Abstract: A surgical tool handle for holding, securing and portioning orthopedic tools is described. The surgical tool handle having a tool attachment mechanism comprising a bias member connected to an actuator. The bias member is positioned within a distal end opening within the handle. Rotation of the actuator causes rotation of the bias member such that when a connection member of a tool, such as a broach, rasp or other cutting tool, is positioned within an opening of the bias member, the bias member wraps around and tightens onto the connection member. Rotating the actuation cable in an opposite direction rotates the bias member in the opposite direction, which thereby releases the tool connection member, and the tool, from the handle.

Abstract: The invention relates to a template for implanting a housing of an implantable unit of a partially implantable hearing instrument, comprising a template plate comprising an implant position marking opening and a template position indicating element which extends substantially normal with regard to the surface of the template plate, wherein the implant position marking opening is designed to mark the position of a receptacle to be created in the patient's temporal bone for receiving an elevated housing positioning portion of the housing, and wherein the template position indicating element is a projection designed to be seen or felt by a surgeon through the patient's skin when the template plate is positioned at the patient's skull to mark the position of said receptacle.

Abstract: The invention relates to a template for implanting a housing of an implantable unit of a partially implantable hearing instrument, comprising a template plate comprising an implant position marking opening and a template position indicating element which extends substantially normal with regard to the surface of the template plate, wherein the implant position marking opening is designed to mark the position of a receptacle to be created in the patient's temporal bone for receiving an elevated housing positioning portion of the housing, and wherein the template position indicating element is a projection designed to be seen or felt by a surgeon through the patient's skin when the template plate is positioned at the patient's skull to mark the position of said receptacle.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: In one embodiment, a surgically implantable adjustable ring comprises a ring body, which includes a closure system having first and second end parts. The ring body is designed to be closed around a tubular organ by the closure system, constricting the tubular organ by forming a loop. The first end part is shaped like a sleeve having a first and second end portions, and is designed to receive the second end part of the ring. The sleeve is substantially perpendicular to the main direction of the first end part of the ring, and the second end part of the ring includes a locking protrusion adapted to hold the sleeve in position, securing the ring in a closed position by engaging the locking protrusion in an opening disposed on the sleeve.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: In one embodiment, a surgically implantable adjustable ring comprises a ring body, which includes a closure system having first and second end parts. The ring body is designed to be closed around a tubular organ by the closure system, constricting the tubular organ by forming a loop. The first end part is shaped like a sleeve having a first and second end portions, and is designed to receive the second end part of the ring. The sleeve is substantially perpendicular to the main direction of the first end part of the ring, and the second end part of the ring includes a locking protrusion adapted to hold the sleeve in position, securing the ring in a closed position by engaging the locking protrusion in an opening disposed on the sleeve.

Abstract: In one embodiment, a surgically implantable adjustable ring comprises a ring body, which includes a closure system having first and second end parts. The ring body is designed to be closed around a tubular organ by the closure system, constricting the tubular organ by forming a loop. The first end part is shaped like a sleeve having a first and second end portions, and is designed to receive the second end part of the ring. The sleeve is substantially perpendicular to the main direction of the first end part of the ring, and the second end part of the ring includes a locking protrusion adapted to hold the sleeve in position, securing the ring in a closed position by engaging the locking protrusion in an opening disposed on the sleeve.

Abstract: In one embodiment, a surgically implantable adjustable ring comprises a ring body, which includes a closure system having first and second end parts. The ring body is designed to be closed around a tubular organ by the closure system, constricting the tubular organ by forming a loop. The first end part is shaped like a sleeve having a first and second end portions, and is designed to receive the second end part of the ring. The sleeve is substantially perpendicular to the main direction of the first end part of the ring, and the second end part of the ring includes a locking protrusion adapted to hold the sleeve in position, securing the ring in a closed position by engaging the locking protrusion in an opening disposed on the sleeve.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: Apparatus and methods are provided comprising an implantable non-hydraulic ring that encircles and provides a controllable degree of constriction to an organ or duct and an external control that powers and controls operation of the ring. The ring includes a rigid dorsal periphery that maintains a constant exterior diameter, and a compliant constriction system that reduces intolerance phenomena. A high precision, energy efficient mechanical actuator is employed that is telemetrically powered and controlled, and maintains the ring at a selected diameter when the device is unpowered, even for extended periods. The actuator provides a reversible degree of constriction of the organ or duct, which is readily ascertainable without the need for radiographic imaging. Methods of use and implantation also are provided.

