The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 20, 2022

Filed:

Dec. 19, 2019
Applicant:

Boston Scientific Scimed, Inc., Maple Grove, MN (US);

Inventors:

Michael J. Bonnette, Minneapolis, MN (US);

Jason T. Anderson, Deephaven, MN (US);

David B. Morris, Anoka, MN (US);

Assignee:

Boston Scientific Scimed, Inc., Maple Grove, MN (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61B 17/22 (2006.01); A61B 17/3203 (2006.01); A61M 25/09 (2006.01); A61M 5/142 (2006.01); A61M 5/178 (2006.01); A61M 25/00 (2006.01); A61B 17/221 (2006.01);
U.S. Cl.
CPC ...
A61B 17/22 (2013.01); A61B 17/32037 (2013.01); A61M 5/142 (2013.01); A61M 5/178 (2013.01); A61M 25/007 (2013.01); A61M 25/0052 (2013.01); A61M 25/0054 (2013.01); A61M 25/09 (2013.01); A61B 2017/2217 (2013.01); A61B 2017/22038 (2013.01); A61B 2017/22084 (2013.01); A61M 25/0015 (2013.01); A61M 2025/0057 (2013.01); A61M 2025/0063 (2013.01); A61M 2025/0915 (2013.01); A61M 2205/0266 (2013.01);
Abstract

An infusion catheter system may deliver a therapeutic agent to a desired location in the body. The system may include an elongate catheter shaft having a proximal end region, a distal end region, a distal opening, and a lumen extending between the proximal end region and distal opening. The distal end region may include a coiled portion having a preformed coiled configuration including a plurality of helically wound rings. A plurality of apertures may be formed through a sidewall of the coiled portion. A guidewire may be configured to be slidably disposed within the lumen of the catheter shaft. The guidewire may include a proximal end region having a first cross-sectional dimension, an enlarged distal end region having a second cross sectional dimension greater than the first cross-sectional dimension, and an intermediate region disposed between the proximal end region and the distal end region.


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