| TERUMO KABUSHIKI KAISHA Patent applications |
| Patent application number | Title | Published |
|---|
| 20130123740 | CLAMP AND BLOOD BAG SYSTEM - A clamp for a blood bag system includes a protrusion section which presses a tube, a locking section having a first engagement section and a second engagement section that form therebetween an engagement groove in which the protrusion section is positioned and by which engagement can be made, a first engagement release section which releases an engaged state between the first engagement section and the protrusion section; and a second engagement release section which releases an engaged state between the second engagement section and the protrusion section. | 05-16-2013 |
| 20130121821 | CENTRIFUGAL PUMP APPARATUS - This centrifugal blood pump apparatus includes an impeller provided in a blood chamber, a first permanent magnet provided in one surface of the impeller, and a second permanent magnet provided in an inner wall of the blood chamber, for attracting the first permanent magnet. The attractive force between the first permanent magnet and the second permanent magnet on the opening side of a sidewall of the blood chamber is set to be smaller than the attractive force between the first permanent magnet and the second permanent magnet on the opposite side of the opening. As a result, inclination of the impeller with respect to a dividing wall during pump operation can be prevented. | 05-16-2013 |
| 20130116725 | METHOD TO STOP BLEEDING AT A PUNCTURE SITE OF AN ARTERY OF A PATIENT'S WRIST - A method to stop bleeding at a puncture site of an artery on a wrist of a patient comprises wrapping a flexible band of a hemostatic device around the wrist of the patient, wherein the hemostatic device also includes a curved plate, a balloon and a marker used to position the balloon at the puncture site, and wherein the flexible band, the curved plate and the balloon are substantially transparent. The wrapping of the flexible band around the wrist of the patient involves wrapping the flexible band around the wrist of the patient while the balloon is in an uninflated state. The wrapping can also take place while an introducer sheath is in place at the puncture site. The method also involves using the marker to position balloon relative to the puncture site such that the balloon overlies the puncture site, introducing a fluid into the balloon and inflating the balloon, and maintaining inflation of the balloon and compression against the puncture site. | 05-09-2013 |
| 20130116721 | Medical Device - A medical device configured to provide a space, allowing a medical instrument to move, in an area of the brain in which the medical instrument is otherwise difficult to move. The medical device includes a catheter provided with an expandable member, wherein the expandable member is expanded to provide a space in which at least a part of a second medical instrument is insertable and movable. | 05-09-2013 |
| 20130116684 | PFO CLOSING DEVICE - A PFO closing device for bringing the septum primum and the septum secundum into contact with each other and joining them together includes a clamping mechanism and energy supplying device. The clamping mechanism includes a needle part for puncturing the septum primum, and a clamping member for cooperating with the needle part in clamping therebetween tissue of the septum primum and the septum secundum. The energy supplying device supplies energy for joining the tissues clamped by the needle part and the clamping member. The clamping mechanism is mounted in a catheter so as to be protrudable from and retractable into the catheter. | 05-09-2013 |
| 20130116651 | CATHETER AND METHOD - The presently disclosed subject matter relates to a catheter and method. The catheter can be configured as a guiding catheter with a flexible shaft section, a hub disposed at a proximal portion of the shaft section, and a strain relief section that surrounds a predetermined proximal-side range of the shaft section. A distal end of the strain relief section can be moved along an axial direction of the shaft section at least toward the side where the hub is located. | 05-09-2013 |
| 20130116622 | MEDICAL DEVICE - A medical device includes a catheter having an opening formed in a side portion of the catheter, an infusion tubing extending within the catheter along an axial direction of the catheter; an infusion needle disposed at a distal portion of the infusion tubing, a connecting part which bendably connects the infusion needle to the distal portion of the infusion tubing, and a bending unit by which the infusion needle located inside the catheter so as to face the opening is bent at the connecting part at essentially a right angle with respect to the distal portion of the infusion tubing. | 05-09-2013 |
| 20130096502 | INJECTION NEEDLE ASSEMBLY AND DRUG INJECTION DEVICE - Objects are to ensure a required depressing force and puncture speed when a needle tube is punctured in the skin, and to be able to reliably situate a needle tip of a needle tube in the upper layer of skin. A needle injection assembly | 04-18-2013 |
| 20130095226 | METHOD FOR PRODUCING MEDICAL DEVICE - A method for firmly fixing a hydrophilic polymer on a polyamide surface involves applying a solution containing a phenolic compound to a base material of which at least a part of the surface is a polyamide, and coating the base material with a hydrophilic polymer after applying the solution. | 04-18-2013 |
| 20130091686 | GUIDE WIRE - A guide wire includes a first wire disposed on the distal side of the guide wire and a second wire disposed on the proximal side. The second wire has an elastic modulus larger than the first wire. The first wire is joined to the second wire at a welded portion by welding. A coil is disposed on the distal side of the first wire. A cover layer is formed on the outer peripheral surface of the wire member in such a manner as to cover at least the welded portion. The cover layer is made from a material capable of reducing the friction of the cover layer, for example, a fluorocarbon resin or a hydrophilic material, to thereby improve the sliding performance of the guide wire. Such a guide wire is excellent in operationality and kink resistance. | 04-18-2013 |
| 20130090589 | TRANSFUSION TUBE AND TRANSFUSION TUBE SET - A transfusion tube set includes: a transfusion tube; and a transfusion tube which does not have a filter and a transfusion tube which has the filter, wherein the transfusion tubes and are detachable from the transfusion tube. The transfusion tube includes a tube and a reservoir needle provided at a upstream end of the tube, and a drip tube, a roller clamp, an upstream connector and a downstream connector are provided downstream of the reservoir needle of the tube. A filter mesh is disposed at the upstream end of a main tube of the downstream connector. | 04-11-2013 |
| 20130085519 | BALLOON FOR CATHETER AND BALLOON CATHETER - A balloon for catheter of the type that has a film body that is inflatable and deflatable by means of a fluid supplied from a catheter, the film body including a hard layer containing a polyamide and a flexible layer formed on the hard layer and containing a polyamide elastomer having a Shore D hardness that is not larger than 62, and the content of the amide units of the polyamide elastomer in the flexible layer is not less than 60 wt % | 04-04-2013 |
| 20130079729 | Injection Needle Assembly And Drug Injection Device - A needle does not come off even if a high back pressure occurs at the skin upper section. Thus, the drug leakage from the skin can be prevented. A drug administration device | 03-28-2013 |
| 20130079631 | MOTOR DRIVE APPARATUS AND IMAGING APPARATUS FOR DIAGNOSIS - A motor drive apparatus including a scanner unit, a scanner moving unit, and a detection unit for detecting that the scanner unit has reached a position apart by a predetermined distance from the forward end position of the scanner unit in case of axially operating or moving the scanner unit toward the forward direction, wherein in case of operating the scanner unit axially toward the forward direction, the scanner moving unit carries out speed control based on a first speed set value until the detection by the detection unit achieves a detection, and after the detection by the detection unit, the scanner moving unit carries out the speed control based on a second speed set value smaller than the first speed set value. | 03-28-2013 |
| 20130079630 | IMAGING APPARATUS FOR DIAGNOSIS - An imaging apparatus for diagnosis includes a display unit for displaying a plurality of generated cross-sectional images sequentially in chronological order, first and second operation members which are arranged on an operation panel and which are for appending a bookmark to the cross-sectional image, and a control unit for appending a bookmark to a cross-sectional image during display in response to a user operation toward at least one of the first and second operation members during the display of the cross-sectional image by the display unit, wherein the first operation member is provided on the right side seen from the center portion in the right and left direction with respect to a user in a case in which the user directly-faces the operation panel, and the second operation member is provided on the left side seen from the center portion of the operation panel. | 03-28-2013 |
| 20130078144 | LIQUID COLLECTION CONTAINER AND EXTRACORPOREAL CIRCUIT - A liquid collection bag is used as a part of an extracorporeal circuit and is connected via a tube to a storage container containing a priming solution. The collection container collects the priming solution from the storage container by a pressure differential between the pressure inside the collection container and the pressure inside the storage container. The liquid collection container is a flexible bag body having a partition part dividing the inside of the bag body into a first space and a second space. In addition, a communication part communicates the first space with the second space. | 03-28-2013 |
| 20130076019 | CONNECTOR AND CONNECTOR ASSEMBLY - A first connector has a first connector main body configured from an outer tube having a cylindrical shape, an inner tube having a cylindrical shape and a hub, a hollow needle supported on the hub, a first sealing member supported on the inner tube, a coil spring serving as puncturing portion biasing means for biasing the first sealing member in a direction toward the distal end thereof, and a clamping member disposed on the outer tube. The hub is disposed at a proximal end portion of the outer tube. The hub is disposed such that, although the hub is initially connected to the outer tube by a breakable welded portion, when the welded portion is broken, the hub is permitted to rotate around an axis of the outer tube with respect to the outer tube. | 03-28-2013 |
| 20130072893 | CONNECTOR AND CONNECTOR ASSEMBLY - A first connector includes a first connector main body configured from an outer tube of cylindrical shape, an inner tube of cylindrical shape, a hub disposed at a proximal end portion of the outer tube, and a clip disposed so as to be removable at the proximal end portion of the outer tube, a hollow needle supported on the hub, a first sealing member supported on the inner tube, a coil spring serving as puncturing portion biasing means for biasing the first sealing member toward the distal direction, and a clamping member disposed upon the outer tube. In a state in which the clip is mounted to the proximal end portion of the outer tube, a protrusion of the clip engages with a protrusion of the hub, and thereby rotation of the hub is prevented. If the clip is removed, the hub becomes rotatable with respect to the outer tube. | 03-21-2013 |
| 20130056387 | MEDICAL TRAY - To provide a medical tray which can be made more compact upon discarding, the medical tray has a bottom portion, a side wall provided along an outer periphery of the bottom portion, and a pair of side wall deformation guiding portions provided at opposing positions of the side wall for guiding the side wall when the side wall is deformed into a convex state toward the bottom portion. | 03-07-2013 |
| 20130046241 | INTRODUCER ASSEMBLY - An introducer assembly is composed of an introducer sheath and a dilator which have been previously integrated with each other to permit the hemostatic valve to exhibit its hemostatic function over an extended period of time without significantly adversely affecting the inherent function of the dilator tube. The introducer assembly includes a dilator tube passing through a passage of a hemostatic valve. The introducer assembly has a deforming member arranged between the hemostatic valve and a cap. As the cap is pushed toward the proximal end surface of a sheath hub for engagement with the sheath hub, the cap presses the hemostatic valve and applies a compressive force to the hemostatic valve in such a direction as to close the passage. | 02-21-2013 |
| 20130046129 | Non-Invasive Diagnostics for Ventrical Assist Device - A circulatory assist system has a pump with a motor coupled to rotate the pump at a selectable speed. A controller drives the motor at a target speed and collects blood flow measurements during operation of the pump. An impaired flow condition is identified when a plurality of successive blood flow measurements are between an expected minimum flow and a low flow threshold, such that the low flow would necessitate issuing an alert. During the impaired flow condition, it is detected whether an inflow obstruction exists by determining whether a reduction in speed of the pump is correlated with a predetermined increase in the blood flow measurements. If the inflow obstruction is detected, then the speed of the pump is further reduced to further increase the blood flow measurements. | 02-21-2013 |
| 20130037727 | FLUORESCENCE SENSOR - A fluorescence sensor includes a silicon substrate on which a PD element that converts fluorescence into an electric signal is formed, an LED substrate having a first principal plane on which an LED element that generates excitation light is formed, a reflective film that averages a light amount distribution of the excitation light radiated from a second principal plane of the LED substrate, and an indicator layer that receives the excitation light averaged by the reflective film and generates the fluorescence having a light amount corresponding to an analyte amount. | 02-14-2013 |
| 20130030380 | MEDICAL APPLIANCE HAVING A SLIDABLE COATING LAYER AND SYRINGE - A medical appliance having a slidable coating layer that moves in contact with an inner surface of a medical member or that of a lumen and has the slidable coating layer formed at a part thereof which contacts the medical member or the lumen. The slidable coating layer is formed of a composition which does not contain solid fine particles and contains a silicone-based resin which is a product of an addition reaction between silicone having a vinyl group and silicone having a hydrogen group bonded to a silicon atom. | 01-31-2013 |
| 20130023982 | STENT - A stent is configured to facilitate directional proliferation of cells on the inner surface of the stent to relatively quickly coat the stent surface with the cells so that the onset of late stent thrombosis or restenosis can be reduced or prevented. The stent includes a cylindrical stent main body having openings at both ends and extending along the longitudinal direction between the openings at both ends. A coating layer is provided on the inner surface of the stent main body and contains a substance having a cell adhesion ability to promote the adhesion of cells. The coating layer is formed by arranging multiple linear coating parts, each extending linearly in a striped manner. | 01-24-2013 |
| 20130023977 | STENT DELIVERY SYSTEM AND MANUFACTURING METHOD FOR THE SAME - A stent delivery system, and associated manufacturing method, are such that the outer diameter of the distal portion of the stent delivery system is relatively small. The stent delivery system includes a hollow shaft portion, an inflatable balloon disposed on the outer periphery of a distal portion of the shaft portion, and a stent disposed on the outer periphery of the balloon and having struts expanded by inflation of the balloon. The balloon has a ridge portion with which the stent is engaged. The ridge portion is sandwiched in a space between the struts, and a top portion of the ridge portion has a concave portion recessed toward the axis of the shaft portion | 01-24-2013 |
| 20130023860 | MEDICAL MANIPULATOR SYSTEM - A medical manipulator system includes an operation unit that has motors, a composite input unit and a tip operating unit that is operated by a driving force of the motors, a working unit that may by attached to and detached from the operating unit, and a console. The motors are driven based on an input operation to the composite input unit. The tip operating unit performs at least a rotation operation along an axial direction or a swing operation that crosses the axial direction. The console changes a driving speed of the motors and includes a speed setting unit that changes an operating speed of the rotation operation or the swing operation of the tip operating unit. | 01-24-2013 |
| 20130018405 | PUNCTURE NEEDLE AND PUNCTURE DEVICEAANM Onishi; SyuuichiAACI ShizuokaAACO JPAAGP Onishi; Syuuichi Shizuoka JPAANM Jokaji; MitsuruAACI YamanashiAACO JPAAGP Jokaji; Mitsuru Yamanashi JP - A puncture needle is constituted of a resin material. The puncture needle comprises: an elongated main body having a sharp needlepoint at a distal end thereof; and at least three cutting parts provided so as to project from the elongated main body to a direction perpendicular to a central axis of the elongated main body, extending along the central axis, and arranged around the central axis. Adjacent cutting parts in the three cutting parts are arranged so as to shift to each other in a direction of the central axis, so that the adjacent cutting parts make an incision on a biological surface in a time difference. Further, a height of a distal portion of each cutting part from the central axis is gradually decreased toward a distal direction. | 01-17-2013 |
| 20130018280 | GUIDE WIRE - A guide wire includes a core wire which forms a line shape formed from a flexible metal material. A distal portion of the core wire is arranged in an axial line direction of the core wire and includes a plurality of deformable portions, which are easily-deformable in a specific direction on a plane (x-y plane) with the axial line of the core wire being a normal line, and easily-deformable directions of the adjacent easily-deformable portions among the respective easily-deformable portions are different from each other. | 01-17-2013 |
| 20130012967 | REPAIRING MATERIAL FOR LUMENS OF LIVING BODY - A stent graft is an example of a repairing material for lumens such as aorta and other blood vessels and trachea of a living body. The stent graft includes warp yarns of plastic material and weft yarns including filaments of at least one of shape-memory plastic, shape-memory alloy, and super-elastic metal, the warp yarns and weft yarns being interwoven into a tubular shape such that the weft yarns extend in the circumferential direction and the warp yarns extend in the axial direction. Either or both of the warp yarns and weft yarns are formed from yarns capable of swelling by body fluid or from yarns with a coating capable of swelling by body fluid. | 01-10-2013 |
