An enteral feeding apparatus comprises a pod having an expansile pouch which defines a reservoir for enteral fluid and a gas impermeable barrier surrounding the pouch. The pod has an inlet port for delivery of enteral fluid into the pouch and an outlet port having a seal which is pierceable to release enteral fluid from the pouch for delivery to a PEG via a feeding line. The expansile pouch provides the sole force by which enteral fluid is delivered from the pouch through a regulator. The system can accommodate a range of enteral fluids with a wide range of viscosities.

An enteral feeding apparatus comprises a pod having an expansile pouch which defines a reservoir for enteral fluid and a gas impermeable barrier surrounding the pouch. The pod has an inlet port for delivery of enteral fluid into the pouch and an outlet port having a seal which is pierceable to release enteral fluid from the pouch for delivery to a PEG via a feeding line. The expansile pouch provides the sole force by which enteral fluid is delivered from the pouch through a regulator. The system can accommodate a range of enteral fluids with a wide range of viscosities.

A medicinal infusion system includes a safety valve for isolating residual medication by providing a single point of fluidic disconnect to encapsulate a residual fluid volume prone to spillage. The safety valve couples a medicinal repository such as an infusion pump to a medicinal supply, typically from a syringe or tubing. The safety valve includes a resilient, deformable, or hinged surface for isolating and sealing the medicinal flow to eliminate and/or isolate any residual volume in tubing and connectors. The isolating surface accommodates an inserted fitting or coupling for allowing the medicinal flow to fill the infusion pump. Upon disconnection, fluids on either side of the safety valve are therefore isolated on the respective fill or source sides, and residual volume prone to spillage is eliminated.

A medicinal infusion system includes a safety valve for isolating residual medication by providing a single point of fluidic disconnect to encapsulate a residual fluid volume prone to spillage. The safety valve couples a medicinal repository such as an infusion pump to a medicinal supply, typically from a syringe or tubing. The safety valve includes a resilient, deformable, or hinged surface for isolating and sealing the medicinal flow to eliminate and/or isolate any residual volume in tubing and connectors. The isolating surface accommodates an inserted fitting or coupling for allowing the medicinal flow to fill the infusion pump. Upon disconnection, fluids on either side of the safety valve are therefore isolated on the respective fill or source sides, and residual volume prone to spillage is eliminated.

A catheter system may include a catheter assembly and a catheter delivery device. The catheter assembly may include a catheter adapter, which may include a catheter adapter distal end, a catheter adapter proximal end, and a catheter adapter lumen extending through the catheter adapter distal end and the catheter adapter proximal end. The catheter assembly may include a primary catheter extending from the catheter adapter distal end. The catheter delivery device may include a housing, which may include a housing distal end coupled to the catheter assembly, a housing proximal end, and a housing lumen extending through the housing distal end and the housing proximal end. A secondary catheter may be disposed within the housing. The secondary catheter may be configured to move distally through the catheter assembly in response to a fluid pressure provided by a fluid delivery device coupled to the housing proximal end.

A medical tube holder is proposed. The medical tube holder includes: holder bodies and surrounding an outer surface of a medical tube; and fluid pockets provided in the holder bodies to form a predetermined space and discharge fluid stored therein to the outer surface of the medical tube while at least a part of the fluid pockets is broken when pressed by an external force. The fluid pockets are formed in the medical tube holder, and when the fluid pockets are pressed by the external force, the fluid pockets are broken and a fluid (i.e., a lubricant) stored therein is discharged to an outer surface of the medical tube. Accordingly, a user may easily apply the fluid such as the lubricant by using the medical tube holder.

In some examples, a conduit system includes a conduit defining a conduit lumen configured to provide a flow path for a fluid between a container and a medical machine. A flexible member secured to the conduit is configured to substantially occlude (e.g., close) the conduit lumen when deformed by a force acting on the flexible member toward the lumen. The conduit system includes a clamp head configured to pass through an opening defined by the conduit and exert the force on the flexible member, such that the flexible member occludes the conduit lumen. In examples, the conduit is substantially rigid conduit configured to provide a relatively constant geometry and/or flow path for the discharge of a nozzle.

In some examples, a conduit system includes a conduit defining a conduit lumen configured to provide a flow path for a fluid between a container and a medical machine. A flexible member secured to the conduit is configured to substantially occlude (e.g., close) the conduit lumen when deformed by a force acting on the flexible member toward the lumen. The conduit system includes a clamp head configured to pass through an opening defined by the conduit and exert the force on the flexible member, such that the flexible member occludes the conduit lumen. In examples, the conduit is substantially rigid conduit configured to provide a relatively constant geometry and/or flow path for the discharge of a nozzle.

An automatic line reel includes a flexible line wound onto a motor-driven reel assembly. A processor controlling the motor detects contact pressure between the flexible line and a triangular pressure transducer, automatically extending the flexible line when the contact pressure exceeds a preset threshold. Line extension stops when contact pressure falls below a second preset threshold. The flexible line may be retracted and rewound around the reel assembly by activation of a switch on a wireless remoted control, by a switch on the automatic line reel, or by activation of a smart phone application program in data communication with the processor controlling the reel assembly. A reel assembly is optionally configured to maintain uninterrupted fluid communications through the automatic line reel as the reel assembly rotates. The reel assembly may optionally be configured to maintain uninterrupted electrical signal communication through the automatic line reel.

A system for improving central line hygiene, including a chamber for containing central line hubs that protects the central line hubs from germs, and optionally including a wand for irradiating the chamber and measuring parameters of the chamber. A kit including the chamber and wand of the system, and instructions for use. A method of protecting a central line hub from germs by enclosing the central line hub with the chamber, and preventing germs from entering the chamber.