40th week of 2017 patent applcation highlights part 14 |
Patent application number | Title | Published |
20170281915 | MEDICAL CATHETER SYSTEM - In some examples, a catheter may include a catheter body, a first expandable member, and a second expandable member. The catheter body may define a first lumen, a second lumen, a delivery port, and a surface extending from the delivery port into the first lumen. The first lumen may define a first central longitudinal axis. The second lumen may define a second central longitudinal axis spaced from the first central longitudinal axis in a direction orthogonal to the second central longitudinal axis. The delivery port may be in fluid communication with the first lumen. The surface extending from the delivery port into the first surface may be oriented at an obtuse or acute angle relative to the first central longitudinal axis. | 2017-10-05 |
20170281916 | TUNNELING GUIDEWIRE - A medical device tunneling system, and a method of using the same, to subcutaneously route trocars, also commonly referred to as tunnelers, or introducers, having a cannula, stylet, and a guidewire stylet, inside a patient during a surgical procedure, such as a ventriculoperitoneal hydrocephalus shunt implantation, from a proximal entry point to a distal end point, in order to subcutaneously route and implant a medical device, such as shunt tubing, in a patient. | 2017-10-05 |
20170281917 | URETHROTOME-DILATOR - Urethrotome dilators for dilating a urethral stricture, and methods for forming and using the same are disclosed. In some embodiments, the urethrotome dilator includes a first distal end with a dilating head, a second proximal end with a handle, and a stem for connecting the first end to the second end. The dilating head may have a first region, a second region, and a channel for receiving a guidewire. The first region of the dilating head may have a substantially conical surface, with a vertex at its distal end and a base at its proximal end. The second region may have a substantially flat surface and a blade for stretching tissue. The blade may be integrally formed within the second region and may extend from the flat surface. The top edge of the blade may be tapered and blunt, while the two opposing sides of the blade may be formed with sharp corners for cutting tissue. | 2017-10-05 |
20170281918 | Nasal Dilator - A nasal dilator. The nasal dilator includes a hollow, tubular body having open first and second ends that allows air to pass through. The tubular body is adapted to be positioned within a user's nostril, or nasal passageway, to maintain or increase the capacity to breathe through one's nostrils. The tubular body includes apertures positioned at intervals that allow hair and other nasal objects to extend within the tubular body. These apertures provide comfort in use. The nasal dilator remains within the nostril by friction fit, and may be selectively utilized in either, or both nostrils. | 2017-10-05 |
20170281919 | NEEDLE-SHAPED BODY - A needle-shaped body including a support section having a tubular shape with a center axis being a reference line, the support section having a proximal end and a distal end, a support substrate positioned in the support section and movable in a direction along the reference line, a needle section positioned on a main surface of the support substrate and protruding in a direction from the proximal end toward the distal end, a connecting section that detachably attaches the support substrate to the support section, and a guiding section that guides the support substrate along the reference line. | 2017-10-05 |
20170281920 | MEDICAL VALVE WITH A VARIABLE DIAMETER SEAL - A medical valve assembly includes a tube extending between a first tube end and a second tube end to define a passageway extending along a longitudinal axis between the ends. A plunger plate extends radially from the second tube end of the tube, and a valve housing surrounds the tube about the second tube end and extends from a first valve housing end to a second valve housing end. The valve housing includes a housing flange extending radially inwardly from the second valve housing end and disposed in spaced relationship with the plunger plate to define a distance dimension D extending therebetween. An elastomeric seal is compressed between the plunger plate and the housing flange, and one of the valve housing and the tube is axially movable relative to the other to vary the distance between said plunger plate and said housing flange and adjust an inner diameter of the elastomeric seal. | 2017-10-05 |
20170281921 | ASEPTIC CONNECTOR - The invention relates to a An aseptic connector comprising a first connection unit ( | 2017-10-05 |
20170281922 | INTRAVENOUS CATHETER APPARATUS WITH AN INTEGRATED THREE WAY STOP COCK - The present invention relates to a stopcock for use in intravenous catheter apparatus and infusions of intravenous fluid to a patient. An intravenous catheter apparatus ( | 2017-10-05 |
20170281923 | CLAMP AND BLOOD BAG SYSTEM - A blood bag system includes a clamp installed in a flexible first tube. The clamp includes: a base section having a protrusion section, an opening/closing section having a pressing protrusion section that presses a side surface of the first tube, and a bent section that connects the base section and opening/closing section. The base section is provided with a pair of cutout sections opened to a side surface where the first tube can be inserted by interposing the protrusion section. The clamp is configured such that a portion of the first tube where the clamp is installed is bent while the clamp is released. | 2017-10-05 |
20170281924 | FIBROTIC BAND INTERRUPTER AND IMPLANT INTRODUCING DEVICE - A space in a muscle wall such as the inguinal canal is dilated by a plunger-based mechanism to break up fibrotic bands by divulsion. While the space is dilated a dynamic plug is advanced into it, with the plug expanding and contracting with the space. | 2017-10-05 |
20170281925 | CONFIGURABLE ELECTRODES AND SENSORS - Example defibrillator electrode assemblies compression assemblies are described that may be dimensioned and configured for use on a patient despite physical constraints that limit the area or locations on a patient onto which an electrode assembly may be placed. A cardio pulmonary resuscitation (CPR) assembly is also described that protects a patient with a transthoracic incision from further injury during application of CPR compressions proximate to the incision. | 2017-10-05 |
20170281926 | BIOMEDICAL ELECTRODE COMPRISING DISCONTINUOUS PRIMER LAYER - Articles and methods of making articles are described. In one embodiment, an electrode is described, comprising an ionically-conductive hydrogel layer comprising a first major surface and opposing major surface. The electrode further comprises a discontinuous primer layer disposed on the first major surface ionically-conducting hydrogel layer and an electrically conductive member or a connector component thereof, in contact with the first major surface of the ionically-conducting hydrogel layer. In another embodiment, an article is described comprising a hydrogel layer comprising a first major surface and opposing major surface; a discontinuous hydrophobic primer layer disposed on the first hydrogel layer; and a hydrophobic adhesive or hydrophobic backing bonded to the primer and discontinuous hydrophobic primer layer of the hydrogel. | 2017-10-05 |
20170281927 | Skull-Mounted Optical Implant - A skull-mountable medical device is disclosed. The device includes a housing containing a light source for providing phototherapy to a patient. A light pipe is attached to the housing. The device is configured to be positioned on a patient's skull with the light pipe extending into the patient's brain, such that light from the light source can irradiate a target position within the patient's brain. Once so positioned, the housing may be affixed to the skull via bone screws. The device is powered and controlled by an implantable pulse generator (IPG) that may be implanted into a patient's tissue remotely from the device and connected to the device by wire leads. | 2017-10-05 |
20170281928 | Optical Stimulation Implant - An implantable medical device for providing phototherapy to a patient's brain is disclosed. The device includes a housing containing a light source for providing phototherapy to a patient. A light path is attached to the housing. The implantable medical device is configured to be positioned between a patient's skull and scalp with the light path extending into the patient's brain, such that light from the light source can irradiate a target position within the patient's brain. The implantable medical device is powered and controlled by an implantable pulse generator (IPG) that may be implanted into a patient's tissue remotely from the device and connected to the device by wire leads. | 2017-10-05 |
