transmitting antenna located outside a subject's body;a second coupler arm; anda connector portion comprising a first metal core and a first dielectric coating surrounding at least portions of the first metal core, the connector portion configured to connect the first coupler arm to the second coupler arm and to transport the received electromagnetic energy from the first coupler arm to the second coupler arm such that when the passive implantable relay module is implanted inside the subject's body and the transmitting antenna initiates wireless energy transfer to the first coupler arm through non-inductive coupling, electromagnetic waves carrying the electromagnetic energy received at the first coupler arm propagate along the first metal core to arrive at the second coupler arm, where the electromagnetic energy arriving is wirelessly transferred, again ...

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28-01-2016 дата публикации

METHOD AND APPARATUS FOR SUPPLYING ENERGY TO A MEDICAL DEVICE

Номер: US20160023004A1
Автор: Forsell Peter
Принадлежит:

In a method and apparatus for supplying wireless energy to a medical device () implanted in a patient, wireless energy is transmitted from an external energy source () located outside a patient and is received by an internal energy receiver () located inside the patient, for directly or indirectly supplying received energy to the medical device. An energy balance is determined between the energy received by the internal energy receiver and the energy used for the medical device, and the transmission of wireless energy is then controlled based on the determined energy balance. The energy balance thus provides an accurate indication of the correct amount of energy needed, which is sufficient to operate the medical device properly, but without causing undue temperature rise. 1268-. (canceled)269. An apparatus for controlling the transmission of wireless energy supplied to an electrically operable medical device adapted to be implanted in a mammal patient , comprising:an external energy source adapted to be located outside the patient, comprising a primary coil adapted to transmit wireless energy,an internal energy receiver located inside the patient, comprising a secondary coil adapted to receive the wireless energy inductively, the internal energy receiver being connected or connectable to the electrically operable medical device for directly or indirectly supplying received energy thereto, andat least one stabilizing unit to stabilize the energy in the electrically operable medical device,wherein the electrically operable medical device is adapted to transfer feedback control information to external energy source encoding the feedback control information,wherein the feedback control information is related to the energy for operating the medical device, adapted to be used to control the transmission of wireless energy from the external energy source, andwherein the electrically operable medical device is adapted to consume, store or consume and store the energy after ...

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28-01-2016 дата публикации

DEVICES AND METHODS FOR TREATING UROLOGICAL DISORDERS

Номер: US20160023005A1
Принадлежит:

Some implementations provide a method for treating urological disorders in a patient, the method including: placing an introducer into a patient's body through an incision site on the patient's body, the patient suffering from an urological disorder; placing an implantable wireless device into an inner lumen of the introducer, the implantable wireless device suitable to fit into the inner lumen and configured to receive electromagnetic energy non-inductively from a source located outside the patient's body; through the inner lumen of the introducer, positioning the implantable wireless device adjacent to or near one or more excitable tissue in the patient, the one or more excitable tissue regulating a nerve activity associated with the urological disorder; and causing neural modulation of the one or more excitable tissue through one or more electrodes on the implantable wireless device. 1. A method for treating urological disorders in a patient , the method comprising:placing an introducer into a patient's body through an incision site on the patient's body, the patient suffering from an urological disorder;placing an implantable wireless device into an inner lumen of the introducer, the implantable wireless device suitable to fit into the inner lumen and configured to receive electromagnetic energy non-inductively from a source located outside the patient's body;through the inner lumen of the introducer, positioning the implantable wireless device adjacent to or near one or more excitable tissue in the patient, the one or more excitable tissue regulating a nerve activity associated with the urological disorder; andcausing neural modulation of the one or more excitable tissue through one or more electrodes on the implantable wireless device.2. The method of claim 1 , wherein placing the introducer comprises:placing the introducer through the incision site into a sacral region of the patient.3. The method of claim 2 , wherein positioning the implantable wireless ...

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28-01-2016 дата публикации

SHIELDING DEVICE FOR SIGNAL TRANSMISSION COIL

Номер: US20160023006A1
Принадлежит:

Systems and apparatuses are used to transmit data between external and internal portions of auditory prostheses or other medical devices. The external portion of the auditory prosthesis includes a magnet and an implanted coil that provides stimulation to the device recipient. A shaped shield material can be placed between the external coil and the sound processing hardware to improve efficiency and effectiveness between the external coil and implanted coil. Adverse effects on tuning frequencies can be reduced by disposing the shield material away from the magnet. 1. An apparatus comprising:an annular coil comprising an inner coil diameter and a coil center point;an annular ferrite shield comprising an inner shield diameter and a shield center point, wherein the coil center point and the shield center point are substantially aligned, wherein the annular ferrite shield comprises a first magnetic flux permeability, and wherein the inner coil diameter and the inner shield diameter at least partially define a cylindrical volume;a magnet at least partially disposed within the cylindrical volume; anda gas disposed within the cylindrical volume, wherein the gas comprises a second magnetic flux permeability less than the first magnetic flux permeability.2. The apparatus of claim 1 , wherein the gas comprises air.3. The apparatus of claim 1 , wherein the gas is contained within a material comprising a third magnetic flux permeability less than the first magnetic flux permeability.4. The apparatus of claim 1 , wherein the magnet comprises a magnet center point claim 1 , wherein the magnet center point is substantially aligned with the coil center point and the shield center point.5. The apparatus of claim 1 , wherein the magnet comprises an outer magnet diameter less than the inner coil diameter and the inner shield diameter claim 1 , such that the outer magnet diameter does not contact the annular ferrite shield.6. The apparatus of claim 1 , wherein the annular coil comprises ...

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26-01-2017 дата публикации

SYSTEMS AND METHODS FOR STIMULATION SITE SELECTION

Номер: US20170021175A1
Принадлежит:

Systems and methods for selecting one or more sites at or within at least one heart chamber for cardiac stimulation are disclosed. The system can include a physiologic sensor circuit to sense physiologic signals at two or more candidate stimulation sites. The system can generate respective activation timing indicators corresponding to the two or more candidate stimulation sites, and detect MI indicators indicating the presence of, or spatial proximity of each of the two or more candidate stimulation sites to a MI tissue. The system can use the activation timing indicators and the MI indicators to select at least one target stimulation site or to determine an electrostimulation vector. The system can display the selected target stimulation site to a user, or deliver electrostimulation to the patient at the target stimulation site or according to the determined electrostimulation vector. 1. A system , comprising:a physiologic sensor circuit, including a sense amplifier circuit to sense respective physiologic signals at two or more candidate stimulation sites at or within at least one chamber of a heart of a patient;an activation timer circuit, including a clock circuit coupled to the physiologic sensor circuit to use the sensed respective physiologic signals to produce respective activation timing indicators corresponding to the two or more candidate stimulation sites;a myocardial infarction (MI) receiver circuit to receive respective MI indicators indicating presence of, or relative spatial proximity of each of the two or more candidate stimulation sites to, a MI tissue; and select, automatically or based on a user input, at least one target stimulation site from the two or more candidate stimulation sites using the respective activation timing indicators and the respective MI indicators; or', 'generate a human-perceptible presentation of the two or more candidate stimulation sites with at least some of the respective MI indicators for selection of the at least one ...

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25-01-2018 дата публикации

TRANSCUTANEOUS POWER CONVEYANCE DEVICE

Номер: US20180021586A9
Принадлежит:

Some embodiments of the present disclosure may include a device for conveying power from a location external to a subject to a location within the subject The device may include a flexible carrier, an adhesive on a first side of the carrier, a coil of electrically conductive material associated with the flexible carrier, and a mechanical connector extending from a second side of the carrier opposite the adhesive. The mechanical connector may be configured to be received by and retained by a receiver associated with a housing configured for mounting on the carrier. 115-. (canceled)16. A device for connection to a flexible adhesive patch configured to convey power from a location external to a subject to a location within the subject , the flexible adhesive patch including adhesive on one side thereof and a protrusion extending from a side thereof opposite the adhesive , the device comprising:a housing containing at least one processor and at least one coil of electrically conductive material, the at least one coil being configured for use in wirelessly transmitting power to an implant located at the location within the subject to modulate the branched fibers of the hypoglossal nerve associated with a genioglossus muscle of the subject, the at least one coil having a plurality of windings;a concavity within the housing, the concavity being configured to receive and retain the protrusion extending from the flexible adhesive patch, wherein at least a portion of a side of the housing and a top of the housing are exposed when the housing is mounted on the flexible adhesive patch.17. The device of claim 16 , wherein an electronic circuit is connected to the at least one processor contained within the housing.18. The device of claim 16 , wherein the housing includes a battery.19. The device of claim 16 , wherein the concavity includes a rim configured to engage flexible arms of the protrusion extending from the adhesive patch.20. The device of claim 16 , further comprising ...

