34th week of 2014 patent applcation highlights part 60 |
Patent application number | Title | Published |
20140236024 | MEDICAL PROBE WITH MULTI-FIBER LUMEN - The present invention relates to a medical probe which consists of a cannula with a multilumen stylet inside. The multilumen contains at least two lumen. Both the multilumen as well as the cannula may have beveled ends. In the lumen straight optical fibers (i.e.no angle end face) are present that can be connected at the proximal end to a console. The cannula, multilumen, fiber system forming the medical probe comprises at least in one of the lumen of the multilumen more than one optical fiber. Preferably the source and detector fibers for the fluorescence detection are contained in one single lumen of the multilumen. | 2014-08-21 |
20140236025 | Personal Health Monitoring System - A personal health monitor device comprising memory for collecting and storing attributes from an individual and a processor for quantizing each attribute in such a way as to indicate a normal range for that attribute and for measuring deviations from that normal range. The processor further calculates the well-being of the individual using the deviations measured. The results are displayed indicating the well-being of the individual. | 2014-08-21 |
20140236026 | METHOD AND APPARATUS FOR MULTI-STATE HEART FAILURE DECOMPENSATION DETECTION - Devices and methods for detecting events indicative of heart failure (HF) decompensation status are described. An ambulatory medical device can determine the present physiologic state as being either a drift state or a stable state, and applies an algorithm to detect HF decompensation event according to the physiologic state. In some embodiments, the ambulatory medical device uses the present physiologic state to estimate one ore more expected future signal characteristics, and to detect HF decompensation event using the one or more expected futures signal characteristics. | 2014-08-21 |
20140236027 | NECKLACE-SHAPED PHYSIOLOGICAL MONITOR - The invention provides a neck-worn sensor (referred to herein as the ‘necklace’) that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the necklace can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls. | 2014-08-21 |
20140236028 | BLOOD-PRESSURE SENSOR - A blood-pressure sensor includes a substrate, a first electrode, a magnetization fixed layer, a nonmagnetic layer, a magnetization free layer, and a second electrode. The substrate is bent to generate a tensile stress at least in a first direction. The first electrode is provided on the substrate. The magnetization fixed layer has magnetization to be fixed in a second direction, and is provided on the substrate. The nonmagnetic layer is provided on the magnetization fixed layer. The magnetization free layer has a magnetization direction which is different from the first direction and from a direction perpendicular to the first direction. The second electrode is provided on the magnetization free layer. | 2014-08-21 |
20140236029 | ALGORITHM ADAPTATION TO AN EXTERNAL IMPACT ON THE DATA - Devices and methods for detecting a physiological target event such as events indicative of HF decompensation status are described. An ambulatory medical device is configured to determine the presence and timing of a confounding event, segment a sensed physiological signal into at least two data segments, adjust the physiological signal by removing or lessening the impact of the confounding event on the physiological signal. The adjusted data can be presented to the user, and the ambulatory medical device can detect the target events using the adjusted physiologic signal. In some embodiments, the ambulatory medical device can be configured to detect an event indicative of HF decompensation using a physiological signal and the information of the detected confounding event. | 2014-08-21 |
20140236030 | ECG Rhythym Advisory Method - A method of automatically determining which type of treatment is most appropriate for a cardiac arrest victim, the method comprising transforming one or more time domain electrocardiogram (ECG) signals into a frequency domain representation comprising a plurality of discrete frequency bands, combining the discrete frequency bands into a plurality of analysis bands, wherein there are fewer analysis bands than discrete frequency bands,
| 2014-08-21 |
20140236031 | NECKLACE-SHAPED PHYSIOLOGICAL MONITOR - The invention provides a neck-worn sensor (referred to herein as the ‘necklace’) that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the necklace can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls. | 2014-08-21 |
20140236032 | IMPLANTABLE HEART MONITORING DEVICE - An implantable heart monitoring device including a sensing unit, a signal quality analysis unit, and an evaluation unit. The sensing unit is connected to at least one electrode that picks up electric potentials. The sensing unit processes electrical signals corresponding to the electric potentials, and generates sense signals including events corresponding to myocardial contractions. The signal quality analysis unit determines whether a noise condition (NC) and/or a low signal indication is present for an event and generates an indication signal. The evaluation unit evaluates the sense signals and the indication signals, treats a detected event as non-valid if a NC and/or low signal indication signal is present for that event, and uses only intervals defined by two consecutive events which do not have a NC and/or a low signal indication to determine a rate of events of the sense signal. | 2014-08-21 |
20140236033 | Apparatus and Method for the Detection and Treatment of Atrial Fibrillation - Embodiments of the invention provide methods for the detection and treatment of atrial fibrillation (AF) and related conditions. One embodiment provides a method comprising measuring electrical activity of the heart using electrodes arranged on the heart surface to define an area for detecting aberrant electrical activity (AEA) and then using the measured electrical activity (MEA) to detect foci of AEA causing AF. A pacing signal may then be sent to the foci to prevent AF onset. Atrial wall motion characteristics (WMC) may be sensed using an accelerometer placed on the heart and used with MEA to detect AF. The WMC may be used to monitor effectiveness of the pacing signal in preventing AF and/or returning the heart to normal sinus rhythm (NSR). Also, upon AF detection, a cardioversion signal may be sent to the atria using the electrodes to depolarize an atrial area causing AF and return the heart to NSR. | 2014-08-21 |
20140236034 | METHOD FOR THE DETECTION OF SUBCUTANOUS CARDIAC SIGNALS AND A CARDIAC DEVICE FOR USE IN DETECTING SUBCUTANEOUS CARDIAC SIGNALS - A cardiac device and method for detecting QRS signals within a composite heart signal of a body including providing at least two input heart signals via at least two separate input channels, wherein each of the at least two input heart signals is recorded by pairs of sensing electrodes that have one electrode in common and provided coincidental in time. The cardiac device and method include generating estimated signals from the input heart signals, combining the input heart signals and the estimated signals to a combined input stream (SECG), and detecting the QRS signal by comparing the combined input stream (SECG) to an adaptive detection threshold (ATHR) which adapts throughout time. | 2014-08-21 |
20140236035 | METHOD AND SYSTEM FOR AUTOMATED VENTILATOR MONITORING TO ENSURE LUNG-PROTECTIVE VENTILATION - A method and a system for acquiring patient parameters and automatically monitoring a patient's lung injury risk include a processor and processing instructions executable by the processor to periodically and automatically determine an arterial oxygenation parameter of the patient based on first data acquired from a monitoring device coupled to the patient. The method and system determine that the mechanical ventilator is set to ventilate the patient; evaluate a lung injury risk monitoring protocol associated with the patient, the lung injury risk monitoring protocol including the arterial oxygenation parameter; and provide a lung injury risk indication when the lung injury risk monitoring protocol is satisfied. | 2014-08-21 |
