Patent classifications
A61M11/00
SOLUTION BOTTLE
A solution bottle contains: a body and an applying head. The body includes a holder, a first sleeve, and a second sleeve. The holder has an accommodation chamber configured to accommodate a spray can, the first sleeve is secured on a top of the holder, and the second sleeve is connected with an inner wall of the first sleeve. The second sleeve has a connection hole arranged on a bottom thereof and fitting with the spray can, and the second sleeve has a receiving groove configured to house the applying head and communicating with the fitting hole. Thereby, the solution bottle is capable of massaging and applying the solution (such as medicine agent or cosmetics) on the user's body.
Intranasal administration
A nosepiece for delivering substance to a nasal cavity of a subject, the nosepiece comprising a body part which comprises a base portion which defines a flow passage therethrough, and a projection at a distal end of the base portion which at least in part provides a tip of the nosepiece and confers a rigidity in the sagittal direction, which enables the tip to open fleshy tissue at an upper region of the nasal valve and thereby expand an open area of the nasal valve, and a flexibility in a lateral direction, orthogonal to the sagittal plane, which facilitates insertion of the tip into the nasal valve.
Intranasal administration
A nosepiece for delivering substance to a nasal cavity of a subject, the nosepiece comprising a body part which comprises a base portion which defines a flow passage therethrough, and a projection at a distal end of the base portion which at least in part provides a tip of the nosepiece and confers a rigidity in the sagittal direction, which enables the tip to open fleshy tissue at an upper region of the nasal valve and thereby expand an open area of the nasal valve, and a flexibility in a lateral direction, orthogonal to the sagittal plane, which facilitates insertion of the tip into the nasal valve.
PACIFIER
A pacifier comprising a suction part and a housing part, wherein said suction part comprises a nipple and a shield connected to each other, wherein said suction part comprises a passageway through which a fluid can pass from outside a mouth of a user of the pacifier to inside the mouth of the user of the pacifier, and wherein said housing part comprises a housing, wherein said housing is prefilled with a drug which can pass through the passageway into the mouth of the user when the housing part is connected to said suction part and wherein said drug is a drug to be inhaled through the passageway of the suction part.
Method of Removing Fluid from the Body, and Device Therefore
A method for removing bodily fluid includes drawing bodily fluid that has accumulated in excess, converting the drawn fluid from bulk liquid form to aerosol form, and disposing of the aerosol via evaporation of liquid droplets and absorption and/or diffusion of vapor. Conversion from bulk liquid to aerosol may include collecting the bulk liquid fluid in a reservoir, conveying the bulk liquid bodily fluid to an atomizer, converting the bulk liquid fluid into an aerosol having ultrafine droplets, and ejecting the aerosol into a subcutaneous space for disposal via evaporation of liquid droplets and absorption and/or diffusion of vapors. The method may be performed with a subcutaneous atomizer that may be controlled locally or by an external transmitter for effecting a conversion and mist rate to keep pace with the accumulation of excess bodily fluid.
ENDOTRACHEAL TUBE
A device for irrigation of an oral cavity in a patient includes a suction element configured to be disposed in the oral cavity and configured to suction a fluid out of the oral cavity. The suction element also has one or more irrigation outlets configured to irrigate the oral cavity with the fluid. A suction line is fluidly coupled with the suction element and is configured to be fluidly coupled with a vacuum source. An irrigation line is fluidly coupled with the one or more irrigation outlets and is fluidly coupled with a source of the fluid.
VIBRATING APERTURE PLATE NEBULIZER
A nebulizer has an aerosol generator mounted in a housing, and has a vibratable aperture plate mounted to an annular support and to which is attached a vibration generator piezo. A downstream annular resilient seal is mounted between the housing and the washer on a side of the aperture plate opposed to the liquid supply reservoir. An upstream resilient seal is in the form of a gasket and is mounted between the washer and the housing reservoir, and has an opening forming part of a throat over the aperture plate. The gasket has a washer-shaped body extending radially from a downstream-extending rim adjacent the aperture plate. There are two upwardly-directed ridges for engagement with a housing surface, and the gasket is configured so that when under axial compression the opening internal surface is tapered inwardly in a flow direction to form a funnel shape.
Graphene nano-steam generator
A graphene nano-steam generator and a beauty instrument are provided. The graphene nano-steam generator includes a coarse steam channel, a nano-steam channel and a high-voltage power supply device. The coarse steam channel is connected to a coarse steam manufacturing device and the nano-steam channel. The coarse steam channel is provided with a steam sieving device, and an end of the coarse steam channel is provided with a first electrode and a second electrode. The high-voltage power supply device is coupled to the first electrode and the second electrode. The high-voltage power supply device supplies high-voltage electricity to the first electrode and the second electrode, and forms a high-voltage arc discharge between the first electrode and the second electrode, thus the coarse steam molecular group flowing through is ionized by the high-voltage arc to generate a large amount of active nano-scale steam to be flowed out from the nano-steam channel.
Pixel array medical systems, devices and methods
Systems, instruments, methods, and compositions are described involving removing a portion of the epidermis within a donor site on a subject, and harvesting dermal plugs within the donor site. An injectable filler is formed by mincing the dermal plugs. The injectable filler is configured for injecting into a recipient site on the subject.
CONTROL DEVICE FOR AEROSOL NEBULIZER SYSTEM
Provided is a control device (20, 20a) for controlling an operation of an aerosol nebulizer system (30), said aerosol nebulizer (system 30) comprising an aerosol generator (31) for nebulizing a liquid or an aerosol source for dispensing aerosol, said control device (20), 20a comprising: a communication unit (21, 21a), configured to establish a first wireless communication connection and to perform first data transmission with the aerosol nebulizer system (30), a control unit (22, 22a), configured to evaluate a progression of identifications received via the first data transmission and received in association with aerosol nebulizer data units respectively related to a usage of the aerosol nebulizer system (30).