A blower unit for use as part of an integrated blower/humidification system is described. The blower unit has an outer casing, which encloses and forms part of the blower unit, the casing including an air inlet vent. The blower unit further includes a humidifier compartment for receiving a humidifier unit with a separate gases inlet and outlet, the compartment having a heater base for heating the contents of the humidifier unit. The compartment also has a blower inlet port which aligns with the humidifier unit inlet in use, the blower providing a gases path through the casing between the inlet vent and the inlet port. The blower unit also includes a fan for providing a pressurised gases stream along the gases path, and a power supply unit for powering the fan. The gases path is routed over the power supply unit in order to provide a cooling air flow.

In an embodiment, a sleep mask is provided, which may include a site (such as a pocket near the center of the forehead), for holding electronical components for implementing a circadian rhythm disorder treatment program. Optionally, the sleep mask may also include one or more holes for locating and securing light pipes that are connected to lights for producing lighting that adjust a user's circadian pattern based on the circadian rhythm disorder treatment program. Optionally, the sleep mask also includes adjustable straps.

A method for determining gases proportions to obtain an inhalable medical gaseous composition consisting of a first noble gas, a second noble gas, and oxygen, in order to reach a body temperature value, including determining a proportion of first or second noble gas depending on predetermined parameters, such as the body temperature value and an inhalation temperature value, the determining further including determining, for the inhalation temperature value, two body temperature theoretical values for the first and second noble gas modeled by reference regression lines, calculating a difference between both body temperature theoretical values, calculating a difference between body temperature value and any one of the body temperature theoretical values, calculating a ratio representing proportion of first or second noble gas in the inhalable medical gaseous composition.

Many embodiments of wound filling devices and methods of their use in systems for the application of negative pressure therapy are described herein. In one embodiment, a wound filling device comprises: an inflatable bag member having at least one fluid carrying conduit operably connected thereto to inflate/deflate said bag member; a separate textured covering sock member at least partially covering the inflatable bag member. Another embodiment comprises a three-dimensional wound packing member, and may optionally comprise a plurality of such members linked together. Certain embodiments of wound packing members may comprise a porous bag member adapted to be non-adherent to the wound. Yet other embodiments may comprise a non-porous bag member provided with means to connect a fluid supply to the interior.

The present invention relates to an at least partly implantable system for injecting a substance into a patient's body. The system comprises at least one implantable infusion needle arranged in at least one first housing, the at least one implantable infusion needle having a tip end for injecting a substance into a penetration area of a patient, and at least one drive unit coupled to the at least one implantable infusion needle and arranged for moving the tip end of the at least one infusion needle for varying the penetration site, wherein the at least one drive unit is a drive unit arranged for moving the tip end of the at least one infusion needle using hydraulic force. The system is adapted to use infusion liquid to be injected into the patient's body as hydraulic fluid.

A vaporization apparatus includes an atomizer, a channel, and a cooler. The atomizer is provided to generate vapor from a vaporization substance by heating the vaporization substance, and the channel is in fluid communication with the atomizer, to enable fluid flow through the vaporization apparatus. The cooler is provided to cool the fluid.

There is provided in accordance with an exemplary embodiment of the invention, a device and a method for controlled extraction of at least one active substance from at least one type of plant matter by application of heat, the device comprising: a heating element adapted to apply heat to an area of the plant matter to extract the substance; and a mechanism adapted for moving the plant matter relative to the heating element. Optionally, the active substance is a restricted substance. There is also provided in accordance with an exemplary embodiment of the invention, a method of monitoring and controlling inhalation of a restricted substance. There is provided in accordance with an exemplary embodiment of the invention, a method of manufacturing a tape of plant matter comprising an active substance.

an apparatus, system, and method for contacting blood with ozone to kill microorganisms in the blood are described. The method involves injecting microbubbles of ozone containing gas into a flow of blood, preferably at a temperature of less than 12° C. The apparatus includes a blood flow conduit including a blood ozone contacting portion including a porous ozone injector. Figure to be published with the abstract:

A surgical fluid thermal treatment system can be used during a procedure to heat or cool surgical fluid, e.g., prior to introducing the fluid into the body of a patient. In some examples, the system includes an open basin into which fresh surgical fluid is dispensed and a heater that heats the fluid in the basin. The system may also include a volume measurement device that measures the volume of fluid in the basin. The system may have a user interface that a user interacts with to check fresh fluid into the basin. The user may also interact with the user interface to check medical tools into the basin and check medical tools out of the basin. A controller associated with the system can track the volume of fluid removed from the basin during the course of a procedure.

The pharmaceutical injection device includes a pharmaceutical syringe mounting portion (3) provided within a main body case (2) and to which a pharmaceutical syringe (4) is removably mounted, a piston (5) provided movably with respect to the pharmaceutical syringe (4) mounted to the pharmaceutical syringe mounting portion (3), a drive mechanism (6) for driving the piston (5), a controller (7) that is electrically connected to the drive mechanism (6), a display section (35) that is connected to the controller (7), and an encoder (26) that is connected to the controller (7) and detects the amount of the pharmaceutical remaining inside the pharmaceutical syringe (4). The controller (7) displays a warning on the display section (35) recommending removal of the pharmaceutical syringe (4) from the pharmaceutical syringe mounting portion (3) when the presence of a pharmaceutical is detected by the encoder (26).