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24-01-2019 дата публикации

Efficient back telemetry transmission in cochlear implant systems

Номер: US20190022391A1
Принадлежит: ADVANCED BIONICS AG

A cochlear implant configured to be implanted within a patient may comprise an integrated circuit including a driver configured to generate a back telemetry signal encoded with information to be transmitted over a wireless communication link to a sound processor located external to the patient. The cochlear implant may also comprise a filter network that includes a first plurality of impedance components including a damping resistor, and a first and a second impedance component such as a capacitor or an inductor. The cochlear implant may also comprise an isolation network including a second plurality of impedance components configured to isolate, from the filter network and the driver, a forward telemetry signal received by the cochlear implant from the sound processor.

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24-01-2019 дата публикации

WEARABLE DEVICES

Номер: US20190022400A1
Принадлежит:

Wearable devices are provided herein including wearable defibrillators, wearable devices for diagnosing symptoms associated with sleep apnea, and wearable devices for diagnosing symptoms associated with heart failure. The wearable external defibrillators can include a plurality of ECG sensing electrodes and a first defibrillator electrode pad and a second defibrillator electrode pad. The ECG sensing electrodes and the defibrillator electrode pads are configured for long term wear. Methods are also provided for using the wearable external defibrillators to analyze cardiac signals of the wearer and to provide an electrical shock if a treatable arrhythmia is detected. Methods are also disclosed for refurbishing wearable defibrillators. Methods of using wearable devices for diagnosing symptoms associated with sleep apnea and for diagnosing symptoms associated with heart failure are also provided. 1. A wearable external defibrillator comprising:two or more sensing electrodes configured to engage with a patient's skin to detect a cardiac signal;a first defibrillator electrode pad configured to engage with the patient's skin and to deliver an electrical therapy to the patient, the first defibrillator electrode pad configured to be in continuous contact with the patient's skin;a first patient engagement substrate comprising an adhesive, the first defibrillator electrode pad, a first fluid transport element configured to transport fluid away from the skin to allow the wearable external defibrillator to be worn continuously, and a first vapor permeable layer;a second patient engagement substrate comprising a second defibrillator electrode pad, a second adhesive, a second fluid transport element in fluid communication with the second patient engagement substrate configured to transport fluid away from the skin to allow the wearable external defibrillator to be worn continuously, and a second vapor permeable layer;an energy source;one or more capacitors in electrical ...

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17-04-2014 дата публикации

APPARATUS AND METHOD FOR CONTROLLING ENERGY DELIVERY AS A FUNCTION OF DEGREE OF COUPLING

Номер: US20140107732A1
Принадлежит:

A device for delivering energy as a function of degree coupling may include an external unit configured for location external to a body of a subject and at least one processor associated with the implant unit and configured for electrical communication with a power source. The device may further include a primary antenna associated with the at least one processor. The processor may be configured to determine a degree of coupling between the primary antenna and a secondary antenna associated with the implant unit, and regulate delivery of power to the implant unit based on the degree of coupling between the primary antenna and the secondary antenna. 113-. (canceled)14. A device , comprising:an external unit configured for location external to a body of a subject;at least one processor associated with the external unit and configured for electrical communication with a power source;a primary antenna associated with the at least one processor; andwherein the processor is configured to communicate with an implant unit when the implant unit is implanted beneath skin of the subject, to determine a degree of coupling between the primary antenna and a secondary antenna associated with the implant unit, and to regulate delivery of power from the power source to the implant unit based on the degree of coupling between the primary antenna and the secondary antenna.1516-. (canceled)17. The device of claim 14 , wherein the primary antenna includes a coil antenna.18. The device of claim 14 , wherein the external unit includes a flexible substrate.19. The device of claim 14 , wherein the at least one processor is further configured to receive physiological data via the implant unit and regulate delivery of power from the power source to the implant unit based on both the physiological data and the degree of coupling between the primary antenna and the secondary antenna.20. The device of claim 14 , wherein an upper limit of power delivered from the power source to the implant unit ...

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28-01-2021 дата публикации

SLEEP APNEA TREATMENT DEVICE

Номер: US20210023365A1
Принадлежит:

A sleep apnea treatment device includes a buried breathing stimulation capsule for embedding in a user's lower jaw and the buried breathing stimulation capsule includes a power receiving coil and an output electrode. The power receiving coil is used for receiving a power required for the buried breathing stimulation capsule, and the output electrode is electrically connected to the power receiving coil, and emits a predetermined voltage to a genioglossus muscle of the user to cause contraction of the genioglossus muscle. 1. A sleep apnea treatment device having a buried breathing stimulation capsule configured to be fixed in a lower jaw of a user , the buried breathing stimulation capsule comprising:a power receiving coil receiving an electrical power for the buried breathing stimulation capsule; andan output electrode electrically connected to the power receiving coil to emit a predetermined voltage to stimulate a tongue muscle of the lower jaw of the user so as to cause a contraction of the tongue muscle.2. The sleep apnea treatment device of claim 1 , wherein the buried breathing stimulation capsule further comprises a buck-boost circuit disposed between the power receiving coil and the output electrode to provide a desired voltage for the output electrode.3. The sleep apnea treatment device of claim 1 , wherein the tongue muscle comprises a genioglossus muscle located under a tongue and attached to an inner surface of a mandibular bone.4. The sleep apnea treatment device of claim 1 , further comprising a wireless power supply module to provide the electrical power for the buried breathing stimulation capsule by wireless induction.5. The sleep apnea treatment device of claim 4 , wherein the wireless power supply module comprises:a power output coil wirelessly inducing the power receiving coil to provide the electrical power for the buried breathing stimulation capsule;an inverter connected to the power output coil to adjust an alternating current power for the ...

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29-01-2015 дата публикации

HIGH EFFICIENCY MAGNETIC LINK FOR IMPLANTABLE DEVICES

Номер: US20150028798A1
Принадлежит:

Systems and devices for a high-efficiency magnetic link for implantable devices are disclosed herein. These devices can include a charging coil located in the implantable device and a charging coil located in a charge head of a charger. The charging coils can each include an elongate core and wire windings wrapped around a longitudinal axis of the elongate core. The charging coil of the charge head can be attached to a rotatable mount, which can be used to align the longitudinal axis of the charging coil of the charge head with longitudinal axis of the implantable device such that the axes of the charging coils are parallel. 1. A method of charging an implantable device , the method comprising:positioning a charging head comprising a transmitting coil attached to a rotatable mount proximate to an implantable device comprising a receiving coil;determining a first orientation of the transmitting coil with respect to the receiving coil; androtating the rotatable mount and the thereto attached transmitting coil until the transmitting coil has a second orientation with respect to the receiving coil.2. The method of claim 1 , wherein the transmitting coil has a longitudinal axis and at least one wire wrapped around the longitudinal axis.3. The method of claim 2 , wherein the receiving coil has a longitudinal axis and at least one wire wrapped around the longitudinal axis.4. The method of claim 3 , wherein determining the first orientation of the transmitting coil with respect to the receiving coil comprises determining an angle between the longitudinal axis of the transmitting coil with respect to the longitudinal axis of the receiving coil.5. The method of claim 4 , wherein the angle between the longitudinal axis of the transmitting coil is non-parallel with the longitudinal axis of the receiving coil in the first orientation.6. The method of claim 4 , wherein an angle between the longitudinal axis of the transmitting coil and the longitudinal axis of the receiving coil ...

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04-02-2016 дата публикации

Implantable Medical Device with Multi-Function Single Coil

Номер: US20160030755A1
Принадлежит:

A combination charging and telemetry circuit for use within an implantable device, such as a microstimulator, uses a single coil for both charging and telemetry. In accordance with one aspect of the invention, one or more capacitors are used to tune the single coil to different frequencies, wherein the coil is used for multiple purposes, e.g., for receiving power from an external source and also for the telemetry of information to and from an external source. 1. An implantable medical device , comprising:an implantable housing;a battery within the housing having a battery voltage;electrical circuitry within the housing; anda coil,wherein the electrical circuitry is configurable to form a first circuit with the coil to receive power from an external source to charge the battery, andwherein the electrical circuitry is configurable to form at least one second circuit with the coil to convert the battery voltage to a different voltage level.2. The implantable medical device of claim 1 , wherein the electrical circuitry is configurable to form a third circuit with the coil to receive command information or data information from an external source.3. The implantable medical device of claim 1 , wherein the electrical circuitry is configurable to form a fourth circuit with the coil to transmit data to an external source.4. The implantable medical device of claim 1 , wherein the at least one second circuit with the coil converts the battery voltage to a different voltage level that is lower than the battery voltage.5. The implantable medical device of claim 1 , wherein the at least one second circuit with the coil converts the battery voltage to a different voltage level that is higher than the battery voltage.6. The implantable medical device of claim 1 , wherein the electrical circuitry is configurable to form two second circuits with the coil claim 1 , wherein a first of the second circuits converts the battery voltage to a different voltage level that is lower than the ...

