Abstract: Disclosed herein is a method and apparatus for observing a manufacturing line, wherein the manufacturing line includes at least one robotic element for moving at least one part, the method comprising receiving, at a processor separate from the manufacturing line, sensor data about the at least one robotic element, and when the sensor data exceeds a boundary condition, triggering a feed-back collection event. The feed-back collection event includes identifying a stream of sensor data, capturing feed-back data at a data collection device associated with the at least one robotic element, tagging the feed-back data to reflect the at least one part associated with the boundary condition, identifying, within the feed-back data, when the boundary condition is exceeded by the at least one part in real time, and storing the feed-back data relating to the boundary condition in association with the sensor data and the boundary condition.

Abstract: The present disclosure relates to a stent delivery system that is specifically designed for the treatment of chronic limb-threatening ischemia (CLTI) below the knee (BTK), through ankle, and to be utilized as a primary treatment or as a bailout treatment.

Abstract: Disclosed herein is a method and apparatus for observing a manufacturing line, wherein the manufacturing line includes at least one robotic element for moving at least one part, the method comprising receiving, at a processor separate from the manufacturing line, sensor data about the at least one robotic element, and when the sensor data exceeds a boundary condition, triggering a feed-back collection event. The feed-back collection event includes identifying a stream of sensor data, capturing feed-back data at a data collection device associated with the at least one robotic element, tagging the feed-back data to reflect the at least one part associated with the boundary condition, identifying, within the feed-back data, when the boundary condition is exceeded by the at least one part in real time, and storing the feed-back data relating to the boundary condition in association with the sensor data and the boundary condition.

Abstract: A system and method for treating critical limb ischemia (CLI) including a radiopaque micro stent disposed for cross ankle stenting as well as retrograde pedal/tibial artery access, in conjunction with antegrade access for the recanalization of impaired tibial vessels. A radiopaque medical device is constructed from a tubular-shaped body having a thin wall defining a specific strut pattern. In an additional aspect, the present apparatus introduces a new radiopaque medical device, such as a stent, wherein the tubular body includes a super elastic, nickel-titanium (nitinol) alloy.

Abstract: Systems, methods and accompanying apparatuses to treat critical limb ischemia through the superficial femoral arteries utilizing a specifically designed delivery package for entry proximal to area above the ankle with the capability to antegrade access via PT or AT into ankle and foot and retrograde access via pedal or plantar arch into the dorsalis pedis artery (DP).

Abstract: A stent delivery system, which includes a catheter and a stent stabilizer and pusher mechanism to capture and deploy a braided stent. The stabilizer pusher mechanism has a reinforced polymer shaft with two ends, a hub, a marker band and a braided mesh sock. The stent stabilizer and pusher mechanism further possesses a reinforced polymer shaft, which is constructed to have a low friction lumen. The low friction lumen may be guide wire compatible.

Abstract: A system and accompanying methods for treating a blockage of the superior femoral artery including utilization of a puncture insertion mechanism, an introducer sheath, a guide catheter and an expandable device. Entry into the body is established through the popliteal and advancing retrograde through the popliteal artery toward the lower superior femoral artery region and in some embodiments utilizing an introducer sheath, a guide catheter and a balloon are featured.

Abstract: A medical device such as a catheter may have an elongate shaft that includes a hypotube having a cut formed therein. The elongate shaft may define a lumen that extends within the elongate shaft. A polymer may be disposed over at least a portion of the hypotube. A medical device may include a cut hypotube having a constant pitch and may be configured to reversibly and temporarily alter the pitch of at least a portion of the cut hypotube. In some cases, the medical device may be configured to reversibly and/or temporarily alter a compressive strength of at least a portion of the cut hypotube.

Abstract: The system and method for protecting multiple networked enclaves each having one or more insecure machines. The system may include an attack detector as part of a secure node (e.g., SAFE node) proxy. The system may include an attack detector external to the proxy. The proxy may support multiple detectors and its actions may include isolating an insecure machine, cleansing an insecure machine, or tattling on (impugning the reputation of) an insecure machine.

Abstract: A coil-reinforced medical device delivery mechanism including a stiff proximal end for enhanced pushability and a soft distal end, including a free floating tip portion, for increased maneuverability and decreased breakage. The system utilizes a non-compliant balloon mounted on a flexible, single lumen shaft device with a support mandrel construction.