20140236036 | DEVICE FOR OBTAINING RESPIRATORY INFORMATION OF A SUBJECT - A device and method for reliably and accurately obtaining respiratory information of a subject despite motion of the subject are disclosed. The proposed device comprises a motion signal computing unit for computing a number M of motion signals for a plurality of pixels and/or groups of pixels of at least a region of interest for a number N of image frames of a subject, a transformation unit for computing, for some or all M motion signals, a number of source signals representing independent motions within said images by applying a transformation to the respective motion signals to obtain source signals representing independent motions within said N image frames, and a selection unit for selecting a source signal from among said computed source signals representing respiration of said subject by examining one or more properties of said source signals for some or all of said computed source signals. | 2014-08-21 |
20140236037 | NECKLACE-SHAPED PHYSIOLOGICAL MONITOR - The invention provides a neck-worn sensor (referred to herein as the ‘necklace’) that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the necklace can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls. | 2014-08-21 |
20140236038 | Method For Signal Encoding Evoked Responses - A method and apparatus for utilizing the benefits of encoded signal transmission and reception to enhance the performance of medical testing devices (100) adapted to evoke and measure biological response signals such as auditory evoked potentials (AEP), and the auditory brainstem response (ABR) signals in particular. Auditory stimuli, such as clicks, are presented to the ear of a human patient, in a predetermined encoded sequence, resulting in the generation of auditory responses and bio-electric response signals in the human patient. These response signals from the patient are acquired and observed, and are processed according to the predetermined encoded sequence in which the auditory stimuli were presented to the patient's ear in order to extract the desired auditory evoked potential signals or ABR signals. | 2014-08-21 |
20140236039 | Method of Calibrating and Operating a Direct Neural Interface System - A method of calibrating a direct neural interface system comprising the steps of: | 2014-08-21 |
20140236040 | LOW FREQUENCY STIMULATOR USING MUSIC AND DIET SYSTEM INCLUDING LOW FREQUENCY STIMULATOR - The present invention relates to a low-frequency stimulator using music, and a weight-loss assisting system having a low-frequency stimulator. The low-frequency stimulator according to an embodiment of the present invention includes: a beat extracting unit extracting a beat through a sound pressure magnitude comparison between one or more acoustic signals having different frequencies generated when music is played on a music player; a pulse generator generating a pulse having the same magnitude as that of the extracted beat; and a pair of electrode pads attached to a user's body and applying an electrical stimulus having an intensity corresponding to the magnitude of the generated pulse to the user's body. | 2014-08-21 |
20140236041 | LOCKING TUBE CLIP - A component useable with one or more tube comprises a body engageable with one or more external surface recesses of the one or more tubes. The component has a pair of jaws extending from the body for gripping an item. The component is configured, such that, in use, in a first orientation of the body relative to the respective tube(s) recesses, the component is movable along a length of the tube(s); and, in a second orientation of the body relative to the respective tube(s) recesses, the component is resistive to movement along a length of the tube(s). | 2014-08-21 |
20140236042 | METHOD AND APPARATUS FOR MEASUREMENT OF NEURAL RESPONSE - A method for estimating conduction velocity of a neural response. Measurements of the neural response are obtained from at least two electrodes which are at distinct locations along a neural pathway. A delay between the time of arrival of the neural response at each respective electrode is determined from the measurements. From the delay, and from knowledge of electrode spacing, a conduction velocity of the neural response is estimated. | 2014-08-21 |
20140236043 | Method and Device for Conducting a Pure Tone Audiometry Screening - A method for conducting a pure tone audiometry uses tones of different frequency and intensity utilizing an adaptive procedure. Tone signals with at least two different frequencies are independently changed by delivering to a test person a set of at least three different test stimuli selected from a group of no tone at all, one long tone with a first frequency, and a multitude of short tones of a second frequency. The second frequency is higher than the first frequency. The test person's response corresponds to one of the different test stimuli, and a next test stimulus is presented to the test person after a short delay. A device for conducting an automated pure tone audiometry screening includes a tone generator capable of delivering pure tones of different frequencies and intensities and is able to deliver tones either as a long tone or a set of shorter tones. | 2014-08-21 |
20140236044 | SAMPLING ASSEMBLY - An assembly for sampling bodily fluid, the assembly comprising a membrane penetration device comprising a membrane penetrating element for penetrating a bodily membrane to release a bodily fluid; and, a collector configured in a collection position to take up the released bodily fluid and retain the fluid for delivery to a test element. | 2014-08-21 |
20140236045 | SYSTEM FOR VASCULAR ACCESS IN LABORATORY ANIMALS - A system, and a method for its use, provides for placement of a fluid delivery needle into the tail of a laboratory animal. The system includes an animal receiving portion, structure configured to receive, position and restrain a tail of the animal placed in the animal receiving portion and a hollow needle attached to a fluid transfer device. Positioning structure is provided to align the needle and fluid transfer chamber with the restrained tail for proper automated insertion of the needle into a blood vessel within the tail. A lateral actuator operatively connected to the fluid transfer device moves the hollow needle in a forward direction so that it is inserted into the blood vessel of the properly aligned tail. The system can include a computer programmed to automatically perform all of the functions and operate all the components of the system. | 2014-08-21 |
20140236046 | BLOOD COLLECTION SAFETY DEVICES AND METHODS OF USE AND MANUFACTURE - An automatically locking safety device, e.g., for use in a blood collection procedure, can include a housing, first and second needle covers that are at least partly received in the housing, and a needle that is at least partly received in at least one of the first and second needle covers. The needle can include a proximal tip configured for placement into a patient and a distal tip configured for placement into a blood collection vial. In some embodiments, the first and second needle covers are biased by a biasing member. In some cases, one or both of the first and second needle covers can be locked to prevent axial movement thereof after the blood collection procedure. In certain embodiments, a distal end of the device is configured to connect with a medical connector, such as a needleless IV access device. | 2014-08-21 |
