25th week of 2010 patent applcation highlights part 68 |
Patent application number | Title | Published |
20100160799 | METHODS AND SYSTEM FOR PERFORMING REMOTE ISCHEMIC PRECONDITIONING - A system for remote ischemic preconditioning that includes a cuff, and actuator, and a controller that operates the actuator according to a treatment protocol. The treatment protocol includes a plurality of treatment cycles that each comprise cuff actuation, an ischemic duration, cuff release, and a reperfusion duration. | 2010-06-24 |
20100160800 | SYSTEM AND METHOD FOR MONITORING MYOCARDIAL INSTABILITY - A method of monitoring myocardial stability includes determining a window length representing an acceptable time period between potential start times associated with at least two physiologic indices and monitoring multiple physiologic indices representative of myocardial stability. Predetermined variations in each of the physiologic indices denote the potential start times and potential end times for candidate events that are indicative of myocardial instability. The method further includes identifying the potential start times associated with at least two of the physiologic indices and declaring at least one of the candidate events to be an actual event of myocardial instability based on the window length and a time period between the potential start times identified by the identifying operation. | 2010-06-24 |
20100160801 | CARDIAC FUNCTION CHANGE EVALUATING DEVICE - A cardiac function variation evaluation apparatus includes: a continuous flow type auxiliary artificial heart | 2010-06-24 |
20100160802 | Genetic Variants as Markers for Use in Diagnosis, Prognosis and Treatment of Eosinophilia, Asthma, and Myocardial Infarction - Polymorphic variants (e.g., certain alleles of polymorphic markers) that have been found to be associated with high blood eosinophil counts, conditions causative of eosinophilia (e.g., asthma, myocardial infarction), and/or hypertension are provided herein. Such polymorphic markers are useful for diagnostic purposes, such as in methods of determining a susceptibility, and for prognostic purposes, including methods of predicting prognosis and methods of assessing an individual for probability of a response to a therapeutic agent, as further described herein. Further applications utilize the polymorphic markers of the invention include, screening methods and genotyping methods. The invention furthermore provides related kits, computer-readable medium, and apparatus. | 2010-06-24 |
20100160803 | Multi-channel bio-med electric signals capturing device based on a sound signal generation - A multi-channel bio-med electric signals capturing device includes: a detection channel unit, a control unit, a voice signal generator and a computer device. The detection channel unit is provided to detect bioelectric signals produced from human body and amplify the same. The control unit is provided to capture the amplified bio-med electric signals based on a frequency conforming to a computer acceptable audient signal. The voice signal generator transmits the captured amplified bio-med electric signals to a microphone of the computer device, whereby a recording program built in the computer device records the input audient signal as a voice file. Accordingly, the user is able to monitor the bio-med electric signals by easily and simply using a computer device. | 2010-06-24 |
20100160804 | MONITORING VARIATION PATTERNS IN PHYSIOLOGICAL PARAMETERS ASSOCIATED WITH MYOCARDIAL INSTABILITY - A method of analyzing myocardial instability includes obtaining a physiological parameter representative of myocardial behavior over a set of cardiac cycles and determining reversal points in the physiological parameter over the set of cardiac cycles. The method also includes identifying myocardial instability based on the reversal points in the physiological parameter. A reversal point may correspond to a value of the physiological parameter, during a current cardiac cycle, that exceeds or is less than the values of the physiological parameter during prior and subsequent cardiac cycles. Optionally, the method includes calculating differences between values of the physiological parameter for consecutive cardiac cycles and detecting the reversal points when a current difference exceeds or is less than differences for prior and subsequent cardiac cycles. | 2010-06-24 |
20100160805 | MONITORING SHORT TERM FLUCTUATIONS IN PR INTERVALS FOLLOWING PREMATURE VENTRICULAR CONTRACTIONS - Implantable systems, and methods for use therein, perform at least one of a cardiac assessment and an autonomic assessment. Short-term fluctuations in PR intervals, that follow the premature contractions in the ventricles, are monitored. At least one of a cardiac assessment and an autonomic assessment is performed based on the monitored fluctuations in PR intervals that follow the premature contractions in the ventricles. This can include assessing a patient's risk of sudden cardiac death (SCD), assessing a patient's autonomic tone and/or detecting myocardial ischemic events based on the monitored fluctuations in PR intervals that follow the premature contractions in the ventricles. | 2010-06-24 |
20100160806 | METHODOLOGY FOR AUTOMATED SIGNAL MORPHOLOGY ANALYSIS IN IMPLANTABLE ELECTROTHERAPY AND DIAGNOSTIC SYSTEMS - Systems and related methods for analyzing data sensed from a device implanted in a patient, such as a cardiac pacing system. The system detects and evaluates electric signals within the patient that share a common event marker. By using algorithms and graphical presentation of the collected signals having common event markers, deviations in signals over time can be identified and evaluated in consideration of taking further action related to the patient and the implanted device. The system can also be used in conjunction with an advanced patient management system that includes a programmer or repeater capable of gathering information from the implanted device and transmitting the data to a host via a communications network for evaluation at a remote location. | 2010-06-24 |
20100160807 | Multi Parametric Classfication of Cardiovascular Sound - The present invention relates to a method for classifying a cardiovascular sound recorded from a living subject. The method comprises the steps of:
| 2010-06-24 |
20100160808 | INTERFACE SYSTEM UTILIZING MUSTICATORY ELECTROMYOGRAM - The interface system includes: an output section for visually presenting a manipulation menu for a device; a measurement section for measuring a masticatory electromyogram of a user; a menu presentation section for causing menu items of the manipulation menu to be presented in order via the output section; an amplitude calculation section for determining a maximum amplitude of a potential waveform of the masticatory electromyogram; a latency calculation section for determining a latency based on a point of highlighting each menu item as a starting point, the latency being an amount of time in which the potential waveform arrives at the maximum amplitude; and a determination section for determining whether the maximum amplitude is greater than a previously determined threshold value and the latency is approximately 200 ms or not. In accordance with the determination result of the determination section, the menu presentation section executes a process corresponding to the highlighted menu item. | 2010-06-24 |
20100160809 | Core-Temperature Based Herd Management System and Method - A system and method for managing a herd of animals possibly requiring medical treatment, such as cows in a feedlot. The animals are herded individually into a chute, where identification data is collected from a tag, and core temperature data is collected using a special non-contacting core temperature sensor. The animal is tagged with a color coded tag representing a range of temperatures into which that animal's temperature falls. The animal is then delivered to a pen corresponding to that range of temperatures, where appropriate medicinal treatment is automatically dosed and applied to the animal. | 2010-06-24 |
20100160810 | Multi-Orientation Targeting Set for MRI Biopsy Device - A biopsy device targeting set includes a vertical member, a carriage that is vertically movable along the vertical member, and a cradle coupled with the carriage. The cradle has a pair of substantially perpendicular mounting arms. Each mounting arm has a recess that may receive a rail of the carriage, such that the cradle may be mounted to the same rail in different orientations. Each mounting arm also has a biopsy device mounting feature, which may be a recess or a rail. The biopsy device mounting feature is configured to engage with a complementary feature of a biopsy device, such that a biopsy device may be mounted to either mounting arm. A z-stop feature is operable to selectively restrict longitudinal motion along either or both of the biopsy device mounting features. The targeting set may be used with a biopsy device in an MRI environment. | 2010-06-24 |
20100160811 | Z-Stop Feature of Targeting Set for MRI Biopsy Device - A cradle assembly is configured to support a biopsy device. The cradle assembly comprises first support member and a second support member. A biopsy device may be supported by either the first support member or the second support member. A movement restriction member is operable to restrict the longitudinal distance to which a biopsy device may be advanced relative to the cradle assembly. The movement restriction member may comprise a needle mount, a cannula mount, and/or a z-stop. For instance, a z-stop may be positioned to limit the distance to which a cannula mount may be slid along a rail of the cradle. A screw gear may be used to make fine adjustments to the longitudinal position of the z-stop. A needle mount or cannula mount may also include a ratcheting mechanism to restrict proximal motion of the needle mount or cannula mount along a rail of the cradle. | 2010-06-24 |