20170281929 | NEUROSTIMULATION LEAD WITH CONDUCTIVE ELEMENTS AND METHODS FOR MAKING THE SAME - A lead includes a ribbon cable comprising a distal end portion and a proximal end portion. The ribbon cable has a plurality of conductors disposed within an insulating body and a plurality of electrode apertures selectively disposed along the distal end portion of the insulating body. The ribbon cable further includes a plurality of conductive electrodes, wherein each of the plurality of conductive electrodes is disposed over at least one of the plurality of electrode apertures and in electrical communication with at least one of the plurality of conductors. The lead may optionally include a flexible, flat lead body. A method of making a lead includes the steps of (1) obtaining a ribbon cable comprising a plurality of conductors; (2) selectively removing regions of the insulating body to create a plurality of apertures; and (3) placing a plurality of conductive elements over the plurality of apertures, respectively. | 2017-10-05 |
20170281930 | Methods for Treating a Tibial Nerve-Related Condition - Methods for placing an electrical stimulation lead at a tibial nerve in a subject, and also for treating a tibial nerve-related condition or disease in the subject. The methods include depositing the electrical stimulation lead at a tibial nerve, activating the electrical stimulation lead to modulate the tibial nerve, and thereby treating the tibial nerve-related condition or disease in the subject. | 2017-10-05 |
20170281931 | NERVE CUFF FOR IMPLANTABLE ELECTRODE - A system for functional electrical stimulation can include a cuff and a stimulation device. The cuff can be attachable to a nerve or a muscle filament. The cuff can include an elastic collar configured to exert a force on the nerve or the muscle filament to reshape the nerve or the muscle filament to the internal configuration of an opening in the elastic collar. The stimulation device can be coupled to the cuff and configured to provide a stimulation waveform to the cuff. | 2017-10-05 |
20170281932 | IMPLANTABLE MEDICAL ELONGATED MEMBER WITH ADHESIVE ELEMENTS - The disclosure is directed to securing electrodes of a medical lead adjacent to a target tissue site. The medical lead may include at least one adhesive element disposed along a longitudinal outer surface of the lead body to adhere the adjacent tissue to the lead. Adhesive elements may be disposed proximal to, distal to, or in-between the electrodes of the lead. Each adhesive element may be inactive during lead implantation and activated by removing a covering sheath to expose the adhesive elements to moisture in the tissue or presenting an energy, e.g. ultraviolet light, to the adhesive elements. Once active, the adhesive elements secure the lead to surrounding tissue to prevent migration of the electrodes from the target tissue. | 2017-10-05 |
20170281933 | SPINAL CORD STIMULATION LEADS WITH CENTRALLY-CONCENTRATED CONTACTS, AND ASSOCIATED SYSTEMS AND METHODS - Spinal cord stimulation leads with centrally-concentrated contacts, and associated systems and methods. A representative lead system includes a proximal portion and a distal portion, a plurality of signal delivery contacts carried by the distal portion, with multiple distal-most signal delivery contacts spaced apart by a first distance, multiple proximal-most signal delivery contacts spaced apart by a second distance, and multiple intermediate signal delivery contacts spaced apart by a third distance less than the first and second distances. A plurality of connection contacts is carried by the proximal portion, and individual conductors are connected between individual connection contacts and corresponding individual signal delivery contacts. | 2017-10-05 |
20170281934 | Reducing Motility of Cancer Cells Using Tumor Treating Fields (TTFields) - The spreading of cancer cells in a target region can be inhibited by imposing a first AC electric field in the target region for a first interval of time, with a frequency and amplitude selected to disrupt mitosis of the cancer cells; and imposing a second AC electric field in the target region for a second interval of time, with a frequency and the amplitude selected to reduce motility of the cancer cells. The amplitude of the second AC electric field is lower than the amplitude of the first AC electric field. | 2017-10-05 |
20170281935 | Process for Establishing a Muscular Electrostimulation Protocol, and Respective Portable Muscular Electrostimulation Equipment Using Said Protocol - Process and equipment for muscular performance recovery in patients in general, specifically, ones practicing physical activity and athletes, the process providing the serial application of electrical pulses, transcutaneously, following stimulation steps: vasodilation, recovery and untightening phases. Equipment includes an electronic module containing monolithic cabinet having a body with two halves containing a mounted printed circuit board carrying the electronic circuit and the microcontroller, a power supply having a battery, whose external lower face houses a main electrode, and, with two electric conductor cables with satellite electrodes extending from a distal side, the electrodes having self-adhesive gel plates. An adjustable strip secures the equipment around a user's limb. A control panel has a power button and two intensity selection buttons. Additional internal components provided include: power source, step-up regulator, micro controller, power supply seal, boost source, intensity regulation, H-bridge, and electrode output modules. | 2017-10-05 |
20170281936 | Convertible Implantable Stimulator - A convertible implantable stimulator that provides electrical stimulation therapy during an extended trial stimulation period (or permanently, if desired) in a fully implanted solution is disclosed. The convertible implantable stimulator preferably does not include an internal power supply and is therefore continuously powered by an external charger, such as a powering patch, in a first mode of operation. If the convertible implantable stimulator is determined to be effective and a patient desires more traditional stimulation therapy, a separate power supply module can subsequently be implanted and connected to the convertible implantable stimulator to provide power to the stimulator in a second mode of operation. | 2017-10-05 |
20170281937 | NEUROMODULATION TO TREAT MENOPAUSE-RELATED CONDITIONS - One aspect of the present disclosure relates to a method for treating a menopause-related condition in a subject. One step of the method can include inserting a therapy delivery device into a vessel of the subject. Next, the therapy delivery device can be advanced to a point substantially adjacent a target site of the sympathetic nervous system (SNS) that is associated with the menopause-related condition. The therapy delivery device can then be activated to deliver a therapy signal to the target site of the SNS in an amount and for a time sufficient to effect a change in sympathetic activity in the subject and thereby treat the menopause-related condition. | 2017-10-05 |
20170281938 | Topical Nerve Stimulator and Sensor for Bladder Control - What is provided is a method and apparatus for modifying bladder function comprising: applying a dermal patch having an integral electrode in proximity to a sacral or pudendal nerve; selecting the sacral or pudendal nerve by a sensor integral on the dermal patch; determining a stimulation corresponding to the sacral or pudendal nerve, by logic of the dermal patch; applying the stimulation by the electrodes and a stimulator integral to the dermal patch to produce an electric field; and selectively activating the sacral or pudendal nerve by the electric field. | 2017-10-05 |
20170281939 | SYSTEMS AND METHODS FOR TREATING FEMALE INCONTINENCE AND PELVIC NERVE DYSFUNCTION - Systems and methods for neuromodulation of a female patient suffering from a pelvic condition, such as incontinence, are disclosed. A mechanical stimulus such as pressure, tension, traction, friction, or vibration for example can be applied to one, two, or more clitoral structures sufficient to cause a physiologic stimulus or inhibition, such as neuromodulation to treat or prevent the pelvic condition. | 2017-10-05 |
20170281940 | Process for Establishing an Electrostimulation Protocol for Headache Control, and the Respective Portable Electrostimulation Equipment for Headache Control Using Said Protocol - Process and electrostimulation equipment employed in the control of headaches, said process predicting the development of an electrostimulation protocol in which the variation of electric pulse variation is made in a random manner to reduce the physiological phenomenon of nerve fiber accommodation upon stimuli; portable electrostimulation equipment, formed by an electrostimulation set and support is provided, the former consisting of a cylindrical compartment housing an electric circuit board and disposable coin-shaped lithium-ion battery, model CR20XX, in whose back face there are recesses, which house the respective electrodes, suitably covered by respective gel layers protected by removable protective sheets; the electrostimulation set being engaged with the medial longitudinal groove of the support, which configures the rail along which aid set is moved; the following internal components are also provided: Power source module, step-up regulator module, micro controller module, power supply seal module, boost source module, H-bridge module, and electrode output module. | 2017-10-05 |
