A condom is configured to include a space such that a front glans part of the condom does not excessively come into contact with the penis of a man by selecting a material having moderate elasticity such as soft synthetic resin or synthetic latex rubber or a foamed rubber material conforming thereto or the like for the front part of the condom made from a soft rubber material; and includes embossed sponge layers or fine soft hairs additionally laminated on the inside and outside of the condom, to provide an excellent moisturizing effect such that an excellent contraceptive effect and a sexual pleasure-increasing effect can be simultaneously obtained when a user wears the condom, thereby providing multiple effects such as contributing to the treatment of patients with chronic dyspareunia or patients with anorgasmia and the like.

A package for a condom provided with a main compartment for housing a condom, and an additional compartment separate from the main compartment and having a disposal element that enables the condom to be disposed of after use in an environmentally friendly manner. A package is provided with integrated components, easy for the user to handle and without excessively increasing manufacturing costs compared to a standard commercial individual package.

A discreet packaged sterile hygiene kit for the unexpected menstrual cycle and safe sex. Kit is comprised such as at least sterile scented underwear, or leggings, and either one in addition to the undergarments/leggings and at least tampons, sanitary pads, panty liners, and at least sterile wipes, and at least prophylactic birth control/safe sex. Packaged uniquely in a small confined vacuum packed plastics packaging which fits inconspicuously inside a purse, backpack, locker, desk, vehicle glove box, or any place of choosing; thus allowing its user maximum and or ultimate privacy. Underwear is folded tightly then inserted into the packaging in one pocket followed by the insertion of either tampons, sanitary pads, panty liners, wipes or prophylactic into another pocket. Extra items being provided in its own packaging material. Package is sealed and packaged in a manner that will allow displaying via; vending machines, store racks, or any retail display.

The invention is directed to a packaging film (2) comprising: a top layer (4) with at least one aperture (4.1); a bottom layer (8) adhered to the top layer (4); a tear layer (6) adhered to the bottom layer (8) and extending along the at least one aperture (4.1) so that upon traction on the tear layer, said layer tears the bottom layer (8) through the aperture(s) (4.1). The tear layer (6) extends beyond the at least one aperture (4.1), between the top layer (4) and the bottom layer (8), preferably longitudinally in two opposite directions. The invention also relates to a condom wrapping with such a film and to the manufacturing method for such a film.

The present invention relates to an arrangement comprising an intrauterine system, an inserter for the intrauterine system and a package for the inserter.

Provided, among other things, is a packaged condom comprising: a sealed package; within the package, an polyisoprene condom; and within the package and substantially coating the condom, a lubricant comprising solvent and one or more sensation-providing agents comprising one or more of vanillyl butyl ether, menthyl lactate, and menthol, wherein the solvent comprises non-water soluble silicone oil and 99% or more of the lubricant by weight is the non-water soluble silicone oil.

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.

A sexual accessory pack comprising a transparent or translucent sterile ring pack including a penile ring enclosed therein by a releasable film having a pull tab, where the ring pack is removably attached to the outer surface of a condom pack to provide integral packaging of sexual accessories. One or more sexual accessory packs are packaged in an at least partially transparent or translucent retail, such as a transparent or translucent window, to allow purchasers to visually access various characteristics of the packaged penile rings, such as style, shape and size, prior to completing a purchase.

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.

Delivery systems and methods for forming and delivering biomaterials from two components are described herein. In particular, apparatus and methods for performing controlled delivery of multicomponent delivery of biomaterials into or onto a body part, such as a body lumen are described. More specifically, in some embodiments, the apparatus and methods are directed towards controlled delivery of micro-volumes of biomaterials into or onto a target location, the micro-volumes being defined as 0.001 mL-1 mL (or 1 μL-1,000 μL) of volume.