20100160812 | Fine Needle Aspiration Handle Attachment - A removable attachment for selectively connecting coaxial medical instruments comprises a first instrument having a proximal end, a distal end and a lumen extending therethrough. The first instrument comprises an arm extending from a fulcrum located on the first instrument and a second instrument movably placed within the lumen of the first instrument, the second instrument comprising a hub at a proximal end thereof. The hub comprises a distal edge to engage a proximal end of the first instrument. The arm pivots around the fulcrum and is configured to selectively engage the hub to provide a removable locking connection between the first and second instruments. | 2010-06-24 |
20100160813 | MEDICAL APPARATUS AND LIVING TISSUE FREEZING AND HARVESTING APPARATUS - A first trocar as an medical apparatus includes an insertion hole having a projection opening for leading out a biopsy forceps into a body of a subject, a lid body for blocking the projection opening of the insertion hole, and a cooling sheet for cryogenically cooling a biopsy portion arranged in the vicinity of the lid body in a state where the biopsy forceps is stored in the insertion hole, and is capable of easily harvesting a living tissue while retaining morphological change of tissues in a living body under various hemodynamics. | 2010-06-24 |
20100160814 | Biopsy Device with Telescoping Cutter Cover - A biopsy device comprises a targeting set, a probe assembly, and a holster assembly, which are detachable from one another. The targeting set comprises a needle assembly having a tissue piercing tip, a tissue receiving aperture, and fluid sealing mechanisms. The probe assembly comprises a tissue cutter, a variable external helix, a body, and telescopic cutter cover. The helix may partially retract the cutter within the probe assembly, while a portion of the cutter extends distally from the probe body. The telescopic cutter cover extends from the distal portion of the probe assembly when the probe assembly is detached from the needle assembly. This extension of the telescopic cutter cover shields a user of the biopsy device from the sharp cutter. The telescopic cutter cover further retracts into the probe assembly when the probe assembly is coupled with the needle assembly of the targeting set assembly. | 2010-06-24 |
20100160815 | Biopsy Device with Retractable Cutter - A biopsy device comprises a targeting set assembly, a probe assembly, and a holster assembly, which are detachable from one another. The targeting set assembly comprises a needle assembly having a tissue piercing tip, a tissue receiving aperture, and a fluid sealing mechanism. The probe assembly comprises a tissue cutter and an internal helix mechanism. The internal helix mechanism may fully retract the cutter within the probe assembly to prevent exposure to the sharp distal end of the cutter when the probe assembly is detached from the needle assembly. When the probe assembly and needle assembly are connected, the internal helix mechanism may extend the cutter into the needle to facilitate biopsy of a tissue sample. The helix may have variable pitch for providing a first translational speed for cutting with the cutter and a second translational speed for cutter retraction. | 2010-06-24 |
20100160816 | Mechanical Tissue Sample Holder Indexing Device - A biopsy device comprises a probe assembly, a holster assembly, a tissue sample holder, and a manually operated rotation mechanism configured to rotate the tissue sample holder. The probe assembly comprises a cutter configured to sever a tissue sample. The tissue sample holder includes a plurality of tissue chambers configured to receive discrete severed tissue samples. The holster assembly comprises the non-motorized, manually operated rotation mechanism configured to allow a user to align consecutive chambers to successively collect discrete severed tissue samples. The tissue sample holder rotation mechanism may comprise a first button, a first lever, a first pawl, a first ratchet, an indexing shaft, and a first gear, which are all configured to, ultimately, rotate a tissue sample holder. The tissue sample holder rotation mechanism may alternately include thumbwheels, a worm gear, or a ratcheting lever, among other things. | 2010-06-24 |
20100160817 | Control Module Interface for MRI Biopsy Device - A biopsy system includes a first external device, a second external device and a control module interface. The control module interface is in electrical communication with both the first and second external devices, and the control module interface is in mechanical communication with the second external device. The control module interface is configured to be positioned remotely from at least one of the first and second external devices. The control module interface comprises a motor, operational electronics, a shaft connector assembly, an electrical connector and a cabinet configured to house the motor and operational electronics. The motor is in mechanical communication with the second external device via a mechanical cable. The operational electronics are configured to permit control of the motor and a motorized component of the second external device. In some embodiments, the mechanical cable comprises a flexible shaft cable, such as a speedometer cable. | 2010-06-24 |
20100160818 | MRI Biopsy Device - A magnetic resonance imaging (MRI) compatible core biopsy system uses a biopsy device having intuitive graphical displays and a detachable remote keypad that advantageously allows convenient control even within the close confines afforded by a localization fixture installed within a breast coil that localizes a patient's breast and guides a probe of the biopsy device relative to the localized breast. A control module for interactive control and power generation are remotely positioned and communicate and transmit rotational mechanical energy via sheathed cable. | 2010-06-24 |
20100160819 | Biopsy Device with Central Thumbwheel - A biopsy device comprises a probe and a holster. The probe has a distally extending needle and a central thumbwheel coupled with the needle. The needle has a transverse tissue receiving aperture. A cutter is translatable relative to the needle to sever tissue protruding through the aperture. The central thumbwheel is manually operable to rotate the needle to reorient the angular position of the aperture about the longitudinal axis defined by the needle. The central thumbwheel is positioned coaxially with the longitudinal axis. An elongate sleeve unitarily couples the needle with the central thumbwheel. A cable driven mechanism in the holster drives the cutter. A rotatable tissue sample holder is coupled with the probe, and has chambers configured to receive tissue samples communicated proximally through a lumen defined by the cutter. A piezoelectric motor in the holster drives the tissue sample holder. | 2010-06-24 |
20100160820 | Biopsy Device with Variable Side Aperture - A biopsy device and method are provided for obtaining a tissue sample, such as a breast tissue biopsy sample. The biopsy device may include an outer cannula having a distal piercing tip, a cutter lumen, a side tissue port communicating with the cutter lumen, and at least one fluid passageway disposed distally of the side tissue port. The inner cutter may be advanced in the cutter lumen past the side tissue port to sever a tissue sample. After the tissue sample is severed, and before the inner cutter is retracted proximally of the side tissue port, the cutter may be used to alternately cover and uncover the fluid passageway disposed distally of the side tissue. | 2010-06-24 |
20100160821 | Biopsy Device with Sliding Cutter Cover - A biopsy device comprises a targeting set, a probe assembly, and a holster assembly, which are detachable from one another. The targeting set comprises a needle assembly having a tissue piercing tip and tissue receiving aperture. The probe assembly comprises a tissue cutter, a body, cutter driving mechanism components, and a sliding cutter cover. The cutter extends from a distal portion of the probe assembly. The sliding cutter cover extends from the distal portion of the probe assembly when the probe assembly is detached from the needle assembly of the targeting set assembly. This extension of the sliding cutter cover shields a user of the biopsy device from the sharp cutter. The sliding cutter cover further retracts into the probe assembly when the probe assembly is coupled with the needle assembly of the targeting set assembly. The cover may be resiliently biased to extend distally from the probe assembly. | 2010-06-24 |
20100160822 | Biopsy Device with Detachable Needle - A biopsy device comprises a targeting set assembly, a probe assembly, and a holster assembly, which are detachable from one another. The targeting set assembly comprises a needle assembly having a tissue piercing tip and tissue receiving aperture. The needle assembly further comprises a needle portion, a needle hub, and a connecting member. The connecting member permits attachment of the needle assembly to the probe assembly. The needle portion may include one or more ceramic inserts, and further is provided with a dual lumen structure. The needle hub comprises features to permit access to the dual lumen structure of the needle portion, while managing fluid and vacuum within the device. | 2010-06-24 |