20140236047 | ADJUSTABLE CONNECTOR, IMPROVED FLUID FLOW AND REDUCED CLOTTING RISK - Methods and systems for determining the concentration of one or more analytes from a sample such as blood or plasma are described. The systems described herein can be configured to withdraw a sample from a source of fluid, direct a first portion of the withdrawn sample to an analyte monitoring system and return a second portion of the sample. The analyte monitoring system can be connected to the fluid source via a connector that is configured to improve fluid flow and reduce blood clotting risk. These goals can be accomplished, for example, by employing coatings in or on a connector, positioning a resilient substance at or near the junction, by reducing dead space volume, by using resiliency to improve fit, by extending a portion of one connector to better mate with a portion of another connector, etc. | 2014-08-21 |
20140236048 | EXTERNAL AUTONOMIC MODULATION - In some embodiments, nerves surrounding arteries or leading to organs are targeted with energy sources to correct or modulate physiologic processes. In some embodiments, different types of energy sources are utilized singly or combined with one another. In some embodiments, bioactive agents or devices activated by the energy sources are delivered to the region of interest and the energy is enhanced by such agents. | 2014-08-21 |
20140236049 | SYSTEM AND METHOD FOR VARIABLE DEPTH ULTRASOUND TREATMENT - A non-invasive variable depth ultrasound treatment method and system comprises a variable depth transducer system configured for providing ultrasound treatment to a patient. An exemplary variable depth transducer system can comprise a transducer configured to provide treatment to more than one region of interest, such as between a deep treatment region of interest and a superficial region of interest, and/or a subcutaneous region of interest. The variable depth transducer can comprise a transduction element having a piezoelectrically active layer, matching layers and/or other materials far generating radiation or acoustical energy. The variable depth transducer may be configured to operate at moderate frequencies within the range from approximately 750 kHz to 20 MHz or more. In addition, the transduction element may be configured with a variable depth device comprising one or more materials configured to allow tor control and focusing/defocusing of the acoustic energy to more than one region of interest. | 2014-08-21 |
20140236050 | METHOD, APPARATUS, AND HIFU SYSTEM FOR GENERATING ULTRASOUND THAT FORM MULTI-FOCI IN REGION OF INTEREST - Provided is a method of generating ultrasound that forms focus points in a region of interest. Additional embodiments include related apparatuses and system embodiments. The method includes: setting focus patterns that each indicate focus points to be formed by radiating therapeutic ultrasound to a region of interest of an object; calculating a parameter of the therapeutic ultrasound based on characteristics of tissue in the region of interest existing on a path through which the therapeutic ultrasound moves; and generating therapeutic ultrasound set at different frequencies to form the focus patterns, based on the calculated parameter. | 2014-08-21 |
20140236051 | APPARATUS AND METHOD OF TRANSMITTING ULTRASOUND - Provided are methods and apparatuses of transmitting ultrasound by adjusting positions of a plurality of ultrasound generating elements within an applicator to direct the ultrasound waves at a position desired by a user. | 2014-08-21 |
20140236052 | METHOD AND APPARATUS FOR THE TREATMENT OF HEADACHE - A battery-operated transcutaneous electrical nerve stimulator (TENS) to treat headache pain in an abortive and/or preventive manner. The TENS unit and its electrodes are built into a unitary device which facilitates a self-administered treatment. In some embodiments, the pulses are monophasic. In other embodiments, pairs of biphasic pulses are provided, wherein each pair of biphasic pulses includes a first pulse having a first polarity separated by a gap in time from a second pulsed having an opposite polarity. In some embodiments, each pulse in each biphasic pair is of a duration equal to that of the other pulse of the pair. In some embodiments, the duration of each pulse is between about 50 microseconds and about 400 microseconds, and the gap in time between pulses of a pair is between about 50 and 100 microseconds. | 2014-08-21 |
20140236053 | CPR QUALITY ASSESSMENT ACCOUNTING FOR PAUSE ASPECT - Devices, systems, software and methods for CPR quality assessment. Patient data is received, derived from a session of administering sets of CPR chest compressions to a patient. The sets can be separated by pauses. In some embodiments, a penalty value can be determined for at least one of the pauses, from at least one control factor unrelated to a constant linear dependence on the pause duration. An Indicative value can be derived from the penalty value. In some embodiments, at least some of the pauses are classified in one or more pause groups, depending on how well they meet one or more classification criteria. The indicative value can be derived for one of the pause groups. The indicative value can be output, and/or an alarm can be emitted if it exceeds a threshold. CPR quality assessment can be improved in real time, and provide feedback for training/ | 2014-08-21 |
20140236054 | PORTABLE AUTOMATIC CHEST COMPRESSION DEVICES - An automated chest compression device has a housing for supporting a patient and a motor within the housing. A conical drive spool is operatively connected to the motor and a cable, is operatively connected to the conical drive spool. The cable is adapted to extend at least partially around the chest of the patient. A controller is operable to control the motor to compress the chest to variable thresholds. | 2014-08-21 |
20140236055 | RESUSCITATION DEVICE - The present invention relates to an apparatus ( | 2014-08-21 |
20140236057 | METHODS AND DEVICES FOR TREATING HYPERTENSION - Devices, systems and methods are described which control blood pressure and nervous system activity by stimulating baroreceptors. By selectively and controllably activating baroreceptors and/or nerves, the present invention reduces blood pressure and alters the sympathetic nervous system; thereby minimizing deleterious effects on the heart, vasculature and other organs and tissues. A baroreceptor activation device or other sensory activation device is positioned near a dermal bone to provide the treatment. | 2014-08-21 |
20140236058 | COMPRESSION VEST FOR PATIENTS UNDERGOING HEMODIALYSIS AND IN CRITICAL CARE - A method of inhibiting hypotensive symptoms in a patient undergoing treatment or a procedure involves elastically constraining the internal organs within the abdomen of the patient while applying non-pulsating, compressive pressure to the internal organs within the abdomen of the patient. The method may also involve one or more of infusing fluid, applying the compressive pressure using compression device, or applying the compressive pressure based upon bio-indicator measurement parameters. | 2014-08-21 |
20140236059 | CARPAL TUNNEL RELIEF DEVICE - A carpal tunnel relief device is configured for adhesive application to a skin area above the median nerve of the distal forearm, wrist or a palm of the subject and includes a middle curved portion shaped to pull the skin and surrounding soft tissues away from the median nerve therefore releasing compression of the median nerve and pain associated with carpal tunnel syndrome. Resilient flexible member may be incorporated with the device or inserted in a pocket of a flexible fabric after its adhesion to the skin. | 2014-08-21 |
