A medical device having a time-controlled start function and a control unit, which enables user-friendly operation of the medical device, is described. The medical device has a control unit, which is equipped for automatic start-up of the medical device at a predetermined point in time and for checking on whether, after start-up of the medical device, a predetermined event has occurred, and has a display screen for display of information when the check reveals that the event has not occurred. Furthermore, a corresponding process for user-friendly operation is described.

Apparatus and methods for delivering medicament to a patient. The apparatus may include elements with different capacities to attenuate or absorb sterilizing radiation. The apparatus may include a medicament delivery assembly with interactive elements for dose-setting, priming and medicament ejection. The assembly may include a chamber housing a radiation-sensitive medicament present in the apparatus during sterilization by electron beam. The assembly may include an actuator chassis, a drive mechanism, a needle-priming mechanism and a fluid-displacement mechanism including a fluid-displacement member. The chassis may be fixed, relative to an outlet, to the chamber. The member may be slidingly and/or threadingly engaged with the chassis, and may be configured to move relative to the outlet to deliver the medicament through the outlet. Assembly elements may be nested coaxially and/or stacked axially. The assembly may include at least one hollow region. The hollow region may reduce beam attenuation or reduce radiation absorption.

Provided herein are methods and compositions for the reduction of endospore contamination of a substrate with percarboxylic acid-based compositions. The methods can include the step of continuously monitoring the oxidation-reduction potential of the percarboxylic acid-based compositions.

A medical device with a valve for autoclavability is disclosed. The medical device may include a cavity. A channel connects the cavity to an autoclave environment. The channel has a distal end and proximal end. The distal end of the channel may open to the autoclave environment and the proximal end may open to the cavity. A valve may be positioned in or near the channel. The valve may permit gas to flow from the cavity when a pressure inside the cavity is greater than a pressure in the autoclave environment outside the cavity. The valve may also prevent gas from flowing into the cavity when the pressure in the autoclave environment outside the cavity is greater than the pressure inside the cavity.

Systems, methods, and devices for disinfecting tonometer probes are described. One example provides a specialized container that allows easy catching of a used probe without having to touch the probe, allows for the storage of multiple used probes, allows for simple disinfection of the probes without having to handle the probes or remove them from the container, allows for rinsing of the probes and container without handling the probes, and then allows for the simple insertion of the disinfected probes directly from the container without having to touch the probes or reinsert them into their specialized tubes.

Seal integrity indicators for sterilization containers are provided. For example, a seal indicator may indicate whether the container is sufficiently sealed to prevent an ingress of contaminants into the container. If the container is sufficiently sealed, the seal indicator is visible, but if not, the seal indicator is not visible. Thus, the seal indicator undergoes a change in state when the sterilization container transitions from unsealed to sealed, or vice versa, such that a user may ascertain whether the container is properly sealed to maintain the container's sterility. An exemplary seal indicator includes an invertible projection formed with the container gasket that is not visible from outside the container until inverted, due to force applied by the lid, to extend through an opening in the container body. Closure mechanisms for sterilization containers also are provided.

Embodiments of a system and method for endoscope cleaning and inspection are disclosed. In an example, an endoscope cleaning and inspection unit includes cleaning and testing capabilities operated via control equipment and a display screen, to operate leak testing equipment, flush control equipment, and optical inspection equipment for leak testing, flushing, rinsing, and inspection of an endoscope interior chamber (lumen) and exterior surfaces. In a further example, the endoscope cleaning and inspection unit may further operate and receive information from a borescope imaging device or a magnification imaging device, using an imaging sensor to capture images of an endoscope lumen or surface respectively, as captured or output on the display screen. Further embodiments provide for control, monitoring, data collection, data input, and data output with such imaging devices via the endoscope cleaning and inspection unit.

The invention relates to an item-to-be-cleaned carrier for the cleaning of items to be cleaned, which have at least one cavity, the cleaning being performed in a conveyor washer. The item-to-be-cleaned carrier can be used in particular for cleaning personal protective equipment. The item-to-be-cleaned carrier comprises at least one base element and at least one nozzle tube, which is connected to the base element. The nozzle tube has at least one inlet opening having at least one catching funnel . The nozzle tube has at least one outlet nozzle. The nozzle tube tapers, at least in parts, from the inlet opening to the outlet nozzle. The invention further relates to a cleaning system and to a method for cleaning items to be cleaned, which have at least one cavity, using the cleaning system.

A free radical sterilization system having a chamber defining a region, and a generator for generating free radical reach effluent from a free radical electric generator and/or a vaporizer. A closed loop circulating system without a free-radical destroyer is provided for supplying the mixture of free radicals from the electric generator mixed with the hydrogen peroxide solution in the form of the effluent to the chamber. The free-radical sterilization system is used in sterilizing items in the chamber and, with an open-bottomed wound chamber, in treating wounds on a body.

A system includes a containment vessel configured to receive and hold one or more pieces of personal protection equipment to be heated and decontaminated during a decontamination process. The system also includes a solar collection device configured to heat the containment vessel based on received solar energy. The solar collection device includes a body having a first portion and a second portion. The first portion includes a solar aperture configured to receive the solar energy. The second portion is configured to receive the containment vessel within the body of the solar collection device. The solar collection device also includes louvered slats across the solar aperture. The louvered slats are configured to be rotated in order to control an amount of solar energy passing through the solar aperture into the body of the solar collection device.