Patent application number | Description | Published |
20090132601 | Identifying Opportunities for Effective Expansion of the Content of a Collaboration Application - Within a document collaboration system, such as a wiki application, a logging component operates in association with a server. The logging component automatically creates and maintains a log of interactions between the server and users of the document collaboration system. The content of the log has a predictable format. In one embodiment, an analysis component identifies, from the log, entries associated with a failed search for a document in the collaboration system database. The terms not represented in the database are identified from the failed search entry. In this manner, statistics related to frequently unsuccessful search terms are generated and utilized as a basis for identifying opportunities for effective expansion of the content of the collaboration application. | 05-21-2009 |
20090132651 | Sensitive Information Handling On a Collaboration System - On a document collaboration system, such as a wiki, the content of postings to the collaboration system is monitored for sensitive information. Under some embodiments, when instances of such sensitive information are detected, an e-mail is sent to the user that posted the collaboration page posting. In other embodiments, a message is then sent to a person associated with the entity that indicates that the information placed on the collaboration page is confidential information or is related to an asset of the entity. In further embodiments, individual people are assigned responsibility for monitoring the use of certain instances of sensitive information on the collaboration system. Each user is only notified when the instances they are responsible for appear on a collaboration page. In other embodiments, if a collaboration page includes an instance of sensitive information, access to the collaboration page is changed such that fewer people can access the collaboration page. | 05-21-2009 |
20120159649 | Sensitive Information Handling on a Collaboration System - On a document collaboration system, such as a wiki, the content of postings to the collaboration system is monitored for sensitive information. Under some embodiments, when instances of such sensitive information are detected, an e-mail is sent to the user that posted the collaboration page posting. In other embodiments, a message is then sent to a person associated with the entity that indicates that the information placed on the collaboration page is confidential information or is related to an asset of the entity. In further embodiments, individual people are assigned responsibility for monitoring the use of certain instances of sensitive information on the collaboration system. Each user is only notified when the instances they are responsible for appear on a collaboration page. In other embodiments, if a collaboration page includes an instance of sensitive information, access to the collaboration page is changed such that fewer people can access the collaboration page. | 06-21-2012 |
Patent application number | Description | Published |
20090221781 | POLYESTER BASED DEGRADABLE MATERIALS AND IMPLANTABLE BIOMEDICAL ARTICLES FORMED THEREFROM - A method of making an aliphatic polyester prepolymer, comprising: reacting, alone or in combination with other reactants, a diol with at least a first diacid (or a diester of said first diacid) to produce an aliphatic polyester prepolymer. The first diacid is preferably a trans-beta-hydromuconic acid (HMA). In some embodiments, the diol contains at least one ether linkage. In some embodiments the diol is further reacted with at a second diacid, or a diester of said second diacid, wherein said second diacid is different from said first diacid. Prepolymers produced from such processes and articles formed therefrom are also described. | 09-03-2009 |
20120027719 | Polyester Based Degradable Materials and Implantable Biomedical Articles Formed Therefrom - A method of making an aliphatic polyester prepolymer, comprising: reacting, alone or in combination with other reactants, a diol with at least a first diacid (or a diester of said first diacid) to produce an aliphatic polyester prepolymer. The first diacid is preferably a trans-beta-hydromuconic acid (HMA). In some embodiments, the diol contains at least one ether linkage. In some embodiments the diol is further reacted with at a second diacid, or a diester of said second diacid, wherein said second diacid is different from said first diacid. Prepolymers produced from such processes and articles formed therefrom are also described. | 02-02-2012 |
20120228219 | SPIRAL WOUND MEMBRANE ELEMENT AND TREATMENT OF SAGD PRODUCED WATER OR OTHER HIGH TEMPERATURE ALKALINE FLUIDS - A spiral wound module is suitable for use with high temperature water that is also very alkaline or has a high pH, for example SAGD produced water. The module uses a polyamide-based membrane with a polysulfone or polyethersulfone backing material. For other components, the module uses primarily one or more of, EPDM; polyamide; polyphenylene oxide; polyphenylene sulfide; polysulfone; polyethersulfone; polysulfonamide; polyvinylidene fluoride; mylar; fiberglass; and, epoxy. Polyester is not used. Polypropylene is not used for the feed spacer. For example, a module may use a PVDF feed spacer, a nylon permeate spacer and a polysulfone center tube. The center tube may be provided with 4 rows of 0.063″ diameter holes and be rolled under high tension. | 09-13-2012 |
20140217163 | TEAR TAB CLOSURE STRIP - A closure device may include a backing and a closure strip removably provided on the backing, wherein the closure strip includes a permanent adhesive on a back face thereof adapted to affix the closure strip to a package, wherein a breakout portion of the backing is configured to separate from the backing and remain adhered to the closure strip when the closure strip is removed therefrom. A product package may include a carton having a flap movable between an open position and a closed position, and a closure device affixed to a portion of the flap and a separate portion of the carton when the flap is in the closed position, wherein a first portion of the closure device is removable from the separate portion of the carton while the first portion remains attached to the portion of the flap. | 08-07-2014 |
Patent application number | Description | Published |
20090149906 | METHOD AND APPARATUS FOR DISCONNECTING THE TIP ELECTRODE DURING MRI - A medical device includes a pulse generator, a lead, and an electrode. The lead includes an electrode and a lead conductor connecting the pulse generator with the electrode via first and second conductive paths. The medical device includes first and second switches. The first switch includes a non-conductive state in the presence of a magnetic field, the non-conductive state preventing formation of the first conductive path between the pulse generator and the electrode. The second switch includes a non-conductive state that prevents formation of the second conductive path between the pulse generator and the electrode. The first switch in the non-conductive state and the second switch in the non-conductive state electrically shields the electrode from electromagnetic radiation and induced voltages during a magnetic resonance imaging procedure. | 06-11-2009 |
20110276104 | METHOD AND APPARATUS FOR DISCONNECTING THE TIP ELECTRODE DURING MRI - A medical device includes a pulse generator, a lead, and an electrode. The lead includes an electrode and a lead conductor connecting the pulse generator with the electrode via first and second conductive paths. The medical device includes first and second switches. The first switch is disposed along the first conductive path and includes an open state in the presence of a magnetic field and a closed state in the absence of the magnetic field. The second switch is disposed along the second conductive path and includes an open state when a voltage applied across the second switch is at or below a threshold voltage and a closed state when the voltage applied across the second switch exceeds a threshold voltage. | 11-10-2011 |
20110319776 | CARDIAC CONTRACTION DETECTION USING INFORMATION INDICATIVE OF LEAD MOTION - Systems and methods for cardiac contraction detection using information indicative of lead motion are described. In an example, an implantable medical device can include a receiver circuit configured to be electrically coupled to conductor comprising a portion of an implantable lead and be configured to obtain information indicative of a movement of the implantable lead due at least in part to a motion of a heart. The device can include a processor circuit configured to determine whether a cardiac mechanical contraction occurred during a specified interval included in the obtained information indicative of the movement of the implantable lead. The processor circuit can be configured to determine information about the cardiac mechanical contraction using the obtained information indicative of the movement of the implantable lead. | 12-29-2011 |
20110319778 | CARDIAC FUNCTION MONITOR USING INFORMATION INDICATIVE OF LEAD MOTION - Systems and methods to monitor cardiac function using information indicative of lead motion are described. In an example, a system including an implantable medical device can include a receiver circuit configured to be electrically coupled to conductor comprising a portion of an implantable lead and be configured to obtain information indicative of a movement of the implantable lead due at least in part to a motion of a heart. The system can include a sensing circuit configured to obtain information indicative of cardiac electrical activity. The system can include a processor circuit configured to construct a template representative of a contraction of the heart, where the template can be constructed using the information indicative of the movement of the implantable lead due at least in part to the motion of the heart during the contraction, and using the information indicative of the cardiac electrical activity sensed during the contraction. | 12-29-2011 |
