3482results about How to "Avoid passing" patented technology

A filter pack includes a filter construction and a sealing system for sealing the construction within a duct or housing. The filter construction has first and second opposite flow faces and is configured for a straight-through flow. The sealing system includes a frame construction and a compressible seal member. The compressible seal member is molded around a portion of the frame construction. The compressible seal member is sufficiently compressible to form a radial seal between and against the frame construction and a surface of a housing when the filter pack is inserted within the housing.

A filter pack includes a filter construction and a sealing system for sealing the construction within a duct or housing. The filter construction has first and second opposite flow faces and is configured for a straight-through flow. The sealing system includes a frame construction and a compressible seal member. The compressible seal member is molded around a portion of the frame construction. The compressible seal member is sufficiently compressible to form a radial seal between and against the frame construction and a surface of a housing when the filter pack is inserted within the housing.

Devices and methods for treating intraocular pressure are disclosed. The devices include shunts for draining aqueous humor from the anterior chamber to the uveoscleral outflow pathway, including the supraciliary space and the suprachoroidal space. The shunts are preferably implanted by ab interno procedures.

A stent for application within an aneurysm the stent comprising an elongated tubular member having a proximal end and a distal end. The stent has a proximal portion expandable from a first diameter to a second diameter. The distal end of the stent may be expandable to a third diameter, which third diameter is larger than the second diameter. The stent may be left disposed across the neck of the aneurysm.

A filter pack includes a filter construction and a sealing system for sealing the construction within a duct or housing. The filter construction has first and second opposite flow faces and is configured for a straight-through flow. The sealing system includes a frame construction and a compressible seal member. The compressible seal member is molded around a portion of the frame construction. The compressible seal member is sufficiently compressible to form a radial seal between and against the frame construction and a surface of a housing when the filter pack is inserted within the housing.

Disclosed is a system for assisting in preventing over heating of the internal electrical components of a computer in the event of a failure of one of the adjacent fans of an array of fans employed to circulate cooling air over the components. The fans include openings through which air is forced from their inlet sides to their outlet sides. The system includes a vent for each fan arranged adjacent to and aligned with the fan opening at its outlet side. The vents are open and closed by vanes, having hinged slats construction to allow them to fall downwardly by their own weight or additional assistance. The vanes are kept open by the airflow created by the fans. Upon the failure of a fan, the absence of airflow through the opening thereof allows the slats of the vane to drop to close off the fan opening and prevent airflow into the fan opening from its outlet side.

A device for connecting a bone fastener to a longitudinal rod is disclosed. The apparatus may have two bores spaced a distance apart and having generally parallel axes. A holding member may be associated with one bore, the member configured to engage a bone fastener such as a bone screw or pedicle hook. A rod coupling member may be associated with the other bore, the member configured to engage a longitudinal rod. The holding member and rod coupling member both are configured to articulate within their respective bores, thus allowing the rod and rod coupling, as well as the holding member and bone fastener, to rotate about the both the first and second axes. The holding member and rod coupling member further may be separately lockable to allow independent locking of the bone fastener and the rod to the connector, thereby preventing or enabling relative rotation as desired.

An inferior vena cava filter (340) for use in the inferior vena cava (4) to capture thrombus (8) passing through the inferior vena cava (4) towards the heart and lungs to prevent pulmonary embolism comprises a proximal support hoop (302), a distal support hoop (312) and a plurality of support struts (303) extending between the proximal support hoop (302) and the distal support hoop (312). The filter (340) also comprises a plurality of capture arms (121) which are movable from a capturing configuration to an open configuration. The capture arms (121) are biased towards the open configuration. A biodegradable suture holds the capture arms (121) in the capturing configuration.

A device for connecting a bone fastener to a longitudinal rod has two bores spaced a distance apart and generally parallel axes. A holding member may be associated with one bore, the holding member configured to engage a bone fastener such as a bone screw or pedicle hook. A rod coupling member may be associated with the other bore, the coupling member configured to engage a longitudinal rod. The holding member and rod coupling member both are configured to articulate within their respective bores, thus allowing the rod and rod coupling, as well as the holding member and bone fastener, to rotate about both bore axes. The holding member and rod coupling member also separately lockable to allow independent locking of the bone fastener and the rod to the connector, thus preventing or enabling relative rotation as desired.

A sheath attached to a guide wire, a tubular shaft member slidable on the guide wire and a filtering assembly constricted within the sheath are movable in a vessel to a position distal to a lesion in the direction of fluid flow. The filtering assembly may be formed from a plurality of angularly spaced splines and a mesh disposed on the splines having properties of passing fluid in the vessel while blocking the passage of emboli in the fluid. The splines may be provided with shape memory for expanding against the wall of the vessel when released from constriction by the sheath. The sheath may be moved relative to the filtering assembly and the support member to release the filter for expansion against the vessel wall. An interventional device can be used to treat the lesion. Any emboli released into the vessel as a result of the interventional treatment are blocked by the filter member while fluid is allowed to pass there through.