| 20130012959 | MEDICAL MANIPULATOR - A medical manipulator includes a trigger lever operated by hands, a shaft that extends from a body in which the trigger lever is provided, and a tip operating unit that is provided at a tip of the shaft. The tip operating unit includes an end effector to which the operation of the trigger lever is mechanically transmitted and in which the operation is performed, and a detection mechanism that detects an operation state of the first input unit. | 01-10-2013 |
| 20130012888 | Prefilled Syringe - A gasket of a prefilled syringe is disclosed, which includes a gasket body and a plunger-mounting member. The gasket body has a plunger-mounting member removal prevention rib formed on an inner surface of the gasket body. The plunger-mounting member has an outer projected part, which engages the plunger-mounting member removal prevention rib of the gasket body, a plurality of elastically deformable inner projected parts which are extended obliquely from an inner portion of a proximal side of the plunger-mounting member toward a central and distal end of the plunger-mounting member, and plunger removal prevention locking parts formed at free ends of the inner projected parts. The plunger has a distal end part capable of entering the plunger-mounting member and an outer projection part which engages the plunger removal prevention locking parts of the plunger-mounting member. | 01-10-2013 |
| 20130012834 | GUIDE WIRE - The guide wire is a guide wire includes a distal portion and a main body portion. This guide wire is provided with a first curve portion; a second curve portion included on the distal side of aforesaid first curve portion and curved to the opposite direction with respect to aforesaid first curve portion; a third curve portion included on the distal side of aforesaid second curve portion and curved to the opposite direction with respect to aforesaid second curve portion, wherein a line contacting with both aforesaid first curve portion and aforesaid third curve portion has an obtuse angle with respect to an axis line of aforesaid main body portion. | 01-10-2013 |
| 20130012810 | PROBE AND OPTICAL IMAGING APPARATUS FOR DIAGNOSIS - A probe including a catheter sheath, a shaft inserted inside the catheter sheath, and an attachment portion detachably attached to a rotational drive unit, wherein the attachment portion includes an isolation member isolating the inside of the attachment portion into a first area in which a member for transmitting the drive force generated by the rotational drive unit to the shaft is rotatably held and a second area in which the catheter sheath is fixedly held; the isolation member includes: an insertion hole through which the shaft is inserted between the first area and the second area and an ejection hole provided in a surface to which an end portion on the rotational drive unit side of the catheter sheath is connected and which is approximately perpendicular to the rotation axis of the shaft; and the ejection hole defines a flow path extending to the outside of the isolation member. | 01-10-2013 |
| 20130008438 | OXYGEN CONCENTRATOR - To provide an oxygen concentrator that can ensure safety by interrupting oxygen in a case where the oxygen concentrator is exposed to fire or an abnormal high-temperature environment when a user thereof is inhaling oxygen with a cannula. The oxygen concentrator includes: a compressor separating compressed air by compressing raw air; an oxygen outlet for discharging oxygen acquired from the compressed air; a coupler mounted on a tube of a cannula and removably connecting the tube to the oxygen outlet, and moreover having a temperature sensor; and a control unit stopping operation of the compressor to interrupt the supply of oxygen when a temperature sensed by the temperature sensor reaches a predetermined temperature or higher. | 01-10-2013 |
| 20120330401 | STENT DELIVERY SYSTEM - A stent delivery system includes a body and an operation unit disposed at the proximal end of the body. The body includes a self-expanding stent, an inner tube body, and a stent-accommodating tube body in which the stent is accommodated. The inner tube body has a stent-holding part enabling the stent to be re-accommodated into the stent-accommodating tube body. The operation unit includes a rack member fixed to a proximal end of the stent-accommodating tube body, an operation rotary roller having a working gear wheel that engages the teeth of the rack member, thereby causing the rack member to move forward and backward; and a connector fixed to a proximal end portion of a proximal-side tube that penetrates the stent-accommodating tube body and protrudes from the proximal end of the stent-accommodating tube body. | 12-27-2012 |
| 20120330320 | BONE CEMENT INJECTION PUNCTURE NEEDLE - An outer needle of a bone cement injection puncture needle has first side holes near the tip, and second side holes near the base. When an inner needle is removed from the outer needle and an inner tube is inserted into the outer needle in place thereof, a reduced-pressure passage is formed between the outer needle and the inner tube. When bone cement is injected into a bone, gas and liquid in the bone pass through the reduced-pressure passage and are discharged from the body, thereby preventing increased pressure in the bone. As a result, the bone cement can be prevented from leaking to outside of the bone. | 12-27-2012 |
| 20120323182 | INTRODUCER SHEATH AND INTRODUCER ASSEMBLY - An introducer sheath, which is formed from a tubular member provided with a hollow portion through which an elongated body is freely insertable, and which includes a distal portion and a main body portion, wherein the inner diameter of the distal portion is formed to become gradually smaller toward the distal side, and on the inner surface of the distal portion, there is provided a hydrophobic coating having a friction coefficient lower than the friction coefficient of the tubular member. | 12-20-2012 |
| 20120323101 | BODILY FLUID COMPONENT MEASUREMENT SYSTEM - The waterproof property of a bodily fluid component measurement system is improved. A bodily fluid component measurement system according to this invention includes a sensor unit which is indwelled in the skin of a subject and connected to a bodily fluid in the subject to measure a predetermined bodily fluid component, and a transmission unit which is detachably attached to the sensor unit and transmits, to a display unit, a measurement signal obtained by the sensor unit or a calculation result calculated as a concentration of the bodily fluid component in a bodily fluid of the same type as or different type from the bodily fluid based on the measurement signal. The sensor unit measures the bodily fluid component and transmits the measurement signal to the transmission unit by being activated by electromagnetic induction caused by an electromagnetic field generated by the transmission unit. | 12-20-2012 |
| 20120319864 | BODILY FLUID COMPONENT MEASUREMENT SYSTEM - In a bodily fluid component measurement system, the convenience for a subject is improved by achieving reductions in size and weight of a device which is always attached at the position where a sensor is indwelled. A bodily fluid component measurement system includes a sensor unit which is indwelled in the skin of a subject to measure a predetermined bodily fluid component, and a transmission unit which is detachably attached to the subject, and transmits, to a display unit, a measurement signal obtained by the sensor unit. The sensor unit is activated upon receiving power supplied by an electromagnetic wave generated by the transmission unit to measure the bodily fluid component and transmit the measurement signal to the transmission unit. | 12-20-2012 |
| 20120316542 | MEDICAL DEVICE MANUFACTURING METHOD AND MEDICAL DEVICE ASSEMBLY - A medical device in which a part to be secondarily shaped comprises a molded silicone rubber article is subjected to heatless shaping by irradiation with electron-rays. The irradiation with electron-rays enables shaping and, furthermore, sterilization under some conditions. In a medical device comprising a part in which at least a silicone rubber is used and the mechanical properties of the silicone rubber preferentially appear, the shape of the above-described part upon molding is deformed with the use of a correcting member to a level exceeding the desired deformed shape and maintained in this state. Next, electron-ray irradiation is conducted in this state and then the correcting member is eliminated. Thus, the desired deformed shape intermediate between the shape upon the molding and the shape upon the electron-ray irradiation can be obtained. | 12-13-2012 |
| 20120316433 | GUIDE WIRE AND CATHETER ASSEMBLY - A guide wire includes an elongated main body possessing flexibility. The main boy is comprised of a first wire having a core member constituted by a metal material, a second wire having a core member arranged on the proximal side of the first wire and constituted by a metal material, and an optically transmissive member arranged between the first wire and the second wire, and connecting the first and second wires to each other and constituted by a substantially transparent tube shaped body. The optically transmissive member exhibits light permeability such that when light is illuminated from one direction of a lateral side thereof, the light is transmissible to the opposite side through the center axis of the main body. | 12-13-2012 |
| 20120310227 | MEDICAL DEVICE - A medical device includes a steering unit at a proximal portion of a catheter to steer operations of a heating unit at a distal portion of the catheter. The steering unit includes a main body portion interlocked with the catheter; a slide portion interlocked with the heating unit and slidable relative to the main body portion; a guide unit interlocked with the main body portion and fixed to the slide portion for movement therewith; and an input connector electrically connected with the heating unit and connectable with an output connector for supplying electric energy to the heating unit. The guide unit hinders connection between the input connector and the output connector. A cutout portion enables connection between the input and output connectors when the guide unit moves with respect to the main body portion and the heating unit moves to a position at which the biological tissue is heatable. | 12-06-2012 |
| 20120310218 | GUIDE WIRE - A guide wire includes a wire body having a first wire disposed at a distal end and a second wire joined to a proximal end of the first wire at a joint by welding. The joint is curved. In the joint, at least one component (e.g., Ti) of the material of the first wire decreases toward the proximal end and at least one component (e.g., Fe) of the material of the second wire decreases toward the distal end. When a tensile test is conducted on a region of the wire body including the joint, the region of the wire body has, in a tensile load and elongation diagram, an elastic section extending substantially straight upwardly to the right, a yield section extending substantially horizontally or upwardly to the right from the elastic section, and a substantially straight section extending upwardly to the right from the yield section. | 12-06-2012 |
| 20120308363 | CENTRIFUGAL PUMP APPARATUS - This centrifugal blood pump apparatus includes an impeller provided in a blood chamber, a permanent magnet provided in one surface of the impeller, and a permanent magnet provided in an inner wall of the blood chamber, for attracting the permanent magnet. A centerline of the permanent magnet is arranged at a position different from that of a centerline of a sidewall of the blood chamber such that a rotation centerline of the impeller matches the centerline of the sidewall of the blood chamber during pump operation. Therefore, high torque transmission efficiency is obtained. | 12-06-2012 |
| 20120304867 | OXYGEN CONCENTRATOR - To provide an oxygen concentrator that can reduce pressure loss when suctioning raw air and that can increase the amount of suctioned raw air by an amount of reduction in pressure loss, and moreover that can reduce noise without significantly changing a basic structure of a compressor. The oxygen concentrator includes: a compressor that has a plurality of suction ports suctioning raw air and that generates compressed air by compressing suctioned raw air; a conduit through which the compressed air is sent; a silencer that has a suction side end introducing the raw air and a discharge side end discharging the raw air, with the silencer being connected with the conduit; and a plurality of connection conduits directly connecting the discharge side end of the silencer and the respective suction ports of the compressor. | 12-06-2012 |
| 20120302952 | CATHETER - A catheter includes an outer tube, and an inner tube which is disposed inside the outer tube and through which a guide wire is passed via a distal-side opening and a proximal-side opening. The outer tube has, in the axial direction thereof, at least: a first region on the distal side; a second region disposed on the proximal side and higher in rigidity than the first region; and a transition region which is provided between the first region and the second region and of which rigidity varies from the same rigidity as that of the first rigidity to the same rigidity as that of the second rigidity. The outer tube is configured with an opening, to which the proximal-side opening of the inner tube is connected, being provided in the second region. | 11-29-2012 |
| 20120296415 | BIOABSORBABLE STENT - A bioabsorbable stent has a relatively high radial force and can be placed directly at the lesion without the possibility or reducing the possibility of occluding the lesion again after placement. The bioabsorbable stent is formed from a mixture composed of a bioabsorbable aliphatic polyester and an aromatic compound having one or more aromatic rings. | 11-22-2012 |
| 20120296409 | STENT DELIVERY SYSTEM - A stent delivery system is provided with a stent which, when inserted into an organism, is compressed in the center axis direction and which, when placed in the organism, can be expanded outward and restored to the shape which the stent has before being compressed; an inner tube body (inner tube); and a stent housing tube body (sheath) in which the stent is housed. The stent can be discharged by moving the stent housing tube body to the proximal side relative to the inner tube body. At least a portion of an inner surface of the stent housing tube body is a substantially polygonal prism-shaped inner surface which extends in the axial direction of the stent housing tube body. | 11-22-2012 |
| 20120296316 | MEDICAL MANIPULATOR AND WELDING METHOD - A wire made up of a plurality of wire strands is wound around a tubular body coupled to a distal end working unit. A fixing pin has a through hole through which the wire is inserted. The fixing pin is fitted into a recess disposed in a side surface of the tubular body. The fixing pin is welded to the tubular body and the wire. The melting point of the wire is higher than the melting point of the fixing pin. In a state where material of the fixing pin flows in between the wire strands, the fixing pin and the wire are joined together. | 11-22-2012 |
| 20120289926 | BLOOD BAG SYSTEM AND BLOOD TREATMENT METHOD - A blood bag system includes: a first bag in which blood containing multiple components is stored; a second bag in which a relative medium-density component is stored; a third bag in which a relative low-density component is stored; a first tube through which the relative low-density component and the relative medium-density component are transported from the first bag to the second bag; and a second tube through which the relative low-density component is transported from the first bag to the third bag. A blood treatment method involves: centrifuging blood containing multiple components in a first bag, transporting a low-density component from the first bag to a third bag through a first tube and transporting a relative medium-density component from the first bag to the second bag through the first tube. | 11-15-2012 |
| 20120283772 | TISSUE CLOSURE AND TISSUE CLOSING DEVICE - A living body tissue closing device includes an elongated body element, a clip (living body tissue closure) for closing a wound hole which penetrates a living body tissue membrane, and a thread. The body element includes a sheath, and elongated feeding and deformation arrangement. The elongated feeding and deformation arrangement includes a covered tube, a pusher tube, a thread anchoring cap, a guide wire, and a stopper. The clip includes a seal portion for covering the wound hole and a peripheral portion of the wound hole from one side of the living body tissue membrane, a deformation portion deformable between a first form in which the deformation portion can pass through the wound hole and a second form in which the deformation portion cooperates with the seal portion to sandwich the living body tissue membrane therebetween, and a fastener portion for retaining the deformation portion in the second form. | 11-08-2012 |
| 20120277849 | ARTIFICIAL BLOOD VESSEL - An artificial blood vessel includes one proximal-end and at least one distal-end communicating with the proximal-end, and an inserting port positioned between the proximal-end and the distal-end. The inserting port is provided with a check valve that permits an intravascular curing device to pass through up to the proximal-end and also prevents body fluid from flowing out from the artificial blood vessel. The proximal-end is connected to the ascending aorta and the at least one distal-end is connected to one of the right brachiocephalic arterial trunk, the left common carotid artery, and the left subclavian artery. | 11-01-2012 |
| 20120271392 | ELECTRIC STIMULATION DEVICE - An electric stimulation device includes a main body portion having a stimulation electrode stimulating nerves or muscles inside the living body, a stimulation circuit portion with a stimulation circuit electrically connected to the stimulation electrode and applying a stimulation signal to the stimulation electrode, and a support body connected to the stimulation circuit portion and holding the implant position of the stimulation electrode inside the living body. The electric stimulation device also includes a fixing body connectable to the base end portion of the main body portion. The fixing body includes a fixing body side coil portion that receives an electromagnetic wave transmitted from an external device. When the fixing body is connected to the main body portion, the fixing body side coil portion is electrically connected to the stimulation circuit to enable power feeding and/or communication with respect to the stimulation circuit in response to the electromagnetic wave. | 10-25-2012 |