20170281941 | ELECTRONIC NERVE STIMULATION - A technology is described for an electronic nerve stimulation system. The electronic nerve stimulation system can include a stimulation device operable to generate a high-frequency alternating current. The electronic nerve stimulation system can include one or more wearable electrodes operable to apply the high-frequency alternating current from the stimulation device to peripheral nerves to provide an electrical stimulation of neuronal tissue to treat pain. The one or more wearable electrodes can interface with the stimulation device via a connection system. | 2017-10-05 |
20170281942 | S-Shaped Coupling Spring for Middle Ear Implants - A loading spring has an inner end that engages the outer end of a middle ear transducer, an outer end that engages a fixed anatomical structure within the middle ear of the recipient patient, and a center of mass located on a common line between the inner end and the outer end. The loading spring also has an s-shape with a central spring axis along the common line. And the loading spring is configured for displacement of the inner end and the outer end along the central spring axis to fit the loading spring between the transducer and the fixed anatomical structure with a loading force that is within a defined range and entirely along a center axis of the middle ear transducer and the central spring axis. | 2017-10-05 |
20170281943 | BIOABSORBABLE OR PARTIALLY-BIOABSORBABLE BONE GROWTH STIMULATOR SYSTEM AND METHOD FOR MANUFACTURING A BIOABSORBABLE OR PARTIALLY-BIOABSORBABLE BONE-REGENERATION STIMULATOR SYSTEM - A bone growth simulator system. A bioabsorbable electric circuit is encapsulated in a modified alginate known-time dissolving capsule having a rate of dissolving proportional to the thickness of the capsule. The electronic circuit is powered by a power source. The power source can be inside the capsule or outside the capsule, and can be bioabsorbable or at least biocompatible. An operational amplifier maintains constant current through the circuit. The current stimulates bone growth in bones adjacent to the circuit. The capsule and electric circuit dissolve after completion of the therapy. | 2017-10-05 |
20170281944 | IMPLANTABLE PULSE GENERATOR THAT GENERATES SPINAL CORD STIMULATION SIGNALS FOR A HUMAN BODY - 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. The IPG also contains circuitry to indicate to a patient that proper alignment exists between the IPG and an external charger to charge a battery in the IPG. | 2017-10-05 |
20170281945 | NERVE STIMULATION TO PROMOTE NEUROREGENERATION - Temporary or sub-threshold electrical stimulation to promote recovery of a damaged or injured nerve. Methods include promoting neuroregeneration of a nerve iatrogenically injured during a medical procedure performed on a target site of a patient's body. Methods include placing an electrical lead in electrical communication with the injured or damaged nerve. Methods further include temporarily stimulating the nerve and/or applying sub-threshold stimulation to the nerve to promote neuroregeneration of the nerve. The nerve can be a peripheral nerve. | 2017-10-05 |
20170281946 | SYSTEMS AND METHODS FOR PATIENT REHABILITATION USING BRAIN STIMULATION - Systems and methods are provided for stimulating the brain of a patient to treat a medical condition. In some aspects, a method includes positioning a stimulating device comprising electrical contacts configured to electrically stimulate locations associated with a patient's brain, and initiating a rehabilitation process to include the patient performing a task. The method also includes acquiring feedback from the patient at least while the patient is performing the task, generating, based on the acquired feedback, electrical stimulations to treat the medical condition of the patient. In some aspects, the method further includes generating a report indicative of a patient performance. | 2017-10-05 |
20170281947 | Method and System for Determining Settings for Deep Brain Stimulation - A method and system are provided for determining a relation between stimulation settings for a brain stimulation probe and a corresponding V-field. The brain stimulation probe comprises multiple stimulation electrodes. The V-field is an electrical field in brain tissue surrounding the stimulation electrodes. The method comprises sequentially applying a test current to n stimulation electrodes, n being a number between 2 and the number of stimulation electrodes of the brain stimulation probe, for each test current at one of the n stimulation electrodes, measuring a resulting excitation voltage at m stimulation electrodes, m being a number between 2 and the number of stimulation electrodes of the brain stimulation probe, from the stimulation settings and the measured excitation voltages, deriving a coupling matrix, an element in the coupling matrix reflecting an amount of electrical impedance between two of the stimulation electrodes, and using the coupling matrix for determining the relation between the stimulation settings and the corresponding V-field. | 2017-10-05 |
20170281948 | NEUROMODULATION SYSTEM AND METHOD FOR PROVIDING MULTIPLE MODULATION PATTERNS IN A SINGLE CHANNEL - A neuromodulation system and method includes delivering first electrical modulation energy to a patient through a timing channel at a relatively high energy level (e.g., at a frequency in the range of 2 KHz-50 KHz) during a first time period in accordance with a stored modulation energy delivery schedule, delivering second electrical modulation energy to the patient through the same timing channel at a relatively low energy level (e.g., at a frequency in the range of 2 Hz to 1500 Hz) during a second time period in accordance with the stored modulation energy delivery schedule. | 2017-10-05 |
20170281949 | DISTRIBUTED ELECTRODE LEAD CONFIGURATIONS AND ASSOCIATED SYSTEMS AND METHODS - Distributed electrode lead configurations for providing electrical therapy, and associated systems and methods. A representative patient therapy system includes at least one implantable signal delivery device having a proximal portion and a distal portion. The proximal portion is configured to be coupled with an implantable pulse generator to direct a pulsed electrical signal at a frequency from about | 2017-10-05 |
20170281950 | Battery Protection and Zero-Volt Battery Recovery System for an Implantable Medical Device - Circuitry useable to protect and reliably charge a rechargeable battery, even from a zero-volt state, is disclosed, and is particularly useful when employed in an implantable medical device. The circuit includes two charging paths, a first path for trickle charging the battery at a relatively low current when the battery voltage is below a threshold, and a second path for charging the battery at relatively higher currents that the battery voltage is above a certain threshold. A passive diode is used in the first trickle-charging path which allows trickle charging even when the battery voltage is too low for reliable gating, while a gateable switch (preferably a PMOS transistor) is used in the second higher-current charging path when the voltage is higher and the switch can therefore be gated more reliably. A second diode between the two paths ensures no leakage to the substrate through the gateable switch during trickle charging. The load couples to the battery through the switch, and preferably through a second switch specifically used for decoupling the load. | 2017-10-05 |
20170281951 | ELECTRICAL CONTACT FOR IMPLANTABLE MEDICAL DEVICE - A one-piece electrical contact ring for use in a lead receptacle of an implantable medical device includes (i) a tubular body defining a cavity extending through the body and (ii) a plurality of resiliently deflectable elements extending from the tubular body into the cavty. The deflectable elements have a lead contacting portion configured to contact the lead when received by the cavity. The lead contacting portions of the deflectable elements in a relaxed state are located in a plane that intersects the tubular body and are configured to deflect along the plane towards the tubular body as the lead is inserted in the contact ring. The contact ring may further include a plurality of stops, each configured to (i) engage a stop portion of the elements when the elements are sufficiently outwardly deflected and (ii) inhibit further outward deflection of the elements when the stops engage the stop portions. | 2017-10-05 |
20170281952 | EXTRACTION DEVICES CONFIGUED TO EXTRACT CHRONICALLY IMPLANTED MEDICAL DEVICES - Extraction devices for extracting chronically implanted devices such as leadless cardiac pacemakers (LCP). In some cases, the extraction devices may be configured to cut or tear through at least some of the tissue ingrowth around and/or over the chronically implanted device such that a retrieval feature on the chronically implanted device may be grasped for removal of the chronically implanted device. | 2017-10-05 |