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24-04-2014 дата публикации

Intermediate Coupler to Facilitate Charging in an Implantable Medical Device System

Номер: US20140114373A1
Автор: Aghassian Daniel
Принадлежит:

An intermediate coupler is used to improve inductive coupling between an external charger and an implantable medical device having a battery requiring charging. The intermediate coupler comprises a coil (inductor) coupled to a capacitor, whose values are chosen to resonate at the frequency of the magnetic field emitted by the external charger. The intermediate coupler preferably contains no power source such as a battery, and can operate passively. When the intermediate coupler receives the magnetic field from the external charger, a current is induced in its coil, and the intermediate coupler generates its own magnetic field which is captured by the implantable medical device and used to charge its battery. 1. A system for charging a battery in an implantable medical device of a patient , comprising:an external charger comprising a first coil, wherein the first coil is configured to emit a first alternating current (AC) magnetic field; anda coupler comprising a second coil, wherein the second coil is configured to receive the first AC magnetic field and generate a second AC magnetic field in response; andan implantable medical device comprising a third coil and a battery,wherein the third coil in the implantable medical device is configured to receive the second AC magnetic field to charge the battery.2. The system of claim 1 , wherein the second coil has a second area claim 1 , the third coil has a third area claim 1 , and the second area is larger than the third area.3. The system of claim 1 , wherein the first AC magnetic field and the second AC magnetic field have the same frequency.4. The system of claim 1 , wherein the external charger is hand-holdable or body-wearable claim 1 , and portable.5. The system of claim 1 , wherein the external charger is stationary.6. The system of claim 1 , wherein the coupler is portable.7. The system of claim 1 , wherein the coupler is integrated into a home furnishing.8. The system of claim 1 , wherein the external charger is ...

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29-01-2015 дата публикации

TRANSCUTANEOUS POWER CONVEYANCE DEVICE

Номер: US20150032177A1
Автор: Mashiach Adi, Ruytjens Tim
Принадлежит:

Some embodiments of the present disclosure may include a device for conveying power from a location external to a subject to a location within the subject The device may include a flexible carrier, an adhesive on a first side of the carrier, a coil of electrically conductive material associated with the flexible carrier, and a mechanical connector extending from a second side of the carrier opposite the adhesive. The mechanical connector may be configured to be received by and retained by a receiver associated with a housing configured for mounting on the carrier. 115-. (canceled)16. A device for connection to a flexible adhesive patch configured to convey power from a location external to a subject to a location within the subject , the flexible adhesive patch including adhesive on one side thereof and a protrusion extending from a side thereof opposite the adhesive , the device comprising:a housing containing at least one processor and at least one coil of electrically conductive material, the at least one coil being configured for use in wirelessly transmitting power to an implant located at the location within the subject to modulate the branched fibers of the hypoglossal nerve associated with a genioglossus muscle of the subject, the at least one coil having a plurality of windings;a concavity within the housing, the concavity being configured to receive and retain the protrusion extending from the flexible adhesive patch, wherein at least a portion of a side of the housing and a top of the housing are exposed when the housing is mounted on the flexible adhesive patch.17. The device of claim 16 , wherein an electronic circuit is connected to the at least one processor contained within the housing.18. The device of claim 16 , wherein the housing includes a battery.19. The device of claim 16 , wherein the concavity includes a rim configured to engage flexible arms of the protrusion extending from the adhesive patch.20. The device of claim 16 , further comprising ...

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29-01-2015 дата публикации

DELIVERING SCHEDULED AND UNSCHEDULED THERAPY WITHOUT DETRIMENT TO BATTERY LIFE OR ACCURACY OF LONGEVITY PREDICTIONS

Номер: US20150032189A1
Автор: Colborn John C.
Принадлежит:

A method comprises applying a first open-loop electrical signal to a neural structure at a first rate. The method also comprises applying a closed-loop electrical signal to the neural structure in response to an event detection, thus causing an overall rate at which electrical stimulation is applied to the neural structure to exceed the first rate. The method further comprises applying a second open-loop electrical signal to a neural structure at a second rate that is lower than the first rate, thus causing the overall rate to be reduced to the first rate. 1. A method , comprising:applying a first open-loop electrical signal to a neural structure at a first charge delivery rate;applying a closed-loop electrical signal to the neural structure in response to an event detection, thus causing an overall charge delivery rate to the neural structure exceeding the first charge delivery rate; andapplying a second open-loop electrical signal to a neural structure at a second charge delivery rate that is lower than the first charge delivery rate, thus causing said overall charge delivery rate to approach the first charge delivery rate.2. The method of claim 1 , wherein said first open-loop electrical signal comprises a plurality of electrical pulse bursts having a duration defined by a first programmed on-time claim 1 , and separated by a first programmed off-time claim 1 ,and wherein applying said second open-loop electrical signal to said neural structure at the second charge delivery rate comprises waiting for an amount of time sufficient to cause said combined rate to equal said first rate between said application of the closed-loop electrical signal and resuming delivery of said first open-loop electrical signal.3. The method of claim 1 , wherein said first open-loop electrical signal comprises a plurality of programmed electrical pulse bursts having a duration defined by a first programmed on-time claim 1 , and separated by a first programmed off-time claim 1 , ...

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31-01-2019 дата публикации

Portable Composite Waveform Transcranial Electrical Stimulation System

Номер: US20190030336A1
Автор: Kwan Pui Tong
Принадлежит:

The present invention relates to a transcranial electrical stimulation (TES) system in that several sets of manipulated, pre-stored raw data are executed. TES signals are generated and output to user in terms of sessions. The output waveform in each singular session is a composite type and is designed mainly by means of Fourier Transform basis together with numerical analysis and mathematical curves fitting techniques. Hence, the electrical signals' frequencies, amplitudes and phase angles are varying during the time of application within just ONE singular session by one device. The kinds of variations in parameters such as frequencies, amplitudes and phase angles are tailor-made to the needs of improvement required in several brain disorders caused or related neurological disorders symptoms. With the help of the wearing design, the brain can be stimulated in dedicated positions such that the TES signals are continuously monitored by the unit. 1. A non-invasive method , comprising using Composite Waveform as a basis of generating Transcranial Electrical Stimulation (TES) signals that provides significance improvements in penetration power into a brain at a “safely controlled voltage-current level”.2. The method claim 1 , as recited in claim 1 , wherein: by using composite waveform claim 1 , a stimulation profile is pre-programmed at combined frequencies claim 1 , amplitudes and phase angles variations claim 1 , which means the profile is customized according to needs claim 1 , relevant profiles for individuals' needs are retrieved with and same TES signals are re-played again.3. The method claim 2 , as recited in claim 2 , wherein: “ONE SESSION” of stimulation possessing various AC signals in different frequencies & amplitudes claim 2 , DC signals as well by just one-time treatment profile claim 2 , there is no interruption of applied signals due to change of profile like those traditional equipment.4. The method claim 3 , as recited in claim 3 , wherein: improved ...

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31-01-2019 дата публикации

FAR FIELD TELEMETRY COMMUNICATION WITH A MEDICAL DEVICE DURING A RECHARGE SESSION WHERE A PRIOR PAIRING WITH THE MEDICAL DEVICE MAY NOT EXIST

Номер: US20190030348A1
Принадлежит:

Far field telemetry communications are conducted during recharge sessions between an external device and an implantable medical device. The two devices may not have been previously paired together for far field telemetry and may have been paired with other devices for far field telemetry during previous recharge sessions and/or programming sessions. Embodiments provide for temporary bonding of the two devices for far field telemetry during the recharge session. The implantable medical device of the recharge session may maintain a programming bond with an external device other than the external device conducting the recharge session. Safeguards against establishment of inadvertent programming sessions between the external device that has conducted a recharge session and implantable medical devices that may or may not be bonded to that external device are provided. 1. An implantable medical device , comprising:a memory storing an identifier and a programming session key;a recharge circuit;a battery coupled to the recharge circuit;a far field telemetry circuit; anda processor configured to receive a recharge session key from an external device, provide an identifier to the external device, receive recharge energy during a recharge session using the recharge circuit, exchange information related to the recharge session with the external device using the recharge key via the far field telemetry circuit while the programming session key remains stored in the memory, and at times other than during the recharge session exchange programming information with a second external device using the programming session key via the far field telemetry circuit.2. The implantable medical device of claim 1 , wherein the processor discontinues current and future use of the recharge session key upon termination of the recharge session.3. The implantable medical device of claim 1 , wherein the processor exchanges the identifier via the far field telemetry circuit.4. The implantable medical ...

