02nd week of 2010 patent applcation highlights part 49 |
Patent application number | Title | Published |
20100010364 | DEVICE FOR AMBULATORY MONITORING OF BRAIN ACTIVITY - A device for ambulatory monitoring of brain activity includes a patch secured to a head of a monitoring subject and an electrode secured to the head of the monitoring subject. The electrode produces a signal indicating brain activity of the monitoring subject. The device further includes a signal processor that receives the signal produced by the electrode and processes the signal to produce data. The signal processor is secured to the monitoring subject. The device further includes a display that displays the data produced by the signal processor, the display being secured to the monitoring subject. The device also includes a power source secured to the monitoring subject, the power source providing power to the electrode, the signal processor, and the display wherein the monitoring subject may ambulate unimpeded by the patch, the electrode, the signal processor, the display and the power source. | 2010-01-14 |
20100010365 | Apparatus for analyzing brain wave - To increase intensity of the brain wave signal for detection. Provided is an apparatus for analyzing a brain wave which is installed on a vehicle comprising: a detection unit for detecting the brain wave signal, and separating and analyzing the detected brain wave signal; a discrimination unit for generating a control signal according to an intensity of the brain wave signal analyzed by the detection unit; a processing control unit for controlling subsequent processing according to a type of each of the plurality of control signals produced by the discrimination unit; at least one brain wave signal induction unit for generating a graphic inducing a predetermined type of the brain wave; and a display for displaying the generated graphic according to the received signal from the brain wave signal induction unit. | 2010-01-14 |
20100010366 | METHOD TO EVALUATE PSYCHOLOGICAL RESPONSES TO VISUAL OBJECTS - A method of evaluating the response of a subject to visual features of a visual display, the method including the steps of: (a) presenting a visual display having particular visual features to the subject during a first period; (b) determining brain activity of the subject during the first period; (c) presenting reference display material to a subject during a second period; (d) determining reference brain activity of the subject during the second period; (e) tracking the gaze position of at least one of the eyes of the subject on the visual display during the first period; and (f) evaluating the response of the subject to particular visual features of the visual display by determining differences in brain activity determined between steps (b) and (d) when the gaze of the subject is directed at the particular features. | 2010-01-14 |
20100010367 | System and methods for monitoring during anterior surgery - The present invention involves a system and methods for nerve testing during anterior surgery, including but not limited to anterior disc replacement surgery, nucleus replacement, and interbody fusion. | 2010-01-14 |
20100010368 | SYSTEMS AND METHODS FOR TREATING AORTIC LESIONS - Devices, systems, and methods for the localization of body lumen junctions and other intraluminal structure are disclosed. Various embodiments permit clinicians to identify and locate lesions and/or anatomical structures within a lumen and accurately place leads and/or devices within a lumen, through determining the intralumen conductance and/or cross-sectional area at a plurality of locations within the body lumen. | 2010-01-14 |
20100010369 | NERVOUS SYSTEM MONITORING METHOD - A method for monitoring the response of a nervous system of a body to a stimulus. The method comprises collecting a set of voltage measurements between selected areas on a surface of the body whilst current is being passed between selected regions of the surface of the body. The set of voltage measurements is collected over a predetermined measurement period, the predetermined measurement period is based upon a time after application of the stimulus, and the collected voltage measurements are compared with reference measurements to determine normal or abnormal response of the nervous system. | 2010-01-14 |
20100010370 | SYSTEM AND METHOD FOR CALIBRATING AND NORMALIZING EYE DATA IN EMOTIONAL TESTING - A system and method is provided for calibrating and normalizing eye data of one or more subjects prior to and/or during emotional testing of the subjects. In particular, initially performing one or more calibration or normalization operations prior to an emotional test of a subject may result in accurate evaluations of emotional responses based on measurements of eye data. Additionally, further calibration or normalization performed during the emotional test may be used to refine the initial calibration or normalization, further increasing the accuracy of the evaluated emotional responses. | 2010-01-14 |
20100010371 | DEVICE, SYSTEM, AND METHOD FOR TREATING PSYCHIATRIC DISORDERS - Provided are a device, system, and method for treating a patient having posttraumatic stress disorder (PTSD) or other such psychiatric disorder. An event being recounted by the patient is recorded and a sensory environment of the patient is controlled so as to administer exposure therapy to the patient. Patient mental state may be monitored during administration of the exposure therapy to the patient, and the exposure therapy may be varied in correspondence to the monitored mental state of the patient. In one embodiment, hierarchy assembly means creates a treatment hierarchy based on input from the patient, and hierarchy navigation means navigates within the treatment hierarchy in response to the mental state of the patient. | 2010-01-14 |
20100010372 | POROUS MULTIPLE SAMPLE SLEEVE AND BLOOD DRAWING DEVICE FOR FLASH DETECTION - A device for drawing fluid from a lumen, and particularly blood from a blood vessel, is disclosed. The device may provide indication of the entry of an intravenous cannula into the lumen. The device may include a central body having an outer wall and an inner fluid passage. The device may include a luer-type adapter to permit the attachment of sample vial guide tube, or an I.V. infusion set of various lengths (“butterfly needle”) and or any luer-type fitting attached to an existing device. The outer wall of the central body of the flexible sleeve may be transparent or translucent to permit the detection of fluid within the inner passage. A front cannula may extend from one end of the central body and a rear cannula may extend from the other end of the central body. Both the front and rear cannulae may communicate with the inner fluid passage. An air-permeable blood-impermeable flexible sleeve may surround at least a tip portion of the rear cannula. The air-permeable blood-impermeable flexible sleeve acts as a venting member. The venting member permits the passage of air through it, and is substantially impermeable to liquids, such as blood. The flexible sleeve may be comprised of two types of material, a first material which is air-impermeable and a second material which is air-permeable blood-impermeable. | 2010-01-14 |
20100010373 | QUANTITATIVE ANALYSIS OF A BIOLOGICAL SAMPLE OF UNKNOWN QUANTITY - Disclosed is a method for testing a modified specimen such as a dried blood spot, plasma or serum specimen, for an analyte of interest, such as cholesterol. In accordance with the disclosed subject matter, the level of the analyte of interest in the medium from which the modified specimen was obtained (e.g., from a patient's blood) is determined based on the level of an analyte in a solution formed from the modified specimen and on the level of at least one normalizing analyte. The analyte and normalizing analyte each may be an ion, compound, biochemical entity, or property of the specimen. Also disclosed are a fluid collector and a fluid collection device. | 2010-01-14 |
