This invention relates to the technology of sterilizing medical ultrasonic probes, and discloses a portable ultraviolet sterilization case for ultrasonic probe, which includes a sterilization container for disinfecting and storing the ultrasonic probe, and a fixing clamp set configured to the interior of the sterilization container, wherein pairs of clamps trap the ultrasonic probe stably by an elastic structure. Hence the ultrasonic probe can be placed without colliding with the inner wall of the container.

A method of operating a sterilizer includes imaging a load of instruments to obtain an optical image and/or thermal image of the load, and selecting a sterilization cycle to be performed by the sterilizer based on one or more characteristics of the load determined from the image of the load. The characteristics may include the number of instruments, the presence of a diffusion-restricted space, the volume of the load, and the temperature of the load. The method may further include adjusting the sterilization cycle based on the characteristics of the load.

A peritoneal dialysis (PD) disinfection device includes a top made of a material configured to let light pass through the material, a bottom, a printed circuit board (PCB) secured between the top and the bottom, a plurality of ultraviolet light emitting diodes (UV-LEDs) secured to the PCB, and a power source operable to supply power to the plurality of UV-LEDs. At least one of the top, the bottom, and the PCB includes a feature that enables a patient to locate and orient the PD disinfection device so that UV light from the plurality of UV-LEDs is directed towards a connection end of the patient's catheter or a catheter/patient exit site.

Reusable catheter products are provided for storing, transporting, and sterilizing reusable urinary catheters. The products include a case comprising a proximal section, a middle section, and a distal section. The case includes a cavity configured to receive a catheter; the cavity includes a hydration fluid. The catheter comprises a distal end, a proximal end and a tubular section therebetween and includes a hydrophilic coating. When the catheter is inserted into the case, the hydration fluid sterilizes and lubricates the catheter.

A sanitation system for sanitizing an object is disclosed. The system comprises a support surface having a target location arranged to receive the object; an illumination module arranged to radiate the target location with sanitizing electromagnetic radiation (SER); a dosimeter module comprising at least a first dosimeter arranged to measure a dose of SER emitted by the illumination module and received by the dosimeter (the measured dose); a database storing instructions indicating the required dose of SER to reach the target location (the required dose); and a control module in communication with the illumination module, the database and the dosimeter module. The control module is arranged to receive from the dosimeter module the level of the measured dose. The control module is further arranged to control, based on the level of the measured dose, the illumination module such that the required dose reaches the target location.

An improved mobile apparatus for sterilizing surgical trays serves as a self-contained autoclave, allowing sterilization of the interior of the apparatus and its contents. A method of sterilization using the apparatus is presented as well. By means of a dedicated transfer and storage system, the apparatus, integrable with respect to a transfer cart and a lift device, may be moved easily between a location of sterilization, a storage area, and an operating room, and more than one such apparatus may be stacked vertically for storage to enhance storage efficiency.

Aspects of electronic illuminator systems and methods are disclosed herein, including subsystems and methods of use. In one aspect, a sensory system for an electronic illuminator to detect the presence and color of a fiber optic cable is disclosed. The system comprises a fiber optic cable having a proximal end with a fiber funnel cap and a terminal end with a protective cover. An electronic illuminator that further comprises a housing, a printed circuit board (PCB), a light emitting diode (LED), and a power source. The system further comprises an ambient light sensor, configured within the housing of the electronic illuminator, wherein the ambient light sensor converts light intensity to a digital signal. The system further comprises a fiber detection assembly, having a three dimensional magnetic flux density. Lastly, the system comprises a cap color detection assembly, wherein the cap color detection assembly detects the color of the fiber funnel cap on the proximal end of the fiber optic cable.

A medical device processor includes a chemical dosing system including a supply tube extending along a length between a first and second end. A pump is coupled to the supply tube downstream from the first end and configured to pump fluid in the tube. A bubble detector is coupled to the supply tube downstream from the first end, wherein an inner volume of the supply tube between the bubble detector and the second end is equal to or greater than a volume of a dose of liquid to be pumped from the chemical dosing system in a given dose. A controller is configured to run the pump for a predetermined period of time; detect the presence of one or more bubbles in the supply line based on measurement by the bubble detector; upon detection, continue to run the pump for the remainder of the predetermined time; and issue a notification.

An endoscope reprocessor for reprocessing an endoscope. An actuation mechanism of the reprocessor includes an actuator housing and a plunger removably attachable to an elevator guidewire lever of the endoscope. A receiving chamber receives pressurized fluid from a pump to impart a pressurized fluid biasing force that displaces the plunger relative to the actuator housing in a first direction and a return actuator that imparts a return biasing force that displaces the plunger relative to the actuator housing in a second direction. A controller controls the pump to provide the pressurized fluid at a first pressure at which the pressurized fluid biasing force is greater than the return biasing force to displace the plunger lever in the first direction and a second pressure at which the return biasing force is greater than the pressurized fluid biasing force to displace the plunger and the lever in the second direction.

A device for connection to a female medical connector is disclosed, the device includes a cap, a scrubbing foam, an elastic sealing lip, and an absorbent material. The cap is configured to define a chamber to contain an absorbent material and disinfectant or antimicrobial agent. The cap may include one or more threads adapted to engage with a female luer connector. The device may also include a peelable seal to maintain sterility prior to use and to prevent the disinfectant or the antimicrobial agent from exiting the chamber prior to use. Also described are methods of disinfecting a medical connector.