32 results about "Hypodermic needle" patented technology

The present invention relates to a pre-assembled reconstitution and injection device, comprising an injection section having a cartridge for holding a diluent or drug product and a reconstitution section having a vial for holding a drug, whereby the injection section may only be disassembled from the reconstitution section after activation of the device has occurred. In an embodiment for use with a pen needle, the reconstitution section comprises a vial needle hub having a reconstitution needle for piercing both the vial and cartridge. In an embodiment of the invention for use with a hypodermic needle, the injection section comprises a cartridge needle hub with a cartridge needle and male luer connection having threads for securing a hypodermic needle, and the reconstitution section comprises a needle hub with a vial needle and a female luer connection for engagement with the male luer connection.

An apparatus for the automated filling of cartridges of e-vapor devices may include a filling drum configured to receive at least one cartridge of an e-vapor device. The apparatus may additionally include a needle assembly including at least one hypodermic needle. The needle assembly is configured to transition between a lowered state and a raised state. The lowered state is where the hypodermic needle is moved down into the cartridge, while the raised state is where the hypodermic needle is lifted up and away from the cartridge. The apparatus may further include a pump assembly configured to pump a pre-vapor formulation into the cartridge when the needle assembly is in the lowered state. The pump assembly may include a variable amplitude cam system configured to adjust an amount of the pre-vapor formulation for pumping to the cartridge without changing start and stop times for the pumping.

A dosage verification system for use prior to administering an injection of a medicinal fluid drawn into the fluid chamber of a medical syringe, the system comprising a medical syringe having a barrel with an outwardly facing, flat indicia display surface, a plunger having a plunger seal disposed inside and slidably engaging an inwardly facing wall of the barrel and a plunger handle projecting rearwardly from the barrel, and a hypodermic needle projecting forwardly from the barrel, all in combination with an imaging device configured to view and selectively capture, store or transmit a digital image of the plunger position relative to the barrel when a dose of the medicinal fluid is drawn into the fluid chamber of the barrel prior to an injection to verify and provide a record of the dosage drawn, and to alert a user prior to injection when an incorrect dosage is drawn into the fluid chamber of the syringe.

A Hypodermic Needle Safety Guard intended for sharps prevention and safer hypodermic needle use during all stages of an injection process. The Safety Guard may include two symmetrically positioned multi-featured arms that include spring tension, multiple hinges and needle locks. These arms may connect a proximal Luer body and a distal alignment tip thereby enabling the guard to open, close and lock on a needle when manual pressure is applied. The Guard position during hypodermic needle use tends to prevent sharps injury by adjusting the exposure of the Needle tip.

A dosage verification system for use prior to administering an injection of a medicinal fluid drawn into a medical syringe, the system comprising a medical syringe having a barrel with an outwardly facing, flat indicia display surface, plunger having a plunger seal disposed inside and slidably engaging an inwardly facing wall of the barrel and a plunger handle projecting rearwardly from the barrel, and a hypodermic needle projecting forwardly from the barrel, all in combination with an imaging device configured to view and selectively capture, store or transmit a digital image of the plunger position relative to the barrel when a dose of the medicinal fluid is drawn into the fluid chamber of the barrel prior to an injection to verify and provide a record of the dosage drawn, and to alert a user prior to injection when an incorrect dosage is drawn into the fluid chamber of the syringe.

A hypodermic needle may be configured for detection in sonographic imaging of tissue. The needle may comprise a needle tube, a hub, and a collar. The needle tube may comprise an outer surface, a proximate end, and a distal end. The distal end may comprise a needle tip. The hub may comprise a hub bore proximate to a center of the hub. The hub may be in fixed connection to the outer surface of the needle tube at least proximate to the hub bore. The collar may comprise a collar bore proximate to a center of the collar. The collar may be in fixed connection to the outer surface of the needle at least proximate to the collar bore. The collar may be configured to decrease damping of a radiated wave propagated by the needle tip in response to sonographic energy excitation into the tissue.

The invention provides a method and device for testing the vibration performance of a super-emulsion needle, and relates to the technical field of detection equipment of medical instruments.The method for testing the vibration performance of the super-emulsion needle comprises the steps that S1, the tip of the vibrating super-emulsion needle is irradiated with laser, part of the laser is shielded by the tip of the vibrating super-emulsion needle, and part of the laser is not shielded; s2, acquiring the shielding condition of the laser by the tip of the super-emulsion needle; and S3, obtaining the vibration performance of the tip of the super milk needle according to the shielding condition.