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30-01-2020 дата публикации

PATIENT-INTERMEDIATED THERAPY MANAGEMENT

Номер: US20200030618A1
Принадлежит:

In some examples, controlling delivery of therapy includes using an implantable medical device comprising at least one electrode. Processing circuitry of a system comprising the device may receive, from an application running on a patient personal device, a patient request entered by the patient into the application. The processing circuitry may further determine, based on the patient request, a requested value of a therapy parameter, compare the requested value to information stored in a memory of the medical device system, the information indicating one or more allowable values of the therapy parameter, determine that the requested value is one of the allowable values based on the comparison of the requested value of the therapy parameter to the one or more allowable values, and control the implantable medical device to deliver cardiac pacing via the at least one electrode according to the requested value for a period of time. 1. A method for controlling delivery of therapy using an implantable medical device configured for implantation within a patient , the implantable medical device comprising at least one electrode and configured to deliver cardiac pacing to the patient via the at least one electrode , the method comprising , by processing circuitry of a medical device system comprising the implantable medical device:receiving, from an application running on a patient personal device, a patient request entered by the patient into the application, wherein the application runs on the patient personal device to enable the patient to interact with the medical device system, and receipt of the request from the application indicates that the request was made by the patient;determining, based on the patient request, a requested value of a therapy parameter according to which the implantable medical device is configured to deliver the cardiac pacing;comparing the requested value of the therapy parameter to information stored in a memory of the medical device system, ...

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11-02-2016 дата публикации

SYSTEMS AND METHODS FOR REDUCING OR ALTERING ORAL BACTERIA

Номер: US20160038734A1
Принадлежит:

A method and apparatus for the concurrent treatment of multiple oral diseases and defects while promoting general oral hygiene utilizing direct current electricity. Electrodes are used to deliver a direct current to the gingival tissues of a mouth in order to achieve a number of therapeutic, prophylactic, and regenerative benefits. These benefits include killing oral microbes, increasing oral vasodilation, reducing oral biofilm, improving oral blood circulation, reversing oral bone resorption, promoting oral osteogenesis, treating gum recession, and fostering gingival regeneration. Other benefits include the treatment of gingivitis, periodontitis, and oral malodor, and other systemic diseases correlated with oral pathogens. 1. A method comprising:placing a first electrode in physical contact with lingual gingival tissue in an animal mouth;placing a second electrode in physical contact with buccal gingival tissue in the animal mouth; and,conducting direct current electricity between the first and second electrodes to reduce a concentration of bacteria in the animal mouth.2. A method according to claim 1 , wherein the first and second electrodes are carried by a mouthpiece.3. A method according to claim 1 , wherein the animal is a human.4F. nucleatum, P. gingivalisS. oralis.. A method according to claim 3 , wherein the bacteria is at least one of claim 3 , and5. A method according to claim 4 , wherein the human has been diagnosed with a systemic disease.6. A method according to claim 5 , wherein the systemic disease is at least one of cardiovascular disease claim 5 , diabetes claim 5 , pyogenic liver disease claim 5 , osteomyelitis claim 5 , and arthritis.7. A method according to claim 4 , wherein the human is pregnant.8. A method comprising:placing a first electrode in physical contact with lingual gingival tissue in an animal mouth;placing a second electrode in physical contact with buccal gingival tissue in the animal mouth; and,conducting direct current ...

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05-02-2015 дата публикации

Insert Tool for Selectively Powering an Implant Unit

Номер: US20150039056A1
Автор: Mashiach Adi
Принадлежит:

An implant unit delivery tool is disclosed having an implant tool and an implant activator. The implant tool may be configured to retain an implant unit during an implantation procedure in which the implant unit is fixated to tissue. The implant activator may be associated with the implant tool. Additionally, the implant activator may be configured to selectively transfer power to the implant unit during the implantation procedure to cause modulation of at least one nerve in the body of a subject prior to final fixation of the implant unit to the tissue. 112-. (canceled)13. A method of testing the functionality of an implant unit , the method comprising:moving an implant activator from a first position to a second position on a delivery tool, prior to final fixation of an implant unit by the delivery tool; andtransferring power from the implant activator to the implant unit when the implant activator is in the second position,wherein transferring power to the implant unit causes modulation of at least one nerve in the body of a subject.14. The method of claim 13 , wherein power is wirelessly transferred from the implant activator to the implant unit.15. The method of claim 13 , wherein the implant activator includes a power source configured to supply the power to the implant unit.16. The method of claim 15 , wherein the power source is a battery.17. The method of claim 13 , wherein the second position is closer to the implant unit than the first position.18. The method of claim 13 , wherein moving the implant activator from the first position to the second position includes sliding the implant activator along a track on the delivery tool.19. The method of claim 18 , further including selectively activating the implant activator and causing the implant activator to move toward and away from the implant unit with a slidable engagement portion.20. The method of claim 13 , further including:determining that an implant location is suitable based on one or more patient ...

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09-02-2017 дата публикации

Control of bladder function using high frequency pacing

Номер: US20170036020A1
Принадлежит: Boston Scientific Scimed Inc

Systems and methods for the treatment of bladder conditions using direct electrical pacing are provided. The systems and methods generally apply high-frequency pacing stimuli directly to the bladder wall, from one or more of the inner and outer bladder surfaces.

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08-02-2018 дата публикации

MEDICAL DEVICE FOR TREATING CARDIAC ARRHYTHMIA

Номер: US20180036541A1
Принадлежит:

A medical device for treating cardiac arrhythmia is disclosed, including: a microprocessor () and a digital/analog module (). A MCU () configures the medical device to operate in a modified DVI (R) mode in which: when receiving a signal indicating the sensing of an atrial event by a sense control/amplification unit (), the MCU () sets a PANP interval and sends to a time control unit () a signal, controlling a first timing unit () to operate in a timing mode for a duration equal to a duration of the PANP interval; if a scheduled post-ventricular atrial escaping interval is to end at a time not within the PANP internal, the MCU () sends respective signals to a pacing control/generation unit () and the time control unit () to dictate the pacing control/generation unit () to deliver a pacing pulse and control a second timing unit () to use a PAVI as a next ventricular escape interval; and if the scheduled post-ventricular atrial escaping interval is to end within the PANP interval, the MCU () sends a signal to the time control unit (), controlling the second timing unit () to use the PAVI as the next ventricular escape interval. 1. A medical device for treating cardiac arrhythmia , comprising a microprocessor and a digital/analog module in connection with the microprocessor , the microprocessor comprising a main control unit and a time control unit , the digital/analog module comprising a pacing control/generation unit and a sense control/amplification unit , the time control unit at least comprising a first timing unit and a second timing unit , whereinthe main control unit is configured to cause the medical device to operate in a modified DVI (R) mode in which:when receiving a signal indicating sensing of an atrial event by the sense control/amplification unit, the main control unit sets a post-atrial non-pacing interval and sends a signal to the time control unit, controlling the first timing unit to operate in a timing mode for a duration equal to a duration of the ...

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24-02-2022 дата публикации

COCHLEAR IMPLANT SYSTEM WITH OPTIMIZED FRAME CODING

Номер: US20220054836A1
Принадлежит: OTICON MEDICAL A/S

The disclosure relates to a cochlear implant system, and more particularly, the disclosure relates to a processor unit which includes a switching mean configured to switch between using a fixed stimulation frame onset or a variable stimulation frame onset for frame coding a plurality of stimulation pulses into a one or more stimulation frames. 1. A cochlear implant system comprising.a receiving unit configured to receive an acoustical signal and transmit an audio signal based on the acoustical signal,a processor unit configured to receive and divide the audio signal into a plurality of band limited audio signals and to generate a plurality of stimulation pulses based on sampling of the plurality of band limited audio signals, and wherein each of the plurality of band limited audio signals is sampled with a temporal onset, and one or more audio components are determined for each of the sampled plurality of stimulation pulses,an electrode array including a plurality of electrodes,and wherein the processor unit includes a switching mean configured to switch between using a fixed stimulation frame onset or a variable stimulation frame onset for frame coding the plurality of stimulation pulses into one or more stimulation frames, wherein the switching mean is configured to switch between the fixed stimulation frame onset and the variable stimulation frame onset based on the one or more audio components, and wherein the electrode array is configured to stimulate auditory nerves of a user of the cochlear implant system based on the frame coded plurality of stimulation pulses.2. A cochlear implant system according to claim 1 , when using the fixed stimulation frame onset claim 1 , the stimulation frame onset is the same between each of the one or more stimulation frames claim 1 , and when using the variable stimulation frame onset claim 1 , the stimulation frame onset is varying between each of the one or more stimulation frames.3. A cochlear implant system according to ...