| 20120271174 | CATHETER - A catheter includes a catheter main body provided with a window portion through which an inspection wave passes, a drive shaft provided with a detection unit detecting the inspection wave and concurrently installed advanceably and retractably in an axial direction inside the catheter main body, and a bias member biasing a force onto the drive shaft for moving the drive shaft forward toward the distal side thereof. | 10-25-2012 |
| 20120259231 | Excitation, Detection, and Projection System for Visualizing Target Cancer Tissue - A system visually distinguishes diseased tissue from healthy tissue after a treatment is administered to a patient to provide different concentrations of a fluorescent marking substance between the diseased tissue and the healthy tissue. A light source illuminates the tissue with excitation light. A detector detects light returning from the tissue, and a controller characterizes the returning light according to a measured property indicative of the different concentrations. A light projector projects light having a predetermined cue in response to the characterization of the returning light. | 10-11-2012 |
| 20120253447 | BALLOON CATHETER - A balloon catheter includes: an inner tube adapted to receive a guide wire; an outer tube disposed on the outer surface side of the inner tube and cooperating with the inner tube to define an inflation lumen therebetween; and a balloon joined at the distal end thereof to the inner tube and at the proximal end thereof to the outer tube and configured to be expanded by inflation fluid from the inflation lumen. A non-circular region, having a non-circular sectional shape taken in a direction orthogonal to an extending direction of the inner tube, is formed on at least one of an outer surface of the inner tube and an inner surface of the outer tube. The non-circular region at least includes a joint section between the balloon and the outer tube and extends proximally of the joint section. | 10-04-2012 |
| 20120253297 | ULTRASOUND-GUIDED PIERCING NEEDLE AND INDWELLING NEEDLE - An ultrasound-guided piercing needle constituting the internal needle of an indwelling needle has ridged and grooved portions which reflect ultrasonic waves. The ridged and grooved portions comprise grooves, which are disposed on the outer periphery near the tip having a blade face, and ridges, which are arranged on both sides of the grooves. | 10-04-2012 |
| 20120253185 | OPTICAL COHERENCE TOMOGRAPHIC IMAGE FORMING APPARATUS AND CONTROL METHOD THEREOF - An optical coherent tomographic image forming apparatus includes: a first switch for instructing rotation of the optical deflection unit at a first speed; a second switch for instructing rotation of the optical deflection unit at a second speed which is higher than the first speed; and a driving controller which drives the optical deflection unit rotationally at the first speed in case of detecting instruction operation of the first switch and which changes the rotation speed of the optical deflection unit to the second speed, in case of detecting instruction operation of the second switch, under the condition that the optical deflection unit rotates at the first speed when the second switch is instructionally operated. | 10-04-2012 |
| 20120253184 | IMAGING APPARATUS FOR DIAGNOSIS AND DISPLAY METHOD - An imaging apparatus for diagnosis comprises a display unit configured to display a longitudinal-sectional image in a first display area, and display a cross-sectional image corresponding to an arbitrary position in an axial direction in the longitudinal-sectional image in a second display area; a signal processing unit divides the second display area into at least two individual areas in case of accepting an instruction to the effect that a predetermined operation is executed with respect to the first display area; and the signal processing unit displays indicators in the first display area, wherein in a case in which the second display area is divided into at least two individual areas, cross-sectional images corresponding to the axial direction position are displayed by at least two indicators in respective individual areas. | 10-04-2012 |
| 20120253144 | SENSOR - An embeddable sensor includes a sensor body, a detector housed in the sensor body, and a retaining mechanism mounted on a side surface of the sensor body. The retaining mechanism includes at least one projection on the side surface of the sensor body. The projection is of a V shape which is progressively wider and higher from a distal end toward a proximal end of the sensor body. The projection is made of a material whose hardness is lowered upon elapse of a certain period of time within a living body. When the embeddable sensor is inserted in the living body, the projection retains the embeddable sensor within the living body. Upon elapse of the certain period of time within the living body, the projection loses its capability to retain the embeddable sensor within the living body. | 10-04-2012 |
| 20120253123 | OTORHINOLARYNGOLOGICAL TREATMENT DEVICE AND METHOD - An otorhinolaryngological treatment device includes: a flexible elongated body to be introduced into an accessory nasal cavity through a nasal cavity; an expansion body which is provided on the elongated body and has an effective expansive section capable of radial expansive deformation within a natural ostium between the nasal cavity and the accessory nasal cavity to thereby force open a stenosed part of the natural ostium; and imaging unit for obtaining an image on the front side of a distal end of the elongated body, which is provided integrally with the elongated body on the distal side of the elongated body relative to the expansion body. The treatment device enables easy positioning (aligning) of the expansion body inside the nasal cavity, without need for radioscopy. | 10-04-2012 |
| 20120253114 | OTORHINOLARYNGOLOGICAL TREATMENT DEVICE AND METHOD - A sinusitis treatment device includes: a flexible first elongated body to be guided into an accessory; an imaging unit which is provided on the first elongated long body, for obtaining an image on the front side of a distal end of the first elongated body; a flexible second elongated body having a lumen in which the first elongated body is inserted; an expansive body which is provided on the second elongated body and which has an effective expansive section capable of radial expansive deformation within a natural ostium located between a nasal cavity and an accessory nasal cavity to push open a stenosed part of the natural ostium; and a positioning unit which is provided on the second elongated body, for positioning the effective expansive section of the second elongated long body moved along the first elongated body relative to the first elongated body. | 10-04-2012 |
| 20120245670 | STENT DELIVERY SYSTEM AND METHOD USING THE SAME - Disclosed herein is a stent delivery system which includes: a hollow shaft; first and second expandable balloons arranged around of the distal end of the shaft; and a stent which is arranged around the second balloon such that it expands as the second balloon expands; the first balloon having drug release means for releasing a drug at least to prevent the proliferation of endothelial cells, the stent being a bare metal stent to be indwelled at a target position as lesion of stenosis or occlusion in the lumen of a living body. | 09-27-2012 |
| 20120245459 | MOTOR DRIVE APPARATUS AND OPTICAL IMAGING APPARATUS FOR DIAGNOSIS - A motor drive apparatus includes: a transmission unit carrying-out transmission of an optical signal between a rotation unit for rotating a transmitting and receiving unit and a fixation unit for transmitting reflected light to a control apparatus through a signal line, wherein the transmission unit includes: a tubular shaped lens holding member where a collimator lens is held, and a holding member fixing member having first fixation surface by which the end surface of the lens holding member is fixed and second fixation surface fixed by a surface which is formed to be approximately perpendicular to the direction toward which the optical signal is emanated or the optical signal is light-received; the first fixation surface is formed in a spherical shape; and the second fixation surface is formed to be approximately perpendicular to the direction toward which the optical signal is emanated or the optical signal is light-received. | 09-27-2012 |
| 20120244366 | MEDICAL DEVICE AND METHOD FOR PRODUCTION THEREOF - A medical device on which a water-swellable polymeric material is strongly bonded to the surface of the substrate such as an electrically conductive material. A medical device that includes an electrically conductive material and a water-swellable polymeric material having reactive functional groups and being previously crosslinked, the reactive functional groups of the water-swellable polymeric material being chemically bonded with ions existing on the surface of the electrically conductive material. | 09-27-2012 |
| 20120232557 | METHOD FOR IMPROVING BLOOD FLOW IN BONE HEAD - A method for improving the blood flow in the bone head, the method including the steps of extending a long tubular body, which has a cutting tool at its foreend, close to the entrance of the retinaculum artery and performing drilling on the bone head by using the cutting tool. This method makes it possible to improve the blood flow in the bone head with a minimum of burden on the patient. | 09-13-2012 |
| 20120228273 | GUIDE WIRE - A guide wire includes a wire body having a first wire disposed at a distal end and a second wire joined to a proximal end of the first wire at a joint by welding. The joint is curved. In the joint, at least one component (e.g., Ti) of the material of the first wire decreases toward the proximal end and at least one component (e.g., Fe) of the material of the second wire decreases toward the distal end. When a tensile test is conducted on a region of the wire body including the joint, the region of the wire body has, in a tensile load and elongation diagram, an elastic section extending substantially straight upwardly to the right, a yield section extending substantially horizontally or upwardly to the right from the elastic section, and a substantially straight section extending upwardly to the right from the yield section. | 09-13-2012 |
| 20120226292 | Urethrovesical Anastomosis Suturing Method Using Articulating Laparoscopic Device - A suturing method for anastomosis of live bodies and training bodies joins a duct having perimeter positions defined according to clock hour positions to an opening in a bladder using an articulating laparoscopic device having a gripper at a distal end with open and closed positions for loading a suture needle in either a forehand or backhand direction. The gripper has a yaw motion including left and right positions and a roll motion either clockwise or counterclockwise. The open and closed positions, yaw motion, and roll motion are under manual control of a user through manual controls at a proximal end of the articulating laparoscopic device. The perimeter positions include a 12-o'clock position proximal to the user and a 6-o'clock position distal of the user. The method includes driving a suture at about the 6-o'clock position through the bladder and then the duct wherein the suture needle is loaded forehand, the yaw is in a left position, and the roll is clockwise. Orientations and directions are provided for other suturing positions. | 09-06-2012 |
| 20120226263 | GUIDE WIRE - A guide wire is comprised of a flexible elongate wire body. The wire body has a plurality of protruding portions n the external surface and recessed portions between the adjacent protruding portions. The protruding portions possess a friction coefficient smaller than that of the recessed portions. | 09-06-2012 |
| 20120226151 | IMAGING APPARATUS FOR DIAGNOSIS - An imaging apparatus for diagnosis is connected detachably with a probe having a first transmitting and receiving unit repeating electric signal transmission and reception and a second transmitting and receiving unit repeating optical signal transmission and reception, obtains a reflected signal inside a body cavity or lumen from the first or second transmitting and receiving unit by rotationally operating the first and the second transmitting and receiving units inside the body cavity, and can generate a tomographic image inside the body cavity, wherein the apparatus includes an electric rotary connector carrying out transmission of the electric signal while rotationally operating the first and second transmitting and receiving units; and an optical rotary connector carrying out transmission of the optical signal, the electric rotary connector includes a metal surface on the rotational drive unit side and a brush on the fixed unit side that is operable between contact and non-contact positions. | 09-06-2012 |
| 20120221020 | MEDICAL DEVICE AND USING METHOD THEREOF - Disclosed herein is a medical device including: a positioning catheter to be inserted into a blood vessel in the vicinity of an affected region; a treatment catheter to be inserted to reach the affected region; and attracting means provided at respective predetermined positions of both the catheters to apply a magnetic force in a direction of attracting each other; wherein the magnetic force of the attracting means restricts floating of the treatment catheter. | 08-30-2012 |
| 20120221009 | MEDICAL DEVICE AND VASCULARIZATION METHOD - A medical device includes a tubular body having a first lumen so designed as to receive a fluid from an opening at one end of the first lumen and discharge the fluid from an opening at the other end of the first lumen, and an expandable body attached to the tubular body. The first lumen communicates with the space inside the expandable body and the expandable body expands by the internal pressure of the fluid which is injected from the opening at one end and enters the space inside the expandable body through the first lumen. | 08-30-2012 |
| 20120215256 | PFO CLOSING DEVICE - A PFO closing device for bringing the septum primum and the septum secundum into contact with each other and joining them together includes a clamping mechanism and energy supplying device. The clamping mechanism includes a needle part for puncturing the septum primum, and a clamping member for cooperating with the needle part in clamping therebetween tissue of the septum primum and the septum secundum. The energy supplying device supplies energy for joining the tissues clamped by the needle part and the clamping member. The clamping mechanism is mounted in a catheter so as to be protrudable from and retractable into the catheter. | 08-23-2012 |
| 20120215255 | PFO CLOSING DEVICE - A PFO closing device for bringing the septum primum and the septum secundum into contact with each other and joining them together includes a clamping mechanism and energy supplying device. The clamping mechanism includes a needle part for puncturing the septum primum, and a clamping member for cooperating with the needle part in clamping therebetween tissue of the septum primum and the septum secundum. The energy supplying device supplies energy for joining the tissues clamped by the needle part and the clamping member. The clamping mechanism is mounted in a catheter so as to be protrudable from and retractable into the catheter. | 08-23-2012 |
| 20120215091 | IMAGING APPARATUS FOR DIAGNOSIS AND CONTROL METHOD THEREOF - An imaging apparatus for diagnosis and associated control method constructs multiple cross-sectional images in an axial direction inside the body lumen based on line data generated by radially operating a transmitting and receiving unit, and includes a receiving mechanism which receives a count value from a reference position of the transmitting and receiving unit, storage for storing the count value and the line data correlated with each other, an arrangement for constructing a longitudinal-sectional image by aligning the line data based on the count value, a display which displays the longitudinal-sectional image; and a mechanism which reads out line data correlated with the same count value as that of the line data disposed at the position appointed by the user on the displayed longitudinal-sectional image and reconstructing the cross-sectional image. | 08-23-2012 |
| 20120209366 | STENT AND STENT DELIVERY SYSTEM - A stent includes a plurality of annular bodies arrayed in an axial direction, each having a plurality of one-end-side bent sections and other-end-side bent sections, and adjacent ones of the annular bodies being linked by link sections. The stent includes at least three kinds of link sections selected from four kinds of link sections including: a vertex-vertex bent link section; a central part-central part bent link section; a central part-vertex bent link section; and a vertex-central part bent link section, the at least three kinds of the link sections including at least the vertex-vertex bent link section and the central part-central part bent link section, and the adjacent annular bodies being linked by at least two different kinds of the link sections | 08-16-2012 |
| 20120209329 | METHOD FOR DILATING BETWEEN SPINOUS PROCESSES - Disclosed is a method for dilating between spinous processes wherein a filamentous body provided with an expansion body is percutaneously inserted to locate the expansion body between the spinous processes, a filling material is injected into the expansion body to dilate between the spinous processes, and the expansion body is cut off from the filamentous body to be located between the spinous processes. This method exerts very little burden on the patient. | 08-16-2012 |
| 20120209242 | METHOD FOR ALLEVIATING CONDITION OF SPINAL CANAL STENOSIS BY LOCAL ADMINISTRATION OF MEDICINE - Disclosed herein is a method for alleviating the condition of spinal canal stenosis, including: transluminally placing a catheter in a lumbar artery, iliolumbar artery or lateral sacral artery at the proximity of a narrowed area of a spinal canal; and injecting a vasodilator into the artery via the catheter. | 08-16-2012 |
| 20120203269 | MEDICAL MANIPULATOR SYSTEM - A medical manipulator system has an operating unit including a grip handle and a composite input unit, a working unit detachably mounted on the operating unit and including an end effector, and a controller for controlling the operating unit. The controller judges starting and ending of a surgical case and increments the usage count of the working unit based on a manner in which the working unit is mounted and dismounted, and the times at which the working unit is mounted and dismounted, and disables the working unit if the usage count of the working unit exceeds a preset count. | 08-09-2012 |
| 20120203120 | SPHYGMOMANOMETER - The objective of the present invention is to provide a sphygmomanometer that is easy to use. The sphygmomanometer according to the present invention measures blood pressure in accordance with an oscillation in an artery wall, resulting from an arterial pulse correspondent with a change in cuff pressure. It comprises a cuff that is connected to the sphygmomanometer main body by a tube, a display unit for displaying the results of blood pressure measurements, and an air supply unit for supplying air to, and thus pressurizing, the cuff, which is detachable from the sphygmomanometer main body. The air supply unit is screwed into the sphygmomanometer main body with a screw assembly, and the screwed-in state is preserved by a caulking ring. The air supply unit also comprises a filter for keeping dust from entering the sphygmomanometer main body. | 08-09-2012 |