20110319779 | RHYTHM DISCRIMINATION USING INFORMATION INDICATIVE OF LEAD MOTION - Systems and methods for rhythm discrimination using the motion of an implantable lead are described. In an example, an implantable medical device can include a receiver circuit configured to be electrically coupled to an implantable lead and be configured to obtain information indicative of a movement of the implantable lead due at least in part to a motion of a heart. The device can include an arrhythmia detection circuit configured to determine an arrhythmia status using the information indicative of the movement of the implantable lead and an arrhythmia classification circuit configured to determine one or more of a location or a type of an arrhythmia, using the information indicative of the movement of the implantable lead, when the arrhythmia status indicates that an arrhythmia is occurring or has occurred. | 12-29-2011 |
20110319782 | CARDIAC MECHANICAL VIBRATION MONITOR USING INFORMATION INDICATIVE OF LEAD MOTION - Systems and methods to monitor cardiac mechanical vibrations using information indicative of lead motion are described. In an example, a system including an implantable medical device can include an excitation circuit configured to provide a non-tissue stimulating, non-therapeutic electrical excitation signal to a portion of an implantable lead. A receiver circuit can be configured to obtain information indicative of a mechanical vibration of the implantable lead due at least in part to one or more of an impact of at least a portion of the heart to the implantable lead, or friction contact between the implantable lead and cardiac tissue. The system can include a processor circuit configured to determine one or more of a lead mechanical status, or information indicative of valvular activity using the information indicative of the mechanical vibration of the implantable lead. | 12-29-2011 |
20150066102 | UNWANTED STIMULATION DETECTION DURING CARDIAC PACING - The disclosure relates to systems and methods for cardiac rhythm management. In some cases, a system may include a pulse generator for generating pacing pulses for stimulating a heart of a patient; a memory; and a sensor configured to sense a response to a unwanted stimulation and to produce a corresponding sensor signal. A processing circuit may receive the sensor signal for a time after one or more pacing pulses, and may derive a time-frequency representation of the sensor signal based on the received sensor signal. The processing circuit may use the time-frequency representation of the sensor signal to help identify unwanted stimulation. Once unwanted stimulation is detected, the processing circuit may change the pacing pulses to help reduce or eliminate the unwanted stimulation. | 03-05-2015 |
20150066103 | UNWANTED STIMULATION DETECTION DURING CARDIAC PACING - The disclosure relates to systems and methods for cardiac rhythm management. In some cases, a system may include a pulse generator for generating pacing pulses for stimulating a heart of a patient; a memory; and a sensor configured to sense a response to a unwanted stimulation and to produce a corresponding sensor signal. A processing circuit may receive the sensor signal for a time after one or more pacing pulses, and may derive a time-frequency representation of the sensor signal based on the received sensor signal. The processing circuit may use the time-frequency representation of the sensor signal to help identify unwanted stimulation. Once unwanted stimulation is detected, the processing circuit may change the pacing pulses to help reduce or eliminate the unwanted stimulation. | 03-05-2015 |
Patent application number | Description | Published |
20090276014 | EXTERNAL POWER SOURCE, SYSTEM AND METHOD FOR PREDICTING HEAT LOSS OF IMPLANTABLE MEDICAL DEVICE DURING INDUCTIVE RECHARGING BY EXTERNAL PRIMARY COIL - External power source, system for controlling and method for predicting heat loss of implantable medical device during inductive recharging by an external primary coil. A primary coil inductively couples energy to a secondary coil when energized and placed in proximity of the secondary coil. Control circuitry, operatively coupled to said primary coil, determines the energy absorbed in said tissue based on a total applied power by said external power source, power lost in said electronic circuitry, power lost in said electronic circuitry, power lost in said primary coil and power applied to said rechargeable power source and controlling said total applied power based upon said energy absorbed in said tissue. | 11-05-2009 |
20090276016 | CONCENTRIC PRIMARY COILS FOR INDUCTIVELY CHARGING AN IMPLANTABLE MEDICAL DEVICE, EXTERNAL POWER SOURCE AND METHOD - An external antenna with a plurality of concentric primary coils recharges an implantable medical device with a secondary coil when the primary coils are placed in proximity of the secondary coil. Selection circuitry determines which of the plurality of concentric primary coils has the most efficient coupling with the secondary coil and drive circuitry drives the selected primary coil with an oscillating current. During a recharge session, selection circuitry periodically checks at least some of the primary coils to determine whether the primary coil with the most efficient connection has changed. An antenna housing may hold the primary coils in a rigid planar relationship with each other or the primary coils may shift with respect to each other, forming a cup-shape around a bulge in the skin created by the implantable medical device. | 11-05-2009 |
20100076524 | INDUCTIVELY RECHARGEABLE EXTERNAL ENERGY SOURCE, CHARGER, SYSTEM AND METHOD FOR A TRANSCUTANEOUS INDUCTIVE CHARGER FOR AN IMPLANTABLE MEDICAL DEVICE - A mechanism for transferring energy from an external power source to an implantable medical device is disclosed. An antenna is positioned in proximity of the implantable medical device. The position of a core of the antenna is adjusted relative to the implantable medical device while the antenna is maintained substantially stationary. A frequency of transmission of a power source is adjusted, and the antenna is driven at the adjusted frequency to transfer energy transcutaneously to the implantable medical device. In one embodiment, the frequency of transmission is selected based on an amplitude of a signal in the antenna. | 03-25-2010 |
20100198307 | MEDICAL DEVICE PROGRAMMER - In general, the disclosure is directed to a patient programmer for an implantable medical device. The patient programmer may include one or more of a variety of features that may enhance performance, support mobility and compactness, or promote patient convenience. The patient programmer includes an internal antenna mounted on a first circuit board and a display mounted on a second circuit board. The first circuit board includes a substantially contiguous ground plane layer that is interrupted by two or more gaps. The patient programmer may also include one or more of a variety of features that may enhance performance, support mobility and compactness, or promote patient convenience. | 08-05-2010 |
20100268305 | ALIGNMENT INDICATION FOR TRANSCUTANEOUS ENERGY TRANSFER - System for transcutaneous energy transfer. An implantable medical device, adapted to be implanted in a patient, has componentry for providing a therapeutic output. The implantable medical device has an internal power source and a secondary coil operatively coupled to the internal power source. An external power source, having a primary coil, provides energy to the implantable medical device when the primary coil of the external power source is placed in proximity of the secondary coil of the implantable medical device and thereby generates a current in the internal power source. An alignment indicator reports the alignment as a function of the current generated in the internal power source with a predetermined value associated with an expected alignment between the primary coil and secondary coil. | 10-21-2010 |
20110022125 | INDUCTIVELY RECHARGEABLE EXTERNAL ENERGY SOURCE, CHARGER, SYSTEM AND METHOD FOR A TRANSCUTANEOUS INDUCTIVE CHARGER FOR AN IMPLANTABLE MEDICAL DEVICE - Techniques for transcutaneous transferral of energy to an implantable medical device are disclosed. An embodiment includes a system comprising an implantable medical device having a secondary coil. An external device is provided to transcutaneously transfer energy to the secondary coil. The external device comprises a housing having a side adapted to be positioned in proximity to the secondary coil when the external device is transferring energy to the secondary coil. A temperature sensor is coupled to the side to determine a temperature indicative of heat to which the patient is being exposed during the transfer of energy. A control circuit is adapted to control the transfer of energy to the secondary coil based on the temperature. For instance, the control circuit may limit transfer of energy by controlling times at which transfer of energy occurs or controlling an amplitude of a signal within the external device. | 01-27-2011 |
20110245892 | FLEXIBLE RECHARGE COIL TECHNIQUES - Techniques adapted for use with recharging a rechargeable power source of an implantable device. One aspect relates to providing a flexible primary coil that can be transcutaneously coupled to a secondary coil of the implantable device. Multiple adjacent turns of the coil are grouped via lacing to form bundles. The bundles have at least one dimension that is selected to be a same size as a predetermined thickness of the coil. In one embodiment, the dimension is a diameter of the bundle. In another embodiment, the dimension is at least one of a length or width of the bundle. Insulating overmolding may be provided over the coil. In one embodiment, the resulting antenna structure is bidirectional such that substantially the same performance characteristics are obtained during recharge regardless of which of two major surfaces of the antenna is placed in proximity to the patient. | 10-06-2011 |