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06-02-2020 дата публикации

TECHNIQUES FOR HEART MUSCLE REMODELING USING A CARDIAC PACEMAKER AND RELATED SYSTEMS AND METHODS

Номер: US20200038663A1
Автор: Meyer Markus

According to some aspects, a cardiac pacemaker for implantation within a subject is provided, the pacemaker including a housing, at least one sensor configured to detect an activity level of the subject, and at least one processor coupled to the sensor configured to detect inactivity of the subject based on output from the at least one sensor, produce a first signal configured to increase the heart rate of the subject to a first heart rate during a first time period, wherein the first heart rate is above a resting heart rate and below 100 beats per minute, and in response to determining that the first time period has elapsed, producing a second signal configured to increase the heart rate of the subject to a second heart rate during a second time period, wherein the second heart rate is between 100 and 140 beats per minute. 1. A cardiac pacemaker for implantation within a subject , the pacemaker comprising:a housing;at least one sensor configured to detect an activity level of the subject and produce output indicating of the activity level; and detecting inactivity of the subject based on the output from the at least one sensor;', 'when said inactivity of the subject is detected, producing a first signal configured to increase the heart rate of the subject to a first heart rate during a first time period, wherein the first heart rate is above a resting heart rate and below 100 beats per minute; and', 'in response to determining that the first time period has elapsed, producing a second signal configured to increase the heart rate of the subject to a second heart rate during a second time period, wherein the second heart rate is between 100 and 140 beats per minute., "at least one processor inside the housing, the at least one processor being responsive to the output from the sensor and configured to stimulate a remodeling of the subject's heart muscle through modulation of the subject's heart rate by:"}2. The cardiac pacemaker of claim 1 , wherein the at least one ...

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18-02-2021 дата публикации

VOLTAGE CONVERTING DEVICE

Номер: US20210046320A1
Автор: Tan Min
Принадлежит: Shenzhen Dansha Technology Co., Ltd.

A voltage converter for medical devices includes a switch capacitor converter core including a plurality of power transistor switches configured to receive an input voltage and output an output voltage; a switch driver connected with the switch capacitor converter core and configured to turn on corresponding power transistor switches in the switch capacitor converter core so as to supply power to a load receiving the output voltage; a switch signal router connected with the switch driver and configured to selectively transmit signals required by the switch driver; a gain selection decoder connected with the switch signal router; a gain controller connected with the gain selection decoder, the gain selection decoder being configured to decode gain selection instructions transmitted from the gain controller; an input adjusting device connected with the gain controller and configured to receive the input voltage and a reference voltage, to indicate relationship between the input voltage and the reference voltage, and to transmit the relationship to the gain controller; and an output adjusting device connected with the gain controller and configured to receive the output voltage and the reference voltage, to indicate relationship between the output voltage and the reference voltage, and to transmit the relationship to the gain controller. 1. A voltage converting device , the voltage converting device comprising:a switch capacitor converter core comprising a plurality of power transistor switches configured to receive an input voltage and output an output voltage;a switch driver connected with the switch capacitor converter core and configured to turn on corresponding power transistor switches in the switch capacitor converter core so as to supply power to a load receiving the output voltage;a switch signal router connected with the switch driver and configured to selectively transmit signals required by the switch driver;a gain selection decoder connected with the ...

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16-02-2017 дата публикации

IMPLANTABLE PULSE GENERATOR THAT GENERATES SPINAL CORD STIMULATION SIGNALS FOR A HUMAN BODY

Номер: US20170043164A1
Принадлежит:

An implantable pulse generator (IPG) that generates spinal cord stimulation signals for a human body has a programmable signal generator that can generate the signals based on stored signal parameters without any intervention from a processor that controls the overall operation of the IPG. While the signal generator is generating the signals the processor can be in a standby mode to substantially save battery power. 1. A method of generating spinal cord stimulation signals for a human body by an implantable pulse generator (IPG) including a processor and a programmable signal generator , the method comprising:transmitting, by a treatment control module executed by the processor, one or more stimulation signal parameters to the programmable signal generator;placing, by the treatment control module, the processor in a standby mode, wherein the programmable signal generator generates the one or more stimulation signals without intervention from the processor while the processor is in the standby mode.2. The method of claim 1 , further comprising wirelessly receiving through a transceiver module a command from a remote control to power up the processor from the standby mode.3. The method of claim 1 , wherein the step of placing the processor in the standby mode causes a master clock of the processor to be disabled.4. The method of claim 1 , wherein the generation of the one or more stimulation signals include concurrently generating stimulation signal patterns for a plurality of programmable channels with each channel capable of being associated with at least two electrodes among a plurality of electrodes and with each channel representing a stimulation pattern of the associated electrodes.5. The method of claim 4 , wherein each channel is associated with one or more stored signal parameters claim 4 , and wherein the one or more stored signal parameters include:a channel length; anda rising edge time of a pulse in the stimulation pattern associated each channel.6. The ...

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15-02-2018 дата публикации

MANAGING RECHARGE POWER FOR IMPLANTABLE MEDICAL DEVICES

Номер: US20180043167A1
Принадлежит:

Devices, systems, and techniques for estimating energy transfer to tissue of a patient during battery charging for an implantable medical device are disclosed. Implantable medical devices may include a rechargeable power source that can be transcutaneously charged. An external charging device may calculate an estimated energy transfer to tissue of the patient that may include a resistive heat loss from the rechargeable power source and/or electromagnetic energy transfer directly to tissue. Based on the estimated energy transfer, the external charging device may select a power level for charging of the rechargeable power source. In one example, the charging device may select a high power level when the estimated energy transfer has not exceeded an energy transfer threshold and select a low power level when the estimated energy transfer has exceeded the energy transfer threshold. 115-. (canceled)16. A method for controlling charging of a rechargeable power source of an implantable medical device in a patient , the method comprising:determining, by processing circuitry, an estimated power stored in the rechargeable power source during charging of the rechargeable power source, the estimated power stored being separate from a resistive heat loss of the rechargeable power source during charging of the rechargeable power source;calculating, by the processing circuitry, an estimated energy transfer to tissue of the patient during charging of the rechargeable power source, the estimated energy transfer including the resistive heat loss of the rechargeable power source; andcontrolling, by the processing circuitry and based on the estimated energy transfer to the tissue, energy generation by a primary coil of an external charging device for charging the rechargeable power source via a secondary coil of the implantable medical device.17. The method of claim 16 , wherein determining the estimated power stored in the rechargeable power source comprises:determining a charge ...

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07-02-2019 дата публикации

Parametric Resonator for Electrical Transduction

Номер: US20190044459A1
Принадлежит:

A parametric resonator can be driven by varying a parameter of a modulated capacitor or other externally powered type device to achieve transduction. Conventionally, externally powered type devices generally require an external power source or a static charge to achieve transduction. By pumping the parameter of the device at a frequency that is about twice the resonance frequency, and an amplitude that is above a threshold, however parametric resonance can be generated and sustained without requiring an external power source or charge to be applied to the device. 1. An electronic device configured to sustain an electrical signal responsive to varying a capacitance of a capacitor without requiring a permanent charge or a voltage applied to the capacitor.2. The electronic device of further configured to generate the electrical signal responsive to varying the capacitance without requiring a permanent charge or a voltage applied to the capacitor.3. The electronic device of claim 1 , wherein the capacitance is variable in response to a mechanical force.4. The electronic device of claim 1 , further configured to sustain the electrical signal responsive to varying the capacitance at frequency that is between about 16 kHz and 100 MHz.5. The electronic device of claim 1 , further configured to oscillate the electrical signal at an electrical resonance frequency responsive to varying the capacitance at a pump frequency that is equal to about twice the electrical resonance frequency.6. The electronic device of claim 1 , further configured to sustain the electrical signal responsive to varying the capacitance of the capacitor between a first capacitance that is equal to an average capacitance plus a change in capacitance and a second capacitance that is equal to the average capacitance minus the change in capacitance claim 1 , wherein the change in capacitance is equal to or greater than about twice the average capacitance divided by a quality factor of the electronic device.7 ...

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25-02-2016 дата публикации

SYSTEMS AND METHODS FOR ELECTRICAL STIMULATION OF SPHENOPALATINE GANGLION AND OTHER BRANCHES OF CRANIAL NERVES

Номер: US20160051820A1
Принадлежит:

Devices, systems and methods are disclosed for modulating cranial nerves, such as the sphenopalatine ganglion, to treat a medical condition of a patient, such as cluster headache. A stimulation device comprising a dipole antenna is advanced transnasally to a target site at or adjacent to the nasopharyngeal mucosa posterior to the middle turbinate. Electrical impulses are applied through one or more electrodes in the stimulation device to the target nerve sufficient to modulate the nerve and treat the medical condition. 1. A system for modulating a cranial nerve to treat a medical condition of a patient comprising:a stimulation device comprising one or more electrodes configured for advancement through a nostril of a patient to a target site adjacent to or near the cranial nerve and one or more dipole antennas;a power source configured for positioning in proximity to a patient and further configured to transmit electrical energy wirelessly to the stimulation device at the target site, wherein the one or more dipole antennas are configured for receiving the electrical energy from the power source at the target site; anda pulse generator coupled to the power source and the stimulation device and configured to apply one or more electrical impulses to the electrodes sufficient to modulate the cranial nerve.2. The system of claim 1 , wherein the cranial nerve is a sphenopalatine ganglion.3. The system of claim 1 , wherein the medical condition is primary headache.4. The system of claim 1 , wherein the medical condition is cluster headache.5. The system of claim 1 , wherein the dipole antenna is selected from at least one of the following: a helical antenna claim 1 , a coiled antenna claim 1 , and a meandering antenna.6. The system of claim 1 , wherein the one or more dipole antennas are configured for receiving plane wave electromagnetic energy.7. The system of claim 6 , wherein the received plane wave electromagnetic energy comprises frequencies in the range of about 0.3 ...

