Abstract: A protective garment, such as a surgical gown, includes a garment body defining sleeves. A cuff may be secured at respective ends of the sleeves. An elastic fiber layer is disposed on the sleeves beginning at the sleeve or cuff. The elastic fiber layer has a high friction surface such that an end of a glove pulled over the elastic fiber layer is inhibited from rolling or sliding back over the elastic fiber and down the sleeve. The elastic fiber may be formed of a polyolefin or other polymers according to known processes and may include a dye or colorant that may be used to indicate the fluid protection level of, for example, a surgical gown.

Abstract: A patient controlled liquid drug administration device is provided that enables either or both of a continuous flow of a liquid drug, as well as successive, large-volume boluses thereof, to be self-administered to and by a patient while avoiding bolus refill during bolus delivery or after bolus delivery but before an intake stroke of the pump occurs. The device includes an elongated housing having an axial cavity extending through it with a reciprocating pump mounted at a bottom end thereof. The pump defines a closed internal reservoir and includes a first wall, or seat, that is fixed in the cavity, and a second, flexible wall that is axially movable in the cavity in relation to the fixed wall between reservoir-full and reservoir-empty positions. The pump includes an inlet port that is connectable to a source of a pressurized liquid drug by an inlet conduit, and an outlet port subcutaneously connectable to the patient by an outlet conduit, both conduits extending out the bottom end of the housing.

Abstract: A pack of oral care items that allows for simultaneous opening and easy access to the items contained in the pack. The pack of oral care items includes two or more flexible packages. The flexible packages may be arranged in parallel. One flexible package may be an inner package that is located substantially within another flexible package that forms an outer package. The inner package may include an integral burst pouch configured to release a liquid into an interior space of the outer package while keeping the interior space of the inner package dry. Each flexible package includes a frangible region located at or adjacent a top portion and at least one oral care item is disposed within an interior space of each flexible package.

Abstract: A multi-panel sterilization assembly that includes a barrier panel formed of a permeable material, a fold protection panel, and at least one panel attachment means. The barrier panel has a first end and a second end opposite the first end such that the barrier panel has a length that is the distance from the first end to the second end and a midpoint along the length generally delineating the barrier panel into a content receiving region and a content covering region. Panel attachment means are located between the first end and the midpoint of the barrier panel at a pre-determined position to identify the content receiving region.

Abstract: An improved process and material for making elastomeric nitrile rubber articles is disclosed. In particular, the process and material formulation can produce nitrile rubber based articles, which exhibit force-strain characteristics that are comparable to those of natural rubber latex articles, while maintaining the tensile strength properties of nitrile rubber. The process includes an accelerator composition at the pre-cure stage having a dithiocarbamate, a thiazole, and a guanidine compound. The invention also includes an elastomeric nitrile rubber product made by the process, such as examination, surgical, or work gloves.

Abstract: A material for making elastomeric nitrile rubber articles is disclosed. In particular, the process and material formulation can produce nitrile rubber based articles, which exhibit force-strain characteristics that are comparable to those of natural rubber latex articles, while maintaining the tensile strength properties of nitrile rubber. The process includes an accelerator composition at the pre-cure stage having a dithiocarbamate, a thiazole, and a guanidine compound. The invention also includes an elastomeric nitrile rubber product made by the process, such as examination, surgical, or work gloves, which can have an exterior coating over naked rubber selected from either a silicone emulsion or oil, glycerin solution, a combined mixture of silicone and glycerin/glycerol, a fluorocarbon release agent, or a natural or synthetic hydrocarbon-based oil in amounts that do not degrade said substrate rubber material.

Abstract: A stoma dilator is provided which has a base dilator and a plurality of dilators which are coaxially disposed over the base dilator. The base dilator has a hub and an opening therethrough. The base dilator is configured to be positioned over a wire into a patient's tissue. Each of the plurality of dilators has a tapered distal end, a proximal end, and a tubular body, and are held in separated, telescoping position by the dilator positioner such that a portion of each distal end is exposed from beneath another dilator and is graspable by a health care practitioner for movement such that a smaller diameter dilator does not become inaccessible inside of a larger diameter dilator. The stoma dilator may include a hollow sheath positioned over an outermost dilator. The sheath is configured to hold open a tissue opening created by the plurality of dilators. The base dilator and the plurality of dilators may be removed while the sheath remains in a tissue opening.

Abstract: An inflatable retention system for an enteral feeding tube having a base deployed outside the human body and an indwelling retainer which is deployed within a lumen or cavity of the body by insertion through a stoma from outside the body. The retention system includes a tube having a proximal end, a distal end, an external tube diameter, and tube walls defining a feeding lumen and an inflation lumen. The retention system also includes an inflatable balloon located at a distal end of the tube in fluid communication with the inflation lumen, the balloon having thin, flexible walls, a predetermined spheroid shape, and a volume at which a fluid in the balloon is under no pressure such that upon inflation with a fluid to pressurize fluid in the balloon, the balloon assumes a stable spheroid shape and exhibits a substantially linear pressure versus volume curve.

