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33results about How to "Improve ablation" patented technology

Medical device for use in bodily lumens, for example an atrium

A device positionable in a cavity of a bodily organ (e.g., a heart) may discriminate between fluid (e.g., blood) and non-fluid tissue (e.g., wall of heart) to provide information or a mapping indicative of a position and / or orientation of the device in the cavity. Discrimination may be based on flow, or some other characteristic, for example electrical permittivity or force. The device may selectively ablate portions of the non-fluid tissue based on the information or mapping. The device may detect characteristics (e.g., electrical potentials) indicative of whether ablation was successful. The device may include a plurality of transducers, intravascularly guided in an unexpanded configuration and positioned proximate the non-fluid tissue in an expanded configuration. Expansion mechanism may include helical member(s) or inflatable member(s).
Owner:KARDIUM

Catheter with flexible pre-shaped tip section

A catheter for mapping and / or ablating continuous linear or circumferential lesions at the intersection of a generally flat structure, such as the left atrium, and the ostium of generally cavernous regions of the heart, including pulmonary vein and the pulmonary venous antrum, comprises a catheter body with an intermediate section that is connected to a tip assembly by a highly flexible section. The intermediate section has at its distal end a preformed section, e.g., a curve, the intermediate section being deflectable in a direction opposite to the curve. The highly flexible section presets the tip assembly at an off-axis and / or off-plane angles from the preformed section. Accordingly, the preformed section is adapted to sit in the region and the preset angles of the ablation assembly enable contact with surrounding tissue. A high bending modulus enables the flexible section absorb displacement force applied to the ablation assembly, such as when the tip assembly encounters uneven tissue surface, without displacing the curve from the region. The tip assembly can be irrigated as enabled by a plurality of irrigation ports, a coil electrode, and a porous covering to disperse fluid over the outer surface of the tip assembly.
Owner:BIOSENSE WEBSTER INC

Adjustable length and/or exposure electrodes

An ablation system is provided. The ablation system includes an ablation device having a handle assembly and an electrode assembly. The handle assembly includes a housing configured for operable engagement by a user. The electrode assembly includes a tubular electrode having an open proximal end and a closed distal end. The tubular electrode is movable relative to the housing to adjust an insertable length of the electrode assembly.
Owner:TYCO HEALTHCARE GRP LP

Method for direct engraving of flexographic printing members

A method for engraving a flexographic relief member includes providing a laser engraveable flexographic member; providing a thin engraveable control layer on top of the laser and engraveable flexographic member; the flexographic relief member comprises the laser engraveable flexographic member and the thin engraveable control layer; the engraveable control layer has an engraving sensitivity lower than the flexographic member; and scanning a radiation beam on the flexographic relief member to engrave the flexographic relief member.
Owner:EASTMAN KODAK CO

Medical device for use in bodily lumens, for example an atrium

ActiveUS20140214028A1Increase capacityConvenient location informationDiagnostic recording/measuringSensorsProximateFluid tissues
A device positionable in a cavity of a bodily organ (e.g., a heart) may discriminate between fluid (e.g., blood) and non-fluid tissue (e.g., wall of heart) to provide information or a mapping indicative of a position and / or orientation of the device in the cavity. Discrimination may be based on flow, or some other characteristic, for example electrical permittivity or force. The device may selectively ablate portions of the non-fluid tissue based on the information or mapping. The device may detect characteristics (e.g., electrical potentials) indicative of whether ablation was successful. The device may include a plurality of transducers, intravascularly guided in an unexpanded configuration and positioned proximate the non-fluid tissue in an expanded configuration. Expansion mechanism may include helical member(s) or inflatable member(s).
Owner:KARDIUM
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