Surgical drapes reliably maintain sterility in the operating room and enable easy and efficient installation on and removal from a surgical instrument, such as a surgical instrument at the end of a robotic surgical arm. The surgical drape comprises a transitional sheath such that in a deployed configuration a second end of the sheath is spaced relatively away from a first end of the sheath, and in an un-deployed configuration the second end of the sheath is spaced relatively close to the first end of the sheath. The sheath may further include a stiffening member secured to the second end, a pull member coupled to the stiffening member, and at least one access port formed in the first end of the sheath, such that each access port is adapted for the passage of surgical instruments therethrough.

A surgical drape includes a seal connectable with a selected surface of a body disposed with a surgical table. A draping is connected with the seal and a track of the surgical table. The draping is movable relative to the seal to define a sterile region about the body. Surgical instruments, systems and methods are disclosed.

A protective medical sleeve for use with a patient having an intravenous flow that permits easy and quick inspection of the site of the injection, but provides protection and a more sanitary environment for the IV site. The thin-walled tubular element includes a convenient door that provides access to the IV site when needed, and can be closed to prevent contaminants from entering the injection site.

The disclosed technology relates to a rod bending machine for use with a robotic surgical system in an operating room. The system which is capable to bend rods for surgeries directly in the operating room. The rigidity of the rods is such that the robotic arm alone would have to be huge to provide sufficient forces and torques. This invention introduces bending module integrated into robotic system which allows free bending of rods within limits required for surgeries.

A method of preparing a surgical site includes the steps of: disposing a preparation material with a selected surface of a patient body, the selected surface includes a sterile region having a boundary; engaging a first applicator with the selected surface and moving the first applicator along a path from a first incision site of the selected surface to the boundary; engaging a second surgical applicator with the selected surface and moving the second applicator along a path from a second incision site of the selected surface to the boundary, the path of the first applicator intersecting the path of the second applicator. In some embodiments, surgical systems and surgical instruments are disclosed.

A protective barrier for protecting an arm of a patient during a blood pressure measurement is disclosed. The protective barrier includes a waterproof layer defining an exterior waterproof surface of the protective barrier and an absorbent layer defining an interior absorbent surface of the protective barrier. An adhesive layer is disposed between the waterproof layer and the absorbent layer to bond the waterproof layer and absorbent layer together to form the protective barrier. The protective barrier also includes at least one adhesive tab extending outward from an edge of the protective barrier to removably attach the adhesive tab to a portion of the protective barrier to hold the protective barrier around the arm of the patient during the blood pressure measurement.

A portable surgical system including a transparent and flexible plastic enclosure (1) is disclosed. The enclosure is attached reversibly to the patient's body encompassing the surgical site such as to isolate and regulate the immediate environment of the surgical site, and to reduce bodily fluid splatters from the surgical site to the surgical providers. The enclosure is inflated with filtered air. Arm ports (8) are integrated into the enclosure to allow access to the inside of the enclosure by either provider arms or augmenting instrumentation taking the place of arms such as laparoscopes or robots. Material ports (10) maintain enclosure environmental integrity but allow the passing of anatomical specimens, instruments, and other materials into and out of the enclosure (1) during a procedure. The portable surgical system is lightweight and can be used in conventional operating rooms to improve sterility, or in other circumstances where no operating room is available, such as field hospitals.

A portable surgical system including a transparent and flexible plastic enclosure (1) is disclosed. The enclosure is attached reversibly to the patient's body encompassing the surgical site such as to isolate and regulate the immediate environment of the surgical site, and to reduce bodily fluid splatters from the surgical site to the surgical providers. The enclosure is inflated with filtered air. Arm ports (8) are integrated into the enclosure to allow access to the inside of the enclosure by either provider arms or augmenting instrumentation taking the place of arms such as laparoscopes or robots. Material ports (10) maintain enclosure environmental integrity but allow the passing of anatomical specimens, instruments, and other materials into and out of the enclosure (1) during a procedure. The portable surgical system is lightweight and can be used in conventional operating rooms to improve sterility, or in other circumstances where no operating room is available, such as field hospitals.

A multi-layer pre-drape apparatus is applied to a patient before the patient is moved into the operating room. The multi-layer pre-drape apparatus includes a lower layer with a center aperture and an upper layer that covers the aperture. The multi-layer pre-drape apparatus can be placed on a sterilized area of the patient to maintain the cleanliness of the incision area. Alternatively, the multi-layer pre-drape apparatus can be placed on the patient and sterilization fluid can be applied to the skin of the patient through the aperture. The patient can then be moved into the operating room and the upper layer of the multi-layer pre-drape can be removed to expose the sterilized area of the patient in the aperture. Additional drapes can be added to the pre-drape apparatus.

A multi-layer pre-drape apparatus is applied to a patient before the patient is moved into the operating room. The multi-layer pre-drape apparatus includes a lower layer with a center aperture and an upper layer that covers the aperture. The multi-layer pre-drape apparatus can be placed on a sterilized area of the patient to maintain the cleanliness of the incision area. Alternatively, the multi-layer pre-drape apparatus can be placed on the patient and sterilization fluid can be applied to the skin of the patient through the aperture. The patient can then be moved into the operating room and the upper layer of the multi-layer pre-drape can be removed to expose the sterilized area of the patient in the aperture. Additional drapes can be added to the pre-drape apparatus.