A medical device may comprise a handle, wherein the handle includes a movable body and a main body; a cap configured to be coupled to a distal end of a scope; a patch, wherein the patch is moveable relative to the cap; and a petal body. The patch may be removably coupled to the petal body. The medical device may further comprise an actuator body coupling the patch to the moveable body such that movement of the moveable body extends the patch from the cap. The petal body may be configured to transition between a closed configuration in which the patch is retracted, and an open configuration in which the patch is extended radially-outward from a central longitudinal axis of the scope.

The invention relates to porous absorbent Composite Material, which may be used e.g. in the form of a plug or tampon, for instance for controlling bleeding, wound closure, prevent tissue adhesion and/or support tissue regeneration. The invention provides a hydrophilic Self-Dispersive, fragmentable and Bio-Absorbable Porous Composite foams, suitable for packing antrum or other cavities of the body, comprising of composite of polymers, which polymer preferably comprises C(O)O; NH2/3+; OH; CH2OCH2C(O)O groups as functional or CHO (e.g. C2H4O; C6H10O5; C6H8O6); CHNO (e.g. C8H13NO5); OCC (e.g. OCH2-CH2); C(O)N groups in the backbone of the polymers e.g. gelatin, chitosan, collagen, alginate, polyvinyl alcohol, polyethylene glycol, keratin, cellulose.

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.

The present invention provides a device that can move inside a biological conduit such as an intestinal tract for sampling the content therein, and a process thereof. While moving along the intestinal tract, the device can continuously collect the content in the intestinal tract. One or more convoy belts having an adsorbent layer are configured to continuously absorb and preserve the collected intestinal content. The belt loaded with the sample may be used to establish a chemical, biochemical and microbiological spectrum along the length of the intestinal tract.

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.

The present invention relates to a biocompatible, foldable, thin profile, low mass and high surface area, chitosan dressing, optionally modified with catechol, and suitable for treating bleeding in a physiological environment, e.g. bladder, and in particular in connection with the TURP procedure. The characteristics and structures of the chitosan dressing are provided. Methods of making and using the chitosan dressing are also provided.

The present invention comprises methods and devices for collection of fluids, including cells and cellular materials, from the uterus. A device of the present invention comprises a central tubing member to which, at least, a flexible tubing member and an absorbable member are connected at least at one point. The absorbable member is connected to at least one portion of the central tubing member and to at least one portion of the flexible tubing member. The devices of the present invention are useful in methods of collection of uterine fluids, including blood, cells and cellular material.

Devices, systems, and methods for treating wounds in endoluminal spaces of a patient are disclosed. A device may include an elongate tube defining a proximal end, a distal end, and a lumen, an expandable component adjustably positioned at the distal end of the elongate tube, and a tether coupled to the expandable component and extending proximal from the expandable component through the lumen to a location exterior of the elongate tube. The expandable component may be adjustable between a delivery position within the elongate tube and a fully deployed position at least partially exterior of the elongate tube. The expandable member may be absorbent. A proximal end of the elongate tube may couple to a vacuum source to apply a negative pressure at or proximate the expandable component. An inner member may extend through the elongate tube and be configured to adjustably engage the expandable component.

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 medical device may include a conduit and a porous body coupled to a distal end of the conduit. The medical device may have a first loop extending proximally from a proximal end of the porous body. The medical device may have a second loop extending distally from a distal end of the porous body.