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 double packaging structure for an object, which may be a sterile object, includes a hollow external container having a closed first end, an open second end and walls, and an internal container disposed inside the external container. The internal container includes a hollow body and a cap. The object is intended to be received in the body. To close its first end, the external container has a membrane capable of deforming when pressure is applied to the membrane. The membrane is configured so that a pressure applied to its outer face, along the longitudinal axis, pushes its inner face against the inner container and causes the inner container to exit at the second end of the external container in the absence of a closure system at the second end.

A double packaging structure for an object, which may be a sterile object, includes a hollow external container having a closed first end, an open second end and walls, and an internal container disposed inside the external container. The internal container includes a hollow body and a cap. The object is intended to be received in the body. To close its first end, the external container has a membrane capable of deforming when pressure is applied to the membrane. The membrane is configured so that a pressure applied to its outer face, along the longitudinal axis, pushes its inner face against the inner container and causes the inner container to exit at the second end of the external container in the absence of a closure system at the second end.

Devices associated with on-body analyte sensor units are disclosed. These devices include any of packaging and/or loading systems, applicators and elements of the on-body sensor units themselves. Also, various approaches to connecting electrochemical analyte sensors to and/or within associated on-body analyte sensor units are disclosed. The connector approaches variously involve the use of unique sensor and ancillary element arrangements to facilitate assembly of separate electronics assemblies and sensor elements that are kept apart until the end user brings them together.

A disposable glove and a method for making the disposable glove that reduces or eliminates glove cuff roll-down. The disposable glove includes a treated area on the interior surface of the glove that extends from the hand area to a portion of the wrist-forearm area of the glove but such that at least a portion of the interior near the glove opening is untreated. The untreated portion of the interior surface of the disposable glove resists glove cuff roll-down when the glove is positioned on a user's hand and forearm.

A moisture tight container includes a container body and a lid preferably linked to the body by a hinge. The body and lid include at least a first seal and a second seal in series to provide a moisture tight seal between the body and the lid. The first seal includes mating of thermoplastic-to-thermoplastic sealing surfaces of the body and lid respectively. The second seal includes mating of thermoplastic-to-elastomeric sealing surfaces of the body and lid, respectively, or of the lid and body, respectively.

A moisture tight container includes a container body and a lid preferably linked to the body by a hinge. The body and lid include at least a first seal and a second seal in series to provide a moisture tight seal between the body and the lid. The first seal includes mating of thermoplastic-to-thermoplastic sealing surfaces of the body and lid respectively. The second seal includes mating of thermoplastic-to-elastomeric sealing surfaces of the body and lid, respectively, or of the lid and body, respectively.

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 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.