20100160823 | Biopsy Probe and Targeting Set Interface - A biopsy device comprises a targeting set assembly, a probe assembly, and a holster assembly, which are detachable from one another. The targeting set assembly comprises a needle assembly, which comprises a connecting member. The probe assembly comprises components configured to selectively attach to the connecting member of the needle assembly. In some versions, the connecting member comprises a recess, and the probe assembly comprises a protrusion configured to selectively engage the recess. The protrusion may be provided on a rocking member or on a resilient arm. The rocking member or resilient arm may bias the protrusion to enter the recess. The connection of the probe assembly to needle assembly provides a device for use during a biopsy procedure. The connection of the probe assembly to needle assembly may further permit rotation of the needle assembly for indexing. | 2010-06-24 |
20100160824 | Biopsy Device with Discrete Tissue Chambers - A biopsy device includes a probe, a holster, and a tissue sample holder for collecting tissue samples. The probe includes a needle and a hollow cutter. The tissue sample holder includes a housing having a plurality of chambers that are respectively configured to receive a tray. The housing is releasably engageable with the probe. Each tray is configured to receive a tissue sample communicated through the cutter lumen. Each tray is removable from the housing, such as along an axial direction. The tissue sample holder is rotatable to successively index each chamber to the cutter lumen. A tray retainer is operable to selectively secure the trays relative to the housing. The trays may be flexible, resilient, or rigid. | 2010-06-24 |
20100160825 | Targeting Set for MRI Biopsy Device with Probe Holster Support - A support assembly is configured to support a biopsy device. The biopsy device has a probe portion coupled with a holster portion. The probe portion may have an integral or removable needle. The holster portion has a mounting recess and a pair of distally extending mounting arms. The support assembly comprises a cradle and a mount. The cradle has a rail that complements the mounting recess of the holster portion. The mount is configured to move longitudinally along the rail. The mount has a pair of recesses that complement the pair of distally extending mounting arms of the holster portion. A cannula support member may be located at the distal end of the cradle. The cradle, mount, and cannula support may collectively support and stabilize the biopsy device in a rigid fashion. The cradle may be coupled with a targeting assembly such as a grid or pedestal. | 2010-06-24 |
20100160826 | Tissue Biopsy Device with Rotatably Linked Thumbwheel and Tissue Sample Holder - A biopsy device comprises a probe operably coupled with a holster. The probe comprises a needle portion, a body portion, a rotatable thumbwheel, a cutter, and a rotatable tissue sample holder. The needle portion has a tissue receiving aperture. The needle portion extends distally from the body portion. The thumbwheel is fixedly secured relative to the needle portion such that the thumbwheel is operable to rotate the needle portion about its longitudinal axis. The cutter is longitudinally movable within the needle portion and is configured to cut tissue protruding into the aperture. The rotatable tissue sample holder is configured to receive tissue samples severed by the cutter and communicated through the cutter lumen. The holster comprises a linking mechanism. The thumbwheel is coupled with the tissue sample holder via the linking mechanism such that the thumbwheel is manually rotatable to rotate the tissue sample holder via the linking mechanism. | 2010-06-24 |
20100160827 | DEVICE FOR TRANSCUTANEOUS BIOPSY - A biopsy device includes a first hollow cylindrical element, a second hollow cylindrical element inside which the first hollow cylindrical element is insertable and a locking element that is suitable for locking a tissue sample inside the first hollow cylindrical element. The locking element includes a deformable portion of the first hollow cylindrical element that is able to become deformed to enable a cross section of the first hollow cylindrical element to be closed, the deformable portion connecting a distal end of the first hollow cylindrical element to a body of the first hollow cylindrical element. | 2010-06-24 |
20100160828 | FINE NEEDLE ARRANGEMENT FOR CELL SAMPLING - Fine needle arrangement for taking a sample of cells from suspicious lesions by using fine needle aspiration (FNA) technique, including a tubular needle member ( | 2010-06-24 |
20100160829 | Biopsy Needle with Integrated Guide Pin - A biopsy needle assembly for use in a biopsy gun includes coaxially slidably engaged outer needle and inner needles. The inner needle defines a cavity adjacent its distal end for receiving a tissue sample. A first hub is attached to the proximal end of the inner needle, and a second hub is attached to the proximal end of the outer needle. An elongated pin having a first end and a second end is fixedly attached to the first hub at the first end of the pin. The second end is in sliding contact with the second hub so that the second hub and the pin are slidable relative to each other. A stop engagement is provided between the second end of the pin and the second hub and is configured to prevent disengagement of the outer and inner needles and to maintain a specific physical relationship between the hubs. | 2010-06-24 |
20100160830 | CODING FOR A SAMPLE CARRIER - Coding for a sample carrier having at least a swab shaft and a piece of cotton wool or the like as sample collector, characterized in that said swab shaft ( | 2010-06-24 |
20100160831 | NARROW-PROFILE LANCING DEVICE - In combination, a blood glucose testing meter comprising a slot for receiving a test strip, a display, one or more control devices, and a battery compartment and a lancing device for releasable coupling to the blood glucose test meter over the battery compartment. The lancing device releasably couples directly to the testing meter over the battery compartment. Optionally, the lancing device is mounted to a mounting clip releasably coupled to the testing meter over the battery compartment. The lancing device comprises a housing, a lancet opening disposed at one end of the housing, an energizing member for charging the lancing device, and a release button for activating a lancet within the lancing device. | 2010-06-24 |
20100160832 | APPARATUS AND METHOD FOR MEASURING BLOOD VESSELS - An apparatus comprising a blood vessel measuring device is disclosed. The blood vessel measuring device may comprise a handle. A measuring member may be attached to the handle. The measuring member may be dimensioned to wrap around a blood vessel to measure a size of the blood vessel. The blood vessel measuring device may comprise an extension, and a first end of the extension may be attached to the handle. The blood vessel measuring device may comprise a connector attached to a second end of the extension. A method is also disclosed. The method may comprise inserting a measuring device into an incision in a patient. The measuring device may comprise a measuring member. The method may also comprise wrapping the measuring member around a blood vessel of the patient and measuring a dimension of the blood vessel with the measuring member. | 2010-06-24 |
20100160833 | METHOD AND SYSTEM OF SEGMENTATION AND TIME DURATION ANALYSIS OF DUAL-AXIS SWALLOWING ACCELEROMETRY SIGNALS - The proposed invention is a method and system for the segmentation of dual-axis accelerometry signals for the purposed of identifying problematic swallowing events. The method and system employ a sensor, a data collection means including an algorithm for the analysis of the data. The proposed invention considers the stochastic properties of swallowing signals in both directions, A-P and S-I to extract events associated with swallowing. A segmentation algorithm may be applied to the signals to establish the time duration of swallows and swallows may be classified with respect to gender, body mass index, age or types of swallow. | 2010-06-24 |
20100160834 | WEARABLE PORTABLE DEVICE FOR INCREASING USER AWARENESS OF A PARETIC LIMB AND RECORDING THE USER AWARENESS - A wearable portable device ( | 2010-06-24 |
20100160835 | APPARATUS AND METHOD FOR DETECTING UPPER BODY POSTURE AND HAND POSTURE - Provided are an apparatus and method which detect a user's upper body posture and the user's hand postures through at least two cameras to configure a user interface such as computers and home appliances. An apparatus for detecting upper body posture and hand posture includes a stereo vision calculation unit, a color pattern categorization unit, a plurality of position detection units, an upper body posture recognition unit, and a hand posture recognition unit. The stereo vision calculation unit calculates three-dimensional distance information from each image provided from at least two cameras. The color pattern categorization unit categorizes each color and pattern from the image to output color information and pattern information. The position detection units extract three-dimensional position information for each subject based on the three-dimensional distance information, the color information and the pattern information. The upper body posture recognition unit recognizes an upper body posture based on the three-dimensional position information. The hand posture recognition unit recognizes hand postures with hand position information of the three-dimensional position information. | 2010-06-24 |