20100010374 | Body fluid sampling device - sampling site interface - An arrangement for producing a sample of body fluid from a wound opening created in a skin surface at a sampling site includes: a housing, the housing comprising a first opening; a skin interface member disposed in the first opening, the skin interface member comprising an inner member having a second opening, and an outer member at least partially surrounding the inner member and attached to the first opening; and at least one skin-penetration member configured and arranged to project within the second opening. Arrangements having alternatively constructed skin interface members are also described. | 2010-01-14 |
20100010375 | DEVICE AND METHOD FOR ANALYZING BODY FLUIDS - A device for analyzing body fluids comprising a lancing element that can puncture a body part along a lancing axis. The lancing element has a collection volume for collecting body fluid obtained by a puncture and a receiving element that can be loaded with body fluid from the collection volume and that can detect a component of the body fluid. The lancing element and the receiving element are arranged in the lancing axis so that they can be moved relative to one another such that the receiving element dips into the collection volume in the lancing direction during a transfer phase following the puncture. | 2010-01-14 |
20100010376 | Guide wire loading method and apparatus - A device for loading a guide wire into the open end of a tubular instrument such as a catheter. The device can be a block of material having a groove in its surface. The ends of the guide wire and the tubular instrument are placed into the groove and moved toward each other. When the ends meet, the groove guides the guide wire into the open end of the tubular instrument. The groove, or at least a portion of the groove, can have a cross-sectional contour that closely matches the outside radius of the tubular instrument. The groove can have one portion with a shallower depth than the other portion, with the guide wire run in the shallower portion and the tubular instrument in the deeper portion. The guide wire and the tubular instrument can be angled above the device, with just their ends moving along the groove. | 2010-01-14 |
20100010377 | GUIDE WIRE LOADING METHOD AND APPARATUS WITH TOWEL ATTACHMENT MECHANISM - A device for loading a guide wire into the open end of a tubular instrument, such as a catheter. The device can be a block of material having a groove in its surface. The ends of the guide wire and the tubular instrument are placed into the groove and moved toward each other. When the ends meet, the groove guides the guide wire into the open end of the tubular instrument. The groove, or at least a portion of the groove, can have a cross-sectional contour that closely matches the outside radius of the tubular instrument. The groove can have a substantially vertical wall and a substantially non-vertical wall. A variety of attachment mechanisms may be provided for attaching the device to a towel draping a patient. | 2010-01-14 |
20100010378 | Apparatus and Method for Detecting Lung Sounds Using an Implanted Device - Adventitious lung sounds indicative of lung congestion are detected using an implantable sensor. The sensor is adapted to be positioned adjacent to a pulmonary system and to output signals indicative of lung sounds in response to pulmonary system activity. A controller receives the signals and processes the signals to detect the presence of adventitious lung sounds. A respiratory cycle sensor operating in conjunction with the lung-sound sensor enables classification of an adventitious lung sound according to its time occurrence within the respiratory cycle. Posture sensing in conjunction with lung-sound sensing provides valuable additional information as to the severity of the lung congestion. | 2010-01-14 |
20100010379 | DEVICES AND METHOD FOR MONITORING THE FORM OF THREE-DIMENSIONAL OBJECTS - Devices for monitoring the deformation of three-dimensional objects thanks to the presence of sensors integrated in the device are described. | 2010-01-14 |
20100010380 | POSTURE STATE CLASSIFICATION FOR A MEDICAL DEVICE - One embodiment relates to a medical device including a sensor to provide signals indicative of a detected posture state of a patient. A memory stores one or more defined vectors, each defined vector being associated with a tolerance describing a relationship with the defined vector. A processor determines a respective similarity between the detected vector and each of one or more of the defined vectors and classifies a posture state of the patient based on whether any similarity has a relationship to the respective defined vector that is described by the associated tolerance. In one embodiment, the similarity is determined without regard to a coordinate system of the patient. Another embodiment relates to determining the similarity based on at least one of an inner product, a length of the defined posture vector and a length of the detected vector. | 2010-01-14 |
20100010381 | POSTURE STATE RESPONSIVE THERAPY DELIVERY USING DWELL TIMES - Techniques related to classifying a posture state of a living body are disclosed. One aspect relates to sensing at least one signal indicative of a posture state of a living body. Posture state detection logic classifies the living body as being in a posture state based on the at least one signal, wherein this classification may take into account at least one of posture and activity state of the living body. The posture state detection logic further determines whether the living body is classified in the posture state for at least a predetermined period of time. Response logic is described that initiates a response as a result of the body being classified in the posture state only after the living body has maintained the classified posture state for at least the predetermined period of time. This response may involve a change in therapy, such as neurostimulation therapy, that is delivered to the living body. | 2010-01-14 |
20100010382 | BLENDED POSTURE STATE CLASSIFICATION AND THERAPY DELIVERY - Techniques for classification of a posture state of a patient using multiple posture state definitions, and for delivering therapy according to the patient's classified posture state. Detected parameter values describing a patient's posture state are compared to posture state definitions. This comparison is used to determine similarity values describing how similar the patient's posture state is to each of the posture states described by the posture state definitions. Weighting factors may be determined from the similarity values and used to weight therapy parameter values that are associated with each of the posture state definitions. The resulting weighted therapy parameter values may be used to derive a blended therapy parameter value for use in delivering therapy to the patient. The patient's posture state may be expressed in terms of a blending of the multiple posture state definitions. | 2010-01-14 |
20100010383 | REORIENTATION OF PATIENT POSTURE STATES FOR POSTURE-RESPONSIVE THERAPY - In general, the disclosure relates to medical devices and systems configured to deliver posture-responsive therapy to a patient. For example, a medical system may detect a posture state of a patient and deliver therapy based at least in part on the detected patient posture state. In some examples, the system comprises a posture state sensor configured to generate first posture sensor data when a patient is in a first posture state. The system may further comprise a processor configured to define posture state reference data corresponding to the first posture state based at least in part on the first posture sensor data, and redefine the posture state reference data based on second posture data generated by the posture state sensor when the patient is in the first posture state. | 2010-01-14 |
