Abstract: A medical device and method for closure of a puncture in a body lumen are disclosed. The device has an aggregate (10) of a support structure (20) and a substantially fluid tight patch member (30) attached thereto at an attachment unit (40). The aggregate has a first, temporary delivery shape, for delivery to an interior of said body lumen and to be subsequently subjected to a change of shape to a second shape, which is a tubular shape. When delivered in said body lumen, the patch member is arranged radially outside of said tubular support structure and arranged towards an inner tissue wall of the body lumen. The aggregate is the detached from a delivery device and said puncture is intraluminally closed in a leakage tight manner, advantageously supported by a physiological pressure of a body fluid in said body lumen. The device may biodegrade over time.

Abstract: A wound drainage and hemostasis promoting medical device (1) are disclosed. A balloon (15) is temporary inflated and arranged outside a sheath (10), in contact with tissue surrounding a wound cavity for hemostasis promotion. The drainage device comprises a fluid communication channel for wound exudate from wound. The balloon is deflated and retracted into said sheath for removal from said wound cavity. Thus the medical device is percutaneously retractable from said confined wound.

Abstract: A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. A plurality of suction units allows for a atrial approach and symmetric implantation of said implant.

Abstract: A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. The annuloplasty implant (3) is arranged to be releasable in said hollow and has said resilient anchoring elements (300) arranged in a restrained spring loaded delivery conformation in said hollow, and wherein said resilient anchoring elements (300) when released are arranged in a tissue engaging conformation protruding out of said opening.

Abstract: A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. The annuloplasty implant (3) is arranged to be releasable in said hollow and has said resilient anchoring elements (300) arranged in a restrained spring loaded delivery conformation in said hollow, and wherein said resilient anchoring elements (300) when released are arranged in a tissue engaging conformation protruding out of said opening.

Abstract: An interchangeable concrete cutting chainsaw cutting assembly adapted for installation upon a drive assembly in exchange for a removed, different type cutting head assembly. The chainsaw cutting assembly includes a housing that has fasteners that releasably attach the housing to a drive assembly in an installed configuration. A ration transmission has a plurality of interconnected rotation member, each rotatable member having a mounting shaft positioned at a fixed location on the housing by a bearing assembly. The driven member has a receiver that interconnects with a driveshaft of the driver assembly in the installed configuration whereby the driven member is rotated by the drive assembly. The cutting chain drive member operatively interconnected with a drive sprocket whereby rotation of the cutting chain drive member rotates the drive sprocket. The chainsaw cutting assembly is pivotable relative to the drive assembly.

Abstract: A seal assembly includes a stator attached to a housing and a rotor attached to a shaft. A static sealing member is attached to the stator presenting a contact with the rotor at stand-still. An electromagnetic is attached to the stator at a distance from an end of the static sealing member. The static sealing member is activated and moved away from the rotor by the magnetic force exerted by the electromagnet as the shaft rotates. The electromagnet is controlled by a control system for controlling the equipment in which the bearing isolator is used. To deactivate the static sealing member during shaft rotation, the bearing isolator may have its own control system with a sensor to indicate if the shaft is rotating. As the shaft rotates, contaminants are expelled through gaps between the stator and the rotor.

Abstract: A shaft sealing assembly for static and dynamic sealing includes a stator member attached to a housing and a rotor member attached to a shaft rotatable about an axis. The rotor member includes first and second pocket sections extending from upper and lower radial flanges extending in a cantilevered fashion from a tubular member. At least one static sealing member is attached to and encapsulates each pocket section. Each static sealing member presents a core portion and a pair of radial lips extending from the core portion. The stator member presents an annular wall extending to inner walls inclined conically to a central radial rim or flange separating two pocket portions and the static sealing members presenting a contact and frictionally engaging with the central radial rim as the rotor member is at a stand-still or static position.

Abstract: A method of detecting urine and/or feces is disclosed, which includes detecting the concentration of at least one gas component indicative of urine and the concentration of at least one gas component indicative of feces. The method also includes registering, for each gas component, a characteristic corresponding to the variation over time of the concentration of each gas component; comparing the registered characteristic with a predetermined characteristic for the corresponding gas component; indicating a presence of urine if the registered characteristic of at least one gas component indicative of urine generally conforms with the predetermined characteristic of the same gas component; and indicating a presence of feces if the registered characteristic of at least one gas component indicative of feces generally conforms to the predetermined characteristic of the same gas component. A system for detecting urine and/or feces is also disclosed.

Abstract: A medical device and method for closure of a puncture in a body lumen are disclosed. The device has an aggregate (10) of a support structure (20) and a substantially fluid tight patch member (30) attached thereto at an attachment unit (40). The aggregate has a first, temporary delivery shape, for delivery to an interior of said body lumen and to be subsequently subjected to a change of shape to a second shape, which is a tubular shape. When delivered in said body lumen, the patch member is arranged radially outside of said tubular support structure and arranged towards an inner tissue wall of the body lumen. The aggregate is the detached from a delivery device and said puncture is intraluminally closed in a leakage tight manner, advantageously supported by a physiological pressure of a body fluid in said body lumen. The device may biodegrade over time.

