Medtronic, Inc.

Covidien LP

Donald R Sandmore

Frederick Alan Shorey, Jr

David Philip Besko

Robert J Lawrence

David Edward Weston

Rebecca Lynn Engel

Ernest J Rodriguez

David Bruce DeWindt

Jean-Aubert Barra

Carolyn Rose Bocheff

William Morris Booth

Friso Schlottau

Sarah L Hayman

Kenneth R Jonkman

Mark R Behlmaier

Neville DeWitt Pierrat

Stanley B Kaus

Jonathan Snyder

Vida Keene

Teresa A Teunis

Katherine Rose Joseph

Heather Harrison

John Mrachek

Remanufactured medical sensors and methods for remanufacturing used medical sensors are provided. Such a remanufactured sensor may include certain components from a used medical sensor and certain new components. For example, a remanufactured regional oximetry sensor may include a padding layer, an emitter and a pair of detectors, a flexible circuit coupled to the emitter and detectors, and a patient-contacting adhesive layer. The flexible circuit, the emitter, the first detector, the second detector, or any combination thereof, are from a used medical sensor, and the padding layer, the patient-contacting adhesive layer, or a combination thereof, are new.

Technique for remanufacturing a medical sensor

Remanufactured BIS sensors and methods for remanufacturing used BIS sensors are provided. Such a remanufactured sensor may include certain components from a used medical sensor and certain new components. For example, a remanufactured BIS sensor may include a backing layer and at least first, second, and third electrodes disposed on the backing layer having a conductive ink. The first, second, and third electrodes are adapted to be in electrical contact with a patient to perform BIS measurements. A foam layer may be disposed on at least a portion of the backing layer, and an adhesive may be attached to the foam layer and is configured to secure the remanufactured BIS sensor to the patient. The first electrode, the second electrode, the third electrode, the backing layer, or a combination thereof, may be new and the foam layer, the adhesive, or a combination thereof, may be from a used medical sensor.

Technique for remanufacturing a BIS sensor

Various embodiments of a tracheal tube having a shaped divider disposed therein for separation of a tracheal tube into multiple ventilation lumens are provided. In some embodiments, the divider divides a tracheal ventilation lumen from a bronchial ventilation lumen. In some embodiments, the shaped divider provides an irregular inner diameter that allows a relatively bulky device to be inserted into one or both lumens.

Dual-lumen tracheal tube with shaped lumen divider

Embodiments of the present disclosure relate to sensors for applying pressure to a patient's tissue. According to certain embodiments, the sensors may include one or more deformable elements that hold the optical components of the sensor against the tissue with an appropriate amount of pressure. In additional embodiments, such sensors may include a rigid one-piece sensor body that incorporates a deformable element to facilitate fine-fitting of the sensor against the tissue.

Sensor system with pressure application

A cannula has a body with a proximal end and a distal end and a tip on the distal end. The tip has an outer wall defining a lumen opening at the end of the tip and extending to the proximal end of the cannula. The tip further comprises one or more ribs extending into the lumen to support the outer wall from kinking when the cannula is flexed. The outer wall has a inner surface defining the lumen and a plurality of non-circular apertures formed in the tip extending into the lumen. The apertures having a major axis and a minor axis. The major axis aligned in relation to a circumference of the outer wall to prevent puckering or buckling when the tip is bent. This alignment is also designed to support the outer wall from kinking when the tip is bent.

Kink resistant cannula having buckle resistant apertures

A retrograde coronary sinus perfusion catheter including a tubular catheter body having a proximal end, a distal end, and an inner lumen, and an inflatable balloon spaced proximally from the distal end of the catheter body, wherein the balloon is echogenically enhanced.

Retrograde coronary sinus perfusion cannula and methods of using same

According to embodiments, a headcovering hat-based, and/or headband sensor assembly may provide an output to indicate when the sensor experiences abnormal forces or pressure. The sensor assembly may include features to increase the pressure against the tissue to allow the sensor to contact the tissue with sufficient force to obtain accurate measurement, but not so much force as to cause any discomfort for a patient.

Medical sensor and technique for using the same

Embodiments of the invention provide a cannula having a body with a first outer diameter, a proximal end, a distal end, a lumen extending between the proximal and distal ends, and a portion outward of the first outer diameter having a second outer diameter greater than the first outer diameter that is adapted to space tissue from the fluid inlet to maintain fluid flow. Such a cannula is particularly useful for cardiopulmonary bypass procedures using a kinetically assisted venous drainage system.

Cannula system and method

A malleable cannula has a body with a proximal end and a distal end, the body having a wall defining a lumen extending from the proximal end to the distal end. A reinforcement member extends along the lumen, the reinforcement member having an interior side facing the lumen and an exterior side facing away from the lumen. A malleable member extends along a portion of the exterior side of the reinforcement member. The malleable member may be constructed of a tube with a wire slidably received within the tube and may include an anchor.

Malleable cannula

An improved balloon catheter has a catheter body with an expandable member, such as a balloon, mounted to the exterior surface thereof. Preferably, means for preventing sticking of the expandable balloon to the exterior surface of the catheter body are provided. In one aspect, the catheter has an expandable member, preferably a balloon, positioned substantially equidistant from the proximal and distal ends of the catheter body. The retention catheter is positioned externally of the heart and partially surrounds the heart so that the balloon is positioned immediately adjacent the coronary sinus and when inflated, the balloon bears against the coronary sinus and at least one of the inferior vena cava and diaphragm thereby preventing inadvertent movement or removal of the RCSP catheter from the coronary sinus.

Method of administering cardioplegia solution

A cannula for conducting fluid to a body includes a cannula body having proximal and distal ends and a lumen extending therebetween. The lumen is adapted to receive the fluid flowing therethrough. The cannula also includes a cannula tip, which is coupled to the distal end of the cannula body. The canula tip includes a side wall having a plurality of fluid outlets formed therein. Each fluid outlet is directed toward the proximal end of the cannula body to reverse the flow of fluid exiting the cannula by an obtuse angle from the original direction of flow.

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Lyons, CO, United States of America

Donald R Sandmore