Provided is a lancet which comprises: a housing provided with an inner sleeve guiding portion and a first needle core guiding portion; an inner sleeve provided inside the housing; wherein the front end of the inner sleeve has an inner sleeve needle outlet, and the inner sleeve is provided with a second needle core guiding portion; a needle core adapted to move axially along the first needle core guiding portion; a spring provided inside the housing to drive the needle core, wherein the inner sleeve guiding portion has a radial rotation angle at a rotation guiding section thereof away from the inner sleeve needle outlet; by pressing towards the inside of the housing, the inner sleeve is guided by the rotation guiding section to rotate such that the first needle core guiding portion is aligned with the second needle core guiding portion in the radial direction.

An injection needle includes a needle hub and a needle tube. The needle hub is connected to a safety protective cover by an elastic flip mechanism. Two symmetrically-distributed needle hub hooks are provided on a side wall of the needle hub. Two symmetrically-distributed protective cover snaps are provided in a hollow inner cavity of the safety protective cover. The two protective cover snaps cooperates with the two needle hub hooks. Protective cover snap stoppers are provided on outer sides of the two protective cover snaps. The injection needle employs the two needle hub hooks disposed on the side wall of the needle hub and cooperate with the two protective cover snaps disposed in the inner cavity of the safety protective cover.

A needle assembly is disclosed. The needle assembly includes a housing having a flash chamber, and having a distal end and a proximal end engageable with a specimen collection container. The assembly includes a cannula having a patient end, a non-patient end, and a sidewall extending therebetween defining a cannula interior. The patient end of the cannula projects at least partially from the distal end of the housing, and the cannula interior is in fluid communication with the flash chamber. The assembly further includes a shield restrainably engaged with a portion of the housing and axially transitionable over the patient cannula from a retracted position in which the patient end is exposed, to an extended position in which the patient end is shielded by at least a portion of the shield, wherein at least a portion of the flash chamber is visible in the retracted position.

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.

A sample tube holder (40) includes an elongated body (42) with an open end (46) suitable for receiving sample vials. A lid (50) is pivotally attached to body and movable to a position over the open end. The lid includes an aperture (62) that is configured to allow a portion of a vascular access needle assembly to extend through the aperture while an access needle (20) and needle protector (34) portion of the assembly are captured and confined within the body to afford added protection against accidental needle sticks.

A medical device configured as a blood collection tube holder, the device having a body with two spaced-apart, oppositely facing, coaxially aligned needles including a forwardly facing venipuncture needle and a rearwardly facing fluid discharge needle, the two needles being held by first and second needle holders separated by a compressible fluid seal defining part of a fluid path between the two needles and the two needle holders. The body also includes a discharge needle displacement member that is manually repositioned following removal of the last blood tube holder so that the discharge needle displacement member contacts the second needle holder and displaces the second needle holder and the fluid discharge needle laterally inside the body to initiate retraction of the venipuncture needle into a rearwardly projecting needle retraction chamber.

A sample collection device for collecting a blood sample of a patient, the sample collection device including a first partially deformable shell and a second at least partially pierceable shell with a pre-packaged vacuum sealed between the first shell and the second shell. The second shell may additionally hold a sample container and an automatic mechanical cutting mechanism including a rotatable cutting blade and an actuator spring, the actuator spring being actuatable by pressing the first shell, thereby releasing and rotating the cutting blade. By pressing the first shell, the pre-packaged vacuum is released to a collection opening of the second shell such that the vacuum effects a suction effect so that blood coming out of the incision created by the rotatable cutting blade leaks into the sample container.

A blood collection system may include a needle assembly, which may include a needle configured to receive an evacuated blood collection tube. The blood collection system may include a tubing, which may include a distal end and a proximal end. The proximal end may be coupled to the needle assembly. The tubing may include a first flow channel and a second flow channel. The first flow channel may be configured to collapse at a lower pressure differential than the second flow channel.

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 syringe assembly includes (i) a syringe with a cylindrical body, luer tip at a first end, finger grip at a second end and a cannula extending from the luer tip into the cylindrical body, and (ii) a plunger unit having an adapter portion, receiving cavity, finger grip and piston. A channel extends the length of the adapter portion to receive the cannula in one end and a variety of connectors, valves and/or syringes in a second end. The end of the channel accessible in the receiving cavity mates with or engages any number of commercially available valves, connectors and/or syringes while the luer tip similarly connects to any number of valves, catheters, connectors, etc., depending on the task being undertaken with the syringe assembly.