20140236060 | COMPRESSION GARMENT APPARATUS HAVING BASELINE PRESSURE - A compression garment apparatus including a compression garment and a pressurizer. The pressurizer intermittently pressurizes a therapeutic bladder on the compression garment and maintains a baseline pressure in the therapeutic bladder to maintain the therapeutic bladder in position with respect to a target compression zone on a body part on which the garment is worn. The baseline pressure is adjusted in response to sensed physical characteristics. | 2014-08-21 |
20140236061 | METHOD, APPARATUS, AND HIGH INTENSITY FOCUSED ULTRASOUND (HIFU) SYSTEM FOR GENERATING ULTRASOUND THAT FORMS MULTI-FOCI VIA MEDICAL IMAGE IN REGION OF INTEREST - A method of generating therapeutic ultrasound that forms multi-foci by a therapeutic ultrasound probe, the method including: obtaining a medical image including anatomical information of a region of interest in a subject; calculating, by using the medical image, characteristics which influence traveling of therapeutic ultrasound with respect to tissues included in the region of interest; calculating, by using the calculated characteristics, a parameter of the therapeutic ultrasound for forming multi-foci in the region of interest; and generating the therapeutic ultrasound according to the calculated parameter. | 2014-08-21 |
20140236062 | BLOOD FLOW CONDUCIVE BRACE - A limb brace used to promote blood flow is provided. The limb brace may be made of a semi-rigid skeleton made of a plurality of intersecting ribs. A padded lining may surround the skeleton for comfort. The limb brace may be tubular, may be attachable to a user's upper arm. | 2014-08-21 |
20140236063 | ARTERIOVENOUS ACCESS VALVE SYSTEM AND PROCESS - In accordance with certain aspects of the present disclosure, a subcutaneous arteriovenous graft system is described. The system includes an arteriovenous graft having an arterial end and an opposite venous end, at least one of the arterial end and venous end including a support frame. The system further includes a first valve device positioned at the arterial end of the arteriovenous graft and a second valve device positioned at the venous end of the arteriovenous graft and an actuator in communication with both the first valve device and the second valve device, the actuator being configured to cause each valve device to open or close simultaneously. | 2014-08-21 |
20140236064 | DEVICES AND METHODS FOR FORMING AN ANASTOMOSIS - Devices and methods for deploying an anastomotic stent between portions of the gastro-intestinal (GI) tract are disclosed. The anastomotic stents are configured to atraumatically engage the tissue walls and to permit the flow of fluid, partially digested food, and food. The stents can be deployed using endoscopic catheter devices, laparoscopic tools, and combinations of both endoscopic tools and laparoscopic tools. Examples of anastomoses include anastomoses between the stomach and a portion of the intestines such as the jejunum. Anastomoses can also be formed between two closed ends of the intestines, such as two closed ends of the colon formed during a colon resection procedure. Anastomoses can also be formed between a fundal pouch formed during a gastric bypass procedure and the jejunum. Laparoscopic tools are disclosed to deploy a stent by selectively removing a radial restraint on a self expanding stent with the restraint removed through the laparoscopic access points. | 2014-08-21 |
20140236065 | INTRAOCULAR SHUNT DEPLOYMENT DEVICE - An intraocular shunt deployment device can release an intraocular shunt into an eye using a deployment mechanism that coordinates action between a pusher component, a shaft component, and a housing of the device. The deployment mechanism causes axial movement of the components in response to a rotational input force. | 2014-08-21 |
20140236066 | ADJUSTABLE INTRAOCULAR FLOW REGULATION - Methods and devices for adjusting or configuring the flow rate of an intraocular shunt are provided whereby hypotony can be avoided by increasing the flow rate through the device. In some embodiments, the device is a shunt that can have a first flow that can be modified to a second flow by modifying the shunt, such as by cutting the shunt. Additionally, one or more dissolvable portions can be present to provide an initial flow restriction and subsequent increase in flow over time. | 2014-08-21 |
20140236067 | ADJUSTABLE GLAUCOMA IMPLANT - Methods and devices for adjusting or configuring the flow rate of an intraocular shunt are provided whereby hypotony can be avoided by increasing the flow rate through the device. In some embodiments, the device is a shunt that can have a first flow that can be modified to a second flow by modifying the shunt, such as by cutting the shunt. Additionally, one or more dissolvable portions can be present to provide an initial flow restriction and subsequent increase in flow over time. | 2014-08-21 |
20140236068 | GLAUCOMA SHUNTS WITH FLOW MANAGEMENT AND IMPROVED SURGICAL PERFORMANCE - A method of treating glaucoma in an eye by managing fluid flow past an implanted shunt having an elastomeric plate and a non-valved elastomeric drainage tube. The plate is positioned over a sclera of the eye with an outflow end of the elastomeric drainage tube open to an outer face of the plate. An inflow end of the drainage tube tunnels through the sclera and cornea to the anterior chamber of the eye. The plate may have regions of greater propensity for cell adhesion alternating with regions of lesser cell adhesion. For example, regions of texturing around the plate or drainage tube may be provided to control the size of a bleb that forms over the implant. The effective surface area of the plate may be balanced against a number of fenestrations. The drainage tube has a reduced profile and may be shaped with a non-circular external cross-section to reduce its height. A scleral groove may be used to further reduce the height of the drainage tube on the sclera. A flow restrictor for the early post operative period will immediately lower the intraocular pressure (IOP). | 2014-08-21 |
20140236069 | PHARMACOKINETICS OF IONTOPHORETIC SUMATRIPTAN ADMINISTRATION - Improved pharmacokinetic profiles for the iontophoretic delivery of sumatriptan are described. | 2014-08-21 |
20140236070 | LINEAR EXPRESSION CASSETTES AND USES THEREOF - Provided herein are linear nucleic expression cassettes and methods of using same in a non-invasive method of vaccination. The method combines electroporation and linear DNA constructs encoding antigens to elicit antigen-specific immune responses. | 2014-08-21 |
20140236071 | LIGHT-ENABLED DRUG DELIVERY - Conjugates are provided which comprise a membrane permeable drug linked to a moiety that is not membrane permeable. Attachment of the moiety that is not membrane permeable prevents the drug from crossing cell membranes and entering cells. However, exposure to light either i) breaks the linkage, releasing the drug and allowing it to enter cells; or ii) converts the non-membrane permeable moiety to a membrane permeable form, allowing the entire conjugate to enter the cell, where the drug is released from the conjugate by cleavage. The membrane permeable drugs are thus delivered to cells at locations of interest, e.g. cancer cells in a tumor, in a temporally and spatially controlled manner. | 2014-08-21 |
20140236072 | SYSTEMS AND METHODS FOR MAINTAINING BREAST OR UDDER HEALTH - Provided herein are systems and methods for maintaining breast or udder health. The systems include a first container comprising a top and a bottom, one or more cups attached to the top of the container and a first temperature-controlling element for providing vapor from the container to a breast or udder via the cup. | 2014-08-21 |
20140236073 | NITRIC OXIDE THERAPIES - A method for delivering nitric oxide therapy to a subject can include administering a composition including a nitric-oxide releasing agent and silica to the subject and releasing a therapeutic amount of nitric oxide from the composition. | 2014-08-21 |