| 20120197385 | STENT - Provided is a stent wherein the water-swellable polymer fine particles applied thereto rarely peel off even when the stent is deformed or when the water-swellable polymer fine particles are swollen. A stent wherein a plurality of water-swellable polymer fine particles are chemically fixed on the stent surface in a dispersed state is provided. | 08-02-2012 |
| 20120197201 | INDWELLING NEEDLE AND INDWELLING NEEDLE ASSEMBLY - A indwelling needle includes an outer needle, an outer needle hub with a flow path communicating with the inside of the outer needle and configured to connect a connector to the flow path, and a valve mechanism which opens and closes the flow path. The valve mechanism includes a valve element in the middle of the flow path having an openable/closable opening/closing section and an operation member having a side hole and configured to open and close the opening/closing section. The valve mechanism is positionable in a state in which the operation member penetrates through the opening/closing section to protrude therefrom and the side hole is located closer to the front end side than the opening/closing section. When infusion liquid is supplied in this state, the liquid flows to the flow path through the side hole and the dead space within the flow path is filled with the infusion liquid. | 08-02-2012 |
| 20120191102 | MEDICINE INJECTION DEVICE AND METHOD - A medicine injection device includes a medicine ejection unit having a fluid flow-in port for receiving liquid, and a pressure generation unit which includes a pressure generating chamber to generate pressure acting upon a working chamber of the medicine ejection unit through the liquid and which ejects medicine by moving a gasket based on the applied pressure. The pressure generation unit includes a pressure portion cylinder in the pressure generating chamber, a first pusher provided with a hollow gasket defining the inner volume of the pressure generating chamber and a second pusher which generates the pressure inside the pressure generating chamber by pressing a distal end head portion into the inside of the pressure generating chamber. The pressure portion cylinder and the first pusher are coupled through an engagement mechanism in which fixation and fixation release are possible at different pitches in the axial direction. | 07-26-2012 |
| 20120191042 | INJECTION AID AND MEDICATION SYRINGE DEVICE - An injection aid is a tool used by being attached to an injection device having an injection needle and a syringe, and includes an aid main body and a tapered guide. The aid main body includes; an engagement part to be engaged with the syringe; a hollow part through which the injection needle penetrates; and a needle-protruding surface from which a needle tip part of the injection needle protrudes and which is brought into contact with skin when sticking the injection needle into a living body. The tapered guide is arranged in the hollow part of the aid main body and includes an inner surface that becomes continuously reduced in diameter toward the needle-protruding surface. | 07-26-2012 |
| 20120190974 | IMAGING APPARATUS FOR DIAGNOSIS AND CONTROL METHOD THEREOF - An imaging apparatus for diagnosis is connected with a probe including a transmitting and receiving unit transmitting a light transmitted from a light source continuously to the inside of a body cavity and concurrently, receiving a reflected light continuously from the inside of the body cavity, and generates a tomographic image inside the body cavity based on the obtained reflected light by obtaining the reflected light from the transmitting and receiving unit while rotating the transmitting and receiving unit. The apparatus comprises: a mechanism for extracting intensity of the reflected light obtained by a phenomenon that the light transmitted to the transmitting and receiving unit is reflected at the transmitting and receiving unit; and a mechanism for judging whether or not the extracted intensity of each reflected light at each rotary angle of the transmitting and receiving unit lies in a range of a predetermined variation width. | 07-26-2012 |
| 20120190839 | ACTIVE ESTERIFIED POLYSACCHARIDE AND METHOD FOR PRODUCING SAME - A method for producing an active esterified polysaccharide, the method including: subjecting a carboxy group of a carboxy group-containing polysaccharide and an agent for introducing an electrophilic group, to an esterification reaction, wherein an active esterified polysaccharide is formed; bringing the active esterified polysaccharide into contact with a polyvalent carboxylic acid; and after the active esterified polysaccharide is brought into contact with the polyvalent carboxylic acid, precipitating and collecting the resulting active esterified polysaccharide. | 07-26-2012 |
| 20120184920 | PREFILLED SYRINGE - A prefilled syringe has a gasket composed of a gasket body and a plunger-mounting member mounted. The plunger-mounting member has a distal part, spiral ribs formed on an outer surface of the distal part, a flange part, and a plunger-mounting part formed on an inner surface of a hollow part. The gasket body has a spiral screwing part which screws the spiral ribs and an accommodation part for accommodating a portion where the spiral ribs are formed. A plunger has a mounting distal part. The plunger-mounting part has a spiral concave portion and an engaging rib disposed at a side distal from the spiral concave portion. The mounting distal part of the plunger has a spiral projected portion capable of screwing the spiral concave portion and an engaging portion which engages the engaging rib of the plunger-mounting member. | 07-19-2012 |
| 20120179129 | VIAL ADAPTER - A vial adapter is provided with a fitting portion which can be fitted into the head portion of a vial, and a hollow needle with a side hole. The base end portion of the needle is provided with a stopper contact portion which contacts the top surface of a stopper when the fitting portion is fitted in the head portion of the vial. When the fitting portion is fitted in the head portion of the vial, the stopper contact portion contacts the top surface of the stopper, and the fitting portion is fixed to the head portion of the vial by a claw engaging with the head portion of the vial, and further, the region of the side hole nearest the base end portion of the needle is positioned either roughly at the bottom surface of the stopper or inside of the stopper. | 07-12-2012 |
| 20120179128 | CONNECTOR ASSEMBLY - A connector assembly includes a first connector having a tubular first connector body, a hollow needle inside the first connector body and a first sealing component piercable by the needle, and a second connector having a tubular second connector body and a second sealing component. The second sealing component is in the second connector body, is attached to a first piercing section when inserted into the first connector body, and, in that state, is pierced by the needle together with the first piercing section. The connector assembly also includes a restriction which, when the second connector is inserted into the first connector, temporarily interrupts and restricts the insertion operation, but allows resumption of such operation when the restriction is removed, and which, when the second connector is withdrawn from the first connector, temporarily interrupts and restricts the withdrawing operation, but allows such operation to resume when the restriction is removed. | 07-12-2012 |
| 20120179114 | SYRINGE NEEDLE ASSEMBLY AND MEDICATION INJECTION DEVICE - To prevent a coating agent applied to the surface of a needle tube from being infiltrated into the clearance between the needle tube and a needle hub, a device comprises a needle tube that has a needle tip capable of puncturing a living body and that is coated with a coating agent on the surface of a tip-end portion on the side of the needle tip; and a needle hub adapted to hold the needle tube in a state where the needle tip of the needle tube is protruded. The needle hub has a through-hole through which the needle tube is inserted, and a discharge hole extending from the through-hole to the outer surface of the needle hub and adapted to discharge the coating agent infiltrated into the through-hole. | 07-12-2012 |
| 20120179113 | SYRINGE NEEDLE ASSEMBLY AND MEDICATION SYRINGE DEVICE - To make it possible to integrally form a needle tube and a needle hub by reliably holding and fixing the needle tube with a chuck member and then performing insert molding, a device has a needle tube having a needle tip capable of puncturing a living body; and a needle hub that is adapted to hold the needle tube in a state where the needle tip of the needle tube is protruded and that is formed with a retention hole into which a chuck member is inserted, the chuck member being adapted to hold and fix the circumferential surface of the needle tube when performing insert molding. | 07-12-2012 |
| 20120179017 | BLOOD GLUCOSE METER AND BLOOD GLUCOSE LEVEL MEASUREMENT METHOD - An internal temperature sensor for measuring internal temperature of a case of the blood glucose meter is arranged inside the case of the blood glucose meter, and an external temperature sensor configured by components with low heat capacity and adapted for measuring external temperature is arranged at a position separated from the central portion of the case of the blood glucose meter. Further, a microcomputer of the blood glucose meter includes the following processing: judging whether or not the temperature fluctuation falls within the acceptable range based on the difference between the respective temperatures and, if the temperature fluctuation exceeds the acceptable range, temporarily stopping the processing until the temperature fluctuation falls within the acceptable range when in the case where the blood glucose measurement has not yet been performed, or stopping the blood glucose measurement processing when in the case where the blood glucose measurement is being performed. | 07-12-2012 |
| 20120172969 | STENT DELIVERY SYSTEM - A stent delivery system includes a self-expanding stent, an inner tube body which has a guide wire lumen, and a sheath which has the stent contained within the tip section thereof. The stent can be discharged by moving the sheath to the base end side relative to the inner tube body. The inner tube body is provided at a position within the base end section of the stent and is provided with an elastic member for pressing the stent in the direction to the sheath. The stent is gripped by the elastic member and the sheath and is adapted to be slidable relative to the sheath. | 07-05-2012 |
| 20120172846 | CATHETER HOLDER - A catheter holder which is compact and which can be relatively easily released while holding the unhoused portion of the catheter stably includes: an attachment portion for receiving or being attached to a portion of a holding tube housing a portion of the catheter, and a plurality of hold portions integral with the attachment portion and holding an unhoused portion of the catheter, which is exposed outside the holder tube. | 07-05-2012 |
| 20120172841 | POSITION CONFIRMING CATHETER - A catheter includes an inner layer, an outer layer, a reinforcement layer located between the inner layer and the outer layer, and a marker composed of a contrast material for confirming the position of the distal end portion of the catheter from outside the living body. The reinforcement layer is composed of a spiral first filamentous member, with a gap provided between those portions of the first filamentous member which are adjacent to each other along the longitudinal direction of the catheter. The marker is formed by spirally winding a second filamentous member having a filament diameter smaller than the gap, and has a portion in close contact with the inner layer in the gap. | 07-05-2012 |
| 20120172830 | MIXING APPARATUS AND PIERCING METHOD FOR A DOUBLE-ENDED NEEDLE - A mixing apparatus for mixing a first component and a second component comprises: a first vessel which has a negative internal pressure and houses the first component; a second vessel which houses the second component; and a double-ended needle which allows communication between the first vessel and the second vessel when a first stopper element and a second stopper element have been pierced through by the needle. Penetration-resistance increasing parts which have a greater penetration resistance with respect to the first stopper element and the second stopper element than tip end tubes are respectively provided on a first puncture needle and a second puncture needle of the double-ended needle at positions further towards the base end than the tip end tubes. The axial heights of the edge faces of the tip end tubes are both less than the thicknesses of the first stopper element and of the second stopper element. | 07-05-2012 |
| 20120172735 | BLOOD PRESSURE MEASURING APPARATUS AND BLOOD PRESSURE MEASURING METHOD - A blood pressure measuring apparatus includes a cuff which is attached to and around an external ear; a first pulse wave detector and a second pulse wave detector which detect a pulse wave in a part squeezed by the cuff and which are affected differently from each other by a characteristic of body movements; a body movement detecting means which detects the characteristic of body movements; a pulse wave selecting means which selects a pulse wave detected by one of the first pulse wave detector and the second pulse wave detector based on the characteristic of body movements detected by the body movement detecting means; and a blood pressure value deriving means which derives a blood pressure value based on the pulse wave selected by the pulse wave selecting means. | 07-05-2012 |
| 20120168464 | SYRINGE - A syringe includes a syringe outer tube having a spout and a spout-mounted cap. The cap has a cap main body sealing the spout in a liquid-tight manner, a mounting section mounted onto the spout, and a breakable breaking section linking the cap main body and the mounting section to release the link upon breaking. The inner circumferential portion of the mounting section includes protrusions inserted into a groove on the outer circumferential portion of the spout which also has a tilted section tilted relative to the axis of the spout outer circumferential portion. When the cap is rotated along the axial direction of the syringe outer tube, the protrusions move along the tilted section of the groove. The mounting section is thus displaced in the base end direction and the braking section is pulled in the direction and breaks to separate the cap main body from the mounting section. | 07-05-2012 |
| 20120168384 | DRUG-ADSORBING MATERIAL AND MEDICAL DEVICE COMPRISING SAME - A drug-adsorbing material capable of efficiently adsorbing and eliminating drugs (such as carcinostatic agents) from blood with a small amount without causing foreign body recognition reaction, such as blood coagulation, and a medical device provided with said drug-adsorbing material. The drug-adsorbing material is based on polymeric microparticles which swell upon adsorption of plasma components at pH value of 7 or above and keep their shape after swelling. The drug-adsorbing material is incorporated into a drug-administrating device for drug adsorption. | 07-05-2012 |
| 20120165923 | STENT - A stent able to minimize occurrences of strain and stress concentration in a drug coat layer upon expansive deformation of the stent in a radial direction to avoid the possibility of the drug separating from the stent, includes a stent body and a drug coating layer coated on the outside surface of the stent body so that the thickness of the drug coating layer gradually decreases toward a bent portion of the stent. | 06-28-2012 |
| 20120165680 | CATHETER - A catheter includes a sheath insertable inside a body lumen and provided with a window portion permeable to inspection waves, a detection unit movable in the axial direction of the sheath inside the sheath and which detects the inspection waves, and a reinforcement tube positionable to cover the inner surface or the outer surface of the window portion and movable in the axial direction of the sheath. | 06-28-2012 |
| 20120158119 | STENT FOR PLACEMENT IN LIVING BODY AND STENT DELIVERY SYSTEM - A stent for placement in living body is substantially in a tubular form and includes a plurality of wave-shaped struts extending in the axial direction from one end to the other of the stent. The axially-extending wave-shaped struts are arranged in a circumferential direction, and connection struts interconnect the respective circumferentially adjacent wave-shaped struts. The circumferentially adjacent wave-shaped struts include a plurality of closer sections and farther sections. The connection struts interconnect between the closer sections of adjacent wave-shaped struts, and each has at the center thereof a bent portion extending in the axial direction of the stent. | 06-21-2012 |
| 20120157672 | POROUS STRUCTURE - A porous structure includes a polysaccharide and having a multitude of pores wherein an average pore size of the pores is not smaller than 40 μm and a ratio of the number of pores having a pore size not smaller than 50 μm to the total number of the pores is not less than 30%. The porous structure improves the solubility of a polysaccharide in water. | 06-21-2012 |
| 20120143282 | ELECTRIC STIMULATOR - An electric stimulator includes a stimulation circuit block having a stimulation electrode that stimulates nerves or muscles in a living body and a stimulation circuit that is electrically connected to the stimulation electrode to apply a stimulation signal to the stimulation electrode. Additionally, the electric stimulator further includes a support that is connected to the stimulation circuit block to hold the stimulation electrode at an implantation position in the living body. The stimulation circuit block and the support, except for at least one end of the support, have a shape configured to be inserted into the duct of a tubular insertion tool. | 06-07-2012 |
| 20120136340 | CATHETER - A catheter which exhibits excellent anti-kinking properties while avoiding interference with respect to an object moving inside the lumen of the catheter includes: an elongated catheter main body having a longitudinally extending lumen; a tubular-shaped guide wire insertion portion on the distal end of the catheter main body through which a guide wire is insertable, and which includes a distal opening portion and a proximal opening portion; and a reinforcement portion having a coil portion in which at least a portion of the reinforcement portion is arranged proximally of the proximal opening portion and is formed by a wound wire element, and an extension portion extending from the wire element of the coil portion in the distal direction away from the proximal opening portion, and wherein the reinforcement portion is positioned between the inner surface and the outer surface of the lumen of the catheter main body. | 05-31-2012 |
