15th week of 2016 patent applcation highlights part 8 |
Patent application number | Title | Published |
20160101224 | HIGH EFFICIENCY BLOOD PUMP - A high efficiency blood pump includes a pump housing, wherein the pump housing provides an inlet and outlet. The pump includes a motor housing, wherein the motor housing contains a motor. An impeller is housed in the pump housing, wherein the impeller is radially supported by a hydrodynamic bearing providing at least one row of pattern grooves. A diaphragm provided by the pump housing separates the impeller chamber from the motor chamber. A magnetic coupling is provided between the motor and the impeller, wherein the magnetic coupling causes the impeller to rotate when the motor rotates and provides axial restraint of the impeller. | 2016-04-14 |
20160101225 | DIALYSIS SYSTEM - A dialysis system is disclosed. An example dialysis system includes a heat disinfected dialysate fluid path. The example dialysis system also includes a disposable blood fluid path. The example dialysis system also includes an active carbon filter to purify influent water to purified water for dialysis or as a substitution fluid. An example method for dialysis includes providing a heat disinfected dialysate fluid path, providing a disposable blood fluid path, and purifying influent water via an active carbon filter to for dialysis or as a substitution fluid. | 2016-04-14 |
20160101226 | Sensing Negative Pressure with a Pressure Transducer - A medical system includes a medical fluid pumping machine comprising a pressure sensor, a medical fluid line set comprising a fluid line in fluid communication with a fluid passage formed between a diaphragm and a base, the medical fluid line set being configured to be connected to the medical fluid pumping machine in a manner such that the diaphragm of the medical fluid line set aligns with the pressure sensor of the medical fluid pumping machine, and a member configured to apply a positive force to the pressure sensor when the medical fluid line set is connected to the medical fluid pumping machine and the fluid passage is at atmospheric pressure. | 2016-04-14 |
20160101227 | Medical Treatment System and Methods Using a Plurality of Fluid Lines - Improvements in fluid volume measurement systems are disclosed for a pneumatically actuated diaphragm pump in general, and a peritoneal dialysis cycler using a pump cassette in particular. Pump fluid volume measurements are based on pressure measurements in a pump control chamber and a reference chamber in a two-chamber model, with different sections of the apparatus being modeled using a combination of adiabatic, isothermal and polytropic processes. Real time or instantaneous fluid flow measurements in a pump chamber of a diaphragm pump are also disclosed, in this case using a one-chamber ideal gas model and using a high speed processor to obtain and process pump control chamber pressures during fluid flow into or out of the pump chamber. Improved heater control circuitry is also disclosed, to provide added or redundant safety measures, or to reduce current leakage from a heater element during pulse width modulation control of the heater. Improvements are also disclosed in the application of negative pressure during a drain phase in peritoneal dialysis therapy, and to control the amount of intraperitoneal fluid accumulation during a therapy. Improvements in efficiency are also disclosed in the movement of fluid into and out of a two-pump cassette and heater bag of a peritoneal dialysis cycler, and in the synchronization of the operation of two or more pumps in a peritoneal dialysis cycler or other fluid handling devices using a multi-pump arrangement. | 2016-04-14 |
20160101228 | METHOD AND SYSTEM PROVIDING MORE ACCURATE FLUID TEMPERATURE MONITORING WITH SELECTABLE FLUID INPUT AND OUTPUT ARRAGEMENTS FOR BODY CAVITY TREATMENTS - Arrangements of components for use in support of a Hyperthermic Intraperitoneal Chemotherapy (HIPEC) System which conveys fluids from a system to a patient and back to the system in a complete circuit. The described arrangements provide multiple means of rapidly configuring the number of input lines and output lines into and out of the patient. Included are integral temperature probes in the inflow and outflow lines. Also included are various means of introducing and removing the fluids from the patient and additional temperature probes to be used at the discretion of the clinician. | 2016-04-14 |
20160101229 | BLOOD FILTRATION SYSTEM CONTAINING MANNOSE COATED SUBSTRATE - A blood filtration method, system, device and media for removing gram negative bacteria from the blood wherein the media includes a substrate coated with mannose optionally in constitution with substrate coated with heparin. | 2016-04-14 |
20160101230 | Biomedical Apparatus for Pumping Blood of a Human or an Animal Patient through a Secondary Intra- or Extracorporeal Blood Circuit - A biomedical apparatus for pumping blood of a human or an animal patient through a secondary blood circuit is provided, including a blood pump ( | 2016-04-14 |
20160101231 | INFUSION PREPARATION - An object of the present invention is to provide an infusion preparation in which the Maillard reaction between an amino acid and a reducing sugar does not occur during storage and the size of fat particles in the fat emulsion does not increase during storage, and in which various types of vitamins can be incorporated in a stable manner, in spite of the fact that it is a two-chamber infusion preparation. Furthermore, even if only one of the infusions (of the infusion preparation) is administered, the patient is unlikely to develop hyperkalemia, vascular pain, or phlebitis. The present invention provides an infusion preparation containing two chambers separated by a partition that can be communicably opened, wherein a first chamber contains a first-chamber infusion containing a sugar and a fat emulsion, a second chamber contains a second-chamber infusion containing an amino acid and an electrolyte, the first-chamber infusion is substantially free of potassium, and has a relative osmotic pressure of 2.0 to 3.0, the second-chamber infusion has a potassium concentration of 40 mEq/L or less and a relative osmotic pressure of 2.5 to 3.5, and a mixture of the first- and second-chamber infusions has a potassium concentration of 16 mEq/L or more as measured upon communicably opening the partition. | 2016-04-14 |
20160101232 | METHODS AND SYSTEMS FOR PROMOTING GLUCOSE MANAGEMENT - Methods and systems for encouraging interactions with a glucose monitoring system include incrementing a score and/or providing a reward based on a variety of different interactions with the glucose monitoring system. The interactions which improve the score may include initiating or changing displays, downloading data, setting operational parameters and other interactions that are independent of a user's glucose measurements. Encouraging these interactions can enhance success in maintaining healthy glucose concentrations. | 2016-04-14 |
20160101233 | FLUID TRANSFER MECHANISM FOR NEEDLE-FREE INJECTION DEVICE - A needle free injection device for use with a cartridge containing an injectate includes a housing. The housing includes an end wall at its distal end and an inner wall. The inner wall extends in a direction from the proximal end of the housing to the distal end of the housing and separates a first chamber from a second chamber in the housing. The housing includes a first opening disposed in the end wall and is in fluid communication with the first chamber. The housing includes a second opening is in fluid communication with the second chamber. A coupler is disposed in the first chamber for coupling to the cartridge. The first opening and the second opening are in fluid communication via a channel for transfer of fluid between the first chamber and the second chamber. | 2016-04-14 |
20160101234 | SUPPLEMENTAL DEVICE FOR ATTACHMENT TO AN INJECTION DEVICE - A supplemental device for attachment to an injection device including a dosage window covering a sleeve on which dose values are marked is disclosed. The supplemental device comprises a main body; an arrangement for supporting the main body of the supplemental device in a predetermined positional relationship with the injection device; a transparent protection window located at a surface of the main body that is aligned with the dosage window of the injection pen when in use; a sensor arrangement supported in the main body and having a sensor directed at the protection window; an illumination arrangement comprising one or more sources of light, each of the one or more sources of light being directed at the protection window; and a non-transmissive part located on an optical path between a first one of the one or more sources of light. | 2016-04-14 |
