Medical tubes and methods of manufacturing medical tubes. The tube(s) may be a composite structure made of two or more distinct components that are spirally wound to form an elongate tube. For example, one of the components may be a spirally wound elongate hollow body, and the other component may be an elongate structural component also spirally wound between turns of the spirally wound hollow body. The tube(s) need not be made from distinct components, however. For instance, an elongate hollow body formed (for example, extruded) from a single material may be spirally wound to form an elongate tube. The elongate hollow body itself may in transverse cross-section have a thin wall portion and a relatively thicker or more rigid reinforcement portion. The tube(s) can be incorporated into a variety of medical circuits or may be employed for other medical uses.

A suction device includes a negative pressure generator, a connector and a mask; the negative pressure generator comprises a housing and a piston rod, wherein the housing is internally provided with a cavity, an upper end of the housing is provided with an avoidance hole communicated with the cavity, and a lower end thereof is provided with an opening communicated with the cavity; the piston rod comprises a push-pull rod and a piston sleeved on the push-pull rod, an upper end of the push-pull rod runs through the avoidance hole, and the piston is movably and hermetically connected to an inner side wall of the housing by means of a sealing ring; an upper side of the mask is provided with a through first connecting cylinder, and a lower side thereof is provided with a flexible annular pad configured to fit with the face.

A passive valve for use as a fixed leak valve. The valve includes a body having an internal chamber, first and second body ports in fluid communication with the chamber with the first port configured for fluid communication with a patient connection and the second body port configured for fluid communication with a ventilator, a body passageway in fluid communication with the chamber and with ambient air exterior of the body, and a check valve seal positioned to seal the body passageway to permit the flow of gas within the chamber through the body passageway to the exterior of the body and to prevent the flow of ambient air exterior of the body through the body passageway into the chamber. In alternative embodiments, the valve is incorporated into the patient connection or constructed as a separate part connectable to the patient connection.

The present disclosure describes an improved endoscopy scope mask and related methods. One such endoscopy mask comprises a mask body defining an interior cavity that fits over a nose and mouth of a patient, in which the mask body comprises a nasal port in fluidic communication with the interior cavity having a silicone membrane that allows for insertion of an endoscopic instrument; an oral port in fluidic communication with the interior cavity having a soft silicone membrane that allows for insertion of the endoscopic instrument; an oxygen port in fluidic communication with the interior cavity; one or more filtered exhalation ports in fluidic communication with the interior cavity; and a suction port in fluidic communication with the interior cavity, the suction port having a connector for attachment to a suction tool. Other embodiments are also provided.

There is provided a respirator for supplying clean air for a wearer. The respirator comprises a face assembly comprising an oronasal mask configured to seal against and cover a nose region and a mouth region of the wearer. The face assembly may be configured to be interchangeable on the respirator between a half-face assembly and a full-face assembly. The respirator comprises a securing headgear releasably securable with the face assembly, the securing headgear assembly configured to secure the respirator on a head of the wearer. The respirator comprises a facepiece assembly for supplying the wearer with air for inhaling and releasing air exhaled by the wear, the facepiece assembly releasably securable with the face assembly. One or more of the face assembly, the facepiece assembly, or the securing headgear are configured to be released from the respirator, sterilized, and releasably resecured with the respirator.

The present invention relates to an exhalation disposal system for collecting, transporting and properly disposing of a bio-waste exhalation from an infectious patient in a closed system, thereby minimizing, if not completely eliminating, contact between medical personnel and the infectious patient's bio-waste exhalation. The system utilizes a length of flexible vacuum tubing in communication with both a specialized patient mouthpiece and a waste drain, and a check valve positioned along the length of the tubing to prevent backflow of the bio-waste exhalation. In an exemplary embodiment, the disposal system further comprises at least one sensor, a window and an access point for clearing blockages that may arise in the disposal system during use. The disposal system is configured to service multiple infectious patients simultaneously.

A ventilator includes an enclosure, a tubing configured to receive an input gas, and a flow outlet airline in fluid communication with the tubing. The flow outlet airline includes an airline outlet. The ventilator further includes a breath detection airline including an airline inlet. The airline inlet is separated from the airline outlet of the flow outline airline. The ventilator further includes a pressure sensor in direct fluid communication with the breath detection airline. The ventilator includes a controller in electronic communication with the pressure sensor and an internal oxygen concentrator in fluid communication with the tubing. The internal oxygen concentrator is entirely disposed inside the enclosure.

An intubation infection control tent system is described. In an example implementation, an infection control tent includes a cover that forms a space in which a patient can be positioned, the cover creating an infectious barrier between the patient and an external environment, one or more support channels integrated into the cover that provide a rigid structure to the cover, and a drape skirt that connects to an edge of the cover and drapes over a portion of the patient.

The present invention provides devices and methods for creating and/or maintain patency of the upper airway passage. The device is configured to fit under the chin of a subject at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device includes structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the therapy device.

The present invention provides devices and methods for creating and/or maintaining patency of the upper airway passage. The device is configured to fit under the chin of a subject at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device includes structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the therapy device.