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.

A single-use infection control system for a forced air warming machine having hosing connected to the machine including: a closable container having a chamber to receive the machine, the container constructed from air permeable material that prevents infectious airborne particles from entering the chamber; a sleeve having a first end and a second end, the first end engaged to an aperture on the container and the sleeve surrounding the hosing; and a filter cap constructed from the air permeable material, disposed at the second end and covering an opening of the hosing.

A blanket for forced air warming of a patient, the blanket including a non-air permeable outer layer an air permeable inner layer contactable to the patient; the outer layer and inner layer defining an inflatable chamber, the inflatable chamber allowing egress of the forced warming air through the inner layer; wherein in use, the inflated chamber provides visual transparency of the patient.

A dynamic support apparatus. The dynamic support apparatus includes a cushion, at least one actuator wherein the at least one actuator defines an interior volume and wherein the interior volume may be configured to be at least partially filled with a fluid, and a support disposed in the interior volume wherein the support configured to support an occupant when the interior volume is not filled with the fluid such that the support is sufficient to support the occupant.

Methods, systems, and apparatus, including computer programs encoded on computer storage media for treating medical conditions such as neurological disorders. A user device can be used to communicate with a user and can be used to control a treatment device. The treatment device can be an ear pressure treatment device. The system can execute treatment parameter profiles, and selection of the treatment parameter profiles can depend, at least in part, on feedback provided by the user, such as via the user device. One, two, or more nerves associated with target anatomical locations (e.g., one or both ears) can be stimulated. Some embodiments involve combination therapy including stimulating one or more nerves associated with at least one ear with a first stimulus modality, and a second stimulus modality that is the same as, or different from the first stimulus modality.

A retainer with a closure mechanism not removable from the retainer is bonded to each of the air inlet openings of an inflatable convective thermal blanket. The bottom surface of the retainer is bonded to the blanket so that its orifice is in alignment with the opening into the blanket. The closure may be a flexible layer or sheet that is adhesively attached to the top surface of the retainer. An end portion of the flexible layer away from the orifice of the retainer may be press or die cut into the retainer so that the flexible layer is non-removably attached to the retainer when the user peels the releasably secured portion of the flexible layer away from the retainer to expose the air inlet opening. The closure can also be an extension of the retainer that is hingedly connected to the retainer so as to be able to be moved pivotally to cover the retainer. The closure has a configuration that allows it to be releasably secured to the retainer when it covers the orifice opening of the retainer.

In an apparatus for facilitating fatigue reduction of a user, a characteristic identifier identifies at least one personal characteristic item of the user, and a hot-cold stimulus controller instructs a hot-cold stimulator to apply hot and cold stimuluses to the user in accordance with a stimulus condition, and varies, based on the identified at least one personal characteristic item of the user, the stimulus condition of each of the hot stimulus and cold stimulus. The stimulus condition of each of the hot stimulus and cold stimulus include at least one of, one or more parts of the user to which the corresponding one of the hot stimulus and cold stimulus is to be applied, a temperature of the corresponding one of the hot stimulus and cold stimulus, and an application period of the corresponding one of the hot stimulus and cold stimulus to the user.

A blanket for venipuncture or cannulation on a patient's hand using forced air warming, including a non-air permeable outer layer and an air permeable inner layer the outer layer and inner layer defined to form an inflatable chamber, the inflatable chamber allowing egress of continuous forced warming air on the patient's hand; wherein in use, continuous forced warming air dilates and allows for visual identification of the patient's hand veins.

The invention relates to a vasodilation assembly for facilitating intravenous cannulation. The assembly comprises: (i) a flexible plastics sleeve (10); (ii) a heated air supply; and (iii) a conduit for conveying heated air from the air supply into the flexible plastics sleeve. The sleeve comprises an air inlet opening (12) for coupling to the conduit, and an opening (14) for accepting an appendage of a patient. The flexible plastics sleeve (10) is of a double-walled construction comprising transparent inner and outer sleeve layers (16, 18).

The present invention and method, process & system comprises a vaginal drying air pump device/apparatus of a barrel (outer tube), inner tube, easy gripping rubber pipet/syringe air bulb and a permanent rubber seal or rubber gasket; constructed from a re-designed tampon plastic applicator with a uniquely new function and new objective, which is capable of reducing the excessive moisture and excessive heat in the vagina that causes and contributes to bacterial and vaginal yeast infections. The vaginal pump and method/process and system are designed with a manual hand-operated, squeezable syringe air bulb to produce a consistent flow of air within the vagina to dry excessive moisture and reduce excessive heat. In preferred embodiments, the various components of the vaginal pump are constructed into 2-pieces that are easily screwed together at the connecting threads by the end user. The vaginal drying air pump is reusable, easy to clean and portable.