20100160836 | DETERMINATION OF INDICATOR BODY PARTS AND PRE-INDICATOR TRAJECTORIES - The present application relates to a determination method for determining an indicator body part subject to vital movement that is not to be irradiated and that serves as an indicator of the change in position of a body part subject to vital movement that is to be irradiated, in particular a tumor in an anatomical body, and/or for determining an indicator trajectory that describes the vital movement of the indicator body part, comprising the following steps:
| 2010-06-24 |
20100160837 | BROAD-AREA IRRADIATION OF SMALL NEAR-FIELD TARGETS USING ULTRASOUND - An ultrasonic transducer system for treating a portion of tissue. The ultrasonic transducer system includes a frequency generator, an ultrasonic transducer, and a transmitter element. The transducer receives an AC voltage from the frequency generator and produces an ultrasonic energy pulse at an ultrasonic frequency for a pulse width. The transmitter element is coupled to the transducer and is for irradiating a portion of skin tissue. The transmitter element has a chilled surface in contact with the skin tissue and an acoustic aperture for producing a substantially collimated energy beam. The beam has a width greater than 4 mm. | 2010-06-24 |
20100160838 | TWO STEP MAMMALIAN BIOFILM TREATMENT PROCESSES AND SYSTEMS - A two-step mammalian biofilm treatment process can have a first step of disrupting or dispersing an undesired biofilm present at a treatment site in or on a mammalian host by suitable mechanical action for example, by applying irrigation fluid, sonic or other vibration, a mechanical instrument or laser-generated mechanical shockwaves to the biofilm. The treatment can also have a second step comprising applying an antimicrobial treatment to the mammalian host to control possible infection related to biofilm dispersed in the first step or to residual biofilm at the treatment site. Usefully, the second step can be performed within a limited time period after the first step. The process can also include additional steps The antimicrobial treatment can employ light or an antibiotic material. Included are implants cleaned of biofilm by a described process. | 2010-06-24 |
20100160839 | Synchronization of Repetitive Therapeutic Interventions - A medical device of the type used for assisting a user in manually delivering repetitive therapy to a patient (e.g., chest compressions or ventilations in cardiac resuscitation), the device comprising a feedback device configured to generate feedback cues to assist the user in timing the delivery of the repetitive therapy, at least one sensor or circuit element configured to detect actual delivery times, at which the user actually delivers the repetitive therapy, and a processor, memory, and associated circuitry configured to compare the actual delivery times to information representative of desired delivery times to determine cue times at which the feedback cues are generated by the feedback device. | 2010-06-24 |
20100160840 | Massage Device - A massage device comprising: a housing with a removable cover; a wheel rotatably mounted inside the housing so that it can rotate about an axis of rotation, the wheel having a series of tongues; wherein the cover can be removed to form an opening in the housing and the wheel can be rotated so that at least part of each tongue periodically protrudes from the opening. The massage device is particularly useful for genital stimulation. | 2010-06-24 |
20100160841 | Massaging Device That Is Assembled and Disassembled Easily and Quickly - A massaging device includes a support base, a drive member rotatably mounted on the support base, a rotation disk rotatable relative to the support base and provided with a driven member which is detachably mounted on and rotated by the drive member to drive the rotation disk to rotate relative to the support base, and a massaging head mounted on the rotation disk to rotate in concert with the rotation disk and rotatable relative to the rotation disk. Thus, the massaging head is directly attached to the rotation disk, and the rotation disk is directly attached to the support base without needing aid of any hand tool. | 2010-06-24 |
20100160842 | Weight shifting apparatus for an orthopedic sling - An apparatus for laterally constraining the shoulder strap of an arm supporting orthopedic sling includes an armband for encircling and attaching to the well arm of the wearer and an anchor strap interconnected between the armband and the shoulder strap for pulling the shoulder strap laterally away from the wearer's neck and holding that strap such that the weight of the supported arm is borne at least primarily by the shoulder rather than the neck. | 2010-06-24 |
20100160843 | Inflatable cast for treating a patient and method of making cast - A cast comprising a shell of bendable material with opposed ends and opposed edges, the shell being bent into a conical shape that is adapted to surround and form a gap with a part of a patient. The edges are fastened on and sealed to each other, and the cast includes a layer of casting material about the shell. A stretchable membrane is disposed in the gap and sealed on the shell forming a fluid tight bag which when inflated engages the patient's part. Metal particles on the membrane surface opposite the shell produce an oligodynamic effect. | 2010-06-24 |
20100160844 | High Torque Active Mechanism for Orthotic and/or Prosthetic Devices - A high torque active mechanism for an orthotic and/or prosthetic joint using a primary brake which can be provide by magnetorheological (MR) rotational damper incorporating and an additional friction brake mechanism driven by the braking force generated by the MR damper. This combination of MR damper and friction brake mechanism allows an increase in torque density while keeping the same level of motion control offered by the MR damper alone. The increased torque density achieved by this high torque active mechanism allows to minimize the size of the actuating system, i.e. its diameter and/or breath, while maximizing its braking torque capability. In this regard, the friction brake mechanism is advantageously positioned around the MR damper, such that the dimension of the package is minimized. | 2010-06-24 |
20100160845 | INGROWN NAIL CORRECTING DEVICE - The ingrown nail correcting device made of a resilient hard synthetic resin comprises an ingrown nail correcting device main body, an engaging member part curved into a hook shape to engage the ingrown nail and arranged at the front end of the ingrown nail correcting device main body, and a lever member inclined obliquely upward at an angle of 5 to 25 degrees with respect to the ingrown nail correcting device main body, and continuously arranged at a base end of the ingrown nail correcting device main body. The part between the ingrown nail correcting device main body and the lever member which are continuously arranged, is formed to serve as a fulcrum part. | 2010-06-24 |
20100160846 | Ultrasonic Material Removal System For Cardiopulmonary Bypass and Other Applications - Devices, systems, and methods manipulate target materials within fluids, and may be useful for removing microbubbles and other materials from blood. Ultrasound or acoustic filtering waves may be directed across a flow of blood, and differences in density between the target microbubbles and the blood may enhance separation by driving the lighter matter upward for removal from the blood stream. A disposable acoustically transmissive conduit can replaceably engage an ultrasound transmitter to facilitate sterilization. Exemplary conduits have elongate lumen cross-sections and an axial path resembling a portion of a Mobius strip. | 2010-06-24 |
20100160847 | SYSTEMS, APPARATUSES, AND METHODS FOR CARDIOVASCULAR CONDUITS AND CONNECTORS - A cardiovascular conduit system may comprise a connector. The connector may comprise a proximal end adapted to attach to a cardiovascular organ. The proximal end may comprise a first plurality of expandable members, and each member in the first plurality of expandable members may be deployable from a delivery position to a deployed position. The first plurality of expandable members may be dimensioned to deploy inside the cardiovascular organ to secure the connector to the cardiovascular organ. The connector may comprise a distal end adapted to attach to a conduit and an opening extending through the connector. Connectors for cardiovascular conduit systems may also include expandable stents. Connectors may be rotateably secured to a conduit, and the conduit may be reinforced. Methods for forming and using cardiovascular conduit systems are also disclosed. | 2010-06-24 |
20100160848 | Ureteral Stent - In some embodiments, a ureteral stent includes an elongate member having a first portion and a second portion, which is coupled to the first portion. The first portion of the elongate member is configured to be disposed within a kidney of a patient. The second portion of the elongate member, which has a sidewall that defines a lumen, is configured to deliver fluid from a first location of the sidewall of the second portion to a second location of the sidewall of the second portion via capillary action. The second portion of the elongate member is configured to be disposed within at least one of a bladder and a ureter of the patient. | 2010-06-24 |