20100010384 | POSTURE STATE DETECTION USING SELECTABLE SYSTEM CONTROL PARAMETERS - Techniques for detecting and classifying a posture state of a patient are disclosed, wherein a posture state includes at least one of a posture and/or an activity state related to motion. In one embodiment, one or more signals indicative of at least one of posture and activity state of the patient may be sensed by a sensor. Control logic may be provided to process the one or more sensed signals in a selectable manner. This selectable manner may be based on current posture state data describing a posture state in which the patient has previously been classified. Alternatively or additionally, this current posture state data may describe a posture state transition previously undergone by the patient. The one or more signals that are so processed may then be used to classify a posture state of the patient. | 2010-01-14 |
20100010385 | GENERATION OF SLEEP QUALITY INFORMATION BASED ON POSTURE STATE DATA - This disclosure describes techniques for generation of sleep quality information based on posture state data. The techniques may include obtaining posture state data sensed by a medical device for a patient, generating sleep quality information based on lying posture state changes indicated by the posture state data, and presenting the sleep quality information to a user via a user interface. | 2010-01-14 |
20100010386 | DATA REJECTION FOR POSTURE STATE ANALYSIS - The disclosure describes techniques for data rejection for posture state analysis. The techniques may include storing posture state data sensed by a medical device for a patient, rejecting any portion of the posture state data that was stored during a session that was shorter than a session threshold, and generating posture state output for the patient based on a portion of the posture state data that was not rejected. | 2010-01-14 |
20100010387 | OBTAINING BASELINE PATIENT INFORMATION - The disclosure relates to a method and system for obtaining baseline patient information. In some examples, a method may include acquiring first patient data, wherein the first patient data comprises at least one of first posture state data indicative of a plurality of posture states of a patient during a first time period or first therapy adjustment data indicative of a plurality of patient therapy adjustments made during the first time period; generating baseline patient information based at least in part on the first patient data; and comparing the baseline patient information to patient information generated based on second patient data. Therapy is not delivered to the patient according to a detected posture state of the patient during the first time period, and therapy is delivered to the patient according to the detected posture state of the patient during the second time period. | 2010-01-14 |
20100010388 | ASSOCIATING THERAPY ADJUSTMENTS WITH INTENDED PATIENT POSTURE STATES - The disclosure described techniques for associating therapy adjustments with intended patient posture states. The techniques may include receiving a patient therapy adjustment to a parameter of a therapy program that defines electrical stimulation therapy delivered to the patient, identifying a posture state of the patient, and associating the patient therapy adjustment with the posture state when the patient therapy adjustment is within a range determined based on stored adjustment information for the identified posture state. | 2010-01-14 |
20100010389 | Generation of proportional posture information over multiple time intervals - The disclosure describes techniques for generation of proportional posture information over multiple time intervals. The techniques may include obtaining posture state data sensed by a medical device for a patient during delivery of therapy by the medical device, determining durations for which the patient occupied each of a plurality of posture states based on the posture state data, generating proportional posture information for a plurality of different time intervals based on the durations, wherein the proportional posture information for each of the time intervals indicates proportional amounts of the respective time interval in which the patient occupied the posture states, and presenting the proportional posture information to a user via a user interface. | 2010-01-14 |
20100010390 | DWELL TIME ADJUSTMENTS FOR POSTURE STATE-RESPONSIVE THERAPY - A medical device detects a patient posture state and adjusts therapy based on the detected posture state. A patient posture state may be transient. To avoid adjusting therapy in response to transient posture states, a dwell time may be imposed. Using the dwell time, only those posture states that are assumed by a patient for a minimum length of time will result in therapy adjustment. To help ensure that the dwell time is set to an appropriate length of time, patient therapy adjustment data may be analyzed. Therapy adjustments made during the dwell time may indicate that the dwell time is too long. Therapy adjustments made prior to the initiation of the dwell time may also indicate that the dwell time is too long. Therapy adjustments made by the patient after expiration of the dwell time may indicate that the dwell time is too short. Based on analysis of the therapy adjustment data, the dwell time can be adjusted to a length that is appropriate for the patient and/or posture state. | 2010-01-14 |
20100010391 | POSTURE STATE REDEFINITION BASED ON POSTURE DATA - The disclosure is directed towards posture-responsive therapy. To avoid interruptions in effective therapy, an implantable medical device may include a posture state module that detects the posture state of the patient and automatically adjusts therapy parameter values according to the detected posture state. A system may include a memory that stores posture state definitions, a posture state module that records a plurality of postures of a patient over a period of time, and a processor that identifies a set of the plurality of postures that fall within a posture state, and redefines a boundary of the posture state based on where the postures fall within the posture state. | 2010-01-14 |
20100010392 | MODIFICATION PROFILES FOR POSTURE-RESPONSIVE THERAPY - In general, the disclosure describes techniques for modifying therapy provided to a patient by a medical device. The techniques may be applicable to electrical stimulation therapy or other therapies. Modification of therapy may include adjustment of one or more therapy parameter values that define one or more characteristics of stimulation therapy delivered to a patient. The therapy modification may be based on activity of a patient that is detected by an IMD, such as a change in a detected posture state occupied by the patient. Different therapy modifications may be applied for different changes in detected posture state. An IMD may modify therapy based on a transition from one posture state to another posture state, and apply different modifications for different transitions. In some aspects, the modification may include a profile, such as a ramp up or ramp down in a parameter value over a period of time. The profile may be different for different posture transitions. A ramp slope may be steeper for one transition than for another transition. When a patient transitions from an upright to a lying posture state, for example, the profile may be especially abrupt. In some examples, a modification profile may define a dwell time. | 2010-01-14 |
20100010393 | Treatment of Occlusions by External High Intensity Focused Ultrasound - An apparatus for treating an occlusion in a vessel inside of a patient. The apparatus includes an external high intensity focused ultrasound transducer configured to be positioned outside of the vessel and to emit ultrasonic waves of energy to the occlusion and to detect ultrasonic waves of energy, an internal ultrasound transducer configured to be positioned inside of the vessel at a position adjacent to or inside the occlusion and to emit ultrasonic waves of energy for detection by the external high intensity focused ultrasound transducer, and a controller configured to control the ultrasonic waves of energy emitted by the external high intensity focused ultrasound transducer based on an electrocardiogram of the patient. | 2010-01-14 |