20110298420 | INDUCTIVELY RECHARGEABLE EXTERNAL ENERGY SOURCE, CHARGER AND SYSTEM FOR A TRANSCUTANEOUS INDUCTIVE CHARGER FOR AN IMPLANTABLE MEDICAL DEVICE - A mechanism for transferring energy from an external power source to an implantable medical device is disclosed. An antenna is positioned in proximity of the implantable medical device. The position of a core of the antenna is adjusted relative to the implantable medical device while the antenna is maintained substantially stationary. A frequency of transmission of a power source is adjusted, and the antenna is driven at the adjusted frequency to transfer energy transcutaneously to the implantable medical device. In one embodiment, the frequency of transmission is selected based on an amplitude of a signal in the antenna. | 12-08-2011 |
20110301667 | INDUCTIVELY RECHARGEABLE EXTERNAL ENERGY SOURCE, CHARGER, SYSTEM AND METHOD FOR A TRANSCUTANEOUS INDUCTIVE CHARGER FOR AN IMPLANTABLE MEDICAL DEVICE - A mechanism for transferring energy from an external power source to an implantable medical device is disclosed. A sensor may be used to measure a parameter that correlates to a temperature of the system that occurs during the transcutaneous coupling of energy. For example, the sensor may measure temperature of a surface of an antenna of the external power source. The measured parameter may then be compared to a programmable limit. A control circuit such as may be provided by the external power source may then control the temperature based on the comparison. The programmable limit may be, for example, under software control so that the temperature occurring during transcutaneous coupling of energy may be modified to fit then-current circumstances. | 12-08-2011 |
20110301669 | Alignment Indication for Transcutaneous Energy Transfer - System for transcutaneous energy transfer. An implantable medical device, adapted to be implanted in a patient, has componentry for providing a therapeutic output. The implantable medical device has an internal power source and a secondary coil operatively coupled to the internal power source. An external power source, having a primary coil, provides energy to the implantable medical device when the primary coil of the external power source is placed in proximity of the secondary coil of the implantable medical device and thereby generates a current in the internal power source. An alignment indicator reports the alignment as a function of the current generated in the internal power source with a predetermined value associated with an expected alignment between the primary coil and secondary coil. | 12-08-2011 |
20120197347 | FAR FIELD TELEMETRY OPERATIONS BETWEEN AN EXTERNAL DEVICE AND AN IMPLANTABLE MEDICAL DEVICE DURING RECHARGE OF THE IMPLANTABLE MEDICAL DEVICE VIA A PROXIMITY COUPLING - Far field telemetry operations are conducted between an external device and an implantable medical device while power is being transferred to the implantable medical device for purposes of recharging a battery of the implantable medical device. The far field operations may include exchanging recharge information that has been collected by the implantable medical device which allows the external device to exercise control over the recharge process. The far field operations may include suspending far field telemetry communications for periods of time while power continues to be transferred where suspending far field telemetry communications may include powering down far field telemetry communication circuits of the implantable medical device for periods of time which may conserve energy. The far field operations may further include transferring programming instructions to the implantable medical device. | 08-02-2012 |
20120197351 | MEDICAL DEVICE RECHARGE SYSTEMS USING A CONTROLLER IN WIRELESS COMMUNICATION WITH A SEPARATE RECHARGE DEVICE - Medical device recharging systems include a controller and a separate recharge device that communicate wirelessly together to provide recharging to an implantable medical device. Either the controller or the recharge device may also communicate wirelessly with the implantable medical device to obtain recharge status and other information. There may be multiple recharge devices present within communication range of the controller, and the controller may determine which recharge device to activate depending upon proximity of each recharge device to the implantable medical device. The controller may allow the recharge device that is active at any given time to change so that the patient having the implantable medical device can move about in the area where the recharge devices are located while recharging continues. | 08-02-2012 |
20120262108 | RECHARGE TUNING TECHNIQUES FOR AN IMPLANTABLE DEVICE - Techniques are disclosed for tuning a frequency at which an external device transcutaneously transfers energy. The transferred energy may be used to charge a rechargeable power source of an implantable medical device (IMD) and/or to power the IMD directly. One embodiment relates to a charging system that may comprise a circuit to drive a primary coil of an external device at a drive frequency and a control circuit to tune the drive frequency based on a characteristic of a monitored signal that is associated with the primary coil. The characteristic is not present when the primary coil is being driven at a resonant frequency of the system. In a specific example, the characteristic comprises a stub pulse and the control circuit is configured to tune the drive frequency based on at least one of a relative timing and a width of the stub pulse. | 10-18-2012 |
20130105115 | REMOVABLE HEAT MANAGEMENT FOR RECHARGE COILS | 05-02-2013 |
20130106347 | HEAT MANAGEMENT FOR RECHARGE COILS FOR IMPLANTABLE MEDICAL DEVICES | 05-02-2013 |
20130193914 | ADAPTIVE RATE RECHARGING SYSTEM - Devices, systems, and techniques for selecting a period for charging an implantable rechargeable power source are disclosed. Implantable medical devices may include a rechargeable power source that can be transcutaneously charged. A system may control a charging module to begin charging the rechargeable power source of the implantable medical device with a high power level. The system may then determine an estimated heat loss based on power initially delivered to the rechargeable power source when beginning the charging. Based on this estimated heat loss during the initial period of recharging, the system may select a boost period that includes a duration of time that the rechargeable power source is charged with the high power level. | 08-01-2013 |
20130197613 | MANAGING RECHARGE POWER FOR IMPLANTABLE MEDICAL DEVICES - Devices, systems, and techniques for controlling charging power based on a cumulative thermal dose to a patient are disclosed. Implantable medical devices may include a rechargeable power source that can be transcutaneously charged. An external charging device may calculate an estimated cumulative thermal dose delivered to the patient during charging over a predetermined period of time. Based on the estimated cumulative thermal dose, the external charging device may select a power level for subsequent charging of the rechargeable power source. In one example, the charging device may select a high power level when the cumulative thermal dose has not exceeded a thermal dose threshold and select a low power level when the cumulative thermal dose has exceeded the thermal dose threshold. | 08-01-2013 |
20130211479 | Alignment Indication for Transcutaneous Energy Transfer - System for transcutaneous energy transfer. An implantable medical device, adapted to be implanted in a patient, has componentry for providing a therapeutic output. The implantable medical device has an internal power source and a secondary coil operatively coupled to the internal power source. An external power source, having a primary coil, provides energy to the implantable medical device when the primary coil of the external power source is placed in proximity of the secondary coil of the implantable medical device and thereby generates a current in the internal power source. An alignment indicator reports the alignment as a function of the current generated in the internal power source with a predetermined value associated with an expected alignment between the primary coil and secondary coil. | 08-15-2013 |
20130278226 | SENSING TEMPERATURE WITHIN MEDICAL DEVICES - Devices, systems, and techniques for monitoring the temperature of a device used to charge a rechargeable power source are disclosed. Implantable medical devices may include a rechargeable power source that can be transcutaneously charged. The temperature of an external charging device and/or an implantable medical device may be monitored to control the temperature exposure to patient tissue. In one example, a temperature sensor may sense a temperature of a portion of a device, wherein the portion is non-thermally coupled to the temperature sensor. A processor may then control charging of the rechargeable power source based on the sensed temperature. | 10-24-2013 |
20130289662 | RECHARGE OF AN IMPLANTABLE DEVICE IN THE PRESENCE OF OTHER CONDUCTIVE OBJECTS - Techniques are disclosed for controlling the transcutaneously transfer of energy to an implantable medical device (IMD) that is in proximity to a conductive object that conducts current in the presence of an electromagnetic field. Various techniques are disclosed for estimating or determining the levels of heat dissipation associated with the object during the transfer of energy. If too much heat is being dissipated, the transfer of energy may be adjusted so that heating remains below acceptable levels. | 10-31-2013 |
20140163648 | Medical Device Recharge Systems Using a Controller in Wireless Communication with a Separate Recharge Device - Medical device recharging systems include a controller and a separate recharge device that communicate wirelessly together to provide recharging to an implantable medical device. Either the controller or the recharge device may also communicate wirelessly with the implantable medical device to obtain recharge status and other information. There may be multiple recharge devices present within communication range of the controller, and the controller may determine which recharge device to activate depending upon proximity of each recharge device to the implantable medical device. The controller may allow the recharge device that is active at any given time to change so that the patient having the implantable medical device can move about in the area where the recharge devices are located while recharging continues. | 06-12-2014 |