20160101235 | Medicament Delivery Device - A medicament delivery device has proximal and distal ends; a medicament container with a plunger, a neck portion, and a delivery member unit; a housing extending along a longitudinal axis with proximal and distal open ends; a drive unit configured to apply a force on the plunger; and a C-shaped tubular body with a longitudinal slit/gap such that body can be attached to the neck portion forming a container unit. The C-shaped body also has an inner support configured to interact with the neck portion and with the delivery member unit and prevent the medicament container from moving relative to the body after the medicament container is attached to the body, and outer support configured to interact with a corresponding support of the housing to prevent the C-shaped tubular body from moving relative to the housing after the container is arranged within the housing through the distal open end. | 2016-04-14 |
20160101236 | INDICATION MECHANISM FOR AN AUTOMATIC APPLICATOR, PARTICULARLY FOR INSULIN - The present disclosure concerns an indication mechanism for an automatic applicator, particularly for insulin or other liquid preparations, particularly for multiple injection administration of set doses of a medicine from an exchangeable container, for example for the self-application of insulin by diabetes patients. An indication mechanism for an automatic applicator, having an assembly of at least two barrels movably coupled to each other has an indication barrel mounted on the driving barrel contains only marking on its external surface and is co-axially connected to the pull-push control nut. | 2016-04-14 |
20160101237 | INDICATION MECHANISM FOR AN AUTOMATIC APPLICATOR, PARTICULARLY FOR INSULIN - The present disclosure concerns an indication mechanism for an automatic applicator, particularly for insulin or other liquid preparations, particularly for multiple injection administration of set doses of a medicine from an exchangeable container, for example for the self-application of insulin by diabetes patients. An indication mechanism for an automatic applicator, having an assembly of at least two barrels movably coupled to each other has an indication barrel mounted on the driving barrel contains only marking on its external surface and is co-axially connected to the pull-push control nut. | 2016-04-14 |
20160101238 | ROTATABLE FINGER FLANGE FOR A SYRINGE - A conventional syringe defines a longitudinal axis and includes a syringe barrel having a syringe barrel flange laterally extending from an open proximal end of the syringe barrel and a plunger advanceable into the syringe barrel. A rotatable finger flange for such a syringe includes identical first and second flange components, each having an attachment member configured to releasably engage the syringe barrel flange and/or the other flange component, and a flange member laterally extending therefrom. The first and second flange component are engageable and rotatable relative to one another about the longitudinal axis between a non-use position, wherein the first flange member overlies the second flange member to reduce the finger flange footprint, and a use position, wherein the first flange member and the second flange member are angularly spaced apart from one another to provide a finger flange having a greater lateral extent than the syringe barrel flange. | 2016-04-14 |
20160101239 | GASKET FOR PREFILLED SYRINGE | 2016-04-14 |
20160101240 | NEEDLE FOR DELIVERING TREATMENT FLUID TO AN AVIAN BIRD, AND ASSOCIATED ASSEMBLY AND METHOD - A needle for delivering a treatment fluid to a target site of an avian bird is provided. Such a needle includes a shaft defining a longitudinal axis and having a proximal end and a distal end. Discrete grooves are defined by the shaft and extend partially along a length thereof. A needle tip extends from the shaft at the distal end thereof. A reservoir assembly includes a body defining first and second holes for receiving the needle therethrough such that the body supports the needle along the length thereof. The reservoir assembly defines a reservoir adapted to receive a treatment fluid through which the grooves pass to carry the treatment substance to the target site. An associated assembly and method are also provided. | 2016-04-14 |
20160101241 | Pen Needle Assembly For Preventing Under-Torquing and Over-Torquing Of Pen Needle - A pen needle hub and cover for a pen needle assembly that provides tactile and/or audible indicia of proper attachment between the hub of the pen needle and the pen is provided. Such indicia substantially prevent under- and over-torquing of the pen needle. The tactile indicia may include a user sensing a wave of a torque of peak value followed by a torque of lesser value. | 2016-04-14 |
20160101242 | SYSTEM AND METHOD FOR DIFFERENTIATING CONTAINERS IN MEDICATION DELIVERY - The present invention relates to a fluid delivery system that comprises a fluid container having a chamber structured to hold a fluid therein and a delivery device operable to control delivery of a fluid from the chamber of the fluid container. The fluid container includes a geometric mating member extending from an outer surface thereof. The delivery device includes a geometric mating receptacle structured to mate with at least a portion of the geometric mating member of the fluid container to verify compatibility of the fluid container with the delivery device. Alternatively or additionally, the fluid container may include a first data fixture component and the delivery device may include a second data fixture component that cooperates with the first data fixture component of the fluid container to verify compatibility of the fluid container with the delivery device. | 2016-04-14 |
20160101243 | Nasal Spray Delivery Guide - A nasal spray delivery guide including a pair of guide elements spaced apart from one another and configured to be at least partially inserted into respective nostrils of a patient, and a flexible connector element attached to and extending between the guide elements. Each guide element includes an aperture extending therethrough from a base end to a tip end of the guide element. A method for delivering a nasal spray into a patient's nose includes the steps of providing the nasal spray delivery guide, inserting the guide elements at least partially into respective nostrils of the patient, inserting at least a portion of a nasal spray delivery device into one of the guide elements, and activating the nasal spray delivery device to deliver a nasal spray to a lateral wall of the respective nasal cavity. | 2016-04-14 |
20160101244 | INHALER FOR A METERED DOSE AEROSOL - An inhaler for delivering a metered dose aerosol, in which a permeable sheet is positioned directly in front of a narrow channel. | 2016-04-14 |
20160101245 | Medical Unit Dose Container - A unit dose container for the containment of an intranasal formulation for use with the POD device. | 2016-04-14 |
20160101246 | APPARATUS AND METHODS FOR PRODUCING AND DELIVERING A VAPOUR MEDICAMENT - Disclosed are apparatus and methods for producing and delivering vapour medicament. An exemplary apparatus disclosed comprises: a gas inlet for receiving a gas from a source of pressurized gas; a chamber for receiving a liquid medicament therein, the chamber being in communication with the gas inlet for permitting entrance and expansion of the gas in the chamber in the presence of the liquid medicament to produce the vapour medicament; and a vapour outlet in communication with the chamber for delivering the vapour medicament. | 2016-04-14 |
20160101247 | Process and Device to control the internal body pressure during use of a medical-technical pump - The present invention relates to a method for controlling the internal body pressure, e.g., the joint pressure using a medical-technical fluid pump, and to a device for carrying out said method. | 2016-04-14 |
20160101248 | Wearable Wrist Inhaler - A wearable wrist inhaler includes a wristband having a first end and a second end configured for wear about a user's wrist. An inhaler unit is coupled to the wristband displaced from the first end and the second end, the inhaler unit including a housing having a plurality of walls defining an interior area and an outlet port in communication with the interior area. A watch assembly is positioned atop the housing of the inhaler unit, the watch assembly energized by a battery and includes a display configured to indicate a time of day. A dosage chamber including a medicament is positioned in the interior area of the housing. A dispensing assembly is communication with the inhaler medicament that is configured to dispense an individual portion of the medicament via the outlet port upon demand by a user. | 2016-04-14 |
20160101249 | NASAL DELIVERY DEVICES - A nasal delivery device for and a method of delivering substance to a nasal airway of a subject, the nasal delivery device comprising a mouthpiece ( | 2016-04-14 |
20160101250 | AUTOTITRATING METHOD AND APPARATUS - An apparatus and method of controlling the delivery of therapeutic gas delivered to a patient undergoing positive airway pressure therapy is described. The method includes providing a flow of gas to a patient's airway at a pressure, obtaining information from the range of 0 to 25 Hz of the frequency domain of the flow, and adjusting the pressure based on the information. The apparatus includes a blower for providing a flow of gas to a patient's airway at a pressure, a sensor to measure a characteristic of the flow, a controller to obtain information from the range of 0 to 25 Hz of the frequency domain of the characteristic, and a pressure regulator for adjusting the pressure based on the information. | 2016-04-14 |
