Patent application number | Description | Published |
20110006104 | INSTRUMENT FOR APPLYING A SURGICAL FASTENER - An instrument for applying one or more surgical fasteners includes a tubular shaft having a distal end through which each fastener is deployed. A delivery system is contained within the tubular shaft for advancing the surgical fasteners along, and out of, the instrument. An actuator is operatively associated with the delivery system. On or more wall structure modifications in the tubular shaft, such as openings, reliefs or cut-outs, interact with the delivery system. An outer tubular shaft is mounted over the wall structure modifications to reinforce the instrument against permanent deformation or inward distortion if excessive forces are encountered. | 01-13-2011 |
20110071578 | METHOD AND APPARATUS FOR SURGICAL FASTENING - A surgical fastener system includes a plurality of fasteners having a throughbore with a non-circular cross section portion. The fasteners may engage with a splined mandrel that passes through the throughbore of the fasteners and rotates the fasteners relative to the mandrel to move at least one of the fasteners along the mandrel, e.g., along the mandrel's longitudinal axis. A distal end of the mandrel may be inserted into a material, such as a tissue, prosthetic or other, and a fastener may be deployed from the distal end of the mandrel while the distal end is positioned in the material. | 03-24-2011 |
20130231526 | SOFT TISSUE REPAIR PROSTHESIS AND EXPANDABLE DEVICE - A hernia repair device is provided which may include a soft tissue repair prosthesis and an expandable device configured to be removably connected with the soft tissue repair prosthesis. Attachment components may be used to removably connect the soft tissue repair prosthesis with the expandable device. The hernia repair device may be manipulated into a reduced configuration for insertion into the body. When expanded, the expandable device may be configured to position the soft tissue repair prosthesis adjacent a hernia defect. The expandable device and/or the attachment components may be shaped and/or configured to minimize the maximum dimension of the hernia repair device in its reduced configuration. | 09-05-2013 |
20140236196 | METHOD AND APPARATUS FOR SURGICAL FASTENING - A surgical fastener system includes a plurality of fasteners having a throughbore with a non-circular cross section portion. The fasteners may engage with a splined mandrel that passes through the throughbore of the fasteners and rotates the fasteners relative to the mandrel to move at least one of the fasteners along the mandrel, e.g., along the mandrel's longitudinal axis. A distal end of the mandrel may be inserted into a material, such as a tissue, prosthetic or other, and a fastener may be deployed from the distal end of the mandrel while the distal end is positioned in the material. | 08-21-2014 |
20140263544 | SURGICAL INSTRUMENT WITH AN ACTUATION LOCKOUT - Embodiments of a surgical instrument and its methods of use are disclosed. The disclosed embodiments of a surgical instrument may include a handle and an elongated shaft assembly distally extending from the handle. The elongated shaft assembly may include an articulable portion. An articulation control may be associated with the elongated shaft assembly. The articulation control may be movable between a first position in which the elongated shaft assembly is arranged in a first articulation position and a second position in which the elongated shaft assembly is arranged in a second articulation position. The surgical instrument may include a fastener deployment system with a locking member. The articulation control may block movement of the locking member when the articulation control is located in the first position. The articulation control may also permit movement of the locking member when the articulation control is located in the second position. | 09-18-2014 |
20140276963 | POWER ASSIST DEVICE FOR A SURGICAL INSTRUMENT - A surgical instrument including a power assist device, and its method of use for deploying surgical fasteners, is disclosed. The surgical instrument may include a handle, an elongated shaft extending from the handle, and a surgical fastener deployment system including a driveshaft. The driveshaft is actuatable between at least a first proximal position and a second distal position. A striker is movable relative to the driveshaft and an impact surface is associated with the driveshaft. The impact surface is constructed and arranged to be struck by the striker member to displace the driveshaft to the second distal position and deploy the surgical fastener. | 09-18-2014 |
20140276964 | HANDLING OF FASTENERS WITHIN A SURGICAL INSTRUMENT - Surgical instruments and their methods of use are disclosed. In some embodiments, the surgical instrument may include a handle and an elongated shaft assembly extending distally from the handle. The surgical instrument may also include a fastener deployment system for deploying fasteners from the elongated shaft assembly including a reciprocating driveshaft disposed within the elongated shaft assembly. The driveshaft may include an internal channel and at least one guide surface shaped and arranged to maintain an orientation of at least one fastener in the channel of the driveshaft. In other embodiments, the fastener deployment system may include a follower disposed within the elongated shaft assembly for displacing one or more fasteners within the elongated shaft assembly towards a distal fastener deployment position. | 09-18-2014 |
20140276965 | HANDLING OF FASTENERS WITHIN A SURGICAL INSTRUMENT - Surgical instruments and their methods of use are disclosed. In some embodiments, the surgical instrument may include a handle and an elongated shaft assembly extending distally from the handle. The surgical instrument may also include a fastener deployment system for deploying fasteners from the elongated shaft assembly including a reciprocating driveshaft disposed within the elongated shaft assembly. The driveshaft may include an internal channel and at least one guide surface shaped and arranged to maintain an orientation of at least one fastener in the channel of the driveshaft. In other embodiments, the fastener deployment system may include a follower disposed within the elongated shaft assembly for displacing one or more fasteners within the elongated shaft assembly towards a distal fastener deployment position. | 09-18-2014 |
20140276966 | ARTICULATING SURGICAL INSTRUMENTS - A surgical instrument and its method of use are disclosed. In one embodiment, the surgical instrument may include a handle and an elongated shaft assembly extending distally from the handle. The elongated shaft assembly may include an articulable portion with an articulation direction. The elongated shaft assembly may also include a tubular member with a flexible portion with a preferential bending direction and a direction of bending resistance. The tubular member may permit articulation of the elongated shaft assembly when the preferential bending direction is aligned with the articulation direction. | 09-18-2014 |