20170281953 | LEADLESS SPINAL CORD STIMULATION SYSTEM AND METHOD INCLUDING SAME - A leadless neurostimulation (NS) device and method to manufacture the device is described. The leadless NS device has a first sub-unit (FU) and a second sub-unit (SU) separately and individually hermetically sealed. The FU and SU also include a flexible inter-connect that physically interconnects the FU and SU to one another. The leadless NS device also includes electrodes provided along the exterior surface of at least one of the first and second sub-units. The electrodes are configured to interface with nervous tissue in an epidural space of a patient and deliver stimulation pulses along the nervous tissue. At least partially housed within the FU includes a first subset of a power source, an energy management components, an electronics sub-system and telemetry component. Further, a second subset of the power source, energy management components, electronics sub-system and telemetry component are at least partially housed within the SU. | 2017-10-05 |
20170281954 | ULTRASOUND POWERED PULSE DELIVERY DEVICE - An implantable device system for delivering electrical stimulation pulses to a patient's body includes a pulse delivery device having a piezoelectric element that is enclosed by a housing and produces voltage signals delivered to the patient's body in response to receiving ultrasound energy. The pulse delivery device includes a circuit having a rate limiter configured to filter voltage signals produced by the piezoelectric element a rate faster than a maximum stimulation rate. | 2017-10-05 |
20170281955 | IMPLANTABLE MEDICAL DEVICE WITH RECHARGEABLE BATTERY - Implantable medical devices such as leadless cardiac pacemakers may include a rechargeable power source. In some cases, a system may include an implanted device including a receiving antenna and an external transmitter that transmits radiofrequency energy that may be captured by the receiving antenna and then be converted into electrical energy that may be used to recharge a rechargeable power source. Accordingly, since the rechargeable power source does not have to maintain sufficient energy stores for the expected life of the implanted device, the power source itself and thus the implanted device, may be made smaller while still meeting device longevity expectations. | 2017-10-05 |
20170281956 | External Charger with Customizable Magnetic Charging Field - Improved external chargers for charging an implantable medical device, and particularly useful in charging a plurality of such devices, are disclosed. Each of the various embodiments include a plurality of field customization coils for customizing the magnetic charging field generated by the external charger such that the magnetic charging field is not radially symmetric. For example, one embodiment includes a primary coil with a plurality of field customization coils distributed radially with respect to the coil. The generated magnetic charging field can be rendered radially asymmetric by selectively activating or disabling the field customization coils in response to data quantifying the coupling between the various implants and the field customization coils in the charger. If there is a relatively high coupling between a particular implant and a particular customization coil for example, that customization coil can be activated to counter the magnetic charging field at that location, while still maintaining a relatively high magnetic charging field at the location of other implants that may have lower couplings. | 2017-10-05 |
20170281957 | Far-Field Short-Range Radio-Frequency Antenna on the Side of an Implantable Medical Device Case - An Implantable Medical Device (IMD) is disclosed having a bi-directional short-range far-field Radio-Frequency (RF) data antenna, operable in accordance with a short-range RF standard such as Bluetooth for example. The antenna is neither located inside the conductive case of the IMD, nor in the non-conductive header of the IMD that includes the lead connectors. Instead, the antenna is outside of the case, proximate to and generally planar with a flat planar side of the case that faces outward of the patient when the IMD is implanted. Dielectric materials keep the antenna from shorting to the case and to the patient's tissue. Because the antenna is not located within the conductive case, data communications to and from the antenna are less subject to attenuation. Not locating the antenna in the header reserves room for the header's lead connectors, thus simplifying IMD design. | 2017-10-05 |
20170281958 | System to Estimate the Location of a Spinal Cord Physiological Midline - Techniques for determining the location of a physiological midline are disclosed. A first technique evaluates the response to stimulation of spinal electrodes at peripheral electrodes on different sides of the body. In this technique, a spinal electrode's position relative to a physiological midline is determined based on a relationship between responses to its stimulation observed on different sides of the body. A second technique evaluates the response of spinal electrodes to stimulation of peripheral electrodes on different sides of the body. In this technique, a spinal electrode's position relative to a physiological midline is determined based on the different responses that it observes to stimulation on different sides of the body. | 2017-10-05 |
20170281959 | System to Estimate the Location of a Spinal Cord Physiological Midline - Techniques for determining the location of a physiological midline are disclosed. A first technique evaluates the response to stimulation of spinal electrodes at peripheral electrodes on different sides of the body. In this technique, a spinal electrode's position relative to a physiological midline is determined based on a relationship between responses to its stimulation observed on different sides of the body. A second technique evaluates the response of spinal electrodes to stimulation of peripheral electrodes on different sides of the body. In this technique, a spinal electrode's position relative to a physiological midline is determined based on the different responses that it observes to stimulation on different sides of the body. | 2017-10-05 |
20170281960 | SYSTEM AND METHOD FOR ANALYZING MEDICAL DEVICE PROGRAMMING PARAMETERS - The technology disclosed herein relates to a system and method for analyzing medical device programming parameters. One aspect of the current technology is a method where an overall performance metric is detected for a cardiac medical device that is outside of a threshold at a first cardiac location in a patient. Processing circuitry identifies a first operating condition and sensing circuitry measures a first sensor response during the first operating condition. An adjustment is proposed to one or more programming parameters of the medical device based on the performance metric, the first operating condition, and the sensor response to the operating condition. | 2017-10-05 |
20170281961 | MEDICAL DEVICE SYSTEMS AND METHODS WITH MULTIPLE COMMUNICATION MODES - Medical device systems and methods with multiple communication modes. An example medical device system may include a first medical device and a second medical device communicatively coupled to the first medical device. The first medical device may be configured to communicate information to the second medical device in a first communication mode. The first medical device may further be configured to communicate information to the second medical device in a second communication mode after determining that one or more of the communication pulses captured the heart of the patient. | 2017-10-05 |
20170281962 | CARDIAC-SAFE ELECTROTHERAPY METHOD AND APPARATUS - A multi-modal electrotherapy apparatus including circuitry for administering defibrillation therapy and for administering medium voltage therapy (MVT) adapted to reduce the side effects of MVT. The electrotherapy apparatus is configured to selectively deliver MVT to vectors not involving the ventricles and defibrillation therapy to vectors involving the ventricles. The apparatus can use biphasic waveforms configured to avoid capture of cardiac cells during MVT. The electrotherapy apparatus can minimize the risk of applying MVT at inappropriate times, such as during atrial fibrillation or where conventional ventricular tachycardia or ventricular fibrillation therapy is more appropriate. | 2017-10-05 |
20170281963 | MULTI-WAVE SIGNAL KEEP-FIT ENERGY CHAMBER - The present invention discloses a multi-wave signal keep-fit energy chamber. The keep-fit energy chamber is a multi-wave signal emission chamber, 90-150 multi-wave signal emission elements ( | 2017-10-05 |
20170281964 | THERAPEUTIC BIOELECTROMAGNETIC FIELDS - Methods for treating pain, inflammation, and skin conditions comprise exposing at least a portion of the body of a subject having pain, inflammation, or a skin condition to a bioelectromagnetic field having low frequency and low voltage for a period of time sufficient to treat the pain, inflammation, or skin condition. Bioelectromagnetic fields may be generated by the interaction of an electromagnetic field generated by a device or composition with the natural electromagnetic fields produced by the body. Such generated bioelectromagnetic fields treat the pain, inflammation, and skin conditions. | 2017-10-05 |
