A collecting unit, which receives secretion from a patient. The collecting unit comprises a cover (2) and a bag (3), which is mechanically connected to the cover (2). The bag (3) can be converted from a folded state, in which a portion of the bag (3) is folded about a fold axis (FA), into an unfolded state. Two overlapping overlap areas (3.1, 3.2) of the bag (3) that have each a connection area (VB.1, VB.2), are formed in the folded state. These connection areas (VB.1, VB.2) are detachably connected to one another, and preferably in a positively connected. The fold axis (FA) forms a common edge of the two overlap areas (3.1, 3.2).

A waste liquid receptacle includes first and second cover members for covering first and second openings, respectively. The first cover member is made of a material that is configured to: (i) be plastically deformed upward by a first suction force in a state where a second negative pressure is generated in an upper space; and (ii) plastically deform downward by a depressing force against the first cover member downward in a state where an openable and closable lid is open and the second negative pressure is released. The second cover member is made of a material that is configured: (i) not to be plastically deformed by a second suction force in a state where a first negative pressure is generated in a waste liquid receipt space; and (ii) to be broken without being plastically deformed when a depressing force is applied to the first cover member.

This invention relates to the design of tissue covering elements for use in vacuum assisted tissue apposition systems, wherein the geometry of the covering elements favours the application of contractile forces over compressive or extensive forces at the tissue interface.

A collection device and a collection process provide the capability of receiving secretions, which have been suctioned out of a patient (P). A collecting unit including a bag (3) and a cover (2) encloses a collecting unit interior space (In1). The suctioned secretions flow through a patient-side fluid connection and through a patient-side port (4) in the cover into the collecting unit interior space. A backflow barrier includes a blocking body, which is fastened to a surface of the cover of the collecting unit interior space. In a blocking state, the blocking body closes the patient-side port. A restoring force generator exerts a restoring force on the blocking body, to hold the backflow barrier in the blocking state. A flow of secretions through the patient-side port into the collecting unit interior space brings about a transference of the backflow barrier into a flow stat e against the restoring force.

A collection liner for a medical or a surgical operation includes a closed flexible bag portion. The closed flexible bag portion has a width direction (W) and a length direction (L). The closed flexible bag portion includes an upper part of the bag portion in the length direction and a lower part of the bag portion in the length direction. The lower part of the bag portion is folded inside the upper part of the bag portion in such a manner that the entire lower volume of the lower part is upside down inside the upper part.

An evacuated bottle system including a bottle defining a hollow interior, the bottle having a neck with a rim defining an opening; a cap assembly supported on the bottle, the cap assembly including a funnel having a first portion and a second portion, the first portion being insertable within the interior of the bottle and the second portion engaging a portion of the bottle to support the funnel above the rim, the funnel defining a bore that fluidly communicates with the hollow interior of the bottle; a self-sealing membrane that covers the bore formed by the funnel to selectively seal the hollow interior of the bottle; a cap attachable to the bottle, the cap including a cover portion that extends at least partially over the self-sealing membrane to restrain movement thereof, the cover portion being axially spaced from the self-sealing membrane to define a gap that permits axial movement of the self-sealing membrane to selectively open the bottle to fluid communication outside of the bottle.

A cap assembly including a self-sealing membrane that overlaps an opening to an interior of a container. The cap assembly further includes a cap having a cover portion that includes an annular wall that defines a central opening, and at least one evacuating opening located radially outward of the central opening. The cover portion defines a gap above the self-sealing membrane. The gap is configured to allow the self-sealing membrane to be at least partially displaced from the opening to allow fluid communication between the interior of the container and an outside atmosphere when a suction is applied to the cap.

A collection liner for a medical or a surgical operation is disclosed which includes a closed bag portion and inlets opening into the bag portion. The collection liner can include a handle which includes at least one of the inlets inside the handle.

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.

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.