Abstract: A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

Abstract: Engine systems and methods for performing a new chemical/thermodynamic cycle, termed a Chemo/thermodynamic Closed Combined (CCC) cycle, are proposed herein. The CCC cycle is composed of an Endothermic Chemo/thermodynamic Open cycle (En-C-O) and an Exothermic Chemo/thermodynamic Open cycle (Ex-C-O), which together complete the larger CCC cycle. CCC cycles may operate as a Combined Heat and Power (CHP) cycle. Since the En-C-O and the Ex-C-O cycles are able to operate independently of one another, they can be distanced from one another in time and/or space. To complete the larger CCC cycle, the En-C-O and Ex-C-O chemical working fluids are stored and/or transported between one another. An Exothermic Reactor Exhaust Compressor (EREC), for permitting otherwise-waste CCC heat to convert said chemical working fluids from liquid/frozen pressurized states into pressurized vapors and/or gases, is also proposed herein. Finally, various En-C-O and Ex-C-O cycles are proposed herein.

Abstract: A battery configured to have improved thermal management and structural stability. The battery including a battery pack construction with at least one battery cell spacer having a first surface contacting substantially all of the bottom surface of a first battery cell and a second surface contacting substantially all of the top surface of a second battery cell, the battery cell spacer including an adhesive component. Additionally, the battery may include a battery management system (BMS) in electrical communication with the first and second battery cells, the BMS having one or more thermal components configured to disperse heat from the BMS, and a thermal epoxy contacting the one or more thermal components and a battery housing. The battery further including a stability cage at least partially enclosing the battery pack construction and positioned between the battery cells and the battery housing.

Abstract: A medical system includes an introducer device having an elongate shaft defining a shaft lumen and a hub secured to a proximal region of the elongate shaft. The hub includes a primary channel extending through the hub and fluidly coupled with the shaft lumen and a secondary channel extending through the hub and fluidly coupled with the shaft lumen. A guide catheter is adapted to be advanced through the secondary channel and into the shaft lumen. A guidewire is adapted to be advanced through the secondary channel and into the shaft lumen. A working catheter is adapted to be advanced through the primary channel and into the shaft lumen when the guide catheter is positioned with a distal end of the guide catheter within the secondary channel, the working catheter including a catheter shaft including a distal region that is adapted to releasably engage the guidewire.

Abstract: The present invention proposes methods and apparatus for improving the technology disclosed in U.S. Pat. No. 3,225,538, U.S. Pat. No. 3,067,594, and U.S. Pat. No. 3,871,179, wherein are detailed techniques for creating a unique thermochemical cycle, termed the Bland/Ewing Cycle (B/E Cycle) after the co-inventors, involving “molecular expansion” and “molecular compression”. The advantage of the B/E Cycle is best exemplified in FIG. 3 and FIG. 4 of U.S. Pat. No. 3,225,538, where P/V and T/S charts indicate the potential for increased “power density”. This power density is a result of the reduced compression work following exothermic conversion of a single mole of gas relative to the increased expansion work following endothermic conversion of multiple moles of gas. The present invention improves power density and/or overall heat engine thermal efficiency by capturing otherwise-waste heat in the exhaust of a B/E Cycle heat engine.

Abstract: For efficiently exchanging heat between two streams of fluid at approximately equal pressure while simultaneously reducing the internal volume and general overall mass of the heat exchange means per quantity of heat exchanged over time, a means termed a Synchronized Thermal Regenerator Exchange Pump (STREP) is proposed.

Abstract: The present invention proposes a thermochemical battery cycle, termed a Benzene Battery cycle, for efficiently storing electric and/or thermal energy for later and/or distant use. The methods and apparatus herein proposed utilize reversible endothermic fluid and exothermic fluid thermochemical means for efficiently storing H2 in a liquid state at STP. The present invention is generally based on the technology disclosed in U.S. Pat. Nos. 3,225,538, 3,067,594, and 3,871,179, wherein techniques are described for creating a unique thermochemical cycle, termed the Bland/Ewing Cycle (B/E Cycle) after the co-inventors, involving “molecular expansion” and “molecular compression”. The present invention is also based on US Patent Application #18-0954634 which proposes optimizing endothermic and exothermic “segments” for the creation of either Combined Heat and Power (CHP) or Combined Cycle (CC) applications.

Abstract: An intravascular articulating retrieval apparatus may be used to move objects within the vasculature, such as to remove an intravascular filter, tissue and other items from the vasculature. The apparatus has a user interface to manipulate a first and second actuating portion that are coupled to the distal end of the apparatus conduit. A retrieval apparatus may include forceps coupled to the second actuating portion whereby the retrieval actuator opens and closes the forceps for retrieval of an IVF or other device, such as stent or stent graft. An intravascular articulating retrieval apparatus may be used to dissect thrombus from the interior of the vascular wall, move a stent or remove a portion of a stent or stent graft to provide better blood flow or to allow blood flow into a branched vessel.

Abstract: A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

Abstract: An intravascular articulating retrieval apparatus may be used to move objects within the vasculature, such as to remove an intravascular filter, tissue and other items from the vasculature. The apparatus has a user interface to manipulate a first and second actuating portion that are coupled to the distal end of the apparatus conduit. A retrieval apparatus may include forceps coupled to the second actuating portion whereby the retrieval actuator opens and closes the forceps for retrieval of an IVF or other device, such as stent or stent graft. An intravascular articulating retrieval apparatus may be used to dissect thrombus from the interior of the vascular wall, move a stent or remove a portion of a stent or stent graft to provide better blood flow or to allow blood flow into a branched vessel.

Abstract: A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

Abstract: An intravascular articulating retrieval apparatus may be used to move objects within the vasculature, such as to remove an intravascular filter, tissue and other items from the vasculature. The apparatus has a user interface to manipulate a first and second actuating portion that are coupled to the distal end of the apparatus conduit. A retrieval apparatus may include forceps coupled to the second actuating portion whereby the retrieval actuator opens and closes the forceps for retrieval of an IVF or other device, such as stent or stent graft. An intravascular articulating retrieval apparatus may be used to dissect thrombus from the interior of the vascular wall, move a stent or remove a portion of a stent or stent graft to provide better blood flow or to allow blood flow into a branched vessel.

Abstract: A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: In at least one embodiment, the present invention relates to a method and system of painting an article having two or more base coats, and to articles prepared in accordance therewith. In at least one embodiment, the method comprises applying a primer composition to a first and second area of the article; applying a first base composition to the first area of the article; curing the primer composition and the first base composition to form a primer and a first base coat; masking at least a portion of the first base coat; applying a second base composition to the second area of the article; removing the masking; applying a clear coat composition to the first and second area of the article; and curing the second base and the clear coat compositions. In at least one embodiment, the article is a vehicle and the compositions are applied via automated spray equipment.