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公开(公告)号：US20240350319A1
公开(公告)日：2024-10-24
申请号：US18640439
申请日：2024-04-19
IPC分类号： A61F13/00 , A61B46/00 , A61F13/01 , A61F13/02 , A61F13/05 , A61M1/00 , A61M3/02 , A61M37/00 , A61N5/06 , A61N7/00
CPC分类号： A61F13/00063 , A61F13/0279 , A61F13/05 , A61M1/77 , A61M1/85 , A61M1/915 , A61M1/92 , A61M1/966 , A61M3/0279 , A61M3/0283 , A61M37/00 , A61N5/0624 , A61N7/00 , A61B46/00 , A61F13/00 , A61F13/00085 , A61F2013/00357 , A61F2013/00536 , A61F13/01021 , A61F13/023 , A61M1/916 , A61M2205/15 , A61M2205/18 , A61M2205/3344 , A61M2205/3553 , A61M2205/3584 , A61M2205/3592 , Y10T29/49826
摘要： A mechanical wound therapy (MWT) system includes a connection for a vacuum source, which is routed through an airtight covering to a porous material positioned over the wound. The porous material may be a tubing network interspaced by a netting material constructed of biologically inert or bioabsorbable material. Alternatively, the porous material may be a layered unified dressing in which layers of mesh, netting or thin perforated film are separated and fixedly attached to functional elements of the dressing (e.g., irrigation tubing) or spacers. The vacuum and irrigation systems may be completely separated. An airtight sealing layer or foldable adhesive sealing layer may seal the dressing and facilitate sealing the dressing to the wound margins. Additional modular devices such as a wound approximating system, positive pressure bladders and adjuvant therapy modules as well as enhanced monitoring technology can be added to synergistically increase the capabilities of each dressing.
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2.发明公开公开(公告)号：US20240341785A1
公开(公告)日：2024-10-17
申请号：US18750634
申请日：2024-06-21
申请人： Penumbra, Inc.
发明人： Nicole Trosper , Stephen Pons
CPC分类号： A61B17/22 , A61M1/75 , A61M1/76 , A61M1/77 , A61M1/774 , A61B17/00 , A61B2017/00022 , A61B2017/00561 , A61B17/32037 , A61B17/3498 , A61B90/06 , A61B2090/064 , A61B2217/005 , A61M39/105 , A61M2205/3334 , A61M2205/3344
摘要： An aspiration thrombectomy system includes an aspiration catheter configured to accommodate fluid and having a proximal end and a distal end. The system includes connection tubing coupled to the aspiration catheter and configured to act as a common conduit for fluid communication. The system further includes controllable valves operable to control a level of pressure, and pressure sensors positioned downstream from the distal end of the aspiration catheter. A controller is configured to determine a vascular pressure level of the patient, and to determine one or more therapeutic-benefit metrics associated with continuance of the aspiration thrombectomy procedure.
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公开(公告)号：US12115333B2
公开(公告)日：2024-10-15
申请号：US17244324
申请日：2021-04-29
申请人： MuPharma Pty Ltd
发明人： Harry Unger , Mark Unger , Sean Michael Langelier
CPC分类号： A61M37/0092 , A61K39/12 , A61K39/21 , A61K41/0047 , A61M37/0015 , A61N1/30 , A61N7/00 , C12N7/00 , A61K2039/5256 , A61K2039/54 , A61M2037/0007 , A61M2037/0023 , A61M2205/3344 , A61M2205/3375 , C12N2710/24021 , C12N2710/24043 , C12N2710/24143 , C12N2740/16034 , C12N2740/16071
摘要： There is disclosed systems and methods for non-invasive delivery of an agent to biological tissues. Delivery of the agent to the tissues can be by one or more modalities. In some embodiments the systems and methods use agent carrier body including a tissue contacting surface for non-invasively engaging tissues under treatment. The tissue contacting surface can be at least partly defined by a plurality of protrusions that are in fluid communication with one or more reservoirs forming part of the agent carrier body. The protrusions may extend outward from an inside of a void and terminate at said tissue contacting surface.
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公开(公告)号：US12115298B2
公开(公告)日：2024-10-15
申请号：US16994182
申请日：2020-08-14
申请人： Smith & Nephew, Inc.