20150073509 | REMOVABLE HEAT MANAGEMENT FOR RECHARGE COILS - Devices, systems, and techniques for managing heat generated in coils for wireless energy transmission are disclosed. Inductive coupling between two coils (e.g., a primary coil and a secondary coil) may be used to recharge the power source of an implantable medical device. A phase change material may be thermally coupled to the primary coil to absorb heat generated during the inductive coupling and reduce temperature increases of the primary coil. In one example, the phase change material may be configured to absorb heat from an energy transfer coil. A housing may be configured to contain the phase change material and a coupling mechanism may be configured to removably attach the housing to the energy transfer coil. | 03-12-2015 |
Patent application number | Description | Published |
20110198413 | PORTABLE AIRLESS SPRAYER - A handheld airless fluid dispensing device comprises a pump, a drive element and an orifice element. The pump directly pressurizes a fluid. The drive element supplies power to the pump. The orifice element is connected to the pump and atomizes un-thinned architectural coating to a particle size of no greater than approximately 150 microns. The pump generates orifice pressures up to approximately 2.48 MPa and the orifice has an area of approximately 18.7 mm2. In one embodiment, the pump, drive element and orifice element are integrated into a handheld housing. In one embodiment, the pump comprises a reciprocating piston fluid pump comprising at least two pumping chambers configured to be actuated out of phase by at least one piston. In another embodiment, the reciprocating piston fluid pump comprises two pistons having different displacements that are linearly actuated by a wobble assembly driven by a gear reducer and an electric motor. | 08-18-2011 |
20130206856 | PORTABLE AIRLESS SPRAYER - A portable airless sprayer comprises a housing, a motor, a pump, a spray tip and a trigger. The motor is mounted to the housing. The pump is mounted to the housing and is driven by the motor. The spray tip assembly receives pressurized fluid from the pump. The trigger is configured to actuate the spray tip assembly and activate the motor. A method of operating a portable airless sprayer comprises moving a lever over a stroke, displacing a valve pin, and activating a motor. The valve pin is displaced with the lever to actuate a spray valve. The motor is activated with the lever to drive a pump that provides fluid to the spray valve. | 08-15-2013 |
20130277455 | PORTABLE AIRLESS SPRAYER - A sprayer attachment for a hand-supported power tool comprises a motion converting mechanism, a pumping mechanism, a spray assembly and a housing. The motion converting mechanism has an input shaft. The pumping mechanism is driven by the motion converting mechanism. The spray assembly is fluidly coupled to the pumping mechanism. The housing assembly couples the motion converting mechanism, the pumping mechanism and the spray assembly. The sprayer attachment may further comprise an anti-rotation bracket extending from the housing. The sprayer attachment may further be coupled to a handheld power tool, such as a cordless drill or a reciprocating saw, with the anti-rotation bracket. | 10-24-2013 |
20140034754 | PORTABLE AIRLESS SPRAYER - A fluid dispensing device comprises a housing body, a fluid container, a reciprocating piston fluid pump, a primary drive element and a spray tip. The housing body is configured to be carried and supported by an operator of the hand held airless fluid dispensing device during operation. The fluid container is supported by the housing body. The reciprocating piston fluid pump is coupled to the housing body and comprises at least two pumping chambers configured to be actuated out of phase by at least one piston. The primary drive element is coupled to the housing body and connected to the reciprocating piston fluid pump to actuate the at least one piston. The spray tip is connected to an outlet of at least one of the pumping chambers. | 02-06-2014 |
Patent application number | Description | Published |
20090029274 | METHOD FOR REMOVING CONTAMINATION WITH FLUORINATED COMPOSITIONS - A method of removing contamination from a substrate having an ion-implanted region is described. The method comprises applying a composition comprising a fluorinated solvent and a co-solvent to the substrate in an amount sufficient to assist in the removal of contamination from the substrate. As contaminant is removed, metal patterns or other desired features on the substrate remain. Additionally, the composition for removing contamination is not harmful to the user or the substrate (i.e., non-flammable and/or non caustic). | 01-29-2009 |
20120273000 | SULFONATE-FUNCTIONAL COATINGS AND METHODS - A coated article having a substrate coated with a layer of a sulfonate-functional coating, and methods of making and using. | 11-01-2012 |
20130216820 | HYDROPHOBIC FLUORINATED COATINGS - Articles having hydrophobic fluorinated coatings are provided. More specifically, the articles include a substrate, a primer layer of acid-sintered silica nanoparticles, and a hydrophobic fluorinated layer. The hydrophobic fluorinated coatings can be used on a large variety of substrate and tend to be quite durable even when subjected to repeated rubbing and/or cleaning. | 08-22-2013 |
20130229378 | OPTICAL DEVICE SURFACE TREATMENT PROCESS AND SMUDGE-RESISTANT ARTICLE PRODUCED THEREBY - A surface treatment process comprises (a) providing at least one optical device; (b) providing a curable surface treatment composition comprising (1) at least one fluorinated organosilane compound comprising (i) a monovalent segment selected from polyfluoroalkyl, polyfluoroether, polyfluoropolyether, and combinations thereof and (ii) a monovalent endgroup comprising at least one silyl moiety comprising at least one group selected from hydrolyzable groups, hydroxyl, and combinations thereof, and (2) at least one fluorinated organosilane compound comprising (i) a multivalent segment selected from polyfluoroalkane, polyfluoroether, polyfluoropolyether, and combinations thereof and (ii) at least two monovalent endgroups, each independently comprising at least one silyl moiety comprising at least one group selected from hydrolyzable groups, hydroxyl, and combinations thereof; (c) applying the curable surface treatment composition to the optical device; and (d) curing the applied, curable surface treatment composition. | 09-05-2013 |
20140287248 | FLUORINATED COATINGS WITH LUBRICIOUS ADDITIVE - Fluorinated coatings having a lubricious additive, articles with the fluorinated coatings, and methods of making articles with the fluorinated coatings are provided. More specifically, the fluorinated coatings are prepared from a curable coating composition that includes both a fluorinated silane and a fluorinated polyether oil. The curable coating composition is typically applied adjacent to a siliceous substrate and then cured. The resulting cured articles can have an outer surface that has a good tactile response, that is abrasion resistant, that is easy to clean, or a combination thereof. | 09-25-2014 |
20150038642 | OLEOPHOBIC COATINGS - A polymeric coating for a glass substrate includes a hexafluoropropylene oxide derived silane polymer. The hexafluoropropylene oxide derived silane polymer has a molecular weight of greater than about 5500, a thickness of between about 2 and about 15 nanometers and a coefficient of friction constant of less than about 0.35. A water contact angle of the polymeric hexafluoropropylene oxide derived silane coating decreases by less than about 27% after being subjected to 10000 abrasion cycles. | 02-05-2015 |
Patent application number | Description | Published |
20090301604 | PORTABLE FLUID TREATING AND DISPENSING DEVICE, SYSTEMS, ARTICLES, AND METHODS - Disclosed are portable fluid treating and dispensing devices, systems, articles, and methods particularly adapted for use in treating potable liquids, such as drinking water, and dispensing it into a plurality of portable potable liquid containers, such as water bottles. | 12-10-2009 |
20100065503 | PORTABLE WATER TREATMENT APPARATUS AND METHODS - Herein are disclosed apparatus and methods that can be used to receive a volume of potable water from a source and to treat the volume of water so as to improve the perceived or actual aesthetic quality of the water, and to thereafter contain the treated water such that it can be used or consumed. | 03-18-2010 |
20110079317 | WATER TREATMENT DEVICE FOR PRODUCING BOTTLED WATER - A water treatment device for filling at least one bottle with treated tap water includes a housing unit having a reservoir, and at least one valve arranged in fluid communication with the reservoir, the valve having a water inlet/air exit port arranged adjacent to the housing unit, and a water exit/air inlet port arranged opposite the water inlet/air exit port, whereby when the valve is actuated to its open condition, water flows through the valve and into the bottle, and air entrapped in the bottle flows through the valve and into the surrounding environment. When the valve is in its closed condition, air and water do not flow through the valve. | 04-07-2011 |
20110079551 | WATER TREATMENT CARTRIDGE - A water treatment cartridge, or insert, for use in connection with a water treatment device such as a gravity-fed water pitcher or the like includes a support structure and water treatment material arranged in combination with the support structure. The support structure may, for example, generally enclose the water treatment material, or the support structure may be integrated into the structure of the water treatment material | 04-07-2011 |
