A number of variations may include a sterile kit that may include a tray constructed and arranged to hold the necessary items to access an Ommaya reservoir and the tray may define a plurality of other resources or indentations constructed and arranged to seat, hold, or house additional components of the sterile kit. The sterile kit may additionally include a paper towel, a fenestrated drape, a plurality of sponge applicators, at least one pouch of povidone-iodine, at least one retractable winged butterfly needle, at least one luer lock syringe, a 3-way stopcock, a plurality of collection vials with tops which may be screwed on to prevent the contents thereof from leaking or escaping, sterile pads, bandages including adhesive bandages, and other components.

An anesthetic equipment storage and waste air management module configured to housing electronic and electromechanical surgical equipment including a system to measure and record administration of one or more IV medications or fluids for IV administration. The module can include a housing having a lower section and a tower-like upper section, wherein the lower section is configured to house unrelated waste heat-producing electronic and electromechanical surgical equipment. The module can also include a cowling that substantially confines waste heat generated by the unrelated waste heat-producing electronic and electromechanical surgical equipment, and can include a system for measuring and recording the administration of the one or more IV medications and fluids.

A surgical draping system includes an under-draping, an over-draping, and a connecting draping connected between the under-draping and the over-draping. The surgical draping system is used to establish and maintain a surgical corridor to a surgical site or sites on a patient supported by a surgical table. The surgical draping system can accommodate rotation of the patient on the surgical table, such that the sterile surgical corridor is maintained even during such rotation. The sterile surgical corridor extends through an aperture formed in the over-draping, through an enclosed passageway formed through the connecting draping, and through an aperture formed in the under-draping.

A surgical draping system includes an under-draping, an over-draping, and a connecting draping connected between the under-draping and the over-draping. The surgical draping system is used to establish and maintain a surgical corridor to a surgical site or sites on a patient supported by a surgical table. The surgical draping system can accommodate rotation of the patient on the surgical table, such that the sterile surgical corridor is maintained even during such rotation. The sterile surgical corridor extends through an aperture formed in the over-draping, through an enclosed passageway formed through the connecting draping, and through an aperture formed in the under-draping.

A protective drape for a medical procedure may include a protective sheet including an interior surface, an exterior surface, a first end, a second end, a first side, and a second side. A first flap is coupled to the interior surface of the protective sheet so as to form a pocket at the first end of the protective sheet. The first flap includes an outer edge positioned away from the second end of the protective sheet and connected to the protective sheet, and a first lateral edge that is connected to the protective sheet so as to form a sealed periphery of the pocket that extends over the outer edge and a first lateral edge of the first flap.

A protective drape for a medical procedure may include a protective sheet including an interior surface, an exterior surface, a first end, a second end, a first side, and a second side. A first flap is coupled to the interior surface of the protective sheet so as to form a pocket at the first end of the protective sheet. The first flap includes an outer edge positioned away from the second end of the protective sheet and connected to the protective sheet, and a first lateral edge that is connected to the protective sheet so as to form a sealed periphery of the pocket that extends over the outer edge and a first lateral edge of the first flap.

A dressing for treating a tissue site with negative pressure may comprise a cover having an adhesive, a manifold, a perforated polymer film, and a perforated silicone gel having a treatment aperture. The cover, the manifold, the perforated polymer film, and the perforated silicone gel may be assembled in a stacked relationship with the cover and the perforated silicone gel enclosing the manifold. The perforated polymer film may be at least partially exposed through the treatment aperture, and at least some of the adhesive may be exposed through the perforated silicone around the treatment aperture.

A dressing for treating a tissue site with negative pressure may comprise a cover having an adhesive, a manifold, a perforated polymer film, and a perforated silicone gel having a treatment aperture. The cover, the manifold, the perforated polymer film, and the perforated silicone gel may be assembled in a stacked relationship with the cover and the perforated silicone gel enclosing the manifold. The perforated polymer film may be at least partially exposed through the treatment aperture, and at least some of the adhesive may be exposed through the perforated silicone around the treatment aperture.

Disclosed is herein a medical drape, and more particularly, a drape capable of preventing sprays generated from the mouth of a patient during dental treatment from being diffused by a first guard or the like to improve hygiene and fixation.

Disclosed is herein a medical drape, and more particularly, a drape capable of preventing sprays generated from the mouth of a patient during dental treatment from being diffused by a first guard or the like to improve hygiene and fixation.