The present invention enables the completion of preparation of liquid medicine injection to be easily and quickly checked with the naked eye based on a color change in an endcap for a liquid medicine-injecting tube. As long as a medical staff checks a color change in the endcap with the naked eye, the medical staff can immediately perform an operation of connecting the tube to a catheter (or injection needle) or the like after removal of the endcap without unnecessarily draining off a large amount of the liquid medicine.

A connector for medical fluid vessels includes a fluid-seal fitting such as a male plug defining a lumen and mating with a cooperating connector, a mechanical fastener such as a screw thread for mating with the cooperating connector, and an outer housing positioned around the plug to form an annular space. Optionally, a cap can be provided with a fluid-seal fitting such as a male plug for mating with the lumen of the connector. The connector includes one or more vent openings for drainage and air-drying of any residual fluid in the annular space when capped, as well as for breaking a vacuum to prevent fluid backflow and thus ensure more accurate dosing. In some embodiments, the vent openings are provided in the outer housing. And in some embodiments, the vent openings are provided in the cap.

A valve for use in manufacturing of implantable medical devices is insertable into a bore of the medical device during a manufacturing process. The valve is configured to remain closed while the pressure differential between an internal volume of the implantable medical device and a surrounding environment is below a particular threshold and to open when the threshold is reached, thereby allowing air or other fluids to escape from the internal volume into the surrounding environment. The valves are particularly useful during certain types of coating processes that must be performed at or near vacuum and provide an effective way to prevent ingress of coating material into the internal volume of the implantable medical device.

A flushing apparatus according to embodiments of the present disclosure includes: a main body configured to connect a connection pipe for guiding a hazardous medicinal liquid harmful to a human body when exposed to an ambient air and a patient connection module for injecting the hazardous medicinal liquid into a patient, the main body configured to form a first flow path for guiding the hazardous medicinal liquid from the connection pipe to the patient connection module, the main body including a flushing portion forming a second flow path connected to a predetermined connection point located between both ends of the first flow path; and a flow rate reduction part disposed at upstream side of the connection point in the first flow path and configured to reduce a flow rate of the hazardous medicinal liquid flowing through the first flow path. The present disclosure shows various embodiments of the flushing apparatus.

A connector for medical fluid vessels includes a fluid-seal fitting such as a male plug defining a lumen and mating with a cooperating connector, a mechanical fastener such as a screw thread for mating with the cooperating connector, and an outer housing positioned around the plug to form an annular space. Optionally, a cap can be provided with a fluid-seal fitting such as a male plug for mating with the lumen of the connector. The connector includes one or more vent openings for drainage and air-drying of any residual fluid in the annular space when capped, as well as for breaking a vacuum to prevent fluid backflow and thus ensure more accurate dosing. In some embodiments, the vent openings are provided in the outer housing. And in some embodiments, the vent openings are provided in the cap.

A priming cap includes a conduit housing and a resilient member. The conduit housing further includes an upper housing, a lower housing coupled to the upper housing, a fluid passageway extending through the upper housing and the lower housing; and a plug positioned within the upper housing. The conduit housing can define a valve activation member configured to open and close a medical connector. The resilient member can include a retaining feature to secure the priming cap to the medical connector.

A medical fluid connector, having a first body with a tube section with an inlet and a first thread, a second body with an outlet and a second thread that engages the first thread to move the first and second bodies between closed and opened positions. The second body has a third thread that is configured to rotate in the opposite direction in relation to said first and second threads. The connector has a closure cap with a fourth thread that, in a delivery state of the fluid connector, is detachably screwed to the third thread of the second body, wherein the fluid connector assumes the open position, and wherein the outlet is closed off in an air-permeable and liquid-tight manner by means of the closure cap.

An intravenous delivery system may operate by gravity feed, and may have a liquid source containing a liquid, a drip unit that receives the liquid from the liquid source, and tubing that receives the liquid from the drip unit for delivery to a patient. A flow rate sensor may be used to measure a flow rate of liquid through the intravenous delivery system, and may generate a flow rate signal indicative of the flow rate. A controller may receive the signal, and may compare the flow rate with a desired flow rate. If the flow rate is more or less than the desired flow rate, the controller may transmit a control signal to a flow rate regulator. The flow rate regulator may receive the control signal and, in response, modify the flow rate to bring the flow rate closer to the desired flow rate.

Devices used to drain fluid are disclosed. The devices may be configured to drain fluid from a body cavity using a vacuum pressure. The devices include a reservoir and a vacuum generating member configured to expand the reservoir and generate a vacuum pressure within the reservoir. The devices can be configured to be shipped in a collapsed state.

An infusion set employing a spike cap, arranged at which there is an opening configured to prevent passage therethrough of solid or liquid but to allow passage therethrough of gas at interior of the cap, hydrophobic filter being arranged at a location inward from where a tip of spike is inserted at interior of the cap by way of an insertion port, and a lid exterior of the opening for closing the opening; and in which there are hook(s) for anchoring to infusion tubing and a clip equipped with a catch for a flange arranged at the spike. Employing the cap at the infusion set makes it possible to carry out preprocessing including priming and backpriming by a simple operation without leakage of liquid.