20170281965 | ASSEMBLY FOR PHOTODYNAMIC THERAPY - An assembly for photomedicine therapy comprising: (a) at least partially transparent body having an internal cavity; the internal cavity provided with input and output pipes configured for circulating a cooling agent via said internal cavity; and (b) at least one electrically energizable light source disposed within said internal cavity such that radiation from said at least one light source propagates to the ambient surroundings. | 2017-10-05 |
20170281966 | Device to Kill Micro-Organisms Inside the Respiratory Tract - A present idea relates to a device to kill micro-organisms inside the patient's respiratory tract using UV light, specifically UV-C. It is particularly used to treat patients with Coronaviruses family such as Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (MERS). The device consists of a triple-lumen catheter and UV control unit. The distal end of one of the catheter's lumen has a curved UV chamber while the proximal end has a cable with a socket to be connected to the UV control unit. The second lumen of the catheter is used for oxygen supply, and the third lumen of the catheter is used for suction. | 2017-10-05 |
20170281967 | SYSTEM AND ASSOCIATED METHODS FOR DYNAMICALLY ADJUSTING CIRCADIAN RHYTHM RESPONSIVE TO CALENDARED FUTURE EVENTS - A method is for dynamically adjusting a circadian rhythm of an observer via a user device that includes control circuitry and an associated memory. The method includes accessing a calendar, identifying future events to precondition for and determining a preconditioning schedule for at least one of the identified future events. Determining the schedule includes identifying a circadian shift needed for the at least one identified future event, determining a magnitude of the circadian shift, determining a timeframe for preconditioning, determining a magnitude of a per-day shift based upon the timeframe, and determining if the per-day shift exceeds a maximum allowed per-day shift. Also, the method includes, upon a determination that the per-day shift exceeds the maximum allowed per-day shift, setting the preconditioning schedule responsive to the determination, establishing communication between the control circuitry and a light source, and operating the light source to emit light based upon the preconditioning schedule. | 2017-10-05 |
20170281968 | SCANNING SYSTEM - An example particle therapy system includes: a particle accelerator to output a beam of charged particles; and a scanning system to scan the beam across at least part of an irradiation target. An example scanning system includes: a scanning magnet to move the beam during scanning; and a control system (i) to control the scanning magnet to produce uninterrupted movement of the beam over at least part of a depth-wise layer of the irradiation target so as to deliver doses of charged particles to the irradiation target; and (ii) to determine, in synchronism with delivery of a dose, information identifying the dose actually delivered at different positions along the depth-wise layer. | 2017-10-05 |
20170281969 | CATHETER APPARATUS, BRACHYTHERAPY SYSTEM AND METHOD USING THE SAME - The present application relates to a catheter apparatus including a tubular member, and four or more fluid-flow pipe members, each having a proximal end and a distal end, and each being disposed around a periphery of the tubular member along an axial direction thereof. Each of the four or more fluid-flow pipe members is provided with an independent positioning member at the distal end thereof, and the number of positioning members is four or more. A brachytherapy system and a method of reducing area of radiation exposure of normal tissue in a brachytherapy treatment using the catheter apparatus are also disclosed. | 2017-10-05 |
20170281970 | System and Method for Inducing Respiration - A system for inducing respiration according to one embodiment of the present invention comprises: an imaging unit for picking a respiration image of a patient; a respiration signal conversion unit for obtaining a respiration signal of the patient by image processing, and tracking and analyzing the respiration image of the patient obtained from the imaging unit; and a respiration determination unit for determining one or more of whether the obtained respiration signal is suitable for radiation treatment, whether the obtained respiration signal is stable, and whether a matching score between the respiration signal of the patient and a guide respiration is greater than a predetermined reference value; and a respiration guide unit for providing the respiration signal of the patient, obtained from the respiration signal conversion unit, together with a stored guide signal. | 2017-10-05 |
20170281971 | Method and Apparatus Pertaining to Radiation-Treatment Plan Optimization - A radiation-treatment plan that comprises a plurality of dose-delivery fractions can be optimized by using fraction dose objectives and at least one other, different dose objective. This use of fraction dose objectives can comprise accumulating doses delivered in previous dose-delivery fractions. The other, different dose objective can comprise a remaining total dose objective, a predictive dose objective, or some other dose objective of choice. An existing radiation-treatment plan having a corresponding resultant quality and that is defined, at least in part, by at least one delivery parameter can be re-optimized by specifying at least one constraint as regards that delivery parameter as a function, at least in part, of that resultant quality and then applying that constraint when re-optimizing the existing radiation-treatment plan. | 2017-10-05 |
20170281972 | MULTI-LEAF COLLIMATOR AND DRIVING SYSTEM - The present disclosure relates to a collimator. The collimator may include a motor, a transmission unit having a first end and a second end, and a leaf unit having a leaf. The first end of the transmission unit may be connected to the motor and the second end of the transmission unit may be connected to the leaf. The present disclosure also relates to a collimator system. The collimator system may include a leaf module having a leaf, a driving module having a motor configured to drive the leaf, and a processing module to generate a movement profile of the leaf. The movement profile of the leaf may include a first speed during a first stage, a second speed of the leaf during a second stage, and a third speed of the leaf during a third stage. | 2017-10-05 |
20170281973 | Radiotherapy and imaging apparatus - Radiotherapy apparatus comprises a source of radiation mounted on a chassis, the chassis being rotatable about a rotation axis and the source being adapted to emit a beam of radiation along a beam axis that intersects with the rotation axis; a patient support, moveable along a translation axis; a set of magnetic coils located on either side of the beam, for establishing a magnetic field at the point of intersection, spaced from that point along a first direction; the translation axis, the rotation axis, and the first direction being substantially parallel; and further comprising a multi-leaf collimator fixed in its orientation with respect to the source of radiation, the multi-leaf collimator comprising a plurality of elongate leaves disposed with their longitudinal directions substantially aligned with the first direction and movable in that direction between a withdrawn position in which the leaf lies outside the beam, an extended position in which the leaf projects across the beam and a plurality of intermediate positions therebetween. | 2017-10-05 |
20170281974 | Method and Apparatus Pertaining to Treating a Patient Using Heavy Particles - A heavy-particle treatment system exposes a patient's treatment volume, during the course of a single treatment session, to beams of heavy particles from a variety of different angles. The source of heavy particles may rotate about the patient to facilitate that variety of different angles. The foregoing can occur pursuant to a treatment plan that accounts for a penetration range as corresponds to the beams of heavy particles and for using at least one lateral beam controlling device to control at least one of the beams of heavy particles. | 2017-10-05 |
20170281975 | COLLISION AVOIDANCE FOR RADIATION THERAPY - An outline of at least a patient on a patient support is determined. Based on at least one image of the patient, a plurality of orientations of the patient support and of at least one device are determined. The at least one device is capable of delivering a radiation treatment to the patient or of performing imaging associated with the radiation treatment. Based on the outline and the plurality of orientations of the patient support and of the at least one device, a clearance zone that no portion of the at least one device will occupy when the at least one device or the patient supported by the patient support is in motion is calculated. | 2017-10-05 |
20170281976 | SYSTEMS AND METHODS FOR DETECTING AND/OR MEASURING MOTION AND POSITION ASSOCIATED WITH A PATIENT - An apparatus for patient position or motion monitoring includes: an energy source configured to emit energy from a first location to a second location, or vice versa, wherein the second location that is moveable relative to the first location in response to a movement by a patient; and a processing unit coupled to receive an input that is based on the emitted energy, and to determine a characteristic associated with the patient based on the input. | 2017-10-05 |
