Implementations of a capillary tube syringe are provided. In some implementations, a capillary tube syringe comprises an elongated hollow outer tube having a proximal end and a distal end and a needle extending from the first end of the outer tube outside the outer tube and extending inside the outer tube. In some implementations, an elongated hollow capillary tube having a proximal end and a distal end extend along the inside of the outer tube. In some implementations, a normally compressed spring is operatively connected to the needle. In some implementations, the spring is configured to expand when activated to retract the needle inside the elongated hollow tube. In some implementations, the capillary tube diameter is less than or equal to 0.865 inches.

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 push-type blood collection needle includes a housing having an accommodating cavity therein, a rear cover and a needle body disposed in the accommodating cavity. The rear cover is movably disposed on the housing, and the rear cover has a supporting leg extending into the accommodating cavity. The needle body is provided with a rib. The accommodating cavity is internally provided with a projecting part that cooperates with and blocks the bottom of the rib. The supporting leg is provided with a stopper that cooperates with and blocks the side wall of the rib. And an elastic member is disposed between the needle body and the rear cover.

The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Methods and apparatus are provided for manufacturing an analyte detecting device. In one embodiment, the apparatus comprises a housing; a penetrating member driver; a cartridge containing a plurality of penetrating members; a display on the cartridge; a linear slider on the housing, the slider coupled to a rod; and the rod moving with the slider, the rod having at least one roller. The device uses the linear motion of the slider to rotate the cartridge, punch open a new cavity and load a new penetrating member.

The present invention generally relates to systems and methods for delivering and/or receiving a substance or substances such as blood from subjects. In one aspect, the present invention is directed to devices and methods for receiving or extracting blood from a subject, e.g., from the skin and/or from beneath the skin, using devices containing a substance transfer component (for example, one or more needles or microneedles) and a reduced pressure or vacuum chamber having an internal pressure less than atmospheric pressure prior to receiving blood. In some embodiments, the device may contain a “snap dome” or other deformable structure, which may be used, at least in part, to urge or move needles or other suitable substance transfer components into the skin of a subject. In some cases, for example, the device may contain a flexible concave member and a needle mechanically coupled to the flexible concave member such that the needle may be urged or moved into the skin using the flexible concave member. Other aspects of the present invention are directed at other devices for receiving blood (or other bodily fluids, e.g., interstitial fluid), kits involving such devices, methods of making such devices, methods of using such devices, and the like.

A tube segment sampler system (10) for withdrawing a fluid sample from a tube segment (100), the sampler (10) having a first tube piercing member (28) for piercing the tube segment at a first location and a second tube piercing member (28) for piercing the tube segment at a second location so as to allow air to be drawn into the tube segment (100) through one of the openings made by one of the piercing members (28) whilst fluid is withdrawn through the other of the openings.

The present invention discloses a push-type safety protection mechanism of a blood collection needle. The push-type safety protection mechanism comprises a sleeve member and a valve core member, wherein the valve core member is provided with three parts, namely a needle seat part, a sleeving part and a stopping part; a plurality of limiting grooves is formed in the stopping part; the sleeve member is provided with two parts, namely a first sleeve part positioned at a front section and a second sleeve part positioned at a rear section; an elastic button higher than the side wall of the first sleeve part is arranged on the side wall of the valve core member; a limiting opening matched with the elastic button is formed in the side wall of the first sleeve part; a limiting sliding cavity for accommodating the elastic button and the valve core member is formed from a position of the first sleeve part from the limiting opening to the inner side of the second sleeve part, and the limiting sliding cavity guides and limits front-back movements of the elastic button and the valve core member; and a plurality of elastic limiting protrusions matched with the limiting grooves is arranged on the inner wall of the tail sliding cavity of the second sleeve part. Through the design of the elastic button, medical staff can operate the blood collection needle with the left hand or the right hand alone during use.

The present invention generally relates to systems and methods for delivering and/or receiving a substance or substances such as blood from subjects. In one aspect, the present invention is directed to devices and methods for receiving or extracting blood from a subject, e.g., from the skin and/or from beneath the skin, using devices containing a substance transfer component (for example, one or more needles or microneedles) and a reduced pressure or vacuum chamber having an internal pressure less than atmospheric pressure prior to receiving blood. In some embodiments, the device may contain a “snap dome” or other deformable structure, which may be used, at least in part, to urge or move needles or other suitable substance transfer components into the skin of a subject. In some cases, for example, the device may contain a flexible concave member and a needle mechanically coupled to the flexible concave member such that the needle may be urged or moved into the skin using the flexible concave member. Other aspects of the present invention are directed at other devices for receiving blood (or other bodily fluids, e.g., interstitial fluid), kits involving such devices, methods of making such devices, methods of using such devices, and the like.

A kit for separating and concentrating body fluid cells is provided. The kit includes a first sealing cap provided with a first close contact body; a first cap connection housing having a first inner connection body in which a first elastic body having a first slit line formed at an end thereof, with which the first close contact body comes into elastic contact when coupled to the first sealing cap, is inserted and disposed in an inner hole so that the first inner connection body is assembled with the first sealing cap; a first housing having one end screw-coupled to the first cap connection housing, and having an inner partition wall formed therein so that a first connection hole corresponding to the inner hole is formed through the inner partition wall; a central housing having one end screw-coupled to the other end of the first housing.