A hand-held electromechanical surgical device is configured to selectively connect with a surgical accessory. The surgical device includes a power-pack, an outer shell housing, and a gasket. The power-pack is configured to selectively control a surgical accessory. The outer shell housing includes a distal half-section and a proximal half-section, the distal half-section and the proximal half-section together defining a cavity configured to selectively encase substantially the entire power-pack therein. The gasket is located between the distal half-section and the proximal half-section of the outer shell housing. The gasket is configured to create a seal between the distal half-section and the proximal half-section and to provide a sterile barrier between the power-pack and an outside environment outside the outer shell housing.

A nasal cannula cover which includes a body having a cavity adapted to receive at least the prongs of a nasal cannula to protect the same from contaminants when the nasal cannula is not in use. Vents are present in the body to facilitate moisture removal from the cavity and discourage bacterial growth. The cover contains a nasal cannula connector with a fastener that temporarily connects the nasal cannula to the cover. The cover further includes an attachment fixture that facilitates connection of the cover to a surface, such as, but not limited to a strap of a bag that a portable oxygen concentrator is carried in, a cart that carries an oxygen tank or concentrator or even a surface in the home, for example a chain, doorknob or home oxygen source, so that the nasal cannula does not come in contact with any unsanitary surface.

A device for forming a liquid aliquot, the device including: a first layer; an elastic second layer overlapping the first layer; a first passageway to receive and hold a volume of liquid, the first passageway formed from the first and second layers; a first actuator to press on the elastic layer thereby dividing the liquid filled passageway into a series of liquid aliquots; a series of vents associated with the series of aliquots; a second actuator to control flow of liquid aliquots through the associated vents; and an attachment structure for attachment of aliquot receptacles to receive liquid aliquots that flow through the vents.

A method for preparing a prosthetic valve and a delivery system for an implantation procedure. The method comprises (a) obtaining a tray, the tray containing the delivery system, the prosthetic valve coupled to the delivery system, and a valve cover in which the prosthetic valve is disposed. The tray comprises a storage cavity comprising an open end, a floor, and a peripheral side wall defining the depth of the cavity, wherein the prosthetic valve and the valve cover are disposed in the storage cavity; and a mounting surface that substantially immobilizes and maintains the valve cover and prosthetic valve within the storage cavity. The method further comprises (b) at least partially filing the storage cavity with a first hydrating fluid to completely immerse the prosthetic valve; and (c) removing the delivery device with the prosthetic valve from the tray, including disengaging the prosthetic valve from the mounting surface.

A sterile packaging assembly configured to receive a surgical instrument is disclosed. The sterile packaging assembly comprises a vacuum-molded tray and a particulate trap. The vacuum-molded tray comprises an instrument cavity configured to receive the surgical instrument, and a trap cavity. The particulate trap is positioned in the trap cavity. The particulate trap comprises a housing including a funnel shaped side terminating in an opening. The opening is in communication with a chamber defined in the particulate trap.

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 sterile packaging assembly configured to receive a surgical instrument is disclosed. The sterile packaging assembly comprises a vacuum-molded tray and a particulate trap. The vacuum-molded tray comprises an instrument cavity configured to receive the surgical instrument, and a trap cavity. The particulate trap is positioned in the trap cavity. The particulate trap comprises a housing including a funnel shaped side terminating in an opening. The opening is in communication with a chamber defined in the particulate trap.

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.

The present invention relates to packages and methods of using packages that provide a sterile enclosure for an implant so that the implant can be transported and retrieved without being contaminated. In one embodiment, the package includes an insert with an implant disposed therein and a tray. The insert includes a first engagement feature and the tray includes a second engagement feature corresponding to the first engagement feature. The insert is sized to fit within and engage with the tray through engagement of the first and second engagement features, where in a first position the implant is secured within the package and in a second position, the implant is retrievable from the insert. The insert moves relative to the tray between the first and positions, but remains secured to it in both positions.

A package for a product and method of retaining and releasing a product, where a container body is configured to support the product and includes a key support and a retaining key that is supported by the key support. The retaining key is movable between locked and released configurations, while in the locked configuration the retaining key retains a portion of the product and while in the released configuration the retaining key retracts to facilitate removal of the product from the container body.