Abstract: A clot retrieval device 1 for removing occlusive clot from a blood vessel, the device comprises an inner elongate body 3 having a collapsed delivery configuration and an expanded deployed configuration and an outer elongate body 2 at least partially overlying the inner elongate body 2. The outer elongate body 2 is expandable to a radial extent which is greater than the radial extent of the inner body 3 in the deployed configuration to define a clot reception space 11. The outer elongate body 2 comprises a distal end portion 24,49 and the inner elongate body 3 comprises a main body portion 10 and a distal portion which extends in the deployed configuration towards the outer elongate body 2 to a greater extent than the main body portion. The distal portion 10 of the inner elongate member 3 and the distal end portion 24,49 of the outer elongate body 2 together define a three dimensional protective structure to substantially prevent distal egress of clot or clot fragments from the device.

Abstract: A clot retrieval device may include an elongate shaft and an expandable section. The expandable section may include a framework of interconnected strut elements. The connection region between adjacent strut elements may include crown elements. Additionally, the framework may be formed from a substrate material and at least a portion of a plurality of said strut elements may be coated with a coating material. Further, at least a portion of a plurality of said crown elements may not be coated with said coating material.

Abstract: A clot retrieval device may include an elongate member and an expandable clot engaging element configured to extend across the clot in its expanded state. The expandable clot engaging element may include a first monolithic structure and a second monolithic structure. The first monolithic structure may encircle the second monolithic structure over at least a portion of its length. The second monolithic structure may include a proximal section, an intermediate section, and a distal section. The distal section may include an expansion.

Abstract: A system may comprise a clot engagement element having a collapsed delivery configuration and an expanded configuration for engaging with a clot and for dislodging the clot from a first vessel segment. An elongate member may be configured to apply a pull force to the clot engaging element to dislodge the clot from the first vessel segment. A clot removal catheter may include a lumen at its distal end sized to receive the clot and configured to maintain a stable position in a second blood vessel segment proximal of and larger in diameter than the first blood vessel segment. A distal end of the elongate member may be configured to protect a third blood vessel segment between the first and second blood vessel segments from tractive forces transmitted by the elongate member during clot dislodgement from the first vessel segment.

Abstract: Non-return valve, in particular for medical purposes, consisting of a first hose connection housing and a second hose connection housing and a membrane disk which is made from flexible material, is arranged between the two hose connection housings, and can be raised up from an annular valve seat which results in an inlet space which is connected to an inlet passage. A medium-permeable formation which faces the membrane disk is arranged on the inlet side into the inlet space, which formation supports the membrane disk against overextension in the case of high return pressures.

Abstract: A clot retrieval device (9501) for removing occlusive clot from a blood vessel comprises an inner elongate body (9503) and an outer elongate body (9504) at least partially overlying the inner elongate body (9503). The device also comprises an elongate member or shaft (9502) having a proximal end which extends exterior of a patient so that a user can retrieve the stent-basket device and captured clot by retracting the shaft (9502). The outer elongate body (9504) and the inner elongate body (9503) are connected to the distal end of the shaft (9502) and are expandable relative to the shaft (9502) from a collapsed delivery configuration to an expanded deployed configuration. The outer elongate body (9504) is expandable relative to the inner elongate body (9503) to a radial extent which is greater than the radial extent of the inner body (9503) in the deployed configuration.

Abstract: A clot retrieval device (9501) for removing occlusive clot from a blood vessel comprises an inner elongate body (9503) and an outer elongate body (9504) at least partially overlying the inner elongate body (9503). The device also comprises an elongate member or shaft (9502) having a proximal end which extends exterior of a patient so that a user can retrieve the stent-basket device and captured clot by retracting the shaft (9502). The outer elongate body (9504) and the inner elongate body (9503) are connected to the distal end of the shaft (9502) and are expandable relative to the shaft (9502) from a collapsed delivery configuration to an expanded deployed configuration. The outer elongate body (9504) is expandable relative to the inner elongate body (9503) to a radial extent which is greater than the radial extent of the inner body (9503) in the deployed configuration.

Abstract: An embolic filter having a filter support frame with a collapsed and an expanded configuration and a collapsible filter body supported by the support frame. The filter body has inlet and outlet ends. The filter body includes a proximal section having a longitudinally extending cylindrical shape and a distal section having a longitudinally extending conical shape that tapers in the distal direction. The support frame includes a plurality of alternating first segments such that, when the support frame is in the expanded configuration, the alternating first segments circumferentially extend in a first zigzag path to support the proximal, cylindrically shaped section of the filter body. The support frame includes a plurality of alternating second segments such that, when the support frame is in the expanded configuration, the alternating second segments circumferentially extend in a second zigzag path to support the proximal, cylindrically shaped section of the filter body.

Abstract: A clot retrieval device (9501) for removing occlusive clot from a blood vessel comprises an inner elongate body (9503) and an outer elongate body (9504) at least partially overlying the inner elongate body (9503). The device also comprises an elongate member or shaft (9502) having a proximal end which extends exterior of a patient so that a user can retrieve the stent-basket device and captured clot by retracting the shaft (9502). The outer elongate body (9504) and the inner elongate body (9503) are connected to the distal end of the shaft (9502) and are expandable relative to the shaft (9502) from a collapsed delivery configuration to an expanded deployed configuration. The outer elongate body (9504) is expandable relative to the inner elongate body (9503) to a radial extent which is greater than the radial extent of the inner body (9503) in the deployed configuration.