20110079572 | BOTTLE FOR WATER TREATMENT DEVICE - A water bottle for use in connection with a water treatment device includes an opening with a diameter of at least about 0.87 inches, a diameter of no greater than about 1.06 inches, and a height of at least about 6.56 inches, and a height of no greater than about 8.02. | 04-07-2011 |
20140353455 | REMOVABLE WALL DECORATION KITS, SYSTEMS AND METHODS - Systems and kits for decorating walls include a plurality of décor assemblies and a plurality of complementary fastening structures. The décor assemblies include a décor element and a releasable fastening structure providing first fastening elements. The complementary fastening structure includes a base, a pressure sensitive adhesive disposed on the base, and second fastening elements. The first fastening elements are releasably mateable with the second fastening elements to define a releasable fastening system. During use, a complementary fastening structure is releasably applied to a wall, and is connected to and supports one of the décor assemblies via the releasable fastening system. The releasable fastening system can comprise low profile hooks and loops, exhibiting relatively low holding power. | 12-04-2014 |
Patent application number | Description | Published |
20080305366 | Magnetic recording tape configured for improved surface lubricity - A magnetic recording tape configured for increased surface lubricity includes an elongated substrate and a magnetic side disposed on the substrate. The magnetic side includes a magnetic recording layer defining an exposed magnetic recording surface opposite the substrate, and a support layer deposited on the substrate between the substrate and the magnetic recording layer. The support layer includes nano-particles configured to release lubrication to the exposed magnetic recording surface. In this regard, the support layer configures the exposed magnetic recording surface to have a surface lubrication to total lubrication ratio (SL ratio) of greater than about 5%. | 12-11-2008 |
20090162701 | Magnetic recording tape having large particles in magnetic recording layer - A magnetic recording tape includes an elongated substrate and a magnetic film coated over the elongated substrate, where the magnetic film includes a first magnetic recording layer. The first magnetic recording layer includes particles having a diameter that is between a factor from about 2 to 5 greater than a thickness of the first magnetic recording layer. | 06-25-2009 |
20110242698 | Barium Ferrite Magnetic Storage Media - Magnetic storage media that include a multilayer structure are described. In general, the magnetic storage media include a substrate, an underlayer that includes a plurality of underlayer particles formed over the substrate, and a magnetic layer that includes a plurality of magnetic particles formed over the underlayer. The magnetic layer may define a saturated magnetization and thickness product less than or equal to approximately 1.00 memu per square centimeter, and the magnetic particles may be selected from the group consisting of magnetic platelet-shaped particles and magnetic particles with an aspect ratio less than or equal to approximately 1.5. In addition, the described magnetic storage media may exhibit minimal interlayer diffusion between the underlayer and magnetic layer. Reduced interlayer diffusion between different layers of a magnetic recording medium may result in an improved magnetic recording surface for recording and storing data. | 10-06-2011 |
20110244114 | Barium Ferrite Magnetic Storage Media with Uniform Magnetic Particle Distributions - Magnetic storage media and methods for constructing magnetic storage media that include a multilayer structure are described. In some examples, a magnetic recording medium can be formed by forming an underlayer over a substrate, drying the underlayer, milling a plurality of magnetic particles, and forming a magnetic layer that includes the plurality of magnetic particles over the underlayer. The magnetic particles may be selected from the group consisting of magnetic platelet-shaped particles and magnetic particles with an aspect ratio less than or equal to approximately 1.5. In addition, the milling process may include milling the plurality of magnetic particles so a magnetic medium formed in the absence of an applied magnetic field exhibits a longitudinal squareness less than or equal to approximately 0.40. | 10-06-2011 |
20110244118 | Method of Forming Barium Ferrite Magnetic Storage Media - Magnetic storage media and methods for constructing magnetic storage media that include a multilayer structure are described. In general, the magnetic storage media include a substrate, an underlayer formed over the substrate, and a magnetic layer that includes a plurality of magnetic particles formed over the underlayer. In some examples, a magnetic recording medium can be formed by forming an underlayer over a substrate, drying the underlayer, and heat-curing the underlayer prior to forming a magnetic layer over the underlayer. A magnetic layer can then be formed over the underlayer. The magnetic layer may includes a plurality of magnetic particles selected from the group consisting of magnetic platelet-shaped particles and magnetic particles with an aspect ratio less than or equal to approximately 1.5, may then be formed over the underlayer. By heat-curing the underlayer prior to forming the magnetic layer over the underlayer, the formed magnetic recording medium may exhibit an improved magnetic recording surface for recording and storing data. | 10-06-2011 |
20120314318 | Continuous Biasing and Servowriting of Magnetic Storage Media having Perpendicular Anisotrophy - Magnetic storage tape and techniques for erasing and writing to magnetic storage tape having a perpendicular squareness greater than 50 percent and a longitudinal squareness less than 50 percent are described. In general, the magnetic tape may be biased with a remanence magnetization, or magnetic orientation, in any direction. One or two head systems may use various magnetic field patterns to create the desired remanence magnetization. Servo marks may have a remanence magnetization in an opposite magnetic orientation than that of the remaining bias on the servo track, e.g., substantially perpendicular to the magnetic tape. In some examples, a write head may alternate the direction of the magnetic field to continuously bias and write servo patterns to the magnetic tape. In addition, a symmetrical servo mark may be created in the magnetic tape with a write head having a gap width approximately equal to the length of the servo mark. | 12-13-2012 |
20120314319 | Servo Mark Length Matched to Write Head Gap for Magnetic Storage Media - Magnetic storage tape and techniques for erasing and writing to magnetic storage tape having a perpendicular squareness greater than 50 percent and a longitudinal squareness less than 50 percent are described. In general, the magnetic tape may be biased with a remanence magnetization, or magnetic orientation, in any direction. One or two head systems may use various magnetic field patterns to create the desired remanence magnetization. Servo marks may have a remanence magnetization in an opposite magnetic orientation than that of the remaining bias on the servo track, e.g., substantially perpendicular to the magnetic tape. In some examples, a write head may alternate the direction of the magnetic field to continuously bias and write servo patterns to the magnetic tape. In addition, a symmetrical servo mark may be created in the magnetic tape with a write head having a gap width approximately equal to the length of the servo mark. | 12-13-2012 |
20120314320 | Erasure of Magnetic Storage Media having Perpendicular Anisotropy - Magnetic storage tape and techniques for erasing and writing to magnetic storage tape having a perpendicular squareness greater than 50 percent and a longitudinal squareness less than 50 percent are described. In general, the magnetic tape may be biased with a remanence magnetization, or magnetic orientation, in any direction. One or two head systems may use various magnetic field patterns to create the desired remanence magnetization. Servo marks may have a remanence magnetization in an opposite magnetic orientation than that of the remaining bias on the servo track, e.g., substantially perpendicular to the magnetic tape. In some examples, a write head may alternate the direction of the magnetic field to continuously bias and write servo patterns to the magnetic tape. In addition, a symmetrical servo mark may be created in the magnetic tape with a write head having a gap width approximately equal to the length of the servo mark. | 12-13-2012 |
20120314322 | Erasure and Servowriting of Magnetic Storage Media having Perpendicular Anisotropy - Magnetic storage tape and techniques for erasing and writing to magnetic storage tape having a perpendicular squareness greater than 50 percent and a longitudinal squareness less than 50 percent are described. In general, the magnetic tape may be biased with a remanence magnetization, or magnetic orientation, in any direction. One or two head systems may use various magnetic field patterns to create the desired remanence magnetization. Servo marks may have a remanence magnetization in an opposite magnetic orientation than that of the remaining bias on the servo track, e.g., substantially perpendicular to the magnetic tape. In some examples, a write head may alternate the direction of the magnetic field to continuously bias and write servo patterns to the magnetic tape. In addition, a symmetrical servo mark may be created in the magnetic tape with a write head having a gap width approximately equal to the length of the servo mark. | 12-13-2012 |
20140139944 | INFORMATION STORAGE USING SERVO PATTERNS - Storage media, systems, and techniques for storing and accessing information in a servo band are described. For example, the distances between adjacent servo patterns written to the servo band may be varied to represent the supplemental information stored in the servo band. Each of the varied distances may be selected to represent physical parameters of the storage medium, servo recording conditions, or data unrelated to the servo patterns, for example. The supplemental information may be recovered from the servo band by demodulating a signal generated from a servo read head. The distances between each servo pattern in the track may be calculated from the time periods detected in the signal between servo marks of subsequent servo patterns. In some examples, a controller may adjust one or more parameters associated with reading or writing servo marks or data marks of the storage media. | 05-22-2014 |
