Abstract: A sealed fluid transfer device comprised of tubing, a proximal fitting, and a distal needle assembly is provided. The needle assembly includes a needle hub secured to a needle cannula. A cantilevered actuator arm extends outwardly from the needle hub having an actuator button at its free end. The needle assembly is disposed in a barrel and can move from a distal position, where the needle is exposed, to a proximal position, where the needle is shielded. The barrel includes a septum which seals the barrel. A spring is disposed in the barrel for propelling the needle assembly to the proximal position. The barrel includes an aperture that receives the actuator button for locking the spring in a compressed condition. Depression of the actuator button enables the spring to propel the needle assembly into its proximal position. A safety mechanism prevents inadvertent depression of the actuator button.

Abstract: A catheter system may include a catheter assembly and a needle assembly. The catheter assembly may include a catheter adapter, which may include a distal end, a proximal end, a lumen, and a side port. The catheter assembly may include a catheter extending from the distal end of the catheter adapter and an extension tube. A distal end of the extension tube may be integrated with the side port of the catheter adapter. The needle assembly may include a needle safety element, which may be disposed within the safety housing or the catheter adapter. The needle assembly may include a guidewire advancement device coupled to the safety housing or the catheter adapter, and an introducer needle having a proximal end coupled to the guidewire advancement device.

Abstract: An infusion system having an integrated inserter and infusion set (10) for containing and placing a flexible catheter (40), and a retractable introducer needle (26), wherein the catheter (40) is isolated from movement after placement. The integrated inserter and infusion set (10) includes a hub (20), having a user push button (30) to activate the device for catheter (40) placement. An adhesive liner (34) can be provided to cover an adhesive layer (36), such as pressure sensitive adhesive (PSA), on the bottom of the device (10).

Abstract: An IV catheter system may have a catheter component and a needle component. The catheter component may have a catheter hub, a cannula extending distally from the catheter hub, and a push feature extending outward from the catheter hub. The push feature may have an outer surface that receives contact from a digit to move the IV catheter system from an insertion configuration, in which the needle is within the cannula, to a fluid delivery configuration, in which the needle is outside the catheter hub. The needle component may have a needle hub and a needle extending distally from the needle hub along an axis. The push feature may be formed of a flexible material that causes the push feature, in response to pressure exerted on the outer surface by a dressing securing the catheter component to a patient, to deflect the outer surface toward the cannula axis.

Abstract: A catheter assembly may include a catheter adapter, a septum housing, and a septum. The catheter adapter may include a distal end, a proximal end, an inner wall extending between the distal end and the proximal end, and a lumen formed by the inner wall. The septum housing may include one or more protrusions and may be secured to the inner wall by one or more of the following: an interference fit between the one or more protrusions and the inner wall, a snap fit between the one or more protrusions and the inner wall, and bonding between the one or more protrusions and the inner wall. The septum may be at least partially disposed within the septum housing and configured to at least substantially seal the lumen.

Abstract: An integrated intravenous catheter includes a catheter adapter having a catheter and an inlet, with the catheter configured to be inserted into a patient's vasculature, a needle-free connector comprising a first port, a second port positioned opposite the first port, and a side port positioned the first port and the second port, with the second port including a valve member, intermediate tubing extending between the inlet of the catheter adapter and the first port of the needle-free connector, and extension tubing extending from the side port of the needle-free connector.

Abstract: A medical instrument or device, such as a catheter, has echogenic properties, in addition to or as an alternative to radiopaque properties, to facilitate detection of the medical instrument or device during medical procedures using suitable imaging methods, such as ultrasound imaging and/or x-ray imaging methods. In example embodiments, an example catheter has a relatively increased radiopacity and echogenicity to facilitate a clinician with detecting the catheter with ultrasound imaging and/or x-ray imaging methods to assist the clinician with the insertion, placement, and/or maintenance of the catheter, for example.

Abstract: An IV access device can include a needle hub that incorporates a flash chamber. The flash chamber can be used to provide visual confirmation of proper catheter placement within a vein. The flash chamber can include a path-defining structure to facilitate identifying whether blood is continually flowing into the flash chamber. The flash chamber may also be removable from the needle hub. In some cases, the needle hub may include a paddle grip that facilitates insertion of the catheter and separation of the needle hub from the catheter adapter.

Abstract: Provided herein is a dressing for use with a catheter assembly, including a base defining a perimeter and an interior, the base comprising a bottom surface configured to contact skin of a patient and comprising a first opening in the perimeter, and a cover portion attached to the base and configured to cover a site of a catheter insertion, the cover portion comprising a second opening, the second opening configured to align with the first opening in the base when the dressing is applied to a patient’s skin.

Abstract: Pinch-style clamps can be designed for use in clamping or occluding plastic tubing, such as intravenous tubing. These pinch clamps can include a soft, polymer material applied to various surfaces of the pinch clamp to prevent abrasion or irritation to the patient, increase friction between the pinch clamp and the user operating said pinch clamp, increase friction between engaged surfaces of the pinch clamp to prevent premature or unintended disengagement of the clamp, or increase friction between the outer surfaces of the tubing and the clamping surfaces of the clamp. Various features or components can be employed to prevent lateral disengagement of the pinch clamp. A pinch clamp may also be configured with rounded outer edges to enhance patient comfort.

