An adapter for an evacuator for increasing a suction power of the evacuator includes a suction assembly adapted to be coupled with the evacuator. The suction assembly has a housing, an impeller arranged inside the housing and configured to provide a suction, and an inlet conduit to facilitate a flow of fluid to the impeller. The suction assembly also includes an outlet conduit arranged inside the housing and adapted to be coupled to the evacuator. The outlet conduit is in fluid communication with the impeller and facilitates a flow of the fluid from the suction assembly to the evacuator.

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.

An airborne pathogen extraction system that provides for continuous airborne pathogen particle extraction from a specifically targeted area in a room or a specifically targeted area proximate to a user. The pathogenic particles are filtered and/or disinfected before the air is returned proximate to the originating location, or are directed an area away from the user(s). The airborne pathogen extraction systems and methods lower the chances of contagion or infection from airborne pathogens, such as viruses.

In a trauma, emergency room/department (ER/ED) or similar exigent treatment environment, an emergency airway evacuation device includes a vacuum body adapted for receiving a suctioned volume, and an actuator engaged with the vacuum body for inducing a lowered pressure therein for suctioned removal of airway blockage matter. An elongated extraction tube is fluidically coupled to the vacuum body for transporting the suctioned volume from a respiratory blockage region, and includes a curved, tapered tip for insertion into the blockage region. The device is small and portable for use as an “on person” accessory suitable in cost and size for widespread distribution to medical treatment providers.

An anesthetic equipment storage and waste air management module configured to housing electronic and electromechanical surgical equipment including a system to measure and record administration of one or more IV medications or fluids for IV administration. The module can include a housing having a lower section and a tower-like upper section, wherein the lower section is configured to house unrelated waste heat-producing electronic and electromechanical surgical equipment. The module can also include a cowling that substantially confines waste heat generated by the unrelated waste heat-producing electronic and electromechanical surgical equipment, and can include a system for measuring and recording the administration of the one or more IV medications and fluids.

An adapter for an evacuator for increasing a suction power of the evacuator includes a suction assembly adapted to be coupled with the evacuator. The suction assembly has a housing, an impeller arranged inside the housing and configured to provide a suction, and an inlet conduit to facilitate a flow of fluid to the impeller. The suction assembly also includes an outlet conduit arranged inside the housing and adapted to be coupled to the evacuator. The outlet conduit is in fluid communication with the impeller and facilitates a flow of the fluid from the suction assembly to the evacuator.

An anesthetic equipment storage and waste air management module configured to housing electronic and electromechanical surgical equipment including a system to measure and record administration of one or more IV medications or fluids for IV administration. The module can include a housing having a lower section and a tower-like upper section, wherein the lower section is configured to house unrelated waste heat-producing electronic and electromechanical surgical equipment. The module can also include a cowling that substantially confines waste heat generated by the unrelated waste heat-producing electronic and electromechanical surgical equipment, and can include a system for measuring and recording the administration of the one or more IV medications and fluids.

A system, method, and air purification device. Air is taken in from an environment into the air purification system. The air is prefiltered. The air is filtered with a primary filter. The filtered air is treated with vacuum ultraviolet radiation in a primary reaction chamber to generate irradiated air. The irradiated air is treated with ultraviolet-C radiation in a secondary reaction chamber to remove ozone. Ozone and other contaminants are removed from the irradiated air utilizing a carbon filter to generate purified air. The purified air is emitted back into the environment from the air purification system.

Arrangements for capturing aerosol during dental procedures include an extraoral suction device and a blower arrangement to induce an airflow zone to push aerosol to the suction device. Blower arrangements can include plenums in the form of a tube, or a face mask, or attached to safety glasses. Extraoral suction devices can be wearable in the form of appliances to be fitted onto either the patient or the dental professional. Improved extraoral suction devices can include a screen secured to a nozzle of the device.

A device, and method of using same, to evacuate aerosols generated proximate to teeth of a patient during dental procedures, including a central housing having a proximal end and a distal end. The proximal end defines a proximal housing opening and the distal end defines a distal housing opening having a first open area. The housing defines (i) at least one housing side port on each side of the housing and (ii) at least one internal passage in fluid communication with the distal housing opening, the proximal housing opening, and the housing side ports. The proximal end of the housing is shaped to be connectable to a conduit for a source of negative pressure. The device further includes a right-side cheek retractor and a left-side cheek retractor, each retractor defining a concave buccal-side surface, a convex oral-side surface, a retractor chamber, and at least a first arc of retractor openings (i) positioned along a portion of the oral-side surface, (ii) communicating with the retractor chamber, and (iii) having a first distribution of total open area along that retractor. A right-side arm extends between the housing and the right-side cheek retractor to support the right-side cheek retractor at a substantially fixed distance from the housing, and a left-side arm extends between the housing and the left-side cheek retractor to support the left-side cheek retractor at a substantially fixed distance from the housing. At least one right-side passageway connects one of the housing side ports with the retractor chamber of the right-side cheek retractor, and at least one left-side passageway connecting one of the housing side ports with the retractor chamber of the left-side cheek retractor.