Abstract: A reusable urinary intermittent catheter comprising: a catheter tube; a funnel connected to the catheter tube; and one or more near-field communication (NFC) tags embedded in the catheter that contain authentication information and validate the authentication information and usage information. The catheter tube may be configured to be inserted into a male or female urethral tract to facilitate drainage of urine from a bladder into a receptacle. The funnel may be curved to facilitate a flow of urine through the catheter tube and slow the flow of the urine exiting the funnel while minimizing splashing of the urine and reducing material strain on the catheter tube when stored with an insertion aid.

Abstract: 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.

Abstract: A filter media can include a fiber coated with a barrier coating that is substantially non-reactive to reactive species, and a photocatalytic coating disposed on the barrier coating, wherein the photocatalytic coating generates reactive species in response to illumination with optical radiation.

Abstract: A system and method for controlling microbial growth on and in medical devices and implants, especially biofilm infections, involves using pulsed electric fields (PEF). To eradicate at least a portion of a biofilm on a medical implant, for example, 1500 volts can be applied through an electrode system, with pulse duration of 50 ?s and pulse delivery frequency of 2 Hz. In the clinical setting, systemic microbial therapy can be combined with PEF to achieve a synergistic effect leading to improved eradication of infections.

Abstract: 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.

Abstract: The present invention is directed to a method of inactivating virus that is present during production of a polypeptide of interest. In particular, the present invention is directed to a method of on-column virus inactivation using a low pH and high salt wash solution that effectively inactivates viruses with minimum recovery loss of the polypeptide.

Abstract: An on-body injector system includes a drug container assembly including a container, a seal member, and a sealing interface between the seal member and the container. The container includes an opening and the seal member at least partially covers the opening in the container. A fluid pathway assembly is coupled to the drug container assembly and includes a needle that is movable between a storage position, in which a point of the needle is spaced from the seal member, and a delivery position, in which the point of the needle is disposed at least partially through the seal member. A radiation generator is configured to emit rays of radiation to sterilize and/or disinfect the sealing interface. A barrier is disposed adjacent to the sealing interface and has an opening. At least a portion of the drug container assembly is positioned adjacent to the opening in the barrier.

Abstract: Methods, devices and systems are described for digitally creating new scents or digitally dispensing gas, vapor, or liquid substances.

Abstract: Systems for extracting solute from a source material are shown and described. Each of the systems includes: a solvent source container configured to store a cooled solvent, a canister configured to contain the source material and receive solvent to produce an extract solution, and one or more extract containers in communication configured to receive and distill the extract solution, the solvent source container being configured to receive a post-extraction portion of the solvent. In some examples, the one or more extract containers are first and second extract containers that are each selectively coupleable to the canister and are selectively removable for storage of the extract mixture or the solute. In some other examples, the system further includes a cooling mechanism coupled to the solvent source container for cooling the recycled solvent within the solvent collection container.

Abstract: A method and apparatus for reducing pathogens in successive pre-measured units of a flowable food product without substantially increasing the head height requirement of a feed production system. A plurality of containers are moved about a path within a housing. The path has a plurality of stations, such as a receiving station, one or more sanitizing stations, and a dispensing station, and a container cleaning station. A pre-measured unit of the flowable food product is received at the receiving station into a container. The pre-measured unit of the flowable food product is exposed to one or more sanitizing agents at one or more sanitizing stations. The pre-measured unit of the flowable food product is dispensed into the 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-quantified unit of the flowable feed product.

Abstract: A method and device for the remote eradication of pathogens comprising a light source for emitting UV light in the pathogen killing wave length range, and a tangible transmission medium, which is at least initially resistant to degradation by the UV light. An optical interface between the UV light source and the tangible transmission medium is provided whereby the emitted UV light is collected from the light source and transmitted through the tangible transmission medium, whereby UV light emitted from the tangible transmission medium and directed against a pathogen in proximity thereto is at a power level sufficient to substantially effectively kill the pathogen within a reasonable period of time. The device is used for sanitization of biopsy channels of endoscopes and for treating of pathogens within humans and animals.

Abstract: Various embodiments of the present invention relate to, among other things, a nano carrier platform for generating enhanced engineered water nanostructures (iEWNS) encapsulating and delivering reactive oxygen species (ROS) and, in some instances, other active ingredients, methods for inactivating at least one of viruses, bacteria, bacterial spores, and fungi on a substrate by applying iEWNS to the substrate.

