Systems and methods for delivering a drug or other therapy over an extended period of time (e.g., several hours, days, weeks, months, years, and so forth) are disclosed herein, as are systems and methods for monitoring various parameters associated with the treatment of a patient. Systems and methods are also disclosed herein that generally involve CED devices with various features for reducing or preventing backflow.

A surgical tool for use with a robotic system that includes a tool drive assembly that is operatively coupled to a control unit of the robotic system that is operable by inputs from an operator and is configured to robotically-generate output motions. A drive system is configured to interface with a corresponding portion of the tool drive assembly for receiving the robotically-generated output motions and applying the output motions to a drive shaft assembly which is configured to apply control motions to a surgical end effector operably coupled thereto. A manually-actuatable control system operably interfaces with the drive shaft assembly to facilitate the selective application of manually-generated control motions to the drive shaft assembly.

A stool management system having a tubular body including a first end section disposable in a rectum of a patient and a second end section including a first connector which detachably mates with a second connector coupled to a collection container which receives waste matter passed through the tubular body from the bowel of the patient.

Disclosed is a medical fluid connector configured to receive and dispense medical liquid. The medical connector can be structured to include an initial stage in which medical liquid is infused into the connector and dispensed out of the connector essentially unchanged. The medical connector also can be structured to include a subsequent stage in which medical liquid is not infused into the connector and a volume of therapeutic liquid is dispensed out of the connector. The therapeutic liquid can include a portion of the volume of the medical liquid that was infused into the connector in the initial stage plus a therapeutic additive.

A connection device includes a tube that is branched to two passages from a branch portion and includes a first and second branch tubes provided on one end side as a liquid-feeding destination, a first protruding plate that includes, on another end side, first another end edge provided in a direction orthogonal to an axis line of the first branch tube and that is provided so as to protrude from an outer circumference portion of the tube, and a second protruding plate that is provided so as to face the first protruding plate across the tube and protrude in a diameter direction of the tube and that includes, on the other end side, second another end edge provided so as to be orthogonal to an axis line of the second branch tube.

A connector assembly for connecting medical lines (3, 4) to each other comprises a first connector (1) having an insertion shaft (12), and a second connector (2) having an insertion opening (22). For connecting the first connector (1) and the second connector (2) to each other, the insertion shaft (12) of the first connector (1) is insertable along an insertion direction (I) into the insertion opening (22) of the second connector (2). For releasing the first connector (1) and the second connector (2) from each other, the insertion shaft (12) of the first connector (1) is removable from the insertion opening (22) of the second connector (2). The first connector (1) comprises an elastic member (14) arranged on the insertion shaft (12), wherein the elastic member (14) comprises an abutment portion (141) abutting a surface (121) of the insertion shaft (12) and being displaceable along the insertion direction (I) relative to the surface (121) of the insertion shaft (12) upon releasing the first connector (1) and the second connector (2) from each other. In this way a connector assembly is provided which, in an easy way, allows for the cleaning of at least the first connector.

Fluid flow manifold assemblies for use in fluid flow sets are provided. The fluid flow manifold assembly includes a body having a main fluid channel and a reinforcing plate, the main fluid channel having a fluid inlet, a fluid outlet and a drug port. A flow control assembly is disposed opposite the main fluid channel from the drug port. The flow control assembly is configured to shut off fluid flow through the drug port into the main fluid channel with a plunger of the flow control assembly in a closed position and to allow incremental levels of fluid flow through the drug port into the main fluid channel by variably retracting the plunger based on rotation of a knob of the flow control assembly.

There is provided a medicinal liquid injection port to be implanted subcutaneously. A housing main body is provided with a medicinal liquid storage portion therein, an opening portion that opens the medicinal liquid storage portion, and a discharge hole that communicates with the medicinal liquid storage portion and configured to be connected with a tube. A septum attached to the opening portion of the housing main body and provided with a puncturable region that can be punctured with a puncture needle. A contrast portion is disposed in the septum over a thickness direction of the septum so as to detect the puncturable region of the septum with the ultrasonic wave. The contrast portion is provided in the septum within a thickness region of the septum and all of the contrast portion is positioned at an inner side of the septum in the thickness direction of the septum.

This document describes fluid coupling devices for fluid systems and methods of using the fluid coupling devices. Some fluid coupling devices described herein are configured for use in fluid systems for the purpose of providing a sterile connection. Such a sterile connection can be useful for the delivery and/or processing of therapeutic agents, or ingredients thereof, and other purposes.

An extravascular system is provided which includes a catheter adapter having a blood control septum configured to control flow of a fluid through the catheter adapter, the catheter adapter further having a catheter configured for intravenous insertion. The extravascular system further includes a septum activator slidably inserted within the catheter adapter and configured for advancement through the blood control septum to provide a fluid pathway through the blood control septum. Further still, the extravascular system includes an external safety mechanism comprising a needle hub and a needle shield interconnected via a tether, wherein the needle shield includes a safety clip that is configured to retain a sharpened end of the introducer needle within the needle shield. Some implementations further comprise an access port forming a portion of the catheter adapter and providing selective access to the lumen of the catheter adapter.