Patent application number | Description | Published |
20080243185 | SPINAL STABILIZING SYSTEM - A bone stabilizing system includes a collar that has a tubular sidewall with an interior surface and an exterior surface each extending between a first end and an opposing second end, the interior surface at least partially bounding a longitudinal passage extending therethrough. The collar also includes a pair of opposing spaced apart channels transversely extending through the sidewall at the first end thereof and a pair of spaced apart bayonet prongs projecting from the first end of the tubular sidewall. A screw has a threaded portion and a head disposed on an end thereof, the head of the screw being disposed within the longitudinal passage of the collar. A locking cap has a hole extending therethrough and a pair of spaced apart bayonet slots formed thereon, the bayonet slots being configured to receive and engage with the pair of bayonet prongs. | 10-02-2008 |
20090287253 | POLYAXIAL SCREW SYSTEM - A polyaxial screw system includes a drive cap having a partition wall with a first side and an opposing second side, a passage extending through the partition wall. A sleeve projects from the second side of the partition wall, the sleeve and partition wall bounding a socket. A shaft outwardly projects from the first side of the partition wall. A screw has a threaded portion and a head formed on an end thereof. The head of the screw is at least partially disposed within socket of the drive cap. A collet is at least partially disposed within the socket of the drive cap. At least a portion of a compression cap movably extends through the opening in the partition wall so that the compression cap can selectively move the collet relative to the drive cap. | 11-19-2009 |
20090326588 | CROSS CONNECTOR - A cross connector that can be used with a spinal implant includes a first rod clamp having a first end and an opposing second end, the first rod clamp having a first clamp arm crossing a second clamp arm so as to form a scissor coupling. The cross connector also includes a second rod clamp and a cross bar assembly extending between the first rod clamp and the second rod clamp. | 12-31-2009 |
20100063550 | RADIOLUCENT SCREW WITH RADIOPAQUE MARKER - A bone screw includes an elongate shaft extending longitudinally between a proximal end and an opposing distal end, the shaft bounding a first passageway at least partially extending between the proximal end and the distal end, the shaft being comprised of a radiolucent material. A core is disposed within the first passageway of the shaft, the core being comprised of a radiopaque material. A rounded head or a substantially U-shaped collar is either integrally formed with or is rigidly attached to the proximal end of the shaft. | 03-11-2010 |
20100191290 | SPINAL STABILIZING SYSTEM - A spinal stabilizing system includes a collar having a tubular sidewall with an interior surface and an exterior surface, the interior surface at least partially bounding a longitudinal passage extending therethrough. A shoulder radially inwardly projects from a second end of the sidewall so as to at last partially encircle the longitudinal passage. A pair of spaced apart channels transversely extend through the sidewall at the first end thereof. The system further includes a screw having a threaded portion and an enlarged head mounted on the end thereof, the head of the screw resting against the shoulder of the collar so that the head can pivot on the shoulder, a locking slot being formed on the head of the screw. A pin is secured to the collar and projects into the locking slot on the head of the screw such rotation of the collar facilitates rotation of the screw. | 07-29-2010 |
20110060365 | RADIOLUCENT STABILIZING ROD WITH RADIOPAQUE MARKER - A stabilizing rod includes an elongate shaft extending between a proximal end and an opposing distal end. The shaft is comprised of a radiolucent material and bounds a passageway that at least partially extends between the proximal end and the distal end. A core is disposed within the passageway of the shaft. The core can be comprised of a radiopaque material. The stabilizing rod can also include a radiopaque marker disposed on or within the shaft. | 03-10-2011 |
20110118840 | SPINAL IMPLANT WITH STAPLES - A spinal implant having a spinal cage and a plurality of staples. The spinal cage is configured to be positioned in an intervertebral space between adjacent vertebrae. The plurality of staples are moveably disposed on the spinal cage and configured to be inserted into the adjacent vertebrae so as to secure the spinal cage in the intervertebral space when the spinal cage is positioned therein. A method of securing the spinal implant within the intervertebral space. | 05-19-2011 |
20110172718 | RADIOLUCENT SCREW WITH RADIOPAQUE MARKER - A bone screw includes an elongate shaft extending longitudinally between a proximal end and an opposing distal end The shaft bounds a first passageway at least partially extending between the proximal end and the distal end. The shaft is comprised of a radiolucent material. A core is disposed within the first passageway of the shaft. The core can be comprised of a radiolucent or radiopaque material. A head is either integrally formed with or secured to the proximal end of the shaft or the proximal end of the core. The head can also bound a second passageway that extends through the head and is aligned with the first passageway. The core can also be disposed within the second passageway. | 07-14-2011 |
20110218570 | RADIOLUCENT BONE PLATE WITH RADIOPAQUE MARKER - A bone plate has a main body configured to position adjacent bones with respect to each other. The main body includes a plurality of separate layers bonded together. Each layer is comprised of a radiolucent material and has a first aperture and a second aperture that extend through the layer. The layers are all stacked such that the first apertures of all of the layers are aligned with each other and the second apertures of all of the layers are aligned with each other. An insert can be positioned within the first aperture. | 09-08-2011 |
20120083851 | METHOD FOR POLYAXIAL SCREW SYSTEM - A method for mounting a polyaxial screw into a bone includes rotating a drive cap so that a screw mounted to the drive cap is screwed into a bone, the drive cap having a socket in which a portion of the screw is pivotably disposed, at least a portion of a collet being disposed within the socket between the screw and the drive cap. A stabilizing structure and a fastener are positioned onto a shaft projecting from the drive cap. The fastener is advanced along the shaft so as to push a portion of a compression cap against the collet which in turn wedges the collet within the socket of the drive cap and causes the collet to bias against a portion of the screw, thereby locking the position of the screw, the collet, and the drive cap relative to each other. | 04-05-2012 |
