Funnel Body Overlap Guide for Percutaneous Implant Folding

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Solution Overview

Problem

Current minimally invasive surgical procedures face complications due to the invasive methods used for closing large puncture holes or access sites in blood vessels, which can lead to tissue trauma and healing issues.

Innovation Solution

A device and method for folding an implant with a wing into an overlapped configuration using a funnel body and overlap guide, allowing for precise sealing of apertures in tissues with a polymer-based implant that remains shelf-stable after sterilization, and a delivery system to maneuver the implant into a sealing position within a blood vessel.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If cut-down surgical repair is used to close large puncture holes, then the access site can be closed, but tissue trauma and complications increase

Engineering Contradiction:
Improveclosure reliabilityVSAvoidtissue trauma
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent extracts the harmful cutting and suturing actions from the closure process by introducing a sutureless implant device that seals the puncture hole through mechanical compression and tissue approximation, eliminating the need for invasive surgical repair

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent replaces the mechanical cutting and suturing system with a compression-based sealing system that uses radial force to approximate tissue edges and create a seal without incisions or stitches

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Ease of operation

If percutaneous access is used to reach target sites, then invasiveness is reduced, but access site closure becomes problematic

Engineering Contradiction:
Improveaccess easeVSAvoidclosure complexity
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The patent introduces a sutureless implant as an intermediary device that facilitates closure of percutaneous access sites, bridging the gap between the need for percutaneous access and the requirement for safe closure without adding surgical complexity

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The implant device is self-contained and self-deploying, requiring no additional surgical instruments or techniques for installation or removal, thereby maintaining the simplicity of percutaneous access while solving the closure problem

Inventive Principle:
Principle #25Self-service

3Adaptability or versatility

If large puncture holes are created for instrument insertion, then instrument access is enabled, but closure risk increases

Engineering Contradiction:
Improveinstrument accessVSAvoidclosure safety
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent employs a dynamic compression mechanism where the implant can be deployed and adjusted to match varying puncture hole sizes and shapes, adapting to different access requirements while maintaining reliable sealing

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The implant device changes its physical parameters (compression force, radial expansion) to effectively seal puncture holes of varying sizes, transforming the closure approach from size-specific surgical repair to a universal sutureless solution

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentEP2996573B1Loading devices for percutaneous perforation closure systems
Publication Date: 2022.04.27 VIVASURE MEDICAL LTD
  • EP2996573B1 patent drawingFigure 1A
  • EP2996573B1 patent drawingFigure 1B
  • EP2996573B1 patent drawingFigure 1C

AI summary

A device for folding an implant 5 having a wing 60 into an overlapped configuration includes a funnel body 500 comprising: a first portion configured to receive and protect the implant when the wing of the implant is in a flat or relaxed state, a second portion proximal to the first portion and configured to engage and fold opposite first and second side portions of the wing of the implant in a predetermined direction when the implant is retracted proximally from the first portion of the funnel body and into the second portion of the funnel body, and an overlap guide configured to direct the path of a first one of the side portions of the wing such that the first and second side portions of the wing are overlapped in a predetermined manner and to prevent respective edges of the first and second side portions of the wing from butting into each other as the first and second side portions of the wing are guided into the overlapping configuration during proximal retraction of the implant relative to the funnel body.