20140236074 | PNEUMATIC DEVICE FOR TREATING INTUSSUSCEPTION - The pneumatic system for intussusception treatment, i.e., invagination of a segment of the intestine into an adjacent segment, includes a pressurized gas supply connected to a series of filters, valves, regulators, and sensors connected to a rectal insertion tube to introduce gas at moderate pressure into the intestine of the patient. A computerized control and monitoring subsystem is included. The system preferably includes a heating system to warm the gas as desired. The system also preferably includes an exhaust portion to relieve internal intestinal pressure as required or desired. The exhaust portion of the system preferably includes a filter to absorb undesirable fecal odors that accompany the exhausted gas. At least the rectal insertion tube and the odor filter may be separable from the remainder of the system for convenient disposal. An alarm may be provided to alert the doctor or medical professional of conditions other than normal. | 2014-08-21 |
20140236075 | HOLLOW NEEDLELIKE OBJECT AND METHOD FOR MANUFACTURING HOLLOW NEEDLELIKE OBJECT - According to one embodiment, a method for manufacturing a hollow needlelike object including a hollow part inside includes: a step of preparing a first needlelike-object base having a face comprising a groove forming at least a part of the hollow part; and a step of covering the face of the needlelike-object base with a covering member. | 2014-08-21 |
20140236076 | INJECTION DEVICES - An injection device operable to deliver a dose of medicament from a syringe or cartridge includes a temperature-sensitive arrangement for inhibiting operation thereof under predetermined temperature conditions. This may include a thermally responsive element that adopts a position in which operation of the device is inhibited when a temperature level is passed. | 2014-08-21 |
20140236077 | Body-Associated Receiver and Method - Receivers, which may be external or implantable, are provided. Aspects of receivers of the invention include the presence of one or more of: a high power-low power module; an intermediary module; a power supply module configured to activate and deactivate one or more power supplies to a high power processing block; a serial peripheral interface bus connecting master and slave blocks; and a multi-purpose connector. Receivers of the invention may be configured to receive a conductively transmitted signal. Also provided are systems that include the receivers, as well as methods of using the same. Additionally systems and methods are disclosed for using a receiver for coordinating with dosage delivery systems. | 2014-08-21 |
20140236078 | TRANSPLANTED CELL CONTAINMENT AND NUTRITION DEVICE - The present invention provides an implanted device that promotes the protection and maintenance of transplanted cells in a host body. The system would provide the transplanted cells with a safe, nutritious environment for survival and would also be suitable for removal of the waste products generated by the cells | 2014-08-21 |
20140236079 | METHOD AND APPARATUS FOR CONTROLING FLOW RATES AND PATTERNS OF HUMAN MILK SECRETION BY A BREAST PUMP - The invention relates to an apparatus and method to control the flow rates and pattern of human milk secretion while using a breast pump. The apparatus comprises a breast pump having a linear source of vacuum and a communication port for communicating with an external source of information on milk flow rates and patterns of a breastfeeding baby, through an external control circuit. | 2014-08-21 |
20140236080 | PARY-XYLENE BASED MICROFILM ELUTION DEVICES - This invention is in the field of controlled elution devices for therapeutic delivery. There exists a need for a stand-alone capable device for the localized and extended delivery of a therapeutic. This need is overcome by the present invention having an examplary embodiment comprised of a microfilm base ( | 2014-08-21 |
20140236081 | Fistula Catheter - A fistula catheter that can prevent separating from the fistula by an inner balloon even if an outer balloon collapses by configuring an internal fixed part with an inner side balloon and an outer side balloon is disclosed. The fistula catheter A has an external fixed part, a supply tube with a primary cavity and a secondary cavity, and an internal fixed part on the tip end side outer periphery of the supply tube, expandable by a compound liquid that includes barium sulfate and distilled water supplied though the secondary cavity. The internal fixed part can be an inner balloon and an outer balloon that communicate with the secondary cavity through filler ports on the peripheral surface of the supply tube. A filter on the filler port can enable distilled water in the compound liquid to be filled into the outer balloon from the secondary cavity through the filter, and the compound liquid can be filled into the inner balloon. | 2014-08-21 |
20140236082 | Biocompatible Carrier Containing A Bioadhesive Material - A biocompatible carrier for delivery of a therapeutic substance or an active agent is disclosed. The carrier contains a bioadhesive material allowing for increased residence time of the active agent at the treatment site. | 2014-08-21 |
20140236083 | MEDICAL TUBING - A medical tube has a tube wall, a first end and a second end. At least one heater wire is wrapped around the wall. Near or at one of the first end or the second end, there is at least one recess in an outer surface of the wall. The heater wire passes over the at least one tube recess such that the wire does not contact the wall in the area of the tube recess. Also disclosed are methods of making the tube and components used in making the tube. | 2014-08-21 |
20140236084 | Automatic Injection Device With Delay Mechanism Including Dual Functioning Biasing Member - An automatic injection apparatus including a delay mechanism for properly delivering medication prior to the needled syringe of the apparatus being retracted. In one form, the delay mechanism includes a shuttle for the syringe, a follower, a locking member, a damping compound between the follower and a supporting surface to dampen rotation of the follower relative to the shuttle, and a dual functioning biasing member acting between the shuttle and the follower. When the locking member moves to a release position during an injection, the dual functioning biasing member first provides a torsional force to force the follower to rotate relative to the shuttle from a latching position to an unlatching position, and then the dual functioning biasing member provides an axial force to force the shuttle axially relative to the follower to move the shuttle for retracting the syringe needle into the housing of the apparatus after injection. | 2014-08-21 |
20140236085 | DEVICE FOR A SYRINGE - The invention provides an accessory ( | 2014-08-21 |
20140236086 | Fluid Delivery Device Needle Retraction Mechanisms, Cartridges and Expandable Hydraulic Fluid Seals - A fluid delivery device includes an automatic needle retraction mechanism configured to automatically retract a delivery end of a needle into a housing. In one embodiment, the needle assembly is configured to automatically withdraw the delivery end of the needle into the housing upon an actuator moving from the first position to the second position. In one embodiment, the needle assembly is configured to automatically withdraw the delivery end of the needle into the housing upon decoupling a bottom surface of the housing from a skin surface. | 2014-08-21 |
