According to an aspect, a bodily implant includes a connector configured to connect a first tube member and a second tube member such that fluid can be transferred through the first tube member and the second tube member. The connector includes a first clip member having an inner surface, a second clip member having an inner surface, a hinge member coupled to the first clip member and the second clip member, a retaining member coupled to the inner surface of the second clip member, and an inner connector coupled to the retaining member.

An automatically bidirectionally-sealable breakaway intra-medical tubing connector assembly for use with first and second luer-actuated valve assemblies connected to opposite intermediate ends of a medical tube, the assembly comprising a first and second snap-fit fittings adapted to be connected to the first and the second luer-actuated valve assemblies respectively, the snap-fit fittings being arranged for tensile force responsive disconnectable snap fit connection with each other; and a connector element, having first and second ends and defining a fluid flow path therethrough, the connect or element being at least partially located within the snap-fit fittings, the snap-fit fittings and the connector element being configured upon connection of the luer-actuated valve assemblies thereto for opening of the luer-actuated valve assemblies and upon disconnection of the snap-fit fittings from each other for automatic closing of the luer actuated valve assemblies.

According to an aspect, a bodily implant includes a connector configured to connect a first tube member and a second tube member such that fluid can be transferred through the first tube member and the second tube member. The connector includes a first clip member having an inner surface, a second clip member having an inner surface, a hinge member coupled to the first clip member and the second clip member, a retaining member coupled to the inner surface of the second clip member, and an inner connector coupled to the retaining member.

The disclosure provides a method for preventing infection and microbial ingress in medical device connections between peritoneal dialysis transfer sets and peritoneal dialysis catheters. A peritoneal dialysis transfer set includes a male connector with a distal tip and a recess at the distal tip configured to deliver and confine an antimicrobial composition into solution within a cavity formed by the recess. The surface of the recess includes an antimicrobial composition. In certain implementations the antimicrobial composition contains chlorhexidine acetate.

Keep vein open (KVO) infusion flow control devices are provided. The KVO infusion flow control device couples to intravenous (IV) tubing and includes a flow controller that provides a full open fluid flow rate through an outlet portion of the IV tubing when the flow controller is in an open position, and a KVO fluid flow rate through the outlet portion of the IV tubing when the flow controller is in a KVO position. Visual indicators are disposed on the KVO infusion flow control device.

A device for connection to a medical connector, the device includes an outer cap, an inner cap and a peelable seal. The outer cap configured to define a chamber to contain an absorbent material and disinfectant or antimicrobial agent. The outer cap including one or more threads adapted to engage with a female luer connector. The inner cap including one or more thread-tabs adapted to engage a male luer connector. The peelable seal prevents the disinfectant or the antimicrobial agent from exiting the chamber.

One aspect of the present disclosure pertains to a connector for conveying a suspension of particles through a system, comprising: a housing (10) comprising an internal cavity (12) and a first passageway (14) for conveying fluid; two or more inlet conduits (16a, 16b, 16c, 16d) formed in the housing and arranged radially with respect to a longitudinal axis of the first passageway; and a rotatable component (18) received in the internal cavity of the housing and rotatable about the longitudinal axis of the first passageway such that a continuous flow path can be established between the first passageway and a selected inlet conduit; wherein an angle between each of the inlet conduits and the first passageway (22) is greater than 90 degrees. Other aspects pertain to systems that employ such a connector and to methods of using such systems.

A cap for disinfecting a needleless connector is described herein. The cap includes a housing having a cavity and an insert disposed within. The insert includes one or more cantilevered prongs disposed on a distal wall of the insert. The one or more cantilevered prongs are configured to bend upon insertion of the needleless connector. On an outer sidewall of the one or more cantilevered prongs are one or more ledges extending at essentially a right angle to the one or more cantilevered prongs, the one or more ledges being configured to push against the sidewall of the housing to resist further bending of the one or more cantilevered prongs upon advancement of the needleless connector.

Embodiments described herein relate to apparatuses, systems, and methods for the treatment of wounds, for example using multiple wound dressings in combination with negative pressure wound therapy. A negative pressure would therapy apparatus can include a negative pressure source and a controller. The negative pressure source can include inlets configured to couple via fluid flow paths to wound dressings. The fluid flow paths can include pressure sensors configured to measure pressure in the fluid flow paths. The pressure sensors can include a first pressure sensor configured to measure pressure in the first fluid flow path and a second pressure sensor configured to measure pressure in the second fluid flow path. The controller can be configured to operate the negative pressure source and provide, based on measured pressure, indication of at least one operating condition associated with at least one of the fluid flow paths.

The present invention provides an adaptor that is suitable for attachment to an endoscopic device for delivery of a secondary gas. The adaptor generally comprises an adaptor body with first and second fluid transport components and can include a gas inlet on one of the fluid transport components suitable for attachment to a secondary gas source. A scaling member can be included to prevent leakage of any fluid (e.g., liquid or gas) that is transported through channels extending through the fluid transport components. The adaptor may be used in endoscopy methods and is particularly useful for adding a secondary gas source in an endoscopy procedure.