Disclosed herein is a dental anesthetic delivery device. The dental anesthetic delivery device may comprise a handle and a body having a trough with a concave, horseshoe-shaped inner cavity. The inner cavity, which may be positioned over and around the area of a painful tooth, may further provide a soft or otherwise non-irritating interior surface which may comprise materials such as mesh, gauze, padding, or similar. The interior surface may act as a carrier of and delivery platform for various dental anesthetic substances. The dental anesthetic delivery device may incorporate a temperature modulation system that allows for the delivery of heat or cold to the affected area.

A melting device is provided that melts a bio-derived frozen product contained in a container including a heat transfer section comprising at least two heating bags, each of which is filled with a heating liquid and is capable of sandwiching the container between the at least two heating bags and a suction mechanism that sucks air from a space between the at least two heating bags and surrounding the container.

A melting device is provided that melts a bio-derived frozen product contained in a container. The melting device includes a main body capable of supporting the container in a vertically oriented state and a heating unit that heats only an upper portion of the container supported in the vertically oriented state. A liquid (bio-derived liquid product) obtained as the bio-derived frozen product melts in the upper portion of the container and then flows to a lower portion of the container. The bio-derived frozen product that has not been melted in the container floats in the liquid, and thus, is heated in the upper portion of the container to be melted.

Methods, devices and systems for improving sleep (including reducing sleep onset and maintenance of sleep duration), enhancing, or increasing sleep, including (but not limited to) treating sleeping disorders such as insomnia.

A method for treatment of a brain and/or spinal cord includes inserting a flexible catheter into a cerebrospinal fluid space, the flexible catheter including two lumens adapted to allow a fluid to circulate therein in a closed loop within the flexible catheter and the flexible catheter being adapted to be connected to a device for cooling and circulating the fluid. The cerebrospinal fluid in the cerebrospinal fluid space is cooled with the flexible catheter to enable selective central nervous system cooling. The functional status of the brain and/or spinal cord is monitored, and the treatment of the brain and/or spinal cord is modified to adjust for any change in the functional status of the brain and/or spinal cord.

In manufacturing an oxygenator (10), an intermediate spacer (18) is arranged between an inner cylinder unit (13) configured by winding a first hollow fiber membrane (14a) and an outer cylinder unit (15) configured by winding a second hollow fiber membrane (16a) so that a first gap (100a) is formed between one end portions of the inner cylinder unit (13) and the outer cylinder unit (15), and a first partition section (62a) is inserted into the first gap (100a). A first end portion (18a) of the intermediate spacer (18) is located at a region which does not overlap the first partition section (62a) in a radial direction. The intermediate spacer (18) independently supports the outer cylinder unit (15) in a state in which a gap (Sa) is formed between an inner peripheral surface of the intermediate spacer (18) and an outer peripheral surface of the inner cylinder unit (13).

In a method for manufacturing an oxygenator, an intermediate spacer is disposed between a cylindrical heat exchange unit configured by winding a first hollow fiber membrane and a cylindrical gas exchange unit configured by winding a second hollow fiber membrane so that a first gap is formed between one end portions of the heat exchange unit and the gas exchange unit, and a first partition section of a first cover member is inserted into the first gap. In such an oxygenator, a first end portion of the intermediate spacer is located at a part that does not overlap the first partition section in a radial direction in the heat exchange unit and the gas exchange unit. The intermediate spacer is formed by winding an intermediate hollow fiber membrane.

Methods and for treatment of cancer and other diseases including complications from late stage viral infections by inducing hyperthermia in a patient relying on withdrawing blood from the patient and returning the withdrawn blood to the patient to establish an extracorporeal flow circuit. Blood is heated by passing through the extracorporeal circuit at a controlled rate until a target body core temperature in is achieved. Usually, the blood will be subjected to a continuously re-circulating dialysis to balance electrolytes. Additionally, the blood will be subjected to a continuously recirculating regeneration through a carbon sorbent column where toxins and contaminants are removed. The blood temperature is maintained at the target blood temperature for a treatment period, and the blood is cooled after the treatment period has been completed. The method can also be effective in treating rheumatoid arthritis, scleroderma, hepatitis, sepsis, the Epstein-Barr virus, and patients with life threatening complications from other viruses, including the COVID-19 virus. A method for removing viruses from the blood supply in an external circuit is also presented.

In some additional aspects, an apparatus for generating nitric oxide (NO) can include one or more pairs of electrodes configured to initiate a series of electric arcs to synthesize a reactant gas into a product gas comprising NO, a sensor configured to measure a flow of a gas in a respiratory system into which the product gas is provided, a controller in communication with the one or more pairs of electrodes and the sensor. The controller is configured to adjust at least one of a pulse width, pulse period, pulse count per pulse group, pulse groups per second, energy generated by the one or more pairs of electrodes, arc frequency, arc current, and a voltage supplied to the one or more pairs of electrodes based on the measured flow to control a concentration of nitric oxide in the product gas.

A system for generating nitric oxide can include an apparatus positioned in a trachea of a mammal, the apparatus including a respiration sensor for collecting information related to one or more triggering events associated with the trachea, an oxygen sensor for collecting information related to a concentration of oxygen in a gas, and one or more pairs of electrodes for initiating a series of electric arcs to generate nitric oxide, and the system for generating nitric oxide can also include a controller for determining one or more control parameters based on the information collected by the respiration sensor and the oxygen sensor, wherein the series of electric arcs is initiated based on the control parameters determined by the controller.