| 20120135384 | PORTABLE TERMINAL, CALORIE ESTIMATION METHOD, AND CALORIE ESTIMATION PROGRAM - A portable terminal including: an imaging portion; a storage portion configured to store a database in which a plurality of foods and the calories thereof are associated with the shapes of containers and with the colors of the foods; a container detection portion configured to detect, from an image taken of a food slantwise at a predetermined angle to a horizontal direction, a container on which the food is placed; a container shape classification portion configured to classify the shape of the container detected by the container detection portion; a color detection portion configured to detect the container having been detected by the container detection portion; and a food estimation portion configured to estimate the food and the calories thereof from the database. | 05-31-2012 |
| 20120116493 | STENT DELIVERY SYSTEM - A stent delivery system includes a distal-side tube, a proximal-side tube, a fixing tube, a stent containing tubular member, a stent in the stent containing tubular member, and a pulling wire for moving the stent containing tubular member to the proximal side. The distal-side tube includes a distal-side priming slit provided in a side wall in proximity to a stent proximal end lock section and a proximal-side priming slit provided in a side wall on the proximal side of the distal-side tube. The slits are opened by injecting liquid, with the distal opening or the rear end opening of a guide wire lumen of the distal-side tube closed. | 05-10-2012 |
| 20120116430 | CATHETER HAVING AN ARRANGEMENT FOR REMOVING AN OCCLUDING OBJECT - Exemplary embodiments of the present disclosure can provide a catheter which can include a removal mechanism which can excavate a tubular-organ occluding object. For example, the exemplary catheter can include: a sheath portion which can have a elongated lumen insertable into a tubular-organ. The catheter can further include an insertion member which can have a second elongated lumen which can be arranged free, slidably, and rotatably with respect to the lumen of the sheath portion. The catheter can also include a removal mechanism configured to remove a occluding object of the tubular-organ. The removal mechanism can include a support portion arranged at a distal portion of the insertion member and a plurality of rotating arrangements having at least one blade edge configured to excavate the occluding object. The support portion can have an axis of rotation that intersects an axis of extension of the insertion member. | 05-10-2012 |
| 20120109125 | METHODS AND ELECTRODE APPARATUS TO ACHIEVE A CLOSURE OF A LAYERED TISSUE DEFECT - Methods for treating anatomic tissue defects such as a patent foramen ovale generally involve positioning a distal end of a catheter device at the site of the defect, exposing a housing and energy transmission member from the distal end of the catheter, engaging the housing with tissues at the site of the defect, applying suction or other approximating tool to the tissue via the housing to bring the tissue together, and applying energy to the tissue with the energy transmission member or to deliver a clip or fixation device to substantially close the defect. Apparatus generally include a catheter body, a housing extending from a distal end of the catheter body for engaging tissue at the site of the defect, and further adapted to house a fusing or fixation device such as an energy transmission member adjacent a distal end of the housing, or a clip or fixation delivery element. | 05-03-2012 |
| 20120106589 | BODY TEMPERATURE MEASURING SYSTEM, DATA READING DEVICE, AND DRIVING CONTROL METHOD THEREOF - In a body temperature measuring system, power consumption of a data reading device is reduced. A clinical thermometer of this invention is a body temperature measuring system including a body temperature tag and a data reading device. A processing unit of the body temperature tag includes a power supply circuit, a semiconductor temperature sensor for detecting a band gap voltage, and a storage unit configured to store calibration data to calibrate the detected band gap voltage, and is configured to, upon activating the power supply circuit, send the detected band gap voltage via the antenna unit together with the calibration data. The data reading device includes an excitation unit, and a sensing unit configured to sense a change in a magnetic field generated by excitation. The power level of the excitation unit is changed upon sensing the change in the magnetic field. | 05-03-2012 |
| 20120083749 | NEEDLE TUBE, MEDICAL INSTRUMENT AND METHOD FOR MANUFACTURING MEDICAL INSTRUMENT - A syringe needle assembly includes a needle tube and a hub. The needle tube has a needle body provided with a needlepoint configured to puncture a living body. To prevent the needle tube from dropping out of a holding member in which the needle tube is held, the needle body also includes an axially press-worked enlarged portion that is continuous in the circumferential direction of the needle body. The hub includes a fitting portion to which the enlarged portion of the needle tube is fitted, and holds the needle tube. | 04-05-2012 |
| 20120082706 | MEDICAL DEVICE FOR DRUG DELIVERY - A medical device for safe and sure delivery of drugs to the lesion and a method for production thereof. The medical device has at least part of its surface in contact with the lumen wall tissue of the living body coated with a drug releasing layer containing a drug and a phospholipid, the drug and the phospholipid forming a solid dispersion. | 04-05-2012 |
| 20120078051 | GUIDE WIRE FOR ENDOSCOPE - A guide wire includes a wire having an elongated body section and a distal portion decreasing in outer diameter from the body section. The guide wire may have a resin coating portion coating the body section and the distal portion and having a smooth outer surface; and a visually discernible mark provided at the resin coating portion. The body section may have a flexible portion which constitutes a part of the body section and lower in flexural rigidity than other portions of the body section different from the part, and the visually discernible mark is provided at a position of the resin coating portion at which the flexible portion is coated with the resin coating portion | 03-29-2012 |
| 20120075266 | HOME MEDICAL APPARATUS - A home medical apparatus can give explanations corresponding to the levels of proficiency in operation when explaining to a patient about operation procedures. A home medical apparatus according to this invention includes a selection unit which selects an explanation mode corresponding to the level of proficiency in operation, a storage unit which stores a plurality of display windows classified to the respective explanation modes upon associating them with each other between adjacent levels, and a display control unit which displays the display windows classified to the selected explanation mode in a predetermined order. When a detailed explanation button is pressed, the display control unit makes transition to a display window classified to an explanation mode one level lower than the current explanation mode. | 03-29-2012 |
| 20120071960 | ARTIFICIAL BLOOD VESSEL AND ARTIFICIAL BLOOD VESSEL SYSTEM - An artificial blood vessel includes a flexible tube and a structure provided at one end portion of the tube and capable of being deformed to a first outside diameter and a second outside diameter greater than the first outside diameter, wherein the tube is provided with a lock part which is locked at a desired position when the tube is folded back from its other end portion to the inside. | 03-22-2012 |
| 20120063570 | IMAGING APPARATUS AND CONTROL METHOD THEREOF - The present invention discloses an imaging apparatus radial-operating a transmitting and receiving unit and generating cross-sectional images inside the body cavity by a plurality of images, which includes: an X-ray image memory holding a plurality of X-ray images obtained by X-ray imaging the transmitting and receiving unit inside the body cavity by a predetermined imaging cycle, an image processing unit generating a cross-sectional moving image by setting the rotation cycle of the transmitting and receiving unit to be frame rate, and an image processing unit reading out an X-ray image, obtained from X-ray imaging just previously at every timing for every rotation cycle of the transmitting and receiving unit, from the X-ray image memory and generating an X-ray moving image by the frame rate. | 03-15-2012 |
| 20120059317 | METHOD OF MANUFACTURING BALLOON CATHETER AND BALLOON CATHETER - A method of manufacturing a balloon catheter involves applying a first application liquid, which contains a hydrophilic coating material, to the outer periphery of a balloon which is disposed on an elongated catheter and is held in an expanded state; folding the balloon; and applying a second application liquid, which contains the hydrophilic coating material, to the balloon with the balloon folded. | 03-08-2012 |
| 20120046383 | SILICONE RUBBER COMPOSITION - The silicone rubber composition disclosed here is formed a configuration in which vitamin E or a derivative thereof, or a salt of any one thereof is dispersed at least at a portion of the silicone rubber. Also disclosed is a method of manufacturing a medical apparatus that involves mixing a silicone rubber precursor with vitamin E or a derivative thereof, or a salt of any one thereof and hardening the obtained mixture, or a process of infiltrating a silicone rubber into vitamin E or a derivative thereof, or a salt of any one thereof in a liquid state. Further, the method of manufacturing a medical apparatus as disclosed here includes installing the obtained silicone rubber composition onto a medical apparatus; hermetically packaging the obtained medical apparatus; and irradiating radiation to the hermetically packaged medical apparatus. | 02-23-2012 |
| 20120041261 | BALLOON CATHETER AND BALLOON CATHETER ASSEMBLY - A balloon catheter includes: an outer catheter; an inner catheter inserted in the outer catheter, capable of moving relative to the outer catheter in the longitudinal direction thereof, and permitting a flexible medical elongate member to be inserted therethrough; an inflatable and contractible balloon constructed from a film member, having one end portion and the other end portion fixed respectively to a distal portion of the outer catheter and a distal portion of the inner catheter, and projecting from a distal end of the outer catheter by an amount which varies according to the amount of movement of the inner catheter relative to the outer catheter; and a position restrictor for restricting the position of a distal end of the medical elongate member, which is inserted through the inner catheter, relative to a distal end of the balloon. | 02-16-2012 |
| 20120029478 | GUIDE WIRE FOR MEDICAL TREATMENT - A guide wire for medical treatment includes a straight-line shaped proximal section and a distal section which is continuous with the distal side of the proximal section and whose most distal portion faces toward the proximal direction. The distal section includes a curved portion continuous with the proximal section and a distal portion continuous with the distal side of the curved portion, the proximal section and at least a portion on the proximal side of the curved portion continuous with the proximal section are positioned on an identical plane, and the distal portion is extended toward a direction backing away from the plane and includes the most distal portion in a section of a direction to which the curved portion is curved with respect to an plane n an axis core of the proximal section orthogonal to the plane. | 02-02-2012 |
| 20120029328 | FLUORESCENCE SENSOR, NEEDLE-TYPE FLUORESCENCE SENSOR, AND METHOD FOR MEASURING ANALYTE - A needle-type fluorescence sensor that measures glucose based on fluorescence produced by excitation light is provided. The needle-type fluorescence sensor includes a needle body section including a sensor portion disposed in a needle distal end portion and metal lines disposed from the sensor portion to a needle proximal end portion, and a connector which is integrated with the needle body section and in which the metal lines extend. The sensor portion includes a silicon substrate having first and second principal surfaces, a PD device that converts fluorescence into an electric signal, an LED device that transmits fluorescence and emits excitation light, and an indicator layer that interacts with an analyte under the excitation light to produce fluorescence. The PD device, the LED device, and the indicator layer overlap with each other above the first principal surface of the silicon substrate. | 02-02-2012 |
| 20120028231 | BIOLOGICAL MODEL FOR TRAINING AND PRODUCTION METHOD OF BIOLOGICAL MODEL FOR TRAINING - Disclosed is a biological model for training which is in a tubular shape having an inner cavity, has a narrowing or closing portion at a mid portion of the tube, and is provided with a artificial lesion member simulating a lesion occurring in a tubular tissue. In this biological model for training, the artificial lesion member includes, at least in a portion thereof, a plastic and deformable material. The biological model for training is used in expansion training for implementing expansion. As the plastic and deformable material, a material including, as the main component, at least one member selected from among a silicone clay, a resin clay and an oil clay can be specifically used. Such a material is preferred because of ensuring the maintenance of a expanded state in the expansion training. | 02-02-2012 |
| 20120027628 | COMPRESSOR AND OXYGEN CONCENTRATOR - A compressor that generates compressed air by compressing raw air has a case section; a driving motor that is provided in the case section and that has an output shaft; head sections operated by the rotation of the output shaft of the driving motor and that suck and compress raw air to generate thereby compressed air; and a raw air intake section formed of a plurality of raw air intake holes for taking raw air into the case section and supplying the raw air to the head sections. | 02-02-2012 |
| 20120024779 | SURFACE TREATING AGENT, FILTERING MATERIAL FOR FILTER, AND BLOOD TREATMENT FILTER - A surface treating agent is comprising a copolymer including: a monomer (A) having a hydrophilic functional group of formula ( | 02-02-2012 |
| 20120022635 | STENT DELIVERY SYSTEM - A stent delivery system includes: a distal-side tube; a proximal-side tube; a tubular member which contains a stent; a wire which has one end fixed to the tubular member; and an operating section which has a wire winding mechanism and a wire winding amount restriction mechanism for restricting the length of wire which is pulled. The operating section has an operating rotary roller; a winding shaft section and driving gear which are provided coaxially and integrally with the roller; and a driven gear which is intermittently rotated by the driving gear. The driving gear and the driven gear have the stopper function by which rotation of the driving gear is stopped after the driving gear is rotated a predetermined amount. | 01-26-2012 |
| 20120022503 | GUIDE WIRE - A method of making a guide wire involves butting a connection end face at a proximal end of a first wire against a connection end face at a distal end of a second wire while applying voltage and a pressing force to weld together the first and second wires at a welded portion. The welded portion forms a projection that projects outwardly in an outer peripheral direction relative to portions of the first and second wire adjacent the projection. The outer dimension of the projection at the welded portion is adjusted so that upon completing adjusting the outer dimension of the projection the projection still projects outwardly in the outer peripheral direction relative to the portions of the first and second wire adjacent the projection. | 01-26-2012 |
| 20120022470 | MEDICAL ELONGATE MEMBER HOUSING TOOL AND MEDICAL ELONGATE MEMBER HOUSING TOOL ASSEMBLY - An elongate member housing tool assembly includes a distal end side tubular member disposed on the distal end side and a proximal end side tubular member disposed on the proximal end side, which accommodate an elongate member, and a liquid inlet port to which a liquid supplying tool for supplying liquid into the distal end side tubular member is removably connected and which is provided on the distal end side tubular member. The distal end side tubular member and the proximal end side tubular member are wound spirally, and the proximal end of the distal end side tubular member and the distal end of the proximal end side tubular member are disposed in a spaced relationship from each other. A distal portion of the guide wire is accommodated in the distal end side tubular member, except possibly the most distal portion of the elongate member. | 01-26-2012 |
| 20120020815 | COMPRESSOR AND OXYGEN CONDENSING DEVICE - Provided is a compressor, and an oxygen concentrator, that achieve low noise by which the noise does not leak directly to the exterior upon generation of compressed air through suction of raw air, and that allow reducing power consumption of a driving motor. | 01-26-2012 |
| 20120016344 | ASPIRATION CATHETER - An aspiration catheter includes an aspiration tube and an aspiration lumen extending between and opening to the distal and proximal ends of the aspiration tube, and a guidewire tube bonded to the outer surface of the aspiration tube on a distal end portion of the aspiration tube, with at least a portion of the guidewire tube being parallel to the aspiration tube. A guidewire lumen extends through the guidewire tube and opens at a proximal opening located at a proximal end of the guidewire tube. The outer surface of the aspiration tube has a flat portion where the outer surface is parallel to an axial direction of the aspiration lumen, and the proximal opening of the guidewire lumen is located at the flat portion of the outer surface of the aspiration tube. | 01-19-2012 |
| 20120016314 | GASKET AND SYRINGE - A gasket configured so that a pusher having a male screw thread on the outer periphery of its tip is connected to the gasket through the male screw thread and so that the gasket slides within a syringe outer tube when the pusher is operated in the longitudinal direction. The gasket includes: a gasket body having a hollow section and a female screw thread in the inner peripheral section of the hollow section engaged by the male screw thread; and projections on the outer peripheral section of the gasket body extending circumferentially of the outer peripheral section and axially arranged in spaced relation to each other. When the gasket is not yet inserted into the syringe outer tube, a screw thread located in a portion on the inner side of and in direct proximity to the projection has a smaller height than a screw thread located in the remaining portion. | 01-19-2012 |
