A device set designed for PCNL surgery includes a puncture needle, a guidewire, a dilator, a balloon catheter, a sheath, and a drainage catheter which are all placed in a single package. A tip length of the dilator is substantially the same as a tip length of the balloon catheter. The device set may include a puncture needle, a guidewire, a plurality of dilators having different sizes, a sheath, and a drainage catheter, which are all placed in a single package, wherein all the dilators have substantially the same tip length.

A percutaneous nephrostomy catheter system includes a nephrostomy catheter lumen, an extension tubing and a collection bag. The extension tubing is inserted into the nephrostomy catheter lumen. The collection bag is fluidly coupled to the extension tubing. A percutaneous nephrostomy catheter system also includes a catheter hub which employs a Luer valve in order to facilitate nephrostomy care so that when the percutaneous nephrostomy system is in place urine flows from the renal pelvis into the nephrostomy catheter lumen, the extension tubing and the collection bag. The Luer valve employs a scalloped Luer-style male connector which, when screwed into the catheter hub allows flow.

A dual fluid injection device is provided that includes at least two syringes. A hub is provided, to which a first syringe and a second syringe are simultaneously connected. The hub includes a fluid delivery member at an end thereof for injection at a site. The first syringe and the second syringe are actuated independently at a directional control valve.

Apparatus and methods of dispensing fluid intravenously to a subject, and of flushing a line of an intravenous fluid administration apparatus, are provided. The apparatus may include a reservoir pump configured to operate in fluid communication with an upstream source of a first fluid and a downstream pressure-operated valve. The apparatus may also include a port connector configured to operate in fluid communication with at least the pressure-operated valve. The reservoir pump may also be configured to, during operation, automatically refill itself with the first fluid from the first upstream source. The downstream pressure-operated valve may be configured to operate in fluid communication with the reservoir pump and a second fluid source upstream of the pressure-operated valve, and to, during operation, dispense the first fluid to tubing downstream of the pressure-operated valve based on a pressure condition within the pressure-operated valve exceeding a threshold pressure.

Methods and devices are provided for various insufflation sealing approaches for a trocar. For example, a trocar is provided that has a housing and a cannula extending therefrom. The housing and the cannula have a tool pathway extending therethrough for receiving a surgical tool, and the housing has an insufflation port therein. A variety of seal elements are provided that seal the insufflation port to prevent fluid flow into the port. The port and seal elements are configured to have a reduced profile to prevent interference between the trocar and a tissue surface during use.

A fluid injector system includes at least one fluid reservoir having at least one interior surface and defining an internal volume, at least one actuator configured to change the internal volume of the at least one fluid reservoir, and at least one processor. The at least one processor may be programmed or configured to drive the actuator to at least partially fill the at least one fluid reservoir with a fluid from a fluid source, drive the actuator to generate a least a partial vacuum within the internal volume to dislodge one or more gas bubbles adhered to the at least one interior surface and to cause the one or more gas bubbles to coalesce into a coalesced bubble, and drive the actuator to expel the coalesced bubble from an outlet of the at least one fluid reservoir.

The subject matter of the invention is a medical device for assisting self-catheterization and instillation of drug-solutions into the bladder in female patients, consisting of switchable light force (6), of power supply (7), of mirror (8) and/or of one or more cameras (13). The device can be fixed on the dosing syringe (1) itself and beside or instead of the mirror (8) is consisting also of one or more cameras (13). The catheter (2) and the urine drainage bag (13) is connected through a three-way tap (9). A holder element (12) is fixed on the grip element (11). On or in the holder element (12) a micro switch (5), a light source (6), power supply (7) can be found. Further on a mirror (8) or a camera (13) is fixed expediently to the holder element (12) by a fixation element (15).

A method and system for forming a hemostatic hydrocolloid for dispensing into a wound site includes a polymer of oxidized derivatized esterified cellulose in solid form comprising a chain of monomers, wherein, for a first plurality of the monomers in the chain: R is OCH.sub.2(COO)CH.sub.2CH.sub.3, R1 is OCH.sub.2(COO)CH.sub.2CH.sub.3, and R2 is CH.sub.2OCH.sub.2(COO)CH.sub.2CH.sub.3; and wherein, for a second plurality of monomers in the chain: R is OCH.sub.2(COO)CH.sub.2CH.sub.3, R1 is OCH.sub.2(COO)CH.sub.2CH.sub.3, and R2 is (COO)CH.sub.2CH.sub.3 and a liquid mixed with the polymer to form a hemostatic gel for dispensing into a wound site.

A fluid collection and measurement container includes a first wall and a second wall disposed opposite the first wall. The second wall is secured to the first wall and the first wall and the second wall define an expandable volume therebetween. A first electrolytic element is disposed on the first wall and a second electrolytic element is disposed on the second wall. A first terminal is connected to the first electrolytic element and a second terminal is connected to the second electrolytic element.

An apparatus includes a cannula assembly, a housing, a fluid reservoir, a flow control mechanism, and an actuator. The housing includes an inlet port removably coupled to the cannula assembly and defines an inner volume. The fluid reservoir is fluidically coupled to the housing and configured to receive and isolate a volume of bodily fluid from a patient. The flow control mechanism is at least partially disposed in the inner volume. The actuator is operably coupled to the flow control mechanism and is configured to move the flow control mechanism between a first configuration, in which bodily fluid can flow, via a fluid flow path defined by the flow control mechanism, from the cannula assembly, through the inlet port and into the fluid reservoir, to a second configuration, in which the fluid reservoir is fluidically isolated from the cannula assembly.