Improved securement devices for use with intracardiac blood pump assemblies are provided. The present technology provides securement devices that may be used with a sheath assembly (e.g., an introducer sheath assembly, repositioning sheath assembly), and which are configured to restrict movement of an object (e.g., the catheter of the pump assembly) within the sheath assembly except when a mechanism (e.g., button) of the securement device is actively being actuated (e.g., pressed, held, etc.).

A manifold associated with a contrast injector system. The manifold may include a first fluid inlet, a second fluid inlet, a fluid outlet, a main passageway, and a valve. The first fluid inlet, second fluid inlet, and fluid outlet may be in fluid communication with the main passageway. The first fluid inlet, second fluid inlet, or fluid outlet can be connected to a conduit for communicating fluid, such as a fluid at high pressure. At least one of the first fluid inlet, second fluid inlet, or fluid outlet can have a surface finish that is in contact with the conduit.

A connector connection indicator is mounted in a Luer male connector, or in a Luer female connector, to indicate proper mating of the two Luer connectors. The connection indicator may be or include a light source, a sound producing device (e.g., buzzer), a switch, a tactile connection indicator or an electronic chip. The electronic chip may be interposed between two conductive elements that are mounted in the Luer female connector. When the two Luer connectors are properly engaged, the electronic chip is powered via two electrical terminals. While the electronic chip is powered up it communicates with an external system via two electrical terminals. The external system interprets the communication with the electronic chip as an indication to proper engagement of the two Luer connectors. Some of the connection indicators may be mounted on a circuit board that is embedded in a void in the Luer male connector.

Some embodiments comprise a connector including a rigid housing having a first end and a second end. A second member can be positioned at a second end portion of the housing and be engageable with a second device. The second member can have a body portion having a first body portion, a second body portion, and a flow lumen extending axially through the body portion, an annular covering portion extending in a radial direction away from the body portion, a receiving portion extending away from the covering portion in an axial direction, and at least one protrusion extending radially away from an outside surface of the body portion. In some embodiments, the second member can be supported by the housing such that, in an assembled state, the first body portion is positioned within the housing and such that the annular covering portion and the second body portion are positioned outside the housing.

A needle free connector for fluid passage having a valve body with a first port; a second port; a hollow resilient membrane disposed in the valve body and having: a first end and a second end is disclosed. A flank is provided and extends between the first end and the second end fitting with the internal surface of the valve body. A slit of the first end is closed when the first end is disposed in the first port or opened when the first end is pushed into the valve body. The disclosure also proposes a drug recipient including a bottle or a bag designed to store drug and the needle free connector. The disclosure offers a needle free connector with a slitted resilient membrane having reduced priming volume.

Formation of a sterile connection includes inserting a first aseptic coupling device into a second aseptic coupling device while a locking ring of the first aseptic device is in an indexed initial position, rotating the locking ring to a secured position in which a compressive force is created and in which a first membrane from the first aseptic coupling device and a second membrane from the second aseptic coupling device can removed thereby resulting in a first a first sealing member of the first aseptic coupling device sealing with a second sealing member of the second aseptic coupling device to form a sterile fluid passageway.

The invention relates to a method of increasing the leak tightness of a mechanical connector of an extracorporeal blood treatment machine, wherein the mechanical connector has a pair of connection parts which have corresponding sealing surfaces, with at least one of the two sealing surfaces being wetted at least sectionally by a viscous fluid before the joining together of the connection parts and/or with the connection gap between the connection parts being covered by a sheath after their joining together. The invention further relates to an extracorporeal blood treatment machine comprising a mechanical connector which has a pair of connection parts which have corresponding sealing surfaces, with the sealing surfaces being at least sectionally wetted with a viscous liquid with a closed connector and/or with the connection gap between the connection parts of the closed connector being covered by a sheath.

A medical device including a connector portion having a distal end and a proximal end, and a screw groove configured for fluid communication between the connector portion and another medical device. The screw groove has a first side wall provided close to the distal end and a second side wall provided close to the proximal end. The first side wall has a stop portion whose lead angle has been reduced or eliminated.

Luer lock connectors are provided that include an inner core of a hard material, the inner core sized and shaped to mate with an inner portion of an opposing luer lock connector, an outer layer of a soft material disposed on an outer surface of the inner core, and a plurality of grip features disposed on an outer surface of the outer layer, wherein the plurality of grip features are configured to provide a slip resistant grip surface. Infusion sets and infusion set luer lock connectors are also provided.

An attachment arrangement has a housing and a needle located within the housing. The arrangement allows administration ports of different sizes to be inserted into and secured within the housing. In certain embodiments, compliant retainers secure the administration port within the housing. In certain other embodiments, the administration port is secured within the housing when the housing is compressed against the administration port by a housing compression element. Once the administration port is secured within the housing, a fluid-tight seal is formed between the attachment device and the administration port.