| 20120010608 | ENERGY BASED DEVICES AND METHODS FOR TREATMENT OF PATENT FORAMEN OVALE - Methods and apparatus for treatment of patent foramen ovale (PFO) provide for applying energy to tissues adjacent the PFO with a catheter device to substantially close the PFO acutely. Apparatus generally includes a catheter device having at least one energy transmission member at or near its distal end configured to apply energy to PFO tissues to acutely, substantially close the PFO. Applied energy may be monopolar or bipolar radiofrequency energy or any other suitable energy, such as laser, microwave, ultrasound, resistive heating or the like. Some embodiments of a catheter device fuirther include one or more tissue apposition members near the distal end for helping bring PFO tissues together, such as a PFO covering member, a vacuum applying member and/or the like. PFO closure via energy-based approaches of the invention may help prevent stroke, treat migraine headache, and possibly treat or prevent other medical conditions. | 01-12-2012 |
| 20120010607 | ENERGY BASED DEVICES AND METHODS FOR TREATMENT OF PATENT FORAMEN OVALE - Methods, devices and systems for treating patent foramen ovale (PFO) involve advancing a catheter device to a position in a heart for treating a PFO, bringing tissues adjacent the PFO at least partially together, and applying energy to the tissues to substantially close the PFO acutely. Catheter devices generally include an elongate catheter body, at least one tissue apposition member at or near the distal end for bringing the tissues together, and at least one energy transmission member at or near the distal end for applying energy to the tissues. In some embodiments, the tissue apposition member(s) also act as the energy transmission member(s). Applied energy may be monopolar or bipolar radiofrequency energy or any other suitable energy, such as laser, microwave, ultrasound, resistive heating or the like. | 01-12-2012 |
| 20120007974 | IMAGE APPARATUS AND CONTROL METHOD THEREOF - An imaging apparatus generates a cross-sectional image in the longitudinal direction inside a body cavity (e.g., blood vessel) by using an interference signal. The apparatus includes an obtaining unit for obtaining line data, and a judgment unit for judging whether or not the optical probe unit operates in a normal state based on existence or non-existence of intensity change in at least a portion of signals within the obtained line date, based on existence or non-existence of change of position in the depth direction in which the portion of signals appear, or based on change quantity per unit time with respect to the position in the depth direction in which the portion in the depth direction of signals appear. | 01-12-2012 |
| 20120003108 | CENTRIFUGAL PUMP APPARATUS - A centrifugal blood pump apparatus includes an impeller provided in a blood chamber, first and second permanent magnets provided in one surface and the other surface of the impeller respectively, a third permanent magnet provided in an inner wall of the blood chamber, and a magnetic element and a coil for driving the impeller to rotate with a diaphragm being interposed. First and second grooves for hydrodynamic bearing different in shape and depth from each other are formed in the inner wall of the blood chamber facing the impeller, and third and fourth grooves for hydrodynamic bearing different in shape and depth from each other are formed in the diaphragm facing the impeller. The second and fourth grooves for hydrodynamic bearing generate high hydrodynamic pressure when the impeller is activated to rotate, while the first and third grooves for hydrodynamic bearing generate high hydrodynamic pressure when the impeller steadily rotates. | 01-05-2012 |
| 20120002928 | COUPLING DEVICE AND OPTICAL IMAGING DEVICE - A coupling device for coupling optical fiber cables reduces contact with the internal parts when coupling a connector. The coupling device includes a projection of a connector device housing insertable into a groove of an adapter device groove of an adapter device housing. The coupling device which connects optical fiber cables compresses an elastic member, and connects an optical fiber connector of the connector device and the optical fiber end on the adapter device side. | 01-05-2012 |
| 20120002699 | ELECTRONIC CLINICAL THERMOMETER ATTACHMENT UNIT AND CONTROL METHOD THEREFOR - An electronic clinical thermometer attachment unit, which is configured to be attached to an electronic clinical thermometer, inputs an external sound, determines whether the external sound is a buzzer sound notifying completion of measurement by the electronic clinical thermometer, based on whether the input external sound has a pattern of a buzzer sound notifying completion of the measurement, and performs notification output for notifying a user when it is determines that the external sound is a buzzer sound notifying completion of the measurement. | 01-05-2012 |
| 20120000745 | BIOLOGICAL GRAFT TRANSFERRING INSTRUMENT AND METHOD FOR TRANSFERRING BIOLOGICAL GRAFT - A biological graft transferring instrument for transferring a biological graft includes a main body, a displacement member capable of being displaced relative to the main body, and a belt-shaped member which is wound around the forward end and base end of the displacement member and is joined to the main body. The biological graft is placed on the belt-shaped member at the forward end of the displacement member. | 01-05-2012 |
| 20110321181 | DEVICE TO BE PLACED IN BLOOD VESSEL, ANGIOSTENOSIS MODEL USING SAME AND METHOD FOR MAKING MODEL - An indwelling vascular device is constructed such that a vascular stenosis model can be controlled from the partial stenosis to the total occlusion. There is also described a vascular stenosis model of such non-human animal, and a method for making the same. The model can be used for diagnosis or therapy of a disease resulting from the stenosis or total occlusion in a blood vessel or further for the development of therapeutic approaches. The indwelling vascular device includes a device substrate containing a metal and/or metal compound which elutes toxic metal ions at least from a surface thereof and having a structure ensuring a vascular flow immediately after indwelling in a blood vessel, and a polymer coating layer formed on at least a metal and/or metal compound containing surface of the substrate. | 12-29-2011 |
| 20110300020 | OXYGENATOR - An oxygenator that inhibits or prevents bubbles in blood from exiting through a blood outlet includes an oxygenator part which performs gas exchange on blood and a heat exchanging part which performs heat exchange on the blood. The oxygenators part has a housing that is generally in a rectangular parallelepiped form, with a hollow fiber membrane bundle positioned in the housing. The hollow fiber membrane bundle is formed by a multiplicity of hollow fiber membranes adapted to perform gas exchange. Blood flows along a blood passage comprised of gaps between the hollow fiber membranes and contacts the surface of the hollow fiber membranes where gas exchange occurs with gas flowing through the lumens of the hollow fiber membranes. In addition, a filter member is arranged on a downstream side of the hollow fiber membrane bundle so that bubbles present in the blood are caught by the filter member. | 12-08-2011 |
| 20110295360 | STENT - A stent includes a plurality of wavy annular bodies each formed in an annular shape from a wavy linear member, and a connection part provided between the adjacent wavy annular bodies, interconnecting the adjacent wavy annular bodies coaxially, weaker than the wavy annular bodies and rupturable. The connection part extends in a slanting manner relative to an axial direction in which the wavy annular bodies are aligned, and interconnects that one inflexed part of one wavy annular body which is curved in a shape projected toward the other wavy annular body adjacent to the one wavy annular body and that the other inflexed part of the other wavy annular body which is curved in a shape projected toward the one wavy annular body. | 12-01-2011 |
| 20110288441 | CLAMP AND BLOOD COLLECTING DEVICE - A clamp is provided in a blood collecting device that includes a first tube having one end and another end connected to a blood collecting needle and a blood bag, respectively, a second tube branched from a halfway of the first tube through a branched portion, and a block-off member which is provided in the first tube at the blood-bag side beyond the branched portion and which allows the first tube in a blocked state to be opened when torn, in which the clamp is arranged at the branched portion, and is configured to change a state between a first state in which the second tube is opened and a tearing operation of the block-off member is disabled and a second state in which the second tube is closed and a tearing operation to the block-off member is enabled. | 11-24-2011 |
| 20110278264 | GUIDE WIRE - A guide wire includes a first wire disposed on the distal side of the guide wire and a second wire disposed on the proximal side. The second wire has an elastic modulus larger than the first wire. The first wire is joined to the second wire at a welded portion by welding. A coil is disposed on the distal side of the first wire. A cover layer is formed on the outer peripheral surface of the wire member in such a manner as to cover at least the welded portion. The cover layer is made from a material capable of reducing the friction of the cover layer, for example, a fluorocarbon resin or a hydrophilic material, to thereby improve the sliding performance of the guide wire. Such a guide wire is excellent in operationality and kink resistance. | 11-17-2011 |
| 20110275994 | INJECTION NEEDLE ASSEMBLY AND DRUG INJECTION DEVICE - To securely position a needle tip and a blade face of a needle tube inserted into the skin in a predetermined site of a living body, such as the upper layer of skin, an injection needle assembly includes a needle tube having a needle tip capable of puncturing a living body, a hub holding the needle tube, a stabilizer, and a guide portion. The stabilizer is formed in a tubular shape surrounding the circumference of the needle tube, and an end face is pressed against the skin, and thereby a raised portion of the skin is formed in a tube hole. The guide portion is arranged on the stabilizer, and is adapted to recognize a press-in distance y of the stabilizer to the skin. | 11-10-2011 |
| 20110274918 | MEDICAL DEVICE HAVING SURFACE LUBRICITY IN WET STATE - A medical device wherein a metal base and a surface lubricating layer are fixed with each other more firmly. The medical device permanently exhibits excellent surface lubricity when in use. A medical device which has a lubricating surface when wet, is characterized by comprising a base layer which is composed of a metal material, an intermediate layer which covers at least a part of the base layer and is composed of a compound that has a plurality of thiol groups in each molecule, and a surface lubricating layer which covers the surface of the intermediate layer and is composed of a hydrophilic polymer that has a reactive functional group. The medical device is also characterized in that the surface lubricating layer is bonded to the base layer via the intermediate layer by reacting the compound having thiol groups with the hydrophilic polymer. | 11-10-2011 |
| 20110274917 | MEDICAL DEVICE HAVING SURFACE LUBRICITY IN WET STATE - A medical device wherein a surface lubricating layer and one of various polymer bases are fixed with each other firmly by a relatively simple technique. The medical device permanently exhibits excellent surface lubricity when in use. The medical device has a lubricating surface when wet, and includes a base layer at least the surface of which is composed of a polymer material, a compound (thiol compound) which is supported on at least a part of the base layer and has a plurality of thiol groups in each molecule, and a surface lubricating layer which covers the thiol compound and is composed of a hydrophilic polymer that has a reactive functional group. | 11-10-2011 |
| 20110257338 | HYDROPHILIC MATERIAL, MEDICAL MATERIAL AND SUSTAINED DRUG RELEASE MATERIAL - A hydrophilic material having a hydrophilic nature and being biocompatible and processable into nanoparticles wherein a hydrophilic monomer such as threitol or a hydrophilic polymer such as polyethylene glycol is attached to the βposition of an α, β-unsaturated carboxyl group of a (co)polymer comprising an aromatic compound such as 4-hydroxycinnamic acid in which an aromatic ring is substituted by the α, β-unsaturated carboxyl group and one or more hydroxyl groups. In particular, a hydrophilic material having a nanoparticle size which is highly dispersible in water, can well migrate into the blood and is useful as a drug carrier, a medical material and a sustained drug release material. | 10-20-2011 |
| 20110245844 | MEDICAL ROBOT SYSTEM - A medical robot system includes a forceps arm provided with a forceps manipulator and a camera arm provided with an endoscope. The forceps manipulator and the endoscope are inserted into a living body through a common insertion implement. The system further includes an operating unit that generates a control signal to control the forceps manipulator and the forceps arm, a forceps motion control unit that controls motions of the forceps manipulator and the forceps arm according to the control signal from the operating unit, an endoscope motion control unit that controls motions of the endoscope and the camera arm, and an interference avoiding unit that controls an interference avoiding motion of the camera arm to avoid interference between the camera arm and the forceps arm while a visual point of the endoscope is kept constant. | 10-06-2011 |
| 20110245684 | OPTICAL IMAGING DIAGNOSTIC APPARATUS AND THE DISPLAY CONTROL METHOD THEREOF - An optical imaging diagnostic apparatus including: a designating unit for designating a predetermined circumferential-direction position at the circumference of the transmitting and receiving unit on the cross-sectional image displayed; an extraction unit for extracting, within the plurality of line data used for the generation of the cross-sectional image, line data corresponding to circumferential-direction position designated in the designating unit from the storage unit; a calculation unit for calculating attenuation rate in a predetermined region in a radial direction of a body lumen with respect to the extracted line data; and a display unit for displaying the calculated attenuation rate. | 10-06-2011 |
| 20110245683 | OPTICAL IMAGING DIAGNOSTIC APPARATUS AND THE DISPLAY CONTROL METHOD THEREOF - An optical imaging diagnostic apparatus includes a calculation unit for respectively calculating signal-intensity change in the circumferential direction of the circumference of the transmitting and receiving unit and signal-intensity change in the radial direction of a body lumen respectively with respect to a plurality of line data used for generation of a cross-sectional image displayed; a specifying unit for judging, based on the calculated result in the calculation unit, whether or not there exists scatter which scatters the light transmitted from the transmitting and receiving unit in an blood flow area of the body lumen and for specifying the position on the displayed cross-sectional image of the scatter in case of being judged that there exists the scatter; and a display unit for displaying a marker indicating that the scatter exists at the specified position on the displayed cross-sectional image. | 10-06-2011 |
| 20110238101 | PUNCTURE INSTRUMENT - A puncture instrument includes a movable body movably disposed in a case, and a needle unit held by the movable body and having a needle. When a distal end face of the movable body is brought into abutment against a region to be punctured and the case is advanced toward the region to be punctured, the case is advanced together with the needle unit, and the tip end of the needle becomes protruded from the movable body and punctures the region to be punctured. An arm of the needle unit is abutted against and turned about a fulcrum member, thereby withdrawing the needle rearwardly. | 09-29-2011 |
| 20110238030 | BLOOD BAG SYSTEM AND BLOOD TREATING METHOD - The blood bag system includes: a blood treating filter for treating a blood; a first bag for containing therein a blood to be supplied to the blood treating filter; a second bag for containing therein the blood treated by the blood treating filter; storage solution supply means for supplying a blood component storage solution to the blood treating filter; a third bag into which a blood remaining in the blood treating filter replaced by the blood component storage solution is transferred and in which the recovered blood is temporarily contained; and a fourth bag to which a blood component separated from the treated blood contained in the second bag is transferred and in which the thus transferred blood component is contained. | 09-29-2011 |
| 20110238029 | BLOOD BAG SYSTEM AND CASSETTE - A blood bag system includes a BC pooling bag for centrifugation of a buffy coat, a filter for removing white blood cells from a supernatant liquid transferred from the BC pooling bag, a platelet preserving bag for reserving the supernatant liquid that has passed through the filter, a first tube connecting the BC pooling bag and an inlet of the filter, a second tube connecting the platelet preserving bag and an outlet of the filter, and a cassette to be fixed in the centrifugation and separation apparatus. The first tube and the second tube are disposed within the cassette. The cassette includes a first clamp section for closing and opening the first tube, and a second clamp section for closing and opening the second tube. | 09-29-2011 |
| 20110237958 | OPTICAL COHERENT CROSS-SECTIONAL IMAGE FORMING APPARATUS AND CONTROL METHOD FOR CONTROLLING SUCH APPARATUS - An optical coherent cross-sectional image forming apparatus in which light outputted from a light source is divided into a measurement light and a reference light inside the apparatus and in which a cross-sectional image is formed based on a coherent light, produced from a reflected light obtained by emitting the measurement light to a biological tissue through a probe inserted into a body lumen, and the reference light, wherein the apparatus includes a detector for detecting that a transmitting and receiving unit entered inside a guiding catheter for guiding the probe by using data during the axial-direction movement and a controller for stopping at least a portion of a process associated with from generation to holding of the cross-sectional image based on the optical coherence in a case in which it is detected by the detector that the transmitting and receiving unit entered inside the guiding catheter. | 09-29-2011 |
| 20110224650 | CATHETER - A catheter comprising a sheath to be inserted into a living body, wherein the sheath includes a tubular reinforcement layer of at least one layer, which is formed with a spiral slit continuous from the distal side to the proximal side thereof; a termination end of the spiral slit is provided on the proximal side of the slit proximal portion at the site of the proximal side of the spiral slit; and at the same time, there is formed a slit termination portion in which inclination angle of the spiral slit with respect to the circumferential direction of the reinforcement layer is larger than that of the slit proximal portion | 09-15-2011 |
