An automatic pet feeder includes a food container, a feeder body, and a bottom shell in sequence from top to bottom. A food-container bottom shell in communication with the food container is arranged at a bottom of the food container, and a bottom of the food-container bottom shell is a food supply passage having a gradually narrowing opening. A food releasing assembly is arranged on a side of the food supply passage, and a sliding passage for reciprocating movement of the food releasing assembly is arranged on a sidewall of the food-container bottom shell. A feeder main shell is arranged below the food supply passage, and a food exit assembly is arranged inside the feeder main shell. The food exit assembly includes a food pushing member matching with a food outlet and configured to move in a reciprocating manner below the food supply passage.

This invention serves to repurpose existing ethylene oxide sterilization chambers utilizing a novel chemical means of sterilization. Ethylene oxide is a longstanding gaseous sterilant for medical devices but has increasing problems associated with its hazards. Ethylene oxide is a carcinogenic and explosive chemical, and its emissions can be very harmful and cause serious health risks. Due to this, the FDA and many medical device manufacturers are trying to reduce or eliminate the use of the gas. Chlorine dioxide gas is a nearly identical alternative mode of sterilization that is non-carcinogenic and non-explosive. If firms choose to eliminate the use of ethylene oxide but do not want to waste the capital expenditure on existing sterilizers, they can instead utilize the ethylene oxide-to-chlorine dioxide conversion system of the present invention and use an effective and environmentally friendly form of sterilization in a system they already possess.

The invention relates to a patient interface comprising a plenum chamber, a seal-forming structure, and a positioning and stabilizing structure, as well as the method of operating the patient interface. The patient's interface is configured to leave a patient's mouth uncovered or if the seal-forming structure is configured to seal around a patient's nose and mouth, the patient interface is configured to allow the patient to breath from the ambient in an absence of the flow of pressurized. The positioning and stabilizing structure includes headgear, and the seal-forming structure and at least a portion of the headgear is formed from a one piece construction of textile material. In another embodiment, the seal-forming structure and/or the positioning and stabilizing structure includes an adaptive portion that adjusts based on usage conditions. In another embodiment, the positioning and stabilizing structure, the seal-forming structure and/or the plenum chamber includes and/or is formed of a textile material, and the textile material includes at least one magnetic thread constructed of magnetic material to provide a magnetic interaction between a first part of the patient interface and a second part of the patient interface. In another embodiment, a stiffener is coupled to the plenum chamber, the seal-forming structure, and/or the positioning and stabilizing structure. In another embodiment, at least one of the plenum chamber and the seal-forming structure includes a textile material; and wherein the textile material includes a surface structure that limits adhesion of debris. A UV cleaning receptacle of the patient interface is also disclosed.

Disclosed are a sterilization fabric processing equipment and a product manufactured by the processing equipment. The processing equipment includes a processing cavity, a steam device, a chemical tank, a pump set, and an automatic control device. The processing cavity has a working door and an interior for putting a frame and a base fabric overlaid on the frame. The steam device is for delivering steam to the processing cavity. The chemical tank is provided for containing a functional ion chemical and communicated with the steam pipeline through the chemical pipeline. The pump set is for delivering the steam and functional ions into the processing cavity. Under the effect of the predetermined pressure, the functional ions are closely combined to the heated base fabric fiber. The automatic control device is telecommunicatively connected to the steam device and the pump set for controlling their operation.

Exemplary embodiments of tabletop dispensers are disclosed herein. An exemplary tabletop dispenser for dispensing soap, sanitizer or lotion includes a bottle. The bottle has a neck that has a neck diameter. A pump assembly having a cylindrical housing is also included. The cylindrical has a cylindrical housing diameter that is less than the neck diameter. A controller board, a battery, a motor and a pump are at least partially located within the cylindrical housing. The pump assembly is configured to be located within the neck and the bottle. A sensor for sensing an object and an outlet nozzle are also included.

Disclosed is a self-sanitizing enclosure for installation onto a table-top. The self-sanitizing enclosure includes a UVC light source, where the UVC radiation emitted from the UVC light source is configured to sterilize components that are stored within the self-sanitizing enclosure.

Systems and methods for cleaning and maintaining artificial airways sized for insertion within pediatric or neonatal patients (e.g., external diameters of less than 5 mm) are disclosed. The system includes a multi-port ventilator manifold configured to couple to a ventilation source, thereby forming a ventilator circuit with the patient. The manifold includes an occluder configured to advantageously reduce an amount of dead space in the manifold so as to prevent less of positive end expiratory pressure of the ventilator circuit and reduce the likelihood of broncho-pulmonary dysplasia of the patient, or even premature death.

The present invention provides a breathing assistance apparatus that has a convenient and effective method of cleaning internal conduits inside the apparatus. The breathing assistance apparatus is preferably a gases supply and humidification device. The cleaning method is a method of disinfection that is automated so minimal training is required to disinfect in particular an internal elbow conduit within the device. It is therefore not necessary to dismantle the gases supply and humidification device, therefore, inadvertent damage to the internal parts of the device is avoided. The present invention also provides a method of disinfecting a heated breathing conduit and a patient interface.

An excimer bulb assembly including an excimer bulb and a pass filter such that the excimer bulb assembly does not emit substantial UV radiation in wavelengths longer than 231 nm, 232 nm, 233 nm, 234 nm or 235 nm. The wavelengths are measured at an incident angle of zero (0) degrees to the filter plane. The pass filter is preferably constructed of a plurality of layers of hafnium oxide, and most preferably constructed of less than seventy five (75)layers of hafnium oxide. The excimer bulb, pass filter, and two electrical connectors may be adapted to form a cartridge which may be adapted to swivel along its main axis. The cartridge may further include a smart chip. The smart chip may retain and store information regarding the assembly and preferably retains hours of use of the excimer bulb.

Provided is an apparatus for treating a surface of a medical metal. The apparatus includes a lamp unit in which a through-hole is formed and which irradiates the through-hole with ultraviolet rays, a lifting unit on which a container accommodating a medical metal is detachably disposed and which is disposed to be movable in the through-hole, and a case unit which accommodates the lamp unit and the lifting unit and includes an outer case in which an outer hole corresponding to the through-hole is formed and an inner case which is disposed inside the outer case and in which the lamp unit or the lifting unit is disposed.