A device, method, and system are provided for treating pleural effusion by administration of a chemical agent through a pleural catheter to achieve pleurodesis. A first embodiment includes a dual barreled syringe to deliver the sclerosing agent; one barrel includes a sclerosing agent, and the other barrel includes a flushing fluid. A kit of the invention comprises a plurality of syringe devices each preloaded with a sclerosing agent matched with a presumptive diagnosis regarding the etiology of the pleural effusion to be treated. A device of the invention includes a handheld, disposable, electronic delivery device with preloaded chambers holding selected medicaments and flushing fluid. Automatic delivery of medicaments is achieved in which a microcontroller of the device controls evacuation of the selected chambers by one or more actuators that communicate with the chambers.

A multi-chamber syringe for delivering a plurality of fluids to a central venous catheter includes a barrel and a plunger. The barrel includes a plurality of chambers, and a first one of the plurality of chambers has a predefined volume of a saline flush stored therein. Actuation of the plunger causes the predefined volume of the saline flush to be dispensed from the barrel into the central venous catheter.

The present invention relates to a syringe, and more particularly, to an apparatus obtained by improving a conventional syringe formed with an injection flow passage including an injection needle, so as to share a portion of the injection flow passage except the injection needle or to form a suction flow passage completely independent of the injection flow passage, thereby further smoothing suction of a liquid medicine. The syringe is configured such that the separate suction flow passage bypassing the injection needle is formed in the conventional syringe to more smoothly perform suction of the liquid medicine, thereby maximizing user's convenience and marketability of the conventional syringe, and further configured to forcibly close the suction flow passage upon injection of the liquid medicine.

A pressure based vessel locating system including a pressure based vessel locator device coupled to a needle or catheter. The pressure based vessel locator device can include a proximal end having an air permeable membrane, and a first chamber and a second chamber. The first chamber can be separated from a second chamber by an interior wall. Each of the first chamber and the second chamber include a proximal opening and a chamber opening having a pressure activated valve disposed therein. The pressure based vessel locator device can further include an air permeable membrane configured to cover proximal openings of the first chamber and the second chamber. Each of the chambers include a window enabling a user to observe the contents of each chamber. A method of identifying a blood vessel includes visually inspecting each chamber for the presence or absence of blood therein.

A syringe is provided having a hub with an orifice, first and second barrels having interior surfaces to form respective lumens, a slider, and an optional test indicator. The first and second barrels slideably receive respective first and second plungers for movement therein. The slider is operable to provide a fluidly communicative path between the orifice of the hub and the first and second barrel lumens. The optional test indicator is responsive to at least one characteristic of bodily fluid, the test indicator positioned to be exposed to any bodily fluid drawn into the first barrel lumen and visible from an exterior of the first barrel.

A fluid delivery device includes an automatic needle retraction mechanism configured to automatically retract a delivery end of a needle into a housing. In one embodiment, the needle assembly is configured to automatically withdraw the delivery end of the needle into the housing upon an actuator moving from the first position to the second position. In one embodiment, the needle assembly is configured to automatically withdraw the delivery end of the needle into the housing upon decoupling a bottom surface of the housing from a skin surface.

The present relates to a filter needle coupled between a fixation member having a needle for injecting a medical fluid after filtering foreign substances contained in the medical fluid and a disposable syringe, the filter needle includes an outer housing having a front end portion to which the fixation member is coupled and a rear end portion to which the disposable syringe is coupled and a filtering unit which is disposed inside the outer housing, and in which a medical fluid supplied from the fixation member to the disposable syringe is passed through as is, while a medical fluid supplied from the disposable syringe to the fixation member is filtered.

A multi-chamber injection device includes multiple syringes. The multiple syringes may be arrayed in a circular, linear, or other format. In some implementations, a needle, port, or similar may be shared by all the syringes in configuration that allows only one syringe to deliver contents at a time while blocking the other syringes from delivering their respective contents. In some implementations, the syringes may be all stored in the same container. One or more of the chambers of a multi-chamber injection device may be preloaded with medication. Different medications may be loaded into different chambers. The medications may be selected to treat the same medical condition.

An auto-disable prefillable integrated package apparatus includes a first chamber, a second chamber, a connection configured to form a communicable channel between the first chamber and the second chamber, a frangible membrane configured to form a rupturable barrier within the connector that separates the first chamber and the second chamber, and a hub configured to be communicably coupled to the second chamber.

A syringe-based device includes a housing, the housing including a port, and an actuator mechanism including a first member and a second member configured to be movably disposed within the housing. The first member includes a syringe body and a plunger movably disposed within the syringe body and including a first plunger seal. The second member includes a second plunger seal defining a channel and a valve fluidically coupled with the channel of the second plunger seal. The device also includes a first fluid reservoir and a second fluid reservoir. The device transitions from a first configuration to a second configuration in which a first type of fluid in the first fluid reservoir is delivered through a port, to a third configuration in which a second type of fluid within the second fluid reservoir is delivered through the port.