20120150230 | CROSS CONNECTOR WITH CENTRAL HUB - A spinal implant cross connector includes a central hub. Four spaced apart arm assemblies outwardly project from the central hub, each arm assembly having an adjustable length extending between a first end coupled to the central hub and an opposing second end. The arm assemblies extend in a substantially X-shaped pattern with two of the arm assemblies being pivotable relative to the other two. A rod clamp assembly is disposed at the second end of each arm assembly. | 06-14-2012 |
20140276829 | MODULAR BONE FIXATION PLATE ASSEMBLY - A bone fixation plate assembly includes a proximal plate having a proximal body with a first arm projecting therefrom, the first arm having an elongated expansion slot extending through a portion thereof and a threaded bore formed thereon so as to communicate with the expansion slot. A set screw is received within the threaded bore and has a top surface with a driver engaging feature formed thereon and an encircling perimeter edge. A distal plate has a distal body with a first sleeve projecting therefrom. The first sleeve bounds a socket with the first arm received therein. An access opening is formed on the first sleeve and is configured so that the driver engaging feature of the set screw is accessible through the access opening while at least a portion of the perimeter edge of the set screw is covered by the first sleeve. | 09-18-2014 |
Patent application number | Description | Published |
20150057368 | CLOSED CELL FOAMS INCLUDING POLY-4-HYDROXYBUTYRATE AND COPOLYMERS THEREOF - Methods to produce substantially closed cell foams with densities less than 0.75 g/cm | 02-26-2015 |
20150112434 | ABSORBABLE IMPLANTS FOR PLASTIC SURGERY - Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and/or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy/breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast. | 04-23-2015 |
20150182670 | Medical Implants Including Laminates of Poly-4-Hydroxybutyrate and Copolymers Thereof - Methods to produce laminates including layers of constructs made from P4HB and copolymers thereof have been developed. These laminates may be used as medical implants, or further processed to make medical implants. The laminates are produced at a temperature equal to or greater than the softening points of the P4HB or copolymers thereof. The layers may include oriented forms of the constructs. Orientation can be preserved during lamination so that the laminate is also oriented, when the laminates are formed at temperatures less than the de-orientation temperatures of the layers. The laminate layers may include, for example, films, textiles, including woven, knitted, braided and non-woven textiles, foams, thermoforms, and fibers. The laminates preferably include one or more oriented P4HB films. | 07-02-2015 |
20150223928 | ABSORBABLE IMPLANTS FOR PLASTIC SURGERY - Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and/or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy/breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast. | 08-13-2015 |
20160022416 | Absorbable Implants for Plastic Surgery - Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and/or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the ingrowth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy/breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast | 01-28-2016 |
Patent application number | Description | Published |
20120088999 | Ambulatory Electrocardiographic Monitor With Jumpered Sensing Electrode For Providing Ease Of Use In Women And Method Of Use - An ambulatory electrocardiographic (ECG) monitor with a jumpered sensing electrode and method of use for female and large-girthed patients is provided. Self-powered ECG sensing circuitry is fully enclosed in a housing with electrode receptacles on a bottom surface. A flexible and stretchable electrode mounting panel is provided with a layer of skin adhesive. A standoff pad is placed between the housing and the electrode mounting panel. Sensing electrodes are mounted on opposite ends of the mounting panel. Each sensing electrode includes an electrode pad facing the skin contacting surface and an oppositely-facing electrode plug. Each plug is removably and pivotably couplable into the receptacles. A jumper wire assembly includes a jumper plug electrically connected to a jumper receptacle. The jumper plug is removably and pivotably couplable into the receptacles and the jumper receptacle is removably and pivotably couplable into the plugs on the mounting panel opposite from the standoff pad. | 04-12-2012 |
20120089000 | Ambulatory Electrocardiographic Monitor For Providing Ease Of Use In Women And Method Of Use - A method for performing ambulatory electrocardiographic monitoring on an adult female is provided. An ambulatory ECG monitor, that includes a plurality of sensing electrodes coupled to self-powered sensing circuitry, is provisioned. A monitoring site is located on the surface of a patient's chest at midline and above the body of the sternum adjacent to the fourth and fifth intercostal spaces between the breasts in the upper portion of the intermammary cleft. The electrodes are aligned and placed along the midline. Interference from breast tissue with placement of the ambulatory monitor at the monitoring site is evaluated. The ambulatory ECG monitor is removably adhered to the monitoring site clear of any breast tissue interference for the duration of monitoring. ECG data is sensed through the sensing electrodes at the monitoring site and the sensed ECG data is recorded into the sensing circuitry. | 04-12-2012 |
20120089001 | Ambulatory Electrocardiographic Monitor And Method Of Use - A method for performing ambulatory electrocardiographic monitoring is provided. An ambulatory ECG monitor, that includes a plurality of sensing electrodes coupled to self-powered sensing circuitry, is provisioned. A monitoring site is located on the surface of a patient's chest at midline and above the body of the sternum adjacent to the fourth and fifth intercostal spaces. The electrodes are aligned and placed along the midline. The ambulatory ECG monitor is removably adhered to the monitoring site for the duration of monitoring. ECG data is sensed through the sensing electrodes at the monitoring site and the sensed ECG data is recorded into the sensing circuitry. | 04-12-2012 |
20120089036 | Microcontrolled Electrocardiographic Monitoring Circuit With Feedback Control - A microcontrolled electrocardiographic monitoring circuit with feedback control is provided. An input signal path includes an electrode, a low pass filter, and an amplifier connected in-line. The electrode senses an input signal and the amplifier outputs a filtered amplified output signal. A microcontroller circuit includes an input codec, analog-to-digital converter, and feedback generation module. The analog-to-digital converter converts the filtered amplified output signal into a data stream of discrete digital values. The feedback module identifies a pairing of drive resistor settings matched to each discrete digital value, which are output as a digital feedback signal. The output signal path includes an electrode and a buffer connected in-line. A pair of drive resistors is connected in parallel to an input terminal of the buffer and to the output terminals of the feedback module. Each drive resistor is adjusted according to the digital feedback signal, and the electrode provides an output signal. | 04-12-2012 |