Suture Locks, as well as related systems and methods, are provided for fixing strands of one or more sutures relative to tissue. The suture locks, systems and methods are simple and reliable in use, facilitate complete perforation closure and adjustment of the suture strands, and are adaptable to a variety of suture fixation and perforation closure situations. The suture lock includes a locking pin and a retaining sleeve. The locking pin has a main body and a grip. The retaining sleeve has a tubular body with an internal wall defining an internal passageway sized to receive the locking pin therein. The suture lock is operable between a locked configuration and unlocked configuration. In the locked configuration, the suture strands are compressed between the grip and the internal wall of the tubular body.

A fat removal device includes a screen which includes passages through which fat can be extruded, to be cut or melted away from the surface of an internal organ. The device includes a blade to cut the fat or radiofrequency monopolar or bipolar electrodes to melt the fat, aspiration to remove the fat away from the screen and blade, irrigation to irrigate the screen and blade, and an electrocautery member to cauterize the capillary bed of the fat. Methods of using removing the fat layer from the surface of an internal body organ are also described.

A system for treating a selected dermatologic problem and a head for use with such system are provided. The head may include an optical waveguide having a first end to which EM radiation appropriate for treating the condition is applied. The waveguide also has a skin-contacting second end opposite the first end, a temperature sensor being located within a few millimeters, and preferably within 1 to 2 millimeters, of the second end of the waveguide. A temperature sensor may be similarly located in other skin contacting portions of the head. A mechanism is preferably also provided for removing heat from the waveguide and, for preferred embodiments, the second end of the head which is in contact with the skin has a reflection aperture which is substantially as great as the radiation back-scatter aperture from the patient's skin. Such aperture may be the aperture at the second end of the waveguide or a reflection plate or surface of appropriate size may surround the waveguide or other light path at its second end. The portion of the back-scattered radiation entering the waveguide is substantially internally reflected therein, with a reflector being provided, preferably at the first end of the waveguide, for returning back-scattered light to the patient's skin. The reflector may be angle dependent so as to more strongly reflect back scattered light more perpendicular to the skin surface than back scattered radiation more parallel to the skin surface. Controls are also provided responsive to the temperature sensing for determining temperature at a predetermined depth in the patient's skin, for example at the DE junction, and for utilizing this information to detect good thermal contact between the head and the patient's skin and to otherwise control treatment. The head may also have a mechanism for forming a reflecting chamber under the waveguide and drawing a fold of skin therein, or for providing a second enlarged waveguide to expand the optical aperture of the radiation.

A fat removal device includes a screen which includes passages through which fat can be extruded, to be cut or melted away from the surface of an internal organ. The device includes a blade to cut the fat or radiofrequency monopolar or bipolar electrodes to melt the fat, aspiration to remove the fat away from the screen and blade, irrigation to irrigate the screen and blade, and an electrocautery member to cauterize the capillary bed of the fat. Methods of using removing the fat layer from the surface of an internal body organ are also described.

A film deposition apparatus includes a turntable having a substrate mounting area, a first plasma gas supplying part, a second plasma supplying part, a first plasma gas generating part to convert the first plasma generating gas to first plasma, and a second plasma generating part provided away from the first plasma generating part in a circumferential direction and to convert the second plasma generating gas to second plasma. The first plasma generating part includes an antenna facing the turntable so as to convert the first plasma generating gas to the first plasma, and a grounded Faraday shield between the antenna and an area where a plasma process is performed, and to include plural slits respectively extending in directions perpendicular to the antenna and arranged along an antenna extending direction to prevent an electric field from passing toward the substrate and to pass a magnetic field toward the substrate.

A spinal implant is provided which maintains intervertebral spacing and stability within the spine. The spinal implant may include a body and an insert. The body of the spinal implant may be formed of a ceramic material. In some embodiments, the body may be formed of beta tricalcium phosphate. The body may include an opening that is complementary to the insert. The insert may fit within the opening. The insert may include a number of passageways. Some of the passageways may intersect to form a scaffold for bone growth. Bone growth promoting material may be introduced into the insert before the insert is positioned in a body and inserted in a patient between two vertebrae.

The present invention is directed towards methods and apparatus for handling powder in a 3D printer. The invention includes a means of transporting powder from multiple sources to a powder dispensing apparatus with minimal user intervention, thus reducing contamination of the 3D printer and surrounding area with loose powder, while also providing a means of improving the recycling of powder for re-use.