发明人： Edward Armstrong , Carrie Lee Childress , William W. Gregory , William Joseph Jaecklein , Felix C. Quintanar , John P. Racette , Christopher Rouseff , Matthew Smith , W. Len Smith
CPC分类号： A61M1/602 , A61F13/05 , A61M1/73 , A61M1/732 , A61M1/734 , A61M1/74 , A61M1/96 , A61M1/98 , A61M1/982 , A61F2013/00357 , A61M1/985 , A61M2205/15 , A61M2205/18 , A61M2205/3334 , A61M2205/3344 , A61M2205/3365 , A61M2205/3382 , A61M2205/3584 , A61M2205/50 , A61M2205/502 , A61M2205/505 , A61M2205/52 , A61M2205/581 , A61M2205/587 , A61M2209/084
摘要： Embodiments of a negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a pump assembly, canister, and a wound dressing configured to be positioned over a wound. The pump assembly, canister, and the wound dressing can be fluidically connected to facilitate delivery of negative pressure to a wound. The pump assembly can present graphical user interface screens for controlling and monitoring delivery of negative pressure. The system can be configured to efficiently deliver negative pressure and to detect and indicate presence of certain conditions, such as low pressure, high pressure, leak, canister full, and the like. Monitoring and detection of operating condition can be performed by measuring one or more operational parameters, such as pressure, flow rate, and the like.
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公开(公告)号：US20240325621A1
公开(公告)日：2024-10-03
申请号：US18742392
申请日：2024-06-13
IPC分类号： A61M1/00
CPC分类号： A61M1/96 , A61M1/962 , A61M1/92 , A61M2205/18 , A61M2205/3344 , A61M2205/3553 , A61M2205/502 , A61M2205/584 , A61M2205/75
摘要： A wound therapy system includes a canister configured to contain fluid removed from a wound site, a primary conduit having a first end coupled to the canister and a second end coupled to the wound site, and a pump fluidly coupled to the wound site via the primary conduit. The pump is configured to apply negative pressure to the wound site via the primary conduit. The system includes a pressure indicator configured to indicate a negative pressure at the pressure indicator and a secondary conduit having a first end coupled to the pressure indicator and a second end coupled to the wound site such that the negative pressure at the wound site is fluidly transmitted to the pressure indicator via the secondary conduit. A blockage in the primary conduit causes the negative pressure indicated by the pressure indicator to differ from the negative pressure applied by the pump.
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公开(公告)号：US12102755B2
公开(公告)日：2024-10-01
申请号：US16428473
申请日：2019-05-31
申请人： Vapotherm, Inc.
发明人： Scott A. Leonard
CPC分类号： A61M15/085 , A61M11/04 , A61M11/042 , A61M16/0666 , A61M16/109 , A61M16/14 , A61M2205/0294 , A61M2205/3344
摘要： Systems and methods for providing respiratory therapy are disclosed. One device includes a nasal cannula comprising at least at one nasal prong, tubing and a breathing gas conduit. The nasal prong has a proximal tip and a distal end connected to the breathing gas conduit. The breathing gas conduit has an inlet port, an outlet port, and a walled flow path connecting the inlet and outlet ports, such that the conduit directs the breathing gas from the tubing to the proximal tip of the nasal prong. A nebulizer is secured to the nasal cannula and operable to aerosolize a medicament via a vibrating mesh. The vibrating mesh is secured to the nasal cannula and is positioned adjacent to the breathing gas conduit such that the aerosol is entrained with the breathing gas at proximal tip of the nasal prong.
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公开(公告)号：US12102341B2
公开(公告)日：2024-10-01
申请号：US17549351
申请日：2021-12-13
发明人： Matthew F. Ogle
IPC分类号： A61B17/22 , A61M1/00 , A61M25/00 , A61M25/09 , A61M25/10 , A61M27/00 , A61B17/00 , A61B17/221 , A61B17/3207 , A61B90/00
CPC分类号： A61B17/22 , A61M1/00 , A61M1/71 , A61M1/732 , A61M1/84 , A61M25/0068 , A61M25/0074 , A61M27/006 , A61B17/00234 , A61B2017/00331 , A61B2017/22079 , A61B17/221 , A61B2017/2212 , A61B2017/320716 , A61B2090/064 , A61B2217/005 , A61M1/74 , A61M1/85 , A61M25/09 , A61M25/10 , A61M2205/3344 , A61M2210/0693
摘要： A suction catheter system is described with a suction extension interfaced with a guide catheter to form a continuous suction lumen extending through a portion of the guide catheter and through the suction extension. The suction extension can be positioned by tracking the suction nozzle through a vessel while moving a proximal portion of the suction extension within the lumen of the guide catheter. The suction extension can comprise a connecting section with a non-circular cross section for interfacing with the inner lumen of an engagement section of the guide catheter. The tubular body of the guide catheter can have a reduced diameter distal section the can be useful to restrain the movement of the suction extension. Proximal fittings attached to the guide catheter can facilitate safe removal of the catheter system from the patient by allowing for the removal of some or all of a tubular extension of the suction extension from the guide catheter behind a hemostatic seal. Pressure sensors connected to the proximal fittings can help to guide the procedures with reduced risk of embolizing thrombus.
