Integrated IV catheters can have a side port that facilities drawing blood. The side port provides separate fluid pathways for drawing blood and for injecting fluids via an extension set. The side port can be configured to allow the extension set to be primed while a blood sample is collected. In this way, the collection of a blood sample at the time of catheter insertion is facilitated.

Bodily fluid sample collection systems, devices, and method are provided. The device may comprise a first portion comprising at least a sample collection channel configured to draw the fluid sample into the sample collection channel via a first type of motive force. The sample collection device may include a second portion comprising a sample container for receiving the bodily fluid sample collected in the sample collection channel, the sample container operably engagable to be in fluid communication with the collection channel, whereupon when fluid communication is established, the container provides a second motive force different from the first motive force to move a majority of the bodily fluid sample from the channel into the container.

Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.

A blood collection device may include a tubular container, which may include a closed end and an open end opposite the closed end. The blood collection device may include a plug sealing the open end and a partition within the tubular container. The partition may separate the tubular container into a first chamber and a second chamber. The first chamber and the second chamber may be evacuated such that a pressure within the first chamber and a pressure within the second chamber are lower than ambient pressure and equal to each other. In response to blood being drawn into the first chamber, the pressure within the first chamber may increase, and the partition may slide towards the closed end such that a size of the first chamber increases and a size of the second chamber decreases.

A vacuum tube receiver can include a housing that has a proximal end and a distal end. The housing can include a hollow interior and a proximal opening for receiving a vacuum tube into the hollow interior. The distal end of the housing can form an adapter for coupling the vacuum tube receiver to an intravenous system. The vacuum tube receiver may also include one or more spikes that extend proximally into the hollow interior to form a blood flow path. The vacuum tube receiver can include a number of features to control the pressure and/or flowrate of blood into a vacuum tube.

A catheter system may include a catheter adapter, a catheter extending distally from the distal end of the catheter adapter, and a needle hub coupled to the catheter adapter. The needle hub may be transparent, and a needle may be secured within the needle hub. The catheter system may also include a flow control plug coupled to the proximal end of the needle hub. In some embodiments, a flashback pathway may be disposed between an outer surface of the flow control plug and an inner surface of the needle hub. In some embodiments, the catheter system may include an inner barrel and an outer barrel, and the inner barrel and the needle hub may be configured to move proximally within the outer barrel to retract the needle. The flashback pathway may be disposed between an outer surface of the needle hub and an inner surface of the inner barrel.

A biological fluid collection device that allows a blood sample to be collected anaerobically is disclosed.

A catheter system may include a catheter adapter, which may include a distal end, a proximal end, a lumen extending through the distal end and the proximal end, and a side port in fluid communication with the lumen. A catheter may extend distally from the catheter adapter. A septum may be disposed within the lumen. The septum may include a first slit generally aligned with a longitudinal axis of the catheter and a second slit offset from the longitudinal axis of the catheter. An introducer needle may be secured within a needle hub and may extend through the catheter and the first slit of the septum. A winged needle set may include: a body; a needle extending distally from the body and through the second slit of the septum; an extension tube extending from the body; and a blood collection device coupled to the extension tube.

A catheter system may include a catheter assembly, which may include a catheter adapter and a catheter extending distally from a distal end of the catheter adapter. The catheter system may also include a needle assembly, which may include a needle hub and an introducer needle. The needle hub may include: a distal end coupled to the proximal end of the catheter adapter; a proximal end; a wall disposed between the distal end of the needle hub and the proximal end of the needle hub; and a flashback chamber proximate the wall. The introducer needle may be press-fit within a through-hole of the wall. The catheter system may also include a plug coupled to the proximal end of the needle hub. A blood collection device may be coupled to a proximal end of the plug to collect blood from a patient.

A regulator for in-line modulation of the flow rate of fluid during blood collection includes a fluid transfer device for transferring fluid from a patient to a collection device. The fluid transfer device comprises a fluid passageway defined by a tubular sidewall and a flexible member associated with a portion of the tubular sidewall. The flexible member is configured for movement with respect to the fluid passageway upon exposure of the fluid transfer device to a differential pressure during a blood collection procedure to prevent collapse of a patients blood vessel. The flexible member of the regulator can be a frame surrounding a flexible diaphragm. Alternatively, the flexible member can include a flexible material integrally formed within the tubular sidewall of the pressure regulator.