20100010394 | Noninvasively low-frequency ultrasonic apparatus for the brain therapy - Ultrasonic energy has been proven that at suitable frequency range (670-kHz to 2-MHz), ultrasound can be focused to a specific target, and the concentrated energy has sufficient high acoustic pressure so that capable of inducing localized blood-brain barrier (BBB) disruption, which has an important implication on noninvasively delivering drug into brain. | 2010-01-14 |
20100010395 | ULTRASOUND EMITTING SYSTEM AND ULTRASOUND TREATMENT MACHINE COMPRISING SAID SYSTEM - An ultrasound emission system comprising a substantially cylindrical body and, inside said body: a piezoelectric assembly for producing ultrasound along the axial direction of said body, a sonotrode assembly, a prestress ring, and further comprising electrical power supply and control means; said piezoelectric assembly being constituted by a stack of layers of piezoelectric material, each layer being provided with excitation electrodes and presenting thickness lying in the range 20 μm to 100 μm. The system, generally fitted with a cannula enabling the ultrasound treatment to be applied to a determined area, can itself be incorporated in such a manner as to make an ultrasound treatment machine serving in particular to perform phacoemulsification. | 2010-01-14 |
20100010396 | SHOULDER EXTENSION CONTROL DEVICE - Methods and apparatuses for providing range of motion control devices, and particularly relates to an apparatus for providing control of the range of motion of a human shoulder. | 2010-01-14 |
20100010397 | PASSIVE EXERCISE ASSISTING DEVICE - A housing is adapted to be placed on a floor and is provided on its top face with a left foot support | 2010-01-14 |
20100010398 | FOOT COMPRESSION SYSTEM - Methods and systems for dynamic compression of venous tissue enable improved blood movement in the extremities. In accordance with an exemplary embodiment, a pressure pad provides a compressive force to the venous plexus region of the foot. The pressure pad is successively withdrawn and re-pressed against the foot. Improved blood circulation may reduce the occurrence of undesirable complications such as deep vein thrombosis, ulcers, and the like. | 2010-01-14 |
20100010399 | HYDRO DRIVEN MASSAGING APPARATUS - A water pressure driven massage apparatus for massaging portions of the human body includes a housing adapted to be placed in an ordinary shower enclosure while a user is in the shower. A water pressure operated power device is rotatably mounted in the housing, and a shower water diverter valve selectively delivers water under pressure to a nozzle that directs a jet of water to impinge upon and rotatively drive the water pressure operated power device. The power device is connected to a gear reduction drive train that converts the rotary motion of the water pressure operated power device to reciprocal motion A rod extends through the housing of the massage apparatus, and the rod is reciprocally driven by the gear reduction drive train. The outer end of the reciprocating rod is adapted to be attached to, or configured into the shape of, a variety of massaging devices. | 2010-01-14 |
20100010400 | Method of brain activation - A method of activating the brain of a subject by delivering at least one gas pulse or fluid pulse of a predetermined amplitude and duration to a predetermined area or areas on the subject's body. | 2010-01-14 |
20100010401 | Device for Treating, in Particular Massaging, the Connective Tissue of the Skin - This device ( | 2010-01-14 |
20100010402 | CLAMPING DEVICE FOR THERAPEUTIC APPLICATIONS - A clamping device for therapeutic applications can comprise an extended handle, a powered linear actuator mounted to the extended handle, and a C-shaped clamp attached to the extended handle and including a stationary jaw. The actuator can be configured to provide reversible axial movement of a movable member. The clamping device can further include a pair of applicators attached to the stationary jaw and to the movable member, respectively. The applicators can be made of an hypoallergenic material configured not to cause an adverse reaction when applied to a human skin. The clamping device can further include a switch configured to control the linear actuator. The linear actuator can be configured, responsive to switching the switch, to axially move the second applicator towards and away from the first applicator, thus applying pressure to a targeted body area. | 2010-01-14 |
20100010403 | Mechanical back scratcher / tickler - A rolling tray with dangling stimulators beneath it moves horizontally back and forth over a human who is lying face-down on a floor or bed. The rolling tray is built into a table-shaped housing with legs that are of adjustable height so that the dangling stimulators can make contact with persons of various sizes. The rolling tray moves back and forth via a simple belt and pulley mechanism driven by a low rpm electric motor. Interchangeable dangling stimulators include pointed shapes, rounded shapes, and rollers to achieve various pleasant skin sensations on the back of the user. | 2010-01-14 |
20100010404 | SELF-CONTAINED COMPRESSION DEVICEWITH SPRING-BIASED HOUSING MEMBERS AND METHOD - A self-contained compression device and related method for cyclically compressing the limb of a patient to improve blood flow in the limb. In one embodiment, the compression device includes a compressive section sized and shaped for extending around a portion of the limb for applying compressive pressure and a housing operatively connected to the compressive section. The housing includes first and second housing members movable relative to each other between contracted and expanded positions. A non-pneumatic mechanical actuator is provided in the housing for cyclically moving the first and second housing members from their contracted position to their expanded position. The housing members are spring-biased toward the contracted position. | 2010-01-14 |
20100010405 | SELF-CONTAINED COMPRESSION DEVICE WITH PNEUMATIC BLADDER AND METHOD - Apparatus and methods for cyclically compressing the limb of a patient to improve blood flow in the limb. In one embodiment, a compression device includes a compressive section sized and shaped for extending around a portion of the limb for applying compressive pressure and a housing operatively connected to the compressive section. The housing includes first and second housing members movable relative to each other between contracted and expanded positions. A non-pneumatic mechanical actuator is provided in the housing for cyclically moving the first and second housing members from their contracted position to their expanded position to apply compressive pressure to the limb portion. At least one pneumatic bladder is positioned for distributing the compressive pressure over a surface of the limb portion. | 2010-01-14 |
20100010406 | SELF-CONTAINED COMPRESSION DEVICE WITH CAM-MOVABLE HOUSING MEMBERS AND METHOD - A self-contained compression device and related method for cyclically compressing the limb of a patient to improve blood flow in the limb are disclosed. In one embodiment, the compression device includes a compressive section sized and shaped for extending around a portion of the limb for applying compressive pressure and a housing operatively connected to the compressive section. The housing includes first and second housing members movable relative to each other between contracted and expanded positions. A non-pneumatic mechanical actuator is provided in the housing for cyclically moving the first and second housing members from their contracted position to their expanded position. In one embodiment, the actuator comprises a prime mover and at least one cam movable by the prime mover for effecting relative movement between the first and second housing members. | 2010-01-14 |