20160101251 | VENTILATOR WITH INTEGRATED BLOWER TO PROVIDE NEGATIVE OR POSITIVE PRESSURE IN A VENTILATOR SYSTEM - A ventilator system and method for medical use includes an integrated blower. The ventilator system may include an inspiration port for connection to an inspiratory limb of a dual-limb patient circuit, and an expiration port for connection to an expiratory limb of the dual-limb patient circuit. The system also includes a gas delivery device connected to the inspiration port to supply a pressurized flow of gas to the inspiration port to generate a positive pressure, and a blower having an inlet that is operatively connected to the expiration port and configured to be controlled to selectively supply a negative pressure level between 4 and 120 cmH | 2016-04-14 |
20160101252 | Bag/Valve/Mask Resuscitator Stabilizer Arm and Method of Use - A stabilizer arm for a BVM resuscitator and method of use is disclosed. The stabilizer arm provides the necessary support to the reservoir bag to enable the user to exert downward pressure on the BVM resuscitator while simultaneously squeezing the reservoir bag. Due to the presence of the stabilizer arm, this pressure pushes the facial mask downward to assist in forming a tight mask to face seal. Multiple embodiments of the stabilizer arm are disclosed. The stabilizer arm may be internal, external or integrated into the wall of the reservoir bag of the BVM resuscitator and may be retro-fitted or original equipment manufactured. The external stabilizer arm may be designed to engage the neck of the outlet port of the BVM resuscitator with an open collar or a closed collar. The internal stabilizer arm may be configured to fit BVM resuscitators having single piece or multiple piece outlet valve design. | 2016-04-14 |
20160101253 | PROTECTIVE ENDOTRACHEAL TUBE - Embodiments include a tracheal tube having a proximal end and a distal end. In certain embodiments, a plurality of spaced-apart cuffs disposed around the tracheal tube. The plurality of spaced-apart cuffs being configured to seal the tracheal airway of a patient and to capture tracheal secretions or debris. Also, at least two pilot balloons are connected to the plurality of cuffs, the at least two pilot balloons being configured to inflate and deflate the plurality of cuffs. Further, at least two injection lumens connected to at least two injection distal ports configured to administer fluids to the bronchi of the patient and at least one evacuation lumen connected to a plurality of evacuation ports, the at least one evacuation lumen being connected to a vacuum source. The plurality of evacuation ports are disposed proximal the plurality of evacuation ports to remove the captured fluids or debris. | 2016-04-14 |
20160101254 | LARYNGEAL MASK - A laryngeal mask for use in a patient comprises an airway tube having an inner lumen and a distal end; and a mask portion connected at a proximal end thereof to the distal end of the airway tube and having a distal tip opposite the proximal end. The mask portion comprises an inflatable cuff including an anterior cuff surface configured to contact the patient's tissue when the inflatable cuff is inflated; and a wedge portion including a stabilization surface and two walls connected to the inflatable cuff and extending therefrom toward from the stabilization surface, the stabilization surface extending from the distal tip of the mask portion toward the distal end of the airway tube at a wedge angle of between about 12 and 30 degrees, the wedge angle formed between the stabilization surface and the anterior cuff surface when the inflatable mask is inflated, whereby the stabilization surface is transversely and longitudinally substantially flat to stabilize the laryngeal mask in use. The laryngeal mask has a gastric tube with a varying inner tube diameter. | 2016-04-14 |
20160101255 | Novel airway tube stabilizer - A novel tube stabilizer with a collar | 2016-04-14 |
20160101256 | METHOD AND APPARATUS FOR INCREASING THERAPY COMPLIANCE - A breathing assistance unit for providing pressurized heated humidified air to a user is configured to increase user compliance. The breathing assistance unit comprises means for generating positive emotional and cognitive states of a user about the therapy. | 2016-04-14 |
20160101257 | HUMIDIFYING DEVICE FOR BREATHING MASK - The present invention relates to a humidifying device for a breathing mask. The breathing mask includes a breathing tube assembled thereto. The humidifying device includes a body, a liquid discharger, a liquid receiver, and a water-absorbent member. The body is connected to the breathing tube. The body includes a passage communicating with the breathing tube. The liquid discharger is fixed to the body. The liquid discharger includes a liquid outlet communicating with the passage. The liquid receiver is fixed to the body and is disposed below the liquid discharger. The liquid receiver includes a liquid inlet communicating with the passage. The water-absorbent member consists of a filtering material. The water-absorbent member is accommodated in the passage and disposed between the liquid outlet and the liquid inlet. | 2016-04-14 |
20160101258 | CAPILLARY HEATER WIRE - A heater wire including at least one extending component disposed thereon. The heater wire is positioned within a respiratory gas conduit. | 2016-04-14 |
20160101259 | VENTILATOR CIRCUIT, ADAPTER FOR USE IN VENTILATOR CIRCUIT AND METHODS FOR THE USE THEREOF - An adapter includes a housing having an inlet port defining a flow path and an outlet port. An interior wall has an inner surface defining an interior passageway communicating with the outlet port and an exterior surface defining an exterior passageway communicating with the inlet port. The interior wall defines a mouth communicating between the interior and the exterior passageways. The interior wall is positioned transverse to the flow path of the inlet port. A medicament delivery port opens into the mouth. A valve is moveable between a closed position, wherein the valve closes the medicament delivery port, and an open position, wherein the medicament delivery port is open. A ventilator circuit and method of delivering a medicament are also provided. | 2016-04-14 |
20160101260 | Human Performance Enhancement Method And Apparatus - A human body support, such as a chair, has a plurality of electrodes arranged in an array and spaced longitudinally with respect to the human body. The array extends from an inferior position to a more superior position along the body. A sensor measures a parameter of the human body that is capable of indicating the presence of drowsiness. A controller has an input connected to the sensor for receiving a signal representing the sensed parameter and has outputs connected to each of the electrodes. The controller detects whether the sensed parameter is within a range indicating the presence of drowsiness and applies a wave of electrical stimuli against the human body in response to detection of a sensed parameter within the range. The electrical stimuli cause periodic tightening and relaxing of proximate muscles as the wave progresses in a direction from an inferior location on the human body toward a more superior location. | 2016-04-14 |
20160101261 | CATHETER TIP - Catheters and related methods for supporting a guidewire or delivering an agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a polymer tip member disposed at a distal end of the shaft body. The shaft body and the tip member can include a liner, one or both of a braid member or a coil member surrounding the liner, and a polymer cover surrounding the braid member or the coil member. The tip member can further include one or more filaments extending from a position overlapping, underlapping, or abutting a distal end of the braid member or the coil member on their proximal ends to a position distal to the braid member or the coil member on their distal ends. The one or more filaments can include a plurality of filaments arranged in a series of contacting helical windings about the liner, the braid member, or the coil member. | 2016-04-14 |
20160101262 | CATHETER - Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. The multi-layer coil can include first and second coil layers wound in opposing directions. An outer surface portion of the polymer cover can include one or more helical threads. In an example, the one or more helical threads are positioned around a distal end portion of the shaft body. The tip member can be made from a metal or a polymer and can also include one or more helical threads around its outer surface. | 2016-04-14 |
20160101263 | SYSTEMS AND METHODS FOR REDUCING MEASUREMENT ERROR USING OPTICAL FIBER SHAPE SENSORS - An apparatus comprises an instrument including an elongated, flexible body and a shape sensor including an optical fiber extending at least partially along the elongated, flexible body. The apparatus also includes a radiopaque material incorporated with the optical fiber at least partially along a length of the optical fiber. | 2016-04-14 |
