Two cylindrical parts (2, 3) are provided which are able to be coupled to each other with an axial sliding movement, of which, a first outer part (2) includes securing means (21) for the menstrual cup (4) to be placed, and a second inner part (3), which includes pushing means (31) which deploy the menstrual cup (4) from the securing means (21). The outer part (2) has an inner through hollow (22) suitable for receiving the inner part (3) in a fitted manner. The securing means (21) are made up of corresponding elastic arms which emerge parallel from the distal end (2a) of said part (2). The proximal end (2b) of the external part (2) has a smooth section (23). The appendages (31) of the inner part (3) have a perimeter edge and a length. The inner part (3) has an inner perforation (34) for inserting a thread-like element of the menstrual cup (4) as extraction means (4a).

A device for the delivery and/or application of a therapeutic composition in a delivery form into the rectal and/or vaginal cavity, the device includes an externally wearable pad; a non-absorbent platform for receiving the delivery form of therapeutic composition; and a sheath joining the platform to the pad such that a user's finger can be received in the sheath.

Urinary incontinence devices generally include a body configured to be inserted into a vagina. The body may have a proximal insertion portion, a plurality of legs coupled to and extending distally from the insertion portion, and a distal retrieval portion. The plurality of legs may each have a length, a width, and a distal end, and the distal ends of the plurality of legs may be coupled together. The body may have a compressed configuration, an expanded configuration, and a lateral cross-sectional diameter, and the lateral cross-sectional diameter of the body may be largest at the widest point of each of the plurality of legs. Methods of treating urinary incontinence may include loading a urinary incontinence device into an applicator, inserting the applicator into the vagina, advancing the incontinence device out of the applicator to position a distal end of the device past the pelvic floor, and removing the incontinence device from the vagina using the distal retrieval portion.

In one example, a medical system may comprise a delivery tube configured to couple to a vacuum source and provide negative pressure to a distal portion of the delivery tube; and a porous body at a distal portion of the delivery tube, the porous body including a first section and a second section removable from the first section.

An application device for positioning an absorptive matrix (AM) element within a body cavity includes a tube, the AM element, a release element and a deflector. The AM element is disposed inside the tube in a stored state before exiting the tube towards the distal end in a released state. The release element slides inside the tube along a longitudinal axis of the tube and pushes the AM element out of the tube towards the distal end of the tube as the release element slides farther into the tube. The deflector is disposed at the distal end of the tube and bends the AM element away from the longitudinal axis of the tube as the AM element is pushed out of the tube. The deflector is an extension of the wall of the tube that protrudes from the distal end and bends inward towards the longitudinal axis of the tube.

A pad body integrally molded from a thermoplastic resin foam material with high compressibility includes a foam absorbent body, an outer film layer formed on an outer portion of the foam absorbent body, and a pull string connected to the outer film layer. A tampon is also disclosed, and includes a tubular sleeve unit and the pad body. The tubular sleeve unit includes an outer tube and a push rod. The foam absorbent body and the outer film layer constitute an absorption section of the pad body. The absorption section is constrained by the outer tube in a compressed state, and is transformed to an expanded state when pushed by the push rod to move out of the receiving hole via the exit opening.

A tampon applicator has a barrel and a plunger. The barrel extends from a proximal end to a distal end, the distal end having a base opening, and the proximal end having an upper opening exposing an inner chamber. A window formed in the barrel is shaped to receive a tampon. A set of protrusions extends inwardly from the inner chamber proximate the distal end of the barrel, and an inner ring of the inner chamber is proximate the distal end of the barrel. The plunger extends from a first end to a second end, the first end having a base. A top ring is on the base of the plunger, wherein the inner ring of the barrel is adapted to removably snap into the top ring. A annular ridge is on the second end of the plunger for threaded engagement with the set of protrusions of the barrel.

A delivery system, including an inner member, an outer tube surrounding the inner member and movable axially relative to the inner member, wherein a space is defined between an outer surface of the inner member and an inner surface of the outer tube, an expandable element disposed in the space at a distal portion of the system, and a patch disposed in the space at the distal portion of the system, wherein the patch is radially outward of the expandable element.

An insertion end for a tampon applicator assembly. The insertion end has an insertion tip region and optionally an inflection region. The insertion end of the tampon applicator assembly is unique in one or more ways, including one or more of the following: having a unique degree of closure, an inflection region length that is different than an insertion end region length, petal slits that form a tear-drop shape, petals having multiple radii of curvature, the insertion end having a unique radius of curvature, the insertion end having a unique part thickness.

Some implementations can include a tampon/suppository hybrid having at least one composition (e.g., pharmaceutical, medicinal plant, herbal composition, vitamin supplementation, and/or essential oil) applied to, attached to, or contained in the tampon (e.g., at or near an insertion point or tip of the tampon). When the tampon/suppository hybrid is inserted, the tampon/suppository hybrid works to provide the composition to the user, for example, to establish/re-establish the microbial flora of the host, while still absorbing secretions and or blood from menstruation flow.