20170281977 | HADRON RADIATION INSTALLATION AND VERIFICATION METHOD - A hadron radiation installation adapted to subject a target to irradiation by a hadron radiation beam includes a target support configured to support, preferably immobilize, a target; a hadron radiation apparatus adapted to emit a hadron radiation beam along a beam axis to irradiate the target supported by the target support, the radiation beam penetrating into the target. The radiation apparatus has a control system at least comprising a beam penetration depth control allowing at least to control and vary the penetration depth of the radiation beam into the target. The installation has a radiation beam range sensor device adapted to determine the penetration depth of said radiation beam into the target, where the range sensor device includes a gamma camera responsive to prompt gamma rays that are emitted while the hadron radiation beam penetrates into the target. | 2017-10-05 |
20170281978 | DOSE-DISTRIBUTION ESTIMATION IN PROTON THERAPY - A system for estimating a dose from a proton therapy plan includes a memory that stores machine instructions and a processor coupled to the memory that executes the machine instructions to subdivide a representation of a volume of interest in a patient anatomy traversed by a planned proton field into a plurality of voxels. The processor further executes the machine instructions to determine the distance from the source of the planned proton beam to one of the voxels. The processor also executes the machine instructions to compute the discrete contribution at the voxel to an estimated dose received by the volume of interest from the planned proton beam based on the distance between the source and the volume of interest. | 2017-10-05 |
20170281979 | Radiation Treatment Platform and Method Using a Portal Imaging Device to Automatically Control Therapy Administration - A portal imaging device is used to determine an amount of radiation that is delivered to at least one point while administering a radiation treatment therapy to a patient. Upon detecting that the amount of radiation that is delivered to that at least one point exceeds a predetermined amount of radiation (for example, a planned amount of radiation per the radiation treatment plan), administration of radiation treatment therapy to the patient can be automatically halted. | 2017-10-05 |
20170281980 | ADAPTIVE PENCIL BEAM SCANNING - Embodiments of the present invention disclose methods and systems for producing an adaptive pencil beam having an adjustable lateral beam size and Bragg-peak width. According to one disclosed embodiment, an apparatus for producing an adaptive pencil beam is disclosed. The apparatus includes a set of momentum band expanders configured to widen a momentum spread of a pencil beam, where a momentum band expander is selected from the set of momentum band expanders to receive the pencil beam, and a slit at dispersive focus of two dipole magnets to adjust a width of a Bragg-peak of the pencil beam. According to another disclosed embodiment, a method for producing an adaptive pencil beam with an adjustable lateral beam is disclosed. The method includes selecting a scatter foil, or setting of a defocusing/focusing magnet, and adjusting a lateral size of the pencil beam. | 2017-10-05 |
20170281981 | RADIATION THERAPY SYSTEMS AND METHODS - A radiation therapy system includes an accelerator and beam transport system that generates a beam of particles. The accelerator and beam transport system guides the beam on a path and into a nozzle that can aim the beam toward an object. The nozzle includes a beam energy adjuster that can adjust the beam by, for example, placing different thicknesses of material in the path of the beam to affect the energies of the particles in the beam to deliver a dose to the object with a Spread Out Bragg Peak. | 2017-10-05 |
20170281982 | METHODS AND SYSTEMS FOR GENERATING AN OCCLUSION USING ULTRASOUND - An intra-cavity ultrasound imaging and therapy system is provided. The system includes an intra-cavity ultrasound probe including a housing configure to be inserted into a cavity proximate to a region of interest (ROI). The housing includes a transducer array located proximate to a distal end of the housing. The system also includes a diagnostic control circuit configured to direct the transducer array to collect diagnostic ultrasound signals from the ROI. The diagnostic control circuit is configured to generate an ultrasound image based on the diagnostic ultrasound signals. The diagnostic control circuit is further configured to direct the transducer array to deliver a high intensity focused ultrasound (HIFU) therapy at a treatment location based on target information derived from the ultrasound image. | 2017-10-05 |
20170281983 | SYSTEM FOR THE ABLATION OR THE MONITORING OF A ZONE OF THE HEART BY ULTRASOUNDS AND ASSOCIATED METHODS - A system for ablating or monitoring a zone of the heart, includes a system to measure the heart electrical activity; a phased array for generating a beam of focussed ultrasound signals on a targeted zone of the heart; an imaging system determining an image of a transcostal wall projected in an image plane of the phased array by taking into consideration a position and direction of the phased array and making it possible to deactivate elements of the phased array in accordance with the position of the elements with regard to the position of the projected image of the transcostal wall; a positioning system to control the position of a focussed zone of a beam of focussed ultrasound signals on the targeted zone, a monitoring system to measure a temperature and tissue deformation in the targeted zone; and a device for measuring a level of cavitation in the targeted zone. | 2017-10-05 |
20170281984 | FOCUSSED ULTRASOUND CARDIAC STIMULATION SYSTEM, PORTABLE DEVICE AND CARDIAC STIMULATION, AND ASSOCIATED METHODS - An ultrasound cardiac stimulation system includes: a system for measuring the heart electrical activity; a system for generating a beam of focussed ultrasound signals focussed on a targeted zone, the signals being calibrated to generate electrical stimulation in a zone of the heart, the beam generation being synchronised with a first selected time of the electrocardiogram, the generation of the beam corresponding to a pulse with a duration of less than 80 ms; a system for locating the targeted zone coupled with a system for positioning the system for generating the focussed beam to control the beam of focussed ultrasound signals in the targeted zone, the location system being synchronised with the system for generating the beam of focussed signals; a single monitoring system following in real time a temperature and tissue deformation in the targeted zone, the monitoring system taking measurements in synchronisation with the rhythm of the electrocardiogram. | 2017-10-05 |
20170281985 | CONTROLLED RELEASE MICROCAPSULES - A method of forming microcapsules having improved physical properties and release control as well as the microcapsules formed by the process wherein the capsule wall is formed by the concurrent polymerization of monomers, oligomer and/or prepolymers on the inside of the capsule wall and different monomers, oligomers and/or prepolymers on the exterior of the capsule wall as it forms. | 2017-10-05 |
20170281986 | CONTROLLED RELEASE MICROCAPSULES - A method of forming microcapsules having improved physical properties and release control as well as the microcapsules formed by the process wherein the capsule wall is formed by the concurrent polymerization of monomers, oligomer and/or prepolymers on the inside of the capsule wall and different monomers, oligomers and/or prepolymers on the exterior of the capsule wall as it forms. | 2017-10-05 |
20170281987 | ANTIPERSPIRANT PRODUCTS - Antiperspirant products are described that include a dispensing package and an antiperspirant product contained within a chamber component of the dispensing package. The portion of the chamber component that comes into contact with the antiperspirant composition is made from a polymeric resin that is substantially devoid of phosphorus compounds. | 2017-10-05 |
20170281988 | Skin Care and Cosmetic Composition - A skin care composition and product having beneficial effects on skin conditions/symptoms, such as reducing wrinkles and skin roughness and improving skin elasticity, etc. The composition has three separate parts: a powder part, an aqueous part and an emulsion part. The power part comprises Oligopeptide-1 and | 2017-10-05 |
20170281989 | FireCoat FEDS (Fullbody Emergency Descent System) - A full body emergency descent system (EDS) for incorporating into the coat and pants of a firefighter for allowing for safe escape from elevated heights. The EDS includes: a panel housing flame resistant rope or cable into the coat, outside of its internal protective liner, with a pair of chest straps, and leg straps having lower buckles that can be fastened through pocket accesses to buckle connectors extending from each of a pair of leg loops incorporated into the pants to form a full body harness. The EDS further includes a purposefully designed control descent rack in and through which the rope/cable is wound and a friction braking handle. Preferred embodiments further incorporate a drag strap loop. | 2017-10-05 |