A respirator 10 that has a mask body 14 and a malleable nose clip 12. The mask body 14 is adapted to fit at least over the nose and mouth of a person to define an interior gas space that is separate from the exterior gas space. The mask body 14 has the nose clip 12 secured to it and can include at least one layer of filter media 20. The malleable nose clip 12 comprises a semi-crystalline polymeric material that has an integrated diffraction intensity ratio of at least about 2.0. The nose clip 12 can be deformed into a desired configuration that enables the mask body 14 to maintain a snug fit over a person's nose when the respirator is worn for extended time periods. Because the nose clip 12 does not need to contain metal, the whole respirator 10 can be easily processed as waste in an incinerator when its service has ended.

A humidification unit adapted to be disposed in a patient circuit for humidifying the flow of breathing gas delivered to the patient via the patient circuit by an artificial ventilator system. The humidification unit includes an exothermic member having an outer surface and a plurality of hollow fibers disposed on the outer surface of the exothermic member. Each hollow fiber is defined by a peripheral wall having minute openings large enough to allow a gas to pass therethrough yet small enough to prevent a liquid from passing therethrough. Liquid delivered to the hollow fibers is heated by the exothermic member and the as vapor resulting from the heating passes through the hollow fiber walls and humidifies the flow of breathing gas delivered to the patient.

A tamper-resistant coaxial terminator includes an inner body rotatably captivated within an outer shield. A deformable portion of the inner body extends within an annular recess formed in the outer shield. An optional RF port, containing a resistor, is press-fit within the inner body. The RF port, or alternatively, the inner body, is internally-threaded for engaging the outer conductor of an equipment port. A seal ring extends over the outer conductor of the equipment port and is urged by the outer shield to directly engage the internally-threaded portion of the terminator. A seal is also optionally disposed between the outer shield and the inner body to minimize moisture induced corrosion. A shipping cap, usable at either end of the terminator, helps protect the terminator during shipment and prevents entry of debris.

A printed wiring board has a first switch contact pattern, a second switch contact pattern, and a cutting portion that cuts a plating bar formed thereon. A metal dome is arranged to be in contact with the first switch contact pattern and allows the first switch contact pattern and the second switch contact pattern to be conductive by being deformed. A first sheet attached to the printed wiring board via an adhesive has a first opening portion formed in a region where the metal dome is arranged and a second opening portion formed in the region where a cutting portion is formed. A second sheet is attached to the first sheet via the adhesive to cover the first opening portion and the second opening portion.

A method and apparatus for closing a vascular wound includes an apparatus that can be threaded over a guidewire into place at or adjacent the wound. The apparatus includes a chamber that encloses a hemostatic material therein. When the apparatus is positioned adjacent the wound as desired, the hemostatic material is deployed from the chamber. Blood contacts the hemostatic material, and blood clotting preferably is facilitated by a hemostatic agent within the material. Thus, the vascular puncture wound is sealed by blood clot formation.

The embodiment of the invention discloses an image prediction method and a relevant device. The image prediction method comprises the following steps: determining the motion vector predictors of K pixel samples in a current image block, wherein K is an integer greater than 1, the K pixel samples comprise a first vertex angle pixel sample of the current image block, the motion vector predictor of the first vertex angle pixel sample is obtained on the basis of the motion vector of a preset first spatial domain adjacent image block of the current image block, and the first spatial domain adjacent image block is adjacent to a first vertex angle pixel sample spatial domain; and predicting the pixel value of the current image block on the basis of a non-translational motion model and the motion vector predictors of the K pixel samples. According to the scheme in the embodiment of the invention, the computation complexity of image prediction based on the non-translational motion model is lowered.

A system for thermal cycling a plurality of samples. The system includes a case having a fluid-tight cavity defining an interior volume. A microfluidic array is disposed in the interior volume, the array including a sheet of material having a pair of opposed surfaces, a thickness, and a plurality of through-holes running through the thickness between the surfaces. A thermal cycler having at least one thermally controlled surface is adapted to thermally contact the case.

A modular outdoor grill for cooking over a bed of combustible fuel or by means of convection heating from an externally mounted firebox. The modular grill comprises a housing with an outwardly, horizontally pivotal food-supporting tray, a vertically extending standard for supporting said housing, and either a horizontally reciprocating fuel-supporting grate or an externally mounted firebox.

A medical electrode designed to prevent the passage of harmful electric current to a patient, thereby preventing tissue damage and electrocution. In the preferred embodiment, the inventive medical electrode is comprised of a proximal end, a distal end, a conductive lead connecting the proximal and distal ends, and a fuse located upon the medical electrode for preventing the passage of harmful electric current to a patient. For additional protection from induction current, the preferred location of the fuse is aft of the conductive lead element of the electrode. While a fuse is used in the preferred embodiment, the fuse could be replaced with a diode or a circuit breaker.