Various embodiments relate to a syringe for separating nucleic acids from a blood sample and systems that include the syringe and a portable PGR device. The syringe may include a shell defining a central aperture extending through a longitudinal axis of the syringe, a plunger disposed within the central aperture of the shell, and a core rotatably disposed within the central aperture. The syringe may further include a needle fluidically connectable to the inlet of the shell. Various embodiments relate to a method for separating nucleic acids from a blood sample, the method comprising drawing the blood sample from a patient using the syringe according to any of the embodiments described herein.

A syringe assembly includes a syringe body, needle assembly, retaining clip, gasket, needle latch, and needle hub. The syringe body has a syringe interior, longitudinal axis, proximal and distal ends, and needle attachment interface disposed at the distal end thereof. The gasket is configured to be compressed to provide a liquid-tight seal around an outer diameter of the needle assembly and the distal end of the syringe body. The needle latch assembly includes first and second latching tabs configured to retain the needle assembly in a close state and to be plastically deformed to an open state to release the needle assembly, and a gasket backstop configured to provide a flat surface for compression of the gasket, where the first and second latching tabs are spaced apart from the gasket such that neither of the first and second latching tabs contact the gasket during compression of the gasket.

A rigid needle shield for a syringe includes a main body comprising an internal sidewall defining a bore, and an end cap attached to the main body. The end cap includes at least one frangible tab connected to the sidewall of the main body. The rigid needle shield further includes an elastomeric insert extending through the bore and engaging the end cap. The at least one frangible tab is configured to break from the internal sidewall and advance through the bore upon application of a force to the end cap.

A needle hub assembly for coupling to a pen needle delivery device includes an outer cover having a first well receiving the needle hub and inner shield covering a cannula of the needle hub. A second well is spaced from the first well and receives the inner shield. In use, the pen delivery device is coupled to the connecting end of the needle hub to withdraw the needle hub and inner shield from the first well. The inner shield is inserted into the second well where the inner shield is gripped so that the inner shield can be separated from the needle hub without the user handling the outer cover or the inner shield. After use, the needle hub is inserted into the first well and the pen needle delivery device is separated from the needle hub. The needle hub is retained within the first well where the outer cover containing the used needle hub and inner shield can be discarded as a single unit.

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 removal device (121, 221) for removing and disposing of a pen needle (113, 213) connectable to a drug delivery device (111, 211) includes a body (123, 223) having a cavity (141, 241) for receiving the pen needle of the drug delivery device such that a patient end (116, 216) of a needle (115, 215) of the pen needle is covered by the body. An ejector (151, 251) is movably connected to the body (123, 223) for engaging the received pen needle (113, 213) and selectively ejecting the engaged pen needle from the body. The pen needle (113, 213) is securely retained within the removal device (121, 221) without exposing the needle (115, 215) of the pen needle until the pen needle (113, 213) can be properly disposed of, such as in a sharps container, thereby substantially preventing an accidental needle stick.

A device for the treatment of periodontal disease includes a handle that has a configuration familiar to dental professionals, and a detachable tip or cartridge, that is locked into the handle when use. The device provides for automatically delivering a single dose of medicament, such as a powdered preparation of antibiotic, to a periodontal pocket for treatment of infection or disease.

The invention relates to a gripper apparatus for a cannulation robot and for gripping a cannula having a cannula holder. The gripper apparatus comprises two gripper elements and a moving device. The two gripper elements can be moved relative to each other and work in concert to grip the cannula holder. The moving device is designed to move the two gripper elements relative to each other and at least one of the gripper elements relative to the cannula holder. The gripper apparatus can thereby be brought into a gripping state, in which at least one of the gripper elements is engaged with the cannula holder, by means of the moving device.

An apparatus for entirely removing a medical sharp from a holder to which it is connected, including a body (102), a heating unit (104) disposed in the body, a receiving unit (114) fixedly disposed in the body and configured to receive the holder, and a collet (122) movably disposed within the body and configured to receive the medical sharp. The apparatus also includes a first biasing member (130) disposed within the body, and a user interface (136) coupled to the collet and configured to displace the collet away from the receiving unit, actuate the first biasing member to increase a bias on the collet toward the receiving unit, and actuate the heating unit.

A safety syringe includes a needle seat, an adapter disposed on the needle seat, and an injection barrel penetrated into the needle seat and the adapter. When an outer sleeve is located at a first position, a first annular rib of the outer sleeve is engaged with an elastic wing of the adapter, such that the needle seat protrudes from the front end of the outer sleeve. A push rod penetrated into the injection barrel is used to take in and expel liquid medicine. When the outer sleeve is located at a second position, the outer sleeve accommodates the needle seat and the adapter inside and pushes against the elastic wind of the adapter through a second annular rib, such that the outer sleeve is detachable from the injection barrel together with the needle seat and the adapter, The injection barrel can be used for needle-free dosing injection.