20100010407 | SPLINT, PARTICULARLY FOR THE WRIST, AND PRODUCTION METHOD THEREFOR | 2010-01-14 |
20100010408 | BODY LIMB CAST INCLUDING AN OUTER RIGID SHELL AND INNER DYNAMIC MEMBERS IN COMBINATION WITH AIR CIRCULATION AND MASSAGE FEATURES - A cast for supporting a limb includes a rigid outer shell, such as provided as first and second assembleable halves interconnected by a plurality of latches. An inner conforming foam insole is supported within the shell and is interconnected by pluralities of linearly extending passageways in combination with radially extending rings and which communicate with additional breathing holes extending through a cross sectional thickness of the insole for introducing an airflow for relieving patient discomfort. A toe attachable fan unit creates the airflow within the insole in communication with a plurality of vents positioned at upper terminating ends of each of the linear extending passageways. A plurality of airbags encircle the insole and are iteratively inflated and deflated to achieve a pulsing massage effect. | 2010-01-14 |
20100010409 | Brace hinge with telescoping condyle pad - A knee brace assembly is provided having an adjustable, pressure-applying gear system mounted to a portion of the hinge assembly. Through selective adjustment of the gear system, the knee brace assembly can apply pressure to a portion or portions of the knee joint, thereby relieving pressure on the knee joint. A method of treating a knee joint using a knee brace assembly including a planetary gear system is also provided. | 2010-01-14 |
20100010410 | VERSATILE ORTHOPAEDIC LEG MOUNTED WALKER - An orthopedic walker for mounting on the lower leg of a patient includes a walker base having a central area for receiving the foot of a patient and a spaced lower surface including an outer sole, and a pair of struts connected to the walker base. Each of the struts has a frame member of high strength material secured to the first end of the walker base and a supporting component integrally secured and adjacent to the frame member. The supporting component defines laterally extending side wings generally corresponding to the second end of the frame member, and is constructed from a material less rigid than the high strength material of the frame member. The supporting component has a main body and a border portion that are integrally secured and contiguous with one another. The border portion is formed from a material having a lower hardness than the material forming the main body. | 2010-01-14 |
20100010411 | Articles Incorporating Preparing Selectively-Releasable Adhesives - In one embodiment, an article incorporating a selectively-releasable adhesive includes a substrate having a surface and a layer of selectively-releasable adhesive provided on the surface of the substrate, the selectively-releasable adhesive comprising a copolymer formed from a multifunctional alcohol and a multifunctional carboxylic acid that has been cured. | 2010-01-14 |
20100010412 | APPARATUS FOR EXTRACORPOREAL BLOOD TREATMENT - An apparatus ( | 2010-01-14 |
20100010413 | Needle for Subcutaneous Port - This disclosure relates to a new type of needed for a subcutaneous port or for any use where blood is recycled, and more precisely to a needle with reduced friction openings for easing blood and its elements along a passageway made of a through bore in the body of a needle. The needle includes an oval shape opening for increased mechanical resistance of the needle while allowing a greater passage curvature of the blood cells at the greatest zone of passage. In other embodiments, a plurality of staggered openings is used to reduce the flow through any single opening where damage occurs, the openings can be made in a curved area, or a plurality of smaller openings or a grid made of openings can be used to further reduce the interference of the needle tip and the needle openings on blood. | 2010-01-14 |
20100010414 | METHOD OF DELIVERING AN IMPLANT FOR TREATING AN OCULAR DISORDER - Surgical methods and related medical devices for treating ocular disorders are disclosed. Some methods relate to delivering an implant within an eye, and involve providing an elongate guide device, such as, a flexible guide member or a guide wire. A distal end of the guide device can be advanced into an anterior chamber of an eye, or through at least a portion of a site of resistance along a physiologic outflow pathway of the eye, or from an anterior chamber of the eye to a location proximate a physiologic outflow pathway of the eye. The implant is advanced along the guide device toward the guide device distal end, and is positioned to conduct aqueous humor between the anterior chamber and the physiologic outflow pathway. | 2010-01-14 |
20100010415 | HIGH PRESSURE RANGE HYDROCEPHALUS VALVE SYSTEM - A valve for use in a shunt system to drain fluid from one part of a patient's body to another is provided. In an exemplary embodiment, the valve is operable at a threshold pressure that is selectively adjustable up to at least about 400 mm H | 2010-01-14 |
20100010416 | GLAUCOMA TREATMENT DEVICE - Methods and devices are adapted for implanting into the eye. An incision is formed in the cornea of the eye and a shunt is inserted through the incision into the anterior chamber of the eye. The shunt includes a fluid passageway. The shunt is passed along a pathway from the anterior chamber through the scleral spur of the eye into the suprachoroidal space and positioned in a first position such that a first portion of the fluid passageway communicates with the anterior chamber and a second portion of the fluid passageway communicates with the suprachoroidal space to provide a fluid passageway between the suprachoroidal space and the anterior chamber. | 2010-01-14 |
20100010417 | Radiation sensitizer or anti-cancer chemotherapy sensitizer - The present invention provides a novel radiosensitizer or anti-cancer chemotherapy sensitizer. In particular, the invention provides a radiosensitizer or anti-cancer chemotherapy sensitizer that can relieve the irritation of an affected area caused by hydrogen peroxide, is safe when injected into a human body, and can delay or reduce the degradation of hydrogen peroxide and thereby can efficiently exert a radiation sensitizing effect and an anti-cancer chemotherapy sensitizing effect. The radiosensitizer or anti-cancer chemotherapy sensitizer comprises a combination of (a) hydrogen peroxide and (b) hyaluronic acid or salt thereof. | 2010-01-14 |
20100010418 | ELECTRICALLY ACTIVATED GEL ARRAY FOR TRANSDERMAL DRUG DELIVERY - A transdermal drug delivery system ( | 2010-01-14 |
20100010419 | Phacoemulssification Needle Tips - A phacoemulsification needle has tip geometries configured to operate efficiently in both the longitudinal and torsional modes. In one variation, the needle tip has a sharpened edge formed on at least a portion of the needle lip. In other variations the lip geopmetry is selected to create cutting surfaces in both the torsional and longitudinal directions. | 2010-01-14 |
20100010420 | SYSTEM AND METHOD FOR TREATING SUBCUTANEOUS TISSUES - An apparatus and method for treating subcutaneous tissues using acoustic waves in the range of low acoustic pressure ultrasound waves is disclosed. The method includes injections of enhancing agents, wherein disruption of subcutaneous tissues and subcutaneous cavitational bioeffects are produced by ultrasound waves having a power that will not produce tissue cavitation in the absence of the enhancing agents. The apparatus and method of use is useful for treatment of subcutaneous abnormalities including cellulite, lipomas, and tumors. | 2010-01-14 |
