Various aspects of the subject disclosure relate to a compounder system having a cartridge that includes controllable fluid pathways. The cartridge may include a syringe pump for moving fluid and/or gas, and one or more syringe valves or rotary valves for controlling which of the controllable fluid pathways is open for flow of the fluid and/or gas.

An exemplary compounding system and method can include a transfer set that includes a manifold for assisting in transferring a plurality of ingredients from supply container(s) to a final container. The manifold can include a first channel in fluid communication with at least one primary ingredient, and a second channel in fluid communication with a plurality of secondary ingredients. The first channel and second channel can be in fluid isolation from each other such that the at least one primary ingredient does not mix with the plurality of secondary ingredients within the manifold. The transfer set can include a plurality of inlet lines in fluid communication with the manifold and two outlet lines configured for connection to two separate pumps and eventually being in fluid communication with the final container.

A valve assembly for a fluid injector system includes a valve housing, a first port configured for fluid communication with a fluid injector, a second port, a third port, and a fourth port configured for fluid communication with a patient line. The valve assembly includes an air detection region associated with the first port, a fluid path length having a proximal end in fluid communication with the second port and a distal end in fluid communication with the third port, and a valve element defining a first fluid path and a second fluid path. The first fluid path provides fluid communication between the first and second ports in a delivery position of the valve housing. The second fluid path provides fluid communication between the third and fourth ports in the delivery position. The third port is isolated from the fourth port in a stop position of the valve housing.

A wearable ultrafiltration apparatus is provided. The apparatus can include a first dialyzer for filtering a patient's blood along a first fluid path and a second dialyzer for filtering the patient's blood along a second fluid path. The apparatus can also include a valve being positionable in a first position for directing the patient's blood along the first fluid path. The valve can also be positioned in a second position for directing the patient's blood along the second fluid path. When the valve is in the first position, blood can flow along the first fluid path and prevent blood from flowing along the second fluid path. When the valve is in the second position, blood can flow along the second fluid path and prevent blood from flowing along the first fluid path. When the valve is in the first position, the second dialyzer can be idle and capable of being serviced or replaced and when the valve is in the second position, the first dialyzer can be idle and capable of being serviced or replaced. Therefore, when a dialyzer fouls, blood can be directed to the other dialyzer while the fouled dialyzer is being serviced or replaced.

A unified X-bar stopcock, including a bidirectional stopcock having a first port, second port, third port, and fourth port; and a three-way stopcock having a fifth port, sixth port, and seventh port. The bidirectional stopcock is fluidly coupled to the three-way stopcock via the first port and the fifth port. A method of using the X-bar stopcock includes providing a Swan-Ganz catheter, an X-bar stopcock, a transducer, a monitor, and at least one bag of saline. The method includes connecting the X-bar stopcock to at least two lumens of the Swan-Ganz catheter. The method additionally includes connecting at least one port of the X-bar stopcock to the transducer connected to the monitor, connecting at least one port of the X-bar stopcock to the bag of saline, and connecting the transducer to the bag of saline. The unified X-bar stopcock may also include a protective case.

An exemplary compounding method of controlling a compounding device to prepare an admixture of at least two distinct material sources can include examining material source solutions for incompatibility of the ingredients and operating a first and a second pump to prevent one of the incompatible source solutions from entering a common flow path. The processing method can detect degradation of a fluid line by evaluating one or more of calibration error rate data, cumulative volumetric flow data, or cumulative pump operation data. The processing method can also selectively transfer a first group of source solutions using the first pump, receiving pump data from one or more sensors that sense actions of the pumps, applying fluid correction factors and calculating discrete pump movements, the pump movements being indicative of an amount of source solution displacement by a pump, and operating the pumps to selectively dispense the source solution amounts according to a preparation order.

Certain aspects are directed to a housing and cap to provide protection of medical devices having one or more percutaneous connection (e.g., a three-way stopcock or catheter port).

A fat harvesting system and related methods of harvesting and reinjecting fat that provides a medical professional with multiple technique options. Harvested fat can be subjected to a variety of pre-reinjection preparation steps within a single, self-contained reservoir such that the potential for contaminating the harvested fat is avoided. The fat harvesting system can be completely self-contained kit requiring no additional external systems or alternatively, can utilize available surgical suite systems, for example, vacuum to successfully harvest, prepare and reinject fat cells. The fat harvesting system can size harvested fat cells so as to be especially desirable for different injection locations in the body. The fat harvesting system is a single use, disposable system that requires no sterilization equipment and recovered and sized fat cells are maintained in a sanitary environment so as to avoid contamination that could result in having to discard recovered fat cells.

A surgical access port or trocar is provided. The trocar has a trocar seal housing and a trocar cannula with an optical obturator insertable through the trocar seal housing and the trocar cannula. The trocar is configured to access a body cavity, to maintain positive pressure and to prevent loss of surgical insufflation gas used in laparoscopic procedures. The trocar seal housing can be releasably attached to the trocar cannula. The trocar seal housing may also have a shield and/or alignment channel that provide protection or assist in operation of instrument and zero seals housed in the trocar seal housing.

A stopcock for a channel that guides a flux medium in a medical endoscope, the stopcock having a housing accommodating a plug rotatable about an axis in a conical seat penetrated by the channel, wherein the housing has a bearing collar adjacent to the conical seat in the direction of the axis, in which bearing collar a handle body is mounted to be rotatable about the axis, the handle body supporting a handle outside the housing and rotationally coupled to the plug displaceable in direction of the axis and resiliently supported relative thereto, wherein the handle body has a radially elastic detent device engaging a circumferential inner groove of the bearing collar to be locking in direction of the axis, wherein the plug is arranged and configured bring the detent device out of engagement with the bearing collar upon displacement in direction of the axis into an unlocked position.