A surgical access device has a housing and a tubular member extending from the housing. A collar includes proximal and distal walls along with first and second sidewalls. The first and second sidewalls have a circular configuration and join the proximal and distal walls. The collar is repositionable along a length of the tubular member. A cavity is defined between the proximal and distal walls and the first and second sidewalls. The cavity is configured to store a quantity of a fluid therein. Pores extend through the distal wall and each pore is configured to allow a predetermined quantity of the fluid to flow therethrough. A port is disposed through the proximal wall and is in fluid communication with the cavity. The port is configured to allow the fluid to be introduced into the cavity.

A method of forming a balloon for a surgical access device includes positioning a molding material into a channel defined in a first mold half of a mold and mounting a second mold half onto the first mold half to cover the channel and form a cavity within the mold. The first and second mold halves each includes vent holes extending therethrough that are in fluid communication with the cavity. The method also includes expanding the molding material to conform to the shape of the cavity to form a balloon including protrusions extending radially outwardly therefrom. The protrusions are formed by engagement of the molding material with the vent holes.

Disclosed is a percutaneous transabdominal port that provides access to a hollow visceral organ. The percutaneous transabdominal port is hollow and has a channel connecting the external surface of the abdomen to the inside of an organ. A catheter or other instrument may pass through this channel into the organ. The percutaneous transabdominal port has a hollow tube which spans an abdominal wall tract, an internal retainer to prevent unintended removal, and an external retainer to prevent withdrawal into the body. If the internal retainer does not rely on inflation, the hollow tube may be cut to length. An optional seal prevents fluid leakage while permitting passage of catheters or instruments. An optional closure cap is described. A method of inserting, utilizing, and removing the percutaneous transabdominal port is described.

A perineal prostate biopsy apparatus comprising a cannula for reaching a prostate gland of an adult human male through his perineum; and a coaxial needle comprising a hollow needle shaft having an open piercing tip at its distal end and being arranged to lie within the cannula so that the piercing tip protrudes from a distal end of the cannula; and, a stylet adapted to lie within the hollow needle shaft so that a distal tip of the stylet closes the piercing tip of the needle.

A collection device (1) for minimising dispersal of pathogens into the environment during insufflating of the peritoneal cavity (12) of a subject (3), and which are entrained in insufflating gases and other gases escaping through an incision (8) in the abdominal wall (9) of the subject (3), through which a trocar is entered into the peritoneal cavity (12) comprises a patch (5) supported on a support framework (30). The patch (5) terminates in an outer peripheral portion (20) with a pressure sensitive adhesive (21) coated thereon for sealably securing the outer peripheral portion (20) to the abdominal wall (9). A central access opening (24) formed in the patch (5) tightly and sealably engages the trocar (10). With the trocar (10) extending through the access opening (24) of the patch (5) and with the patch (5) bonded by the pressure sensitive adhesive (21) to the abdominal wall (9) of the subject, the patch (5) defines with the trocar (10) and the abdominal wall (9) of the subject an annular collection chamber (17) for collecting insufflating and other gases leaking through the opening (8) in the subject. An outlet port (25) extending from the patch (5) and communicating with the collection chamber (17) is connected through a filter (29) to a vacuum system (27) for drawing gases from the collection chamber (17) where they are filtered in the filter (29) for removing pathogens therefrom, and clean filtered gases are dispersed into the atmosphere from the vacuum system (27). Other access devices and apparatus for collecting and filtering insufflating gases and other gases leaking through an incision formed in the body of a subject or through other body orifices are also disclosed.

A retractor/protector suitable for use in a surgical incision or a natural orifice comprises a longitudinal axis defining an instrument access channel extending from a proximal end to a distal end; a flexible outer ring; an inner ring; a flexible sheath extending between the outer ring and the inner ring; and at least one rigid segment adapted to attach to the flexible outer ring to thereby increase the rigidity of the outer ring. Embodiments of the retractor/protector are described that have interlocking and non-interlocking rigid segments. Embodiments are also described that have bases that insert into or under the flexible outer ring in addition to or in lieu of rigid segments to increase rigidity and/or provide support for a detachable cap.

A depth limiter that is configured to couple with a cannula of a surgical access device. The depth limiter includes first and second user contact portions and first and second biasing features. The first biasing feature includes a first resilient portion and a first gripping surface. The second biasing feature includes a second resilient portion and a second gripping surface. The first and second resilient portions are configured to move the respective first and second gripping surfaces from a fixed configuration to a movable configuration when the respective first and second user contact portions are actuated. In the fixed configuration, the first and second gripping surfaces collectively restrict axial movement of the depth limiter by directly contacting the cannula. In the movable configuration, the first and second gripping surfaces extend parallel to a longitudinal axis and allow for axial movement of the depth limiter relative to the cannula.

An intra-body system and method of inserting a flexible sleeve as a passageway into an internal organ. The method comprises inserting a channel into an organ by perforating the wall of the organ; releasing a distal fixation portion of the passageway sleeve inside the organ; fixating the distal fixation portion to the wall of the organ; pulling a proximal portion of the passageway sleeve outside the body to stretch the sleeve. The stretched sleeve: a) generates a passageway between the proximal end of the sleeve at the outer body portion and the distal portion of the sleeve inside the organ, and b) seals the perforation rim at the organ.

A surgical instrument access port assembly and method of use, the surgical instrument access port a surgical instrument has a needle lumen and a surgical access port. The needle lumen extends in a longitudinal direction and includes a needle tip at a distal end, and a body portion at a proximal end, the body portion having at least one recess or finger. The surgical access port has a cannula defining a hollow cannula shaft, and a tapered hub attached to a proximal end of the cannula. The tapered hub includes at least one inner ring configured to abut against the at least one recess or finger while the surgical instrument is inserted into the cannula of the surgical access port.

Various trocars and trocar supports are provided for allowing an insufflation port on the trocar to be coupled through the trocar support to an insufflation fluid. In one embodiment, the trocar includes a housing, a cannula extending through the housing, and an insufflation port projecting from the housing. A trocar support is provided having an opening that receives the insufflation port on the housing such that the insufflation port is unobtrusive during use and can be connected and disconnected rapidly.