Patent application number | Description | Published |
20080207794 | POLYMERIC FIBERS AND METHODS OF MAKING - Polymeric fibers and methods of making the polymeric fibers are described. The polymeric fibers are crosslinked hydrogels or dried hydrogels that are prepared from a precursor composition that contains polymerizable material having an average number of ethylenically unsaturated groups per monomer molecule greater than 1.0. The polymeric fibers can contain an optional active agent. | 08-28-2008 |
20080300339 | POLYMERIC BEADS AND METHODS OF MAKING POLYMERIC BEADS - Polymeric beads and methods of making the polymeric beads are described. The polymeric beads are crosslinked hydrogels or dried hydrogels. The polymeric beads are formed from droplets of a precursor composition that are exposed to radiation. The droplets are totally surrounded by a gas phase. The precursor composition contains a polar solvent and a polymerizable material miscible in the polar solvent. The polymerizable material has an average number of ethylenically unsaturated groups per monomer molecule equal to at least 1.2. | 12-04-2008 |
20090130157 | Antimicrobial Adhesive Films - A multi-layer film for reducing microbial contamination on a surface. The multi-layer film can include a core layer having a first surface and a second surface opposite the first surface, an adhesive layer disposed adjacent the first surface of the core layer, and an antimicrobial layer disposed adjacent the second surface. The antimicrobial layer can include a cross-linked matrix and an antimicrobial agent dispersed within the cross-linked matrix, where the cross-linked matrix is derived from a polymerizable precursor comprising a material selected from the group consisting of a polymerizable monomer, a polymerizable polymer having a molecular weight of about 1,000 or less, and combinations thereof. | 05-21-2009 |
20090155451 | ANTIMICROBIAL COATING SYSTEM - An antimicrobial coating system, a film-forming composition, and an antimicrobial film. In some embodiments, the antimicrobial coating system can include a film-forming composition comprising a polymer having an effective molecular weight, and an effective amount of an antimicrobial agent dispersed within the polymer. The film-forming composition can form a water-insoluble, biocidal antimicrobial film when applied to a surface. | 06-18-2009 |
20120045498 | ANTIMICROBIAL COATING SYSTEM - An antimicrobial coating system, a film-forming composition, and an antimicrobial film. In some embodiments, the antimicrobial coating system can include a film-forming composition comprising a polymer having an effective molecular weight, and an effective amount of an antimicrobial agent dispersed within the polymer. The film-forming composition can form a water-insoluble, biocidal antimicrobial film when applied to a surface. | 02-23-2012 |
Patent application number | Description | Published |
20110004285 | SYSTEM AND METHOD FOR CARDIAC LEAD - An implantable medical device (IMD) can include implantable pulse generator (IPG) devices, implantable cardioverter-defibrillators (ICD), cardiac resynchronization therapy defibrillator devices, neurostimulators or combinations thereof. In one example, the IMD can include a body assembly, which can provide at least one electrical signal corresponding to a therapy. The IMD can also include a cardiac lead assembly, which can have a proximal portion and a distal portion. The proximal portion of the cardiac lead assembly can be in communication with the body assembly to receive the therapy and the distal portion can be adapted to be coupled to an anatomical structure to transmit the at least one electrical signal to the anatomical structure. The proximal portion of the cardiac lead assembly can have a first stiffness and the distal portion can have a second stiffness. The first stiffness can be greater than the second stiffness. | 01-06-2011 |
20110004286 | SYSTEM AND METHOD FOR CARDIAC LEAD - An implantable medical device (IMD) can include implantable pulse generator (IPG) devices, implantable cardioverter-defibrillators (ICD), cardiac resynchronization therapy defibrillator devices, neurostimulators or combinations thereof. The IMD can also include a cardiac lead assembly in communication with the body assembly to transmit the at least one electrical signal to an anatomical structure. The cardiac lead assembly can include a first sleeve, which can have a distal end, a proximal end, and a surface therebetween. The surface can define a plurality of annular ribs along the distal end and can have a channel defined between each pair of adjacent ribs. An electrode can be coupled to the surface of the first sleeve adjacent to the distal end such that at least one channel is fillable with an adhesive to couple a second sleeve to the first sleeve. | 01-06-2011 |
20120239124 | IN-LINE CONNECTOR TERMINALS FOR IMPLANTABLE MEDICAL ELECTRICAL LEADS - An implantable medical electrical lead includes a plurality of conductors that extend continuously, without any intermediary junctions, between a plurality of electrodes and a corresponding plurality of contact members of an in-line connector terminal. A junction between each conductor and the corresponding contact member is preferably formed by first fitting a conductive sleeve, which is coupled to a proximal portion of the conductor, into an eyelet feature of the contact member, which is mounted on a strut member, and then welding the sleeve to the contact member at a pre-formed slot of the contact member, which extends along an external recessed surface thereof. The assembly of the connector terminal preferably completes the construction of the lead, wherein the proximal portion of each conductor is positioned in a helical path, which extends between an elongate body of the lead and the connector terminal, and along which a grip zone is formed. | 09-20-2012 |
20140052228 | IN-LINE CONNECTOR TERMINALS FOR IMPLANTABLE MEDICAL ELECTRICAL LEADS - An implantable medical electrical lead includes a plurality of conductors that extend continuously, without any intermediary junctions, between a plurality of electrodes and a corresponding plurality of contact members of an in-line connector terminal. A junction between each conductor and the corresponding contact member is preferably formed by first fitting a conductive sleeve, which is coupled to a proximal portion of the conductor, into an eyelet feature of the contact member, which is mounted on a strut member, and then welding the sleeve to the contact member at a pre-formed slot of the contact member, which extends along an external recessed surface thereof. The assembly of the connector terminal preferably completes the construction of the lead, wherein the proximal portion of each conductor is positioned in a helical path, which extends between an elongate body of the lead and the connector terminal, and along which a grip zone is formed. | 02-20-2014 |
Patent application number | Description | Published |
20080269837 | IMPLANTABLE MEDICAL LEAD FOR IMPLANTATION IN A PATIENT, SUCH AS A PATIENT'S NECK - Implantable leads implantable in a patient, such as patient's neck. The lead includes a first lead segment and a second lead segment. The second lead segment extends from the first lead segment at a first junction point and includes first, second, and third legs each defining a longitudinal length in extension from the first junction point to a distal end. A length of the first leg is greater than a length of the second leg, and a length of the second leg is greater than a length of the third leg. With this configuration, each of the legs are adapted to support at least one electrode at the distal end thereof, and are appropriately dimensioned relative to one another for locating the corresponding electrode at a desired target tissue site in the patient's neck. Targeted tissue can include, for example, muscles of the neck. | 10-30-2008 |
20080269857 | IMPLANTABLE MEDICAL LEADS AND LEAD ASSEMBLIES WITH FLEXIBILITY, EXTENSIBILITY AND BRANCHED STRUCTURES - Implantable medical leads that are flexible and extensible in a controllable manner to facilitate subject body movements and that are bundled to create a branched lead to permit lead body ends on one or both ends of the lead to be movable relative to one another so as to be positionable in different locations. Implantable medical leads advantageously include individual lead portions, sub-bundles, and bundles that are able to be selectively positioned and implanted within a subject body and that are useful, in particular, for use in the neck region of a subject body and other regions of any subject's body that may benefit from increased flexibility, extensibility and positionability. | 10-30-2008 |
20080269859 | METHODS FOR CUSTOMIZING IMPLANTABLE MEDICAL LEADS AND LEAD ASSEMBLIES WITH IMPROVED FLEXIBILITY AND EXTENSIBILITY - Implantable medical leads that are customizable and that are flexible and extensible in a controllable manner to facilitate subject body movements. In particular, implantable medical leads include the ability to be customized by selective and controllable separation of lead bodies from one another, which leads are also able to permit and withstand multiple degree of freedom of movement that are useful for use in the neck region of a subject body and other regions of any subject's body that may benefit from increased flexibility and extensibility. | 10-30-2008 |
