Various concepts relate to treatment systems for medical devices delivered into patients in medical procedures. The treatment system may include a proximal valve configured to receive the endoluminal device, an optional distal valve configured to receive the endoluminal device, and a treatment chamber configured to receive a portion of the endoluminal device.

A flow sensor sub-assembly includes a flow tube having a lumen, an outside diameter, a first end, and a second end. An inlet fitting includes a conical orifice sized for insertion in either end of the flow tube, such that an internal passage of the inlet fitting is coaxial and concentric with the lumen and the end of the flow tube abuts a shoulder. An outlet fitting includes a conical orifice sized for insertion in either end of the flow tube, such that an internal passage of the inlet fitting is coaxial and concentric with the lumen and the end of the flow tube abuts a shoulder. A first piezo element integrated with the inlet fitting is arranged at an upstream position of the flow tube assembly and a second piezo element integrated with the outlet fitting is arranged at a downstream position of the flow tube assembly.

An injection setup kit can include a manifold connector, a first packaging container, and a fluid line. The first packaging container can define a first closed interior volume that includes a patient interface connector having a patient interface inlet, a first patient interface outlet, and a valve configured to selectively permit fluid communication through the patient interface connector. The patient interface inlet can be fluidly connected to the manifold outlet. The fluid line can have a first fluid line end and a second fluid line end. The first fluid line end can be connected to the patient interface inlet within the first closed interior volume. The second fluid line end can extend outside of the first closed interior volume and be connected to a manifold outlet outside of the first closed interior volume.

Fluid flow manifold assemblies for use in fluid flow sets are provided. The fluid flow manifold assembly includes a body having a main fluid channel and a reinforcing plate, the main fluid channel having a fluid inlet, a fluid outlet and a drug port. A flow control assembly is disposed opposite the main fluid channel from the drug port. The flow control assembly is configured to shut off fluid flow through the drug port into the main fluid channel with a plunger of the flow control assembly in a closed position and to allow incremental levels of fluid flow through the drug port into the main fluid channel by variably retracting the plunger based on rotation of a knob of the flow control assembly.

Disclosed herein is an implantable port and an implantable port-detecting device (“IPDD”). The implantable port includes a housing and a septum over a portion of the housing. At least one of the housing or the septum incorporates a contrast agent for locating the septum of the implantable port when the implantable port is implanted in a patient. The IPDD includes a light source, a light detector, and a display configured to display a presence of the implantable port. The light source is configured to emit light in a near-infrared (“NIR”) range of wavelengths as incident light for absorption by the contrast agent. The light detector is configured to detect light in the NIR range of wavelengths including luminescent light emitted by the contrast agent. The display is configured to display a presence of the implantable port when the luminescent light from the contrast agent is detected by the light detector.

A needleless connector may include a housing having an inlet port, an outlet port, and an inner surface defining an internal cavity extending between the inlet and outlet ports, and a compressible valve reciprocally disposed within the internal cavity. In a closed state, a top section of a head portion of the compressible valve may have a planar shape configured to contact and seal against the inner surface of the housing. In an open state, where the compressible valve is subject to an axial force, the top section of the head portion may be lodged between two pinch points between opposing walls of an inwardly angled portion of the internal surface. Additionally, in the open state, the top section of the head portion may have a non-planar shape defining a fluid path extending at least partially between opposing walls on an outwardly angled portion of the internal surface.

A catheter system may comprise an elongated access assist device configured to receive a guidewire during a thrombectomy. The device may include a hemostasis valve coupled to a proximal end of the device, whereby the valve controls fluid flow between a proximal portion and a distal portion of the device. The device may also include a flush port coupled to the proximal portion, where the flush port is configured to couple to a fluid supply source and facilitate the release of fluid from the fluid supply source through the elongated access assist device. The fluid may be configured to be released through a plurality of microperforations located along the body of the device, as well as on a distal tapered portion of the device. The distal tapered portion, combined with the release of fluid through the microperforations, may ease navigation of the system through the vasculature.

The invention discloses a multi-tube body adapter which is connected to a plurality of outer tubes for application to a digestive system and a respiratory system of a human body. The multi-tube body adapter includes a housing to form an accommodating space of the multi-chamber. The plurality of chambers is not in communication with each other. One end of the plurality of chambers respectively provides a connection port and the other end of the plurality of chambers is commonly connected to an extension having a plurality of openings. By connecting with the chamber, the connection port and the opening, a supply path for separately providing the supply path of the respiratory system and the digestive system can be formed.

A solution for injecting one or more fluids into a patient is proposed. A corresponding injection system comprises: at least one supply station for supplying a fluid to be injected into a patient's vasculature; a pressurizing unit comprising a motor for pressurizing the fluid received from said at least one supply station; a delivery arrangement in fluid communication with said at least one supply station, the delivery arrangement comprising a connector having a connecting element and a latching mechanism; a patient set assembly in fluid communication with said delivery arrangement, said patient set assembly comprising a peristaltic pump component and at least one delivery tube for delivering the pressurized fluid to the patient, said peristaltic pump component having a connecting element for fluidically engaging the connecting element of the connector of the delivery arrangement at said port of the pressurizing unit, characterized in that said latching mechanism comprises an elongated flap integral with said connector, and said latching mechanism engages a corresponding port of the pressurizing unit.

Systems and methods for locally engaging tissue using suction. In at least one catheter device embodiment, the catheter device comprises an engagement catheter having a proximal end, a distal end, and a vacuum lumen therethrough operably coupling the proximal and distal ends; an elongated tube of a shape memory material having a plurality of elongated strips removed from a length of the elongated tube to form elongated shape memory tines at a distal end of the tube, wherein the shape memory tines flare outward away from a central axis to form a fluted distal end; and an elastomeric coating disposed over the elongated shape memory material tines to form a suction cup shape.