An identification system for medical sterile containers and mesh trays for accommodating medical instruments. The system includes one or more sterile containers, one or more mesh trays, and one or more identification plates. Each identification plate includes an interface. At least one counterpart interface is complementary to the interface and formed or arranged on each sterile container and each mesh tray. The interface and the counterpart interface are designed to retain at least one identification plate on one of the sterile containers or on one of the mesh trays.

A sanitizing apparatus includes a main housing, a dispensing member, a supporting platform, and a sanitizing fluid pouch. the main housing comprises a front wall, a first sidewall, a second sidewall, a rear wall, a bottom wall, and an opening. The front wall, the first sidewall, the second sidewall, the rear wall, the bottom wall of the main housing together form an internal space accessible through the opening of the main housing. The dispensing member is inserted into the internal space through the opening of the main housing. The dispensing member comprises a dispensing mechanism. The sanitizing fluid pouch is filled with a sanitizing fluid and is flexible and deformable. The supporting platform is placed within the dispensing member. The supporting platform comprises a supporting plate on which is seated the sanitizing fluid pouch. The supporting platform further comprises a pressure-applying member.

A sterile container for sterilizable medical goods includes a receiving space for the medical goods and a data acquisition unit for acquiring parameter data of influencing variables that act on the sterile container. The sterile container includes an NFC module with at least one sensor for acquiring sterility-relevant and/or sterilization-relevant data and a data logger for recording and storing data from the sensor at a recording interval. The sterile container can be monitored by a method that is automatic and sterile-container-specific.

A modularly structured lid for a sterile container includes a lid component, which has at least one gas exchange portion, on which, on the inner side of a lid, at least one filter device can be arranged, and at least one filter covering by which the at least one gas exchange portion can be completely covered on an outside of the lid. The lid component has at least one standardized clip receiving portion and the filter covering has at least one standardized clip portion, by which the filter covering and the lid component can be interlockingly fixed to each other, and can be mounted and removed without tools. A sterile container can include such a lid and a filter covering for such a lid.

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.

A sanitizing apparatus includes a main housing, a dispensing member, a supporting platform, and a sanitizing fluid pouch. the main housing comprises a front wall, a first sidewall, a second sidewall, a rear wall, a bottom wall, and an opening. The front wall, the first sidewall, the second sidewall, the rear wall, the bottom wall of the main housing together form an internal space accessible through the opening of the main housing. The dispensing member is inserted into the internal space through the opening of the main housing. The dispensing member comprises a dispensing mechanism. The sanitizing fluid pouch is filled with a sanitizing fluid and is flexible and deformable. The supporting platform is placed within the dispensing member. The supporting platform comprises a supporting plate on which is seated the sanitizing fluid pouch. The supporting platform further comprises a pressure-applying member.

A combination storage and sterilization device for fake eyelashes is a portable device that houses and disinfects all types of fake eyelashes including eyelash extensions and eyelash tools. The device includes a casing, a drawer, a cover, and a sterilization mechanism. The sterilization mechanism may include a UV bulb, a power source such as batteries, and a control circuit with a timer to automatically turn on and off the sterilization mechanism. The device may further include additional compartments for storing tools and accessories associated with fake eyelashes.

A decontamination system, method, and sterilant kit for a device, such as a lumen device, is depicted. The decontamination system, in some embodiments, includes a device container, a wicking pad, and a sterilant fluid delivery device. The device container, such as a terminal package or a decontamination chamber, defines a device receiving area. The wicking pad is in fluid communication with the device receiving area. The sterilant fluid delivery device is in fluid communication with the wicking pad. The sterilant fluid delivery device is configured to wet the wicking pad with sterilant fluid. The wicking pad is configured to evaporate sterilant fluid into the device receiving area.

A packaging for a bioprocessing bag includes a housing having an open interior space, and a support base attached to an external side of the housing, the support base having a recess for receiving an impeller base plate of a bioprocessing bag.

Indicators for indicating the integrity of a seal of a sterilization container 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 in one state and displays a first indicium, and if the sterilization container is not sufficiently sealed, the seal indicator is in another state and displays a second indicium. Thus, the seal indicator undergoes a visible change in state when the sterilization container transitions from unsealed to sealed, such that the user may be assured that the container is properly sealed to maintain sterility of the articles post-sterilization. Further, the seal indicator undergoes a visible change in state if the seal is subsequently broken, to signal to the user that the seal and the sterility of the container interior has been compromised.