Abstract: A catheter assembly may include a catheter adapter, a septum housing, and a septum. The catheter adapter may include a distal end, a proximal end, an inner wall extending between the distal end and the proximal end, and a lumen formed by the inner wall. The septum housing may include one or more protrusions and may be secured to the inner wall by one or more of the following: an interference fit between the one or more protrusions and the inner wall, a snap fit between the one or more protrusions and the inner wall, and bonding between the one or more protrusions and the inner wall. The septum may be at least partially disposed within the septum housing and configured to at least substantially seal the lumen.

Abstract: A blood draw device for delivery of a probe into a patient's vascular system, the blood draw device including a housing having a proximal end and a distal end, and an advancement wheel, wherein the advancement wheel is operably coupled to the probe to advance and retract the probe based on a direction of rotation of the advancement wheel. The blood draw device also includes an advancement stop member, wherein the advancement stop member is positionable by a user via an interface portion external to the housing and is configured to selectively limit rotation of the advancement wheel.

Abstract: A blood draw device for delivery of a probe into a patient's vascular system, the blood draw device including an introducer body having a proximal end and a distal end, and an actuator. The actuator is displaceable along at least a portion of the introducer body, and the actuator is operably coupled to the probe to advance and retract the probe based on direction of displacement of the actuator. The blood draw device also includes an advancement stop member, wherein the advancement stop member is displaceable along at least a portion of the introducer body and is configured to selectively limit travel of the actuator along the introducer body.

Abstract: An IV access device can include a needle hub that incorporates a flash chamber. The flash chamber can be used to provide visual confirmation of proper catheter placement within a vein. The flash chamber can include a path-defining structure to facilitate identifying whether blood is continually flowing into the flash chamber. The flash chamber may also be removable from the needle hub. In some cases, the needle hub may include a paddle grip that facilitates insertion of the catheter and separation of the needle hub from the catheter adapter.

Abstract: Disclosed herein is an intravascular catheter assembly, including a catheter adapter having a distal end; a proximal end; a first lumen arranged between and in fluid communication with the distal end and the proximal end; a catheter arranged at the distal end of the catheter adapter and in fluid communication with the lumen; and a first side port in fluid communication with the lumen; a first fluid conduit having a distal end and a proximal end, the distal end of the fluid conduit coupled to the side port; and a connector having a proximal end, a distal end connected to the fluid conduit, and a second lumen therethrough, the connector comprising a manually-actuable valve.

Abstract: A catheter adapter includes a body having a first end and a second end positioned opposite the first end, with the body including an inlet port positioned between the first end and the second end and defining a longitudinal axis extending between the first end and the second end of the body, a catheter configured to be inserted into a patient's vasculature, with the catheter positioned at the first end of the body, and a stabilizer including a first wing member and a second wing member, with a portion of the stabilizer extending beyond the inlet port of the body in a direction extending along the longitudinal axis from the first end of the body to the second end of the body.

Abstract: Pinch-style clamps can be designed for use in clamping or occluding plastic tubing, such as intravenous tubing. These pinch clamps can include a soft, polymer material applied to various surfaces of the pinch clamp to prevent abrasion or irritation to the patient, increase friction between the pinch clamp and the user operating said pinch clamp, increase friction between engaged surfaces of the pinch clamp to prevent premature or unintended disengagement of the clamp, or increase friction between the outer surfaces of the tubing and the clamping surfaces of the clamp. Various features or components can be employed to prevent lateral disengagement of the pinch clamp. A pinch clamp may also be configured with rounded outer edges to enhance patient comfort.

Abstract: A pinch clamp for use in occluding intravenous tubing or other similar tubing can include patient comfort features and/or lateral disengagement prevention features. These features can also be designed in a manner that allows the pinch clamps to be more easily manufactured. A pinch clamp can include a first arm that is coupled to a second arm by hinges. Each of the first and second arms can form a clamping surface that are aligned when the first arm is positioned overtop the second arm. The first arm can include opposing openings and the second arm can include opposing tabs which insert through the openings when the first arm is positioned overtop the second arm. The retaining tabs interface with the openings to prevent the first arm from separating from the second arm.

Abstract: A vein simulator can enable a clinician to perform a PIVC workflow. This workflow can include preparation of simulated skin, insertion of a PIVC into a simulated vein, flushing a line of the PIVC and dressing and securing the PIVC to the simulated skin. The vein simulator may be formed of simulated tissue, simulated skin that is integrated into the simulated tissue and an embedded simulated vein that may be positioned within a protruding vein channel. Because the simulated skin is integrated into the simulated tissue, the vein simulator will provide a more realistic experience while practicing the workflow. A vein simulator may include one or more sensors to provide real-time feedback to a clinician while practicing the workflow.