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:
Oct. 11, 2022

Filed:

Feb. 07, 2022
Applicant:

Sequana Medical NV, Zwijnaarde, BE;

Inventors:

Ian Crosbie, London, GB;

Andreas Wirth, Simbach am Inn, DE;

Oliver Goedje, Strasslach, DE;

Assignee:

Sequana Medical NV, Sint-Denijs Westrem, BE;

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61M 1/28 (2006.01); A61P 7/08 (2006.01); A61K 33/14 (2006.01); A61K 9/00 (2006.01); A61K 9/08 (2006.01); A61K 31/7004 (2006.01); A61K 31/716 (2006.01); A61M 27/00 (2006.01); A61M 31/00 (2006.01); A61L 2/00 (2006.01);
U.S. Cl.
CPC ...
A61M 1/282 (2014.02); A61K 9/0019 (2013.01); A61K 9/08 (2013.01); A61K 31/7004 (2013.01); A61K 31/716 (2013.01); A61K 33/14 (2013.01); A61M 1/28 (2013.01); A61M 1/285 (2013.01); A61M 1/287 (2013.01); A61M 27/002 (2013.01); A61M 31/002 (2013.01); A61P 7/08 (2018.01); A61L 2/0047 (2013.01); A61L 2202/21 (2013.01); A61M 2205/18 (2013.01); A61M 2205/3317 (2013.01); A61M 2205/3337 (2013.01); A61M 2205/3344 (2013.01); A61M 2205/3368 (2013.01); A61M 2205/3379 (2013.01); A61M 2205/3569 (2013.01); A61M 2205/3576 (2013.01); A61M 2205/502 (2013.01); A61M 2205/52 (2013.01); A61M 2205/587 (2013.01); A61M 2205/6009 (2013.01); A61M 2205/70 (2013.01); A61M 2205/8206 (2013.01); A61M 2205/8243 (2013.01); A61M 2209/086 (2013.01); A61M 2209/088 (2013.01); A61M 2210/1017 (2013.01); A61M 2210/1085 (2013.01);
Abstract

Systems and methods for performing Direct Sodium Removal (DSR) therapy are provided in which an implantable device includes a pump coupled to an inlet catheter designed for placement in a patient's peritoneal cavity, an outlet catheter designed to be coupled to the patient's bladder, and is operably coupled to an analyte sensor, the pump programmed to transfer and/or cease transfer of fluid from the patient's peritoneal cavity to the patient's bladder for voiding responsive to a level of analyte detected by the analyte sensor. In addition, the system may include a processor that computes an amount of analyte transferred per pumping session.


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