20080269863 | LEAD OR LEAD EXTENSION HAVING A CONDUCTIVE BODY AND CONDUCTIVE BODY CONTACT - An implantable medical device that includes a body that includes a proximal end portion configured to be at least partially received by an apparatus, and a distal end portion; a stimulating electrical element at the distal end portion of the body; a stimulating contact at the proximal end portion of the body, wherein the stimulating contact is positioned such that, when received by the apparatus, at least a portion of the apparatus is capable of electrically coupling to the stimulating contact; a stimulating conductor that electrically couples the stimulating electrical element to the stimulating contact; a conductive body, wherein the conductive body is not utilized for application of stimulation; a conductive body contact, wherein the conductive body is electrically connected to the conductive body contact. Systems that include devices are also disclosed. | 10-30-2008 |
20090312712 | Medical Device Anchor and Method of Manufacture Thereof - A medical device anchor for use with electrical stimulation leads or catheters, and method of manufacture thereof. The anchor may include a gripping structure and a body portion molded on the gripping structure. The gripping structure forms a serpentine arrangement of a continuous nature with axial segments alternately interconnected between shoulder segments and bridging segments. The shoulder segments extend radially outward relative to the through hole further than the axial segments. The body portion may be formed by molding to securely capture the shoulder in the body portion, with the body portion being molded of material that is softer and more compliant than the gripping structure. | 12-17-2009 |
20110172606 | Implantable Retention System and Method - An implantable anchor for anchoring a lead or catheter relative to biological tissue, implantable system including such an anchor and a lead or catheter, and a method of use of such anchor. The anchor comprises a body having a channel adapted to receive a catheter or lead, and a cover mounted on the body for pivoting motion along a lateral axis, that is an axis that extends generally in the lateral direction perpendicular to the catheter or lead, between an open position in which the anchor is adapted to allow a lead or catheter to be placed in or moved along the channel, and a locked position in which the anchor is adapted to retain a lead or catheter within the channel. | 07-14-2011 |
20120197367 | ANCHORS INCLUDING RIGID BODIES DEFINING FULL LENGTH SLOTS FOR USE WITH IMPLANTABLE MEDICAL LEADS - Anchors for use with implantable medical leads include an elastic body containing one or more rigid bodies that have longitudinal free edges. The longitudinal free edges run from end to end to define full length slots. Partial length slots may also be included within the one or more rigid bodies. The full length and partial length slots allow for deflection of the rigid bodies against the body of an implantable medical lead to hold the anchor in place on the lead. The full length slots allow a blade to pass through and cut a slit in the elastic body which allows the anchor to be removed from the lead. | 08-02-2012 |
20120277760 | MEDICAL TUNNELING DEVICE AND METHOD - A medical device assembly includes a tunneler having a proximal end and a distal end and a carrier element fixed to the distal end of the tunneler. In various embodiments the carrier element is configured to be slidably disposed within a lead connection lumen. In various embodiments the carrier element includes a plurality of recesses configured to engage a lead extension set screw. In various embodiments the carrier element can freely rotate relative to the rest of the tunneler. | 11-01-2012 |
20130296991 | LEAD OR LEAD EXTENSION HAVING A CONDUCTIVE BODY AND CONDUCTIVE BODY CONTACT - An implantable medical device that includes a body that includes a proximal end portion configured to be at least partially received by an apparatus, and a distal end portion; a stimulating electrical element at the distal end portion of the body; a stimulating contact at the proximal end portion of the body, wherein the stimulating contact is positioned such that, when received by the apparatus, at least a portion of the apparatus is capable of electrically coupling to the stimulating contact; a stimulating conductor that electrically couples the stimulating electrical element to the stimulating contact; a conductive body, wherein the conductive body is not utilized for application of stimulation; a conductive body contact, wherein the conductive body is electrically connected to the conductive body contact. Systems that include devices are also disclosed. | 11-07-2013 |
20140107746 | LEAD OR LEAD EXTENSION HAVING A CONDUCTIVE BODY AND CONDUCTIVE BODY CONTACT - An implantable medical device that includes a body that includes a proximal end portion configured to be at least partially received by an apparatus, and a distal end portion; a stimulating electrical element at the distal end portion of the body; a stimulating contact at the proximal end portion of the body, wherein the stimulating contact is positioned such that, when received by the apparatus, at least a portion of the apparatus is capable of electrically coupling to the stimulating contact; a stimulating conductor that electrically couples the stimulating electrical element to the stimulating contact; a conductive body, wherein the conductive body is not utilized for application of stimulation; a conductive body contact, wherein the conductive body is electrically connected to the conductive body contact. Systems that include devices are also disclosed. | 04-17-2014 |
20140288626 | LEAD OR LEAD EXTENSION HAVING A CONDUCTIVE BODY AND CONDUCTIVE BODY CONTACT - An implantable medical device that includes a body that includes a proximal end portion configured to be at least partially received by an apparatus, and a distal end portion; a stimulating electrical element at the distal end portion of the body; a stimulating contact at the proximal end portion of the body, wherein the stimulating contact is positioned such that, when received by the apparatus, at least a portion of the apparatus is capable of electrically coupling to the stimulating contact; a stimulating conductor that electrically couples the stimulating electrical element to the stimulating contact; a conductive body, wherein the conductive body is not utilized for application of stimulation; a conductive body contact, wherein the conductive body is electrically connected to the conductive body contact. Systems that include devices are also disclosed. | 09-25-2014 |
20140290029 | Medical Device Anchor and Method of Manufacture Thereof - A medical device anchor for use with electrical stimulation leads or catheters, and method of manufacture thereof. The anchor may include a gripping structure and a body portion molded on the gripping structure. The gripping structure forms a serpentine arrangement of a continuous nature with axial segments alternately interconnected between shoulder segments and bridging segments. The shoulder segments extend radially outward relative to the through hole further than the axial segments. The body portion may be formed by molding to securely capture the shoulder in the body portion, with the body portion being molded of material that is softer and more compliant than the gripping structure. | 10-02-2014 |
Patent application number | Description | Published |
20090088685 | Endovascular devices and methods for exploiting intramural space - The present disclosure is directed to a device. The device may include a distal shaft defining a central lumen and an orienting element comprising at least one inflatable member. Wherein a first portion of the orienting element extending from the shaft in a first direction and a second portion of the orienting element extending from the shaft in a second direction. Further, wherein the second direction is substantially opposite the first direction. | 04-02-2009 |
20090124899 | Methods and devices for crossing chronic total occlusions - The present disclosure is directed to a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing an intravascular device having a distal portion and a longitudinal axis and inserting the intravascular device into the vascular lumen. The method may further include positioning the distal portion in the vascular wall, rotating the intravascular device about the longitudinal axis, and advancing the intravascular device within the vascular wall. | 05-14-2009 |
20090209910 | Crossing occlusions in blood vessels - The present disclosure is directed a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing a first intravascular device having a distal portion and at least one aperture and positioning the distal portion of the first intravascular device in the vascular wall. The method may further include providing a reentry device having a body and a distal tip, the distal tip having a natural state and a compressed state and inserting the distal tip, in the compressed state, in the distal portion of the first intravascular device. The method may further include advancing the distal tip, in the natural state, through the at least one aperture of the first intravascular device. | 08-20-2009 |
20090270890 | Methods and apparatus for crossing occlusions in blood vessels - Exemplary embodiments of the present disclosure are directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device further includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Further rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Still further, rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque. | 10-29-2009 |
20100063534 | ENDOVASCULAR DEVICES AND METHODS FOR EXPLOITING INTRAMURAL SPACE - Devices and methods for exploiting intramural (e.g., subintimal) space of a vascular wall to facilitate the treatment of vascular disease, particularly total occlusions. For example, the devices and methods disclosed herein may be used to visually define the vessel wall boundary, protect the vessel wall boundary from perforation, bypass an occlusion, and/or remove an occlusion. | 03-11-2010 |
20120283759 | METHODS AND APPARATUS FOR CROSSING OCCLUSIONS IN BLOOD VESSELS - This disclosure is directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Further rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque. | 11-08-2012 |