Abstract: A catheter with a self-expanding stent of a permeable mesh of stiff intersecting fibers is provided. A tubular outer catheter shaft holds the stent under tension at its distal end and from which the stent can be released for placement. A displaceable inner catheter inside the tubular outer catheter shaft supports the stent axially at its proximal end. In order to release the stent, the outer catheter shaft is retracted with respect to the inner catheter. A process for producing this catheter is also described. The stent is secured by gripping it at its proximal end in such a way that it forms a permeable mesh cone that expands automatically together with the stent and has a radius that increases gradually to the radius of the relaxed stent. The stent is securely anchored on the inner catheter with the help of the mesh cone.

Abstract: A catheter with a self-expanding stent of a permeable mesh of stiff intersecting fibers is provided. A tubular outer catheter shaft holds the stent under tension at its distal end and from which the stent can be released for placement. A displaceable inner catheter inside the tubular outer catheter shaft supports the stent axially at its proximal end. In order to release the stent, the outer catheter shaft is retracted with respect to the inner catheter. A process for producing this catheter is also described. The stent is secured by gripping it at its proximal end in such a way that it forms a permeable mesh cone that expands automatically together with the stent and has a radius that increases gradually to the radius of the relaxed stent. The stent is securely anchored on the inner catheter with the help of the mesh cone.

Abstract: A resilient, elastic self-expanding prosthesis comprising a flexible tubular body, the diameter of which is variable under axial movement of the ends of the body relative to each other, said body being composed of several individual rigid but resiliently flexible thread elements with spring properties each of which extends in helix configuration with the center line of the body as a common axis, a number of elements having same direction of winding but being axially displaced relative to each other crossing a number of elements also axially displaced relative to each other but having the opposite direction of winding to form a braided structure, characterized in that the residual tension of the thread elements as they form the structural elements of the tubular body, at least at the end sections thereof, is such that the diameter of the unloaded helix-shaped thread element, at least at the end sections thereof, when removed from the other elements forming the tubular body is not more than about 60% and prefer

Abstract: A device for implantation by insertion into a difficulty accessible location of a substantially tubular, radially expandable prosthesis including in combination such prosthesis and concentric therewith a flexible probe provided with an arrangement for maintaining said prosthesis in a radially contracted state and for releasing same at the desired location. The arrangement includes a hose concentrically surrounding the probe and radially surrounding the prosthesis to form a compartment therefor. The probe has a central axial channel enabling supply of a liquid flushing medium at its other end and the probe is provided with at least one radial aperture opening into the prosthesis compartment to enable flushing of the prosthesis compartment to remove gases therefrom before implantation.

Abstract: A device for transluminal implantation of a substantially tubular, radially expansible prosthesis (2), comprising in combination such prosthesis (2) and concentric therewith a flexible probe (1) with means (200) for maintaining said prosthesis (2) in a radially contracted state and for releasing same at the desired location, said means for maintaining and releasing the prothesis comprising a hose (5) concentrically surrounding said probe (1), one end of said hose being connected to the probe (1), and the hose (5) being folded inside itself to form a double-walled section (51, 52) radially surrounding the prothesis (2), the latter being releasable by axial relative movement of the ends of the hose, characterized by inflatable balloon means (30) positioned between said probe (1) and said prosthesis (2) and substantially coextensive with the latter, whereby after releasing the prosthesis at the desired location in the lumen controlled expansion of the prosthesis and the surrounding lumen wall can be achieved by

Abstract: A device and method for implantation of a prosthesis provides for insertion of the prosthesis in a location which is difficult to access. The prosthesis is held in a radially contracted state by the device. An expandable chamber within the device permits relative movements between elements of the devices as to permit the prosthesis to be inserted and radially expanded in the location.

Abstract: A converter and method of converting thermal images into secondary images, e.g. visible images. The infrared radiation emitted by an object is focused by an optical system to form a thermal image on the free surface of a thermal radiation absorbing layer to one side of a liquid-liquid interface which has low surface tension and is a mixture of two liquid partially miscible at operating temperature and pressure. To convert the thermal image to a visible a parallel beam of light or a beam of light from a point source in the visible range is directed to the other side of the interface and, depending on the selected indices of the interface liquids and whether a prism is used or not; is either transmitted or reflected. The emerging transmitted or reflected beam is then received on a screen or in a detection system where variations of the optical properties of the emerging beam are observed.