A blood collection apparatus is provided with a blood collection assembly including a casing tube including a forward nose, a plurality of connectors and a rear flange having a flexible projection, a plunger slidably disposed in the casing tube and including a forward plug and an elongated arm having a plurality of cavities, a blood collection tubes, an adapter assemblies each including a tube body, a first tube extending out of one end and insert into a related connectors of the casing tube, a second tube extending out of the end to insert into one of the blood collection tubes, and a butterfly needle assembly mounted to the nose of the casing tube. A pulling of the plunger moves the plug rearward and pivots the projection to engage in one cavity of the elongated arm and an orifice of the each related connectors is not blocked by the plug so as to flow blood from the tube casing to one of the blood collection tube via one connector and one adapter assembly.

Fluid collection/injection device comprises a body having a front end, a back end, and a main hollow section arranged between the front and back ends and a needle hub securing section arranged on the front end and being structured and arranged to receive therein a needle member. The fluid collection/injection device is structured and arranged to utilize at least an operational mode, an operational mode, and a post-use mode. In the installation mode, the needle member is coupled to the body via the needle hub securing section. In the operational mode, fluid passes through the needle member and into or out of a receptacle inserted into the main hollow section.

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.

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.

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.

A needle protection device and a safety needle assembly are described. The needle protection device comprises a connecting portion and a protection arm rotatable relative to the connecting portion. A pair of holding members are respectively formed on a proximal end portion of the protection arm and the connecting portion and configured to engage with each other in an unretreatable manner. A pair of positioning arms are respectively formed on the proximal end portion of the protection arm and the connecting portion and formed with at least one pair of complementary snap-fitting features. The paired snap-fitting features are configured to engage each other in a separable manner. The needle protection device and the safety needle assembly not only reliably prevents medical instruments from incurring accidental needle-sticks after use and ensures such medical instruments disposable, but also exhibits a simple structure and low costs.

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 blood collection assembly includes a hub with a distal end, a proximal end, a hub outer surface and an internal opening extending therethrough. The assembly also includes a holder housing defining a receiving chamber and having a rearward end adapted to receive a sample collection tube within the chamber and a forward end including a receiving port extending into the chamber, where the receiving port receives a portion of the proximal end of the hub therein. An internal opening of the hub accommodates a puncturing element at the proximal end thereof for providing passage of a fluid therethrough, and the puncturing element contacts the sample collection tube. The hub and the holder housing include an interengaging structure extending substantially perimetrically therearound for axially locking the hub with the holder housing.

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.