20120089037 | Ambulatory Electrocardiographic Monitor With Jumpered Sensing Electrode And Method Of Use - An ambulatory electrocardiographic (ECG) monitor with a jumpered sensing electrode and method of use is provided. Self-powered ECG sensing circuitry is fully enclosed in a housing that provides electrode connection receptacles on a bottom surface of the housing. A flexible and stretchable electrode mounting panel having an elongated shape is provided with a layer of skin adhesive on a skin contacting surface. Sensing electrodes are mounted on opposite ends of the mounting panel. Each sensing electrode includes an electrode pad facing the skin contacting surface and an oppositely-facing electrode connection plug. Each connection plug is removably and pivotably couplable into the connection receptacles. A jumper wire assembly includes a jumper connection plug electrically connected to a jumper connection receptacle. The jumper connection plug is removably and pivotably couplable into the connection receptacles and the jumper connection receptacle is removably and pivotably couplable into the connection plugs on the mounting panel. | 04-12-2012 |
20120089039 | Microcontrolled Electrocardiographic Monitoring Circuit With Differential Voltage Encoding - A microcontrolled electrocardiographic monitoring circuit with differential voltage encoding is provided. An input signal path includes an electrode, a low pass filter, and an amplifier, which are each connected in-line. The electrode senses an input signal via a conductive surface and the amplifier outputs a filtered amplified output signal. A microcontroller circuit includes an input codec, an analog-to-digital converter, and an encoder. The analog-to-digital converter is connected to the input signal path through an output of the amplifier and converts the filtered amplified output signal into a data stream of discrete digital values. The encoder determines a differential voltage between a current discrete digital value and a prior discrete digital value in the data stream. Persistent memory is connected to the microcontroller circuit via a peripheral serial interface bus, wherein the differential voltages for each of the discrete digital values in the data stream are stored into the persistent memory. | 04-12-2012 |
20120302906 | Computer-Implemented Electrocardiographic Data Processor With Time Stamp Correlation - A computer-implemented electrocardiographic data processor with time stamp correlation is provided. A monitoring circuit includes a persistent memory and power supply that powers an encoder that determines a differential voltage between a current discrete digital voltage value and a prior voltage value. The differential voltage is stored into the persistent memory in a digitized data stream representative of analog cardiac action potential signals. Digitally-encoded voltage values and time stamps are retrieved from the persistent memory. A post-processing application executes. A set of output voltages and voltage differences that each correspond to lower and upper bounds of voltage is stored. Each retrieved voltage value is compared to the voltage bounds and the voltage differences within which each retrieved voltage value falls is identified. The output voltages corresponding to the voltage differences is selected. A display depicts the output voltages as reproduced analog cardiac action potential signals and correlates the time stamps. | 11-29-2012 |
20140200472 | COMPUTER-IMPLEMENTED ELECTROCARDIOGRAHIC DATA PROCESSOR WITH TIME STAMP CORRELATION - A computer-implemented electrocardiographic data processor with time stamp correlation is provided. A monitoring circuit includes a persistent memory and power supply that powers an encoder that determines a differential voltage between a current discrete digital voltage value and a prior voltage value. The differential voltage is stored into the persistent memory in a digitized data stream representative of analog cardiac action potential signals. Digitally-encoded voltage values and time stamps are retrieved from the persistent memory. A post-processing application executes. A set of output voltages and voltage differences that each correspond to lower and upper bounds of voltage is stored. Each retrieved voltage value is compared to the voltage bounds and the voltage differences within which each retrieved voltage value falls is identified. The output voltages corresponding to the voltage differences is selected. A display depicts the output voltages as reproduced analog cardiac action potential signals and correlates the time stamps. | 07-17-2014 |
20150082623 | Method For Constructing A Stress-Pliant Physiological Electrode Assembly - A method for constructing a stress-pliant physiological electrode assembly is provided. An electrode backing is formed from a stretchable woven textile material compatible to contact the skin on at least one surface. A pair of flexile wires is provided to serve as electrode circuit trace and electrode signal pickup. At least one of the flexile wires is sewn into the textile material which provides a stress-pliant malleability. Each of the flexile wires has an electrically-contacting area functioning for electric signal pickup. The electrically-contacting area may be sewn into the woven textile or affixed to the woven textile via conductive adhesives. The stress-pliant physiological electrode assembly is applicable for a wide array of physiological monitors, including ECG monitors, and especially is suitable for long-term wear. The method disclosed is both environmentally friendly and low-cost. | 03-26-2015 |
20150087921 | Remote Interfacing Of Extended Wear Electrocardiography And Physiological Sensor Monitor - Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline (or immediately to either side of the sternum) benefits extended wear by removing the requirement that ECG electrodes be continually placed in the same spots on the skin throughout the monitoring period. The wearable monitor can interoperate wirelessly with other physiology and activity sensors and mobile communications devices, to download monitoring data either in real-time or in batches. The monitor recorder can provide data or other information to, or receive data or information from, an interfacing physiology or activity sensor, or mobile communications devices for relay to a further device, such as a server, analysis, or other purpose. | 03-26-2015 |
20150087922 | Self-Contained Personal Air Flow Sensing Monitor - Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally (in the midline) on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline (or immediately to either side of the sternum) benefits extended wear by removing the requirement that ECG electrodes be continually placed in the same spots on the skin throughout the monitoring period. Instead, the patient can place an electrode patch anywhere within the general region of the sternum. Power is provided through a battery provided on the electrode patch, which avoids having to open the monitor recorder's housing for battery replacement. The monitor further includes sensors for monitoring patient's air flow and respiratory measures contemporaneously with the ECG monitoring. | 03-26-2015 |
