Medical devices and related methods useful for EVAC procedures are described. The medical device may include a sponge. The sponge may include a plurality of perforations that form one or more tear surfaces. The one or more tear surfaces may define a predefined location for removing a first portion of the sponge from a second portion of the sponge. The one or more tear surfaces may form a boundary between a radially inner surface of the first portion and a radially outer surface of the second portion. The medical device may further include a tube coupled to a proximal portion of the sponge.

A tampon product including an applicator with a hollow barrel portion and an ejection plunger within the barrel portion, is disclosed. One or both of the barrel portion and the ejection plunger may have a cylindrical form and be formed of a paper, and have a coating applied to the paper, wherein the coating is not predominately constituted by a material derived from petroleum. The coated paper barrel portion and/or ejection plunger may be manufactured to as to exhibit a static Relative Sliding Resistance Coefficient (CSR) no greater than 0.250 and/or a kinetic CSR no greater than 0.210, for purposes of smooth manufacturing. In combination or alternatively, the coated paper barrel portion and/or ejection plunger may be manufactured to as to exhibit a static Gripping Slip Resistance Coefficient (CGSR) no less than 0.190 and/or a kinetic CGSR no less than 0.170, for purposes of consumer satisfaction.

A tubular shaped tampon can include an absorbent body defining a cylindrical shape having a hollow interior, a porous protective sleeve surrounding the absorbent body, and a string that holds the protective sleeve in place against the absorbent body and facilitates removal of the tampon after use. The absorbent body and protective sleeve can combine to define an overall tubular structure having an inner hollow region, providing increased surface area. Methods of manufacturing the tampon can include cutting a fluid absorbent material, rolling the cut material around elongated machine prongs to form an absorbent body, rolling a porous sheet around and extending beyond both distal ends of the absorbent body, pinching together distal ends of the porous sheet, pushing at least one distal end through the hollow interior of the absorbent body, stitching the distal ends of the porous sheet together, and punching a string through the protective sleeve and absorbent body.

A device for collection of vaginal discharge or menstrual blood as an analyte of medical testing, comprising a filter configured to separate cells of interest from other material and a nanomaterial cartridge comprising a nanomaterial configured to passively adsorb DNA and segregate cells of different sizes. The nanomaterial is a silica sol gel with templated macropores

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent. The primary absorbent including at least one of rayon fibers and cotton fibers and having improved fluid handling due to dynamic expansion of the tampon at a relatively reduced dry tampon mass.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent. The primary absorbent including at least one of rayon fibers and cotton fibers and having improved fluid handling due to dynamic expansion of the tampon at a relatively reduced dry tampon mass.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent.

The present disclosure relates to a gastrointestinal delivery device of a chitosan dressing, where the delivery device is capable of stop bleeding, in particular in connection with TURP procedures. The delivery device may be used in all gastrointestinal bleeding applications and can be used with a biocompatible, foldable, thin profile, chitosan dressing. Various aspects of the device and its uses are provided herein.

The present invention introduces a tampon with an integrated device designed for improved insertion, and removal, and leak prevention. The device comprises a flexible, nonpermeable wall, hollow to enable finger-assisted insertion and featuring a removal aid element attached to the bottom end of the wall for easy, hygienic extraction. Additionally, the wall is equipped with ridges that conform to the vaginal wall, enhancing the seal to prevent menstrual fluid leakage and block the absorption of external fluids. In other embodiments, a smoothed wall is offered. This invention eliminates the need for separate applicators, allows the device to compact for discrete portability, and significantly enhances user comfort and effectiveness in fluid management.

Bi-directionally positionable tampon configured to be disposed in a vaginal opening adjacent to a cervical os for absorbing and collecting vaginal discharge. The tampon includes an elastomeric ring to support an absorbent pad for collecting and absorbing bodily fluids. To support the absorbent pad, the elastomeric ring has a first circular-shaped edge and a second circular-shaped edge that surrounds the central aperture. A covering comprising a first pervious layer and a second pervious layer disposed adjacent to the first pervious layer is attached to the elastomeric ring and disposed at least partially in the central aperture of the ring. An absorbent pad is disposed in a cavity formed between the first fabric layer and the second fabric layer of the covering. When the elastomeric ring is disposed in a vaginal opening, bodily fluid can pass through either the first and/or second pervious layers to reach the absorbent pad.