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25-02-2016 дата публикации

MEDICAL IMPLANT

Номер: US20160051824A1
Принадлежит: BIOTRONIK SE & Co. KG

A medical implant including an implant body for insertion into a human and/or animal body. The implant body includes at least one first and at least one second contact portion, wherein the at least one first and the at least one second contact portions contact two tissue regions performing a relative movement with respect to one another. The at least one first and the at least one second contact portions are movable relative to one another, wherein a relative movement of the contact portions may be converted into an electrical signal. 1. A medical implant for insertion into the human and/or animal body , comprising:an implant body, wherein the implant body comprises at least one first and at least one second contact portion;wherein the at least one first and the at least one second contact portions are configured to contact two tissue regions performing a relative movement with respect to one another, and,wherein the at least one first and the at least one second contact portions are movable relative to one another and a relative movement of the at least one first and the at least one second contact portions is converted into an electrical signal.2. The medical implant as claimed in claim 1 , wherein one or more of the at least one first contact portion and the at least one second contact portion is coupled directly or indirectly to an electric generator in or on the implant body.3. The medical implant as claimed in claim 1 , wherein the at least one first contact portion comprises a fixing element to fasten the implant body to one of the two tissue regions.4. The medical implant as claimed in claim 1 , wherein one or more of the at least one first contact portion and the at least one second contact portion is mechanically connected to a movable element of a generator provided in or on the implant body.5. The medical implant as claimed in claim 1 , wherein the implant body comprises a number of parts claim 1 , wherein at least two parts of the number of parts are ...

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25-02-2021 дата публикации

VOLTAGE CONVERTER FOR MEDICAL DEVICES

Номер: US20210052905A1
Автор: Tan Min
Принадлежит: Shenzhen Dansha Technology Co., Ltd.

A voltage converter for medical devices includes a switch capacitor converter core including a plurality of power transistor switches configured to receive an input voltage and output an output voltage; a switch driver connected with the switch capacitor converter core and configured to turn on corresponding power transistor switches in the switch capacitor converter core so as to supply power to a load receiving the output voltage; a switch signal router connected with the switch driver and configured to selectively transmit signals required by the switch driver; a gain selection decoder connected with the switch signal router; a gain controller connected with the gain selection decoder, the gain selection decoder being configured to decode gain selection instructions transmitted from the gain controller; an input adjusting device connected with the gain controller and configured to receive the input voltage and a reference voltage, to indicate relationship between the input voltage and the reference voltage, and to transmit the relationship to the gain controller; and an output adjusting device connected with the gain controller and configured to receive the output voltage and the reference voltage, to indicate relationship between the output voltage and the reference voltage, and to transmit the relationship to the gain controller. 1. A voltage converter for medical devices , the voltage converter comprising:a switch capacitor converter core comprising a plurality of power transistor switches configured to receive an input voltage and output an output voltage;a switch driver connected with the switch capacitor converter core and configured to turn on corresponding power transistor switches in the switch capacitor converter core so as to supply power to a load receiving the output voltage;a switch signal router connected with the switch driver and configured to selectively transmit signals required by the switch driver;a gain selection decoder connected with the ...

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25-02-2021 дата публикации

EXTERNAL ENERGY TRANSFER SYSTEM FOR AN IMPLANTABLE MEDICAL DEVICE AND METHOD THEREFOR

Номер: US20210052906A1
Принадлежит:

User interface for external power source, recharger, for an implantable medical device. At least some of patient controls and display icons of an energy transfer unit are common with at least some of the patient controls and the display icons of a patient control unit. An energy transfer unit is operable by the patient with less than three operative controls to control energy transfer from the external energy transfer unit to the implantable medical device. An external antenna having a primary coil can inductively transfer energy to a secondary coil of the implantable medical device when the external antenna is externally placed in proximity of the secondary coil. An energy transfer unit has an external telemetry coil allowing the energy transfer unit to communicate with the implantable medical device through the internal telemetry coil in order to at least partially control the therapeutic output of the implantable medical device. 1. An implantable medical device system , comprising:an implantable medical device having a secondary coil, said implantable medical device being configured to communicate transcutaneously using telemetry; andan external unit comprising a primary coil configured to inductively transfer energy to said secondary coil of said implantable medical device when said primary coil is externally placed in proximity of said secondary coil and said external unit drives said primary coil;said external unit being configured to communicate with said implantable medical device by way of telemetry during the process of transferring, via said primary coil, energy to said implantable medical device;wherein said external unit is configured to time division multiplex between said telemetry and said process of transferring energy.2. The implantable medical device system as m wherein said external unit comprises circuitry and wherein said circuitry of said external unit drives said primary coil to inductively transfer energy to said implantable medical device.3 ...

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23-02-2017 дата публикации

EXTERNAL AND IMPLANTABLE COILS FOR AUDITORY PROSTHESES

Номер: US20170050023A1
Принадлежит:

Certain medical devices, such as auditory prostheses, have an implantable portion and an external portion. The implantable portion and external portion each include a transmission/receiver coil that communicates signals between the two portions. The implanted coil is implanted about the ear canal while the external coil is disposed about the pinna or in the ear canal itself. The proximity of the two coils allows for signal transmission between the implantable and external portions. 1. A system comprising: a housing;', 'a stimulator unit disposed within the housing for generating an stimulus;', 'a flexible sleeve connected to the housing; and', 'a wire disposed within the sleeve, wherein the wire comprises a connector disposed at an end of the wire; and, 'an implantable portion includingat least one transmission element extending from the implantable portion for transmitting the stimulus.2. The system of claim 1 , wherein the stimulator unit comprises a port for detachably receiving the connector claim 1 , and wherein when the connector is received in the port claim 1 , the sleeve defines an annulus.3. The system of claim 1 , further comprising: an external housing disposed remote from the implantable housing; and', 'an external coil configured to communicate with the implantable coil, 'an external portion includingwhen disposed proximate a head of a recipient.4. The system of claim 3 , wherein the external housing comprises a behind-the-ear portion of an auditory prosthesis claim 3 , and wherein the external coil is sized to be disposed about a pinna of the recipient.5. The system of claim 3 , wherein the external housing comprises an in-the-ear portion of an auditory prosthesis claim 3 , and wherein the external coil is sized to be disposed about a pinna of the recipient.6. The system of claim 3 , wherein the external housing comprises an in-the-ear portion of an auditory prosthesis claim 3 , and wherein the external coil is disposed within the in-the-ear portion.7 ...

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22-02-2018 дата публикации

FULLY IMPLANTABLE MODULAR COCHLEAR IMPLANT SYSTEM

Номер: US20180050198A1
Принадлежит:

Cochlear implant systems can include a cochlear electrode, a stimulator in electrical communication with the cochlear electrode, and a signal processor in communication with the stimulator. The signal processor can receive an input signal from an input source and output a stimulation signal to the stimulator based on the received input signal and a transfer function of the signal processor. The signal processor can be connected to the stimulator via a first detachable connector configured to detachably connect and provide communication between the signal processor and the stimulator. The signal processor can be connected to the input source via a second detachable connector configured to detachably connect and provide communication between the signal processor and the input source. A modular signal processor can be detached from the stimulator and the input source for repair or replacement. 1. A modular cochlear implant system comprising:a cochlear electrode;a stimulator in electrical communication with the cochlear electrode;a signal processor in communication with the stimulator;an input source in communication with the signal processor; anda first detachable connector configured to detachably connect the signal processor and the stimulator and to provide communication between the signal processor and the stimulator when attached; whereinthe signal processor is configured to receive an input signal from the input source and output a stimulation signal to the stimulator based on the received input signal and a transfer function of the signal processor;the stimulator provides an electrical stimulus to the cochlear electrode based on the stimulation signal; andthe cochlear electrode, the stimulator, the signal processor, and the input source are fully implantable into a patient.2. The implant system of claim 1 , further comprising a second detachable connector configured to detachably connect the signal processor and the input source and to provide communication ...