20150087923 | Event Alerting Through Actigraphy Embedded Within Electrocardiographic Data - Physiological monitoring can be provided through an actigraphy sensor imbedded into an electrocardiography monitor, which correlates movement and electrocardiographic data. Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally on the patient's chest along the sternum. The patient can place an electrode patch anywhere within the general region of the sternum. The occurrence of actigraphy events are monitored by the monitor recorder through an actigraphy sensor. Actigraphy becomes a recordable actigraphy event occurrence when the movement of the wearable monitor and, therefore, the patient, exceeds a certain criteria threshold of acceleration or deceleration as detected by the actigraphy sensor. Certain actigraphy event occurrences as recorded by the monitor recorder are considered to be actionable, that is, of sufficient importance to warrant flagging for further consideration to a following physician. | 03-26-2015 |
20150087948 | Extended Wear Electrocardiography Patch - Physiological monitoring can be provided through a wearable monitor that includes a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally on the patient's chest along the sternum, which significantly improves the ability to sense cutaneously cardiac electric signals, particularly those generated by the atrium. The electrode patch is shaped to fit comfortably and conformal to the contours of the chest approximately centered on the sternal midline. To counter the dislodgment due to compressional and torsional forces, non-irritating adhesive is provided on the underside, or contact, surface of the electrode patch, but only on the distal and proximal ends. To counter dislodgment due to tensile and torsional forces, a strain relief is defined in the electrode patch's flexible circuit using cutouts partially extending transversely from each opposite side of the flexible circuit and continuing longitudinally towards each other to define in ‘S’-shaped pattern. | 03-26-2015 |
20150087949 | Extended Wear Ambulatory Electrocardiography And Physiological Sensor Monitor - Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally (in the midline) on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline (or immediately to either side of the sternum) benefits extended wear by removing the requirement that ECG electrodes be continually placed in the same spots on the skin throughout the monitoring period. Instead, the patient can place an electrode patch anywhere within the general region of the sternum. Power is provided through a battery provided on the electrode patch, which avoids having to open the monitor recorder's housing for battery replacement. | 03-26-2015 |
20150087950 | Self-Authenticating Electrocardiography Monitoring Circuit - Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally (in the midline) on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline (or immediately to either side of the sternum) benefits extended wear by removing the requirement that ECG electrodes be continually placed in the same spots on the skin throughout the monitoring period. Instead, the patient can place an electrode patch anywhere within the general region of the sternum. Ensuring that the quality level of ECG recording remains constant over an extended period of time is provided through self-authentication of electrode patches. The monitor recorder implements a challenge response scheme upon being connected to an electrode patch. Failing self-authentication, the monitor recorder signals an error condition. | 03-26-2015 |
20150087951 | Extended Wear Electrocardiography Patch Using Interlaced Wire Electrodes - Physiological monitoring can be provided through a wearable monitor that includes a flexible extended wear electrode patch and a removable reusable monitor recorder. A pair of flexile wires is interlaced or sewn into a flexible backing, serving as electrode signal pickup and electrode circuit traces. The wearable monitor sits centrally on the patient's chest along the sternum, which significantly improves the ability to sense cutaneously cardiac electric signals, particularly those generated by the atrium. The electrode patch is shaped to fit comfortably and conformal to the contours of the chest approximately centered on the sternal midline. To counter the dislodgment due to compressional and torsional forces, non-irritating adhesive is provided on the underside, or contact, surface of the electrode patch, but only on the distal and proximal ends. Interlacing the flexile wires into the flexile backing also provides structural support and malleability against compressional, tensile and torsional forces. | 03-26-2015 |
20150088007 | Computer-Implemented System And Method For Providing A Personal Mobile Device-Triggered Medical Intervention - Physiological monitoring can be provided through a wearable monitor that includes two components, a flexible extended wear electrode patch and a removable reusable monitor recorder. The wearable monitor sits centrally on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline (or immediately to either side of the sternum) benefits extended wear by removing the requirement that ECG electrodes be continually placed in the same spots on the skin throughout the monitoring period. The wearable monitor can interoperate wirelessly with other physiology and activity sensors and mobile devices. An application executed by the sensor or device can trigger the dispatch of a wearable monitor to the patient upon detecting potentially medically-significant events. The dispatched wearable monitor would then be capable of providing precise medically-actionable data, not merely an alert that some abnormality may be present. The patient can then use the sensor or device to physically record the placement and use of the medically-actionable wearable monitor, thereby facilitating the authentication of the data recorded. | 03-26-2015 |
20150088020 | System and Method For Interactive Processing Of ECG Data - A system and method for interactive processing of ECG data are presented. An electrocardiogram is displayed. A user selection of a portion of the displayed ECG is received. Digitized signals corresponding to the selection are obtained. A list of digital filters for filtering the selection are displayed. A user selection of one or more sets of the digital filters is received, with each of the sets including one or more of the filters from the list. The selected sets are applied to the digitized signals for the selection. A filtered ECG for the selection is generated for each of the sets based on the signals filtered by that set. The filtered selection ECG for each of the sets are presented on the display. | 03-26-2015 |
Patent application number | Description | Published |