20160101264 | CUTANEOUS CATHETER ANCHORING DEVICE AND METHOD OF STABILIZING A CATHETER SITE - A cutaneous catheter anchoring device and method to prevent occlusion of an indwelling peripheral intravenous catheter and to do so in a way that does not require immobilization of, or significant reduction in the range of motion of, the joint of the particular extremity. The device and method accomplish this by immobilizing multiple areas of the skin's surface relative to the indwelling catheter. The device is in close proximity to the indwelling catheter and maintains a smooth, rather than bent or creased, skin surface above the catheter thus preventing creasing or kinking of the catheter itself during times when the patient bends the extremity. | 2016-04-14 |
20160101265 | MEDICAL GUIDE ELEMENT WITH DIAMETER TRANSITION - Improved methods for percutaneously creating, entering and/or dilating an opening in the wall of a blood vessel or other anatomic structure. The improvement comprises deploying a guide element having a proximal segment and a distal segment, the diameter of said distal segment being greater than the diameter of said proximal segment at their juncture, and which at said juncture forms an abrupt circumferential step comprising a proximally-facing surface. Said proximally-facing surface abuts the catheter's tip and shields said tip, thereby facilitating passage of said catheter as it enters and passes through said opening in said wall of a blood vessel or other anatomic structure. | 2016-04-14 |
20160101266 | Medical Instrument Clamp - A medical instrument clamp for removably securing an elongated medical instrument within a housing to be conductively connected to a conduit. The present invention generally includes a housing having a first opening at its first end and a second opening at its second end. The first opening leads to a first channel adapted to receive an elongated medical instrument such as a catheter guide wire. The second opening leads to a second channel adapted to receive a conduit such as a connection conduit for a medical device. A contact internal to the housing is positioned between the first and second channels to conductively connect the medical instrument with the conduit. A pair of arms and clamp are included which may be transitioned to open or close in response to manipulation of a knob. By closing the arms and clamp, the medical instrument may be removably secured within the first channel. | 2016-04-14 |
20160101267 | Anchoring Device and Methods for Use - An anchoring guide wire and methods for use are provided, where the guide wire comprises a non-coiled segment, a first expandable segment, and a leading segment, wherein the first expandable segment is configured to transition between a constrained state and a deployed state. | 2016-04-14 |
20160101268 | ANGIOPLASTY DEVICE - The invention relates to an angioplasty device for treating stenoses or occlusions that facilitates the diagnosis and visualisation of the stenosis and the treatment control having a duct dedicated to the injection of the contrast product. | 2016-04-14 |
20160101269 | Apparatus For A Medical System Inflation Syringe - The medical system inflation syringe of the present invention enables a fluid communication selective interconnection of a male connector with a subset of certain female connectors, while preventing interconnection of said male connector with other subsets of female connectors, for the purpose of providing secure interconnection to achieve fluid (including gas or air) communication only with medical systems with which the inflation syringe is intended to be interconnected. | 2016-04-14 |
20160101270 | DRAINAGE SYSTEMS FOR EXCESS BODY FLUIDS AND ASSOCIATED METHODS - Drainage systems for excess body fluids and associated methods are disclosed herein. A body fluid drainage system in accordance with an embodiment of the present technology, for example, can include a catheter that has an exterior surface, a proximal portion, and a distal portion opposite the proximal portion. The body fluid drainage system can further include a valve device, a pressure sensor, and a controller operatively coupled to the valve device and the pressure sensor. The valve device can include an actuator positioned over the exterior surface of the catheter. The actuator is movable between an open position that allows body fluid flow through the catheter, a closed position that at least substantially obstructs the body fluid flow through the catheter, and intermediate positions that partially obstruct the body fluid flow through the catheter. The controller can change the position of the actuator in response to a predetermined condition of the pressure sensor. | 2016-04-14 |
20160101271 | CATHETER-ASSISTED TUMOR TREATMENT - A method for treating a subject diagnosed with a cancer or other disorder comprising a hyperproliferative tissue is described herein. The method includes localized delivery of a material which contains a therapeutically effective agent and/or moiety. The localized delivery of the agent is achieved using a catheter-based delivery system and an implant. An implant can include a support component, a cover component, and a valve component. The valve component can be operable to permit flow through the implant. The implant can be delivered on a catheter, with one of the ends of the implant being selectively expanded to permit temporary occlusion of a vessel while delivering a material through the valve component to a downstream target region. The other end of the implant can thereafter be released such that the implant occludes the vessel, or the implant can be removed from the vessel entirely. | 2016-04-14 |
20160101272 | MICRONEEDLE PATCH APPLICATOR SYSTEM - A method and apparatus for application of a microneedle patch to a skin surface of a patient includes use of an applicator. The applicator includes a housing, a slidably disposed applicator plate, and a compression spring. The applicator plate is moveable between a retracted position and a deployed position, and has an engaging surface suitable for mashing up against a microneedle patch and pressing it against a skin surface. A docking system transfers the microneedle patch from a support to the applicator without requiring a user to handle the microneedle patch directly. Once mounted in the applicator, the microneedle patch is deployed against a skin surface of a patient for delivery of a desired agent via a microneedle array contained on the patch. | 2016-04-14 |
20160101273 | NON-INVASIVE AGENT APPLICATOR - An agent carrier delivers an agent to biological tissues by one or more modalities. The modality of delivery may be one or more transportation stimulus that causes the agent to be transported through the agent carrier. The transportation stimulus also enhances or permits penetration of the agent into the tissue. The agent carrier has an agent carrier body that is configured to retain the agent within the agent carrier body. The agent carrier body has a tissue-contacting surface for engaging tissues under treatment. Application of the transportation stimulus causes transportation of the agent through the agent carrier body to the tissue-contacting surface. | 2016-04-14 |
20160101274 | Method of Manufacturing Percutaneous Ports with Wire Coils - The various implementations described herein include methods used to manufacture a percutaneous port for promoting tissue in-growth around the percutaneous port. In one aspect, the method includes providing a tubular structure having an outer surface and providing a coil having an outer surface and comprised of a plurality of loops. The method further includes joining at least a portion of the outer surface of the coil to the outer surface of the tubular structure. | 2016-04-14 |
20160101275 | Percutaneous Ports with Wire Coils - The various implementations described herein include a percutaneous port for promoting tissue in-growth around the percutaneous port. In one aspect, the percutaneous port includes a tubular structure having an outer surface, and a coil having an outer surface and comprised of a plurality of loops. Furthermore, at least a portion of the outer surface of the coil is joined to the outer surface of the tubular structure. | 2016-04-14 |
20160101276 | Methods and Apparatus for Disinfecting and Reflux Prevention Flush Syringe Assembly - Embodiments of the invention are directed to flush syringe assemblies comprising an integrated contamination-prevention device integrated with device connector flushing positioned so that the practitioner cannot forget to apply disinfectant. The flush syringe assemblies comprise a barrel with an elongate plunger rod disposed therein and a cap comprising a passageway. The plunger rod includes a stopper of which at least a portion can be embedded in the passageway of the cap to form a plug in the cap. | 2016-04-14 |
