Abstract: The present invention generally provides a device for inserting needles and alleviating the discomfort associated with needle insertion. In certain embodiments, the device is suited for injecting butterfly needles and particularly butterfly needles that are attached to infusion tubing. The patient or caregiver loads a butterfly needle with tubing attached into the base of the drive plunger. The needle with tubing attached is retracted into the housing of the device by retracting the inner plunger. Once retracted, the device is activated and ready to administer a needle into the tissue of a patient. The device is then placed on the location of the skin where injection is desired. The surface that contacts the skin may be textured and may include a contact switch that causes the device to vibrate when slight pressure is applied through contact with the skin.

Abstract: The present invention generally provides a device for inserting needles and alleviating the discomfort associated with needle insertion. In certain embodiments, the device is suited for injecting butterfly needles and particularly butterfly needles that are attached to infusion tubing. The patient or caregiver loads a butterfly needle with tubing attached into the base of the drive plunger. The needle with tubing attached is retracted into the housing of the device by retracting the inner plunger. Once retracted, the device is activated and ready to administer a needle into the tissue of a patient. The device is then placed on the location of the skin where injection is desired. The surface that contacts the skin may be textured and may include a contact switch that causes the device to vibrate when slight pressure is applied through contact with the skin.

Abstract: The present invention generally provides a device for inserting needles and alleviating the discomfort associated with needle insertion. In certain embodiments, the device is suited for injecting butterfly needles and particularly butterfly needles that are attached to infusion tubing. The patient or caregiver loads a butterfly needle with tubing attached into the base of the drive plunger. The needle with tubing attached is retracted into the housing of the device by retracting the inner plunger. Once retracted, the device is activated and ready to administer a needle into the tissue of a patient. The device is then placed on the location of the skin where injection is desired. The surface that contacts the skin may be textured and may include a contact switch that causes the device to vibrate when slight pressure is applied through contact with the skin.

Abstract: The present invention generally provides a device for inserting needles and alleviating the discomfort associated with needle insertion. In certain embodiments, the device is suited for injecting butterfly needles and particularly butterfly needles that are attached to infusion tubing. The patient or caregiver loads a butterfly needle with tubing attached into the base of the drive plunger. The needle with tubing attached is retracted into the housing of the device by retracting the inner plunger. Once retracted, the device is activated and ready to administer a needle into the tissue of a patient. The device is then placed on the location of the skin where injection is desired. The surface that contacts the skin may be textured and may include a contact switch that causes the device to vibrate when slight pressure is applied through contact with the skin.

Abstract: Provided is a system and method for a high flow at low pressure infusion system needle set for delivering a liquid from a reservoir to a patient. More specifically, provided is a high flow at low pressure infusion system needle set including a flexible tubing element having a first length and a first end structured and arranged to connect to the reservoir, and a second end opposite thereto, the flexible tubing element having a first internal diameter. A needle having a second length and a second internal diameter is coupled to the second end of the flexible tubing, the needle having a first portion providing a sharpened distal end for penetration of the patient's tissue and a second portion providing a second end in fluid communication with the second end of the flexible tubing element, the first portion and second portion generally normal to each other.

Abstract: Provided is a precision variable flow rate infusion system and method for delivering a liquid from a reservoir having an initial potential outflow rate to a patient. The system includes at least a first flexible flow rate tubing having a pre-defined flow rate selected at a maximum dosage flow rate for the liquid from the reservoir, the pre-defined flow rate being less than the initial potential outflow rate of the reservoir. Also provided is an adjustable flow rate controller having an inlet and an outlet, at least one internal fluid pathway there between and a fluid pathway modifier structured and arranged to modify the internal fluid pathway from the inlet to the outlet from a closed pathway to a maximum flow pathway with a plurality of different flow rate pathways there between.

Abstract: Provided is a system and method for an anti-foaming needle assembly for avoiding foam generation when extracting a liquid from a vessel having a chamber with a bottom and opposite thereto an opening sealed with a penetrable and re-sealable stopper providing an inner surface above the chamber.

Abstract: Provided is a precision variable flow rate infusion system and method for delivering a liquid from a reservoir having an initial potential outflow rate to a patient. The system includes at least a first flexible flow rate tubing having a pre-defined flow rate selected at a maximum dosage flow rate for the liquid from the reservoir, the pre-defined flow rate being less than the initial potential outflow rate of the reservoir. Also provided is an adjustable flow rate controller having an inlet and an outlet, at least one internal fluid pathway there between and a fluid pathway modifier structured and arranged to modify the internal fluid pathway from the inlet to the outlet from a closed pathway to a maximum flow pathway with a plurality of different flow rate pathways there between.

