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Closure device for closing a percutaneous opening in a blood vessel

A closed-membrane, mid-zone technology used in the field of closed systems to address discomfort, restricted or interrupted blood flow, prolonged immobility, and requiring close monitoring by hospital staff

Active Publication Date: 2020-06-12
TELEFLEX LIFE SCI LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Whether the patient is hypertensive or anticoagulated, using external pressure to control bleeding has several disadvantages
For example, human hand pressure would be uncomfortable for the patient, cause excessive blood flow restriction or disruption, and consume expensive time and effort on the part of hospital staff
Other compression techniques, such as compression bandages, sandbags, and clamps, also have disadvantages, including requiring the patient to remain still for long periods of time and requiring hospital staff to monitor the patient closely to ensure the effectiveness of these techniques

Method used

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  • Closure device for closing a percutaneous opening in a blood vessel
  • Closure device for closing a percutaneous opening in a blood vessel
  • Closure device for closing a percutaneous opening in a blood vessel

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 26

[0117] In Example 26, a method for closing a hole extending between an inner vessel surface and an outer vessel surface can include inserting an inner member through the hole and into the lumen of the vessel. The inner member may be drawn against the inner vessel surface, and the portion of the connecting member and closure membrane coupled to the inner member at its first end may be arranged to extend at its second end to the exterior of the vessel. The outer member in the delivery configuration can then be inserted through the second end of the closure membrane such that the closure membrane at least partially surrounds the outer member. A compressive force can be applied to the outer member in a distal direction to expand the delivery configuration into a closed configuration. The expansion may push the middle region of the closure membrane radially outward so that its outer surface contacts and conforms to the edge of the hole.

[0118] In Example 27, the method of Exampl...

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PUM

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Abstract

Closure systems, kits, and methods for closing percutaneous punctures or other openings in vessel walls, body cavities, or biopsy tracts are disclosed. A closure system can include an implant assembly, a delivery assembly, and an introducer sheath. The closed system may further include a valve bypass and a dilator. The implant assembly can comprise an inner member, a closure membrane and an outer member, each of which can be delivered by the delivery assembly. The inner member can extend through the puncture or opening and be placed adjacent to an internal tissue surface. The outer member can be placed adjacent to an external tissue surface. The closure membrane may have a distal end attached to the inner member, a proximal end including an opening configured to receive the outer member, and an intermediate region therebetween. When expanding from the delivery configuration to the closed configuration, the outer member can push the intermediate region of the closure membrane radially outward so that its outer surface can contact and conform to the peripheral edge of the puncture or opening.

Description

[0001] priority claim [0002] U.S. Provisional Patent Application Serial No. 62 / 114,101, entitled "IMPLANT ASSEMBLY FOR SEALING PERCUTANEOUS OPENING IN A VESSEL," filed February 10, 2015, is hereby requested priority interest, the entire contents of which are incorporated herein by reference. technical field [0003] This patent document relates to medical devices. More specifically but not limitedly, this patent document relates to closure systems, kits and methods. [0004] Background of the invention [0005] Catheterization and interventional procedures such as angioplasty and stenting are typically performed by inserting a hollow needle into a blood vessel of the vasculature through the patient's skin and any intervening tissue. A guidewire may then be passed through the lumen of the needle into the blood vessel entered through the needle. The needle can be removed and an introducer sheath, with or behind the dilator, can be advanced over the guide wire and into the ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61B17/00
CPCA61B17/0057A61B2017/00619A61B2017/00623A61B2017/00004A61B2090/3966A61B2017/00646
Inventor 彼得·雅各布斯托马斯·霍尔曼查德·库格勒
Owner TELEFLEX LIFE SCI LTD