20100160849 | Methods for Identifying Areas of a Subject's Skin that Appear to Lack Volume - The present embodiments relate to methods and systems for identifying areas of a subject's skin that lack sufficient volume. In some embodiments, this can be used to direct the administration of filler compositions or the application of techniques that increase the volume or firmness of the area. In some embodiments, the methods and systems provide for improved aesthetic benefit as well as suitability for instruction and training. In some embodiments, the methods are especially useful in the administration of dermal fillers to a subject. | 2010-06-24 |
20100160850 | GELS WITH PREDETERMINED CONDUCTIVITY USED IN ELECTROPORATION OF TISSUE - Gel compositions with adjusted conductivity are disclosed which compositions are used for directing reversible electroporation and irreversible electroporation of cells and tissue. The gel compositions are also used in a similar manner in order to carry out thermotherapy on cells and tissues. | 2010-06-24 |
20100160851 | Gilled phacoemulsification irrigation sleeve - A phacoemulsification irrigation sleeve includes an elongated, resilient, tubular body section configured to surround a portion of a shaft of a phacoemulsification needle, the tubular body section having a distal end and a proximal end, and an inner surface and an outer surface. An enlarged section formed on the proximal end of the tubular body portion surrounds a hub of the phacoemulsification needle and connects the irrigation sleeve to a phacoemulsification handpiece. The irrigation sleeve further comprises at least one slitted irrigation port formed adjacent to the distal end of the body section and configured to splay in response to a drop in pressure between the inner surface and the outer surface. | 2010-06-24 |
20100160852 | VARIABLE FREQUENCY PHACOEMULSIFICATION HANDPIECE - A phacoemulsification system includes a phacoemulsification handpiece having a horn coupled to a transducer configured to convert alternating current into mechanical oscillation of the horn. The phacoemulsification handpiece further includes a phacoemulsification needle attached to the horn. The phacoemulsification needle vibrates by oscillation of the horn, to provide for mechanical cutting of tissue and inducing cavitation proximate a tip of the phacoemulsification needle. The phacoemulsification system further includes a control system with associated drive circuitry in connection with the transducer of the phacoemulsification handpiece. The control system is configured to adjust an operating frequency of the transducer to increase or decrease a mechanical cutting performance and a cavitational-induced performance of the phacoemulsification needle. | 2010-06-24 |
20100160853 | Method for dressing a wound - A method for dressing a wound is provided including providing a wound dressing pad of hydrophobic fabric that is treated to bind microorganisms; placing the hydrophobic fabric so that it faces the wound; and applying negative pressure therapy to the wound dressing so that microorganisms in the wound surface adhere to the dressing through hydrophobic interaction. The negative pressure therapy may be alternated with hyperbaric oxygen treatments of the wound dressing. | 2010-06-24 |
20100160854 | INTEGRATED PATIENT MANAGEMENT AND CONTROL SYSTEM FOR MEDICATION DELIVERY - An integrated patient monitoring and control system is provided which includes a SITS, the SITS being adapted for coupling to the patient to obtain a specimen from the patient, a sensor, the sensor being adapted to receive the specimen from the SITS and to analyze the sample, a medication control unit, the medication control unit receiving information from the sensor, and utilizing that information to determine medication dosing information for the patient, and a medication administration system, the medication administration system receiving the dosing information from the medication control unit, and adapted to cause administration of the medication to the patient. If the SITS is adapted for blood draw, the system advantageously is performed in conjunction with a pneumatic pressure cuff, inflated so as to aid in blood draw. | 2010-06-24 |
20100160855 | PORTABLE DRUG ADMINISTRATION DEVICE AND METHOD FOR CONTROLLING A PORTABLE DRUG ADMINISTRATION DEVICE - A portable drug administration device includes a pump and a controller configured to control operation of the pump according to a standard administration mode and a suspend mode in which drug administration is temporarily suspended. The device is configured to generate an event trigger on the occurrence of at least one of an error condition and/or the beginning of a maintenance action by the user. The controller is configured to detect the occurrence of the event trigger, and to store, in response to the event trigger, administration data, the administration data comprising all information that characterizes the current administration according at the time of occurrence of the event trigger automatically in a memory and to switch the device from the standard administration mode to the suspend mode. The controller is further configured to detect the occurrence of a restoring trigger and to retrieve, in response to the restoring trigger, the administration data from the memory, to switch the device from the suspend mode to the standard administration mode and to control the pump to resume administration according to the retrieved administration data. | 2010-06-24 |
20100160856 | Oral Care Implement - An oral care implement with a handle includes a head with a releasable material (e.g., an oral medicament) and a tissue cleaner for cleaning the soft tissues and removing odor-causing bacteria from the mouth. In one arrangement, the releasable material is disposed on the surface of the tissue cleaner. In one arrangement, the releasable material is disposed behind the tissue cleaner. In one arrangement, the releasable material is incorporated in the composition of the tissue cleaner. | 2010-06-24 |
20100160857 | Hand-Held Electronically Controlled Injection Device For Injecting Liquid Medications - A medication delivery device includes a housing, a door coupled to the housing and moveable between a closed position and an open position. The door permits insertion of a medication container, containing liquid medication, into the housing in the open position. A door opening mechanism is coupled to the door. A push member is axially moveable between a retracted position and a non-retracted position and located external to the medication container. The push member enters the medication container and pushes the liquid medication out of the medication container. A lock mechanism is coupled to the door opening mechanism and prevents opening of the door when the push member is in the non-retracted position inside the medication container, wherein the lock mechanism automatically unlocks the door opening mechanism when the push member is in the retracted position. | 2010-06-24 |
20100160858 | DEFLECTABLE CATHETER STEERING AND LOCKING SYSTEM - A deflectable catheter includes a catheter shaft having a deflectable distal tip. A support member is coupled around a proximal portion of the catheter shaft, and the support member includes a first brake portion extending along at least a portion of the support member. A handle is coupled around the support member. The deflectable catheter includes a carriage moveably coupled along the handle, and the carriage includes a second brake portion sized and shaped to engage with at least a portion of the first brake portion. A flexible element is coupled between the deflectable distal tip and the carriage. A biasing device is adapted to bias the second brake portion into engagement with the first brake portion. | 2010-06-24 |
20100160859 | TEMPLATE SYSTEM FOR MULTI-RESERVOIR IMPLANTABLE PUMP - A template system for use in conjunction with a multiple reservoir or chambered implantable infusion pump is disclosed. The template system preferably includes at least one template having opening(s) for guiding a needle or syringe to various ports of the multiple reservoir pump. Preferably, each template includes at least two surfaces for cooperating with a like portions of the implantable pump, for properly seating the template on the pump. A kit is also disclosed including three templates for guiding injections into different ports of the pump. | 2010-06-24 |
20100160860 | Apparatus and method for remotely controlling an ambulatory medical device - An electronic device may remotely control a medical device. The electronic device may include a wireless communication circuit configured to wirelessly communicate with the medical device, and a processor that receives from the medical device via the wireless communication circuit screen data generated by the medical device for display on a display device thereof and to control a display device of the electronic device according to the received screen data to display on the electronic device display the screen data generated by the medical device, to emulate at least some of a plurality of user keys of the medical device with selected ones of a plurality of user buttons of the electronic device, and to control the display device of the electronic device to display a map that relates emulated ones of the plurality of user keys to selected ones of the user buttons. | 2010-06-24 |
20100160861 | Control Tabs for Infusion Devices and Methods of Using the Same - An external infusion device that infuses a fluid into an individual's body includes a housing, a reservoir, a drive system, a power supply, electrical elements, and a tab. The reservoir contains the fluid, and the drive system forces the fluid from the reservoir. The electrical elements control the power to the drive system to regulate the rate that fluid is forced from the reservoir. The tab mates with the housing, and contains at least one electrical element. The tab is removable, and may be replaced with a different tab. The different tab may change the rate fluid is forced from the reservoir. A tab may be removed from one external infusion device and installed in a different external infusion device. The tab may be limited to use in a predetermined number of external infusion devices and may include a power supply. | 2010-06-24 |
