A biopharmaceutical flow port, a biopharmaceutical liquid container assembly, and a method for manufacturing the biopharmaceutical flow port and the biopharmaceutical liquid container assembly are described. The biopharmaceutical flow port includes a hose barb coupled to an elliptic body. The hose barb includes a bore. The elliptic body includes a flow passage, a first edge, and a second edge. The flow passage is fluidly coupled to the bore. The first edge extends from the elliptic body away from the flow passage in a first direction and the second edge extends from the elliptic body away from the flow passage in a second direction opposite the first direction. The biopharmaceutical liquid container assembly includes a biopharmaceutical liquid container with an opening and the biopharmaceutical flow port coupled to the biopharmaceutical liquid container within the opening and in fluid communication with a volume of the biopharmaceutical liquid container.

A method for improved controlling of a thermic infusion system having a one tubal segment and a thermal element to heat an infusion fluid carried within the tubal segment, and having at least one sensor positioned within the thermic infusion system comprising regulating energy provided to the sensor for a first period of time to sense a self-heating effect of the at least one sensor due to a dry tube; responsive to detecting a dry tube, preventing energizing the thermal element; responsive to detecting a non-dry tube, regulating energy provided to the sensor for a second period of time to sense a temperature of an infusion fluid carried within the at least one tubal segment.

The present disclosure is directed to a device for delivering an antimicrobial composition into an infusion device. The disclosure provides a method for preventing infection and microbial ingress in medical device connections. The device includes a male connector with a distal tip and a recess at the distal tip. The surface of the recess includes an antimicrobial composition. In certain implementations a male luer comprises a tapered sealing member further comprising a recess containing chlorhexidine acetate.

A drug delivery system includes a delivery container including a container body adapted to accommodate a drug therein, a supply line, a flow rate sensor, and a flow controller. The delivery container further includes an outlet port and is constructed from a resilient material. The container body is adapted to exert an urging force on the drug to expel the drug from the outlet port. The supply line is operably coupled to the outlet port to deliver the drug to a user. The flow sensor senses a flow rate of the drug within the supply line. The flow controller is configured to regulate a flow rate of the drug; the flow controller includes a supply line restrictor and a controller for adjusting the supply line restrictor between at least two settings.

A patient support apparatus includes a frame. A vertical transport structure may be coupled with the frame. A grip is coupled with the vertical transport structure and at least one grip sensor is coupled to the grip on the vertical transport structure. A controller determines a vertical position of a user applied force applied to the at least one grip sensor and the controller activates a power drive mode upon determining that the push force has reached a threshold value corresponding to the vertical position of the user applied force and propel patient support apparatus.

An infusion system includes a chamber for accommodating an infusion fluid and an infusion line for transferring the infusion fluid from the chamber. The infusion line includes at least a rotor module or is connected to a rotor module at least at a downstream end of the infusion line. The rotor module includes a rotor that is drivable by the infusion fluid.

Systems and methods for determining the position of a fluid within a fluid source and infusion line coupled to an infusion flow control device are described herein. An exemplary system and method includes sampling fluid pressure upstream of an infusion pump, and calculating fluid pressure slope profiles. By sampling fluid pressure upstream of an infusion pump at discrete intervals and monitoring fluid pressure slope profiles, conditions of fluid flow, including unintentional fluid flow through an infusion line or a defective check valve in an infusion line, are detected, and fluid flow through an infusion pump is controlled.

A prepackaged needleless intravenous line assembly is provided as well as a method of delivering intravenous medication and/or fluid to a patient while maintaining sterility of needleless access ports. The pre-packaged needleless intravenous line assembly is a sterile intravenous line with at least one sterile access port, each access port having a disinfection cap installed thereon, sealed within a pouch with at least one strip of multiple sealed disinfection caps. An intravenous tubing kit, having sterile intravenous tubing with capped sterile access ports as well as sealed replacement disinfection caps, is removed from the package and attached to a patient's intravenous catheter. A disinfection cap is removed from the sterile access port. Medication and/or fluid is administered into the access port. A replacement disinfection cap is installed onto the access port.

There is disclosed a heating device which is adapted to be used to warm medical solutions contained within medical devices such as an intravenous bag, intravenous tube or respiratory circuit. The heating device includes an elongated flexible material tube having an interior medical solution channel and a pair of heat channels. The heat channels are filled or coated with a flexible, electrically conductive substance, which forms an electrical resistor. The conductive substance is electrically coupled to an electric power source controller. Electric current passing through the conductive substance creates heat which is transferred from the heat channels to the medical solution contained within the interior medical solution channel.

An automated dose-response record system including a module for housing waste-heat producing electronic and electromechanical medical equipment including at least one physiologic monitor, and including a system to measure, temporally correlate and record dose and response events.