Abstract: An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a probe formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the probe out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.

Abstract: An IV catheter device can include or being configured to employ a probe assembly having an integrated fluid flushing mechanism. The probe assembly can be configured in a variety of ways to cause flushing fluid to be injected through a fluid permeable structure of the probe as the probe is advanced distally from a catheter. In this way, the fluid permeable structure can be kept clear of any occlusion that may otherwise form. With the probe extending distally from the catheter, a blood sample may be collected.

Abstract: An extension set may include a tube having an outer surface. An instrument, such as a tubing or a probe, may be disposed within the tube and may include a proximal end and a distal end. A translation handle may be coupled to the outer surface of the tube and may move along the outer surface between a proximal position and a distal position to translate the distal end of the instrument between a retracted position and an advanced position. In the advanced position, the distal end of the instrument may extend beyond the distal end of the tube and into a catheter assembly and/or vasculature of a patient.

Abstract: An extravascular system is provided which includes a catheter adapter having a blood control septum configured to control flow of a fluid through the catheter adapter, the catheter adapter further having a catheter configured for intravenous insertion. The extravascular system further includes a septum activator slidably inserted within the catheter adapter and configured for advancement through the blood control septum to provide a fluid pathway through the blood control septum. Further still, the extravascular system includes an external safety mechanism comprising a needle hub and a needle shield interconnected via a tether, wherein the needle shield includes a safety clip that is configured to retain a sharpened end of the introducer needle within the needle shield. Some implementations further comprise an access port forming a portion of the catheter adapter and providing selective access to the lumen of the catheter adapter.

Abstract: A delivery device to deliver a tubular instrument into a catheter extending distally from a catheter adapter. The delivery device may include a housing configured to couple to the catheter adapter. The delivery device may include a tubular instrument configured to insert through the catheter. The tubular instrument may include a distal end, a proximal end, and a lumen extending between the distal end and the proximal end. The distal end may include a distal tip, which may be closed. The proximal end may be secured within the housing. The tubular instrument may be configured to advance distally with respect to the housing. A portion of the distal end proximate the distal tip may include a first material and maybe stiffer than the distal tip, which may include a second material. A durometer of the first material may be greater than a durometer of the second material.

Abstract: Inserts can be formed with elution characteristics to cause the inserts to elute an antimicrobial agent when subject to a fluid within a medical device. An insert can be formed with a desired geometry to allow the insert to be compression fit within a medical device to prevent the insert from moving or becoming dislodged once inserted into the medical device. The material may also be hygroscopic so that the insert swells when subject to a fluid thereby enhancing the compression fit of the device within the medical device. In some cases, the material can be reinforced using an internal structure. Inserts can be formed in many ways including by casting, thermoforming, or extrusion. In some cases, the inserts can be formed using a peel-away sleeve or material. The peel-away sleeves can be formed of a non-sticky material which facilitates removal of the inserts once the inserts have cured.

Abstract: A cap is configured to provide antimicrobial protection to a female luer port of an intravenous device. The cap distributes an antimicrobial solution within the intraluminal surfaces of the port when the cap is connected to the port. A cap may also be designed to distribute an antimicrobial solution around the exterior surfaces of the port. Once connected to a port, the cap can form a seal that minimizes the evaporation of the antimicrobial solution from within the lumen of a port. The cap can therefore provide antimicrobial protection against another device that is connected to the port once the cap is removed.

Abstract: Provided herein is a probe delivery device for advancing a probe into a vascular access device. The probe delivery device includes an outer housing, a connector, a shield assembly, and a probe assembly. The shield assembly includes a shield sleeve movable within an inner volume of the housing and a shield advancer coupled to the proximal end of the shield sleeve, the shield advancer having a shield handle configured to slide along an outer surface of the housing to move the shield sleeve distally from a first sleeve position to a second sleeve position. The probe assembly includes a probe movable within the shield sleeve and a probe advancer coupled to the proximal end of the probe, the probe advancer having a probe handle configured to slide along an outer surface of the housing to move the probe distally from a first probe position to a second probe position.

Abstract: A catheter assembly may include a catheter adapter, a catheter, and a dressing to securely apply traction to the catheter where the catheter is disposed within a vasculature of a patient. The catheter adapter may include a proximal end, a distal end, and a lumen extending between the proximal end and the distal end. The catheter may extend from the distal end of the catheter adapter. The dressing may include a first section adjustably coupled to a second section. The first section may be configured to secure the catheter adapter and/or the catheter to the patient. The second section may be configured to be adjustably positioned relative to the first section to apply the traction to the catheter within the vasculature.

Abstract: A system to detect a position of a cannula may include a cannula, which may include a distal tip and an inner lumen. Also, the system may include an optical fiber, which may be disposed within the inner lumen of the cannula and may include a first end, a second end, and a U-shaped portion disposed between the first end and the second end. The U-shaped portion may be at least proximate the distal tip. Further, the system may include a light emitter, which may be coupled with the first end of the optical fiber, and a light receiver, which may be coupled with the second end of the optical fiber. Moreover, the system may include an electronic processor. The electronic processor may be coupled with the light receiver and configured to detect a decrease in an intensity of light received at the light receiver.

