A device and associated method for the dispensation of mists for therapeutic use, comprising: a dispensing member (2) for dispensing an air flow (3) within which micronized particles of a liquid or solid therapeutic substance are dispersed; a chamber (11) having at least one inlet (12) for said air flow (3) generated by the dispensing member (2) and at least one outlet (13) for said air flow (3) present inside the chamber (11) itself; and a communication conduit (10) interposed between said dispensing member (2) and said chamber (11) in order to introduce the air flow (3) into the chamber (11) itself; said chamber (11) being switchable between an operative condition of maximum volume in which it internally defines a space (20) for containing at least one user, and a non-operative condition of minimum volume suitable for transport and/or storage.

The invention relates to a method for controlling an electrostatic atomizer for liquids, the atomizer comprising a liquid tank and a delivery device for liquid from the liquid tank, a high-voltage source and also at least one atomizer nozzle for the atomization of liquid, the at least one atomizer nozzle being connected to the high-voltage source. Here, the voltage and/or the current intensity at at least one of the atomizer nozzles are detected by sensors of control electronics and/or the voltage and/or the current intensity at the high-voltage source are detected by sensors of the control electronics.

A handle device for use with a hand held portable skin care device has a gas emitting portion that is configured to be proximate to the head of the skin care device during use with the skin care device. The gas emitting portion of the handle device has one or more gas openings. The handle device also includes an inlet that is fluidly coupled to the one of more gas openings through a channel in the handle device. During use, oxygen can be provided to the inlet, and emitted through the one or more gas openings as the skin care device is used to provide therapeutic light to the user's skin.

A wound care device for delivering topical oxygen therapy and negative pressure wound therapy for treatment of a wound. The wound care device may include an oxygen supply membrane electrode device (MEA), a vacuum pump and motor, a pressure sensor, and a power supply and electronic controls. A dressing may be connected to the wound care device for administering topical continuous oxygen therapy and negative pressure wound therapy to a wound. The wound care device may be operated to provide simultaneous topical oxygen therapy and negative pressure wound therapy, continuous oxygen therapy with intermittent negative pressure wound therapy, and alternating oxygen therapy and negative pressure wound therapy.

A wound care device for delivering topical oxygen therapy, negative pressure wound therapy, and a low intensity vacuum therapy for treatment of a wound. The wound care device may include an oxygen supply mea, an oxygen consuming mea, a vacuum pump and motor, a pressure sensor, and a power supply and electronic controls. A dressing may be connected to the wound care device for administering topical continuous oxygen therapy and simultaneous negative pressure wound therapy to a wound. A canister or exudate trap may be positioned between the dressing and the vacuum supply port of the vacuum pump to collect and store exudates from the wound. The canister may be combined with the dressing.

A medicated patch applicator includes a portable handle having a centrally registered longitudinal axis, a flexible frame pivotally connected to the handle and selectively articulated relative thereto, and an implement adjustably coupled to a distal end of the handle and disposed at a proximal end of the frame. Such an implement is located adjacent to a juncture of the frame and the handle such that the implement linearly protrudes outwardly from the handle along the centrally registered longitudinal axis. Advantageously, the implement is capable of removing an existing back liner of an existing medicated patch during an application process of the existing medicated patch.

The present disclosure relates to a connector device for a negative pressure wound therapy system having a connector housing, a fluid outlet connected to the connector housing, an air feeding port and an air filter and coupling means. The fluid outlet is adapted to be connected to a negative pressure source. The connector device is adapted to be engaged with a wound side connector of a wound side assembly by means of the coupling means. The wound side assembly includes a fluid removing conduit and an air supplying conduit, wherein a portion of each one of the fluid removing conduit and the air supplying conduit is connected to the wound side connector. The connector device when engaged with the wound side connector, the fluid removing conduit is fluidly connected to the fluid outlet and the air supplying conduit is fluidly connected to the air feeding port such that air ambient of the connector device can be fed to the air supplying conduit via the air feeding port and the air filter.

A system for treatment of a wound area of a patient including a first treatment pad comprising a plurality of Light Emitting Diodes (LEDs) for cleaning and exposing a wound area to ultraviolet light, a second treatment pad comprising removal ports for exposing the wound area to a negative pressure, and a control unit interoperably connected to the first and second treatment pads for providing a negative pressure and the ultraviolet light to the wound area.

Systems, methods, and connectors are provided that introduce a working gas at certain times into a reduced-pressure dressing into order to break or avoid vacuum locks in the conduits removing fluids. In one instance, a reduced-pressure connector includes a connector body for applying a reduced pressure to the tissue site. The connector body is formed with a venting port, a body conduit, and a receptacle to receive a reduced-pressure delivery conduit. The reduced-pressure connector includes a flexible member coupled to the connector body over the venting port. The flexible member is formed with at least one venting aperture. The flexible member is biased away from the venting port and is configured to collapse and seal the venting port under a reduced pressure greater than a threshold pressure. Other systems, apparatuses, and methods are disclosed.

A system and method for cosmetic treatment of a region of a biological surface using cold atmospheric plasma is presented. In one embodiment, a method of treatment of a region of a biological surface with cold plasma includes: selecting a post-treatment formulation; and applying the post-treatment formulation to the region pre-treated by the cold plasma.