A61H23/04

Inflation Pressure Garments and Connectors

A connector for an inflatable garment that detects a valid connection with a pump.

HANDHELD ACOUSTIC SHOCK WAVE OR PRESSURE PULSE APPLICATION DEVICE AND METHODS OF USE
20200306132 · 2020-10-01 ·

A handheld acoustic shock wave or pressure pulse applicator device has a body structure and an applicator head. The body structure has a proximal end and a distal end with a longitudinal axis extending between the ends. The applicator head is at the distal end. the head emits pressure pulses or shock waves at an inclined angle relative to the longitudinal axis of the body structure. The applicator head has a balloon or lens or membrane through which the emitted pressure pulses or shock waves pass. The lens or membrane is configured to be coupled directly or indirectly to an exposed soft tissue surface of a palate inside a patient's mouth to direct emitted pressure pulses or shock waves to the brain. The applicator device can be configured with the inclined obtuse angle fixed between 150 degrees and 90 degrees or can be adjustable between 180 degrees and 90 degrees.

HANDHELD ACOUSTIC SHOCK WAVE OR PRESSURE PULSE APPLICATION DEVICE AND METHODS OF USE
20200306132 · 2020-10-01 ·

A handheld acoustic shock wave or pressure pulse applicator device has a body structure and an applicator head. The body structure has a proximal end and a distal end with a longitudinal axis extending between the ends. The applicator head is at the distal end. the head emits pressure pulses or shock waves at an inclined angle relative to the longitudinal axis of the body structure. The applicator head has a balloon or lens or membrane through which the emitted pressure pulses or shock waves pass. The lens or membrane is configured to be coupled directly or indirectly to an exposed soft tissue surface of a palate inside a patient's mouth to direct emitted pressure pulses or shock waves to the brain. The applicator device can be configured with the inclined obtuse angle fixed between 150 degrees and 90 degrees or can be adjustable between 180 degrees and 90 degrees.

INSERTABLE STIMULATION DEVICE

An example stimulation device for stimulation of an area inside a human body includes a first portion configured to at least partially be inserted into the human body, a pressure field generation device configured to generate a pneumatic pressure alternating field, and a pressure chamber coupled with the pressure field generation device, the pressure chamber configured to accommodate a pressure alternating field generated by the pressure field generation device. The pressure chamber is disposed in the first portion and includes an opening formed in the first portion, the pressure alternating field in the pressure chamber to be applied via the opening to the area to be stimulated inside the human body.

INSERTABLE STIMULATION DEVICE

An example stimulation device for stimulation of an area inside a human body includes a first portion configured to at least partially be inserted into the human body, a pressure field generation device configured to generate a pneumatic pressure alternating field, and a pressure chamber coupled with the pressure field generation device, the pressure chamber configured to accommodate a pressure alternating field generated by the pressure field generation device. The pressure chamber is disposed in the first portion and includes an opening formed in the first portion, the pressure alternating field in the pressure chamber to be applied via the opening to the area to be stimulated inside the human body.

Lounger having a pneumatic lounging system
10765219 · 2020-09-08 · ·

A pneumatic lounging system includes an inflatable support unit and an inflatable unit. The inflatable support unit includes an inward layer, an outward layer, and a support air nozzle. The inward layer and the outward layer define an air cavity, and the outward layer is attached to the inward layer. The support air nozzle is attached and adapted to provide direct fluid communication of air with the air cavity. The inflatable unit includes an inward wall, an outward wall, and an air nozzle. The inward wall and the outward wall define at least one air chamber, and the inward wall is attached to the outward layer. The air nozzle is adapted to provide direct fluid communication of air with one of the at least one air chamber. There is no fluid communication between the inflatable support unit and the first inflatable unit.

Lounger having a pneumatic lounging system
10765219 · 2020-09-08 · ·

A pneumatic lounging system includes an inflatable support unit and an inflatable unit. The inflatable support unit includes an inward layer, an outward layer, and a support air nozzle. The inward layer and the outward layer define an air cavity, and the outward layer is attached to the inward layer. The support air nozzle is attached and adapted to provide direct fluid communication of air with the air cavity. The inflatable unit includes an inward wall, an outward wall, and an air nozzle. The inward wall and the outward wall define at least one air chamber, and the inward wall is attached to the outward layer. The air nozzle is adapted to provide direct fluid communication of air with one of the at least one air chamber. There is no fluid communication between the inflatable support unit and the first inflatable unit.

Treatment of headache disorders

A method for treatment of a headache disorder in a human subject, including selecting at least one treatment area in the nasal cavity of the human subject, said treatment area being selected from a posterior part of the nasal cavity or an anterior part of the nasal cavity, providing a device including a stimulation member arranged for vibration stimulation of the selected treatment area, and at least one expansion member provided with a channel having a plurality of openings arranged for fluid communication with the stimulation member, introducing the stimulation member into a nasal cavity of the human subject, expanding the stimulation member to a volume such that the stimulation member abuts against the tissue to exert a pressure on tissue of the selected treatment area and bringing the stimulation member to vibrate in the nasal cavity to impart vibrations to the selected treatment area, wherein the vibrations are imparted to a posterior part of the nasal cavity, to an anterior part of the nasal cavity, sequentially to a posterior and an anterior part of the nasal cavity; or simultaneously to a posterior and an anterior part of the nasal cavity.

Treatment of headache disorders

A method for treatment of a headache disorder in a human subject, including selecting at least one treatment area in the nasal cavity of the human subject, said treatment area being selected from a posterior part of the nasal cavity or an anterior part of the nasal cavity, providing a device including a stimulation member arranged for vibration stimulation of the selected treatment area, and at least one expansion member provided with a channel having a plurality of openings arranged for fluid communication with the stimulation member, introducing the stimulation member into a nasal cavity of the human subject, expanding the stimulation member to a volume such that the stimulation member abuts against the tissue to exert a pressure on tissue of the selected treatment area and bringing the stimulation member to vibrate in the nasal cavity to impart vibrations to the selected treatment area, wherein the vibrations are imparted to a posterior part of the nasal cavity, to an anterior part of the nasal cavity, sequentially to a posterior and an anterior part of the nasal cavity; or simultaneously to a posterior and an anterior part of the nasal cavity.

CARE INSTRUMENT
20200260834 · 2020-08-20 ·

The present technical solution relates to the technical field of face and body care, and more particularly to a care instrument. In care instrument of the present technical solution, by arranging the storage container and the peristaltic pump, with the storage container accommodating the care product, the peristaltic pump is configured to draw the care product from the storage container and deliver the care product to a surface of the housing. In this way, the user can apply care products while using the care instrument. In addition, by controlling the peristaltic pump by the control component, the care product is delivered to the surface of the housing in a timed and quantitative manner, thereby achieving precise and accurate delivery of the care product. The massaging component and the peristaltic pump can operates independently. When only the massaging component works independently, the care instrument functions in massaging; and when the massaging component and the peristaltic pump work together, the care product delivered to the surface of the housing may be further uniformly dispersed by the massaging component, for better application of the care product onto the face or the body, and therefore effectively improving the user experience.