Patent classifications
A61M5/346
Apparatus for Rapid Collection of Blood from Livestock
An apparatus useful for the rapid collection of blood from a subject (e.g., a blood vessel, such as the vein, artery or capillary bed of a bovine subject) and dispensing the blood therefrom into a test or collection device. In general, the apparatus comprises: (a) a body having a chamber formed therein, said chamber having an inlet and outlet, with said chamber configured to draw blood therein; (b) a hollow barrel connected to said chamber outlet; (c) an ejector operatively associated with said barrel; (d) a hollow needle connected to said body, with said hollow needle in fluid communication with said chamber through said inlet, so that blood can be rapidly drawn into said chamber through said needle. The needle is optionally removed and blood dispensed from the body into a test or collection device by actuating the ejector.
APPARATUS FOR RAPID COLLECTION OF BLOOD FROM LIVERSTOCK
An apparatus useful for the rapid collection of blood from a subject (e.g., the vein of a bovine subject) and dispensing the blood therefrom into a collection device includes: (a) a capillary body having a capillary chamber formed therein, with the chamber having an inlet and outlet, and with said chamber configured to draw blood therein through the inlet by capillary action; (b) a hollow barrel connected to the chamber outlet; (c) a plunger positioned in the barrel; and (d) a hollow needle connected to the capillary body, with the hollow needle in fluid communication with the capillary chamber through the capillary inlet, so that blood can be rapidly drawn into the capillary chamber through the needle by the combined action of vein pressure (or other pressure, if present, such as arterial pressure) and capillary action.
Injection needle having shield activated valve
The present invention relates to a needle assembly having a build-in valve (30). The needle assembly is built up from a hub (20) carrying a needle cannula (10) and a telescopically movable shield (40) which axially covers the distal tip (13) of the needle cannula (10) between injections. The valve (30) is operated by the shield (40) and is arranged such that it is closed when the distal tip (13) of the needle cannula (10) is covered by the shield (40) and is opened when the telescopically movable shield (40) has been retracted a specific distance (X) proximally to the distal tip (13) of the distal cannula part (11).
SYRINGE INCLUDING DIFFERENT MATERIALS
A syringe includes a syringe body, a syringe cone having a distal opening, and a connection arranged in the region of the syringe cone, wherein the syringe body includes a first material and the connection includes a second material, and wherein the first material is different from the second material and the second material is a softer material than the first material.
FOLLICULAR ASPIRATION NEEDLE
The invention refers to a needle for follicular aspiration, comprising a base with a through-hole, inside of which a needle cannula is coupled, the needle cannula having a front aspiration end which protrudes from a front end of the base, and a rear end which freely protrudes from the rear end of the base, the through-hole of the base having a frustro-conical segment tapering from the rear end towards the front end of the base, forming a gap between the inner surface of the base and the outer surface of the needle cannula for coupling a biological sample collecting line.
System and method for safety syringe
One embodiment is directed to a system for injecting, comprising a syringe body defining an interior medicine chamber; a stopper member configured to be inserted into the interior medicine chamber to contain medicine within the medicine chamber; a plunger member configured to be manually manipulated to insert the stopper member relative to the syringe body; and a needle having proximal and distal ends, the proximal end comprising an anchoring geometry configured to be at least partially inserted into the stopper member such that upon retraction of the stopper member, the needle is pulled proximally along with the stopper to be at least partially contained within the interior medicine chamber.
Dental Syringe with Stabilizer for Removable Needle
A cartridge syringe system includes a syringe (5). The syringe has a tip-ward direction and a ring-ward direction. The syringe (5) has a syringe body (9) and an actuator ring (7). A shaft (10) slidably mounts the actuator ring (7) to the syringe body (9), with a harpoon (11) at a tip-ward end of the shaft (10). The syringe body (9) has a spiral mount external to the syringe body (9) for removably mounting a sheath (20) to the syringe body (9), on a cooperating internal spiral sheath mount. The syringe body (9) and the sheath have similar openings. The sheath opening can be rotated to coincide with the syringe body opening, for inserting a needle assembly into the syringe body, or for removing the needle assembly. The sheath opening can be rotated to obstruct the syringe body opening, for retaining the needle assembly in the syringe body.
Dental Syringe with Stabilizer for Removable Needle
A needle assembly (14), for use with a syringe (3) and a medicine cartridge (12); has a molded body (14B). A needle (14A) is housed in, affixed to, and reinforced by the molded body (14B). The needle (14A) has a single tube which includes a tip (311), and a tip-ward needle (31) extending ring-ward from said tip into the molded body (14B). The tip-ward needle becomes a cartridge needle (531) within the molded body (14B). The cartridge needle (531) extends tip-ward from the molded body (14B). The molded body (14B), is molded as a single structure, and includes: a domed cylinder (248), at the molded body (14B)'s tip-ward end; a flange (22) ringward of the molded body (14B); and fins (251). The fins are molded radially from the domed cylinder (248). The fins are vertically molded from the flange (22); and reinforce the fins to the flange. A second cylinder (244), is extended ringward from the flange (22). A conical portion (15) is molded ringward from the second cylinder (244). The cone flares out ring-ward to a widest part (631) of the conical portion (15), at a ringward end (500) of the molded body to an annular surface (510) at the widest part (631) of the conical portion (15). The cartridge needle (531) has a molded support located tip-ward of the annular surface (510). A needle shaft (514) is at a central longitudinal axis of the molded body (14B). The needle (14A) passes through needle shaft.
Apparatus and methods for ocular injection
An apparatus includes a housing coupled to a medicament container, which is coupled to a needle. An injection assembly is disposed within the housing and includes an energy storage member and an actuation rod. A distal end portion of the actuation rod is disposed within the medicament container. The energy storage member can produce a force on a proximal end portion of the actuation rod sufficient to move the distal end portion of the actuation rod within the medicament container. This can convey at least a portion of a substance from the medicament container via the needle when a distal tip of the needle is disposed within a first region of a target location. The force is insufficient to move the distal end portion of the actuation rod within the medicament container when the distal tip of the needle is disposed within a second region of the target location.
System and method for safety syringe
One embodiment is directed to a system for injecting, comprising a syringe body defining an interior medicine chamber; a stopper member configured to be inserted into the interior medicine chamber to contain medicine within the medicine chamber; a plunger member configured to be manually manipulated to insert the stopper member relative to the syringe body; and a needle having proximal and distal ends, the proximal end comprising an anchoring geometry configured to be at least partially inserted into the stopper member such that upon retraction of the stopper member, the needle is pulled proximally along with the stopper to be at least partially contained within the interior medicine chamber.