Disclosed is a tube connector for medical treatment including a housing including an internal channel configured to allow an inflow pipe disposed at the front end thereof and an outflow pipe disposed at the rear end thereof to fluidly communicate with each other, an insertion hole formed from the outer surface of the rear end of the housing to the internal channel, and at least one branch pipe disposed so as to fluidly communicate with the internal channel, a push button having a through hole, the push button being disposed in the insertion hole so as to be movable upwards and downwards, and an elastically deformable dome-shaped balloon configured to surround the insertion hole of the housing, the lower part of the balloon being open, wherein the internal channel of the housing is opened and closed through the upward and downward movement of the push button.

A medication container adapter that utilizes a push-pull valve for adapting medication containers for use with syringes that are filled on semi-automatic and automatic filling machinery. The syringes are filled when the medication container is in the inverted filling position. The push-pull valve comprises of a stationary portion and a poppet slidably inserted into the stationary portion. The poppet is an annular member having a central channel and a fluted axial outlet from the central channel. The push-pull valve can be configured to be pressed onto an existing medication container adapter or manufactured as an integrated part of the medication container adapter so that it can either be screwed onto or pressed into the medication container neck.

A monitoring device provided for monitoring the delivery of fluids through a drip chamber. The device includes an electromagnetic radiation source and a radiation detector. A weight detector is positioned to determine the weight of a fluid reservoir over time, and the detector is positioned with respect to the drip chamber to detect drops falling through the drip chamber. A processor is coupled to the radiation detector and the weight detector to determine flow rate, and is further coupled to a flow restrictor to selectively increase or decrease flow based on the determined flow rate.

A valve system comprises a first valve plunger configured for insertion into a first valve plunger channel. The first valve plunger has a first latch member disposed at a distal end. A first sealing member and a first valve are opening disposed proximally from the first latch member. The valve system also comprises a second valve plunger configured for insertion into a second valve plunger channel. The second valve plunger includes a second valve opening that is longer than the first valve opening. The valve system also includes a valve body having the first and second valve plunger channels. The first and second valve plunger channels are configured to receive the first and second valve plungers, respectively.

A dilution spacer for a metered-dose inhaler comprises an enclosure defining a dilution chamber. An ambient air inlet and an outlet are in fluid communication with the dilution chamber. The ambient air inlet is positioned opposite the outlet whereby suction through the outlet from outside the enclosure draws ambient air into the enclosure through the ambient air inlet to generate an airflow path from the ambient air inlet through the dilution chamber and out of the outlet. The dilution spacer may include an actuator inlet configured to securely releasably interengage a metered-dose inhaler actuator mouthpiece, or may include a receptacle having an actuator nozzle and configured to receive a metered-dose inhaler canister, A metered-dose inhaler plume entering the dilution chamber intersects the airflow path thereto and airflow along the airflow path entrains and redirects at least a portion of the metered-dose inhaler plume toward the outlet.

A cap for intake and delivery of a fluid from a syringe is described. The cap includes an outer cap assembly comprising a fluid inlet path and a fluid outlet path and an inner cap assembly configured for innertion into a fluid nozzle of the syringe and to provide selective fluid communication between an interior of a syringe and the fluid inlet path or the fluid outlet path. The outer cap assembly is slidable relative to the inner cap assembly between a first filling position, where the interior of the syringe is in fluid communication with the fluid inlet path, and a second delivery position, where the interior of the syringe is in fluid communication with the fluid outlet path. The outer cap may further slide, relative to the inner cap assembly, to a third closed position where the interior of the syringe is fluidly isolated from the fluid inlet path and the fluid outlet path. Syringes including the cap are also described.

A valve comprising: a valve body; and a valve stem disposed at least partially within the valve body, the valve stem comprising a sidewall defining a central lumen and at least one opening in the sidewall, wherein the valve is adapted to prevent fluid flow through the lumen when the at least one opening is disposed within the valve body and permit fluid flow through the lumen when the at least one opening is exposed from the valve body, and wherein the valve is essentially free of a spring.

A needle-free connector including a guiding base, a connecting base, a valve member, and a seal member is provided. The guiding base has a conduit, and the conduit extends downward along an axial direction. The connecting base is disposed on the guiding base and has a screw portion and a passage running through the screw portion. A chamber is formed between the guiding base and the connecting base, and the conduit and the passage respectively communicate with the chamber along the axial direction. The valve member is disposed between the guiding base and the connecting base, and is movably located in the chamber. The seal member is disposed at an end of the valve member far away from the conduit, and the seal member and the valve member are adapted to be connected into a whole in a manufacturing process.

A solution is proposed for closing a mouth (125) of a container (110) of a liquid (105). A corresponding closure (135) comprises a cap (205) having fixing means (315) for fixing the cap (205) to the container (110), a delivery port (321) for delivering the liquid (105) from the container (110), a valve member (215) in a closed position wherein the valve member (215) closes the delivery port (321), a cap suction conduit (339) for suctioning air into the container (110) during the delivering of the liquid (105) and a connector (327) for connecting to a delivery device (805) of the liquid (105), the connector (327) being in fluid communication with the delivery port (321), a slider (220) slidebly coupled with the cap (205), the slider (220) having a slider suction conduit (440) for suctioning the air into the container (110) during the delivering of the liquid (105) slidebly coupled with the cap suction conduit (339), and a frangible element (345) closing the cap suction conduit (339) or the slider suction conduit (440), wherein the closure (135) is configured to cause the delivery device (805) during the connecting thereof to move inwards the container (110), in a fixed condition wherein the closure (135) is fixed to the container (110), and thus moving the valve member (215) inwards the container to an open position, wherein the valve member (215) opens the delivery port (321), and moving the slider (220) inwards the container to break the frangible element (345), thereby putting in fluid communication the slider suction conduit (440) with the cap suction conduit (339).

A mechanical fluid pressure modification valve, or MFLP-valve, is set forth. The MFLP-valve can be actuated upon movement of a movable pressure system member of a medical pressure system reaching a selected position. Additionally, the MFLP-valve can be actuated based on a pressure condition of the system. When the MFLP-valve unseals, a pressure differential between a pressure chamber and a volume outside of the chamber can be relieved. Disengagement of the movable pressure system member from the MFLP-valve can enable the MFLP-valve to re-seal. The MFLP-valve may include a flag that indicates the position of the movable pressure system member. The MFLP-valve may be provided in a diaphragm-type pressure source.