20160101277 | Methods and Apparatus for Disinfecting and Reflux Prevention Flush Syringe Assembly - Embodiments of the invention are directed to flush syringe assemblies comprising an integrated contamination-prevention device integrated with device connector flushing positioned so that the practitioner cannot forget to apply disinfectant. The flush syringe assemblies comprise a barrel with an elongate plunger rod disposed therein and a cap comprising a passageway. The plunger rod includes a stopper of which at least a portion can be embedded in the passageway of the cap to form a plug in the cap. | 2016-04-14 |
20160101278 | Medical Treatment System and Methods Using a Plurality of Fluid Lines - Improvements in fluid volume measurement systems are disclosed for a pneumatically actuated diaphragm pump in general, and a peritoneal dialysis cycler using a pump cassette in particular. Pump fluid volume measurements are based on pressure measurements in a pump control chamber and a reference chamber in a two-chamber model, with different sections of the apparatus being modeled using a combination of adiabatic, isothermal and polytropic processes. Real time or instantaneous fluid flow measurements in a pump chamber of a diaphragm pump are also disclosed, in this case using a one-chamber ideal gas model and using a high speed processor to obtain and process pump control chamber pressures during fluid flow into or out of the pump chamber. Improved heater control circuitry is also disclosed, to provide added or redundant safety measures, or to reduce current leakage from a heater element during pulse width modulation control of the heater. Improvements are also disclosed in the application of negative pressure during a drain phase in peritoneal dialysis therapy, and to control the amount of intraperitoneal fluid accumulation during a therapy. Improvements in efficiency are also disclosed in the movement of fluid into and out of a two-pump cassette and heater bag of a peritoneal dialysis cycler, and in the synchronization of the operation of two or more pumps in a peritoneal dialysis cycler or other fluid handling devices using a multi-pump arrangement. | 2016-04-14 |
20160101279 | DIRECTIONAL ELECTRODE DEVICES WITH LOCATING FEATURES - Electrode devices having directional electrodes for use in deep brain stimulation or other uses. In one aspect, an electrode assembly comprises an elongate lead and a lead guide that are engageable with each other in a coaxial relationship. When the elongate lead and the lead guide are engaged with each other; the two components are rotationally fixed in relation to each other. In another aspect, an elongate lead comprises a radiologically-visible feature for indicating the orientation of the elongate lead. In yet another aspect, an electrode system is capable of determining the position and/or orientation of an electrode positioned within a body. In other aspects, methods for electrically stimulating a target site in the body are disclosed. | 2016-04-14 |
20160101280 | APPARATUS AND METHODS FOR ASSISTED BREATHING BY TRANSVASCULAR NERVE STIMULATION - A catheter may include electrodes for transvascular nerve stimulation. The electrodes may be positioned within lumens of the catheter and aligned with apertures in the outer wall of the catheter. The electrodes may produce focused electrical fields for stimulation of one or more nerves. In one embodiment, the catheter may include a set of proximal electrodes and a set of distal electrodes, and the proximal electrodes may stimulate a patient's left phrenic nerve and the distal electrodes may stimulate a patient's right phrenic nerve. | 2016-04-14 |
20160101281 | METHODS,DEVICE,AND SYSTEMS FOR OBESITY TREATMENT - Methods and systems for detecting wall breach in inflatable prostheses rely on intrusion of a body fluid or inflation medium to electrically alter a signaling circuit. In one embodiment, an open portion of a circuit is closed to enable or modify a transmitted signal. In another embodiment, electrical current is generated to power an electrical transmission. | 2016-04-14 |
20160101282 | An arrangement for facilitating wound healing, a method for measuring wound healing and a wound dressing - The present invention relates to the field of electrotherapy and measuring by means of electric currents for diagnostic purposes, and more particularly to an electrode arrangement for facilitating wound healing, a method for measuring wound healing and a wound dressing having an electrode arrangement. A wound dressing according to the present invention comprises at least two impedance reference electrodes, a frame like counter-electrode and stimulation electrodes in a form of an array; and a bioadhesive affinity layer surrounding the stimulation electrodes; said wound dressing being suited for applying on top of the wound so that the stimulation electrode array is on the wound area, and that the at least two impedance reference electrodes and the frame like counter-electrode are suited for placing in contact with the healthy skin surrounding the wound area; which electrodes, are suited for applying LIDC type electrical stimulation current to the wound area and for bioimpedance measurement. The wound dressing according to the present invention provide a continuous, non-invasive and objective solution for monitoring chronic wound healing without disturbing the delicate healing process. | 2016-04-14 |
20160101283 | Method and Apparatus for Stimulating the Vascular System - The present invention provides methods of treating a gastrointestinal condition. In some embodiments, the method generally includes administering a chemical or electrical stimulus to an artery of the gastrointestinal vasculature of the subject, a vein of the gastrointestinal vasculature of the subject, a nerve supplying an artery of the gastrointestinal vasculature of the subject, and/or a nerve supplying a vein of the gastrointestinal vasculature of the subject, wherein the chemical or electrical stimulus is effective for treating a gastrointestinal condition. | 2016-04-14 |
20160101284 | SYSTEMS AND METHODS FOR THERAPEUTIC ELECTRICAL STIMULATION - In various embodiments, the invention disclosed herein provides systems, devices and methods for providing electrical stimulation to a patient. An electrical mechanical interconnection is provided to facilitate user friendly systems and devices. Exemplary therapeutic electrical stimulation devices include a shoe connected mechanically and electrically to a conductor that provides signals for electrical stimulation. | 2016-04-14 |
20160101285 | Neural Coding with Short Inter Pulse Intervals - Arrangements are described for generating electrode stimulation signals for an implanted electrode array having multiple stimulation contacts. An audio input preprocessor receives an input audio signal and generates band pass signals that represent associated bands of audio frequencies. A band pass signal analyzer analyzes each band pass signal to detect when one of the band pass signal components reaches a defined transition event state. A stimulation signal generator generates a set of electrode stimulation signals for the stimulation contacts from the band pass signals such that the electrode stimulation signals to a given stimulation contact: i. use a transition event stimulation pattern whenever a transition event is detected in a band pass signal associated with the given stimulation contact, and ii. use a different non-transition stimulation pattern after the transition event stimulation pattern until a next subsequent transition event is detected. | 2016-04-14 |
20160101286 | METHODS OF TREATMENT OF A NEUROLOGICAL DISORDER USING ELECTRICAL NERVE CONDUCTION BLOCK - Described herein are methods of treating various neurological disorders using electrical nerve conduction block (ENCB) without causing electrochemical damage. Examples of the various neurological disorders can include pain, muscle spasticity, hyperhidrosis, vertigo, sialorrhea, or the like. The methods can include placing an electrode contact in electrical communication with a nerve that transmits a signal related to the neurological disorder. The method also includes applying an ENCB to the nerve through the electrode contact. The electrode contact can include a high charge capacity material that prevents formation of damaging electrochemical reaction products at a charge delivered by the ENCB. The method also includes blocking transmission of the signal related to the neurological disorder through the nerve with the ENCB to treat the neurological disorder. | 2016-04-14 |
20160101287 | IMPLANTABLE LEAD - An implantable wireless lead includes an enclosure, the enclosure housing: one or more electrodes configured to apply one or more electrical pulses to a neural tissue; a first antenna configured to: receive, from a second antenna and through electrical radiative coupling, an input signal containing electrical energy, the second antenna being physically separate from the implantable neural stimulator lead; one or more circuits electrically connected to the first antenna, the circuits configured to: create the one or more electrical pulses suitable for stimulation of the neural tissue using the electrical energy contained in the input signal; and supply the one or more electrical pulses to the one or more electrodes, wherein the enclosure is shaped and arranged for delivery into a subject's body through an introducer or a needle. | 2016-04-14 |
