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公开(公告)号:US12128199B2
公开(公告)日:2024-10-29
申请号:US17813945
申请日:2022-07-21
IPC分类号: A61M29/00 , A61B17/34 , A61B18/14 , A61M25/06 , A61M25/09 , A61B17/00 , A61B17/22 , A61B18/00 , A61B90/00
CPC分类号: A61M29/00 , A61B17/3415 , A61B17/3478 , A61B18/1477 , A61M25/06 , A61M25/09 , A61B2017/00247 , A61B2017/22038 , A61B2017/22042 , A61B2017/22047 , A61B2018/00351 , A61B2018/1425 , A61B2090/033 , A61B2090/062 , A61B2090/0807 , A61M2205/32 , A61M2205/582
摘要: An apparatus is disclosed for an optimized transseptal procedure that reduces the number of devices that are used in order to minimize procedural time, complexity and cost. The apparatus comprises a hybrid dilator that comprises the combined functionality of a transseptal sheath and dilator assembly. The hybrid dilator comprises: a dilator shaft defining a lumen for receiving a crossing device therethrough, a distal tip having an outer diameter which tapers down to an outer diameter of the crossing device for providing a smooth transition and a hub coupled with a side arm coupled to the dilator shaft.
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2.
公开(公告)号:US20240341781A1
公开(公告)日:2024-10-17
申请号:US18579719
申请日:2022-08-09
申请人: BIOTRONIK AG
发明人: Azadeh Mehrabi
IPC分类号: A61B17/22 , A61B17/00 , A61B17/3207 , A61B90/00
CPC分类号: A61B17/22 , A61B17/00234 , A61B17/320758 , A61B90/39 , A61B2017/00238 , A61B2017/00305 , A61B2017/00477 , A61B2017/00831 , A61B2017/22038 , A61B2017/22094 , A61B2090/3966 , A61B2217/007
摘要: A crossing catheter system for crossing chronic total occlusion includes or consists of a support catheter having a support catheter shaft defining a support catheter lumen capable of receiving a dilator. A dilator is arranged within the support catheter lumen. A locking handle is arranged at a proximal support catheter end. The dilator has a proximal segment with a uniform radial circumference and a distal segment that has a radial circumference that is smaller than the radial circumference of the proximal segment.
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公开(公告)号:US12114886B2
公开(公告)日:2024-10-15
申请号:US16926893
申请日:2020-07-13
发明人: Kosuke Nishio , Junichi Kobayashi , Tomonori Hatta , Taiga Nakano
IPC分类号: A61B17/3207 , A61B17/32 , A61B17/00 , A61B17/22
CPC分类号: A61B17/320758 , A61B17/32002 , A61B17/3207 , A61B2017/00845 , A61B2017/22038 , A61B2017/320032
摘要: A medical device for grinding substance inside a body lumen includes a rotatable tubular drive shaft, a treatment member connected to the drive shaft, and a tubular member possessing an axially extending lumen that extends throughout the tubular member. The tubular member is mounted on the treatment member and surrounds a portion of the treatment member so that the treatment member is rotatable relative to the tubular member. The treatment member includes a shearing portion, and the tubular member includes a protrusion that projects toward the lumen of the tubular member. The protrusion is located axially in front of the shearing portion and interacts with the shearing portion during relative rotation between the treatment member and the tubular member to shear debris resulting from the grinding of the substance.
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4.
公开(公告)号:US20240325036A1
公开(公告)日:2024-10-03
申请号:US18741038
申请日:2024-06-12
IPC分类号: A61B17/22 , A61B17/00 , A61B17/221 , A61M25/10
CPC分类号: A61B17/22032 , A61B17/221 , A61B2017/00867 , A61B2017/22038 , A61B2017/22051 , A61B2017/22054 , A61B2017/22072 , A61B2017/22079 , A61B2017/22094 , A61M2025/1013 , A61M2025/1015
摘要: A system for dislodging and removing occlusions from a vascular vessel. The system includes a handle and an elongate member, the elongate member including an occlusion dislodging member adapted to axially move, radially expand and contract, and rotate to dislodge vessel occlusions. The handle is adapted to selectively induce the axial movement, radial expansion and contraction, and rotation of the occlusion dislodging member.
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公开(公告)号:US20240299052A1
公开(公告)日:2024-09-12
申请号:US18273233
申请日:2022-01-20
申请人: SENSOME
发明人: Bruno Carreel
IPC分类号: A61B17/221 , A61B17/00 , A61B17/22 , G16H20/40
CPC分类号: A61B17/221 , A61B17/00234 , G16H20/40 , A61B2017/00022 , A61B2017/00199 , A61B2017/00221 , A61B2017/00238 , A61B2017/00292 , A61B2017/0046 , A61B2017/00477 , A61B2017/00526 , A61B2017/00929 , A61B2017/00951 , A61B2017/22038
摘要: Embodiments described relate to a medical device including an invasive probe that, when inserted into a duct (e.g. vasculature) of an animal (e.g., a human or non-human animal, including a human or non-human mammal), may be used to aid in diagnosing and/or treating a lesion of the duct (e.g. a growth or deposit within vasculature that fully or partially blocks the vasculature). The invasive probe may have one or more sensors to sense characteristics of the lesion, including by detecting one or more characteristics of tissues and/or biological materials of the lesion.
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公开(公告)号:US20240299048A1
公开(公告)日:2024-09-12
申请号:US18665380
申请日:2024-05-15
申请人: Inquis Medical, Inc.
