Abstract: One embodiment of a blood transfusion device includes a drip chamber (10) comprising a bottom outlet (113); a filter (40) fixedly disposed in the drip chamber (10); and a float regulator (20) moveably disposed in the drip chamber (10) under the filter (40). the float regulator (20) comprising an inverted upper cup (21) including a top projection (212), a lower cup (22) secured to the upper cup (21), and a suction cup (23) secured to an underside of the lower cup (22). An inner diameter of the upper cup (21) is greater than an outer diameter of the lower cup (22). The projection (212) contacts an underside of the filter (40) when blood from a blood bag (90) sufficiently fills the drip chamber (10). The suction cup (23) falls to permanently close the outlet (113) when blood in the drip chamber (10) completely drains.

Abstract: An intravenous flow control device includes a flexible drip chamber (20) comprising a fluid entrance (22) and an open bottom (231); a rigid drip assembly (30) secured to the drip chamber (20) and comprising an inner cylinder (31) having a bottom exit (331); and an internal float valve (10) comprising a fastening member (12) including a hollow inner cylinder (121), a plunger (11) slidably disposed through the inner cylinder (121), an upper float member (15) secured to one end of the plunger (11), a lower float member (13) secured to the other end of the plunger (11), and a block member (14) secured to the lower float member (13) for sealingly blocking the exit (331). Fluid flows into the inner cylinder (31) for accumulation so as to float the block member (14), thereby unblocking the exit (331) and moving the plunger (11) upward.

Abstract: A syringe includes in one embodiment a fluid cartridge including a rear sliding member; a syringe barrel; a hypodermic needle assembly releasably secured to the syringe barrel; a nut member releasably secured to the syringe barrel; and a plunger including a rear handle, a front member disposed through the nut member to urge against a rear end of the sliding member, and an arm interconnected the handle and the front member. In response to dispensing fluid disengage the syringe barrel with the hypodermic needle assembly so as to separate the syringe into first and second portions, and wherein the first portion consists of the hypodermic needle assembly and the fluid cartridge and is adapted to discard, and the second portion consists of the nut, the plunger, and the syringe barrel and is adapted to sterilize for a next use.

Abstract: Provided is a non-coring needle for venous access implantatable port. In one embodiment the non-coring needle comprises a puncturing assembly comprising two wings having a central sleeve, an L-shaped needle coupled to the sleeve, the needle including an annular groove or enlargement on its bent portion, and a plastic tubing coupled to the sleeve; and a syringe barrel comprising an internal chamber having a forward opening, and an elongate slot formed on the syringe barrel and being in communication with the chamber. The groove or enlargement is located at a first dent of the slot when the needle is concealed in the chamber in a non-use position, the groove or enlargement is located at a forward second dent of the slot when the needle is fully extended from the opening for use, and the groove or enlargement is permanently locked at a rear triangular recess of the slot when the needle is fully retracted into the chamber.

Abstract: Provided is a non-coring needle for venous access implantatable port. In one embodiment the non-coring needle comprises a puncturing assembly comprising two wings having a central sleeve, an L-shaped needle coupled to the sleeve, the needle including an annular groove or enlargement on its bent portion, and a plastic tubing coupled to the sleeve; and a syringe barrel comprising an internal chamber having a forward opening, and an elongate slot formed on the syringe barrel and being in communication with the chamber. The groove or enlargement is located at a first dent of the slot when the needle is concealed in the chamber in a non-use position, the groove or enlargement is located at a forward second dent of the slot when the needle is fully extended from the opening for use, and the groove or enlargement is permanently locked at a rear triangular recess of the slot when the needle is fully retracted into the chamber.

Abstract: A safety syringe comprises a plunger, a hollow cylindrical, staged adapter fitted on a forward nose of the plunger, a projection on a circumference of the adapter, a hypodermic needle mounted on a forward end of the adapter, and a sheath for enclosing the adapter and the needle, the sheath comprising a T-shaped groove having a left recess with the projection disposed therein in a non-operating position, a right slot, and an intermediate cross piece in a horizontal portion thereof. The projection slides along the groove for causing the needle to dispense fluid through a forward aperture of the sheath. Also, responsive to again disposing the projection in the recess after dispensing fluid, rotate the adapter to move the projection from the recess to and lock in the slot by passing under the cross piece. The sheath is adapted to couple to any typical syringe plunger or IV infusion set.

Abstract: A disposable, safe needle sheath assembly comprises a barrel unit including a hollow barrel, a forward extension adapted to insert through a wing unit into a cap, and a T-shaped slot longitudinally formed thereon, a transverse bar of the slot including a locking device in a right side, and a needle unit including a hollow plunger, a needle, two opposite latched members raised above an edge of a rear end, and a circumferential protrusion, the protrusion being projected from the slot after inserting the needle unit in the barrel unit. Removing the cap and sliding the protrusion from the transverse bar to a distal end of the slot will project the needle from the extension for dispensing medicine. To the contrary sliding the protrusion from the distal end of the slot to the locking device will lock the protrusion therein.

Abstract: A needle sheath assembly comprises a butterfly needle coupled to an IV tubing, and a plastic sheath comprising two rear side slits, two pairs of upper and lower snapping members, a latched member in front of the slits, a slot extended forward from the latched member. The needle is concealed in the sheath. The upper and lower snapping members secured together. In use push the wings forward along the slot until the needle projects from the aperture. After use pull the wings rearward until the needle has concealed in the sheath and a joint of the wings has moved in the slits prior to pushing the wings forward again until being stopped by the latched member. This can eliminate a possibility of accidentally pricking a medical worker after use. Also, criminals are prevented from selling needle sheath assemblies to hospitals again by simply cleaning or even disinfecting the used needles.

Abstract: An intravenous (IV) flow controlling device comprises a flexible open container having a specific gravity less than one and an outer diameter smaller than that of the drip chamber, the container including a spherical bottom portion thinner than the shell upper portion thereof; a first plastic tube coupled to the bottom of the container being in communication with the exit; a flexible reservoir having one end coupled to the first tube; and a second plastic tube coupled to the other end of the reservoir being in communication therewith. The container is submerged as fluid filled in the drip chamber. Fluid flows through the exit, the first plastic tube, the reservoir, and the second plastic tube to cause the container to fall, thereby stopping fluid exiting when the bottom portion of the container clogs the exit and fluid in the drip chamber is used up.