20160101289 | SYSTEMS AND METHODS FOR DELIVERING VAGAL THERAPY - A method may include delivering autonomic neural stimulation (ANS) therapy, including delivering stimulation pulses to evoke physiological responses. The method may further include recording physiological parameter values, including recording first population data, the first population data including evoked response (ER) values corresponding to the evoked physiological responses, and recording second population data, the second population data including reference values that include no effect (NE) values corresponding to times without an evoked physiological response. The method may further include quantifying a relationship between the first population data and the second population data, and analyzing the quantified relationship for a signature to indicate if the stimulation pulses are evoking desired physiological responses. | 2016-04-14 |
20160101290 | SYSTEM AND METHODS FOR IMPROVING DEVICE THERAPY USING MULTIPLE SENSOR METRICS - Devices and methods for improving device therapy such as cardiac resynchronization therapy (CRT) by determining a desired value for a device parameter are described. An ambulatory medical device can receive one or more physiologic signals and generate multiple signal metrics from the physiologic signals. The ambulatory medical device can determine a desired value for a device parameter, such as a timing parameter used for controlling the delivery of CRT pacing to various heart chambers, using information fusion of signal metrics that are selected based on one or more of a signal metric sensitivity to perturbations to the device parameter in response to a stimulation, a signal metric variability in response to a stimulation, or a covariability between two or more signal metrics in response to a stimulation. The ambulatory medical device can program a stimulation using the desired device parameter value, and deliver the programmed stimulation to one or more target sites to achieve desired therapeutic effects. | 2016-04-14 |
20160101291 | APPARATUS AND METHODS FOR CHARGING AN IMPLANTED MEDICAL DEVICE POWER SOURCE - Apparatus and methods for charging an implanted medical device. | 2016-04-14 |
20160101292 | METHOD AND SYSTEM FOR HOSPITAL, EMT/EMS, AND AED GRADE EXTERNAL DEFIBRILLATION AND TRANSCUTANEOUS PACING - A method and apparatus for treating a cardiac condition in a human or animal patient comprises contacting an area of skin spanning the chest area of the patient with at least two patches or electrode paddles that apply low voltages and currents in a rotational manner to pre-stimulate that area, followed by applying a high voltage shock in rapid succession through the patient's heart through at least two electrode pad patches or paddles, wherein an amplifier-based external defibrillation cardioversion system is used. Also, an external pacing system is employed using ascending ramp or any arbitrary ascending or level waveform for transcutaneous pacing which employ a constant current delivery mode. Treatable conditions include atrial fibrillation (AF), atrial tachycardia (AT), ventricular fibrillation (VF), and ventricular tachycardia (VT). | 2016-04-14 |
20160101293 | IMPLANTABLE CARDIO DEFIBRILLATOR (ICD), SUBCUTANEOUS IMPLANTABLE CARDIO DEFIBRILLATOR (SICD), AND WAVEFORM ENERGY CONTROL SYSTEMS - Cardiac defibrillation or cardioversion waveform energy control systems employ transvenous ICDs or subcutaneous SICDs for treating cardiac arrhythmias. The systems comprise differentially driven amplifier circuit operational modes to control the delivery of defibrillation or cardioversion electrical shocks, wherein the shock waveforms are constant current, constant voltage, or constant energy. Biphasic arbitrary shock waveforms deliver increasing and or level energy with increasing time as represented by phase 1 ascending ramp, ascending exponential, ascending chopped, ascending stepped, ascending curved, square, rectilinear or level and or any combination of geometric shaped ascending or level waveforms. | 2016-04-14 |
20160101294 | PORTABLE PHOTOTHERAPY APPARATUS FOR PSORIASIS - A portable phototherapy apparatus for treating a skin disorder in a patient. The apparatus includes an illumination source, an image capture device, a projecting system and a controller. The illumination source is configured to irradiate the patient's skin. The image capture device for capturing an image of lesion areas of the patient's skin needing treatment. The projecting system includes a therapeutic light source for generating UV radiation. The controller configured to cause the projecting system to form a shaped treatment image comprising the UV radiation on the patient's skin based on the image of the lesion areas captured by the image capture device such that the therapeutic light source delivers a dose of the UV radiation only to the lesion areas of the skin. | 2016-04-14 |
20160101295 | Photonic Treatment Apparatus - A photonic treatment apparatus and apparatus for patient care, using a film, such as a phosphorous plate and a casing comprising an aperture provided for films that may be positioned therein to allow for desired treatments of a user, a photonic engine, positioned behind the film, to create photonic pressure. The photonic engine directed toward the film energizes the film achieving a desired wavelength emanation, a first zone of wavelengths that originate from the photonic engine, and a second zone of wavelengths emanating from the film that can be directed toward a target area and used in a method for treating patient conditions. A specific phosphor plate can be used for a desired treatment to customize the output to a specific wavelength necessary for treatment of specific conditions or other possible uses. | 2016-04-14 |
20160101296 | RADIATION TREATMENT COLLIMATOR HAVING MULTILAYERED LINKAGE STRUCTURE - The present invention relates to a radiation treatment collimator having a multilayered linkage structure, the collimator providing various shapes of spaces and configuring a radiation area, which transmits radioactive rays, the collimator including: a fixed frame disposed on a plate; multiple pixel board layers fixedly stacked at predetermined intervals on top of each other inside the fixed frame, each pixel board layer being configured in a lattice form and having pixel covers disposed correspondingly to the respective lattices in such a manner as to be open and closed individually; control units disposed on both sides of the fixed frame to individually control the operations of the pixel covers of the pixel board layers; and power source units disposed on the front and rear sides of the fixed frame to supply the pixel board layers with operating power. The collimator is inexpensive and exhibits good treatment results; each pixel can be open/closed separately to form a radioactive ray radiation area; and the collimator is capable of, in real time, converting the shape of the radiation area and adjusting the intensity of the radioactive rays. | 2016-04-14 |
20160101297 | PARTICLE BEAM TREATMENT DEVICE AND OPERATION METHOD THEREFOR - When an energy of a particle beam to be emitted from an accelerator is set for every slice group including two or more adjacent slices and an attenuation amount is set for each slice in the slice group, the energy to be emitted from the accelerator is set, for every slice group, higher than an energy corresponding to the slice at a deepest location in that slice group so that a transmissive plate has a predetermined thickness for the slice at the deepest location; and, with respect to a thickness of the transmissive plate to be set for every slice group, the thickness set for the slice group at a deep location is larger than or equal to the thickness set for the slice group at a shallow location, and the thickness set for the slice group at a deepest location is thicker than the thickness set for the slice group at a shallowest location. | 2016-04-14 |
20160101298 | PARTICLE BEAM THERAPY SYSTEM - A particle beam transport section comprises a horizontal deflection electromagnet which deflects a particle beam to a direction which is parallel to an accelerator median plane of a circular accelerator, a first perpendicular electromagnet which deflects a particle beam whose travelling direction is deflected by the horizontal deflection electromagnet to a direction which is different from a direction which is parallel to the accelerator median and a second perpendicular electromagnet which deflects the particle beam whose travelling direction is deflected by the first perpendicular deflection to a direction which is parallel to the accelerator median plane, wherein the horizontal deflection electromagnet is provided on a floor which is different from a floor where a particle beam irradiation unit is provided. | 2016-04-14 |
20160101299 | SELECTIVE REMOVAL OF CELLS HAVING ACCUMULATED AGENTS - A method of treating a condition associate with accumulation of an agent in cells in a patient includes exposing the cells to ultrasound, to selectively kill or induce apoptosis in the cells. The cells include the accumulated agent. | 2016-04-14 |
