A sterility-preserving robotic frontend-system, including a flexible trajectory-guide including at least one force- and/or torque-transmitting coupling-member, a baffle-member separating a sterile section from a non-sterile section, and a sterility-sleeve attached to the baffle-member; an actuator unit having a sensor unit that senses at least one of a) whether a trajectory-guide is placed with respect to the actuator unit in a manner that allows engaging-members to accurately engage an actuator interface, and b) whether the engaging-members have accurately engaged the actuator-interface; and a retainer-receptacle adapted to temporarily accommodate the trajectory guide, and to restrain flexibility of the trajectory-guide while it is accommodated. A packaging-container having an inner sterile volume containing the retainer-receptacle and the trajectory-guide and a method of setting up such a sterility-preserving robotic frontend-system.

The invention relates to devices, systems, and methods for conditioning a zirconium oxide sorbent module for use in dialysis after recharging. The devices, systems, and methods can provide for conditioning and recharging of zirconium oxide in a single system, or in separate systems.

Vertical decompression relaxation device with vertical tank, with access ladders, with handrail and stairs for internal access, and tie rods adjustable fasteners to tie rods, mainly in the treatment of muscle and fascia stiffness.

A reverse osmosis (RO) system is described that is connectable to a dialysis machine and is capable of using heated purified water to clean and disinfect an external connection section or portion disposed between the RO system and the dialysis unit (or any other external heat tolerant device) without forming a closed loop system between both systems before and during a heat forward process. This can be accomplished without the need for direct/indirect or wired/wireless communication with the dialysis unit or the need to introduce a chemical cleaner or process that would require further rinsing after chemical disinfection.

An oral sanitation system may include a case including: a support portion defining a lower end of the case; and a container portion extending from the support portion. The container portion may define a wall extending from the support portion to a top end of the container portion. The oral sanitation system may further include a closure including a lid formed with a peripherally-extending wall; a lower cavity defined by the wall of the container portion; an upper cavity defined by the peripherally-extending wall of the closure; and a light-guiding floor that is substantially transparent to UVC light, the light-guiding floor forming a bottom of the container portion that is surrounded by the wall.

A method is provided for vaporized hydrogen peroxide cleaning of a chamber. The method includes altering a temperature of air in the chamber from an initial temperature to a sterilization temperature over a first time period. The method also includes injecting vaporized hydrogen peroxide into air in the chamber to alter a relative humidity of hydrogen peroxide vapor in the chamber to a sterilization level over the first time period. The method also includes maintaining the temperature at the sterilization temperature and the relative humidity at the sterilization level over a second time period. The method also includes reducing the relative humidity from the sterilization level to a safe level over a third time period. In one embodiment, the method is provided for vaporized hydrogen peroxide cleaning of an interior chamber of an incubation container. In other embodiments, the incubation chamber featured in the method is provided.

A sterile Intracervical Insemination (ICI) fertility kit, method of sterilization, and method of use for performing self-insemination. Each sterile kit comprises: up to three sets of individually wrapped sterile, disposable, syringes and semen collection jars; printed instructions; and a QR code. The collection jar comprises a snap-on lid, and an inner surface with seamless edges to prevent semen residue. The syringes and jars are sealed in plastic wraps permeable to air and gas, and impermeable to pathogens; and are sterilized via gamma radiation or ethylene oxide. Fresh or frozen, unwashed or washed, semen is deposited into the jar, pulled into the syringe, and administered cervically during a user's maximum monthly level of luteinizing hormone. The syringe distal end is designed to push all semen out of the syringe then plug the end closed, while preventing semen residue from collecting within the syringe. Large circular syringe handles facilitate stable handling.

An unlocking apparatus for unlocking locking devices of at least two medical ring instruments, and a sieve basket. The locking devices include cooperating locking elements, and the unlocking apparatus includes a first receiving body with at least two ring receptacles for accommodating first rings of the at least two ring instruments. The unlocking apparatus includes an unlocking body with at least two unlocking elements cooperating with second rings of the at least two ring instruments. The unlocking body and the receiving body are movable relative to one another in an actuating direction such that the at least two unlocking elements engage on and move the second rings relative to the first rings in an unlocking direction that is transverse, in particular perpendicular, to a first ring plane and to a second ring plane for transferring the locking devices from a locked position into an unlocked position.

Catheters including thermoplastic polyurethane polymer tubing with improved shape recovery after storage in a substantially coiled configuration are provided.

A cleaning device for a tomography device, in particular an MRT, has an examination tunnel. The cleaning device has a nozzle assembly for applying a liquid cleaning agent to a tunnel inner surface facing toward the tunnel axis, a mounting device, which is configured to mount the nozzle assembly on a structural unit of the tomography device parallel to the tunnel axis and displaceably along the examination tunnel, and a control unit, which is configured, in the intended cleaning operation, to specify the application of the cleaning agent in dependence on the movement of the nozzle assembly.