There is provided a method for controlling a flow of sperms in a uterine tube formed by a uterine tube wall of a patient. The method comprises gently constricting (i.e., without substantially hampering the blood circulation in the uterine tube wall) at least one portion of the uterine tube wall to influence the flow of sperms in the uterine tube, and stimulating the constricted wall portion to cause contraction of the uterine tube wall portion to further influence the flow of sperms in the uterine tube. The method can be used for restricting or stopping the flow of sperms in the uterine tube, or for actively moving the fluid in the uterine tube, with a low risk of injuring the uterine tube.

A condom, container and applicator for a condom, in which the condom is provided in a longitudinally expandable cup having a peel-off lid. The cup is typically formed of plastic material. The side wall of the container is expandable, and can include accordion-like pleats to allow for longitudinal expansion of the cup. The condom is placed in the cup such that it can be directly applied to the penis while still in the cup, and the cup used as an applicator to unroll the condom over at least the head of the penis by expanding the side wall of the cup. The disclosure also relates to a dispenser for storing and dispensing the condom containers.

A case for the storage and easy wearing of condoms emprises-includes a box-shaped casing defining a containment chamber configured to accommodate a plurality of condoms arranged in respective flattened single-use packages arranged to form a stack. A pusher operates in the containment chamber so that a terminal single-use package of said stack is held against a bottom wall of the chamber itself. An extractor movable between a waiting position in which it engages the terminal single-use package inside the containment chamber and an extracted position in which the terminal single-use package is extracted through an outlet slot arranged in proximity to the bottom wall to expose the respective condom outside the box-shaped casing, in a use condition suitable for wearing.

A cervical transfer catheter (10) for transferring a therapeutic substance to an endocervix or other internal mucosal surfaces of a recipient, the catheter (10) comprising: a catheter body (12) having first and second lumens (14) and (16), the second lumen (16) being adapted, in use, to allow passage and retention of a structure containing the therapeutic substance that will be released slowly and continuously. The catheter (10) also comprises an inflatable balloon (20) provided at a distal end of the first lumen (14), the inflatable balloon (20) being designed to be as small as possible in its inflated condition while still being retained in the uterus by virtue of its shape.

A cervical transfer catheter (10) for transferring a therapeutic substance to an endocervix or other internal mucosal surfaces of a recipient, the catheter (10) comprising: a catheter body (12) having first and second lumens (14) and (16), the second lumen (16) being adapted, in use, to allow passage and retention of a structure containing the therapeutic substance that will be released slowly and continuously. The catheter (10) also comprises an inflatable balloon (20) provided at a distal end of the first lumen (14), the inflatable balloon (20) being designed to be as small as possible in its inflated condition while still being retained in the uterus by virtue of its shape.

A packaging system is provided for placement of condoms in a gaze-attracting position of a recipient of a gift or product. The system features a mount for holding the condom where the mount is adapted on one side to engage upon the product or the packaging surrounding it. Required removal of the mount to open the gift or positioning of the mount in a spot viewable after required sequential opening of the packaging insures the gaze of the recipient is captured and the location of the condom thereby ascertained.

Damage indicating packaging is disclosed. A damage indicating material may be applied between inner and outer wrapper layers. When the damage indicating material is exposed to oxygen, excessive heat and/or excessive pressure, the material changes in appearance to thereby alert the user that the package may be compromised. The damage indicating material may include an anti-counterfeiting taggant material. Active and intelligent tamper-evident packaging is thus provided.

A condom, container and applicator for a condom, in which the condom is provided in a longitudinally expandable cup having a peel-off lid. The cup is typically formed of plastic material. The side wall of the container is expandable, and can include accordion-like pleats to allow for longitudinal expansion of the cup. The condom is placed in the cup such that it can be directly applied to the penis while still in the cup, and the cup used as an applicator to unroll the condom over at least the head of the penis by expanding the side wall of the cup. The disclosure also relates to a dispenser for storing and dispensing the condom containers.

A condom comprises, on one or more surfaces thereof, a self-lubricating coating comprising a dry powder having a particle size of 300 microns or less. The self-lubricating coating becomes lubricious when the coating comes into contact with a liquid environment. A method of making a self-lubricating condom comprises providing a dry condom and coating said condom, on one or more surfaces thereof, with a self-lubricating coating comprising a dry powder. The invention also provides the use of a dry powder such as xanthan gum to provide a self-lubricating coating for a condom.

A tray for securing an implantable device to a carrier member includes a slot configured to retain the carrier member and a receptacle adjacent the slot. The carrier member surrounds a shaft of the implantable device. The receptacle has a first width at a proximal end of the receptacle to receive first and second arms of the implantable device in an initial state in which the first and second arms extend substantially perpendicularly from the shaft. The receptacle has a second width at a distal end of the receptacle for receiving the first and second arms of the implantable device in a collapsed state in which the first and second arms are folded against the shaft such that the carrier member can be slid over the first and second arms to retain the first and second arms. The second width is less than the first width.