20160101300 | Safety Airbag System - A safety airbag device for cushioning the free fall of a person or object from an elevated height. The airbag device includes an inflatable base bag capable of sustaining an air pressure and an inflatable structure coupled to the base bag, where the inflatable structure is in air communication with the base bag. A net is coupled to a top portion of the inflatable structure for decelerating and supporting the individual from free fall. A top cover is coupled to the base bag that substantially encloses the inflatable structure. | 2016-04-14 |
20160101301 | RESPIRATOR MASK SPEECH ENHANCEMENT APPARATUS AND METHOD - Speech enhancement apparatus and respirator masks including speech enhancement apparatus, as well as methods of enhancing speech transmission for the wearer of a respirator mask are described herein. In one or more embodiments, the speech enhancement apparatus and methods described herein detect acoustic energy within a first frequency range in the clean air envelope of a respirator mask and deliver compensating acoustic energy outside of the clean air envelope using a speaker. The compensating acoustic energy is, in one or more embodiments, delivered in one or more predetermined attenuated frequency ranges that cover less than all of the detected first frequency range. In one or more embodiments, the compensating acoustic energy may be delivered with an attenuated amplitude profile that uniform or that is non-uniform over the one or more attenuated frequency ranges. | 2016-04-14 |
20160101302 | SNAP HOOK - A snap hook that includes a body, a gate, a connection link and a breakable fastener is provided. A central portion of the body is positioned between an upper portion and a lower portion. The gate is pivotally coupled proximate the central portion of the body. The gate and the body selectively forming a closed configuration that defines a hook connection passage and an open configuration that provides access to the hook connection passage. An upper end of the connection link is pivotally coupled proximate the central portion of the body. A lower end of the connection link includes a body connection aperture. The breakable fastener couples the lower end of the connection link proximate the lower portion of the body. The breakable fastener is configured to break when a select amount of force is applied to the lower end of the connection link to transfer the force from the lower portion of the body to the central portion of the body. | 2016-04-14 |
20160101303 | NONWOVEN MATERIAL AND DRYER WITH NONWOVEN MATERIAL - A non-woven fabric includes flame retardant fibers and binding material mixed with the flame retardant fibers. The binding material sets a thickness of the fabric. Application of a flame to the fabric causes the binding material to degrade and the flame retardant fibers to expand to prevent a flame from passing through a hole in a wall of an appliance, a building, or an appliance and/or to protect wiring of an appliance, a building, or an appliance. | 2016-04-14 |
20160101304 | Multi-Blanket Inert Gas Rail Car Fire Suppression - A container ignition and fire suppression system, comprising means for removing volatile gases present prior to and produced during and after loading the container with a volatile liquid based on a weight capacity of the container; filling a headspace above a level of the volatile liquid with a blanket composition of inert gas(es); pressurizing the volatile liquid and the predetermined composition of inert gas(es) to a predetermined pressure to retard outgassing of the volatile liquid into the head space occupied by the inert gas(es); discharging a fire retardant foam at onset of a rupturing of the predetermined blanket composition, the discharge adapted to smother, extinguish and prevent a fire from igniting via a spark, a rupture and other combustible processes; and a monitor and control apparatus adapted to determine and adjust a plurality of conditions regarding the inert gas(es) and the volatile liquid in the container via telemetry. | 2016-04-14 |
20160101305 | DEVICE FOR ANTI-FIRE PROTECTION OF A STARTER-CONTROLLER DEVICE OF AN ELECTRICAL INSTALLATION - An anti-fire protection device for a starter-controller device of an electrical installation is able to be connected to an electrical power conductor and includes thermal monitoring of the electrical power conductor to detect a temperature rise of greater than a predetermined threshold. This anti-fire protection device can be fixed mechanically to the starter-controller device via at least one mechanical linking member. The thermal monitoring includes at least one temperature sensor and a cartridge including a fire extinguishing agent and at least one injection element, situated on the same face of the protection device as the temperature sensor, the cartridge being situated inside the protection device and connected to the temperature sensor, the injection element being able to inject the fire extinguishing agent towards the electrical power conductors subsequent to a detection, by the temperature sensor, of a temperature of greater than the predetermined threshold. | 2016-04-14 |
20160101306 | FIRE SPRINKLER SYSTEM HAVING COMBINED DETECTION AND DISTRIBUTION PIPING - A fire sprinkler system is described which includes a piping system having at least one dual-use pipe providing both an air conveying inlet and a fire extinguishing fluid conveying outlet. The pipe has at least one air sampling opening allowing ambient air flow into the pipe and at least one fire sprinkler for ejecting a fire extinguishing fluid from the pipe in the event of a fire. An air sampling detector is fluidly connected to the pipe and tests the ambient air within the pipe to detect the presence of the fire. A valve, disposed between the source of the fire extinguishing fluid and the pipe, is in communication with the air sampling detector and operable to open, upon detection of the fire based on the ambient air tested by the air sampling detector, in order to fill the pipe with the fire extinguishing fluid. | 2016-04-14 |
20160101307 | FIRE HYDRANT SECURITY INTEGRATED FLOW CONTROL/BACKFLOW PREVENTER INSERT VALVE - Integrated flow control backflow preventer valve (“IFCBPV”) for new and existing wet- and dry-barrel fire hydrants, with barrel drain assemblies for dry-barrel hydrants, and hydrants equipped with such IFCBPVs, are presented. An exemplary IFCBPV can have a retaining screen comprising equidistant concave radial spokes intersecting at a central ring structure, a freely suspended check ball, and a lower ball seat with a seal. The upper surface of the retaining screen can be affixed to the hydrant's axial shaft, and can thus be used to open and close the hydrant via the ball. Alternatively, the retaining screen can be fixed and the axial shaft provided with a cup on its bottom that mates with the freely suspended ball that is caged between the retaining screen and the ball seat. An exemplary barrel drain assembly can comprise a spring-loaded piston, or alternatively, a check ball design as in the main barrel. | 2016-04-14 |
20160101308 | Drug Disposal System - The present invention comprises a safe and effective system for removal of a range of common pharmaceutical compounds. The formulation comprises activated carbon, accompanied by some larger pebble-like material to help break up capsules and tablets upon shaking, in the presence of an acidified liquid medium. Drugs are added to the bottle and the bottle is shaken so that the drugs are dissolved by the liquid solution and are irreversibly adsorbed onto activated carbon, thereby sequestering them from further use. | 2016-04-14 |
20160101309 | Sports Performance Enhancement System - athletic physical training system is configured to be worn on a human body. The physical training system includes a flexible article of footwear, a torso member, and an elastic resistance band. The flexible article of footwear includes a fabric panel configured to receive a foot of the human body. At least one first strap is connected to the fabric panel and extends over a dorsal side of the fabric panel from a lateral side to a medial side of the fabric panel. The torso member is configured to engage the torso of the wearer. The elastic resistance band extends between the at least one first strap and the torso member. | 2016-04-14 |
20160101310 | ADJUSTABLE SUPPORT FOR EXERCISE SYSTEM - An exemplary exercise device includes, among other things, an attachment structure configured to be mounted to a support assembly, a first arm directly pivotably connected to the attachment structure, a second arm directly pivotably connected to the attachment structure, a bracket directly pivotably connected to the first arm and directly pivotably connected to the second arm, and a catch member configured for accepting a weight bar. The catch member is pivotably connected to at least one of the first arm, the second arm, or the at least one bracket such that the at least one catch member is pivotable relative to the at least one bracket. | 2016-04-14 |