20140236087 | INFUSION DEVICE HAVING GEAR ASSEMBLY INITIALIZATION - Apparatus are provided for infusion devices and related operating methods. An exemplary infusion device includes a housing to receive a shaft coupled to a plunger disposed in a reservoir and a gear assembly including a first gear to engage the shaft, wherein the first gear exhibits rotational freedom in a direction opposite a delivery direction. One exemplary method of operating the infusion device comprises identifying a reset condition and in response to the reset condition, operating a motor having a rotor coupled to the gear assembly to provide the rotational freedom for the first gear. | 2014-08-21 |
20140236088 | EXPANDABLE SHEATH AND SYSTEM FOR INTRAVASCULAR INSERTION OF A MEDICAL IMPLEMENT USING THE SAME - The expandable sheath and system for intravascular insertion of a medical implement includes a cannula for entering a lumen of a vascular vessel of a patient, a guide wire insertable into the lumen, an introducer and dilator adapted to follow the guide wire into the lumen, an expandable sheath positioned on the introducer and dilator, with the expandable sheath being adapted to be positioned in the vessel, and an extension collar. The medical implement is received within the vessel by passing through the sheath upon separating the introducer and dilator therefrom. In one embodiment, a linear array of perforations formed through the expandable sheath allow for expansion. Alternatively, an external slit may be provided for selective expansion of the sheath. | 2014-08-21 |
20140236089 | SYSTEM FOR TRANSPORTING FLUID ACROSS OR INTO A BIOLOGICAL BARRIER, DEVICE AND CAPSULE AS PART OF THE SYSTEM - The invention relates to a system ( | 2014-08-21 |
20140236090 | INTEGRATED MICRONEEDLE ARRAY DELIVERY SYSTEM - The present disclosure provides low-profile systems and methods for delivering a microneedle array. A delivery system includes a housing that may be secured to and temporarily worn on a patient's skin. A carrier assembly coupled to a microneedle array is received in the housing proximate a stored energy device. The stored energy device can be designed to store a predetermined amount of potential energy that is greater or substantially greater than the energy necessary to release said energy. As the stored energy device is potentially capable of releasing substantially more energy than is required to cause the release, the amount of normal force applied to the skin can be minimized while sufficient application velocity is still generated. | 2014-08-21 |
20140236091 | BODY PORTAL ANCHORS AND SYSTEMS - Anchors for securing a therapy device such as a therapy catheter relative to a burr hole, and systems and methods for using the same. Anchors in accordance with embodiments of the present disclosure may include a connector for securing the therapy catheter to a delivery catheter, wherein the connector is independently and removably attachable to the anchor. The connector may secure the therapy catheter relative to the burr hole and isolate forces that may otherwise tend to disrupt the placement of the therapy catheter. | 2014-08-21 |
20140236092 | Display Arrangement for a Drug Delivery Device - The present invention relates to a display arrangement for a drug delivery device, comprising: a first display member comprising numerous surface portions having at least two different but interrelated appearances and being alternately arranged along a first direction, and a second display member comprising a light modulating structure to modulate visible light emanating from the first display member, wherein first and second display members are movably disposed relative to each other along the first direction to simultaneously reveal and/or to conceal at least two surface portions of interrelated appearance. | 2014-08-21 |
20140236093 | HANDHELD MEDICAMENT INJECTION DEVICE WITH ILLUMINATED DOSE BUTTON - A cartridge holder is presented having a first cartridge retainer, at least a second cartridge retainer and a locking device for each cartridge retainer, wherein each cartridge retainer is configured to receive a medicament reservoir and wherein each cartridge retainer is movable between a closed and an open position, wherein the locking devices are configured to lock and unlock the cartridge retainers in the closed position and wherein the locking devices are configured to operate such that only one of the cartridge retainers at a time is movable into the open position. An apparatus is also presented that has a main body and a cartridge holder, wherein the cartridge holder is removably attached to the main body. A method for inserting of a medicament reservoir in a cartridge holder or in an apparatus is also described. | 2014-08-21 |
20140236094 | Medicament Delivery Device and Actuation Mechanism for a Drug Delivery Device - Described is an actuation mechanism for a medicament delivery device having a needle with a distal tip. The actuation mechanism comprises an outer sleeve telescopically relative to the delivery device and an inner sleeve telescopically arranged relative to the outer sleeve. The outer sleeve is axially translatable relative to the delivery device, and the inner sleeve is axially translatable relative to the outer sleeve. In a first state, the inner sleeve protrudes distally from the outer sleeve and the outer sleeve protrudes distally from the delivery device. In a second state, the inner sleeve is contained within the outer sleeve. Movement of the outer sleeve proximally relative to the delivery device in the second state initiates delivery of a medicament in the delivery device. | 2014-08-21 |
20140236095 | Needle Safety Device - Described is a needle safety device comprising a needle hub, a needle coupled to the needle hub and having a distal tip; a needle shield telescopically coupled to the needle hub, the needle shield, a locking element including latch arms adapted to engage the needle hub and engagement elements adapted to engage the needle shield. When the needle shield is in a first axial position (PA | 2014-08-21 |
20140236096 | Drug Delivery Device and Method for a Drug Delivery Device - A drug delivery device is provided comprising a housing comprising a distal end and a proximal end and a cartridge adapted and arranged to contain at least one dose of a drug, a bung being movably arranged within the cartridge. In an initial state of the device, the bung is arranged in a proximal end position with respect to the cartridge. The device further comprises a piston rod adapted and arranged to move the bung in the distal direction with respect to the cartridge for delivering a dose of the drug. The device further comprises a mechanism operable such that, after a dose delivery operation was completed, the piston rod is moved into the proximal direction with respect to the bung by a back off distance (D), wherein in the initial state, a distance between a distal end of the piston rod and a proximal end of the bung is greater than zero, with the distance between the piston rod and the bung in the initial state being defined by the back off distance (D). Furthermore, a method for assembling a drug delivery device is provided. | 2014-08-21 |
20140236097 | Assembly for a Drug Delivery Device - An injection device for injection of set doses of medicine from a cartridge, in which one or more friction wheels engage linear bearing surfaces during dose setting and dose delivery. | 2014-08-21 |
20140236098 | Intraocular Injection Device - Described is a medicament delivery device comprising a needle and a layer of a composition coupled to at least a portion of the needle. The composition has a low viscosity and a low surface tension. | 2014-08-21 |
20140236099 | INDWELLING CATHETER - An indwelling catheter including: a hollow catheter base having a tip and a back end, the back end being able to receive and connect a male connector; a tube provided at the tip of the catheter base; a flexible hemostasis valve installed inside the catheter base; a pusher installed at a back of the hemostasis valve; and a pusher guide installed between the pusher and the catheter base, The pusher has a hollow constitution whose taper reduces in diameter facing its tip. The pusher guide is able to restrict a position of the pusher at a first position where the pusher does not push open the hemostasis valve and a second position where the taper of the pusher is positioned inside the hemostasis valve and pushes open the hemostasis valve. | 2014-08-21 |