发明人: Vahid SAADAT , William Jason FOX , Michael PARE , Eyal AKLIVANH , Neekon SAADAT
CPC分类号: A61B17/22 , A61B17/00234 , A61B2017/00026 , A61B2017/00084 , A61B2017/00119 , A61B2017/00154 , A61B2017/00199 , A61B2017/00238 , A61B2017/00292 , A61B2017/00544 , A61B2017/22038 , A61B2017/22079
摘要: Methods for removing clot material by directional aspiration may include removing clot material from a side vessel while the suction catheter remains in the main vessel. These methods may include a steerable distal end region. In some cases the apparatuses and methods may include the use of a guide catheter and/or a guidewire in orienting the suction catheter to laterally capture clot material from a side vessel without having to enter the side vessel. Any of these methods may include optionally sensing and confirming clot material (e.g., electrically sensing).
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公开(公告)号:US20240225674A1
公开(公告)日:2024-07-11
申请号:US18408177
申请日:2024-01-09
申请人: Inari Medical, Inc.
IPC分类号: A61B17/221 , A61B17/00 , A61B17/22
CPC分类号: A61B17/221 , A61B2017/00336 , A61B2017/00367 , A61B2017/00982 , A61B2017/22038 , A61B2017/2215
摘要: Disclosed herein are catheters for use with clot treatment systems, and associated devices and methods. The catheter can include an outer sheath, an outer sheath drive component operably coupled to the outer sheath, a guidewire sheath slidably disposed within the outer sheath, a guidewire sheath drive component operably coupled to the guidewire sheath and slidably disposed within the outer sheath drive component, and a clot treatment component. During a clot treatment procedure, the outer sheath drive component can be moved proximally and/or the guidewire sheath drive component can be moved distally to cause corresponding movement of the outer sheath and/or guidewire sheath, respectively, and transition the catheter between a first configuration, in which the clot treatment component can be positioned within the outer sheath, and a second configuration, in which at least part of the clot treatment component can extend beyond the outer sheath.
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公开(公告)号:US20240206972A1
公开(公告)日:2024-06-27
申请号:US18595031
申请日:2024-03-04
发明人: JiChao Sun , Parker Hagen , Dannah Dean , Lauren Eno , Brady Hatcher , Curtis Goreham-Voss , Tristan Tieso , Edward Anderson , Scott Nelson , Dean Irwin , Bryan Goh , Charles Anthony Plowe , Randy Beyreis
CPC分类号: A61B18/26 , A61B2017/22038 , A61B2018/0022 , A61B2018/2261 , A61B2018/263 , A61B2018/266
摘要: A medical device may include an elongated body having a distal elongated body portion and a central longitudinal axis. The medical device may include a balloon positioned along the distal elongated body portion. The balloon may be configured to receive a fluid to inflate the balloon such that an exterior balloon surface contacts a calcified lesion within a patient's vasculature. The medical device may include one or more pressure wave emitters positioned along the central longitudinal axis of the elongated body. The one or more pressure wave emitters may be configured to propagate at least one pressure wave through the fluid to fragment the calcified lesion. At least one pressure wave emitter may include an optical fiber configured to transmit laser energy into the balloon. The laser energy may be configured to create a cavitation bubble in the fluid.
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公开(公告)号:US20240197346A1
公开(公告)日:2024-06-20
申请号:US18593795
申请日:2024-03-01
发明人: Robert Chisena , Hitinder Gurm
CPC分类号: A61B17/22012 , A61M5/007 , A61B2017/00022 , A61B2017/00039 , A61B2017/00477 , A61B2017/00964 , A61B2017/22001 , A61B2017/22038 , A61B2017/22054 , A61B2017/22062 , A61B2090/063 , A61B2090/064
摘要: Pulsatile balloon catheter systems are provided. Aspects of the systems include: a pulse generator; and a balloon catheter assembly operably connected to the pulse generator. In embodiments, the balloon catheter assembly includes: a proximal connector operably connecting the balloon catheter assembly to the pulse generator and configured to transduce a first pulse energy generated by the pulse generator to a second pulse energy; a distal balloon; and a catheter component, where the catheter component includes a fluidic passage operably positioned between the proximal connector and the distal balloon, which passage is configured to propagate the second pulse energy from the proximal connector along the fluid passage to the distal balloon. Also provided are balloon catheter assemblies and kits that include the same. Also provided are systems and methods for assessing vessel compliance in-vivo. Also provided are systems and methods for determining system state of balloon catheter systems. The systems, assemblies and kits find use in a variety of different applications, including balloon angioplasty applications.
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公开(公告)号:US20240197332A1
公开(公告)日:2024-06-20
申请号:US18516729
申请日:2023-11-21
CPC分类号: A61B17/12122 , A61B17/12145 , A61B17/1215 , A61B17/12159 , A61B17/12172 , A61B17/12177 , A61B17/12181 , A61B17/00491 , A61B2017/00495 , A61B2017/1205 , A61B17/12136 , A61B2017/22038 , A61B2017/22048 , A61B2090/064
摘要: Devices and methods are described for occluding the left atrial appendage (LAA) to exclude the LAA from blood flow to prevent blood from clotting within the LAA and subsequently embolizing, particularly in patients with atrial fibrillation. An implant is delivered via transcatheter delivery into the LAA. The implant includes a conformable structure comprising a foam body and internal support. The support includes anchors that penetrate the foam body and anchor the implant to the walls of the LAA. The implant provides compliance such that it conforms to the native configuration of the LAA.
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