20170281990 | AIR FILTERING DEVICES AND METHODS - A face mask includes an electrostatically-precipitating filter configured to be removably coupled to a face of a user, a controller operatively coupled to the electrostatically-precipitating filter, and a fastening member configured to removably couple the electrostatically-precipitating filter to the face of the user. The controller is configured to selectively control operation of the electrostatically-precipitating filter in response to an input received by the controller. | 2017-10-05 |
20170281991 | END OF SERVICE LIFE INDICATOR FOR DISPOSAL MASK - Embodiments relate generally to methods and systems for detecting and indicating end-of-service-life in disposable filtration masks. Applicant has proposed incorporating end-of-service-life indicators comprising color changing chemicals into the mask. The indicating chemicals may be incorporated into the nonwoven fabric material of the mask, or may be attached to the nonwoven material of the mask, such as by dipping, spraying, or adhering. The color change of the indicating chemicals may indicate to a user that the use life of the mask has been depleted. | 2017-10-05 |
20170281992 | FLAME AND PARTICULATE RESISTANT KNIT ARTICLE - An article of protective clothing comprising a durable multilayer fabric laminate formed from | 2017-10-05 |
20170281993 | COMPOSITIONS FOR REDUCING INHALATION OF TOXIC AIR POLLUTION COMPONENTS - The present invention relates to a composition, textile, and mask for reducing the inhalation of pollutants. The composition includes an aqueous solution of an inorganic iodide compound, a metal phthalocyanine, and a polymeric binder. The inorganic iodide can be cuprous iodide, the metal phthalocyanine can be iron phthalocyanine, and the polymeric binder can be polyvinylpyrrolidone or polyvinyl alcohol. This pollutant-inactivating composition neutralizes pollutants such as nitrogen dioxide, sulfur dioxide, ozone, volatile organic compounds and other unpleasant airborne agents, without requiring elevated temperatures or bulky canisters containing adsorbents. Optionally, a humectant can also be incorporated into the coating solution to retain moisture in the active filter matrix, which enhances the activity of the composition to inactivate oxidizing gases and other toxic constituents of air pollution. | 2017-10-05 |
20170281994 | FALL CONTROL SYSTEM AND METHOD OF CONTROLLING A MOVEMENT DURING FALL EVENT - A fall control system is described. The fall control system comprises an elongate guide rail extending along an axis, a trolley for moving along the elongate guide rail, a tether attached to the trolley at a first end, a second end of the tether for attaching to a user, and a speed control system for controlling a speed of the trolley along the elongate guide rail. The speed control system comprises one or more than one speed control track attached to the elongate guide rail and extending along the axis, a background speed controller coupled to the trolley and engaged with the one or more speed control track when the speed control system or the trolley is in a travelling orientation and controlling the speed of the trolley along the elongate guide rail to not exceeded a maximum walking speed. The speed control system also includes a speed controller coupled to the trolley and engagable with the one or more than one speed control track, the speed controller displaceable from a first position when the speed control system or the trolley is in the travelling orientation, and the speed controller is not engaged with the speed control track, to a second position when the speed control system or the trolley is in a falling orientation and the speed controller is engaged with the speed control track. The speed controller for controlling the speed of the trolley along the guide rail in the falling orientation to not exceed a maximum fall speed. | 2017-10-05 |
20170281995 | FIRE AND SMOKE COMPOSITIONS AND THE PROCESSES OF MAKING THEM - A method for fire and smoke prevention, suppression or extinction using a composition having sodium polyacrylate and distilled water, wherein the ratio of sodium polyacrylate to distilled water is about 1 to 200, having the step of placing the composition in the path of the fire or smoke. | 2017-10-05 |
20170281996 | FIRE SUPPRESSION SYSTEM AND METHOD - A fire suppression system includes at least one high pressure gas source containing an inert gas, at least one low pressure gas source containing an organic halide gas, a distribution network connected with the high pressure gas source and the low pressure gas source to distribute the inert gas and the organic halide gas, and a controller in communication with the distribution network. The distribution network includes flow control devices configured to control flow of the inert gas and the organic halide gas. The controller is configured to initially release the inert gas in response to a fire threat to reduce an oxygen concentration at the fire threat below a preset oxygen concentration threshold, and release the organic halide gas to increase an organic halide gas concentration at the fire threat above a preset organic halide gas concentration threshold while the oxygen concentration is below the preset oxygen concentration threshold. | 2017-10-05 |
20170281997 | FIRE SUPPRESSION SYSTEM AND METHOD - A fire suppression system includes at least one first gas source containing an inert gas, at least one second gas source containing an organic halide gas, a distribution network connected with the first gas source and the second gas source to distribute the inert gas and the organic halide gas, and a controller. The distribution network includes a common manifold, input lines connecting the first gas source and the second gas source with the common manifold, output lines leading from the common manifold, and flow control devices. The controller is in communication with the distribution network and configured to distribute the inert gas responsive to a fire threat signal and determine whether to distribute the organic halide gas based upon a location of a fire threat. | 2017-10-05 |
20170281998 | AUTOMATIC NOZZLE FOR FIREFIGHTING SYSTEMS - An automatic nozzle for firefighting low-pressure water mist systems comprising a nozzle body and shutter means, said nozzle body comprising a plurality of axial-symmetric components defining an inlet opening and a plurality of inner cavities, which are fluid-dynamic connected each other by means of one or more openings, being said components configured to generate a radial spray through a circumferential opening, which extends all over the circumference of a second component, said circumferential opening being formed between a base of an annular board of the second component and an upper surface of a hollow body of a third component, and two or more full cone sprays by means of the fluid passage through cylindrical openings on a circular and axial-symmetric body of a fifth component, configured to define a turbulent motion of the fluid in at least two correspondent cylindrical cavities of a fourth component. | 2017-10-05 |
20170281999 | Gait Pattern Training Device - A gait trainer adapted for use with a treadmill and, optionally, a spinning cycle, provides greater accessibility for therapeutic and rehabilitative gait pattern training to individuals confronting injury, illness, or disability. The gait trainer is adjustable, to accommodate a wide variety of users with different stride lengths and needs. | 2017-10-05 |
20170282000 | INTERCHANGEABLE ROTATING FREE-MOTION FITNESS HANDLE SYSTEM - A fitness handle which is used as an exercise device that allows a resilient cord or tube to move in a linear direction in order to maintain consistent resistance. The fitness handle includes a grip and a frame. The frame includes an opening which allows the cord to slide. The cord or tube has an adjoining portion which fits into the opening of the handle. | 2017-10-05 |
20170282001 | Barbell Drinking Fluid Container - A drinking fluid container is structured as exercise equipment. The drinking fluid container includes a first enclosure, a second enclosure, and a handle that fixes to the first and second enclosures. | 2017-10-05 |
20170282002 | FITNESS STRUCTURE - A fitness structure includes a bar having a first end portion and a second end portion, a pair of bar support portions provided at each side of the bar and having a plurality of bar support members to place the bar at a plurality of heights, a first load portion and a second load portion spaced apart from the bar to a certain degree and facing each other, a first cable coupled between the first end portion of the bar and the first load portion, a second cable coupled between the second end portion of the bar and the second load portion. Heights of the first load portion and the second load portion vary depending on a height of one of the plurality of bar support members at which the bar is detachably placed. | 2017-10-05 |