Medical devices including an integrated dressing pad assembly. A medical device comprises a hypodermic needle having a distal tip configured to be inserted into a patient at an insertion location and a proximal end attached to a needle hub. An integrated dressing pad assembly is mounted to and positioned with respect the medical device or packaging so that the integrated dressing pad assembly is configured to be slidably engaged along the length of the hypodermic needle and applied to a patient at the insertion location when the medical device is used and the hypodermic needle is removed from the patient.

An assembly of an injector (5) for administering a liquid to a human by injection and a supply holder (4) for one or more of said injectors (5), wherein the supply holder (4) is provided with one or more compartments (12) for containing a said injector (5), wherein the injector (5) is located in a first orientation in a said compartment (12), wherein the first orientation is horizontal or deviates from horizontal by at most 45°, wherein the injector (5) comprises an hypodermic needle (13), wherein the injector (5) is rotatable relative to the supply holder (4) about an horizontal geometric axis of rotation (35) from the first orientation to a second orientation, wherein the second orientation is vertical or deviates from vertical by at most 20°, and wherein the hypodermic needle (13) is located at the bottom of the injector (5) in the second orientation.

Provided herein is a method for modifying the surface texturing of hypodermic needles. The method comprises placing one or more hypodermic needles on a support tool, each of which comprises a cylindrical needle body having a terminal end and a proximal end and defining a lumen inside. The method also comprises directing a laser from one or more laser sources onto the outer surface of each needle body of the one or more hypodermic needles. The laser forms a pattern of depressions on the outer surface of each needle body of the one or more hypodermic needles, thereby forming a textured outer surface on the one or more hypodermic needles.

Disclosed is a suture delivery device for endoscopically passing a suture into biological tissue. The device can include two hypodermic needles that can be manipulated via controls on a handle of the device in order to pass a suture from one needle to the other. For example, the device can include a first needle coupled to at least one loop member that, when deployed from the first needle, provides a target through which a second needle of the device can deliver the suture. Once the second needle intersects the loop member, the user can advance a length of suture out through a distal end of the second needle. The loop member can then be retracted into the first needle, thereby grabbing and securing the suture in the process.

The hypodermic needle is described as having a proximal end, a distal end having a tissue-piercing tip, and a lumen extending from the proximal end to the distal end. The elongate body may have a channel formed in its outer surface. The channel may be concave or formed in the outer wall. The portion having the channel may maintain a circular lumen, or the lumen may be non-circular or conform to the shape of the channel. Additionally, the elongate body may have a flattened portion along its length. The flattened portion may be at the distal-most portion of the elongate body extending proximally from the distal tip. The elongate body may also include a notch formed in the outer wall to communicate with the lumen or open to the lumen. The opening of the notch may traverse the lumen or be aligned with the lumen.

A low-profile universal passive protector for an IV catheter includes a connector having a tubular body and a pair of arms pivotally connected thereto. The tubular body defines an end face and the connector includes a cavity extending from the end face. An elongate sheath is snap engageable to the tubular body. A spring is insertable within the connector cavity to extend between at least one of the pair of arms and the elongate sheath when received within the cavity. A slider is moveably coupled to the sheath. The slider includes a flashback chamber formed therein. A hypodermic needle is connected to the slider and is in fluid communication with the flashback chamber. The slider is moveable along the sheath between a first position and a second position, with the hypodermic needle being drawn into the sheath as the slider moves from the first position toward the second position.

Peritoneal dialysis is delivered via implementation of the total implantable system disclosed. The system is composed of several components. The extended surface area port, equipped with an internal support pillar, is implanted beneath the subcutaneous tissue. The catheter portion is tunneled under the subcutaneous tissue until it reaches the abdomen where it enters the peritoneal cavity. The distal / terminating end of the catheter resides in the peritoneal cavity and is designed with an inner perforated distal catheter, circumferentially enclosed by an outer perforated sheath, creating an anti-occlusion technology system. The distal end of the sheath is designed with an anti-clog tip. Port and system access is achieved via hypodermic needle. Dialysis solution is infused and evacuated via the same modalities.

