Abstract: A method and system for facilitating mirror trading comprising: obtaining first criteria for identifying first target trading position and second criteria for identifying second trading position; automatically opening a first basket of trading positions in accordance with said first criteria, and one or more second baskets of trading positions in accordance with the second criteria; obtaining a liquidation trigger comprising two or more components, each component having a specified percentage weight in respect of the entire liquidation trigger, wherein a first component is applicable to the first basket and a second or more components are applicable to the second or more baskets; and automatically changing the liquidation trigger upon a performance measure satisfying a trigger change criteria, wherein the specified percentage weights are also applicable to said changed liquidation trigger.

Abstract: A method and system for facilitating mirror trading of financial instruments in a trading network comprising a plurality of traders, the method comprising, by a processor operatively coupled to a memory, obtaining from the memory, criteria received from a copying trader for identifying at least one target trading position opened by at least one copied trader in respect of at least one instrument to mirror for the copying trader in a mirror portfolio associated with the copying trader, identifying at least one target trading position satisfying the obtained criteria, automatically opening, in the mirror portfolio, a basket of trading positions comprising one or more mirror positions, each mirror position corresponding to an identified target trading position, obtaining, from the memory, one or more liquidation triggers received from the copying trader to apply to the mirror portfolio, and automatically changing at least one liquidation trigger upon a performance measure for the mirror portfolio satisfying one

Abstract: A stent crimping assembly is provided for crimping a stent from a first diameter to a reduced second diameter. The crimping assembly includes a plurality of movable wedges disposed about a rotational axis to form a wedge assembly. Each wedge includes a respective first side and a second side converging to form a tip portion. The tip portions are arranged to collectively form an iris about the rotational axis thereof. The iris defines a crimp aperture about which the movable wedges are disposed. A control unit is electronically programmed to control the mechanical components. A method of calibrating the control unit includes inserting a quill of known diameter into the iris and reducing the diameter of the iris onto the quill.

Abstract: A stent crimping assembly is provided for crimping a stent from a first diameter to a reduced second diameter. The crimping assembly includes a plurality of movable wedges disposed about a rotational axis to form a wedge assembly. Each wedge includes a respective first side and a second side converging to form a tip portion. The tip portions are arranged to collectively form an iris about the rotational axis thereof. The iris defining a crimp aperture about which the movable wedges are disposed. Each wedge is associated with a stationary structure and an rotational actuation unit such that during rotation of the actuation unit about the rotational axis, the iris is caused to rotate about the rotational axis, relative the stationary structure, for inward movement of the wedges to decrease the size of the aperture and outward movement of the wedges to increase the size of the aperture.

Abstract: A stent crimping assembly is provided for crimping a stent from a first diameter to a reduced second diameter. The crimping assembly includes a plurality of movable wedges disposed about a rotational axis to form a wedge assembly. Each wedge includes a respective first side and a second side converging to form a tip portion. The tip portions are arranged to collectively form an iris about the rotational axis thereof. The iris defining a crimp aperture about which the movable wedges are disposed. Each wedge is associated with a stationary structure and an rotational actuation unit such that during rotation of the actuation unit about the rotational axis, the iris is caused to rotate about the rotational axis, relative the stationary structure, for inward movement of the wedges to decrease the size of the aperture and outward movement of the wedges to increase the size of the aperture.

Abstract: A stent crimping apparatus is provided which includes a crimping assembly adapted to crimp the stent, a clamp assembly configured to secure the medical device; and a control unit configured to control the movement of the crimp assembly. The clamp assembly includes a lower clamp device defining a seating groove formed and dimensioned to seat a portion of the medical device therein, and a retaining assembly having an elastomeric member. This elastomeric member defines a contacting groove oriented in an opposed manner proximate to at least a portion of the seating groove. The clamp assembly further includes an actuation mechanism associated with the retaining assembly and the lower clamp device such that operation thereof causes the retaining assembly to move between an opened condition and a closed condition.

Abstract: A stent crimping assembly is provided for crimping a stent from a first diameter to a reduced second diameter. The crimping assembly includes a plurality of movable wedges disposed about a rotational axis to form a wedge assembly. Each wedge includes a respective first side and a second side converging to form a tip portion. The tip portions are arranged to collectively form an iris about the rotational axis thereof. The iris defining a crimp aperture about which the movable wedges are disposed. Each wedge is associated with a stationary structure and an rotational actuation unit such that during rotation of the actuation unit about the rotational axis, the iris is caused to rotate about the rotational axis, relative the stationary structure, for inward movement of the wedges to decrease the size of the aperture and outward movement of the wedges to increase the size of the aperture.

Abstract: A medical device for vessel occlusion, the medical device including an elongated body having a distal end portion, a proximal end portion, and a lumen disposed therethrough, an balloon disposed at the distal end portion of the elongated body, the balloon in fluid communication with the lumen. An opening defined at the proximal end portion of the elongated body, the opening being in fluid communication with the balloon via the lumen, and a valve body moveably disposed at the proximal end portion of the elongated body, the valve body movable between a closed position and an open position, the valve body configured to engage a surface of the elongated body, distal to the opening, to seal the opening when the valve body is in the closed position.

Abstract: A medical device for vessel occlusion, the medical device including an elongated body having a distal end portion, a proximal end portion, and a lumen disposed therethrough, an balloon disposed at the distal end portion of the elongated body, the balloon in fluid communication with the lumen. An opening defined at the proximal end portion of the elongated body, the opening being in fluid communication with the balloon via the lumen, and a valve body moveably disposed at the proximal end portion of the elongated body, the valve body movable between a closed position and an open position, the valve body configured to engage a surface of the elongated body, distal to the opening, to seal the opening when the valve body is in the closed position.

Abstract: A medical device for vessel occlusion, the medical device including an elongated body having a distal end portion, a proximal end portion, and a lumen disposed therethrough, an balloon disposed at the distal end portion of the elongated body, the balloon in fluid communication with the lumen. An opening defined at the proximal end portion of the elongated body, the opening being in fluid communication with the balloon via the lumen, and a valve body moveably disposed at the proximal end portion of the elongated body, the valve body movable between a closed position and an open position, the valve body configured to engage a surface of the elongated body, distal to the opening, to seal the opening when the valve body is in the closed position.