20160101311 | Resistance Selector for Exercise Apparatus - An exercise apparatus includes a frame, a guide member coupled with a portion of the frame, a weight stack including a plurality of weight plates associated with the guide member and a lifting mechanism. The lifting mechanism has a first end attached to a pull handle and a second end being attached to a weight attachment mechanism. Further, a resistance selector has a pin coupled to the weight attachment mechanism and is displaceable between a first position and a second position relative to the weight attachment mechanism. When the pin is in the first position the weight attachment mechanism is interlocked with a plate of the weight stack and when the pin is in the second position the weight attachment mechanism is freed from the weight plate and the pin has an engagement structure that is shaped to interlock with a profile of an edge of the plate. | 2016-04-14 |
20160101312 | KEYED WEIGHT SYSTEM - Disclosed is a system which prevents weights from being misplaced within an exercise environment. The system prevents a weight from being placed in an incorrect position of a weight rack. By using a keyed weight and weight rack the user is required to place the weight correctly in order for the weight to properly seat on the weight rack. The weights are keyed in such a way as to allow use on any properly sized dumbbell or barbell whilst limiting placement on an incorrect weight rack. This system eliminates the need to sort weights and therefore drastically reduces the amount of effort required to maintain the weight system in addition to reducing the time which is required to locate a specific weight plate. | 2016-04-14 |
20160101313 | BICYCLE TRAINER - A bicycle trainer is adapted to be arranged with a bicycle to simulate riding a bicycle on an outdoor road. The bicycle includes a stand, a roller, a first resistance source and a second resistance source. The stand is adapted to support the bicycle. The roller is pivoted to the stand and is adapted to contact a bicycle wheel of the bicycle. The first resistance source is coupled to the roller and provides resistance to the bicycle wheel via the roller. The second resistance source is coupled to the roller and provides resistance to the bicycle wheel via the roller. | 2016-04-14 |
20160101314 | EXERCISE DEVICE - The exercise device includes a wheel having a side and an axle assembly including an axle and a handle section extending from the axle outwardly of the sides of the wheel. A coil spring is situated within the wheel, surrounding the axle and is operably connected between the wheel and the axle such that the wheel and the axle can move relative to each other to alter the tension on said spring. The handle assembly also has a circular member situated proximate and parallel to the side of the wheel. The member is fixedly mounted to and radially extending from the axle such that the member and the axle move together as a unit. Accordingly, the wheel can move relative to the axle/member unit without irritating the user's hand gripping the handle section. | 2016-04-14 |
20160101315 | JAW EXERCISER - A jaw exerciser for providing passive motion therapy such as that used to treat trismus is provided. The jaw exerciser has a user-adjustable distance between the upper jaw support and the lower jaw support. The jaw exerciser includes a shaft, a first or upper jaw support frame including a first jaw support, a second or lower jaw support frame including a second jaw support, a distance adjuster which may be in the form of a jack screw for manually adjusting the distance between the first jaw support and the second jaw support, and a retaining screw. The jack screw may be received by the second or lower jaw support frame and engage the first or upper jaw support frame. Removable bite pads may optionally be provided for installing on the first jaw support and the second jaw support. | 2016-04-14 |
20160101316 | System, Method and Apparatus for Capturing and Training a Swing Movement of a Club - A system, method and apparatus for training a swing movement of a club includes storing a desired swing data in a measuring device, capturing a training swing data in the measuring device, comparing the training swing data to the desired swing data to determine a set of differential data, outputting a signal to a user corresponding to the set of differential data. | 2016-04-14 |
20160101317 | SWING EVALUATION APPARATUS, SWING EVALUATION METHOD, AND SWING EVALUATION PROGRAM - A swing evaluation apparatus includes an analysis unit which calculates an analytical value relating to a swing based on an output of an inertia sensor; an evaluation unit which evaluates a degree of achievement of the analytical value with respect to a set target value; and a notifying unit which notifies a user of an evaluation result by changing types of notification in accordance with the degree of achievement. In this way, the degree of achievement with respect to a target is notified to the user. | 2016-04-14 |
20160101318 | SWING GROUP ANALYSIS APPARATUS, SWING GROUP ANALYSIS METHOD, AND SWING GROUP ANALYSIS PROGRAM - A swing group analysis apparatus includes a swing analysis unit which calculates an analytical value of a specific item for a swing which belong to a swing group based on an output of an inertia sensor; and an evaluation unit which evaluates the swing group by comparing a set target value and the analytical value. | 2016-04-14 |
20160101319 | ELECTRONIC DEVICE, CONTROL PROGRAM, CONTROL METHOD, AND SYSTEM - An electronic device includes an acceleration sensor configured to detect an acceleration value, an atmospheric pressure sensor configured to detect an atmospheric pressure value, and a controller. The controller is configured to calculate the amount of activity or the number of steps based on the acceleration value detected by the acceleration sensor and the atmospheric pressure value detected by the atmospheric pressure sensor. | 2016-04-14 |
20160101320 | EXERCISE EQUIPMENT AND EXERCISE EQUIPMENT SET - Provided is Exercise equipment including a gripping section that is gripped by a user; a weight section that is connected to the gripping section; a first electrode that is arranged on the gripping section; a second electrode that is arranged on the weight section; a measuring section that measures at least one of body fat percentage of the user and an electrocardiogram waveform of the user, using the first electrode and the second electrode. | 2016-04-14 |
20160101321 | Method and System for Automated Personal Training - Example embodiments may relate to a system, method, apparatus, and computer readable media configured for monitoring a user performing an exercise and generating a avatar of the user and a virtual shadow, wherein the virtual shadow illustrates proper form of the exercise. The example embodiments may further be configured for determining an amount of overlap between the virtual avatar and the virtual shadow, and generating a feedback score based on the amount of overlap. | 2016-04-14 |
20160101322 | Series Elastic Motorized Exercise Machine - The disclosure teaches a novel exercise apparatus. This apparatus does not generate load momentum. The apparatus is based around a series elastic torque sensor and contains an intelligent servo drive with reduction gear to control a variable speed rotating motor shaft. The combination of the motor, gear reducer, spring, angle measurement sensors (position sensors), and intelligent motor controller is a series elastic actuator which is the basis for the exercise device. The exercise device also contains a load transfer mechanism adopted to provide an interface between an individual and the torque sensor. The apparatus allows for isokinetic, isometric, isotonic, and variable force modes of exercise without hardware configuration. | 2016-04-14 |
20160101323 | ORIENTATION DURING SWIMMING - There is provided an apparatus, wherein the apparatus is configured to perform operations comprising: obtaining heading information indicating a target heading to a target; detecting, during swimming, that the swimmer deviates from the target heading; and informing the swimmer, via a user interface element, that the swimmer has deviated from the target heading. | 2016-04-14 |
20160101324 | GOLF BALL INCORPORATING AN INNERMOST HOLLOW PORTION - Golf ball incorporating: spherical or aspherical innermost hollow portion; shell layer, one or more outer core layers, and at least one cover layer. Shell layer has outer surface hardness greater than inner surface hardness by up to about 7 Shore C to define first hardness gradient. Outer core layer has a second hardness gradient. A shell layer surrounding a spherical hollow portion may have an inner surface with a non-uniform contour defining a phantom spherical circumference of the innermost spherical hollow portion at symmetrically spaced locations about the golf ball's geometric center. In golf balls including a spherical or aspherical innermost hollow portions, the outer surface can have non-uniform contour bordering and defining a contour of a second inner surface of outer core layer. The outer surface hardness and a second inner surface hardness of second inner surface differ and alternate symmetrically and circumferentially about the shell layer inner surface. | 2016-04-14 |