A method for performing a surgical procedure on a patient using a robotic system and a navigation system. The robotic system includes a cutting tool. The navigation system has at least one locating device to track a portion of the patient during the surgical procedure. The navigation system provides information as to a position of the portion of the patient. An optical cutting guide is projected onto the portion of the patient to enable cutting of the portion of the patient with the cutting tool of the robotic system while the optical cutting guide is projected onto the portion of the patient.

Disclosed is a surgical drape configured to selectively allow or block a patient's view of the surgical field, as is desired in Caesarean section operations. Generally, the drape includes a main sheet, a substantially transparent sheet attached to the main sheet proximal the patient's head, and a substantially opaque screen attached to the patient-facing side of the substantially transparent sheet. This substantially opaque screen occludes the patient's visual access through the substantially transparent sheet but may be at least partially removed to permit the patient viewing access through the substantially transparent sheet towards the area of the surgery, without compromising the sterility of the surgical field. Desirably, the drape is provided with an adhesive strip disposed on the sheet or screen to permit reconnection to thereby again occlude the patient's view through the sheet.

Devices, systems, and methods facilitating surgery include surgical packaging transitionable from a furled configuration to an unfurled configuration. In the furled configuration, the surgical packaging is configured to enclose at least one surgical component therein. In the unfurled configuration, the at least one surgical component is removed from the surgical packaging and the surgical packaging is configured for use during a surgical procedure.

A surgical drape is configured for covering a patient and an ultrasonography probe during surgical treatment of the patient. The surgical drape may comprise a first portion that comprises a canopy portion. The canopy portion can be sized and shaped to at least partially cover a mechanical arm coupled to the ultrasonography probe and a proximal portion of the ultrasonography probe, and the canopy portion can be configured to move with the proximal portion of the ultrasonography probe when the ultrasonography probe is supported by the mechanical arm. A second portion can be coupled to the first portion, in which the second portion is sized and shaped to cover at least a portion of a torso of the patient.

A surgical drape having an attachable fluid control pouch and geometric alignment feature are described. The surgical drape may be fenestrated and include a base drape panel, an absorbent intermediate panel, and a mounting panel. The mounting panel may have a fluid impervious top surface that forms a higher quality adhesive seal with the adhesive attachment areas of the fluid control pouch. The surgical drape panels may be joined together by a continuous fluid impervious seal surrounding the fenestration. The fluid control pouch attachment edge may include a geometric structure that aligns with a corresponding geometric structure of the fenestration such that the fluid control pouch can be effectively positioned regardless of its rotational orientation relative to the surgical drape.

An examination garment for endoscopy includes a covering portion and a first fluid suppression member. A pants-type covering portion has an insertion port that covers a subject, who is a test object, from a torso portion to a thigh portion, and allows an insertion part of the endoscope to be inserted thereinto. The first fluid suppression member is provided in the insertion port of the covering portion and suppresses passage of the fluid in the insertion port.

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 assembly including a suctioning device suitable for being placed on an incision and/or a wound of a patient to disinfect and/or dry the incision or wound, the device including a drape. The drape includes an outer layer with an upper face and a lower face, the upper face being impermeable, an inner layer, made of non-woven sterile material, including an upper face and a lower face, the lower face to come into contact with the wound and/or the incision. The drape is wound around a limb or around the body of the patient. The assembly also includes a suctioning zone having cavities, a discharge tube connected to the suctioning zone, and a suctioning member is a system for recovering portable or mobile autologous blood.

A fluid infusion system includes an air pump connected to an accumulator tank to produce pressurized air that is stored in the accumulator tank. The system can include one or more fluid bag chambers wherein each fluid bag chamber includes an inflatable bladder positioned inside the fluid bag chamber to apply pressure on the fluid bag supported inside the chamber. The fluid bag can be connected by a tube set to deliver fluid from the fluid bag to a surgical tool at a surgical site. The fluid can, for example, be irrigation fluid or distention fluid. The system can include a controller connected to the pump to control the pump to produce the pressurized air and an adjustable pressure regulator can be connected between the accumulator tank and the inflatable bladder to control the pressure of air delivered to the inflatable bladder and the pressure that the fluid is delivered to the surgical tool. A pressure sensor can be connected between the adjustable pressure regulator and the inflatable bladder to measure the air pressure delivered to the inflatable bladder and send the air pressure measurements to the controller. The controller can configure the system display to show the air pressure measured by the pressure sensor.

Disclosed is a surgical drape configured to selectively allow or block a patient's view of the surgical field, as is desired in Caesarean section operations. Generally, the drape includes a main sheet, a substantially transparent sheet attached to the main sheet proximal the patient's head, and a substantially opaque screen attached to the patient-facing side of the substantially transparent sheet. This substantially opaque screen occludes the patient's visual access through the substantially transparent sheet but may be at least partially removed to permit the patient viewing access through the substantially transparent sheet towards the area of the surgery, without compromising the sterility of the surgical field. Desirably, the drape is provided with an adhesive strip disposed on the sheet or screen to permit reconnection to thereby again occlude the patient's view through the sheet.