20100160862 | VARIABLE STIFFNESS INTRODUCER SHEATH WITH TRANSITION ZONE - An introducer sheath includes a lubricious inner liner having a passageway extending longitudinally therethrough, a reinforcing member positioned over the inner liner, and an outer jacket positioned longitudinally over the reinforcing member and the inner liner. The outer jacket has a higher durometer proximal portion, a lower durometer distal portion, and a transition zone between the proximal portion and the distal portion. The transition zone has a variable durometer from a junction with the outer jacket proximal portion to a junction with the outer jacket distal portion, to provide a transition between the higher durometer proximal portion and the lower durometer distal portion. | 2010-06-24 |
20100160863 | Catheter Introducer System - A catheter introducer system is provided with a catheter sheath having a valve providing for a friction fit around a catheter. The friction fit is selectively adjustable to vary between a first configuration for longitudinal movement of the catheter through the valve and a second configuration for holding the catheter longitudinally in place. The valve may include a chuck to grip the catheter radially. The chuck may include an annular base and an opposed annular clamp, and a washer disposed between the base and the clamp. At least one of the base and the clamp may include a beveled surface that forces the washer radially inwardly as the base and the clamp are drawn together. The system also includes one or more dilators layered within the sheath. One or more of the dilators may include a preformed arcuate portion configured to access a targeted branched vessel. The layered dilators and sheaths are typically softer and more hydrophilic proceeding from the innermost dilator out to the sheath. The dilator may be reinforced by a wire embedded in the body of the dilator. The distal tip of the sheath may be stiffened by a ring affixed adjacent the distal end. The sheath may include in the innermost dilator a trocar formed of a flexible, hollow outer wire and an inner stiff needle, which can extend beyond the wire for piercing and be withdrawn to relax the wire for advancement of the dilator. | 2010-06-24 |
20100160864 | INSERTION DEVICE - An insertion device, generally used with an infusion set, including a needle being adapted for puncturing at one end and including at the opposite end a hub. The hub includes a handle part and a guard part that are capable of securing the needle through the use of locks. Locking structures are used to secure the insertion device in a position where the needle is covered in a locked position, avoiding unintended contact with the needle. | 2010-06-24 |
20100160865 | LUMBAR PUNCTURE DETECTION DEVICE - A device for drawing spinal fluid from a body part or injecting medication into the body part is disclosed. The device may include one or more measurement features (markings) that indicate the subcutaneous depth of the device as well as confirm placement and orientation of the spinal fluid withdrawing or medication injecting end of the device in the body part. The device may include a trocar and a cannula having a patient end, a non-patient end, an outer surface, and a central passage adapted to receive said trocar. One or more windows may be provided in or on the cannula, said windows extending from the outer surface of the cannula to the central passage. The windows may be spaced from the patient end of the cannula and from each other along a specific longitudinal axis of the cannula by a predetermined distance, such as 10 millimeters. Means for venting air from the cannula central passage and/or transparent/translucent material may be disposed in said windows. | 2010-06-24 |
20100160866 | REINFORCED CLOSURE ANCHOR - A reinforced closure anchor includes a first layer having an adhesive side, an opposite non-adhesive side, and an outer edge. An anchor member layer having a reinforcing structure is disposed on the first layer. The anchor member includes an adhesive side and an opposite non-adhesive side. The anchor member adhesive side is adhered to the first layer non-adhesive side or the first layer adhesive side. The anchor member is disposed within the outer edge of the first layer. The anchor member may have a surface area that is in the range of approximately 1-2% of a surface area of the first layer, or the anchor member may have a surface area that is in the range of approximately 99-100% of a surface area of the first layer. | 2010-06-24 |
20100160867 | APPARATUS AND METHOD TO INJECT FLUIDS INTO BONE MARROW AND OTHER TARGET SITES - Apparatus for delivering a quantity of fluid to bone marrow of a bone or providing access to remove fluids from a target site is provided. The apparatus may include a driver, a plunger operating and cartridge assembly mechanism, a cartridge assembly having a fluid reservoir and a bone penetrating needle. | 2010-06-24 |
20100160868 | Apparatus and Method to Inject Fluids into Bone Marrow and Other Target Sites - Apparatus for delivering a quantity of fluid to bone marrow of a bone or providing access to remove fluids from a target site is provided. The apparatus may include a driver, a plunger operating and cartridge assembly mechanism, a cartridge assembly having a fluid reservoir and a bone penetrating needle. | 2010-06-24 |
20100160869 | Medical Needle Assemblies - A safety arrangement for a medical needle 15 has a support 14 for carrying the mount end of the needle, and a sleeve 16 slidably mounted on the support 14 for movement from an initial position to a retracted position and then back to a protecting position where the sleeve 16 covers the tip 21 of the needle 15. A spring 32 urges the sleeve towards its protecting position and a blocking member 23 projects forwardly from the support 14 and is movable between non-blocking and blocking positions. In the non-blocking position the sleeve 16 is free to slide from its initial position to its retracted position. On movement of the sleeve to its protecting position, the blocking member 23 moves to lie between the support 14 and sleeve 16 to prevent subsequent movement of the sleeve away from its protecting position. A control member 27 for the blocking member 23 is slidable within the sleeve from a first position at the rearward end of the sleeve to a second position forwardly therefrom. The sleeve is translucent or transparent and the control member is of a strongly coloured material so that when the arrangement has been used, the control member is clearly visible within the sleeve to indicate the device has been used and the sleeve is locked against rearward movement. | 2010-06-24 |
20100160870 | Two Piece Housing For Drug Loading - A drug loading apparatus has a dispensing chamber housing formed by a top housing part and a bottom housing part. The top housing part is separable from the bottom housing part. A plunger is located in the bottom housing part such that the plunger forms a first fluid seal with an inner wall of the bottom housing part. When the top housing part is coupled to the bottom housing part, a second fluid seal is formed. | 2010-06-24 |
20100160871 | REDUCED-PRESSURE TREATMENT SYSTEMS AND METHODS EMPLOYING DEBRIDEMENT MECHANISMS - Reduced-pressure treatment systems and methods are disclosed that employ debridement mechanisms to remove unwanted tissue. In one instance, a reduced-pressure treatment system for treating a tissue site on a patient includes a manifold member for distributing reduced pressure to the tissue site, a support member for disposing proximate the tissue site and the manifold, and a debridement mechanism coupled to the support member. The debridement mechanism is for debriding the tissue site. The system further includes a sealing drape for placing over the tissue site and manifold member. The sealing drape is operable to form a fluid seal over the tissue site and manifold member. The system also includes a reduced-pressure subsystem for delivering a reduced pressure to the sealing drape. The system may further include a chemical-debridement subsystem. Other systems, manifolds, and methods are disclosed. | 2010-06-24 |
20100160872 | Eye-Guard - The present invention relates to medication applied to the eye, and in particular to an apparatus for applying such medication. An arrangement as described herein enables precise quantities of medication to be administered without the apparatus contacting the eye ball. The application comprises a shield portion ( | 2010-06-24 |
20100160873 | ANTIMICROBIAL GEL DISPENSER - A tube dispenser adapted to apply antimicrobial gel beneath a user's fingernails includes a rotatable knob coupled to a piston with a threaded rod so that rotation of the knob advances the piston, extruding antimicrobial gel through an applicator tip. | 2010-06-24 |
20100160874 | REDUCED-PRESSURE WOUND TREATMENT SYSTEMS AND METHODS EMPLOYING MICROSTRAIN-INDUCING MANIFOLDS - Microstrain-inducing manifolds, systems, and methods are presented that involve microstrain-inducing manifolds that include a plurality of shaped projections for creating microstrain. The shaped projections may be tapered projections. A system may include a sealing member for placing over the tissue site, a microstrain-inducing manifold, and a reduced-pressure subsystem that delivers reduced pressure to the sealing member. The reduced pressure causes the shaped projections to create microstrain at the tissue site. Other methods, apparatuses, and systems are also presented. | 2010-06-24 |
