A therapeutic pouch is provided. The therapeutic pouch defines a cavity for slidably receiving intravenous therapy equipment, such as an IV bag or other fluid dispenser. A front portion of the therapeutic pouch provides a comforting presentation for the patient, while the rear portion of the therapeutic pouch provides a visibility pouch for securing the IV bag and allowing a healthcare provider visibility of the administration of the fluids retained by the IV bag. The visibility pouch may provide an upper opening and an opposing lower opening, both communicating with the cavity for enabling the IV bag to protrude therefrom and access to IV tubing and ports, respectively. An upper portion of the therapeutic pouch provides a hanging loop for working in unison with the IV bag hole for enabling support from an IV stand or the like.

A rotary aromatherapy lamp structure includes an aromatherapy lamp and rotating cover. Abase of the aromatherapy lamp is configured with a control circuit board in electric connection with a fan and heating element and first support, a part of the first support positioned relatively above the fan and heating element is in combination with a container, and the first support above the container is extended with a fulcrum; the rotating cover is covered on the fan, heating element and first support, and the fulcrum is used to prop against an axle center of the fan leaves, allowing a space to be formed between the rotating cover and base and thus allowing the rotating cover to have a rotation mechanism. Whereby, the heating element heats the container to speed the essential oil evaporation, and air flow generated from the fan blows the fan leaves to rotate the rotating cover.

A patient interface comprises a support structure and a seal-forming structure. The support structure is arranged to support the sealing portion and is configured to connect to the frame. The sealing portion comprises textile and is attached to the support structure along an outer perimeter of the sealing portion such that in use the sealing portion may be in tension due to reactive stress of the support structure and/or a resilient stretch characteristic of the textile such that the sealing portion exerts a force against the patient's face.

A masking package (100) for blind testing of materials stored in a syringe, the masking package (100) comprising: an opaque housing (110) defining a syringe chamber (111) adapted to substantially surround a plunger and at least a portion of a barrel of a syringe; and a plunger extender (130) slidably receivable in the syringe chamber (111) and comprising a coupler (132) adapted to couple to the plunger of a syringe received in the syringe chamber (111), wherein movement of the plunger extender (130) relative to the opaque housing (110) moves the plunger of a syringe received in the syringe chamber (111) relative to the barrel of the syringe; and a masking package (200) for blind testing of materials stored in a vial, the masking package (200) comprising an opaque housing (210) defining a chamber (211) for receiving and surrounding a vial, the housing (210) having a length between an upper end and a lower end and comprising a first housing part (212) and a second housing part (214), the first and second housing parts (212, 214) being openable along the length of the housing (210) to define an opening in the chamber (211) that extends the length of the housing (210) for inserting a vial laterally into the chamber (211), wherein the housing is formed with a single piece construction.

A safety needle device is disclosed having a housing configured to couple to a syringe, the housing having a proximal end, a distal end, and a housing body. A first guide path, a second guide path and a third guide path may be disposed on the housing body. A needle hub is disposed on the proximal end of the housing and a needle cannula is attached to the needle hub. The device having a retractable sheath configured to move between an initial position, a retracted position and an extended position with respect to the housing, wherein the initial position partially exposes a distal tip of the needle cannula, the retracted position fully exposes the needle cannula, and the extended position fully covers the distal tip of the needle cannula. The retractable sheath also may have a guide element. The first, second and third guide paths are configured to slidingly receive the guide element. The device also having a first locking member, a second locking member, a rotating cam disposed in the housing body, and a spring element to bias the retractable sheath to an extended state to cover the distal end of the needle cannula upon completion of an injection.

The invention relates to the use of the modulation of an audio and/or visual signal by a variation in the impedance of at least one contact with the skin of at least one user, for the maintenance and/or development of the user's physical and/or mental abilities. The invention comprises the use of a device (100) for controlling the delivery of a medium, said device comprising: a first skin electrode (105) configured to generate electric waves, positioned against the skin of a first user; a second skin electrode (110) configured to capture electric waves, positioned against the skin of a second user, where the second user can be the first user; a detector (115) for detecting the value of an impedance parameter of the junction connecting the electrodes and passing through the contact with the skin of each user; and a control means (120) configured to transmit a medium-delivery command according to the value detected.

The present invention relates to a novel snow globe having an aroma diffuser function, which can obtain indoor air freshening effects without installation of a separate aroma diffuser in the room, the snow globe comprising: a glass globe in which a miniature, a transparent liquid, and white flakes or powder are stored; and a support on which the glass globe is placed, wherein all or a part of the support is formed of an absorbent material, and the portion formed of the absorbent material is impregnated with a fragrance oil.

An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

A personal vapor inhaling unit is disclosed. An electronic flameless vapor inhaler unit that may simulate a cigarette has a cavity that receives a cartridge in the distal end of the inhaler unit. The cartridge brings a substance to be vaporized in contact with a wick. A pH sensor detects a pH value of the substance to be vaporized for preventing use of an improper substance. When the pH value is confirmed, the unit is activated, and the user provides suction, the substance to be vaporized is drawn out of the cartridge, through the wick, and is atomized.

The present invention relates to a position determination device (100) (and system) for determining and registering an injection location of a liquid drug administered on a body part of a user, wherein the position determination device (100) (and system) comprises a position determination element (110) configured to provide a position signal representing a current location of the position determination device (100), and one or more processing units (150) configured to derive data representing an actual injection location based on the user in response to a current location being determined by the position determination unit (110). The position determination device may be further configured for determining a dosage activity performed by a liquid drug administration device (200) based on obtaining at least one vibration signal from a vibration determination element (110).