20100010421 | METHOD AND APPARATUS FOR DELIVERING THERAPEUTIC OXYGEN TREATMENTS - The present invention provides an applicator for directing a flow of medically pure, therapeutic gas onto a selected portion of the body of a patient. The applicator receives the flow of medically pure, therapeutic gas, such as oxygen, from a source, via a conduit coupled to the source and to the applicator. The applicator can be an adhesive bandage having an inlet for receiving the flow of gas, and one or more outlets for directing the flow of gas. The applicator can also be a mask, patch or similar article configured to be applied to the skin of a patient and connected to a source of medically pure, therapeutic gas via a conduit. The applicator can also having other therapeutic materials impregnated therein. The applicator can also be configured to deliver other therapeutic substances introduced into the flow of gas. | 2010-01-14 |
20100010422 | Nanofluid Production Apparatus and Method - The object of the invention is to provide an apparatus and a method for generating a large amount of nanofluid continuously and stably with a relatively simple, inexpensive and easy-to-use structure, and for efficiently performing an intra-apparatus cleaning operation to substantially reduce the nanofluid manufacturing cost. | 2010-01-14 |
20100010423 | DIALYSIS SYSTEM HAVING FILTERING METHOD FOR DETERMINING THERAPY PRESCRIPTIONS - A peritoneal dialysis system includes a logic implementer configured to: (i) generate a number of peritoneal dialysis therapy regimens that meet at least one therapy target input; (ii) accept a filter input; and (iii) filter the generated therapy regimens according to the filter input to refine the number of therapy regimens available for selection. | 2010-01-14 |
20100010424 | DIALYSIS SYSTEM HAVING REGIMEN GENERATION METHODOLOGY - A peritoneal dialysis system includes a logic implementer configured to: (i) accept at least one therapy target input; (ii) accept at least one patient transport characteristic input; (iii) accept at least one solution input; (iv) accept at least one fluid volume input; (v) accept at least one therapy time input, at least one of the inputs (ii) to (v) including an input range; and (vi) generate each therapy regimen using the inputs of (ii), (iii), (iv) and (v), including each of the possibilities within the at least one input range, that satisfy the at least one therapy target input. | 2010-01-14 |
20100010425 | PERITONEAL EQUILIBRATION TEST AND DIALYSIS SYSTEM USING SAME - An ultrafiltration (“UF”) evaluation method includes: (i) determining an amount of UF removed from a patient over a first dwell time; (ii) determine an amount of UF removed from the patient over a second, different dwell time; (iii) determining an amount of UF removed from the patient over a third, different dwell time; and (iv) fitting a curve to the UF removal amounts for the first, second and third dwell time. A peritoneal dialysis therapy generation method using the curve determined according to the “UF” evaluation method to generate at least one peritoneal dialysis therapy regimen. | 2010-01-14 |
20100010426 | DIALYSIS SYSTEM HAVING INVENTORY MANAGEMENT INCLUDING ONLINE DEXTROSE MIXING - A peritoneal dialysis system includes: a plurality of automated peritoneal dialysis (“APD”) machines; and a server computer in communication with the APD machines, the APD machines programmed to inform the server computer of how much dialysate is consumed over a first delivery period, the server computer configured to use the amounts consumed to determine dialysate delivery amounts for the plurality of APD machines for a second delivery period. | 2010-01-14 |
20100010427 | DIALYSIS SYSTEM HAVING TRENDING AND ALERT GENERATION - A peritoneal dialysis system includes: an automated peritoneal dialysis (“APD”) machine configured to remove ultrafiltrate (“UF”) from a patient and record how much UF has been removed; and a logic implementer configured to (i) form a first moving average UF removed trend, (ii) determine a trending range around the first moving average UF removed trend, (iii) determine at least one of an upper and lower UF removed limit from the trending range, (iv) form a second moving average UF removed trend, and (v) alert if the second moving average UF removed trend moves outside of the at least one UF removed limit. | 2010-01-14 |
20100010428 | DIALYSIS SYSTEM AND MACHINE HAVING THERAPY PRESCRIPTION RECALL - In one embodiment an automated peritoneal dialysis (“APD”) machine includes: at least one pump; a logic implementer storing a plurality of therapy prescriptions by which to operate the at least one pump, each therapy prescription pre-approved for a particular patient; and an input device operating with the logic implementer to allow the patient to select one of the therapy prescriptions for a particular therapy. In another embodiment, the input device operating with the logic implementer allows a doctor/clinician to select or approve one of the therapy prescriptions to be run on the APD machine. In a further embodiment, the logic implementer is programmed to select or suggest one of the therapy prescriptions to be run on the is APD machine. | 2010-01-14 |
20100010429 | SYSTEMS AND METHODS FOR PERFORMING PERITONEAL DIALYSIS - A regenerative peritoneal dialysis system includes a dialysis fluid loop; a filter located in the dialysis fluid loop, a first portion of the dialysis fluid sent to the filter rejected by the filter and returned upstream of the filter, a second portion of the dialysis fluid sent to the filter forming permeate, the permeate being rich in urea; and a urea removing apparatus located in the dialysis fluid loop downstream from the filter to receive the permeate and absorb urea from the permeate. | 2010-01-14 |
20100010430 | PERITONEAL DIALYSIS SYSTEMS AND METHODS THAT REGENERATE DIALYSATE - An artificial kidney that regenerates dialysate includes: a catheter having an inflow lumen and an outflow lumen for communication with a peritoneal cavity of a patient; a fluid circuit in fluid communication with the catheter for circulating dialysate into, through and out of the peritoneal cavity; a pump configured to circulate the dialysate; a cleaning cartridge coupled to the fluid circuit for removing solutes from the dialysate, including a therapeutically effective amount of urea from the dialysate as the dialysate circulates along the fluid circuit; and wherein the fluid circuit is configured to receive a volume of ultrafilterate removed from the patient, such that the pump can mix the ultrafiltrate volume with the dialysate to an increase an overall therapy fluid volume. | 2010-01-14 |
20100010431 | Multi Lumen Suction Irrigator - A multi-lumen tube ( | 2010-01-14 |
20100010432 | ASSOCIATING THERAPY ADJUSTMENTS WITH PATIENT POSTURE STATES - A therapy adjustment received from a patient is associated with a sensed patient posture state. Thereafter, a stability indication can be associated with the sensed posture state to indicate that a therapy adjustment specific to the sensed posture state was received and implemented. In addition, therapy parameter values associated with related patient posture states are updated based on the therapy adjustment. In some examples, only the related posture states that are not associated with respective stability indications are updated based on the therapy adjustment. The absence of a stability indication indicates that the patient has not inputted a therapy adjustment specific to the respective related posture state. As a result, the therapy parameter values associated with the related posture states that are not associated with stability indications may float until the patient adjusts the therapy parameter value associated with the respective related posture state. | 2010-01-14 |
20100010433 | MEDICAL SYSTEM WHICH CONTROLS DELIVERY OF A DRUG - A first medical system includes a controller, a plurality of predetermined patient monitors, and a predetermined drug-delivering medical effector. The controller is adapted to choose different groups of the patient monitors for different medical procedures involving the medical effector. A second medical system includes a controller which is adapted to identify, by querying, connected ones of a multiplicity of medical effectors and connected ones of a plurality of patient monitors and is adapted to control at least one connected medical effector using at least some of the connected patient monitors for a predetermined medical procedure. | 2010-01-14 |