20100027849 | Methods and Systems for Administering a Drug Program - Systems and methods are described that provide a fast and simple way of administering a drug program related to an animal. Specifically, systems are provided that can receive, compile and analyze information regarding the condition of an organ in a form that is readily readable, transferable to others, and associated with, or linked to, other information such as the presence or absence of an administered drug, combination of drugs, or drug program. | 02-04-2010 |
20120033858 | Method for Administering a Drug Program to Determine Whether an Animal Has Been Given a Drug - Systems and methods are described that provide a fast and simple way of administering a drug program related to an animal. Specifically, systems are provided that can receive, compile and analyze information regarding the condition of an organ in a form that is readily readable, transferable to others, and associated with, or linked to, other information such as the presence or absence of an administered drug, combination of drugs, or drug program. | 02-09-2012 |
20130156272 | Method for Administering a Drug Program to Determine Whether an Animal Has Been Given a Drug - Systems and methods are described that provide a fast and simple way of administering a drug program related to an animal. Specifically, systems are provided that can receive, compile and analyze information regarding the condition of an organ in a form that is readily readable, transferable to others, and associated with, or linked to, other information such as the presence or absence of an administered drug, combination of drugs, or drug program. | 06-20-2013 |
20140147017 | Method for Administering a Drug Program to Determine Whether an Animal Has Been Given a Drug - Systems and methods are described that provide a fast and simple way of administering a drug program related to an animal. Specifically, systems are provided that can receive, compile and analyze information regarding the condition of an organ in a form that is readily readable, transferable to others, and associated with, or linked to, other information such as the presence or absence of an administered drug, combination of drugs, or drug program. | 05-29-2014 |
Patent application number | Description | Published |
20100251600 | HYDROPYROLYSIS OF BIOMASS FOR PRODUCING HIGH QUALITY LIQUID FUELS - A self-sustaining process for producing liquid fuels from biomass in which the biomass is hydropyrolyzed in a reactor vessel containing molecular hydrogen and a deoxygenating catalyst, producing a partially deoxygenated pyrolysis liquid, which is hydrogenated using a hydroconversion catalyst, producing a substantially fully deoxygenated pyrolysis liquid and a gaseous mixture comprising CO and light hydrocarbon gases (C | 10-07-2010 |
20100251615 | METHOD FOR PRODUCING METHANE FROM BIOMASS - A multi-stage method and apparatus for producing methane from biomass in which the biomass is hydropyrolyzed in a reactor vessel containing molecular hydrogen and a deoxygenating catalyst, the output of which is hydrogenated using a hydroconversion catalyst. The output from the hydroconversion step is provided to a water-gas-shift process providing a mixture of H | 10-07-2010 |
20120260563 | BUBBLING BED CATALYTIC HYDROPYROLYSIS PROCESS UTILIZING LARGER CATALYST PARTICLES AND SMALLER BIOMASS PARTICLES FEATURING AN ANTI-SLUGGING REACTOR - This invention relates to a process for thermochemically transforming biomass or other oxygenated feedstocks into high quality liquid hydrocarbon fuels. In particular, a catalytic hydropyrolysis reactor, containing a deep bed of fluidized catalyst particles is utilized to accept particles of biomass or other oxygenated feedstocks that are significantly smaller than the particles of catalyst in the fluidized bed. The reactor features an insert or other structure disposed within the reactor vessel that inhibits slugging of the bed and thereby minimizes attrition of the catalyst. Within the bed, the biomass feedstock is converted into a vapor-phase product, containing hydrocarbon molecules and other process vapors, and an entrained solid char product, which is separated from the vapor stream after the vapor stream has been exhausted from the top of the reactor. When the product vapor stream is cooled to ambient temperatures, a significant proportion of the hydrocarbons in the product vapor stream can be recovered as a liquid stream of hydrophobic hydrocarbons, with properties consistent with those of gasoline, kerosene, and diesel fuel. Separate streams of gasoline, kerosene, and diesel fuel may also be obtained, either via selective condensation of each type of fuel, or via later distillation of the combined hydrocarbon liquid. | 10-18-2012 |
20130035528 | REMOVAL OF HYDROGEN SULFIDE AS AMMONIUM SULFATE FROM HYDROPYROLYSIS PRODUCT VAPORS - A system and method for processing biomass into hydrocarbon fuels that includes processing a biomass in a hydropyrolysis reactor resulting in hydrocarbon fuels and a process vapor stream and cooling the process vapor stream to a condensation temperature resulting in an aqueous stream. The aqueous stream is sent to a catalytic reactor where it is oxidized to obtain a product stream containing ammonia and ammonium sulfate. A resulting cooled product vapor stream includes non-condensable process vapors comprising H | 02-07-2013 |
20130338412 | HYDROPYROLYSIS OF BIOMASS FOR PRODUCING HIGH QUALITY LIQUID FUELS - A self-sustaining process for producing liquid fuels from biomass in which the biomass is hydropyrolyzed in a reactor vessel containing molecular hydrogen and a deoxygenating catalyst, producing a partially deoxygenated pyrolysis liquid, which is hydrogenated using a hydroconversion catalyst, producing a substantially fully deoxygenated pyrolysis liquid and a gaseous mixture comprising CO and light hydrocarbon gases (C | 12-19-2013 |
20140100395 | DIRECT PRODUCTION OF FRACTIONATED AND UPGRADED HYDROCARBON FUELS FROM BIOMASS - Multistage processing of biomass to produce at least two separate fungible fuel streams, one dominated by gasoline boiling-point range liquids and the other by diesel boiling-point range liquids. The processing involves hydrotreating the biomass to produce a hydrotreatment product including a deoxygenated hydrocarbon product of gasoline and diesel boiling materials, followed by separating each of the gasoline and diesel boiling materials from the hydrotreatment product and each other. | 04-10-2014 |
20140262727 | Rapid Production of Hydrothermally Carbonized Biomass via Reactive Twin-Screw Extrusion - A system for the production of carbonized biomass that includes an infeed for accepting biomass feed material and an associated twin screw extruder. A water heater is connected with respect to at least one inlet along a length of the twin screw extruder and a pressure sustaining valve is connected at an outlet of the twin screw extruder. | 09-18-2014 |