Abstract: An inline drain sanitizing system, includes: a manifold assembly including an inlet port, an outlet port, and a treatment port, wherein: the inlet port is configured to be couplable to a condensate supply line and receive unsanitized condensate, and the outlet port is configured to be couplable to a condensate drain line and provide sanitized condensate; and a treatment subsystem configured to interface with the treatment port and process the unsanitized condensate to generate the sanitized condensate.

Abstract: The invention relates to a facility which has a dirty facility area and an adjacent clean facility area, baskets for receiving the dirty articles, and a wall separating the dirty area from the clean area, the dirty area including an entry door for receiving the dirty articles, pre-processing stations with tables for the pre-washing and/or sorting by a human operator, or even by a robotic operator, of the dirty articles and for arranging the pre-washed and/or sorted articles in the baskets, pick-up points at the pre-processing stations for pick-up of the baskets with the pre-washed and/or sorted articles, a plurality of washers, eg.

Abstract: A multi-use disinfecting cap and method for disinfection and protection of a needleless IV injection port. The disinfecting cap has an upper chamber which contains a sterilizing solution and a low chamber which connects to a needleless IV injection port. The fluid can be manipulated to flow between the two chambers. When in use the cap protects and disinfects a needleless IV injection port when exposed prior to injecting medication into the needleless port and continues to disinfect and protect prior for any subsequent exposures. The cap is re-usable and provides a clear indication of the disinfecting solution and a datable top surface. The multi-use disinfecting cap may be removably clipped to the IV tubing and is shaped to prevent accidental rolling away if dropped.

Abstract: Sterilisation apparatus comprising a sterilisation instrument configured to be inserted through the instrument channel of a surgical scoping device and a withdrawal device for withdrawing the sterilisation instrument from the instrument channel at a predetermined rate. The sterilisation instrument comprises an elongate probe having a probe tip with a first electrode and a second electrode arranged to produce an electric field from received RF and/or microwave frequency EM energy. In operation the instrument may disinfect an inner surface of the instrument channel by emitting energy whilst being withdrawn through the channel.

Abstract: A method of sterilizing material includes receiving the material in a sterilizing chamber, vaporizing sterilant supplied to vaporizer from a sterilant source, exposing the material to the vaporized sterilant by conducting a sterilization cycle in the sterilizing chamber, heating ambient filtered air supplied to the vaporizer from an ambient filtered air source, and removing residuals of the vaporized sterilant absorbed or adsorbed by the material during the sterilization cycle by conducting an aeration cycle in the sterilizing chamber. The removing of the residuals includes conducting a plurality of aeration pulses to provide the sterilizing chamber with an aeration atmosphere comprising the heated filtered air to vaporize the absorbed or adsorbed residuals, and conducting a plurality of aeration vacuum pulses to evacuate the aeration atmosphere and vaporized residuals from the sterilizing chamber.

Abstract: Method that allows surfaces in interior spaces or technical equipments to be cleaned, characterised in that it comprises at least the following step: —the targeted atomization on the surfaces of a liquid with spores of benign bacteria on all or certain types of surfaces by means of an electrically and/or pneumatically powered atomizer, while the space remains accessible to people and animals, with the purpose of speeding up the cleaning of interior spaces and of technical equipments, lowering the cleaning frequency, and lowering the dust deposit.

Abstract: There is provided a system and method of cleaning surfaces of an enclosable environment of a contamination comprising a microbial and viral load. The method includes the steps of sealing the enclosable environment and placing water, and a solid or gel pack, into a container and generating a vortex the container by rotating an impeller. The agitation causes the solid or gel pack to release a gaseous cleaning agent. An air-borne spray exiting from the container spreads throughout the enclosable environment to contact the surfaces to be cleaned within the enclosable environment. The enclosable environment is maintained closed for an effective time period while the air-borne spray dwells on the surfaces to eliminate or substantially reduce the load of the contamination.

Abstract: A portable sterilizer according to an embodiment of the present application is capable of spraying ultra-fine chemicals, and includes a housing in which a space is formed and an injection nozzle is provided at a front end thereof, a chemical tank provided on one side of the space of the housing, a chemical feed pipe formed between the chemical tank and the injection nozzle, and a water pump which is installed on one side of the chemical supply pipe to supply the chemical to the injection nozzle through the chemical supply pipe.