20100160875 | OSTOMY SUCTION SYSTEM - The general purpose of the present invention is to provide a new ostomy drainage system, which generally improves on many of the disadvantages of the ostomy devices mentioned above. To attain this, the present invention generally comprises an ostomy bag (or pouch) connected by tubes to a container. The container is then connected via tubes to a vacuum device whereby the contents of the ostomy bag can be suctioned into the container. This prevents the frequent changing of the ostomy bag thereby improving upon the sanitation and convenience of the ostomy patients. | 2010-06-24 |
20100160876 | REDUCED-PRESSURE WOUND TREATMENT SYSTEMS AND METHODS EMPLOYING MANIFOLD STRUCTURES - Manifold structures, systems, and methods are disclosed that include using longitudinal members and one or more shaped projections to cause microstrain at a tissue site. In one instance a manifold structure includes a plurality of spaced longitudinal members and at least one shaped projection coupled to at least one of the plurality of longitudinal members for creating a microstrain at a tissue site. The at least one shaped projection includes a columnar member having a distal end and includes an enlarged member positioned at the distal end of the columnar member. The columnar member has a first outer diameter (D | 2010-06-24 |
20100160877 | MEMBRANES, SYSTEMS, AND METHODS FOR APPLYING REDUCED PRESSURE TO A SUBCUTANEOUS TISSUE SITE - The illustrative embodiments described herein are directed to apparatuses, systems, and methods for applying reduced pressure to a subcutaneous tissue site. In one illustrative embodiment, the apparatus includes a membrane having a substantially uniform membrane wall thickness and a first, tissue-facing surface. The membrane may be shaped to form a plurality of protrusions on the tissue-facing surface. The plurality of protrusions at least partially defines at least one channel operable to transfer the reduced pressure along the tissue-facing surface. | 2010-06-24 |
20100160878 | WOUND TREATMENT APPARATUS - A therapeutic apparatus for stimulating the healing of a wound site includes a polyurethane foam positioned at the wound site and a connector having a disc-like cup and an elbow-shaped spout. The connector is positioned in contact with the polyurethane foam, and the elbow-shaped spout is configured for connection to a tube that is capable of delivering negative pressure through the elbow-shaped spout and to the polyurethane foam. The therapeutic apparatus further includes a drape having a hole, the drape being positioned over the connector such that the elbow-shaped spout extends through the hole in the drape. | 2010-06-24 |
20100160879 | REDUCED PRESSURE WOUND TREATMENT SYSTEM - A reduced pressure treatment appliance is provided for treating a wound on the body of a patient. In some embodiments, the appliance comprises a cover, which can have a top cup member and an interface member. The interface member can have flow control means, configured to permit exudate from the wound to flow through the flow control means into the volume under the cover, but not in the opposite direction. Also, in some embodiments, the top cup member can have a lid member, a cup body member, and lid attachment means to removably attach the lid member to the cup body member. In some embodiments, the cover can be configured to facilitate access to the wound for monitoring, treatment and other purposes without removing the cover from the body. The wound treatment appliance can have a vacuum system to supply reduced pressure to the site of the wound in the volume under the cover. A suction bulb can be used to provide a source of reduced pressure to the cover. Additionally, methods are provided for using various embodiments of the treatment appliance. | 2010-06-24 |
20100160880 | FLEXIBLE REDUCED PRESSURE TREATMENT APPLIANCE - A wound treatment appliance is provided for treating all or a portion of a wound. In some embodiments, the appliance comprises an impermeable flexible overlay that covers all or a portion of the wound for purposes of applying a reduced pressure to the covered portion of the wound. In other embodiments, the wound treatment appliance also includes a vacuum system to supply reduced pressure to the wound in the area under the flexible overlay. In yet other embodiments, the wound treatment appliance also includes wound packing means to prevent overgrowth of the wound or to encourage growth of the wound tissue into an absorbable matrix comprising the wound packing means. In still other embodiments, the appliance may include a suction drain. In other embodiments, the appliance may include a collection chamber to collect and store exudate from the wound. In yet other embodiments, a suction bulb may be used to provide a source of reduced pressure to an impermeable overlay that covers all or a portion of the wound. Finally, methods are provided for using various embodiments of the wound treatment appliance. | 2010-06-24 |
20100160881 | APPARATUS FOR FLUID COLLECTION - An apparatus for fluid collection is disclosed, which comprises: a frame, composed of a plurality of unit cells, each being made of an absorbent polymer composite; and a bag, for receiving the frame while being connected to a conduit provided for enabling a fluid to flow in and out the bag therethrough. | 2010-06-24 |
20100160882 | HYGIENE APPARATUS, PERSONAL MONITORING SYSTEM, AND METHOD OF USE THEREOF - The present invention includes a hygiene apparatus, more specifically, the hygiene apparatus includes a housing and replaceable absorbent portion. The hygiene apparatus can include an electronic monitoring system and sensory feedback system. The absorbent portion and electronic monitoring system are retained within the housing. The electronic monitoring system includes an electronic portion which detects fluids and activates a sensory feedback signal to the user when fluids contact the system and can thereby warn the user before leakage of fluids beyond the article occurs. The user can remove and replace the absorbent cartridge accordingly. The electronic monitoring system can also include a biosensor to analyze the fluids discharged, process the analyzed information, and provide the physiological information regarding the fluids to the user. The electronic monitoring system can also transfer the information to a remote device so that the user can view the results of system's analysis. | 2010-06-24 |
20100160883 | HIGHLY SWELLABLE ABSORPTION MEDIUM WITH REDUCED CAKING TENDENCY - The present invention concerns highly swellable absorption mediums with a reduced caking tendency at high humidity and/or high temperatures, wherein a swellable polymer is coated with a non-ionic, nitrogen-containing surfactant and optionally a Lewis acid and then reacted by heating. | 2010-06-24 |
20100160884 | WOUND DRESSING - A wound dressing includes an absorbent core defining opposed proximal and distal surfaces including a central portion and a border portion, and a liquid impervious, vapor permeable backing layer connected to the distal surface of the absorbent core. The backing layer defines a border portion extending beyond the periphery of the absorbent core. A skin adherent, perforated facing layer is secured to the proximal surface of the absorbent core. An adhesive layer is applied to at least a proximal segment of the border portion of the backing layer and has greater skin adherence properties than the facing layer. | 2010-06-24 |
20100160885 | ABSORBENT PAD - An absorbent pad including a chassis having a first side edge and a second side edge. The chassis includes a liquid pervious topsheet and a liquid impervious backsheet. An absorbent system is disposed between the topsheet and the backsheet. An elastic element is disposed along each of the first and second side edges of the chassis and attached to at least one of the topsheet and the backsheet, the elastic elements generating a cupping action so that the absorbent pad is biased towards a cup-like shape. A first side adhesive element is attached to the chassis inwardly from the first side edge of the chassis. A second side adhesive element is attached to the chassis inwardly from the second side edge of the chassis. A central adhesive element is attached to the chassis between the first and second side adhesive elements. The absorbent pad has a first configuration in which the central adhesive element is releasably attached to an inner surface of an undergarment so that the absorbent pad retains its cup-like shape and a second configuration in which the first and second side adhesive elements are releasably attached to an outer surface of the undergarment to overcome the cupping action of the elastic elements. | 2010-06-24 |
20100160886 | Pre-expanded tampon pledget - A pre-expanded tampon pledget is formed from cellulosic absorbent fibers. The fibers are not tightly compressed, thus, the pledget has a reduced fiber density. As a result, a softer, more pliable pledget is formed that not only increases user comfort during use, but also affords a user with comparable and/or increased leakage protection over conventional tampons or tampon pledgets. | 2010-06-24 |
