C. R. Bard, Inc.

Venetec International, Inc.

Purewick Corporation

Christopher K Brooks

Kelly J Christian

Matt Loui

Jennifer Stryker

Lyndsay Sweeney

Jason Jishen Cheng

Rafael Victor Andino

Jill Walthall Jones

Jill M Jones

Mark McDermott

David Xu

Fluid collection assemblies () including a sample port (), systems () including the same, and methods of using the same are disclosed herein. An example fluid collection assembly () includes a fluid impermeable barrier () including a first end region (), a second end region () opposite the first end region, and a sump () that forms at least a portion of the first end region. The fluid impermeable barrier also defines at least one opening () between the first end region and the second end region and a fluid reservoir that is defined by at least a portion of the sump. The fluid collection assembly also includes at least one wicking material () disposed in the chamber () and a sample port () extending from the sump. The sample port is configured to be connected to a fluid collector (). The sample port is in fluid communication with the fluid reservoir () such that a sample of the bodily fluids received by the fluid collection assembly may be obtained.

Fluid collection assemblies including a sample port

Disclosed herein is a waste detection system. The waste detection system includes a pad configured to acquire a fluid sample excreted from a patient. The pad includes one or more layers and at least one microfluidic channel configured to receive therein the fluid sample. The waste detection system further includes an intake manifold in fluid communication with the at least one microfluidic channel, the intake manifold configured to receive the fluid sample, the intake manifold having one or more reagents configured to detect the presence of waste within the fluid sample excreted from the patient.

Waste detection system

A retainer includes a first arcuate wall and a second arcuate wall that together define a channel designed to receive a medical article. The retainer has an open configuration wherein a first end of the first arcuate wall is spaced away from a first end of the second arcuate wall, and a closed configuration wherein the first end of the first arcuate wall is adjacent the first end of the second arcuate wall. A second end of the first arcuate wall opposite the first end of the arcuate wall may be spaced away from the base in the open configuration and pressed against the base in the closed configuration. The retainer also may include a first support and a second support fixed to the base, and a first and second flexible coupling connecting the first and second supports to the first and second arcuate walls.

Stabilizing device having a snap clamp

Embodiments disclosed herein are directed to a dynamic pressure response drainage system including control logic configured to enable measuring of residual fluid disposed within the drainage lumen. The residual fluid volume is measured by detecting the magnitude of the dynamic pressure response in the system containing the residual fluid when a sudden displacement (e.g. increase or decrease) of air volume occurs inside the system. The pressure burst magnitude is related to the pressure needed to move the mass of fluid, thus the fluid volume can be calculated from measurements of the burst pressure. The magnitude of the measured air pressure exhibits a dynamic pressure response corresponding to the mass of fluid in the tube. Either positive or negative pressure bursts can be used to produce and measure the corresponding positive or negative dynamic response spike pressure.

Dynamic pressure response system and method for measuring residual fluid

Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient can include one or more wrap assemblies for use in the placement/maintenance procedure. The one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure, such as a urinary catheterization procedure. A wrap assembly can include a wrap body including a front surface defining an aseptic field for the urinary catheterization procedure, a plurality of pockets on the front surface, and urinary catheterization components disposed in the plurality of pockets, the urinary catheterization components arranged in a predetermined order of use for the urinary catheterization procedure. The wrap assembly can be in a rolled configuration. A method of using the wrap assembly includes unrolling the wrap assembly and removing the urinary catheterization components to perform the procedure.

Wrap systems for medical device kits

Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient are disclosed. Such medical device kits can include one or more wrap assemblies for use in the placement/maintenance procedure. In accordance with present embodiments, the one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure. In one embodiment, a medical wrap assembly is disclosed, comprising a foldable wrap body that includes a front surface, wherein the front surface is configured to define a sterile field. A plurality of pockets is included on the front surface of the wrap body. The pockets are configured to contain therein a plurality of medical components. The medical components are arranged in the pockets in a predetermined order of use for the medical procedure.

A balloon-manipulating device for a balloon catheter, methods of making, and methods of use. The balloon-manipulating device includes a tubular body, a longitudinal hole through a least a portion of the tubular body, one or more balloon-compressing pieces of a sidewall of the tubular body, and one or more balloon-letting through holes through the sidewall. The longitudinal hole may extend from an opened proximal end of the tubular body to at least a distal end portion of the tubular body, and is configured for inserting a balloon-catheter shaft therein. Each of the one or more balloon-compressing pieces is configured for compressing a different portion of an inflated balloon-catheter balloon when the balloon-manipulating device is disposed over the balloon. Each of the one or more balloon-letting through holes is configured for allowing therethrough a different portion of an inflated balloon-catheter balloon when the balloon-manipulating device is disposed over the balloon.

Growing community of inventors

Decatur, GA, United States of America

Christopher K Brooks