| 20110223675 | DRUG RELEASE MEANS FROM LIPOSOMES AND METHOD FOR EVALUATING RELEASABILITY - Drug release means from liposomes and a method for evaluating drug releasability of liposome preparations, which are useful for the quality control of a liposome preparation, are simple, accurate and excellent in reproducibility and are able to achieve in vivo/in vitro correlation (IVIVC), are provided. The drug release means from liposomes by causing the shift of chemical equilibrium in the inside of the liposome and the method for evaluating drug releasability by quantitatively determining the drug released to the outside of the liposome. | 09-15-2011 |
| 20110223078 | DEVICE FOR MEASURING BLOOD COMPONENT - A blood glucose meter includes a front attachment part to which a test piece is attached, a measurement part for measuring a component of blood collected via a blood guide passage in the test piece, and a monitor for displaying the measurement results obtained by the measurement part. When the device is placed on a horizontal plane by referring to the display face of the monitor as the upper side and the opposite side as the lower side and placing the display face of the monitor upward, the central axis of the test piece extends obliquely downward toward the front side. The blood glucose meter comprises a main part provided with the monitor and a linking part between the main part and the front attachment part. The top face of the linking part is placed roughly parallel to the central axis line and is provided with an ejector lever. | 09-15-2011 |
| 20110218677 | MEDICAL MANIPULATOR SYSTEM - A medical manipulator system includes a manipulator including a working unit having a distal end at which an end effector for carrying out working is provided and an operating unit including an operating input unit for being operated for an input and a driving source for operating in response to contents of an operation of the operating input unit to drive the end effector, the working unit being removably attached to the operating unit. A controller to which the operating unit can be connected controls at least the driving source. A use history retaining unit is adapted to retain use history data for each working unit. | 09-08-2011 |
| 20110218511 | CONNECTOR, SYRINGE ASSEMBLY, AND CONNECTOR FOR MIXING - A connector is configured to be connected to a syringe assembly provided with at least one syringe having an outer cylinder with a protruding tube-shaped port, and a holder which holds the syringe. The connector includes a connector main body mountable on a container containing a medical solution; a tube-shaped fitting section protruding from the upper section of the connector main body for receiving the syringe to connect the inside of the syringe and the inside of the container when the syringe port is fitted in the fitting section; and fixing means having a lock mechanism that fixes the syringe assembly to the connector main body when the syringe port is fitted in the fitting section, an operating section to release the fixed state provided by the lock mechanism, and a push-out section that pushes out the syringe assembly when the fixing releasing operation is performed. | 09-08-2011 |
| 20110213102 | MEDICAL DEVICE, MEDICAL MATERIAL AND METHOD FOR MAKING SAME - A medical device and medical material using an aromatic biodegradable resin composition, which is not susceptible to decrease in strength and impact resistance during sterilization by ionizing radiation. Provided are ionizing radiation sterilized medical device and medical material, which contain a composition composed of an aromatic polyester-based biodegradable resin and a polylactic acid, with the polylactic acid being 25 to 70 wt % of the weight of the composition. The medical device and medical material are biodegradable, while having excellent strength and impact resistance. | 09-01-2011 |
| 20110202122 | STENT - A stent includes a stent body in which struts are joined mutually while intersecting and which is formed tubularly as a whole, and a drug coat layer on the outer surface of the struts. The strut has a bend which is deformed as the stent body expands/contracts in the radial direction, and the drug coat layer with which the bend is coated is formed in such a manner that the drug coat layer is mountain-shaped in a cross-section perpendicular to the axis of the strut and the ridgeline of the mountain shape extends in a wavy shape along the longitudinal direction of the strut. The drug coat layer deforms relatively easily without using plasticizer as the stent deforms and is not so susceptible to causing problems such as peeling, destruction, damage or falling off of the drug coat later | 08-18-2011 |
| 20110202065 | BONE CEMENT INJECTION NEEDLE - A bone cement injection needle comprises: a hollow outer needle; an outer needle hub affixed to the base end part of the outer needle; an inner needle that can be slidably inserted into the hollow part of the outer needle; and an inner needle hub affixed to the base end part of the inner needle. The outer needle comprises a first side hole located near the tip; a second side hole located near the base end part; and a depressurization passage which connects the first side hole and the second side hole. | 08-18-2011 |
| 20110196475 | STENT FOR PLACEMENT IN LIVING BODY, AND STENT DELIVERY SYSTEM - A stent includes a plurality of first wave-shaped struts extending in the axial direction of the stent and arranged in the circumferential direction of the stent, a plurality of second wave-shaped struts each located between the first wave-shaped struts, and one or more connecting struts each interconnecting the first wave-shaped strut and the second wave-shaped strut which are adjacent to each other, with the one or more connecting struts extending in the axial direction over a predetermined length. The apexes of the second wave-shaped struts are shifted a predetermined distance in the axial direction of the stent relative to the apexes of the first wave-shaped struts which are located close to the apexes in the circumferential direction of the stent and which are curved in the same direction as the apexes. | 08-11-2011 |
| 20110196472 | STENT DELIVERY SYSTEM - A stent delivery system includes a self-expandable stent, a shaft section having a guide wire lumen, and a sheath having distal portion containing the stent. The stent is located at a position which is on the shaft section and near the distal end of the shaft section. The stent delivery system has a stent proximal portion fixing wire and a breaking member. The stent proximal portion fixing wire has one end portion and the other end portion which are fixed to the shaft section, and also has an intermediate portion engaged with a proximal portion of the stent. The breaking member breaks the stent proximal portion fixing wire to release the stent from the engagement. | 08-11-2011 |
| 20110196218 | BLOOD GLUCOSE LEVEL MEASURING APPARATUS AND METHOD, AND MEASUREMENT DATA MANAGEMENT APPARATUS - A blood glucose level measuring apparatus and measurement data management apparatus are provided which can carry out measurement of the blood glucose level of a plurality of patients relatively rapidly and reliably, while also addressing emergency situations. The blood glucose level measuring apparatus includes a patient identifier, blood glucose level measuring device, a date/time counter, a display, and a controller. The controller controls in a normal measurement mode the cross-checking of patient identification information and a patient data table, and then, if patient identification information is not found, measurement of the blood glucose level is inhibited. The controller also controls in an emergency measurement mode in which carrying out of measurement of the blood glucose level is permitted without acquiring the patient identification information by the patient identifier. | 08-11-2011 |
| 20110196217 | BLOOD GLUCOSE LEVEL INFORMATION PROCESSING APPARATUS, BLOOD GLUCOSE LEVEL INFORMATION PROCESSING METHOD AND BLOOD GLUCOSE LEVEL INFORMATION PROCESSING PROGRAM - A blood glucose level information processing apparatus, method and program provide blood glucose values and blood glucose value information within a period or range desired by a user without imposing cumbersome operation on the user. The apparatus, method and program provide blood glucose values and blood glucose value information within a period or desired range by acquiring blood glucose levels measured by a blood glucose level measuring device and date/time of measurement at which the blood glucose levels are measured, displaying a line graph obtained by plotting the blood glucose values within a predetermined period. A slide bar can also be provided, for example on a graph display screen image, whereupon if the slide bar is moved, only the blood glucose values corresponding to a preceding period backdating in response to the amount of movement of the slide bar are plotted on a line graph along a time series. | 08-11-2011 |
| 20110186514 | ARTIFICIAL LUNG - An artificial lung includes a housing, a tubular hollow fiber membrane bundle contained in the housing and providing a multiplicity of hollow fiber membranes having a gas exchange function, a gas inflow port and a gas outflow port communicating with each other through hollow portions of the hollow fiber membranes, and a blood inflow port and a blood outflow port through which blood is distributed. The tubular hollow fiber membrane bundle has a cylindrical overall shape, and a filter member having a bubble-trapping function is provided on an outer peripheral portion of the tubular hollow fiber membrane bundle. | 08-04-2011 |
| 20110184383 | SYRINGE PUMP - A syringe pump includes: a syringe mounting part on which to mount a syringe outer cylinder of a syringe; a clamp which is pulled downward by an elastic member, contacts an upper surface of the mounted syringe outer cylinder and thereby fix the syringe outer cylinder; a slider which holds a plunger flange of a plunger of the mounted syringe by levers and which pushes out the plunger; and a display or monitor of which the display is controlled by the computer. Regarding an operation of mounting the syringe outer cylinder onto the syringe mounting part, an operation of setting the plunger flange into the slider, and an operation of fixing the syringe outer cylinder with the clamp, the display or monitor alternately displays the respective states before and after the operations at a predetermined interval. | 07-28-2011 |
| 20110178506 | PROTECTOR - A protector which is used to cover a distal portion of a guide wire protruding from a distal opening of a tube body includes a first half body and a second half body which are movable between an open state and a closed state. Each of the first half body and the second half body includes a guide wire sandwiching and holding portion which mutually sandwich and hold the distal portion of the guide wire cooperatively in the closed state of the protector. Each of the first half body and the second half body also includes a tube body sandwiching and holding portion which mutually sandwich and hold the tube body cooperatively in the closed state of the protector. | 07-21-2011 |
| 20110166533 | PROTECTOR AND PROTECTOR ASSEMBLY - A protector includes a supporting member mounted on a needle assembly having a needle main body; an outer cover member arranged to incline to the needle main body by having an arm axially supported to the supporting member; and an inner cover member arranged inside the outer cover member. The outer cover member has a cylindrical body having a needle slit extending in an axial direction for insertion of the needle main body. The inner cover member has an arcuate column, which interlocks with the needle assembly when the outer cover member inclines to insert the needle main body into the needle slit, and rotates by sliding on the inner surface of the cylindrical body. The arcuate column has a circular arc cross-section with an area facing at least the needle slit opened to the cylindrical body at an opened position, the needle slit being covered at a closed position. | 07-07-2011 |
| 20110166520 | INJECTION NEEDLE AND DRUG INJECTION DEVICE - A needle tip of a needle tube stuck in the skin is caused to be reliably positioned in the skin upper layer part and the injected drug is caused not to leak to the outside of the body. | 07-07-2011 |
| 20110160693 | MEDICATION-CONTAINING CONTAINER - A medication-containing container includes a container body having at its front end side a mouth section through which liquid can enter and exit the container body and made of a flexible material, and also with a medication contained in the container body and dissolved by the liquid flowing into the container body. In the medication-containing container, the container body has two flat sections facing each other with a gap therebetween in an initial state in which the container body is not filled with liquid, a frame section on the outer peripheries of the flat sections, and an easily deformable section interconnecting at least either of the pair of flat section and the frame section. When the container body is filled with liquid, the easily deformable section deforms to separate the flat sections from each other, increasing the gap between the flat sections to increase the volume of the container body. | 06-30-2011 |
| 20110160671 | INDWELLING NEEDLE ASSEMBLY - An indwelling needle assembly comprises an inner needle, a hollow outer needle receiving the inner needle and secured to an outer needle hub having a resin projection, and an elastic protector which has a connection member with a projecting part engageable with the projection and which is detachably connected to the outer needle hub by the engagement of the projecting part with the projection. The outer needle hub projection includes a sliding surface on which the projecting part slidingly moves. The connection member can take a first state in which the projecting part engages the projection and a second state in which the projecting part is disengaged from the projection. When the connection member changes from the first state to the second state, the projecting part slidingly moves along the projection sliding surface of the projection. A part of the projecting part contacting the sliding surface is formed of resin. | 06-30-2011 |
| 20110152791 | MEDICAL INSTRUMENT - A medical instrument to be inserted into a living body before being used. The medical instrument is provided with a medical instrument main body including a long linear body having flexibility on which a coating layer covering at least the outer periphery on the distal side thereof is formed. The coating layer composes of a first layer which includes a material containing a low-friction resin material capable of lowering friction and a binder resin material serving as a binder; a second layer which is formed on the first layer and includes a material containing a low-friction resin material and a pigment and in which the content of a binder resin material is lower than the binder resin material content of the first layer or nil; and a third layer which is formed on the second layer and includes a material containing a low-friction resin material. | 06-23-2011 |
| 20110137207 | BLOOD COMPONENT MEASUREMENT DEVICE AND TIP FOR BLOOD MEASUREMENT - A blood component measurement device has a puncturing unit provided inside a housing and having a puncture needle; a button unit for advancing and retreating the puncture needle; a contact mechanism coming into contact with the skin of a person to be measured; and a holder for displaceably holding the puncturing unit. The blood component measurement device also has an introduction section at the substantially center of a contact member. After the skin is punctured by the puncture needle provided at the substantially center of the mechanism, the introduction section introduces blood to testing paper when the contact member of the contact mechanism is displaced in a sliding manner along a guide member. | 06-09-2011 |
| 20110137203 | PUNCTURE INSTRUMENT - A puncture instrument includes a needle assembly, a hub passage for axially guiding a hub, a needle passage communicating with the hub passage and having a distal end opening for allowing the tip end of a needle to project instantaneously therethrough, two arms having first junctions connected to the hub and inclined rearward in a direction away from the hub in an initial state, two push rods connected to second junctions of the arms and extending rearward, a button for pushing the push rods forwardly, and fulcrum members disposed more closely to the distal end than the arms for abutment against portions of the arms when the arms are moved. When the push rods are pushed forwardly by the button, the arms push the needle assembly forwardly, thereafter have portions thereof brought into abutment against the fulcrum members, and turn to pull the needle assembly rearward. | 06-09-2011 |
| 20110132482 | CONNECTOR AND INFUSION TUBE SET - A connector includes an inlet port into which liquid is poured and which has a first flow path for the liquid, a liquid discharge port to which a tube body is connectable and which has a second flow path discharging liquid from the first flow path to the connected tube body, a gas discharge which discharges air in the first flow path, and a blocking device which, when the liquid is poured in the first flow path, temporarily stops the liquid flow. Use of the connector involves sealing an opening section of the liquid discharge port, pouring liquid in the inlet port, causing air in the first flow path to be discharged, temporarily stopping the flow of the liquid in the first flow path, unsealing the opening section of the liquid discharge port, connecting the tube body to the liquid discharge port, and resuming flow of the liquid. | 06-09-2011 |
| 20110129373 | BLOOD PUMP APPARATUS - A blood pump apparatus includes a housing having a blood inlet port and blood outlet port, a pump unit including an impeller that rotates within the housing, and an impeller rotational torque generation section. The housing includes a plurality of magnetic members embedded between the impeller and the impeller rotational torque generation section for transmitting a magnetically attractive force generated by the impeller rotational torque generation section to an impeller body. The pump device includes a non-contact bearing mechanism for rotating the impeller without contacting with the inner surface of the housing when the impeller is rotated by the impeller rotational torque generation section. | 06-02-2011 |
| 20110118568 | ASSISTANCE DEVICE - Disclosed is an assistance device which can be used for the puncture into the skin with a puncture tool having a puncture needle and the measurement of a desired component in the blood with a blood glucose monitoring system equipped with a measurement tool. The assistance device comprises a main body which contacts with the skin and a lid which is connected to the main body in a freely openable and closable manner, wherein one of the main body and the lid has a puncture guide for positioning the puncture needle toward a position on the skin to be punctured with the puncture needle, and the other has a blood collection guide for positioning the measurement tool toward the position on the skin punctured with the puncture needle. | 05-19-2011 |
