Ams Research Corporation

Boston Scientific Scimed, Inc.

St. Jude Medical Coordination Center Bvba

St. Jude Medical, Cardiology Division, Inc.

Dean W Hacker

Karl Alan Jagger

Jessica Elizabeth Felton

Benjamin M Wilke

Seth C Kelto

Benjamin Y Arcand

Alex Alden Peterson

James A Alexander

Chaouki A Khamis

Kevin R Arnal

John R Frigstad

Fredrik Mahlin

Mats Hilmersson

Ryan Cerepak

Sara Sundler

Shawn Boye

Stefan Tiensuu

Niklas Borg

Jelica D Wold

Johan Mattsson

Johan Grundin

Richard Charles Gunderson

Emily R Rolfes Meyering

Gerald W Grabowski

Mary Johnson

James A Kazmierkoski

Corey Tillman

Jason Lind

A pressure sensor configured for biological pressure measurement at a distal end portion of an elongated member comprises a dissolvable hydrophilic material coated on a surface of the pressure sensor. A guide wire for biological pressure measurement may include a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube. The first distal opening is larger than the second and third distal openings, and the first proximal opening is larger than the second and third proximal openings.

Pressure sensor and guide wire with hydrophilic material

A guide wire for biological pressure measurement includes a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube. The first distal opening is larger than the second and third distal openings, and the first proximal opening is larger than the second and third proximal openings.

Pressure sensor and guide wire with self wetting tube

Described are implants and dilators useful in a sacral colpopexy procedure, and related methods. The present invention relates to systems, tools, and methods for treating pelvic organ prolapse by use of a pelvic implant to support pelvic tissue. The pelvic treatments include, for example, treatment of vaginal prolapse by laparoscopic or abdominal procedures.

Tools and methods for treatment of pelvic conditions

An assembly for loading a self-expanding prosthetic heart valve into a delivery device, includes a compression member having a longitudinal axis, a first open end with a first diameter, a second open end with a second diameter less than the first diameter, and a wall decreasing in diameter from the first open end to the second open end, a support member having a longitudinal axis, a base and a recess extending along the longitudinal axis and adapted to receive an end of the valve, the support member and the compression member being movable between an initial position and an operative position, and a substantially tubular restrainer disposed within the support member and, in the operative position of the compression member and the support member, defining a passageway for accepting a portion of the delivery device and leaflets of the valve when the valve is assembled on the support member.

System for loading a collapsible heart valve having a leaflet restraining member

A unitary or homogeneous patterned implant is provided. The implant is constructed of patterned cells formed by way of a molding, die casting, laser etching, laser cutting, extruding, and the like. Portions of the implant can be formed into sinusoid or other waveform strut members to control and promote elongation, expansion or contraction along single or multiple axes. As such, controlled and designated stress, tension and compression distribution is promoted across specific or localized areas of the implant.

Patterned implant and method

Various embodiments of an implant devices and systems are provided. The implant devices can include a mesh or implant encapsulated or otherwise coated, in whole or in part, with a film or coating. The coating or film can include methylcellulose or ethylcellulose to provide tissue regeneration as a hydrogel, while also providing a stiff polymer film when dry.

Film encapsulated pelvic implant system and method

A unitary or homogeneous patterned implant is provided. The implant is constructed of patterned cells formed by way of a molding, die casting, laser etching, laser cutting, extruding, and the like. Portions of the implant can be formed into sinusoid or other waveform strut members. One or more undulating anchor arms or rods extend out from the implant for tissue fixation, with the one or more undulating anchor arms including one or more arcuate bends.

Pelvic implant and treatment method

Stent delivery systems, clip members for use with stent delivery systems, and methods for making and using the same are disclosed. An example stent delivery system may include an inner shaft having a distal region. A stent may be disposed about the distal region. A deployment sheath may be slidably disposed about the inner shaft. A handle may be coupled to the inner shaft. The handle may include a clip member having a first holding portion and a second holding portion. The inner shaft may extend through the first holding portion and the second holding portion. A holding cuff may be thermally bonded to the inner shaft. The holding cuff may be positioned between the first holding portion and the second holding portion.

Stent delivery system

Implant

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Minnetonka, MN, United States of America

Dean W Hacker