A catheter devices/systems and methods therefrom are described herein for treating acute kidney injury, especially the contrast-induced acute kidney injury wherein the devices may prevent the contrast dyes from entering into kidney and/or facilitate blood flow of kidney by said catheter system.

A medical filler delivery assembly includes a micro catheter for delivering filler material such as filamentary material into an aneurysm in a vessel, the assembly also including a positioning mechanism which includes a support element made of knitted wires, as well as an expansion mechanism for expanding the support element within the vessel. The wires form an array of polygonal, preferably rhomboidal cells, the wires being intertwined at their junctions by at least one turn around one another, the intertwined regions extending in the longitudinal direction of the support element. The support element is able to trap the micro catheter in position and in practice such that its distal end is disposed within the aneurysm sac.

This invention relates to a hemostatic member using chitosan having superior hemostatic activity, and more particularly to a chitosan-based hemostatic member for the cervix, suitable for use through insertion into an affected part upon cervical biopsy or surgery, configured to include a hemostatic pack having a projection at an upper end thereof through tying with a thread so as to form a spherical shape using chitosan nonwoven fabrics having a hemostatic function, wherein the thread contains an X-ray-sensitive material, thereby realizing effective hemostasis of the affected part upon cervical biopsy or surgery.

A medical device configured for assistance with the cervical cerclage procedure is provided. The medical device includes a barrier structure with a finger and a therebetween. A hub is fixed to a distal end of the catheter and defines an extension with a second void between an end surface of the hub and the extension. The barrier structure and the hub are releaseably attached with the extension disposed within the first void and the finger within the second void. A wire guide withdrawably extends through coaxial holes within the hub, extension, finger, and a portion of the barrier structure to fix the hub and barrier structure together.

An enclosure provides a prophylactic barrier that may be permeable to gases, hormones, proteins, and peritoneal fluid, but restrains tumor cells within the enclosure so as to inhibit ovarian cancer invasion of adjacent tissue, and increase the speed of diagnosis of ovarian dysplasia, including cancer. The enclosure includes one or more of fiducial markers, heat sensors, and blood flow reflectors, which may be imaged non-invasively in order to detect conditions or pathology affecting the ovary. The enclosure may also include an access port that permits sampling of the enclosure's contents to further aid in detecting or treating conditions or pathology affecting the ovary.

A compression stent for applying a localized high stress against a blood vessel wall to cause vessel wall compression and blockage of sympathetic and nerve signal transmission within the wall of a blood vessel. The compression stent can also sever nerves located in the vessel wall. Blockage of sympathetic nerve signal transmission reduces hypertension and improves other clinical problems that are associated with sympathetic nerve signals.

A medical device may include a catheter, an expandable member, a cover, and an actuator. The catheter may include a longitudinal axis, proximal and distal ends, and a cover lumen extending from the proximal to the distal end. The expandable member may include proximal and distal ends and may be disposed on a distal section of the catheter. The cover may include a first region that may be disposed along the expandable member, and a second region that may extend along a length of the catheter beyond the proximal end of the expandable member towards the proximal end of the catheter. A first end of the cover may invert into the cover lumen. The actuator may be coupled to the first end of the cover and configured to move the first end of the cover towards the proximal end of the catheter along the longitudinal axis of the catheter.

The present invention introduces a material, i.e. a device, which is insertable into a vein of a outer parts of a sheath, two-sidedly adhesive tubular material with a supporting material and protrusions, either a balong or an inner protective film, and a control cable for the insertion and extraction of the device along the vein. The supporting material may be compressed initially, and after removal of the outer part of the sheath, the supporting material with protrusions will expand towards the vein walls. After removal of the inner part of the sheath and the control cable, the treated vein area can be manually pressed on top of the skin, thus closing the vein through inner and outer adherence of the material. The protrusions may have a barbed shape.

The invention provides improved medical devices, therapeutic treatment systems, and treatment methods for treatment of the lung. A lung volume reduction system includes an implantable device having an elongate body that is sized and shaped for delivery via the airway system to a lung airway of a patient. The implant is inserted and positioned while the implant is in a delivery configuration, and is reconfigured to a deployed configuration so as to locally compress adjacent tissue of the lung, with portions of the elongate body generally moving laterally within the airway so as to laterally compress lung tissue. A plurality of such implants will often be used to treat a lung of a patient.

A device for percutaneous transcathetral closure of Atrial Septal Defect by deploying a pericardial patch without ardiopulmonary bypass includes a guide, and a head including a distal jaw and a proximal jaw. The guide includes guide knobs which move guide levers of the guide forward and backward via a rod and control the head. Each of the distal jaw and the proximal jaw includes a plurality of alms which closes when a distal disc moves forward and a proximal disc moves backward. The aims of the distal jaw and the arms of the proximal jaw open through a pressure when the distal disc moves backward and the proximal disc moves forward. When the arms of the distal jaw and the aims of the proximal jaw are completely open, pins located on the arm of the distal jaw engage with sockets located on the arm of the proximal jaw.