Extractors and methods of extracting a medication from another medical device, such as an insulin pen. The extractor includes a syringe, a first cap having an open end adapted to be coupled to the syringe, a hypodermic needle protruding from a closed end of the first cap, and a second cap coupled at a closed end thereof to the first cap by the hypodermic needle, which extends through the closed end of the second cap and protrudes into an internal cavity of the second cap such that an internal cavity of the first cap fluidically communicates with the internal cavity of the second cap through the hypodermic needle. An open end of the second cap can be coupled to the medical device so that the internal cavity of the second cap fluidically communicates with the medical device through the hypodermic needle.

A multi-beveled needle point geometry for hypodermic needles such as pen needles. A proximal bevel is formed at a first angle of inclination, a pair of intermediate bevels at a second angle of inclination, and a pair of distal bevels at a third angle of inclination and differing angles of rotation. The second angle of inclination is substantially different than the first angle of inclination to define a marked apex at the intersections between the proximal bevel and the intermediate bevels. At least one smooth transition is typically provided between adjacent bevels, between a bevel and an outer surface of the needle, and / or between a bevel and the lumen of the needle.

The present disclosure provides a method of performing an image guided carpal tunnel release procedure. The method includes directing fluid through a hypodermic needle toward a median nerve of a patient to move the median nerve away from a deep surface of a transverse carpal ligament (TCL) of the patient. The method further includes dissecting the TCL with the hypodermic needle by sliding a cutting edge associated with the hypodermic needle along the TCL.

In the field of medical sharps, particularly subcutaneous injection needles, there is a need for improved needle assemblies. A needle assembly (10;80;100;110;120;130) for engaging with a syringe (58;90) having an elongated hollow syringe body (56) in which a plunger (34;88) is slidably received comprises a needle assembly body (12) having a subcutaneous injection needle (14) coupled to the needle assembly body (12) and extending from the distal end (16) of the needle assembly body (12). The needle assembly (10;80;100;110;120;130) also includes an actuator valve (18;132) movably received within the needle assembly body (12) and formed to define a propellant storage space (22;122). The actuator valve (18;132) is movable between a closed position in which the propellant is held under pressure in the propellant storage space (22;122) and an open position in which the propellant is released from the propellant storage space (22;122) and causes the needle (14) to shroud.

A hypodermic needle having a proximal end, a distal end having a tissue penetrating tip, and a lumen extending from the proximal end to the distal end is described herein. The elongate body may have a channel formed in the outer surface. The channel may be concave or formed in the outer wall. The portion with the channel may retain a circular lumen, or the lumen may be non-circular or conform to the shape of the channel. In addition, the elongated body may be a flat segment along the length of the elongated body. The flat segment may be at a distal-most portion of the elongate body extending proximally from the distal tip. The elongate body may also include a notch formed in the outer wall to provide communication with or open to the lumen. The notch opening may be transverse to or aligned with the lumen.

A die press apparatus and method of operating to fabricate vascular access needles having one or more complex shapes at different locations at or adjacent to or proximal to a tissue penetrating tip along with features along one or more positioned spaced along the body of the needle. In some specific needle configurations, the features are specifically positioned and shaped to cooperate with an article used with the needle such as a handle, catheter, guide element, valve, seal or other component of a vascular access system.

In the field of methods and apparatus for administering drugs, there is a demand for improved closed-loop transfer devices. A closed-loop transfer device (10) comprises a syringe (12) having an elongated hollow syringe body (14), in which a plunger (16) is slidably housed, defining a drug chamber (18) whose size changes depending on the degree of insertion of the plunger (16) within the syringe body (18). The closed-loop transfer device (10) also comprises a needle assembly (28;300) having a needle assembly body (30), to which a subcutaneous injection needle (32) is fixedly attached. The needle assembly body (30) is coupled to the syringe body (14) and maintains fluid communication between the internal conduit (40) of the subcutaneous injection needle (32) and the drug chamber (18). In addition, the closed-loop transfer device (10) also comprises a shield assembly (42) having a shield body (44). The shield body (44) is movably coupled to the syringe body (14), thereby allowing the shield assembly (14) to selectively operate to surround the needle (32). The shield body (44) and the syringe body (14) are provided with mutually cooperative forming parts for restricting the movement of the shield assembly (42) relative to the syringe (12) through a series of positions (200, 210, 220, 230, 240, 250, 260) corresponding to different operating states of the device (10).