Abstract: A stent delivery system, which includes a catheter and a stent stabilizer and pusher mechanism to capture and deploy a braided stent. The stabilizer pusher mechanism has a reinforced polymer shaft with two ends, a hub, a marker band and a braided mesh sock. The stent stabilizer and pusher mechanism further possesses a reinforced polymer shaft, which is constructed to have a low friction lumen. The low friction lumen may be guide wire compatible.

Abstract: A system and method for treating critical limb ischemia (CLI) including a radiopaque micro stent disposed for cross ankle stenting as well as retrograde pedal/tibial artery access, in conjunction with antegrade access for the recanalization of impaired tibial vessels. A radiopaque medical device is constructed from a tubular-shaped body having a thin wall defining a specific strut pattern. In an additional aspect, the present apparatus introduces a new radiopaque medical device, such as a stent, wherein the tubular body includes a super elastic, nickel-titanium (nitinol) alloy.

Abstract: A medical device such as a catheter may have an elongate shaft that includes a hypotube having a cut formed therein. The elongate shaft may define a lumen that extends within the elongate shaft. A polymer may be disposed over at least a portion of the hypotube. A medical device may include a cut hypotube having a constant pitch and may be configured to reversibly and temporarily alter the pitch of at least a portion of the cut hypotube. In some cases, the medical device may be configured to reversibly and/or temporarily alter a compressive strength of at least a portion of the cut hypotube.

Abstract: The system and method for protecting multiple networked enclaves each having one or more insecure machines. The system may include an attack detector as part of a secure node (e.g., SAFE node) proxy. The system may include an attack detector external to the proxy. The proxy may support multiple detectors and its actions may include isolating an insecure machine, cleansing an insecure machine, or tattling on (impugning the reputation of) an insecure machine.

Abstract: The present invention provides a method of determining whether a subject is afflicted with a depressive disorder comprising: (i) introducing into the subject a positron emission tomography (PET) radioligand capable of binding with a serotonin 5-HT1A receptor; (ii) performing one or more PET scans of the subject; (iii) determining, by analysis of the one or more PET images, a receptor binding potential of the PET radioligand for the serotonin 5-HT1A receptor in a region of interest in the subject; (iv) comparing the receptor binding potential value of the PET radioligand in the region of interest in the subject to a predetermined receptor binding potential threshold value; and (v) classifying the subject as having the depressive disorder or as not having the depressive disorder based on the comparison of step (iv), thereby determining whether the subject is afflicted with the depressive disorder.

Abstract: A coil-reinforced medical device delivery mechanism including a stiff proximal end for enhanced pushability and a soft distal end, including a free floating tip portion, for increased maneuverability and decreased breakage. The system utilizes a non-compliant balloon mounted on a flexible, single lumen shaft device with a support mandrel construction.

Abstract: A filtration system to collect debris in the vascular system and/or other systems and a method for using such filter. An internally disposed apparatus for inside a fluid conduit during a medical procedure which includes a filtering membrane and a frame connected to the membrane. In one embodiment of the filtration system, a filter may generally include a membrane, a frame, and a rod.

Abstract: The present invention is a business method for the inventor company which operates through an internet web site a By Owner multiple listing service that pools the multiple listing service data from a multiplicity of By Owner real estate listing companies, both local and national in nature. The company's web site has software with an architecture that contemplates sellers listing their properties with a variety of By Owner LCs who elect to become part of the By Owner multiple listing service database by submitting data on their seller's/customer's listings to the web site searchable database. The database may be accessed by users through the company's web site.

Abstract: An electrical appliance includes a power cord having a GFCI device and an associated remote test/reset unit. The power cord includes a first end portion provided with a plug adapted to be inserted into an electrical outlet. The first end portion extends to a second end portion that is electrically coupled to a plurality of electrical components in the appliance. The test/reset unit is spaced from the GFCI device along the power cord. Preferably, the test/rest unit is connected to the power cord through an extension lead. With this arrangement the test/reset unit is actually remote from the GFCI device, allowing easy access to service personnel.

Abstract: A vending machine includes a storage/display region, a dispensing chamber including a product access opening, and an anti-pilfer device that prevents unauthorized removal of products from the storage/display region through the product access opening. A delivery door is provided which can be shifted from a closed position to an open position to enable the removal of products from the dispensing chamber. The anti-pilfer device includes a plate coupled to a lower portion of the delivery door. When the delivery door is moved from the closed position, the anti-pilfer plate shifts, over a guide element, into a position that prevents products from being withdrawn from the storage/display area. Preferably, the storage/display region and dispensing chamber are separated by a product door, with the anti-pilfer plate preventing the product door from opening when the delivery door is shifted from the closed position.