Porous Media Corporation

Other

Lexion Medical, LLC

Hemostasis, LLC

Spx Corporation

John Henry Burban

Michael R Spearman

Keith Allen Roberts

Majid Zia

Robert Orvin Crowder

John M Shanahan

Craig Jonathan Cuta

Douglas E Ott

Carl Matthew Geisz

Peter Joseph Catalano

Steven T Jersey

Philip M Rolchigo

Duane Earl Lloyd

Mathews J Thundyil

Kevin Carlson

Michael Saveliev

Carl Hahn

John Shanahan

Timothy J Fox

Mark F Honath

Michael J Spearman

Brian M Spearman

Rochelle Marie Mickschl

Jeffrey William Berg

Brent Joseph Steffensmeier

Joseph Charles Tuma

Gabriel P Kern

Darrin Barnette

Ryan A Hoitink

David S Kolstad

David Kolstad

Michael Savellev

Mathews Thundyil

A hand-held device is used to deliver and hydrate a temporary polymeric implant having a length, an outer surface and a cross-section, with a disruptable cover over the implant. A lumen may pass through the entire length, the lumen having a surface forming an equivalent diameter in the polymeric stent. The temporary polymeric implant includes a first aqueous-swellable, biocompatible and biodegradable composition (e.g., polymer) having a thickness. The aqueous-swellable and biodegradable polymer retaining structural integrity for at least 1 hours up to thirty days when swollen and kept moist by a moist aqueous environment. Barrier layers of biodegradable polymer(s) may be used to prevent migration of liquids into the lumen.

Tool for placement of degradable ostial stent

A sponge including one or more hemostatic agents and one or more binding agents. At least one of the hemostatic agents is a pregelatinized potato starch. The collective percentage by weight of the one or more hemostatic agents is within the range of approximately one eighth to approximately sixteen times as great as the collective percentage by weight of the one or more binding agents.

Hemostatic agent and method

A polymeric stent having a length, an outer surface and a cross-section. A lumen passes through the entire length, the lumen having a surface forming an equivalent diameter in the polymeric stent. The polymeric stent includes a first aqueous-swellable, biocompatible and biodegradable composition (e.g., polymer) having a thickness. The aqueous-swellable and biodegradable polymer retaining structural integrity for at least 1 hours up to thirty days when swollen to between 15% and 500% of its dry diameter and kept moist by a moist aqueous environment. Barrier layers of biodegradable polymer(s) may be used to prevent migration of liquids into the lumen.

Degradeable nasal ostial stent

A polymeric stent having a length, an outer surface and a cross-section. A lumen passes through the entire length, the lumen having a surface forming an equivalent diameter in the polymeric stent. The polymeric stent includes a first aqueous-swellable, biocompatible and biodegradable composition (e.g., polymer) having a thickness. The aqueous-swellable and biodegradable polymer retaining structural integrity for at least 1 hours up to thirty days when swollen and kept moist by a moist aqueous environment. Barrier layers of biodegradable polymer(s) may be used to prevent migration of liquids into the lumen.

Degradeable ostial stent

One aspect of the invention is a method of treating a wound to clot blood. A sponge material is applied to the wound. The sponge comprises a starch having hemostatic properties and at least one binding agent. The sponge may further comprise a porous, flexible material.

An apparatus and method for on-the-go humidifying an insufflation gas through water vapor transfer from a liquid to the insufflation gas through a barrier separating the gas from the liquid to enable the gas in a normally trauma inducing state to be brought to a conditioned state. If the gas is at an improper insufflation temperature the temperature of the gas can be brought to the proper insufflation temperature at the same time the gas is humidified through heat transfer through the barrier.

Medical gas humidification system

An antimicrobial solution for disinfecting instruments in an automatic sterilization device, the solution comprising: a peracid reaction product formed in situ from combining a liquid acetyl donor with a solid source of peroxide, wherein the in situ reaction takes place in the sterilization device, along with a containment and delivery ampule for use in an automatic sterilization device, and methods for disinfecting a medical instrument employing the inventive antibacterial solution.

Sterilant composition and system

Embodiments of the invention provide a membrane module including a first plurality of fibers capable of filtering fluids that are helically wound in layers creating a mono helix. Fluids to be treated can flow radially with respect to a longitudinal axis of the mono helix or parallel to the longitudinal axis of the mono helix. The membrane module can further include a second plurality of fibers that are helically wound with the first plurality of fibers to create a dual helix. The second plurality of fibers can have different properties than the first plurality of fibers in order to achieve different filtering functionalities.

Membrane module for fluid filtration

One aspect of the invention is a method to vent gas from a body cavity during an endoscopic procedure. A body cavity is in fluid communication with an exhaust gas inlet of a vacuum break device. The vacuum break device has a chamber in fluid communication with both the inlet and an outlet. The chamber may comprise one or more openings in fluid communication with the atmosphere. A conduit in fluid communication with the exhaust gas outlet may be connected directly or indirectly to a suction source. The suction source may be activated.

System and method to vent gas from a body cavity

Embodiments of the invention provide venting and filtration systems with a membrane that is permeable to gas and substantially impermeable liquid. The systems can remove a gas from a liquid entrained with gas. The systems can include a reservoir in fluid communication with the membrane and a liquid outlet. The membrane can help prevent the gas from reaching the liquid outlet.

Venting and filtration systems with gas permeable membrane

A helically wound hollow membrane module having a core with a plurality of helically wound layers of semi-permeable hollow fibers wound on the core. The fiber wind angle with respect to any one layer of fibers may be essentially constant along the axial length of the module, except in one or both end or tubesheet regions, where the wind angle may be increased, in at least some of the layers relative to the essentially constant wind angle, to produce an area of decreasing diameter.

Membrane module

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Lake Elmo, MN, United States of America

John Henry Burban