Abstract: A gastropexy kit includes a plurality of safety needle assemblies. Each safety needle assembly includes a needle and a stylus. A fastener is positioned in a distal end of the needle. The fastener is coupled to one end of the suture and a suture retention hub is coupled to an opposite end of the suture. The fastener is deployed in a patient's stomach via the needle and stylus which has a blunt distal end which extends through the needle to push the fastener out of the needle and to blunt the needle. The suture retention hub is positioned on a patient's skin and adjustably tensions the suture, which, desirably, is a resorbable suture.

Abstract: The invention describes a closure device for the provision of freshly created gastric feeding fistulas, the basis of the design of the device being an introverted balloon that allows a sealing and hemostatic axial traction movement on the fistula that is to be sealed, the concentric balloon ends which run transmurally through the stomach and abdominal wall being arranged in a special seal-promoting and hemostatic manner.

Abstract: An improved process and material for making elastomeric nitrile rubber articles is disclosed. In particular, the process and material formulation can produce nitrile rubber based articles, which exhibit force-strain characteristics that are comparable to those of natural rubber latex articles, while maintaining the tensile strength properties of nitrile rubber. The process includes an accelerator composition at the pre-cure stage having a dithiocarbamate, a thiazole, and a guanidine compound. The invention also includes an elastomeric nitrile rubber product made by the process, such as examination, surgical, or work gloves.

Abstract: A suture retention hub is provided. It includes a base configured to moveably hold a handle within at least a portion of the base. The base has an aperture which extends through the base. The hub also includes a handle configured to moveably fit into the portion of the base. The handle has an aperture formed therethough as well. When a suture is positioned in the apertures and the base and handle are positioned such that the apertures are substantially in an axial alignment, the suture moves readily through the apertures in the hub. Then the base and handle are positioned such that the apertures are not in a substantial axial alignment, the suture is frictionally crimped and it is prevented from moving through the hub.

Abstract: A face mask for reducing the amount of microbes to which a wearer is exposed is provided. The face mask includes a body portion that has an outer layer that has been treated with a germicidal agent in an effective amount. The layer may be a nonwoven fabric like a spunbond, meltblown or coform layer and may be a laminate of such layers. The face mask having such a germicidal treatment can result in a reduction in microbial activity as compared to another face mask, identical but for the germicidal agent.

Abstract: An enteral feeding unit or system that minimizes the occurrence of gastro-esophogeal-pharynegal reflux during feeding is described. The enteral feeding unit or device includes an automatable feeding pump with a feedback sensor for sensing a relative pressure in a patient's stomach and esophagus, and a regulator system for controlling or monitoring feeding rate to said patient as a function of said relative gastro-esophageal pressure. The system includes a stomach probe that has a fluid-tight closure of the esophagus.

Abstract: A protective garment, such as a surgical gown, includes a garment body defining sleeves. A cuff may be secured at respective ends of the sleeves. An elastic fiber layer is disposed on the sleeves beginning at the sleeve or cuff. The elastic fiber layer has a high friction surface such that an end of a glove pulled over the elastic fiber layer is inhibited from rolling or sliding back over the elastic fiber and down the sleeve. The elastic fiber may be formed of a polyolefin or other polymers according to known processes and may include a dye or colorant that may be used to indicate the fluid protection level of, for example, a surgical gown.

Abstract: The present invention is directed generally to an adapter for assist with the connection of a flexible tubing to a connector, and more particularly to a product that enables the flexible tubing to retain its ability to provide a secure connection even after multiple uses by resisting or limiting permanent deformation thereof.

Abstract: A three-piece surgical drape with fluid diverting channel or sleeve therein and method of making or assembling the same. The drape generally including a first liquid impermeable section attached at either end thereof to second and third sections of the drape, respectively. At least a portion of one end of the first section of the drape folded back upon itself and intermittently tacked or bonded to the first section to create a channel or sleeve adapted to divert fluids. The channel or sleeve may also have a tube or hose placed therein to facilitate or enhance fluid diversion through the channel or fluid removal therefrom.

Abstract: A high pulp content nonwoven composite fabric is disclosed. The composite fabric contains 1) from more than about 0 to less than about 30 percent, by weight, of a nonwoven layer of conjugate spun filaments, the filaments containing at least one low-softening point component and at least one high-softening point component and having at least some exterior surfaces of the filaments composed of at least one low-softening point component; 2) more than about 70 percent, by weight, of pulp fibers; and 3) regions in which the low-softening point component at the exterior surfaces of the filaments is fused to at least a portion of the fibrous component. This high pulp content composite nonwoven fabric may be used as a heavy duty wiper or as a fluid distribution material, cover material, and/or absorbent material in an absorbent personal care product. Also disclosed is a method of making the high pulp content nonwoven composite fabric.