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26-02-2015 дата публикации

NERVE ROOT STIMULATOR AND METHOD FOR OPERATING NERVE ROOT STIMULATOR

Номер: US20150057720A1
Автор: KO Kwang Chon
Принадлежит: LUTRONIC CORPORATION

A nerve root stimulator, according to the present invention, comprises: a body which is installed at the spinal nerve root inside the human body; an antenna, which is provided on the body, for receiving a wireless frequency that is irradiated from outside of the human body; a power generation unit for generating power by using the wireless frequency that is received by the antenna; and electrodes for electrically stimulating the spinal nerve root by using the power that is generated by the power generation unit. 1. A nerve root stimulator , comprising:a body part installed in a spinal nerve root of a human body;an antenna provided in the body part and receiving a radio frequency irradiated outside the human body;a power generating unit generating power by using the radio frequency received to the antenna; andan electrode electrically stimulating the spinal nerve root by using the power generated in the power generating unit.2. The nerve root stimulator of claim 1 , wherein the power generating unit comprises a rectifying unit rectifying the radio frequency received to the antenna to a direct current and a switching unit controlling the power provided to the electrode.3. The nerve root stimulator of claim 1 , wherein a plurality of electrodes is provided claim 1 , and the power generating unit provides power having different sizes to the plurality of electrodes.4. The nerve root stimulator claim 1 , further comprising:a demodulator demodulating a transmission signal at the radio frequency received to the antenna and a control unit controlling an operation of the power generating unit by using data transferred from the demodulator.5. The nerve root stimulator of claim 1 , wherein a plurality of antennas extended in a length direction of the body part is included.6. A method for operating a nerve root stimulator claim 1 , comprising:receiving a radio frequency by a nerve root stimulator installed in a spinal nerve root of a human body;generating power by using the ...

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10-03-2022 дата публикации

IMPLANTABLE APPARATUS

Номер: US20220072318A1
Принадлежит:

Implantable apparatuses are provided, where the implantable apparatus includes a first electrode, a second electrode, an electrode signal transceiver connected to the first electrode and the second electrode, an antenna, a wireless power receiver connected to the antenna, and a conductor case configured to protect the electrode signal transceiver and the wireless power receiver. The antenna be spaced apart from the conductor case and encloses the conductor case, and a plane in which the antenna is disposed is at a same level or at a higher level than a top surface of the conductor case. 1. An implantable apparatus comprising:a first electrode;a second electrode;an electrode signal transceiver connected to the first electrode and the second electrode;an antenna;a wireless power receiver connected to the antenna; anda conductor case configured to protect the electrode signal transceiver and the wireless power receiver,wherein the antenna is spaced apart from the conductor case and encloses the conductor case, and a plane in which the antenna is disposed is at a same level or at a higher level than a top surface of the conductor case.2. The implantable apparatus of claim 1 , further comprising:ferrite disposed between the conductor case and the antenna.3. The implantable apparatus of claim 1 , whereinthe antenna is connected via a feed-through to the wireless power receiver, andthe antenna is electrically insulated from the conductor case.4. The implantable apparatus of claim 3 , wherein the feed-through comprises a conductive wire covered with an insulator.5. The implantable apparatus of claim 4 , wherein the insulator is fastened in a hole claim 4 , and the conductive wire is connected to the antenna and a circuit in the conductor case.6. The implantable apparatus of claim 1 , further comprising:an insulator case configured to protect the first electrode, the second electrode, the antenna, and the conductor case,wherein the insulator case is configured to fix the ...

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03-03-2016 дата публикации

Matrix-Coded AED Maintenance

Номер: US20160058996A1
Принадлежит:

A status monitoring function that simplifies the process of collecting status information for medical devices in a medical device system. Matrix codes are used to associate a medical device with a location. A maintenance application transmits the association information to a centralized tracking system. Status information about the medical device is also transmitted to the centralized tracking system from the maintenance application. 1. A medical device system , comprising:one or more medical devices, each medical device having an associated location at which the medical device is intended to reside, the medical device having a first matrix code encoded with status information about the medical device, the associated location having a second matrix code encoded with location information, the medical device and the associated location being co-located;a tracking system configured to maintain information about an operability status of the medical device system; anda maintenance application configured to scan the first matrix code and the second matrix code, to decode the information encoded within the first matrix code and the second matrix code, and to transmit the information to the tracking system.2. The medical device system recited in claim 1 , wherein the medical device comprises a portable external defibrillator.3. The medical device system recited in claim 1 , wherein the first matrix code comprises a static two dimensional code encoded with the status information.4. The medical device system recited in claim 1 , wherein the first matrix code comprises a dynamically-generated two dimensional code encoded with the status information.5. The medical device system recited in claim 4 , wherein at least a portion of the status information is discovered through one or more tests performed by the medical device and encoded into the dynamically-generated two dimensional code.6. The medical device system recited in claim 1 , wherein the associated location comprises ...

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03-03-2016 дата публикации

Charging System for an Implantable Medical Device Employing Magnetic and Electric Fields

Номер: US20160059021A1
Принадлежит:

A base station for passively recharging a battery in an implant without patient involvement is disclosed. The base station can be hand held or may comprise equipment configured to be placed at a fixed location, such as under a bed, on or next to a wall, etc. The base station can generate electric and magnetic fields (E-field and B-field) that couple with an antenna and a receiving coil within the implant to generate a charging current for charging the implant's battery. No handling or manipulation on part of the patient is necessary; the implant battery is passively charged whenever the patient is within range of either the magnetic or electric charging fields generated by base station. Charging using the B-field occurs when the IPG is at a relatively short distance from the base station, while charging using the E-field occurs at longer distances. 1. An implantable medical device , comprising:a first antenna configured to receive an electric field for powering the implantable medical device;a second antenna configured to receive a magnetic field for powering the implantable medical device; andcontrol circuitry configured to determine whether either or both of the electric field and the magnetic field have been received at the first or second antennas respectively, and for issuing at least one control signal enabling powering the implantable medical device either by the electric field or the magnetic field.2. The device of claim 1 , further comprising a first rectifier coupled to the first antenna for producing a first DC voltage claim 1 , and a second rectifier coupled to the second antenna for producing a second DC voltage.3. The device of claim 2 , wherein the control circuitry is configured to determine whether either or both of the electric field and the magnetic field have been received at the first or second antennas respectively using the first and second DC voltages.4. The device of claim 2 , further comprising charging circuitry claim 2 , wherein the ...

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21-02-2019 дата публикации

IMPLANTABLE NEUROMODULATION SYSTEM FOR CLOSED-LOOP STIMULATION AND RECORDING SIMULTANEOUSLY AT MULTIPLE BRAIN SETS

Номер: US20190054295A1
Принадлежит:

The present disclosure relates to a modular system for deep brain stimulation (DBS) and electrocorticography (ECoG). The system may have an implantable neuromodulator for generating electrical stimulation signals adapted to be applied to a desired region of a brain via an attached electrode array. An aggregator module may be used for collecting and aggregating electrical signals and transmitting the electrical signals to the neuromodulator. A control module may be used which is in communication with the aggregator module for controlling generation of the electrical signals and transmitting the electrical signals to the aggregator. 1. A modular system for deep brain stimulation (DBS) and electrocorticography , comprising:an implantable neuromodulator configured to generate electrical stimulation signals adapted to be applied to a desired region of a brain via an electrically coupled electrode array;an aggregator module configured to be at least one of either carried on a person or implanted in a bodypart of the person, and including implantable electrical connections for collecting and aggregating electrical signals and transmitting the electrical signals to the neuromodulator; anda control module in communication with the aggregator module for controlling generation of the electrical signals and transmitting the electrical signals to the aggregator module.2. The system of claim 1 , wherein the neuromodulator is connected to the electrode array via an electrical cable claim 1 , and wherein the electrode array forms a planar configuration electrode array.3. The system of claim 1 , wherein the neuromodulator is connected to the electrode array via an electrical cable claim 1 , and wherein the electrode array comprises a cylindrical configuration electrode array.4. The system of claim 1 , wherein the neuromodulator includes a multiplexer for distributing electrical signals to and from various units of the electrodes.5. The system of claim 1 , wherein the aggregator ...

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02-03-2017 дата публикации

MACHINE LEARNING TO OPTIMIZE SPINAL CORD STIMULATION

Номер: US20170056642A1
Принадлежит:

An example of a system may include a processor and a memory device comprising instructions, which when executed by the processor, cause the processor to: access a patient metric of a subject; use the patient metric as an input to a machine learning algorithm, the machine learning algorithm to search a plurality of neuromodulation parameter sets and to identify a candidate neuromodulation parameter set of the plurality of neuromodulation parameter sets, the candidate neuromodulation parameter set designed to produce a non-regular waveform that varies over a time domain and a space domain; and program a neuromodulator using the candidate neuromodulation parameter set to stimulate the subject. 1. A system comprising:a processor; and access a patient metric of a subject;', 'use the patient metric as an input to a machine learning algorithm, the machine learning algorithm to search a plurality of neuromodulation parameter sets and identify a candidate neuromodulation parameter set of the plurality of neuromodulation parameter sets, the candidate neuromodulation parameter set designed to produce a non-regular waveform that varies over a time domain and a space domain; and', 'program a neuromodulator using the candidate neuromodulation parameter set to stimulate the subject., 'a memory device comprising instructions, which when executed by the processor, cause the processor to2. The system of claim 1 , wherein the subject is a patient.3. The system of claim 1 , wherein the subject is an animal from a preclinical trial.4. The system of claim 1 , wherein the machine learning algorithm comprises a genetic algorithm.5. The system of claim 1 , wherein the machine learning algorithm comprises a neural network.6. The system of claim 1 , wherein the system is a cloud-based system claim 1 , and wherein the instructions to provide the candidate neuromodulation parameter set comprise instructions to transmit the candidate neuromodulation parameter set to a client device of the cloud- ...