Abstract: A catheter system may include a catheter adapter, which may include a distal end, a proximal end, and a lumen extending through the distal end of the catheter adapter and the proximal end of the catheter adapter. The catheter system may include a catheter extending distally from the distal end of the catheter adapter. The catheter system may include a connector coupled to the catheter adapter and comprising a septum. The catheter system may include a blood collection adapter coupled to the connector. The blood collection adapter may be configured to create a fluid path through the connector. The catheter system may include a blood collection set coupled to the blood collection adapter. The blood collection set may include a needle assembly configured to receive a blood collection container.

Abstract: A blood collection device to reduce hemolysis in a peripheral intravenous catheter system may include a distal end. The distal end of the blood collection device may include a male luer adapter, which may include a distal opening. The blood collection device may include a cannula in fluid communication with the male luer adapter. The cannula may include a distal end and a sharp proximal tip. The blood collection device may include an elongated neck disposed between the male luer adapter and the sharp proximal tip. The blood collection device may include a fluid pathway extending from the distal opening through the sharp proximal tip. A diameter of the fluid pathway may be constant. An entire length of the fluid pathway is represented by L, and the diameter of the fluid pathway is represented by D. D4/L may be equal to or less than a predetermined value.

Abstract: An extension set may include a tube having an outer surface. An instrument, such as a tubing or a probe, may be disposed within the tube and may include a proximal end and a distal end. A translation handle may be coupled to the outer surface of the tube and may move along the outer surface between a proximal position and a distal position to translate the distal end of the instrument between a retracted position and an advanced position. In the advanced position, the distal end of the instrument may extend beyond the distal end of the tube and into a catheter assembly and/or vasculature of a patient.

Abstract: An extension set may include a tube, which may include a distal end, a proximal end, and an outer surface. The extension set may include a distal connector coupled to the distal end of the tube and/or a proximal connector coupled to the proximal end of the tube. The extension set may include a patency instrument disposed within the tube. The extension set may include a translation handle coupled to the outer surface of the tube. The translation handle may be configured to move along the outer surface of the tube between a proximal position and a distal position to translate the distal end of the patency instrument between a retracted position and an advanced position. In response to the distal end of the patency instrument being in the advanced position, the distal end of the patency instrument may extend beyond the distal end of the tube.

Abstract: An introducer needle may include a proximal end, a distal tip, and a needle lumen extending therebetween. The introducer needle may include a wall defining the needle lumen, a first notch formed through the wall, and a second notch formed through the wall. A catheter system may include a catheter adapter, a catheter extending distally from the distal end of the catheter adapter, a flash chamber coupled to the introducer needle, and the introducer needle, which may extend through the catheter. The first and second notches and the flash chamber may facilitate pressure-driven blood flow into the catheter for improved flashback and detection of transfixation when the catheter is primed prior to insertion into vasculature of a patient or otherwise.

Abstract: A method may include coupling a first delivery device to a catheter assembly, which may include a catheter dwelling within vasculature of a patient. The first delivery device may include a first tubular instrument. In response to the first tubular instrument being in a distal position, a distal surface of the first tubular instrument may be disposed at a first distance beyond the distal tip of the catheter. The method may include coupling a second delivery device to the catheter assembly after uncoupling the first delivery device from the catheter assembly. The second delivery device may include a second tubular instrument. In response to the second tubular instrument being in the distal position, a distal surface of the second tubular instrument may be disposed at a second distance beyond the distal tip of the catheter. The second distance may be greater than the first distance.

Abstract: An intravenous therapy system, may include a processor; a data storage device; and a handheld ultrasound probe to detect structures within a patient's body, the handheld ultrasound probe including a video display device physically and operatively coupled to the handheld to display the structures within the patient's body and a magnetic field detector to detect the presence of a vascular access device (VAD) and provide closed-loop feedback to guide the VAD into a blood vessel within the patient's body detected by the ultrasound probe.

Abstract: A vascular access device including a catheter adapter, a port opening, and an elastomeric valve. The catheter adapter extends along a longitudinal axis and includes a proximal end, a distal end, and a lumen extending therebetween. The port opening is formed in a surface of the catheter adapter in fluid communication with a side port of the catheter adapter and the lumen. A structural geometry of the port opening directs a fluid into the lumen in a proximal direction. The elastomeric port valve is disposed within the lumen and configured to deform in response to a transverse force applied thereto. A proximal gap may result between the inner wall forming the lumen and a proximal side of the elastomeric port valve, thereby opening a fluid path.

Abstract: Provided herein is an instrument delivery device for use with an intravenous catheter assembly. The instrument delivery device includes a housing having a proximal end portion and a distal end portion, with the housing including a first housing portion and a second housing portion arranged side-by-side and coupled together to define an inner volume. The instrument delivery device also includes an instrument movably received within the inner volume, a coupling device positioned at the distal end portion of the housing and configured to couple the housing to an access connector of an intravenous catheter assembly, and an advancement member configured to move relative to the housing to advance a distal end of the instrument beyond the distal end portion of the housing and into the intravenous catheter assembly. The housing comprises a visualization aid configured to improve visibility of the instrument within the inner volume of the housing.

Abstract: An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a patency instrument formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the patency instrument out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.