A interconnectable port is provided. The interconnectable port is adapted to be at least partially placed in an incision in a patient's body. The interconnectable port comprises a first and second port adapted be interconnected to form the interconnectable port, wherein the second port is disconnectable from the first port, wherein the first port is connected to a first portion of a flexible wall, and the second port is connected to a second portion of the flexible wall, and wherein the flexible wall is adapted to form a chamber.

A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective barrier from contamination.

A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective barrier from contamination.

A device is provided for enclosing an extremity of a patient for container efficient wound cleaning and for integrating draping prior to surgery. A loose-fitting flexible container with a flexible seal is provided for enclosing the extremity and treating the extremity in a controlled fashion to reduce or eliminate spillage and unwanted dispersion of antiseptic solution. Sealed to the flexible container is a vacuum packed, folded and rolled sterile surgical drape. The combination of a flexible container and a sterile pre-positioned surgical drape in a single device provides the advantage of controlled decontamination of the skin or wound while simultaneously providing the advantage of pre-positioning a surgical drape. The use of the device also provides the advantages of reduced operating room fires and biohazard dispersion risk and reduced cost by reduction of total operating room time per procedure.

The invention encompasses devices and methods that at least partially entrap the droplets and aerosols from a person undergoing an aerosol/droplet-generating procedure, thereby reducing a heath care worker's direct exposure to such health hazards. The device includes a planar cover structure impermeable to aerosols, droplets, fluids and gas. The planar cover structure providing a barrier between a health care worker and the body cavity or orifice of a patient. A hollow tubular extension forming an opening on the planar cover structure and the opening is configured to he positioned approximately on top of the body cavity or orifice of the patient. The opening configured to be reversibly closed via a closure mechanism.

The invention encompasses devices and methods that at least partially entrap the droplets and aerosols from a person undergoing an aerosol/droplet-generating procedure, thereby reducing a heath care worker's direct exposure to such health hazards. The device includes a planar cover structure impermeable to aerosols, droplets, fluids and gas. The planar cover structure providing a barrier between a health care worker and the body cavity or orifice of a patient. A hollow tubular extension forming an opening on the planar cover structure and the opening is configured to he positioned approximately on top of the body cavity or orifice of the patient. The opening configured to be reversibly closed via a closure mechanism.

A protective device that protects against nerve compression and injury during medical procedures. The device includes an elongated body having a base, and a retention flap and a closure flap joined to the base. The device further includes a closure operable to join the closure flap to the retention flap. The closure may be provided as adhesive field, magnets, a living hinge, or matable structures, such as teeth/sockets, snaps, etc., or tape, strings, sutures or other external elements may be used for joining the flaps. The body may be pretensioned to remain open, or to urge the body to assume a closed configuration. The body may be formed of foam or other flexible/compressible material so as to readily bend and conform to the body and to act to enclose and organize/confine wires/lines used in a medical procedure, and to act as a cushion between such wires/lines and the body.

A protective device that protects against nerve compression and injury during medical procedures. The device includes an elongated body having a base, and a retention flap and a closure flap joined to the base. The device further includes a closure operable to join the closure flap to the retention flap. The closure may be provided as adhesive field, magnets, a living hinge, or matable structures, such as teeth/sockets, snaps, etc., or tape, strings, sutures or other external elements may be used for joining the flaps. The body may be pretensioned to remain open, or to urge the body to assume a closed configuration. The body may be formed of foam or other flexible/compressible material so as to readily bend and conform to the body and to act to enclose and organize/confine wires/lines used in a medical procedure, and to act as a cushion between such wires/lines and the body.

A sanitary finger cover that includes a cover body of an elastic material, an outer surface, a first end defining an enclosed cover opening, an inner surface defining an enclosed cover channel, a second end, and a cover length of at least 1″ and separating the first and second ends. The cover body has an enclosed sidewall spanning the cover length and configured to at least partially enclose the finger of the patient and cover the tip of the finger of the patient enclosed and second end adapted to cover the tip of the finger. Additionally, the cover assembly includes a finger probe operably configured to measure user biometrics through, and at least partially superimposed over and directly coupled to, the outer surface of the cover body, thereby enabling the cover body to provide a barrier between the finger of the patient and the finger probe.

A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective harder from contamination.