20100010434 | MECHANISM CAPABLE OF PROVIDING NEAT CLEAVED OPENING SURFACE AND AMPULE WITH MOVABLE GASKET - An ampoule which is hard to crack on a barrel while increasing cleavability required for a hermetical container end. An ampoule ( | 2010-01-14 |
20100010435 | One-piece fluid suctioning device - A mucous suction device, comprising in combination, a longitudinally elongated, generally tubular, one-piece plastic body, the body having an axially elongated tapered, first portion extending toward an inlet proximate one end of the body, the body having an axially elongated second portion extending toward an outlet proximate an opposite end of the body, radially outwardly extending annular retention rings in said body second portion, said rings having sharp annular peripheries and said rings being axially resiliently flexible and axially spaced apart, and there being body side porting between said body first and second portions, said side porting being manually controllable to control suction exertion. | 2010-01-14 |
20100010436 | Double burette syringe - The present invention discloses a device, which comprises a double burette syringe, a stopper, a slidable plate for mixing, and a plurality of mixing bars easily detachable from the mixing plate. This invention relates to devices for storing, delivering, and mixing of a two component double burette syringe. | 2010-01-14 |
20100010437 | STEERABLE CATHETER WITH DISTENDING LUMEN-ACTUATED CURLING CATHETER TIP - A steerable catheter having a catheter tip connected to an elongated catheter body, with the catheter tip having an elastomeric cylindrical body and one or more steering lumens each offset from the longitudinal axis of the elastomeric cylindrical body and extending substantially the length of the elastomeric cylindrical body so that increasing the internal pressure of one or more of the steering lumens using, for example, a pneumatic or hydraulic pressure source or heating a thermally expandable media in the steering lumens, operates to curl the longitudinal axis of the elastomeric cylindrical body towards the internally pressurized steering lumen or lumens for steering the catheter tip. | 2010-01-14 |
20100010438 | Balloon With Dividing Fabric Layers And Method For Braiding Over Three-Dimensional Forms - A medical balloon with a variable diameter that is reinforced with continuous fibers woven to form a fabric with a varying number of layers and fiber densities. Portions of the balloon having a relatively smaller diameter are reinforced with a fabric having a reduced fiber density and an increased number of layers to facilitate the placement of the layers. The fabric also includes a braiding pattern that facilitates the transition from a single layer fabric to a multiple layer fabric. Also described is a manufacturing method for the braiding and layering. | 2010-01-14 |
20100010439 | Medical Device With Varying Physical Properties and Method for Forming Same - A medical device in which a melt processed part has different crystallized properties at different locations. The part is formed of a polymer composition by inclusion a of polymer crystallization modifier in the composition making up at least a portion of such part, the amount of the polymer crystallization modifier is varied at different locations on the part in accordance with the desired difference in crystallization behavior. | 2010-01-14 |
20100010440 | Medical Devices Comprising Nanocomposites - The present invention provides medical devices comprising nanocomposite materials. By utilizing nanocomposites in the production thereof, the inventive medical devices can be produced with various advantageous properties. Methods of producing the inventive medical devices are also provided. Inasmuch as the inventive devices are expected to provide certain advantages in their use, there is also provided a method of medical care including methods of treatment or diagnosis, wherein the inventive devices are brought into therapeutic contact with a body to be treated or diagnosed thereby. | 2010-01-14 |
20100010441 | FLOW-DIRECTED CATHETER GUIDE WITH VARIABLE RIGIDITY SHAFT - A flow-directed catheter guide includes a selectively deployable flow-directed member and a variable rigidity shaft. The variable rigidity shaft can be selectively changed between a flexible state and a rigid state. The flow-directed member can be deployed to direct the distal end of the catheter guide downstream following the blood flow in the vessel. | 2010-01-14 |
20100010442 | ENDOVASCULAR CATHETER AIR BLOCK - This invention is an air block for industrial, medical, and non-medical uses. For example, the air block is connected to the proximal end of a vascular access catheter. The air block is either removably connected to the proximal end of the catheter or it is integral to the proximal end of the catheter. The air block permits introduction of other catheters or instrumentation through its central lumen and on into a lumen of the catheter while minimizing fluid loss or gain into the catheter. The air block further prevents air from entering the catheter and provides for removal of the air or other gas from the central lumen before it can enter the catheter where it could cause harm to the patient. The air block can be attached to various standard proximal catheter terminations including Luer fittings and hemostasis valve outer barrels. | 2010-01-14 |
20100010443 | INSULIN RESERVOIR DETECTION VIA MAGNETIC SWITCHING - A system and method for detecting the presence of a medicament reservoir within the housing of an infusion pump. A medicament reservoir, affixed to a reservoir cap is removably inserted within the housing of an infusion pump. A magnet is affixed to or embedded in one or both of the reservoir or the reservoir cap. Alternately, the cap or the reservoir can be made of magnetic material. A sensing device embedded or otherwise affixed to the pump housing senses the presence or absence of the magnetic field created by the magnet. The presence of the magnetic field indicates that the reservoir is inserted properly within the housing and the absence of the magnetic field indicates that the reservoir has been at least partially withdrawn from the pump's housing. | 2010-01-14 |
20100010444 | SURGICAL SYSTEM HAVING A MAGNETIC ENTRY - A surgical portal apparatus for receiving medical instrumentation includes a portal member adapted for passage through tissue for providing access to an underlying tissue site, and having a longitudinal opening extending therethrough. The portal member has a magnetic material for creating a magnetic field adapted to urge magnetically responsive instrumentation at least toward the longitudinal opening to permit passage therethrough and use of the instrumentation in performing a medical procedure adjacent the tissue site. | 2010-01-14 |
20100010445 | CONNECTOR SYSTEM FOR A PROXIMALLY TRIMMABLE CATHETER - A catheter connector system for a subcutaneously placed catheter. The catheter connector system permits proximal trimming of the placed catheter, which is a procedure that provides numerous advantages over traditional methods of trimming catheter distal ends prior to implantation. The catheter connector system can be configured for a single lumen catheter or a multiple lumen catheter. The catheter connector system facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced functionability and patient comfort. | 2010-01-14 |