A low-profile universal passive protector for an IV catheter includes a connector having a tubular body and a pair of arms pivotally connected thereto. The tubular body defines an end face and the connector includes a cavity extending from the end face. An elongate sheath is snap engageable to the tubular body. A spring is insertable within the connector cavity to extend between at least one of the pair of arms and the elongate sheath when received within the cavity. A slider is moveably coupled to the sheath. The slider includes a flashback chamber formed therein. A hypodermic needle is connected to the slider and is in fluid communication with the flashback chamber. The slider is moveable along the sheath between a first position and a second position, with the hypodermic needle being drawn into the sheath as the slider moves from the first position toward the second position.

A needle assembly 80 for engagement with a syringe having an elongate hollow syringe 90 body within which a plunger 88 is slidably received, comprises a needle assembly body 12 with a hypodermic needl

In the field of medical sharp instruments, particularly in the field of subcutaneous injection needles, an improved needle assembly is needed. A needle assembly (10, 80, 100, 110, 120, 130) for engagement with a syringe (58, 90) having an elongate hollow syringe body (56) within which a plunger (34, 88) is slidably received includes a needle assembly body (12) having a hypodermic needle (14) coupled with the needle assembly body to extend from a distal end (16) of the needle assembly body. The needle assembly (10, 80, 100, 110, 120, 130) also includes an actuator valve (18, 132) movably received within the needle assembly body (12) and formed to define a propellant storage volume (22, 122). The actuator valve (18, 132) is movable between a closed position, in which propellant is held under pressure in the propellant storage volume (22, 122), and an open position, in which propellant is released from the propellant storage volume to shield the needle (14).

A Hypodermic Needle Safety Guard intended for sharps prevention and safer hypodermic needle use during all stages of an injection process. The Safety Guard may include two symmetrically positioned multi-featured arms that include spring tension, multiple hinges and needle locks. These arms may connect a proximal Luer body and a distal alignment tip thereby enabling the guard to open, close and lock on a needle when manual pressure is applied. The Guard position during hypodermic needle use tends to prevent sharps injury by adjusting the exposure of the Needle tip.

A multi-beveled needle point geometry for hypodermic needles such as pen needles. A proximal bevel is formed at a first angle of inclination, a pair of intermediate bevels at a second angle of inclination, and a pair of distal bevels at a third angle of inclination and differing angles of rotation. The second angle of inclination is substantially different than the first angle of inclination to define a marked apex at the intersections between the proximal bevel and the intermediate bevels. At least one smooth transition is typically provided between adjacent bevels, between a bevel and an outer surface of the needle, and / or between a bevel and the lumen of the needle.

In the field of drug delivery methods and devices, improved closed system transfer devices are required. A closed system transfer device (10) includes a syringe (12) having an elongate hollow syringe body (14) within which a plunger (16) is slidably received to define medicament chambers (18) of different sizes depending on the extent of insertion of the plunger within the syringe body (18). The closed system transfer device (10) also includes a needle assembly (28; 300) having a needle assembly body (30) to which the hypodermic needle (32) is securely secured. The needle assembly body (30) is coupled with the syringe body (14) to maintain an internal conduit (40) of the hypodermic needle (32) in fluid communication with the drug chamber (18). In addition, the closure system transfer device (10) also includes a shroud assembly (42) having a shroud body (44). The shroud body (44) is movably coupled with the syringe body (14), whereby the shroud assembly (14) is selectively operable to enclose the needle (32). The shroud body (44) and the syringe body (14) include mutually cooperating formations to constrain movement of the shroud assembly (42) relative to the syringe (12) through a series of positions (200, 210, 220, 230, 240, 250, 260) corresponding to different operating conditions of the device (10).

An apparatus for the automated filling of cartridges of e-vapor devices may include a filling drum configured to receive at least one cartridge of an e-vapor device. The apparatus may additionally include a needle assembly including at least one hypodermic needle. The needle assembly is configured to transition between a lowered state and a raised state. The lowered state is where the hypodermic needle is moved down into the cartridge, while the raised state is where the hypodermic needle is lifted up and away from the cartridge. The apparatus may further include a pump assembly configured to pump a pre-vapor formulation into the cartridge when the needle assembly is in the lowered state. The pump assembly may include a variable amplitude cam system configured to adjust an amount of the pre-vapor formulation for pumping to the cartridge without changing start and stop times for the pumping.

The present disclosure provides a method of performing an image guided carpal tunnel release procedure. The method includes directing fluid through a hypodermic needle toward a median nerve of a patient to move the median nerve away from a deep surface of a transverse carpal ligament (TCL) of the patient. The method further includes dissecting the TCL with the hypodermic needle by sliding a cutting edge associated with the hypodermic needle along the TCL.