The present invention relates to the diagnosis and treatment of urinary incontinence. The diagnosis and treatment involves the use of a multiple sensor-enabled catheter capable of providing real-time data regarding the patient's physiology, such as urinary flow and muscular function of the bladder sphincter, as well as the position and movement of the catheter within the patient.

The present invention discloses a urinary catheter that utilizes balloons to generate a method of urine drainage. The disclosed invention does not implement a traditional drainage port and avoids an exposed catheter tip. Rather, this invention consists of a multi-lumen shaft with a divided tip that generates a horizontal aperture for urine drainage when separated. The invention utilizes retention members that can take the form of multiple expandable balloons or a singular, expandable, central balloon. The balloon element can consists of balloons that are attached separately to each divided tip or one balloon shared with adjacent divided tips so that when the balloon element expands, a communication channel is revealed between the bladder and the central lumen of the shaft, ultimately generating a method of urine drainage.

A packaged intermittent urinary catheter having a longitudinally extending package and a catheter movement control device. The catheter movement control device is disposed within the package and has a monolithic planar locking member and a one-way valve. The monolithic locking member has longitudinally spaced upper and lower surfaces, laterally spaced ends, and transversely spaced front and back edges. The valve is disposed through the upper and lower surfaces of the locking member and configured and arranged for receipt of the catheter tube and to advance the tube through the locking member in the first longitudinal direction only.

A catheter insertable into a urethra to drain urine from a bladder includes a tubular portion, a sleeve disposed relative to the tubular portion, with the tubular portion having a bendable zone that is configured to allow the catheter to fold to a compact length. The catheter has a total catheter length measured between an end of a connector that is attachable to a drainage bag and an insertion end of the tubular portion that is insertable into the bladder. The compact length is less than the total catheter length, and the sleeve is operable to support the tubular portion by removing the bend in the bendable zone to thus align the connector axially with the insertion end of the tubular portion.

Fluid collection assemblies and systems and methods of using the same are disclosed herein. An example fluid collection assembly includes a fluid impermeable barrier. The fluid impermeable barrier at least partially defines a waist opening and two leg openings. The waist opening and the two leg openings are configured to have a waist and two legs of an individual positioned therein, respectively. The fluid impermeable barrier also defines at least one fluid outlet. The fluid collection assembly further includes at least one porous material conforming to at least a portion of the fluid impermeable barrier. The porous material may be adjacent to the outlet defined by the fluid impermeable barrier.

Example fluid collection devices and methods of using the fluid collection devices are described. The fluid collection devices include a fluid impermeable barrier, an enlarged base, and a fluid permeable body. The fluid impermeable barrier has a first lateral dimension and at least partially defining a chamber, an aperture configured to receive a conduit therethrough, and an opening. The base extends from the fluid impermeable barrier distal to the aperture and has a second lateral dimension greater than the first lateral dimension. The fluid permeable body is positioned at least partially within the chamber to extend across at least a portion of the opening.

A medical diagnostic system is provided to automate analysis of samples to predict a medical condition, such as pregnancy or chronic kidney disease. The system may provide test strip usage automation. The medical diagnostic system may include a sample collection component, collection cup contamination protection mechanism, sample volume control component, test strip reader component, which may be manifested as a lateral flow strip reader, flow reader, sample analytic component, data processing component, data communication component, networked data management component, and device cleaning mechanism. A method to automate analysis of samples to predict a medical condition using the medical diagnostic system is also provided.

A device for collecting urine discharged from a body of a user includes a fluid collection assembly having at least one layer for drawing urine discharged from the body into an interior cavity, an external covering that covers a portion of the at least one layer, and at least one fenestration for receiving urine, wherein the fenestration is a portion of the fluid collection assembly that is uncovered by the external covering. The device further includes a cap enclosing a first end of the assembly, a tube having a first end in fluid communication with the cap, and a shape retaining element configured to conform the assembly to a curved configuration and maintain the curved configuration until the configuration is adjusted. The assembly is configured to be disposed against the body of the user, with the at least one fenestration in operative relation with a urethral opening of the user.

Examples of a module for housing unrelated electronic and electromechanical equipment for use during surgery. The module can include a lower section and a tower-like upper section. The lower section can house unrelated electronic and electromechanical equipment. The tower-like upper section can be located on top of the lower section. A water-resistant cowling can enclose at least a portion of the lower section and the tower-like upper section. A cartridge containing one or more ultraviolet-C producing lights can be protectively housed within the tower-like upper section. The cartridge containing one or more ultraviolet-C producing lights can be configured to emerge upward from a top of the tower-like upper section to substantially seat itself on the top of the tower-like upper section when activated allowing the ultraviolet-C light to disinfect the patient and staff-contacting upper surfaces of the equipment in the operating room.

Provided herein are materials and methods of reducing contamination in a biological substance or treating contamination in a subject by one or more toxins comprising contacting the biological substance with an effective amount of a sorbent capable of sorbing the toxin, wherein the sorbent comprises a plurality of pores ranging from 50 Å to 40,000 Å with a pore volume of 0.5 cc/g to 5.0 cc/g and a size of 0.05 mm to 2 cm and sorbing the toxin. Also provided are kits to reduce contamination by one or more toxins in a biological substance comprising a sorbent capable of sorbing a toxin, wherein the sorbent comprises a plurality of pores ranging from 50 Å to 40,000 Å with a pore volume of 0.5 cc/g to 5.0 cc/g and a size of 0.05 mm to 2 cm and a vessel to store said sorbent when not in use together with packaging for same.