A connector for connecting a medical tube set to a medical container, includes a collar connectable to a container, a cap having at least one opening for receiving a tube of a tube set, and an annular seal. The cap is located in the collar between an inner surface of the collar and the seat. The cap is rotatable relative to the collar. The collar includes a generally cylindrical side wall open at its upper and lower ends and an annular flange projects inwardly from the side wall at the upper end. The cap has a disc defining at least one opening and having an outer annular rim which locates between a lower surface of the annular flange on the collar and the seal.

Insufflation systems including a plurality of flow rate sensors are disclosed. Each flow rate sensor is configured to measure flow across a different flow rate range, with the combined flow rate ranges of the sensors encompassing the entire flow rate capability of the insufflation system. A controller selects the most appropriate flow rate sensor based on the gas flow required to be delivered to the patient.

A filter cartridge for a surgical gas delivery system is disclosed which includes a housing having a front end and a rear end and defining a first interior flow path extending downstream from a first inlet at the rear end of the housing to a first outlet at the front end of the housing, and a second interior flow path extending upstream from a second inlet at the front end the housing to a second outlet at the rear end of the housing, a first pleated filter element operatively associated with the first interior flow path, a second pleated filter element operatively associated with the second interior flow path, and a carbon filter disc operatively associated with the second interior flow path and positioned adjacent a downstream side of the second pleated filter element.

A seal anchor member defines a housing defining a longitudinal axis, the housing having leading and trailing ends, and including a plurality of lumens extending between the leading and trailing ends, each lumen being adapted for substantially sealed reception of an object therein and defining a longitudinal axis, wherein at least two of the lumens define longitudinal axes that are non-parallel to facilitate angled, at-rest placement of multiple instruments within the seal anchor member.

A surgical humidification system includes a source of gas flow and a humidifier that receives the gas flow and outputs a humidified gas to a delivery conduit. The delivery conduit has an outlet and a suitable interface, such as a diffuser, is connected to the outlet. The interface can be positioned near or within an open surgical cavity of a patient to supply the humidified gas to the cavity. The system also includes a pressure relief arrangement that operates to relieve pressure from the system above a normal operating pressure. The pressure relief arrangement can be located in a non-sterile portion of the system, such as upstream from the humidifier, for example.

A surgical humidification system includes a source of gas flow and a humidifier that receives the gas flow and outputs a humidified gas to a delivery conduit. The delivery conduit has an outlet and a suitable interface, such as a diffuser, is connected to the outlet. The interface can be positioned near or within an open surgical cavity of a patient to supply the humidified gas to the cavity. The system also includes a pressure relief arrangement that operates to relieve pressure from the system above a normal operating pressure. The pressure relief arrangement can be located in a non-sterile portion of the system, such as upstream from the humidifier, for example.

A leak control system (26) for an evacuation system (12) of an insufflation system (1), for controlling leakage of insufflating gas from a vessel (5) of a subject being insufflated. An evacuation conduit (20) connects a Venturi vacuum creating device (14) to the vessel (5) through a pressure relief valve (27) operable from a closed state to an open state in response to a pressure drop across the pressure relief valve (27) in the direction of the arrow A exceeding a predefined pressure drop value. The vacuum creating device (14) is operable in response to a signal from a pressure sensor (10) detecting pressure in the cavity (5) exceeding a predefined pressure value for applying a vacuum to the evacuating conduit (20) to increase the pressure drop across the pressure relief valve (27) to the predefined pressure drop value, for in turn operating the pressure relief valve (27) into the open state. On the pressure in the vessel (5) being reduced below the predefined pressure value, the vacuum creating device (14) is deactivated, and the pressure relief valve (27) transitions into the closed state, thereby preventing further leakage of insufflating gas though the Venturi vacuum creating device (14).

A system and method for use in surgical procedures. The system includes an endoscope, an imaging device coupled to the endoscope, an imaging processor coupled to the imaging device, and at least one management system coupled to the imaging processor, in which a function of the management system is automatically adjusted upon receipt of a communication from the imaging processor.

The present disclosure relates to a gas injection stabilization device and comprises: a fixed volume part having a first gas space with a fixed volume; at least one variable volume part which is in communication with the fixed volume part, and which has a volume that varies due to a gas introduced to and discharged from the fixed volume part, and which has a second gas space connected to the first gas space; a gas supply part which is connected to the fixed volume part and receives a supply of a gas from an external gas supply device; and a gas discharge part which is connected to the fixed volume part and discharges a gas to an external surgical space.

A method of treatment and delivery device for mixed carbon dioxide, carbonic acid, saline and optional active additives for treating head ailments includes delivery of dosage of the treatment at specified flow rates, using a) main housing having a hollow central area containing the dosage; b) a dosage dispenser head located at the distal end of the main housing, and having at least one flow channel for movement of the dosage from the main housing through the dosage dispenser head and to external of the dosage dispenser head; c) a dosage release control component located between the main housing and the dosage dispenser head to permit flow of the dosage through the dosage dispenser head in response to increased pressure against the dosage; and d) a pressure-changing moveable component on the main housing.