An at-home sterilization and data acquisition and deposition device including a housing having an opening or series of openings for receiving up to six medical devices, a sterilization chamber formed within the housing that is lined with sterilizing radiation reflecting material, and several sources of sterilizing radiation disposed within the sterilization chamber for sufficient emission of radiation to achieve a significant log reduction of any pathogens present on the medical devices, and an RFID scanner and sensor suite configured into the housing that prevents sterilization of non-system components, radiation emission into the environment, and that can pair with a user's mobile device. An individual catheterization system includes an at-home sterilization and data acquisition device, a software-enabled analysis of data acquired through the system, a set of accessories to enable proper lubrication, cleaning, and radiation-based sterilization of medical devices, and a set of RFID-enabled medical devices designed to facilitate sterile emptying of the bladder by providing a tactile interface that prevents direct contact between the individual and the parts of the medical devices that enter the individual's body.

Disclosed are microwave assisted methods and systems for decontaminating a variety of contaminated surfaces. The systems and methods comprise treating the surfaces with benign chemical formulations followed by exposing to microwave irradiation for short periods of time to achieve at least 6-log reduction in biological contaminants including spores of B. anthracis, B. thuringiensis, and P. roqueforti. Chemical formulations may comprise copper (II) chloride in water. The formulations may include a surfactant such as a polyethylene sorbitol ester surfactant.

Disclosed are microwave assisted methods and systems for decontaminating a variety of contaminated surfaces. The systems and methods comprise treating the surfaces with benign chemical formulations followed by exposing to microwave irradiation for short periods of time to achieve at least 6-log reduction in biological contaminants including spores of B. anthracis, B. thuringiensis, and P. roqueforti. Chemical formulations may comprise copper (II) chloride in water. The formulations may include a surfactant such as a polyethylene sorbitol ester surfactant.

A wearable device consists of a smart band and a display unit. The smart band comprises a microbial biosensor, a particulate matter sensor, an enviro sensor, a single board computer, a power supply unit, a band fastener, and a set of watch adapters. The microbial biosensor detects, measures, and monitors beneficial microorganisms and pathogens in a nasal cavity, an oral cavity, or on a surface. The microbial biosensor sterilizer kills pathogens. The particulate matter sensor detects, measures, and monitors a set of suspended particles in the surrounding air comprising beneficial microorganisms, pathogens, pollen grains, dust mite allergens, and an air quality index. The enviro sensor detects, monitors, and measures environmental conditions surrounding the user. A computing system comprises a wearable device, a microbiome mobile application, a user, a mobile device, a laboratory testing facility, a cloud server, and a physician.

Pathogens (e.g., viruses or bacteria) within a volume of air can be killed or deactivated using RF energy. A plurality of phase shifters input an RF signal and output a phase-shifted version of the RF signal at their respective outputs, wherein an amount of phase shift introduced by each of the phase shifters is controllable. A phased array antenna has a plurality of microwave radiators, and each of the respective outputs of the phase shifters drives a respective one of the microwave radiators. A controller controls the phase shifters to drive the phased array antenna such that a beam of RF energy emanates from the phased array antenna and sweeps through a volume positioned in front of the phased array antenna, and the beam of RF energy kills or deactivates the pathogens.

A personal protection and pathogen disinfection system includes personal protective equipment (“PPE”) configured to cover at least a portion of a person's face when worn by the person, a disinfection device configured to be worn or carried by the person, an input device configured to receive input from the person, and at least one processor configured to selectively activate the disinfection device responsive to the input.

A method for sanitizing pre-measured units of a pre-sanitized flowable food product in a sanitizing device installed into an existing food production system without substantially increasing the head height requirement of the feed production system. A plurality of containers are moved about a path with increased retention time through a plurality of stations: a receiving station, one or more sanitizing stations, and a dispensing station, and a container cleaning station. A pre-measured unit measured for packaging is received at the receiving station into a container. The pre-measured unit is exposed to one or more sanitizing agents at one or more sanitizing stations. The pre-measured unit is immediately packaged after sanitization. The pre-measured unit is dispensed into a packaging device at the dispensing station. The containers are then cleaned at the container cleaning station to prepare each container to receive a subsequent pre-measured unit of the pre-sanitized flowable feed product.

A method for sanitizing pre-measured units of a pre-sanitized flowable food product in a sanitizing device installed into an existing food production system without substantially increasing the head height requirement of the feed production system. A plurality of containers are moved about a path with increased retention time through a plurality of stations: a receiving station, one or more sanitizing stations, and a dispensing station, and a container cleaning station. A pre-measured unit measured for packaging is received at the receiving station into a container. The pre-measured unit is exposed to one or more sanitizing agents at one or more sanitizing stations. The pre-measured unit is immediately packaged after sanitization. The pre-measured unit is dispensed into a packaging device at the dispensing station. The containers are then cleaned at the container cleaning station to prepare each container to receive a subsequent pre-measured unit of the pre-sanitized flowable feed product.

A catheter insertion aid may comprise: an insertion tip located at a proximal end of the insertion aid; a flexible bag; a self-sealing mating mechanism on the proximal end of the insertion aid; and a physical interface that helps a user hold and support the insertion aid against the body when inserting the catheter tube into the male or female urethral tract. The catheter insertion aid may mate with a urinary intermittent catheter with a catheter tube to be inserted into a male or female urethral tract to facilitate drainage of urine from a bladder into a receptacle. The flexible bag may surround the catheter tube with a first collar connection mechanism connecting to the insertion aid and a second collar connection mechanism connecting to a catheter funnel. The self-sealing mating mechanism may mate with the catheter funnel to create a hermetic seal that is substantially air- and water-tight. The catheter insertion aid may further comprise a lubrication reservoir that holds a lubricant to coat a thin layer of the lubricant on the catheter tube facilitating insertion of the catheter tube into the male or female urethral tract.

A catheter insertion aid may comprise: an insertion tip located at a proximal end of the insertion aid; a flexible bag; a self-sealing mating mechanism on the proximal end of the insertion aid; and a physical interface that helps a user hold and support the insertion aid against the body when inserting the catheter tube into the male or female urethral tract. The catheter insertion aid may mate with a urinary intermittent catheter with a catheter tube to be inserted into a male or female urethral tract to facilitate drainage of urine from a bladder into a receptacle. The flexible bag may surround the catheter tube with a first collar connection mechanism connecting to the insertion aid and a second collar connection mechanism connecting to a catheter funnel. The self-sealing mating mechanism may mate with the catheter funnel to create a hermetic seal that is substantially air- and water-tight. The catheter insertion aid may further comprise a lubrication reservoir that holds a lubricant to coat a thin layer of the lubricant on the catheter tube facilitating insertion of the catheter tube into the male or female urethral tract.