A sterile packaging for sterile medicinal products, in particular implants, forms at least one, or in case of a multiple sterile packaging, at least one first sterile barrier and an outer second sterile barrier, separate and independent from the first sterile barrier, and which is accommodated in an outer packaging. The outer packaging is made of a composite material that includes cardboard and at least one coating or film, and is designed and intended to form the second sterile barrier of the sterile packaging.

An implant delivery device suitable for delivery of breast implants features a reusable design that can be autoclaved to sterilize between uses. External fluid pressure is selectively delivered to a housing with the implant inside and can be regulated by the surgeon. The application of fluid pressure can be paused with the already applied pressure retained in the housing giving mechanical advantages for easier force application by the surgeon for enhanced control of the position of the implant within the housing and as it exits the outlet of the housing. The housing can be transparent to aid in observing the implant position and orientation as it moves through the housing. The outlet tip can be slant cut to allow for a fixed opening of the incision before delivering the implant to the surgical site. The housing cover is configured for rapid attachment with a seal that is amenable for autoclaving.

A package for a medical tool has a receiving space for the medical tool. The package has a readable data carrier with tool-specific data. The package is usable in a method for automatic identification of a medical tool.

A system for managing female incontinence includes a body of biocompatible material configured to fit between the labia minora and the vestibule floor, the body having a surface configured to occlude the urethral meatus, an adhesive carried on at least a first portion of the surface and configured to provide a sealing engagement between the body and the urethral meatus, and a substance carried by at least one of the body and the adhesive and configured for controlling the odor of the general vaginal-urethral area of a female.

A method of inserting an intervertebral disc implant into a disc space includes accessing a spinal segment having a first vertebral body, a second vertebral body and a disc space between the first and second vertebral bodies. The method includes securing a first pin to the first vertebral body and a second pin to the second vertebral body, using the first and second pins for distracting the disc space, and providing an inserter holding the intervertebral disc implant. The method also desirably includes engaging the inserter with the first and second pins, and advancing the inserter toward the disc space for inserting the intervertebral disc implant into the disc space, whereby the first and second pins align and guide the inserter toward the disc space.

A device retention assembly includes a delivery system and a device retention mechanism retaining the delivery system. The device retention mechanism includes a tray, a base coupled to the tray, and retaining flanges pivotally coupled to the base. The delivery system is enclosed within an opening defined by the base and retaining flanges. A key locks the device retention mechanism in the closed position retaining the delivery system. The key must be removed to unlock the device retention mechanism to release the delivery system.

A spinal implant package includes a tray having a body including spaced apart first and second cavities. The body includes a third cavity between the first and second cavities. The tray includes a first connecting feature that is movable relative to the body. A lid is coupled to the tray by a hinge. The lid includes a second connecting feature that is movable between a first position in which a bottom surface of the second connecting feature directly engages a top surface of the first connecting feature and a second position in which a top surface of the second connecting feature directly engages a bottom surface of the first connecting feature to provisionally fix the lid to the tray.

The present disclosure in one aspect provides a sterile packaging container comprising a container body with a cross-sectional shape that is constant along the majority of the longitudinal axis, a cover and a closure assembly that inhibits the passage of microbial contaminants. The container is configured such that the interior of the container can be sterilized. The sterile packaging container described herein allows one to manufacture a sterile packaging tube exercising the smallest possible volume.

An apparatus includes a flexible container and a port. The container includes a first layer coupled to a second layer to define a storage volume within which a tissue specimen can be contained. The first layer has a first stiffness and the second layer has a second stiffness. An edge of the first layer is spaced apart from an edge of the second layer to define an opening into the storage volume. The edges of the first and second layer form a peelable seal that hermetically seals the storage volume such that the first layer can be peeled away from the second layer to expose the storage volume. The port is coupled to the flexible container and allows fluid communication between the storage volume and an external volume.

A protective device for an elongate catheter carrying a functional element, in particular a stent or a balloon, in particular a balloon coated with an active substance, on a distal end portion of the catheter. The protective device includes a protector configured to be arranged on the distal end portion so that the functional element is surrounded by the protector. A protective sleeve surrounds an interior to receive the catheter together with the protector. The protective sleeve has at least one projection on an inner side of the protective sleeve facing the interior of the protective sleeve. The projection is configured to retain the protector when the catheter together with the protector is arranged in the interior of the protective sleeve and the catheter is withdrawn from the protective sleeve so that the protector is pulled off the distal end portion of the catheter.