20150027184 | REMOVAL OF HYDROGEN SULFIDE AS AMMONIUM SULFATE FROM HYDROPYROLYSIS PRODUCT VAPORS - A system and method for processing biomass into hydrocarbon fuels that includes processing a biomass in a hydropyrolysis reactor resulting in hydrocarbon fuels and a process vapor stream and cooling the process vapor stream to a condensation temperature resulting in an aqueous stream. The aqueous stream is sent to a catalytic reactor where it is oxidized to obtain a product stream containing ammonia and ammonium sulfate. A resulting cooled product vapor stream includes non-condensable process vapors comprising H | 01-29-2015 |
20150141716 | BUBBLING BED CATALYTIC HYDROPYROLYSIS PROCESS UTILIZINIG LARGER CATALYST PARTICLES AND SMALL BIOMASS PARTICLES FEATURING AN ANTI-SLUGGING REACTOR - This invention relates to a process for thermochemically transforming biomass or other oxygenated feedstocks into high quality liquid hydrocarbon fuels. In particular, a catalytic hydropyrolysis reactor, containing a deep bed of fluidized catalyst particles is utilized to accept particles of biomass or other oxygenated feedstocks that are significantly smaller than the particles of catalyst in the fluidized bed. The reactor features an insert or other structure disposed within the reactor vessel that inhibits slugging of the bed and thereby minimizes attrition of the catalyst. Within the bed, the biomass feedstock is converted into a vapor-phase product, containing hydrocarbon molecules and other process vapors, and an entrained solid char product, which is separated from the vapor stream after the vapor stream has been exhausted from the top of the reactor. When the product vapor stream is cooled to ambient temperatures, a significant proportion of the hydrocarbons in the product vapor stream can be recovered as a liquid stream of hydrophobic hydrocarbons, with properties consistent with those of gasoline, kerosene, and diesel fuel. Separate streams of gasoline, kerosene, and diesel fuel may also be obtained, either via selective condensation of each type of fuel, or via later distillation of the combined hydrocarbon liquid. | 05-21-2015 |
20160002540 | HYDROPYROLYSIS OF BIOMASS-CONTAINING FEEDSTOCKS - Various techniques are disclosed for pretreating municipal solid waste (MSW) and other biomass-containing feedstocks that may be of a poorer quality and consequently more difficult, or even impossible, to convert to higher value liquid products (e.g., transportation fuels) using conventional processes. Such conventional processes may otherwise be satisfactory for the conversion of the biomass portion of the feedstock alone. The pretreatment of biomass-containing feedstocks may generally include steps carried out prior to a hydropyrolysis step and optionally further steps, in order to change one or more characteristics of the feedstock, rendering it more easily upgradable. | 01-07-2016 |
Patent application number | Description | Published |
20080202261 | Apparatus and method for maintaining multi-component sample gas constituents in vapor phase during sample extraction and cooling - A dilution apparatus for diluting a gas sample. The apparatus includes a sample gas conduit having a sample gas inlet end and a diluted sample gas outlet end, and a sample gas flow restricting orifice disposed proximate the sample gas inlet end connected with the sample gas conduit and providing fluid communication between the exterior and the interior of the sample gas conduit. A diluted sample gas conduit is provided within the sample gas conduit having a mixing end with a mixing space inlet opening disposed proximate the sample gas inlet end, thereby forming an annular space between the sample gas conduit and the diluted sample gas conduit. The mixing end of the diluted sample gas conduit is disposed at a distance from the sample gas flow restricting orifice. A dilution gas source connected with the sample gas inlet end of the sample gas conduit is provided for introducing a dilution gas into the annular space, and a filter is provided for filtering the sample gas. The apparatus is particularly suited for diluting heated sample gases containing one or more condensable components. | 08-28-2008 |
20080223153 | Method and apparatus maintaining multi-component sample gas constituents in vapor phase during sample extraction and cooling - An apparatus and method for diluting and cooling that is extracted from high temperature and/or high pressure industrial processes. Through a feedback process, a specialized, CFD-modeled dilution cooler is employed along with real-time estimations of the point at which condensation will occur within the dilution cooler to define a level of dilution and diluted gas temperature that results in a gas that can be conveyed to standard gas analyzers that contains no condensed hydrocarbon compounds or condensed moisture. | 09-18-2008 |
20080305948 | METHOD FOR PRODUCING CATALYTICALLY-ACTIVE MATERIALS - A method for producing a catalytically-active material having at least one base component and at least one catalytically-active component in which the at least one base component is heated to a softening or melting temperature to form a softened or molten base component. While the base component is in the softened or molten state, at least one catalytically-active component is incorporated into or onto the base component, forming the catalytically-active material. In accordance with one embodiment, a catalyst precursor is introduced into the base component and subsequently transformed to a catalytically-active component. | 12-11-2008 |
20090011925 | Method for producing catalytically active glass-ceramic materials, and glass-ceramics produced thereby - A catalytically active glass-ceramic and method for producing a catalytically active multi-phase glass-ceramic in which at least one catalyst precursor is mixed with a glass-ceramic precursor formulation to form a catalyst precursor/glass-ceramic precursor mixture. The catalyst precursor/glass-ceramic precursor mixture is then melted to form an amorphous glass material which, in turn, is devitrified to form a polycrystalline ceramic. The polycrystalline ceramic is then activated, forming a catalytically active multi-phase glass-ceramic. | 01-08-2009 |
20150094503 | CATALYST FOR PRODUCING HYDROCARBONS - A hydropyrolysis catalyst and a process using that catalyst are described. The catalyst comprises a support and an active metal component wherein the catalyst is an eggshell type catalyst having the active metal component located in the outer portion of the support. | 04-02-2015 |
20150133704 | PROCESS FOR PRODUCING HYDROCARBONS - A process for converting biomass to products is described. Biomass is contacted with hydrogen in the presence of a fluidized bed of hydropyrolysis catalyst in a reactor vessel under hydropyrolysis conditions; and products and char are removed from the reactor vessel. The products leave the fluidized bed at an exit bed velocity, the char has a settling velocity that is less than the exit bed velocity and hydropyrolysis catalyst has a settling velocity that is greater than the exit bed velocity. | 05-14-2015 |
Patent application number | Description | Published |