20100160887 | Lily pad panty - The present invention relates to a panty for ladies that can be worn during menstruation. These panties are for protection against leakage while swimming, sunbathing, or just relaxing in the hot tub. Thus the name Lily Pad Panty. The present invention Lily Pad Panty is made of a unique absorbent material. They are disposable. Sides can be torn away for ease of removal. | 2010-06-24 |
20100160888 | Flexible Absorbent Article With Improved Body Fit - An absorbent article that has a thin, conformable absorbent core where the core has at least two layers, both of which are substantially free of cellulosic fibers. The absorbent article has a Circular Bend Flexibility of less than about 15 N and an acquisition rate on the third gush of less than about 170 seconds and/or on the fourth gush of less than about 190 seconds. | 2010-06-24 |
20100160889 | VIAL ACCESS SPIKE ASSEMBLY - A spike assembly having an elongate spike defining a hollow cannula that is in fluid communication with the interior of a luer connection portion. The spike assembly provides needleless access to a stopper of a vial to facilitate injection and withdrawal of fluids via a syringe barrel selectively secured to the luer connection portion. The syringe can safely be removed from the spike assembly and then be directly attached to a luer compatible connector. The elongate spike may include a frangible tip portion that can break away from the spike assembly within a vial. The spike assembly may have a neck with a pair of gripping wing members. The spike assembly may have a feature that prevents rotation of the spike in the vial stopper, thereby allowing the syringe to be easily and safely disconnected from the spike assembly without having to grasp the spike assembly. | 2010-06-24 |
20100160890 | Syringe guide - The Syringe Guide is an assistive device that is specially designed to couple a syringe and insulin bottle, providing a handy guide for needle insertion and extraction. Fabricated of a durable plastic material, this product is basically rectangular in shape, measuring approximately 6″ in length and 1.25″ in width and 1.5″ in depth. The length of the unit is expandable and is an open ended cylindrical receptacle, sized appropriately to completely house a standard insulin vial on one end, while the opposite end features a grooved trough, inside of which the user inserts the actual syringe. | 2010-06-24 |
20100160891 | ELASTIC IMPLANTABLE COMPOSITES AND IMPLANTS COMPRISING SAME - Described herein are implantable composites, kits comprising the composites, implant devices comprising the composites, and methods of making and using same, including point of use methods. | 2010-06-24 |
20100160892 | IMPLANTABLE SUCTION CUP COMPOSITES AND IMPLANTS COMPRISING SAME - Described herein are implantable composites, kits comprising the composites, implant devices comprising the composites, and methods of making and using same, including point of use methods. | 2010-06-24 |
20100160893 | METHOD AND SYSTEM FOR MEASURING FLOW AT PATIENT UTILIZING DIFFERENTIAL FORCE SENSOR - A fluid delivery system and method for measuring flow at a patient utilizing a differential force sensor in order to precisely control the flow of fluid at very low flow rates. The system includes a fluid line through which a fluid is conveyed to the patient, and a flow controller that selectively varies a rate of flow of the fluid through the fluid line. The differential force sensor can be mounted very close to a point of entry of the fluid into the patient's body. An onboard communications device is controllably coupled to the flow controller and to the force sensor, responds to an output signal, and provides a feedback to the flow controller in a closed-loop process. The system can pump the fluid at a higher frequency until the flow rate is actually reached at the patient and then adjust to the flow rate needed to ensure patient health. | 2010-06-24 |
20100160894 | Automatic injection device - The invention provides an automatic injection device for providing a subcutaneous injection of a substance into a user, comprising: a housing having an open first end and a second end; a syringe movably disposed in the housing, the syringe including a barrel portion for holding the substance, a hollow needle in fluid communication with the barrel portion for ejecting the substance from the syringe, and a bung for sealing the barrel portion and selectively applying pressure to the substance to force the substance through the hollow needle; a plunger for first moving the syringe towards the first end such that the needle projects from the first end and subsequently applying pressure to the bung, the plunger including a rod connected at a first end to the bung, a compressible expanded central portion and a flange between a second end of the rod and the compressible expanded central portion; and a biasing mechanism for biasing the plunger towards the first open end of the housing, the biasing mechanism disposed about the second end of the rod between the flange and the second end of the housing. The present invention also provides methods and kits for using an automatic injection device, and methods and kits for promoting an automatic injection device comprising a medication based on advantageous properties of the device as compared to a pre-filled syringe. The invention also provides methods and kits for training a recipient on use of the automatic injection device. | 2010-06-24 |
20100160895 | Apparatus and Method for Transdermal Delivery of Parathyroid Hormone Agents - An apparatus and method for transdermally delivering a biologically active agent comprising a delivery system having a microprojection member (or system) that includes a plurality of microprojections (or array thereof) that are adapted to pierce through the stratum corneum into the underlying epidermis layer, or epidermis and dermis layers. In one embodiment, the PTH-based agent is contained in a biocompatible coating that is applied to the microprojection member. | 2010-06-24 |
20100160896 | Blood Flow Bypass Catheters and Methods for the Delivery of Medium to the Vasculature and Body Ducts - A catheterization device that may be designed by use of an adaptive genetic algorithm computational fluid dynamics approach, as well as other Global Optimization methods that may include simulated annealing, multistart and interval methods, continuous branch and bound methods, evolutionary algorithms, and tabu search and scatter search methods, as well as other available Global Optimization methods that is able to maximize/optimize the dwell time of an infused agent in the vicinity of a vascular lesion. The device may have an internal by-pass channel that allows the blood upstream of the lesion to continue its pulsatile flow through the vessel in the part of it occluded by the lesion, while simultaneously allowing the disbursement and maximal dwell time of an antithrombolytic or other diagnostic or therapeutic agent needed to treat the lesion. Different embodiments of the catheterization device are disclosed and indications for the use of these devices in the treatment of vascular diseases are discussed. | 2010-06-24 |
20100160897 | Apparatus and Methods for Containing and Delivering Therapeutic Agents - The present embodiments provide apparatus and methods suitable for containing and delivering a therapeutic agent to a target site. The apparatus generally comprises at least one container for holding a therapeutic agent, and a pressure source for facilitating delivery of the therapeutic agent. In one embodiment, the pressure source may be placed in selective fluid communication with a proximal region of the container and fluid from the pressure source may flow through at least a portion of the container to urge the therapeutic agent through the container towards the target site. In an alternative embodiment, the pressure source may be selectively in fluid communication with either a first hollow tube and the container so that therapeutic agent is urged into a catheter, or with a second hollow tube and a catheter so that a fluid from the pressure source bypasses the container and enters the catheter. | 2010-06-24 |
20100160898 | METHOD AND APPARATUS FOR STORAGE AND/OR INTRODUCTION OF IMPLANT FOR HOLLOW ANATOMICAL STRUCTURE - Apparatus for advancing a vascular implant into a blood vessel. The apparatus comprises a first elongate member, the first elongate member having sufficient column strength to function as a pusher member; and a second elongate member, the second elongate member being thinner than the first elongate member and extending to a distal end located at a first point which is at or near a distal end of the first elongate member. The elongate members form an implant retaining portion while the distal end of the second elongate member is located at the first point. The implant retaining portion is located proximal of the first point. The implant retaining portion comprises a space located between the elongate members and configured for receiving an implant portion, with the first elongate member on one side of the space and the second elongate member on another side. The implant retaining portion further comprises a proximal side and a distal side which further circumscribe the space. The proximal and distal sides are effective to prevent an implant received in the retaining portion from moving out of engagement with the retaining portion as the first elongate member is moved distally and proximally. The implant retaining portion is removable by withdrawing the second elongate member in a proximal direction with respect to the first elongate member, thereby moving the distal end of the elongate member proximally beyond the former location of the implant retaining portion. Associated methods, and other apparatus and methods, are also disclosed. | 2010-06-24 |