US2021275331A1PendingUtilityA1
Endovascular delivery system with an improved radiopaque marker scheme
Est. expiryJun 15, 2032(~5.9 yrs left)· nominal 20-yr term from priority
A61F 2/966A61F 2250/0003A61F 2002/9511A61F 2/95A61F 2002/9665A61F 2230/0069A61F 2/9522A61F 2250/0098
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Claims
Abstract
An endovascular delivery system for an endovascular prosthesis includes a radiopaque marker system for accurate delivery of the prosthesis. The radiopaque marker system is disposed within a prosthesis or stent holder within the delivery system. The radiopaque marker system includes a plurality of radiopaque markers that provide different views rotation of the prosthesis or stent holder.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An endovascular delivery system, comprising:
an elongate outer tubular device having an open lumen and opposed proximal and distal ends with a medial portion therein between; an inner tubular member configured to be disposed within an outer tubular device, said inner tubular member comprising a longitudinal axis and a proximal portion comprising: a rotatable prosthesis holder comprising a body and a plurality of markers; and an outer surface, upon which a prosthesis may be secured prior to delivery, wherein the plurality of markers comprises a first marker having a longitudinal axis aligned in a direction generally parallel to said inner tubular member longitudinal axis and a second marker having a longitudinal axis aligned in a direction generally perpendicular to said inner tubular member longitudinal axis.
2 . The endovascular delivery system of claim 1 , wherein the rotatable prosthesis holder body surrounds an axial guidewire.
3 . The endovascular delivery system of claim 2 , wherein said first marker and said marker are spaced an equal distance from said axial guidewire.
4 . The endovascular delivery system of claim 1 , wherein said prosthesis holder is made of a material that is not fluorescent or radiopaque.
5 . The endovascular delivery system of claim 2 , wherein said axial guidewire is made of a material that is fluorescent or radiopaque.
6 . The endovascular delivery system of claim 1 , wherein said first and second markers are made of a material that is fluorescent or radiopaque.
7 . The endovascular delivery system of claim 1 , wherein at least a portion of said first marker is disposed within a first interior portion of the body of the prosthesis holder.
8 . The endovascular delivery system of claim 1 , wherein at least a portion of said second marker is disposed within a second interior portion of the body of the prosthesis holder.
9 . The endovascular delivery system of claim 1 , wherein said first marker and/or said second marker are made of materials selected from the group consisting of palladium, iridium, gold, tantalum, tungsten, platinum, and combinations thereof.
10 . The endovascular delivery system of claim 1 , wherein said first marker and/or said second marker are made of radiopaque polymeric materials.
11 . The endovascular delivery system of claim 10 , wherein said radiopaque polymeric materials comprise polymeric materials with radiopaque fillers.
12 . The endovascular delivery system of claim 11 , wherein said radiopaque fillers are selected from the group consisting of bismuth, barium, and tungsten.
13 . The endovascular delivery system of claim 2 , wherein said first marker and said second marker are spaced at about a 90° interval as measured around a longitudinal axis formed by said axial guidewire.
14 . The endovascular delivery system of claim 1 , wherein said first marker and said second marker comprise a shape selected from the group consisting of a hollow construction, a partially hollow construction and a solid construction.
15 . The endovascular delivery system of claim 1 , wherein a first interior portion of the body of the prosthesis holder is different from a second interior portion of the body of the prosthesis holder.
16 . An endovascular delivery system, comprising:
an outer tubular device having an open lumen and opposed proximal and distal ends with a medial portion therein between; an inner tubular member configured to be disposed within an outer tubular device, said inner tubular member comprising a proximal portion comprising: a rotatable prosthesis holder comprising a body and a plurality of markers; and an outer surface, upon which a prosthesis may be secured prior to delivery, wherein the plurality of markers comprises a first and a second marker each having a longitudinal axis, wherein the longitudinal axis of the first marker is generally perpendicular with the longitudinal axis of the second marker.
17 . An endovascular delivery system, comprising:
an elongate inner tubular member comprising a proximal portion comprising: a rotatable prosthesis holder comprising a body surrounding and axial guidewire, the body comprising a first radiopaque marker and a second radiopaque marker; and an outer surface, upon which a prosthesis may be secured prior to delivery, wherein said first radiopaque marker and said second radiopaque marker are spaced at about a 90° interval as measured around a longitudinal axis formed by said axial guidewire.
18 . The endovascular system of claim 17 , comprising an outer tubular device having an open lumen and opposed proximal and distal ends with a medial portion therein between, the outer tubular wherein the elongate inner tubular member is configured to be disposed within said outer tubular device.Join the waitlist — get patent alerts
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