20140107446 | FLEXIBLE MICROELECTRODE ARRAY WITH INTEGRATED STIFFENING SHANK, AND METHOD OF FABRICATION - A stiffener-reinforced microelectrode array device and fabrication method having a plurality of polymer layers surroundably encapsulating one or more electrodes connected to one or more metal traces so that the one or more electrodes are exposed. A stiffening shank is also integrally embedded in the polymer layers adjacent an insertion end of the device near the electrodes to provide mechanical support during insertion. | 04-17-2014 |
20140172051 | SINGLE LAYER POLYMER MICROELECTRODE ARRAY - A microelectrode array having one or more electrical conduits surrounded and insulated from each other by only a single layer of polymer (e.g. polyimide), and a method of fabricating the same. Multiple layers of an uncured polymer precursor (such as polyamic acid) are separately formed with metal layers sandwiched in between. Formation of the uncured polymer precursor layers includes deposition and heating to remove solvent only but not polymerize the precursor. Upon completing construction, the array is subjected to a high-temperature curing process that converts the uncured polymer precursor layers into the polymer. The different layers of the polymer precursor are thus covalently bonded together during the curing process to create a single continuous layer (e.g. monolithic block) of polymer, with no polymer-polymer interfaces. | 06-19-2014 |
20140262462 | DEPOSITING BULK OR MICRO-SCALE ELECTRODES - Thicker electrodes are provided on microelectronic device using thermo-compression bonding. A thin-film electrical conducting layer forms electrical conduits and bulk depositing provides an electrode layer on the thin-film electrical conducting layer. An insulating polymer layer encapsulates the electrically thin-film electrical conducting layer and the electrode layer. Some of the insulating layer is removed to expose the electrode layer. | 09-18-2014 |
20140277296 | INCORPORATING AN OPTICAL WAVEGUIDE INTO A NEURAL INTERFACE - An optical waveguide integrated into a multielectrode array (MEA) neural interface includes a device body, at least one electrode in the device body, at least one electrically conducting lead coupled to the at least one electrode, at least one optical channel in the device body, and waveguide material in the at least one optical channel. The fabrication of a neural interface device includes the steps of providing a device body, providing at least one electrode in the device body, providing at least one electrically conducting lead coupled to the at least one electrode, providing at least one optical channel in the device body, and providing a waveguide material in the at least one optical channel. | 09-18-2014 |
20140277317 | FLEXIBLE NEURAL INTERFACES WITH INTEGRATED STIFFENING SHANK - A neural interface includes a first dielectric material having at least one first opening for a first electrical conducting material, a first electrical conducting material in the first opening, and at least one first interconnection trace electrical conducting material connected to the first electrical conducting material. A stiffening shank material is located adjacent the first dielectric material, the first electrical conducting material, and the first interconnection trace electrical conducting material. | 09-18-2014 |
Patent application number | Description | Published |
20100155319 | Density Phase Separation Device - A mechanical separator for separating a fluid sample into first and second phases is disclosed. The mechanical separator includes a float having a passageway extending between first and second ends thereof with a pierceable head enclosing the first end of the float, a ballast longitudinally moveable with respect to the float, and a bellows extending between a portion of the float and a portion of the ballast. The bellows is adapted for deformation upon longitudinal movement of the float and the ballast, with the bellows isolated from the pierceable head. The float has a first density and the ballast has a second density greater than the first density. The bellows is structured for sealing engagement with a cylindrical wall of a tube, and the pierceable head is structured for application of a puncture tip therethrough. The separation device is suitable for use with a standard medical collection tube. | 06-24-2010 |
20120210778 | Specimen Container Label for Automated Clinical Laboratory Processing Systems - A label and labeling system for identifying the volume of a specimen within a specimen collection container are disclosed. The system includes providing a specimen collection container having an open top end, a closed bottom end, and a sidewall extending therebetween forming an interior adapted for receiving a specimen therein. The specimen collection container also includes a label having a label body disposed over at least a portion of the sidewall, in visual alignment with a colored background. At least one of the sidewall of the specimen collection container and the label body have printing disposed thereon having a color that is substantially identical to the colored background against which the specimen collection container will be viewed. At least one of the sidewall of the specimen collection container and the label body may have colorless indicia having a surface enhancement feature for providing visual distinction. | 08-23-2012 |
20130164195 | Density Phase Separation Device - A mechanical separator for separating a fluid sample into first and second phases is disclosed. The mechanical separator includes a float having a passageway extending between first and second ends thereof with a pierceable head enclosing the first end of the float, a ballast longitudinally moveable with respect to the float, and a bellows extending between a portion of the float and a portion of the ballast. The bellows is adapted for deformation upon longitudinal movement of the float and the ballast, with the bellows isolated from the pierceable head. The float has a first density and the ballast has a second density greater than the first density. The bellows is structured for sealing engagement with a cylindrical wall of a tube, and the pierceable head is structured for application of a puncture tip therethrough. The separation device is suitable for use with a standard medical collection tube. | 06-27-2013 |
20150135813 | Specimen Container Label for Automated Clinical Laboratory Processing Systems - A label and labeling system for identifying the volume of a specimen within a specimen collection container are disclosed. The system includes providing a specimen collection container having an open top end, a closed bottom end, and a sidewall extending therebetween forming an interior adapted for receiving a specimen therein. The specimen collection container also includes a label having a label body disposed over at least a portion of the sidewall, in visual alignment with a colored background. At least one of the sidewall of the specimen collection container and the label body have printing disposed thereon having a color that is substantially identical to the colored background against which the specimen collection container will be viewed. At least one of the sidewall of the specimen collection container and the label body may have colorless indicia having a surface enhancement feature for providing visual distinction. | 05-21-2015 |