20100010446 | Surgical sealing element holder for holding a surgical sealing element and surgical sealing system - In order to improve a surgical sealing element holder for holding a surgical sealing element of a surgical sealing system comprising a trocar with a trocar sleeve, the sealing element having an insertion opening which can be widened, such that a sealing element of the sealing system can be replaced in a simple and reliable manner and it is ensured that sealing in relation to a channel of the trocar sleeve is perfect at all times it is suggested that a holder sealing element be provided for sealing the sealing element holder with respect to an inner wall surface of the trocar sleeve. | 2010-01-14 |
20100010447 | FLUSH ENTRANCE HEMOSTASIS VALVE WITH UNOBSTRUCTED PASSAGEWAY - A method of placing a catheter into a patient while preventing disadvantageous escape of fluid from the patient comprises providing a catheter secured to a valve hosing. The catheter has a proximal end, a distal end and an interior lumen. The valve housing has a first port, a second port, and a fluid path running between the first and second ports. The catheter and the valve housing have a hollow needle extending therethrough. The method further comprises piercing the patient's skin, thereby inserting the catheter into the patient. The method further comprises holding the catheter and valve housing in place while removing the hollow needle through the catheter and valve housing. The hollow needle passes through the first and second ports of the valve housing. | 2010-01-14 |
20100010448 | ANCHOR ASSEMBLY - An anchor assembly is used with a medical device to engage the medical device against a body wall. The anchor assembly includes a pivotable anchor and a filament. The anchor is seated in a longitudinal orientation within a recessed channel located at the distal end of the medical device. Pulling on a proximal free end of the filament causes the anchor to pivot from a longitudinal orientation to a perpendicular orientation. The anchor in the perpendicular orientation engages against a body wall to immobilize the medical device. | 2010-01-14 |
20100010449 | Cannula Stabilization Device, System, And Method Of Use - A cannula stabilization device, systems and kits comprising the cannula stabilization device, and methods of using the cannula stabilization device can include a collar removably securable about a longitudinal axis of a cannula. The collar can include a locking mechanism adapted to secure the collar about the cannula. When the collar is positioned on the skin, the collar can stabilize the cannula from at least axial movement in a distal direction. Embodiments of the devices, systems, kits, and methods are useful for stabilizing a cannula during minimally invasive surgery or other percutaneous procedures. | 2010-01-14 |
20100010450 | RETRACTABLE SYRINGE WITH IMPROVED STEM RING AND NEEDLE INTERCHANGEABILITY - A syringe includes a needle assembly at least partially secured within a barrel of the syringe, the needle assembly including a needle stem, a resilient member biasing the needle stem toward a proximal end opening of the barrel, a needle holder connectable to the needle stem during assembly of the syringe and that is further securable to a needle, and a cap that is dimensioned to surround the needle secured to the needle holder and a portion of the needle holder during assembly of the needle holder with the needle stem. In another embodiment, a syringe includes a needle assembly including a section secured within the barrel, the needle assembly including a needle holder, a resilient member biasing the needle holder toward a proximal end opening of the barrel, and a retaining member releasably secured to the needle holder, where the retaining member includes a first material that connects the retaining member to the needle holder and a second material that engages an interior wall section of the barrel, the second material having a hardness or durometer value that is less than that of the first material. | 2010-01-14 |
20100010451 | Huber Needle Assembly and Method of Use - A Huber needle assembly ( | 2010-01-14 |
20100010452 | APPARATUS FOR INTRA-OCULAR INJECTION - The present technology relates to an apparatus for intraocular injection comprising a plate adapted for being brought into contact with an eye and a guide operable to guide a needle into the interior of an eye, characterized in that it comprises means for displacing a superficial layer ( | 2010-01-14 |
20100010453 | Lockable shield for a syringe - The invention is a shield ( | 2010-01-14 |
20100010454 | SUBSTANCE DELIVERY DEVICES - A substance delivery device (autoinjector) for use with a container (such as a syringe) containing the substance includes: a body arranged to house or hold the container; a plunger which is movable with respect to at least a portion of the body, the plunger being arranged to act upon the container so as to move the container with respect to the portion of the body; wherein the plunger is also arranged to expel at least a portion of the substance from the container; and wherein the device includes elements for adjusting the amount of substance to be expelled from the container. The device can also have elements for priming the container, and can accommodate containers of different size or shape. | 2010-01-14 |
20100010455 | Medical Delivery System Adapted to be Locked Axially and Unlocked Rotationally - A medical delivery system ( | 2010-01-14 |
20100010457 | APPARATUS AND METHODS FOR FORMING GASTROINTESTINAL TISSUE APPROXIMATIONS - Apparatus and methods are provided for forming a gastrointestinal tissue fold by engaging tissue at a first tissue contact point, moving the first tissue contact point from a position initially distal to a second tissue contact point to a position proximal of the second contact point to form a tissue fold, and extending an anchor assembly through the tissue fold near the second tissue contact point. | 2010-01-14 |
20100010458 | MAGGOT DEBRIDEMENT THERAPY DRESSINGS AND METHODS - Maggot debridement therapy dressing embodiments and methods are discussed for the treatment of a variety of indications including wound care, including septic wound care and the like. | 2010-01-14 |
20100010459 | UNDERGARMENT FOR INCONTINENT PERSON AND TREATMENT DEVICE CONNECTED TO AN UNDERGARMENT - The present invention relates to an undergarment ( | 2010-01-14 |
20100010460 | DEODORIZING GAS FILTER ASSEMBLY FOR A BODY WASTE COLLECTION POUCH, AND METHOD OF MAKING - A high performance flatus gas filter assembly, and a body waste collection pouch with which it may be used, along with a method for making such an assembly, are disclosed. The assembly includes a filter pad having first and second layers of deodorizing filter media with an imperforate gas and odor barrier layer sandwiched therebetween for blocking the direct flow of gases between the opposing inner faces of the filter layers. An envelope of liquid and gas impermeable material defines a chamber for enclosing the pad. The envelope has walls with first and second openings communicating with central portions of the first and second filter layers, and defines a peripheral space about the pad to permit the outward flow of flatus gases from the peripheral edge surface of one of the filter layers inwardly into the peripheral edge surface of the other of the filter layers. | 2010-01-14 |
20100010461 | Polyamine Coated Superabsorbent Polymers Having Transient Hydrophobicity - Superabsorbent polymer particles having a transient hydrophobicity, excellent gel integrity, and free swell gel bed permeability are disclosed. A method of producing the superabsorbent polymer particles by applying a polyamine coating and a cosolvent to the particles also is disclosed. | 2010-01-14 |
20100010462 | WOUND DRESSING - Provided is a further improved wound dressing suitable for a method for treating a wound while maintaining a moist environment created by exudate oozing from the wound. The wound dressing ( | 2010-01-14 |
20100010463 | ABSORBENT ARTICLE - The invention includes an absorbent article | 2010-01-14 |
20100010464 | ABSORBENT ARTICLE - There is provided an absorbent article having a surface member joined in consideration of absorptivity. | 2010-01-14 |