20140236100 | Needle Safety Device - Described is a needle safety device comprising a needle hub having a radial protrusion, a needle coupled to the needle hub and having a distal tip, and an inner sleeve telescopically coupled to the needle hub. The inner sleeve includes a first track adapted to engage the radial protrusion. The first track includes an axial section and a radial section. When the inner sleeve is in a first advanced position (PA | 2014-08-21 |
20140236101 | Medical tubings made of a polymer material - Medical tubing (T), such as a guidewire, a stent, a catheter or a hollow needle, made of a kinked rigid-rod polyarylene exhibiting a outstanding characteristics including high torqueability, high pushability and high flexibility and which can be easily thin-wall extruded under especially harsh conditions. | 2014-08-21 |
20140236102 | METHOD FOR MANUFACTURING NEEDLE-EQUIPPED OUTER TUBE, AND NEEDLE-EQUIPPED OUTER TUBE - A method for manufacturing a needle-equipped outer tube includes providing a needle; providing a joint member having a needle insertion hole into which the needle is insertable; providing an outer tube comprising a connection section at a first axial end portion of the outer tube; pressing the joint member, with the needle located in the needle insertion hole, toward the connection section, such that the joint member engages with the connection section of the outer tube; and thermally welding the needle and the joint member, as well as the joint member and the connection section, such that the needle is joined to the joint member, and the joint member is joined to the connection section of the outer tube. | 2014-08-21 |
20140236103 | PERI-VASCULAR TISSUE ABLATION CATHETER WITH SUPPORT STRUCTURES - An intravascular catheter for peri-vascular and/or peri-urethral tissue ablation includes multiple needles advanced through supported guide tubes which expand around a central axis to engage the interior surface of the wall of the renal artery or other vessel of a human body allowing the injection an ablative fluid for ablating tissue, and/or nerve fibers in the outer layer or deep to the outer layer of the vessel, or in prostatic tissue. The system may also include a means to limit and/or adjust the depth of penetration of the ablative fluid into and beyond the tissue of the vessel wall. The catheter may also include structures which provide radial and/or lateral support to the guide tubes so that the guide tubes expand uniformly and maintain their position against the interior surface of the vessel wall as the sharpened injection needles are advanced to penetrate into the vessel wall. | 2014-08-21 |
20140236104 | PUNCH-REDUCING CANNULA - The present invention relates to a new bevel or grinding for a punch-reducing cannula, i.e. a cannula which reduces punching particles, and, in particular, to a punch-reducing cannula having a beveled or ground end as well as to a method for manufacturing a cannula which reduces punching particles. | 2014-08-21 |
20140236105 | Dual Reservoir Implantable Access Port - An implantable access port for use in transferring fluid transdermally between an external fluid storage or dispensing device and a site within a patient is disclosed. The access port includes a body, at least two reservoirs defined within the access port body, and at least one septum secured to the body and enclosing the reservoirs within the body. The access port also includes reservoir outlets defined within the reservoirs. The access port also has body conduits defined within the body and in fluid communication with the reservoir outlets and external openings defined in the exterior of the body. An implantable access port and system for use in apheresis is also provided that includes an implantable access port, at least one needle, and a catheter that is fluidly connected to the access port. | 2014-08-21 |
20140236106 | SYSTEM AND METHOD FOR DETERMINING A FILL STATUS OF A CANISTER OF FLUID IN A REDUCED PRESSURE TREATMENT SYSTEM - A reduced pressure treatment system is provided that includes a canister that is fluidly connected to a tissue site and is configured to receive fluid drawn from the tissue site under the influence of a reduced pressure. A reduced pressure source provides the reduced pressure and is fluidly connected to the tissue site by a fluid communication path, which may include a source conduit, the canister, and a target conduit. A sensing device communicates with the source conduit and is configured to sense a pressure in the source conduit. A valve communicates with the source conduit and is configured to vent the reduced pressure. A processing unit communicates with the sensing device and the valve and is configured to open the valve for a selected amount of time, determine a decay of reduced pressure, and determine a fill status of the canister based on the decay of reduced pressure. | 2014-08-21 |
20140236107 | ABSORBENT HYGIENIC OR PERSONAL CARE PRODUCT HAVING A STRIP-LIKE COMPONENT WITH A CONTENT OF AT LEAST ONE HEAVY METAL PRESENT IN ELEMENTAL OR IONIC FORM - The present invention relates to an absorbent hygienic or personal care product having an absorption body with a content of super-absorbent polymer based on acrylates, wherein said hygienic or personal care product further comprises a strip-like component having a content of at least one heavy metal present in elemental or ionic form. | 2014-08-21 |
20140236108 | MULTI-LUMEN CONNECTOR - Apparatus is disclosed for applying negative pressure to a wound site to promote healing. The apparatus includes a porous pad for application to the wound, a suction tube linking the porous pad to a source of negative pressure, a container for collecting fluid exudate from the wound interposed between the porous pad and the source of negative pressure and a quick disconnect connector linking a first section of the suction tube leading to the porous pad with a second section leading to the container, said connector comprising two separable and non-interchangeable parts, said first section of the suction tube comprising a multi-lumen tube, one lumen being provided for applying suction to the porous pad and another being provided for monitoring pressure, said multi-lumen tube being fixedly attached at one end to the container and at the other end to one of said separable parts, said one separable part including sealing means whereby the lumens are connected in air-tight manner to said second section of the suction tube. | 2014-08-21 |
20140236109 | VACUUM ASSISTED WOUND DRESSING - Apparatus for the application of topical negative pressure therapy to a wound site is described, the apparatus comprising: a wound contacting element for retaining wound exudate fluid therein; a wound covering element that provides a substantially airtight seal over the wound contacting element and wound site; a vacuum connection tube connecting a wound cavity to a vacuum source; and a vacuum source connected to a distal end of the vacuum connection tube. | 2014-08-21 |
20140236110 | TISSUE SPECIMEN RETRIEVAL BAG, METHOD FOR RETRIEVING TISSUE - Provided is a tissue retrieval bag. The bag is made primarily of a first material, the bag having a region defining an opening; a pleated fold intersecting the opening. The bag has at least one porthole on at least one side of the bag. The at least one porthole is covered by a second material, the second material being different from the first material. The bag also includes a first hem circumferentially formed around the opening, the first hem forming insertion points adapted to receive a first draw string. | 2014-08-21 |