Abstract: A device including a processor which automatically allocates and transfers funds in a sweep account between a primary on-balance demand account and one or more off-balance accounts in a manner which assists the bank in maintaining an optimal liquidity profile and capital structure. The device is adapted to prepare and analyze current data pertaining to the liquidity profile and capital structure of a bank and compare this data to predetermined reference values stored in data storage means of the device. The device has an allocation unit which utilizes an algorithm in order to allocate an amount of funds to transfer between an on-balance account and one or more off-balance accounts which will provide an optimal liquidity profile and capital structure for the bank.

Abstract: A catheter system 1 has an internal reception space for an embolic protection filter 10 to enable the filter 10 to be transported through a vasculature 20 and a treatment means such as a stent 15 to facilitate treatment. The catheter system may be used for retrieval of a filter 10 and stenting of a lesion with a stent 15. The procedure may also involve post dilatation using an on-board balloon 16.

Abstract: A check valve in particular for medical applications has a first hose connecting casing and a second hose connecting casing and a membrane disk configured between the two hose connecting casings. The membrane disk is made of a resilient material and cooperates with an annular valve seat. The membrane disk is fitted radially outside the valve's seat with apertures leading to a discharge space. The wall of the second hose connecting casing is opposite the apertures and fitted with a surface curved away from the membrane toward the discharge channel. The discharge channel is fitted with an intake mouth in the wall, and conically tapers within a transition segment toward the intake mouth. Recesses communicating with the discharge space are fitted into the transition segment and are dimensioned in a way to substantially compensate the different flow cross-sections between the intake mouth and the discharge channel.

Abstract: The present invention relates to an endoprosthesis having a plurality of web rings coupled by connectors, which include two or more essentially parallel struts and a foot extension protruding from one of the struts. An endoprosthesis constructed according to the principles of the present invention provides an elevated degree of scaffolding to a body lumen while retaining an acceptable degree of flexibility.

Abstract: An embolic protection system comprises an embolic protection filter 1 having a collapsed delivery configuration and an expanded deployed configuration. The filter 1 is housed in the collapsed configuration in a reception space of a delivery catheter 20. The delivery catheter 20 containing the filter 1 is housed in a sealed sterile pouch 35. The filter 1 may be coated with a non-thrombogenic coating and an adhesion preventer 9 such as a silicon gel is used to substantially prevent adhesion of adjacent folds of the filter 1 when the filter is in the collapsed configuration in the delivery catheter 20.

Abstract: The present invention relates to an endoprosthesis having a plurality of web rings coupled by connectors, which include two or more essentially parallel struts and a foot extension protruding from one of the struts. An endoprosthesis constructed according to the principles of the present invention provides an elevated degree of scaffolding to a body lumen while retaining an acceptable degree of flexibility.

Abstract: An embolic protection filter for deployment in a vasculature, the filter having an inlet end and an outlet end, the inlet end having one or more inlet openings sized to allow blood and embolic material enter the filter, and the outlet end of the filter having a plurality of outlet openings sized to allow through passage of blood but to retain undesired embolic material within the filter. The filter is movable between a collapsed configuration for movement through a vasculature, and an outwardly extended configuration for deployment in a vasculature. The filter at least in the collapsed configuration was a guidewire lumen defined at least partially therethrough for passing the filter over a guidewire. The guidewire lumen is defined by a lumen-defining member which is spaced proximally of the distal end of the filter.

Abstract: The method comprises the steps of advancing a guidewire from a first intermediate location to a further intermediate location which is proximal of the treatment location and, subsequently, advancing a medical device over the guidewire toward the further intermediate location. The method may comprise repeating these steps for additional intermediate locations. In one case the treatment location is in the carotid artery. The treatment location may be at or adjacent to the carotid bifurcation. An intermediate location may be at or adjacent to the aortic arch. An intermediate location may be at or adjacent to the carotid take-off. The medical device may be delivered over the guidewire using a delivery catheter. The delivery catheter and the medical device may be advanced through the vasculature without the use of a guide catheter.

Abstract: The present invention relates to an endoprosthesis having a plurality of web rings coupled by connectors, which include two or more essentially parallel struts and a foot extension protruding from one of the struts. An endoprosthesis constructed according to the principles of the present invention provides an elevated degree of scaffolding to a body lumen while retaining an acceptable degree of flexibility.

Abstract: A check valve in particular for medical applications has a first hose connecting casing and a second hose connecting casing and a membrane disk configured between the two hose connecting casings. The membrane disk is made of a resilient material and cooperates with an annular valve seat. The membrane disk is fitted radially outside the valves seat with apertures leading to a discharge space. The wall of the second hose connecting casing is opposite the apertures and fitted with a surface curved away from the membrane toward the discharge channel. The discharge channel is fitted with an intake mouth in the wall, and conically tapers within a transition segment toward the intake mouth. Recesses communicating with the discharge space are fitted into the transition segment and are dimensioned in a way to substantially compensate the different flow cross-sections between the intake mouth and the discharge channel.

Abstract: A check valve is provided, including a first hose connector housing defining an entry passage extending into an entry space at least partially defined by an annular valve seat, a second hose connector housing coupled with the first hose connector housing and defining an exit passage, and a generally flexible perforated membrane disk positioned between the first and second hose connector housings such that the membrane disk selectively engages the valve seat.