20120323251 | CROSSING OCCLUSIONS IN BLOOD VESSELS - The present disclosure is directed a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing a first intravascular device having a distal portion and at least one aperture and positioning the distal portion of the first intravascular device in the vascular wall. The method may further include providing a reentry device having a body and a distal tip, the distal tip having a natural state and a compressed state and inserting the distal tip, in the compressed state, in the distal portion of the first intravascular device. The method may further include advancing the distal tip, in the natural state, through the at least one aperture of the first intravascular device. | 12-20-2012 |
20130296907 | METHODS AND APPARTUS FOR CROSSING OCCLUSIONS IN BLOOD VESSELS - This disclosure is directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Further rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque. | 11-07-2013 |
20140128900 | METHODS AND DEVICES FOR CROSSING CHRONIC TOTAL OCCLUSIONS - The present disclosure is directed to a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing an intravascular device having a distal portion and a longitudinal axis and inserting the intravascular device into the vascular lumen. The method may further include positioning the distal portion in the vascular wall, rotating the intravascular device about the longitudinal axis, and advancing the intravascular device within the vascular wall. | 05-08-2014 |
20140171989 | METHODS AND APPARTUS FOR CROSSING OCCLUSIONS IN BLOOD VESSELS - This disclosure is directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Further rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque. | 06-19-2014 |
Patent application number | Description | Published |
20100328807 | INTEGRATED HEAT ASSISTED MAGNETIC RECORDING DEVICE - An integrated heat-assisted magnetic recording (HAMR) device comprises a slider that has a top surface, a bottom surface, and a trailing end. A waveguide is carried on the trailing end and a near field transducer is positioned to receive energy from the waveguide and produce plasmons for heating a region of a magnetic medium. A write pole is carried by the slider adjacent to the near field transducer. A laser is mounted on the top surface of the slider and produces a laser beam that passes through a beam shaper mounted on the top surface of the slider that collimates or focuses the laser beam. A mirror is mounted on the slider for directing the collimated or focused light beam into the waveguide. | 12-30-2010 |
20120044967 | Capping Method For Laser Diode Protection - A method includes: positioning a laser in the cavity in an end of a slider, wherein the laser has an output facet positioned adjacent to a first wall of the cavity to define a first gap between the output facet and the first wall of the cavity, and filling at least a portion of the first gap adjacent to the output facet. An apparatus including a slider including a cavity in a trailing end of the slider, a laser positioned in the cavity and having an output facet positioned adjacent to a first wall of the cavity to define a first gap between the output facet and the first wall of the cavity, and a sealing material filling at least a portion of the first gap adjacent to the output facet is also provided. | 02-23-2012 |
20120074131 | INTEGRATED RESISTIVE HEATERS FOR MICROELECTRONIC DEVICES AND METHODS UTILIZING THE SAME - A device having a substrate having a first surface and a second opposing surface; and at least one electrical connection assembly, wherein each electrical connection assembly includes: a resistive heater disposed on the first surface of the substrate, wherein the resistive heater is electrically connected to a circuit via a heater electrical connection; an electrical connection precursor, wherein the electrical connection precursor includes a fusible conductive material that is electrically connected to a lead; and a first insulating layer, wherein the resistive heater is disposed beneath the electrical connection precursor, wherein the first insulating layer functions to electrically insulate the resistive heater and the heater electrical connection from the electrical connection precursor and the lead, and wherein activation of the resistive heater functions to at least partially flow the fusible conductive material, wherein each electrical connection assembly can be activated individually by passing a current through the resistive heater. | 03-29-2012 |
20120327754 | Vertical Cavity Surface Emitting Laser With Integrated Mirror And Waveguide - An apparatus includes an extended cavity vertical cavity surface emitting laser producing light and having an active region, a first reflector position adjacent to a first side of the active region, an extended cavity positioned adjacent to a second side of the active region, and a second reflector reflecting a first portion of the light into the extended cavity and transmitting a second portion of the light, a planar waveguide positioned adjacent to the extended cavity vertical cavity surface emitting laser, and a horizontal coupler structured to couple the second portion of light from the extended cavity vertical cavity surface emitting laser into the waveguide. | 12-27-2012 |
20130223462 | SEMICONDUCTOR LASER WITH CATHODE METAL LAYER DISPOSED IN TRENCH REGION - A laser diode includes a substrate and a junction layer disposed on the substrate. The junction layer forms a quantum well of the laser diode. The laser diode includes a junction surface having at least one channel that extends through the junction layer to the substrate. The at least one channel defines an anode region and a cathode region. A cathode electrical junction is disposed on the junction surface at the cathode region, and an anode electrical junction is disposed on the junction surface and coupled to the junction layer at the anode region. A cathode metal layer is disposed in at least a trench region of the channel. The cathode metal layer couples the substrate to the cathode electrical junction. | 08-29-2013 |
20150036467 | CAPPING METHOD FOR LASER DIODE PROTECTION - An apparatus includes a slider with a cavity in a trailing end of the slider. A laser is positioned in the cavity and has an output facet positioned adjacent to a first wall of the cavity. A cap is connected to the trailing end of the slider and covers the laser. | 02-05-2015 |
Patent application number | Description | Published |
20100053621 | Apparatus and method for measuring the concentration of gases in a sterilization chamber - Accurate measurements of the concentration of a sterilant in a sterilization chamber are provided through the use of a light source, a first detector that receives light from the light source that has not passed through the sterilization chamber and a detector that receives light from the light source that has passed through the sterilization chamber. The light contains wavelengths known to be absorbed by the sterilant. A controller receives and processes signals received from the two detectors to cancel changes in the output of the light source and then apply a modified Beer-Lambert law to determine the concentration of the sterilant gas. | 03-04-2010 |
20100313441 | APPARATUS AND METHOD FOR DRYING AND STERILIZING OBJECTS IN A LOAD - The removal of moisture from an object to be sterilized is provided through at least the steps of placing the load in the chamber, reducing the pressure within the chamber to increase the rate of evaporation of moisture from the load, monitoring over a predetermined period of time the increase in the quantity of vapor within the chamber resulting from evaporation of moisture from the load, admitting gas into the chamber and repeating the steps following placing the load into the chamber. | 12-16-2010 |
20100316527 | APPARATUS AND METHOD FOR DRYING AND THEN STERILIZING OBJECTS IN A LOAD USING A CHEMICAL STERILANT - The removal of moisture from an object to be sterilized is provided through at least the steps of placing the load in the chamber, reducing the pressure within the chamber to increase the rate of evaporation of moisture from the load, monitoring over a predetermined period of time the increase in the quantity of vapor within the chamber resulting from evaporation of moisture from the load, admitting gas into the chamber and repeating the steps following placing the load into the chamber. | 12-16-2010 |
20110250677 | Apparatus for Assessing the Effectiveness of a Sterilization Process - A device useful in determining the efficacy of a chemical sterilization process includes a dead end cavity closed by an access cap having a port coupled to a challenge tube defining the only path by which a substantial quantity of sterilant can reach the cavity. A biological indicator is located within the cavity and a chemical indicator is also provided. These indicators, and particularly the biological indicator, provide an indication of whether chemical sterilant would reach all interior exposed surfaces of a load in sufficient concentrations to adequately sterilize the load. | 10-13-2011 |
20120275954 | Sterilization System And Method With Compression and Expansion - An apparatus and method for achieving low temperature vapor sterilization of objects which may involve objects having a lumen. Following evacuation of the sterilization chamber and the introduction of a vaporous or gaseous sterilant, the volume of the chamber is changed by actuation of a movable boundary in the chamber to increase and decrease the pressure in the chamber thus driving the sterilant into and out of such lumens. | 11-01-2012 |
20120297638 | Apparatus and Method for Drying and Sterilizing Objects in a Load - The removal of moisture from an object to be sterilized is provided through at least the steps of placing the load in the chamber, reducing the pressure within the chamber to increase the rate of evaporation of moisture from the load, monitoring over a predetermined period of time the increase in the quantity of vapor within the chamber resulting from evaporation of moisture from the load, admitting gas into the chamber and repeating the steps following placing the load into the chamber. | 11-29-2012 |