20140236111 | METHODS AND SYSTEMS FOR OSTOMY CARE - Disclosed are computer-based systems and media for providing an interactive ostomy treatment guide, and methods of using the same, the guide comprising: a software module configured to receive ostomy assessment information, the assessment information comprising one or more of: condition of skin adjacent an ostomy, topographical location of any peristomal lesion, stoma type, pouching surface type, stoma devices present, and stoma complications; a software module configured to apply a treatment algorithm to the ostomy assessment information to generate an output; and a software module configured to display one or more ostomy management options based on the output. | 2014-08-21 |
20140236112 | WOUND DRESSING - The present application is concerned with an improved wound dressing for use in the treatment of skin wounds with some level of exudation, especially for use in those wounds which are infected or under risk of being infected by microorganisms. | 2014-08-21 |
20140236113 | Absorbent Article - A disposable absorbent article worn about the lower torso of a wearer includes at least one serviceable indicium that facilitates the process of fitting the absorbent article to the wearer by providing an apparent visual and physical indication when the article is not properly fitted. The apparent visual and physical indication includes a detectable distortion of the waist opening, the leg openings or both the waist opening and the leg openings. The detectable distortion includes at least one serviceable indicium disposed on a portion of the waist opening or leg opening or both that becomes flipped in towards an inner surface of the article or flipped out towards the outer surface of the article when the article is not properly fitted. | 2014-08-21 |
20140236114 | Disposable Absorbent Article Having Serviceable Indicia Indicating Improper Fit - A disposable absorbent article worn about the lower torso of a wearer includes at least one serviceable indicium that facilitates the process of fitting the absorbent article to the wearer by providing an apparent visual and physical indication when the article is not properly fitted. The apparent visual and physical indication includes a detectable distortion of the waist opening, the leg openings or both the waist opening and the leg openings. The detectable distortion includes at least one serviceable indicium disposed on a portion of the waist opening or leg opening or both that becomes flipped in towards an inner surface of the article or flipped out towards the outer surface of the article when the article is not properly fitted. | 2014-08-21 |
20140236115 | FASTENING SYSTEMS FOR USE WITH ABSORBENT ARTICLES - A fastener for a disposable absorbent article, having a fixed portion attachable to the article, a connective portion joined to and contiguous with the fixed portion, and a folding line disposed between the fixed and connective portions. The fastener may be free of a release tape. The fastener may further comprise an adhesive disposed upon a surface of the fixed portion of the fastener being attached to the article, the adhesive being offset from each of the edges of the fixed portion including the edge formed by the folding line, the dimensions of the offsets being defined herein. The adhesive may be applied during the assembly of the absorbent article on a converting line. | 2014-08-21 |
20140236116 | FASTENING SYSTEMS FOR USE WITH ABSORBENT ARTICLES - A fastener for a disposable absorbent article, having a fixed portion attachable to the article, a connective portion joined to and contiguous with the fixed portion, and a folding line disposed between the fixed and connective portions, and the fastening member has a plurality of engaging elements outwardly extending from the fastening surface, which are offset from the folding line as defined herein. The fastener may be free of a release tape. The fastener may further comprise an adhesive disposed upon a surface of the fixed portion of the fastener being attached to the article, the adhesive being offset from each of the edges of the fixed portion including the edge formed by the folding line, the dimensions of the offsets being defined herein. The adhesive may be applied during the assembly of the absorbent article on a converting line. | 2014-08-21 |
20140236117 | Disposable Patient Interface - The present invention is directed to a patient interface for use with an injector assembly, the patient interface having a removable cap, wherein removal of the cap after an injection disables the patient interface to prevent re-use. | 2014-08-21 |
20140236118 | DEEP VEIN THROMBOSIS THERAPEUTIC METHODS - The invention provides methods for diagnosing and treating deep vein thrombosis and other conditions associated with occluded or constricted vessels. According to certain aspects, methods of the invention involve inserting a sensing device into a vessel having a thrombus therein, assessing, with the sensing device, one or more functional parameters within the vessel, determining an interventional therapy for treating the thrombus based on the assessing step; and performing the interventional therapy. | 2014-08-21 |
20140236119 | Method for Processing Infusion Data and an Infusion Pump System - A distributed infusion pump system is provided with long-term recording of the type of medication, nutrition or hydration, pump output pressure, corresponding infusion flow, infusion flow resistance, and an automatic or manual alarm in the event that thresholds applied to these parameters or their derivatives are exceeded. | 2014-08-21 |
20140236120 | ADJUSTABLE STIFFNESS CATHETER - The present invention relates to a catheter that has adjustable stiffness that enables a user to select the stiffness of at least one region of the catheter during insertion and navigation through a body lumen. A preferred embodiment of the invention works in combination with a guidewire to enable placement of the catheter at a position within the vascular system, for example, to enable treatment of a variety of medical conditions. The catheter can include segments that undergo relative movement in response to actuation by the user to adjust the flexibility of the at least one region, preferably located at or near the distal end of the catheter. | 2014-08-21 |
20140236121 | SYRINGE - A syringe ( | 2014-08-21 |
20140236122 | Elastic Introducer Sheath - An elastic percutaneous elastic introducer sheath is disclosed which can locally expand and reduce to accommodate a transcatheter medical device. The elastic introducer sheath includes a non-circumferentially continuous elastic frame, a liner, and a jacket. | 2014-08-21 |
20140236123 | Elastic Introducer Sheath - An elastic percutaneous elastic introducer sheath is disclosed which can locally expand and reduce to accommodate a transcatheter medical device. The elastic introducer sheath includes a non-circumferentially continuous elastic frame, a liner, and a jacket. | 2014-08-21 |
20140236124 | CATHETER - A catheter has an intermediate layer with a constant thickness in first and second adjacent portion, and the adhesive strength between the intermediate layer and an inner layer is uniform. When the catheter is curved, the movement of a braid caused by the curving of the catheter can be uniformly suppressed within the adjacent first and second portions. Even if, when the catheter is curved, a tensile stress towards a proximal end acts upon a first outer layer at the first portion and a tensile stress towards a distal end acts upon a second outer layer at the adjacent second portion, the first and second outer layers are caught by an uneven contour of the intermediate layer by an anchor effect, so that it is possible to prevent peeling of the first and second outer layers from the intermediate layer. | 2014-08-21 |