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公开(公告)号：US12097362B2
公开(公告)日：2024-09-24
申请号：US17168817
申请日：2021-02-05
申请人： Stryker Corporation
发明人： Kevin J. Sutter , Douglas L. Carr , Eugene A. Estok , Liliya Fritzsching , Katherine N. Lionetti , Benjamin T. Lorman , Andrew R. Biddinger , Alexander S. Turner
CPC分类号： A61M5/445 , A61M1/73 , A61M1/743 , A61M1/80 , A61M3/0258 , A61M39/08 , A61M39/227 , A61M2205/02 , A61M2205/12 , A61M2205/121 , A61M2205/127 , A61M2205/3317 , A61M2205/3331 , A61M2205/3344 , A61M2205/3368 , A61M2205/3379 , A61M2205/3393 , A61M2205/368 , A61M2205/502 , A61M2205/505 , A61M2205/52
摘要： Fluid management systems are disclosed that include software-controlled, electro-mechanical devices used in combination with single-use or multi-use tubing sets. Functions of the fluid management systems can include fluid pressurization, fluid warming, fluid deficit monitoring (including flow-based and weight-based), suction, fluid collection, and fluid evacuation (including indirect-to-drain and direct-to-drain options). The systems can be configured based on the surgical environment (e.g., operating room or physician office) as well as other user needs and/or preferences.
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公开(公告)号：US12097312B2
公开(公告)日：2024-09-24
申请号：US16971581
申请日：2019-02-20
申请人： Emory University
CPC分类号： A61M1/06935 , A61M1/06 , A61M1/064 , A61M1/74 , A61M1/067 , A61M2205/3344 , A61M2205/3584 , A61M2205/52 , A61M2205/7536 , A61M2205/8206 , A61M2209/088
摘要： The systems, methods, and devices can efficiently express breast milk while being visually and audibly discreet, and portable. The breastmilk expression system for extracting milk from a breast of a female may include an interface configured to deliver suction to a nipple of the breast. The system may include a breastmilk storage container configured to store breastmilk. The system may include a control device operatively coupled to the breastmilk storage container and the interface. The control device may include one or more pressure reservoirs configured to store negative pressure. The control device may be configured to cause passive suction at the interface to cause extraction of the breast milk by controlling delivery of the negative pressure stored in the one or more pressure reservoirs to the interface.
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公开(公告)号：US12089954B2
公开(公告)日：2024-09-17
申请号：US17289866
申请日：2019-11-18
申请人： BIOTRONIK AG
发明人： Bodo Quint
CPC分类号： A61B5/6853 , A61B5/0538 , A61B5/068 , A61B5/25 , A61B5/6886 , A61F2/958 , A61M25/10184 , A61B2562/0209 , A61F2250/001 , A61M2205/3303 , A61M2205/3317 , A61M2205/332 , A61M2205/3327 , A61M2205/3344 , A61M2230/65
摘要： A balloon catheter system has a balloon extending in an axial direction and surrounding a balloon interior. The balloon has an outer side facing away from the balloon interior. A catheter is connected to the balloon and extending in the axial direction, the catheter having a lumen in fluid communication with the balloon interior. First and second annular electrodes are disposed on the outer side, each extending in a circumferential direction of the balloon and being located opposite one another in the axial direction. The electrodes are configured to measure one of more of strain of the balloon in the circumferential direction, strain of the balloon in the radial direction, an impedance of tissue of a patient resting against the electrodes, and a redox potential of tissue of the patient contacting at least one of the electrodes.
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