20170282003 | Adjustable Club - An adjustable club for exercise and art that has an elongate handle, at least one weight and a stud. The elongate handle acts as a counterweight to the removable weights. The elements of the adjustable club may be held together by two different types of frictional fits. The adjustable club may include only the elongate handle and the stud. | 2017-10-05 |
20170282004 | STAIR CLIMBING APPARATUS AND METHOD - A stair stepping apparatus comprising: a plurality of stairs forming a treadmill or endless belt on which a user steps, wherein each stair comprises: a first link comprised of a major step portion joined to a minor riser portion by a rigid elbow, and a second link comprised of major riser portion joined to a minor step portion by a rigid elbow. | 2017-10-05 |
20170282005 | REAR HANDLEBAR ASSEMBLY FOR A STATIONARY BIKE - A rear handlebar assembly in combination with a seat and a supporting member of a stationary bike, includes a seat of a stationary bike for supporting a rider thereon. A supporting member supports the seat of the stationary bike. A joining member includes a vertical bore and a horizontal bore, the vertical bore receiving therein the supporting member, the horizontal bore receiving therein a shaft coupled to flanges of the seat. A clasp holds the joining member against the supporting member. A crossbar forms a rear handlebar adapted to support the hands of a rider in an upright riding position. A rearwardly extending member connects the joining member to the crossbar. A pair of hand grips can be positioned on the crossbar. | 2017-10-05 |
20170282006 | TREADMILL BELTS THAT ENHANCE A USERS COMFORT AND STABILITY - A treadmill comfort belt includes a strap having a first end portion and a second end portion. Each of the first end portion and the second end portion has a securing member. A lumbar support portion is disposed between the first end portion and the second end portion. A compressible sleeve is disposed over the lumbar support portion. A collar is slidingly disposed over the first end portion and the second end portion. The collar is adapted to slide between the securing members and the sleeve. A method of using the belt is also provided. | 2017-10-05 |
20170282007 | EXERCISE DEVICE WITH ELLIPTICAL STEPPING MOTION - An exercise device includes a frame and a crank assembly. A pair of foot links each has a forward end, a rearward end, and a mid-portion. Each foot link has a crank attachment at the forward end that is connected the crank assembly. A foot receiving area is defined at the rearward end of each foot link. Each foot receiving area is longitudinally fixed with respect to the respective foot link and the mid portion of each foot link has a defined support location. The frame supports the support locations of the support links at a generally constant vertical height while allowing horizontal motion relative to the frame. The rearward length of the foot links is at least 1.5 times the forward length such that the foot receiving areas move in a path of travel having more vertical travel than horizontal travel. | 2017-10-05 |
20170282008 | ATHLETIC TRAINING EQUIPMENT - An exercise apparatus may include a rectangular platform, first and second attachment points, first and second rails and friction reducing runners on the rails. The platform may have an upper face, a lower face, two long edges and two short edges. The first attachment point may be disposed along one of the long edges. The second attachment point may be disposed along the other of the long edges. The first rail may be attached to the lower face of the platform proximal to one of the short edges of the platform. The second rail may be attached to the lower face of the platform proximal to the other of the short edges of the platform. The first and second rails may be spaced apart to define a passageway beneath the apparatus, wherein the passageway is configured to allow the apparatus to pass over a standard sprinter's starting block without contacting any part of the starting block. | 2017-10-05 |
20170282009 | Device for Training Abductors and/or Adductors of the Hip Joint - A device for training abductors and/or adductors of the hip joint, having a frame and guided, movable seating. The characterizing feature of the device is that abductors and/or adductors of the hip joint can be trained. To this end, the guiding component of the seating, which is pivotally connected to the frame and can be locked in various positions, has a first rest for at least lateral placement of the knee, at least a lower leg region and/or at least a thigh region of one leg. Furthermore, the guided component of the seating is provided with a seat having a second rest and a third rest for lateral placement of at least the upper region of the pelvis and/or at least a region of the upper body. The second rest and/or the third rest can be adjusted into and locked in its position in order to provide lateral fixing. | 2017-10-05 |
20170282010 | Virtual Golf System and Methods - Virtual golf system for playing golf, comprising a plurality of trackable golf balls, wherein each golf ball comprises transmitting means for broadcasting electromagnetic beacon signals for detecting a position of the golf ball, a position determination unit comprising three receiving antenna's arranged for receiving beacon signals broadcasted by any of said plurality of trackable golf balls, and wherein said position determination unit is arranged to determine a position of said golf ball on a driving range based on time differences of a broadcasted beacon signal received by said receiving antenna's. A plurality of trackable golf balls and a plurality of players may be active at the same time. Trackable golf balls may be paired with specific players. A game controller advances a virtual game of golf each time a trackable golf ball is stroked by a player. | 2017-10-05 |
20170282011 | METHOD AND APPARATUS FOR ASSESSING CARDIOPULMONARY FITNESS - A method and an apparatus for assessing cardiopulmonary fitness of a user are provided. A method of assessing cardiopulmonary fitness involves measuring a biosignal of a user performing an activity, measuring an exercise intensity of the activity, determining a parameter based on the biosignal and the exercise intensity, estimating a cardiopulmonary fitness index based on the parameter, and assessing the cardiopulmonary fitness of the user based on the cardiopulmonary fitness index. | 2017-10-05 |
20170282012 | ELECTRONIC APPARATUS, NOTIFICATION METHOD, AND COMPUTER-READABLE STORAGE MEDIUM - A mobile terminal includes a sensor information acquisition unit, a state calculation unit, and an output control unit. The sensor information acquisition unit successively acquires bio-information relating to a subject. The sensor information acquisition unit acquires activity information relating to activity of the subject. The state calculation unit estimates a physical condition of the subject based on the bio-information acquired and the activity information acquired. The output control unit controls the output unit to perform a notification of information based on the physical condition of the subject estimated. | 2017-10-05 |
20170282013 | Force Measuring Exercise Device - A force measurement device has a motion dampening device having at least two ends. A first end is releasably engaged to a base frame and a second end is releasably engaged to a moveable member. A load cell is in communication with the motion dampening device. The load cell measures a force imparted by a user and the load cell registers the force to a display which depicts the registered force exerted by the user. A method for measuring the force a user imparts onto an exercise apparatus comprises the user imparting force onto a moveable member. The motion dampening device imparts a force substantially opposite to the user force and a load cell measures the force exerted by the user. The force is transmitted to a display wherein the display depicts the registered force imparted by the user. | 2017-10-05 |
20170282014 | MONITORING AND ASSESSING SUBJECT RESPONSE TO PROGRAMMED PHYSICAL TRAINING - In a system for monitoring and assessing subject response to programmed physical training, a client application provides an intake form, into which subject information, such as contact information, demographics and history may be entered. At least part of the subject information may be stored in a central repository for aggregation with other subject data, for analysis and reporting. Parameterized descriptions of exercises produce a binary string for each exercise, the resulting in a binary map of an entire exercise system, such as the PILATES system. Using a digital session planner, a practitioner selects from filtered lists of exercises to generate a customized exercise sequence for a subject. After the training session, the binary strings for the session are aggregated and a summary of the session displayed for user and/or practitioner. Session data may be uploaded to the repository for aggregation with data from other subjects/session for analysis and reporting. | 2017-10-05 |