Abstract: An embolic protection device and medical procedure for positioning the device in the aortic arch is disclosed. The device and method effectively prevent material from entering with blood flow into side branch vessels of the aortic arch. The device is a collapsible embolic protection device devised for temporary transvascular delivery to an aortic arch of a patient, wherein the device has a protection unit that comprises a selectively permeable unit adapted to prevent embolic material from passage with a blood flow into a plurality of aortic side branch vessels at the aortic arch. The protection unit is permanently attached to a transvascular delivery unit at a connection point provided at the selectively permeable unit, and a first support member for the protection unit that is at least partly arranged at a periphery of the selectively permeable unit. In an expanded state of the device, the connection point is enclosed by the first support member or arranged at said support member.

Abstract: A seal assembly includes a stator attached to a housing and a rotor attached to a shaft. A static sealing member is attacked to the stator presenting a contact with the rotor at stand-still. An electromagnetic is attached to the stator at a distance from an end of the static sealing member. The static sealing member is activated and moved away from the rotor by the magnetic force exerted by the electromagnet as the shaft rotates. The electromagnet is controlled by a control system for controlling the equipment in which the bearing isolator is used. To deactivate the static sealing member during shaft rotation, the bearing isolator may have its own control system with a sensor to indicate if the shaft is rotating. As the shaft rotates, contaminants are expelled through gaps between the stator and the rotor.

Abstract: A shaft sealing assembly for static and dynamic sealing includes a stator member attached to a housing and a rotor member attached to a shaft rotatable about an axis. The rotor member includes first and second pocket sections extending from upper and lower radial flanges extending in a cantilevered fashion from a tubular member. At least one static sealing member is attached to and encapsulates each pocket section. Each static sealing member presents a core portion and a pair of radial lips extending from the core portion. The stator member presents an annular wall extending to inner walls inclined conically to a central radial rim or flange separating two pocket portions and the static sealing members presenting a contact and frictionally engaging with the central radial rim as the rotor member is at a stand-still or static position.

Abstract: A method for delivering a bisphosphonate and/or strontium ranelate below the surface of a bone using a mechanical force. The method includes the steps of combining a bisphosphonate and/or strontium ranelate with a carrier to form a delivery composition and delivering an effective amount of the delivery composition below the surface of the bone with a mechanical force. Also provided is a method for strengthening a portion of a bone. This method includes the step of delivering an effective amount of a bisphosphonate and/or strontium ranelate below the surface of a portion of a bone with a mechanical force.

Abstract: An embolic protection device and medical procedure for positioning the device in the aortic arch is disclosed. The device and method effectively prevent material from entering with blood flow into side branch vessels of the aortic arch. The device is a collapsible embolic protection device devised for temporary transvascular delivery to an aortic arch of a patient, wherein the device has a protection unit that comprises a selectively permeable unit adapted to prevent embolic material from passage with a blood flow into a plurality of aortic side branch vessels at the aortic arch. The protection unit is permanently attached to a transvascular delivery unit at a connection point provided at the selectively permeable unit, and a first support member for the protection unit that is at least partly arranged at a periphery of the selectively permeable unit. In an expanded state of the device, the connection point is enclosed by the first support member or arranged at said support member.

Abstract: An embolic protection device and medical procedure for positioning the device in the aortic arch is disclosed. The device and method effectively prevent material from entering with blood flow into side branch vessels of the aortic arch. The device is a collapsible embolic protection device devised for temporary transvascular delivery to an aortic arch of a patient, wherein the device has a protection unit that comprises a selectively permeable unit adapted to prevent embolic material from passage with a blood flow into a plurality of aortic side branch vessels at the aortic arch. The protection unit is permanently attached to a transvascular delivery unit at a connection point provided at the selectively permeable unit, and a first support member for the protection unit that is at least partly arranged at a periphery of the selectively permeable unit. In an expanded state of the device, the connection point is enclosed by the first support member or arranged at said support member.

Abstract: An embolic protection device and medical procedure for positioning the device in the aortic arch is disclosed. The device and method effectively prevent material from entering with blood flow into side branch vessels of the aortic arch. The device is a collapsible embolic protection device devised for temporary transvascular delivery to an aortic arch of a patient, wherein the device has a protection unit that comprises a selectively permeable unit adapted to prevent embolic material from passage with a blood flow into a plurality of aortic side branch vessels at the aortic arch. The protection unit is permanently attached to a transvascular delivery unit at a connection point provided at the selectively permeable unit, and a first support member for the protection unit that is at least partly arranged at a periphery of the selectively permeable unit. In an expanded state of the device, the connection point is enclosed by the first support member or arranged at said support member.

Abstract: A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. A plurality of suction units allows for a atrial approach and symmetric implantation of said implant.

Abstract: A medical device and method for closure of a puncture in a body lumen are disclosed. The device has an aggregate (10) of a support structure (20) and a substantially fluid tight patch member (30) attached thereto at an attachment unit (40). The aggregate has a first, temporary delivery shape, for delivery to an interior of said body lumen and to be subsequently subjected to a change of shape to a second shape, which is a tubular shape. When delivered in said body lumen, the patch member is arranged radially outside of said tubular support structure and arranged towards an inner tissue wall of the body lumen. The aggregate is the detached from a delivery device and said puncture is intraluminally closed in a leakage tight manner, advantageously supported by a physiological pressure of a body fluid in said body lumen. Rotational orientation is detectable by fiducial markers.

Abstract: A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. The annuloplasty implant (3) is arranged to be releasable in said hollow and has said resilient anchoring elements (300) arranged in a restrained spring loaded delivery conformation in said hollow, and wherein said resilient anchoring elements (300) when released are arranged in a tissue engaging conformation protruding out of said opening.