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02-03-2017 дата публикации

SYSTEMS AND METHODS FOR TREATING SHOULDER PAIN RELATED TO SUBACROMIAL IMPINGEMENT SYNDROME

Номер: US20170056645A1
Принадлежит:

Systems and methods are provided for treating chronic pain occurring secondarily to subacromial impingement syndrome in a human body. A system is provided to deliver percutaneous electrical stimulation through at least one electrode to neurological motor points of the posterior and middle deltoid muscles to mediate such pain. One-time, continued and/or periodic dosing of treatment methods according to the present invention may result in a change to central nervous system maladaptive neuroplasticity. 1. A method comprising the steps of:placing an electrode in subepidermal tissue of a human; anddelivering electrical stimulation through the electrode,wherein, after the delivering step, a level of pain perceived by the human, wherein the pain was caused by or occurring secondarily to subacromial impingement syndrome, is reduced.2. A method according to claim 1 , wherein during the delivering step claim 1 , a level of pain perceived by the human claim 1 , wherein the pain was caused by or occurring secondarily to subacromial impingement syndrome claim 1 , is reduced. This application claims the benefit of co-pending U.S. Provisional Patent Application No. 61/419,537, filed 3 Dec. 2010, and entitled “Systems and Methods for Treatment of Pain caused by Subacromial Impingement,” which is incorporated by reference herein in its entirety.This application also claims the benefit of co-pending U.S. Provisional Patent Application No. 61/540,934, filed 29 Sep. 2011, and entitled “Systems and Methods for Treating Shoulder Pain Related to Subacromial Impingement Syndrome,” which is incorporated by reference herein in its entirety.This application is also a continuation in part cf co-pending U.S. Nonprovisional patent application Ser. No. 13/04,616, filed 27 Apr. 2011, and entitled “Systems and Methods for Percutaneous Electrical Stimulation,” which claims the benefit of U.S. Provisional Patent Application 61/343,325, filed 27 Apr. 2010, and entitled “Systems and Methods for ...

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02-03-2017 дата публикации

IMPLANTABLE PULSE GENERATOR THAT GENERATES SPINAL CORD STIMULATION SIGNALS FOR A HUMAN BODY

Номер: US20170056662A1
Принадлежит:

An implantable pulse generator (IPG) that generates spinal cord stimulation signals for a human body includes a timing generator and high frequency generator. The timing generator generates timing signals that represent stimulation signals for multiple channels. The high frequency generator determines whether to modulate the timing signals and modulates them at a burst frequency according to stored burst parameters if the decision is yes. As such, the IPG provides the ability to generate both the low frequency and high frequency stimulation signals in different channels according to user programming. 1. A method of generating spinal cord stimulation signals for a human body , comprising:storing in control registers stimulation signal parameters for a plurality of channels with each channel capable of being associated with at least two electrodes among a plurality of electrodes, each channel representing a stimulation signal pattern of the associated electrodes, the signal parameters including burst parameters;generating timing signals representing stimulation signals for the plurality of channels according to the stored signal parameters;determining whether to modulate the timing signals received from the timing generator; andif it is determined that the timing signals are to be modulated, modulating the received timing signals at a burst frequency according to the stored burst parameters.2. The method of claim 1 , wherein if it is determined that the timing signals are not to be modulated claim 1 , outputting the received timing signals whose frequency is unaltered.3. The method of claim 1 , further comprising:selecting the burst parameters associated with an active channel among the plurality of channels, wherein the step of modulating includes modulating the received timing signals according to the selected burst parameters.4. The method of claim 1 , further comprising:transmitting, by a processor, the stimulation signal parameters to the control registers; ...

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04-03-2021 дата публикации

AUTONOMOUS IMPLANTABLE MEDICAL DEVICE TUNING

Номер: US20210060347A1
Автор: Meskens Werner
Принадлежит:

Presented herein are implantable medical devices that comprise an implantable portion having a resonant tank circuit that is used to receive signals from one or more external devices. The resonant tank circuit is configured to operate at first and second resonant frequencies, where the first resonant frequency is optimized to exchange data with, and potentially receive operating power from, an external device, while the second resonant frequency is optimized to receive charging power. In certain embodiments, upon initiating operation of the implantable portion with at least one external device, the implantable portion is configured to force tune the resonant tank circuit to the first resonant frequency. That is, when the resonant tank circuit first begins receiving signals from an external device, the signals received at the resonant tank circuit are used to initially tune the resonant tank circuit to the first resonant frequency. 120-. (canceled)21. An implantable component , comprising:a resonant circuit including an implantable coil and at least one switch, wherein, at least upon initial operation of the implantable component, the at least one switch is driven by energy transferred to the resonant circuit so as to initially force tune the resonant circuit to a first frequency.2220. The implantable component of claim , further comprising:an implant controller connected to the at least one switch and configured to subsequently selectively activate the at least one switch to override the initial force tuning of the resonant circuit to the first frequency such that the resonant circuit is selectively tuned to a second frequency.23. The implantable component of claim 21 , further comprising a rechargeable battery claim 21 , wherein the second frequency is a frequency that configures the resonant circuit to receive charging power via the implantable coil when recharging the rechargeable battery claim 21 , and wherein the first frequency is different from the second ...

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02-03-2017 дата публикации

Controlled Stimulation Delivery From Neurostimulator

Номер: US20170056676A1

A system for providing neurostimulation includes an external device (“external exciter”) and an implanted device. The external exciter includes an energy source which inductively powers the implanted device. Examples of such external exciters include devices having at least one of: ultrasonic transducers, Radio Frequency (RF) transmitters, and solar cells. The implanted device includes circuitry that limits its maximum energy output to a predetermined saturation threshold such that excess stimulation from the external exciter does not raise the output of the implanted device beyond the saturation threshold. The output signal of the external exciter is then pulse-width modulated in order to produce a desired amount of output stimulation from the implanted device to stimulate the bioelectrically excitable tissue at a desired level. 1. A system for stimulating an electrode configured to deliver an electrical stimulation to tissue of a subject , comprising: an energy acquisition device;', 'a voltage limiting device connected to the energy acquisition device;', 'an electrode connected to the voltage limiting device; and, 'an implantable device, the implantable device includingan exciter that is physically unconnected to the energy acquisition device and configured to radiate a pulse width modulated excitation signal to the energy acquisition device of the implantable device.2. The system of claim 1 , wherein the energy acquisition device includes at least one of a dipole antenna and a piezoelectric material.3. The system of claim 1 , wherein the exciter includes at least one of a radio frequency transmitter claim 1 , an ultrasound emitter claim 1 , and a photic energy emitter.4. The system of claim 1 , wherein the excitation signal includes a plurality of neurostimulation pulses having a duration of approximately 50 microseconds claim 1 , each neurostimulation pulse including a plurality of subpulses claim 1 , each subpulse having a duration of approximately 5 ...

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05-03-2015 дата публикации

METHOD FOR CONTROLLING TELEMETRY IN AN IMPLANTABLE MEDICAL DEVICE BASED ON POWER SOURCE CAPACITY

Номер: US20150066112A1
Принадлежит:

An implantable microstimulator configured for implantation beneath a patient's skin for tissue stimulation to prevent and/or treat various disorders, uses a self-contained power source. Periodic or occasional replenishment of the power source is accomplished, for example, by inductive coupling with an external device. A bidirectional telemetry link allows the microstimulator to provide information regarding the system's status, including the power source's charge level, and stimulation parameter states. Processing circuitry automatically controls the applied stimulation pulses to match a set of programmed stimulation parameters established for a particular patient. The microstimulator preferably has a cylindrical hermetically sealed case having a length no greater than about 27 mm and a diameter no greater than about 3.3 mm. A reference electrode is located on one end of the case and an active electrode is located on the other end. The case is externally coated on selected areas with conductive and non-conductive materials. 1. A method for controlling an implantable medical device , the device having telemetry circuitry to receive both a first type of telemetry and to receive a second type of telemetry , the method comprising:listening for the first and second telemetry types;monitoring a voltage of a power source within the implantable medical device; andif the voltage falls below a first threshold, discontinuing listening for the first telemetry type while continuing listening for the second telemetry type.2. The method of claim 1 , wherein the first telemetry type comprises Frequency Shift Keying (FSK) claim 1 , and wherein the second telemetry type comprises On/Off Keying (OOK).3. The method of claim 2 , wherein the telemetry circuitry comprises an OOK receiver claim 2 , an FSK receiver claim 2 , and an FSK transmitter.4. The method of claim 1 , wherein the first threshold is stored in a first register in the implantable medical device.5. The method of claim 1 , ...

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