| 20110106239 | STENT AND STENT DELIVERY DEVICE - A stent has a plurality of wavy annular members arranged adjacently to each other in an axial direction of the stent, with the adjacent wavy annular members connected with each other. Each of the wavy annular members has a plurality of one-end side bent portions each having an apex at one-end side of the stent in an axial direction thereof and a plurality of other-end side bent portions each having an apex at the other-end side of the stent in the axial direction thereof. An apex of each of the one-end side bent portions of each wavy annular member penetrates into a space formed between the adjacent other-end side bent portions of one of the adjacent wavy annular members. An apex of each of the other-end side bent portions of each wavy annular member penetrates into a space formed between the adjacent one-end side bent portions of the other of the adjacent wavy annular members. The apex of the one-end side bent portion of each wavy annular member and the apex of the other-end side bent portion of the adjacent wavy annular member curve in an approach direction, thus engaging each other. | 05-05-2011 |
| 20110106046 | CONNECTOR ASSEMBLY - A connector assembly is provided with a first connector equipped with a first connector body, a hollow needle supported on the inner side of the first connector body and having a side hole ( | 05-05-2011 |
| 20110098966 | ELECTRONIC CLINICAL THERMOMETER AND OPERATION CONTROL METHOD - The electronic clinical thermometer includes a thermistor, a reference resistor, a voltage switch for selectively applying a voltage in order to accumulate electric charge in a capacitor via the thermistor or reference resistor, an A/D converter for detecting a voltage change occurring when removing the electric charge accumulated in the capacitor, and outputting an ON signal while the capacitor has a voltage equal to or higher than a predetermined voltage, a timer for measuring the duration of the ON signal, and an arithmetic processor for calculating the ambient temperature of the thermistor by using the discharge time when removing the electric charge accumulated in the capacitor via the thermistor, and the average value of the discharge times when removing the electric charge accumulated in the capacitor via the reference resistor immediately before and after removing the electric charge accumulated in the capacitor via the thermistor. | 04-28-2011 |
| 20110092776 | MEDICAL MANIPULATOR - A medical manipulator and a cleaning method therefor are provided. The medical manipulator includes an operation command unit equipped with a motor, and a working unit, which is detachable with respect to the operation command unit. A connector of the working unit is connected to the operation command unit, and includes pulleys that engage with the motor, the connector serving to rotatably retain the pulleys therein. The connector has an elongate shape extending in the longitudinal direction of a connecting shaft, and a first cleaning hole is arranged in an end portion of the connector that is opposite to a side on which the connecting shaft is connected. A second cleaning hole opens into an interior cavity, in the vicinity of an end portion on the side where the connecting shaft is connected. The end portions are shaped substantially hemispherically. | 04-21-2011 |
| 20110077602 | INJECTION NEEDLE ASSEMBLY AND MEDICINE INJECTION APPARATUS - An injection needle assembly includes a needle having a needle point to puncture skin, a needle hub including a first member which holds the needle, and a second member in which a discharge part of a syringe is to be fitted, and an elastic member disposed inside the second member to make liquid-tight close contact with the inner surface of the second member, with the elastic member having an insertion hole in which the needle tube is inserted. | 03-31-2011 |
| 20110077592 | PUNCTURE NEEDLE ASSEMBLY AND MEDICINAL LIQUID INJECTOR - A puncture needle assembly has a needle tube, a protector capable of moving between a first position at which the protector covers the tip of the needle tube and a second position at which the tip is exposed, a body for movably supporting the protector and having an elastic deformable section, and an engagement preventing member removably mounted to the base end of a protector body. The protector has a rib. A portion on the head end side of the rib forms a contact section, and a portion on the base end side of the rib forms an engaging section engaging with the elastic deformable section. When the protector moves from the first position to the second position, the engagement preventing member moves together with the protector to prevent the engaging section from engaging with the elastic deformable section and elastically deforms the elastic deformable section. | 03-31-2011 |
| 20110074148 | CONNECTOR ASSEMBLY - A connector assembly includes a first connector having an outer tube and an inner tube, the outer tube being equipped with a pin having a first flow path, the inner tube being equipped with a first valve element opening and closing the first flow path; a second connector having a second flow path and a second valve element for opening and closing the second flow path; a locking device interconnecting, in an assembled state in which the first and second connectors are assembled together, the inner tube and the second connector; and an unlocking device for unlocking the connection between the inner tube and the second connector effected by the locking device. The first and second flow paths are interconnected in the assembled state. In this interconnected state, the connection between the inner tube and the second connector by the locking device cannot be unlocked by the unlocking device. | 03-31-2011 |
| 20110071501 | MEDICAL DEVICE MANUFACTURING METHOD AND MEDICAL DEVICE ASSEMBLY - A medical device in which a part to be secondarily shaped comprises a molded silicone rubber article is subjected to heatless shaping by irradiation with electron-rays. The irradiation with electron-rays enables shaping and, furthermore, sterilization under some conditions. In a medical device comprising a part in which at least a silicone rubber is used and the mechanical properties of the silicone rubber preferentially appear, the shape of the above-described part upon molding is deformed with the use of a correcting member to a level exceeding the desired deformed shape and maintained in this state. Next, electron-ray irradiation is conducted in this state and then the correcting member is eliminated. Thus, the desired deformed shape intermediate between the shape upon the molding and the shape upon the electron-ray irradiation can be obtained. | 03-24-2011 |
| 20110062616 | TEST PAPER AND POROUS MEMBRANE - A test paper includes a porous membrane capable of separating an object that should be filtered out of a sample by filtration, the porous membrane carrying a reagent capable of reacting with a specified component of the sample to result in coloring. The porous membrane includes a first layer having a surface on which the sample is supplied and a second layer having a surface at which sample percolation and measuring are effected, the first layer composed of large pore portions, the surface of the first layer consisting of a smooth surface having open pore portions, the second layer composed of minute pore portions the surface of the second layer consisting of a surface having open pore portions. The porous membrane has a thickness of 50 to 200 μm and a porosity of 60 to 95%. | 03-17-2011 |
| 20110058982 | METHOD FOR RADIATION STERILIZATION OF HYDROPHILIC POLYMER-COATED MEDICAL DEVICE - A radiation sterilization method of a disposable medical device and a manufacturing method are provided, which method comprising the steps of packaging a disposable medical device, which has applied thereto with hydrophilic polymer coating, with a gas permeable packaging material, controlling a product moisture content of the thus packaged medical device by maintaining the device in a given humidity atmosphere for not less than a time at which an equilibrated moisture content is reached, and subjecting, to radiation sterilization, the medical device whose product moisture content has been controlled, so that an eluted matter is reduced in amount and a sliding performance is ensured according to the radiation sterilization method of the hydrophilic polymer-coated, disposable medical device and the manufacturing method. | 03-10-2011 |
| 20110054404 | MEDICAL INSTRUMENT - An indwelling needle assembly has a hollow outer needle fixed to an outer needle hub, an inner needle in the outer needle and fixed to an inner needle hub, and a protector. A step section of the outer needle hub serves as a speed reducer that reduces the speed, in the direction of the flow path axis of a main pipe, of a liquid portion flowing in the flow path, the portion flowing along that portion of the inner surface of the main pipe located on that side of the main pipe on which a branch flow path is located. The step section has an opening in the inner surface of the main pipe located at a position corresponding to a front end opening of the branch flow path. The step section forms a space between the opening and the front end opening of the branch flow path. | 03-03-2011 |
| 20110054403 | INDWELLING NEEDLE ASSEMBLY AND METHOD OF USING THE SAME - An indwelling needle assembly, includes an inner needle having a sharp needle point at a distal end thereof, an inner needle hub fixed to a proximal portion of the inner needle, a hollow outer needle into which the inner needle is inserted, and an outer needle hub fixed to a proximal portion of the outer needle. The indwelling needle assembly is designed to be used with a thumb in contact with a proximal portion of the inner needle hub. The inner needle hub is provided with a finger hold at the proximal portion thereof. At least a part of the finger hold is formed from a material less liable to slip on a medical glove. | 03-03-2011 |
| 20110054402 | INDWELLING NEEDLE ASSEMBLY AND METHOD OF USING THE SAME - An indwelling needle assembly, including an inner needle having a sharp needle point at a distal end thereof; an inner needle hub which is fixed to a proximal portion of the inner needle and which has a proximal end face; a hollow outer needle into which the inner needle is inserted; and an outer needle hub fixed to a proximal portion of the outer needle, the inner needle is adhered and fixed to the inner needle hub with an adhesive at a proximal portion thereof, and the inner needle hub is provided with a projected part formed by projecting the adhesive toward a proximal side relative to the proximal end face. | 03-03-2011 |
| 20110054065 | MEDICAL INSTRUMENT, MEDICAL MATERIAL, AND METHOD FOR PRODUCTION OF THE MEDICAL INSTRUMENT AND MEDICAL MATERIAL - Disclosed are a medical instrument and a medical material each comprising an aliphatic polyester resin composition, which are hardly reduced in strength and impact resistance upon the sterilization by ionizing radiation or have excellent shape-retaining properties after a heat treatment. Specifically, a medical instrument and a medical material both sterilized by ionizing radiation are provided, each of which contains a biodegradable resin and a polycarbodiimide compound in an amount of 0.1 to 10% by weight on the resin. The biodegradable resin is polybutylene succinate, a copolymer of polybutylene succinate, or a mixture of polybutylene succinate and a copolymer of polybutylene succinate with polylactic acid or poly(3-hydroxyalkanoate). A method of producing such medical instrument and medical material is also provided. | 03-03-2011 |
| 20110046643 | SUTURING AND LIGATING METHOD - A manipulator includes a distal-end working unit having a rolling mechanism and an opening and closing mechanism. A forceps includes a gripper on a distal end thereof. A curved needle of a suture-needle assembly is inserted through an incision in a body cavity within a living body, while leaving a portion of a suture strand of the suture-needle assembly uninserted in the tissue. The gripper grips the curved needle. The suture strand is wound around the gripper a predetermined number of times by turning a proximal end portion of the curved needle with the rolling mechanism. The gripper grips the portion of the suture strand, which has not been inserted into the tissue. The gripper is then withdrawn through loops of the suture strand, which are wound around the gripper. The distal-end working unit and the gripper are moved relatively to each other in order to form a knot across the incision. | 02-24-2011 |
| 20110046309 | BIOABSORBABLE MATERIAL AND IN-VIVO INDWELLING DEVICE MADE THEREOF - A bioabsorbable material which is flexible and degradable at a controlled rate, and an in-vivo indwelling device made thereof. The bioabsorbable material is a copolymer composed of an aromatic compound having an α,β-unsaturated carboxylic group and at least one hydroxyl group as substituents on the aromatic ring, and a polycarbonate or a monomer constituting polycarbonate. Alternatively, it is a copolymer composed of, as the first component, an aromatic compound having an α,β-unsaturated carboxylic group and at least one hydroxyl group as substituents on the aromatic ring, as the second component, an aromatic compound having an α,β-unsaturated carboxylic group and at least two hydroxyl groups as substituents on the aromatic ring, and, as the third component, a polycarbonate or a monomer constituting polycarbonate. | 02-24-2011 |
| 20110040280 | INJECTOR - An injector includes a support tube having one end surface to be brought into contact with skin, a movable tube advanceable in the support tube in the direction of the skin, an injection needle communicating with the movable tube, a plunger advanceable in the movable tube in the direction of the skin to introduce medicinal liquid filled in the movable tube to the injection needle, and a sealing material provided at the tip of the support tube and penetratable by the injection needle to penetrate the sealing material. In an initial state, the tip of the injection needle is sealed by the sealing material. | 02-17-2011 |
| 20110040209 | BODY FLUID SAMPLING UNIT - A body fluid sampling unit includes a puncture device including a needle having a sharp needle point and a drive mechanism for operating the needle to puncture a living body surface with the needle point, a tip including an introducing section for introducing a body fluid flowing out from a puncture portion of the living body surface punctured with the needle point, a test paper for detecting a predetermined component in the body fluid, and a tip body mounted to a component measuring device for measuring the quantity and/or property of the predetermined component detected by the test paper; and a case including a mechanism containing section for containing the puncture mechanism so that the needle point of the puncture mechanism can be moved by the drive means, and a sampling implement containing section for containing the body fluid sampling implement so that the tip can be taken out. | 02-17-2011 |
| 20110034830 | BODY FLUID SAMPLING UNIT - A body fluid sampling unit includes a puncture device including a needle having a sharp needle point and a drive mechanism for operating the needle to puncture a living body surface with the needle point, a tip including an introducing section for introducing a body fluid flowing out from a puncture portion of the living body surface punctured with the needle point, a test paper for detecting a predetermined component in the body fluid, and a tip body mounted to a component measuring device for measuring the quantity and/or property of the predetermined component detected by the test paper; and a case including a mechanism containing section for containing the puncture mechanism so that the needle point of the puncture mechanism can be moved by the drive means, and a sampling implement containing section for containing the body fluid sampling implement so that the tip can be taken out. | 02-10-2011 |
| 20110034412 | VISUALLY OBSERVABLE MATERIAL FOR MEDICAL TREATMENT - A visually observable material for medical treatment, which is preferable as an adhesion preventive material and a hemostatic material for biological organisms includes a crosslinking composition comprising at least two components of a crosslinking polysaccharide derivative with an active ester group reactive with active hydrogen in the co-presence of an alkali, where the active ester group is preliminarily introduced in a side chain of a polysaccharide and the crosslinking polysaccharide derivative is not yet crosslinked, and a carbonate including at least one type of carbonate generating divalent carbonate ion in an amount at a mass ratio of 0.03 or more to the polysaccharide derivative. | 02-10-2011 |
| 20110024929 | APPARATUS FOR PRODUCING LIPOSOMES AND METHOD OF PRODUCING LIPOSOMES - Disclosed herein are an apparatus for producing liposomes and a method of producing liposomes by which it is made possible to produce liposomes under sterile conditions during the manufacturing process while monitoring in line the particle diameter of liposomes. The apparatus for producing liposomes includes a unit for regulating the particle diameter of liposomes, a supply flow channel for supplying the particle diameter regulating unit with a solution under processing containing a liposome-forming lipid, and a discharge flow channel for discharging from the particle diameter regulating unit a solution under processing containing liposomes, the supply flow channel having an input port through which the solution under processing containing the liposome-forming lipid is put into the supply flow channel, wherein the discharge flow channel has a first light transmitting part at least a portion of which is made of material transparent to light, and also has at least a first light transmittance measuring unit which measures the light transmittance of the solution under processing containing liposomes by directing light to the first light-transmitting part from the outside of the first light-transmitting part. A method of producing liposomes by use of the apparatus. | 02-03-2011 |
| 20110021890 | SET FOR DETERMINING BLOOD TYPE AND COVER BODY - Disclosed is a set for determining whether blood obtained in puncture tools by puncturing a blood vessel is venous blood or arterial blood easily, and ensuring handling under a sterile state. A set for determining blood type has a cover body to be attached to a syringe set, and a blood type determination unit to be housed in the cover body. The blood type determination unit comprises a light projecting portion and a light receiving element, and a blue output LED and a red output LED showing a judgment result based on a signal obtained from the light receiving element. The cover body has a body and a lid that are combined with each other to cover the blood type determination unit, a partition for passing blood between the light projecting portion and the light receiving element, and a pair of measurement windows for transmitting light between the light projecting portion and the light receiving element through the partition. | 01-27-2011 |