Abstract: Provided is a system and method for a flared luer connector for medical tubing. More specifically, the flared luer connector includes a tube head adapter formed of a resilient material providing an inlet and opposite thereto an outlet with a longitudinal axis there between. A luer lock fitting is formed proximate to the inlet and structured and arranged to engage a syringe, and at least one flared member disposed between the luer lock fitting and the outlet, the flared member rising from the tube head adapter and angled towards the outlet. The flared member also provides at least one engaging surface between the tube head adapter and a distal edge, the engaging surface acutely angled with respect to the longitudinal axis. The engaging surface is structured and arranged to engage with a corresponding receiving section of a base, the base having a deflector section structured and arranged to deflect a tube head adapter having other than the corresponding flared member.

Abstract: Provided is a system and method for a removable syringe micro pump. The removable syringe micro pump includes a pump housing having a first end and opposite thereto an attaching end, and at least one sidewall there between, the housing having a base proximate to the first end and, the attaching end having an attacher structured and arranged to temporarily engage a syringe. At least one wave spring is nested within the housing and attached proximate to the base. The wave spring having has a compressed first position wherein the wave spring is disposed within the pump housing, and a second extended position wherein, the release of tension extends the spring normally away from the pump housing. The wave spring has a diameter pre-selected to pass within a barrel of the engaged syringe. And engage a plunger seal of the syringe. An associated method of use is also provided.

Abstract: The present disclosure relates to a connector for connecting flow channels, flow regulators and/or reservoirs for directing flow. In some embodiments, the connector is a medical connector for connecting fluid flow controlling elements used in medical applications, particularly in infusion systems, such as tubes, syringes, needles, catheters and fluid reservoirs. The connector reduces the risk of contamination during handling and enhances safety when administering therapeutic solutions into a patient.

Abstract: The present invention generally provides a device for inserting needles and alleviating the discomfort associated with needle insertion. In certain embodiments, the device is suited for injecting butterfly needles and particularly butterfly needles that are attached to infusion tubing. The patient or caregiver loads a butterfly needle with tubing attached into the base of the drive plunger. The needle with tubing attached is retracted into the housing of the device by retracting the inner plunger. Once retracted, the device is activated and ready to administer a needle into the tissue of a patient. The device is then placed on the location of the skin where injection is desired. The surface that contacts the skin may be textured and may include a contact switch that causes the device to vibrate when slight pressure is applied through contact with the skin.

Abstract: Provided is a system and method for a flared luer connector for medical tubing. More specifically, the flared luer connector includes a tube head adapter formed of a resilient material providing an inlet and opposite thereto an outlet with a longitudinal axis there between. A luer lock fitting is formed proximate to the inlet and structured and arranged to engage a syringe, and at least one flared member disposed between the luer lock fitting and the outlet, the flared member rising from the tube head adapter and angled towards the outlet. The flared member also provides at least one engaging surface between the tube head adapter and a distal edge, the engaging surface acutely angled with respect to the longitudinal axis. The engaging surface is structured and arranged to engage with a corresponding receiving section of a base, the base having a deflector section structured and arranged to deflect a tube head adapter having other than the corresponding flared member.

Abstract: Provided is a system and method for a removable syringe micro pump. More specifically, the removable syringe micro pump includes a pump housing having a first end and opposite thereto an attaching end, and at least one sidewall there between, the housing having a base proximate to the first end and, the attaching end having an attacher structured and arranged to temporarily engage a syringe. A volute spring is nested within the housing and attached proximate to the base, the volute spring having a compressed first position wherein coils of the volute spring are concentrically disposed under tension such that an initial height of the volute spring is equivalent to a width of a coil, and an extended second position wherein the release of tension extends the volute spring normally away from the pump housing. The volute spring has a diameter pre-selected to pass within a barrel of the engaged syringe.

Abstract: A compact mechanical pump is provided. The pump is adjustable between a compact form and an expanded form, where the pump can be reduced to a compact form for ease of portability and storage and to the expanded form for use as a pump.

Abstract: Provided is a system and method for a high flow at low pressure infusion system needle set for delivering a liquid from a reservoir to a patient. More specifically, provided is a high flow at low pressure infusion system needle set including a flexible tubing element having a first length and a first end structured and arranged to connect to the reservoir, and a second end opposite thereto, the flexible tubing element having a first internal diameter. A needle having a second length and a second internal diameter is coupled to the second end of the flexible tubing, the needle having a first portion providing a sharpened distal end for penetration of the patient's tissue and a second portion providing a second end in fluid communication with the second end of the flexible tubing element, the first portion and second portion generally normal to each other.

Abstract: Provided is a system and method for an ergonomic needle protector. More specifically, provided is an ergonomic needle protector for a needle having a first curvature. The ergonomic needle protector has a flexible body having a first end and a second end, and an internal channel extending from the first end towards the second end. The flexible body is formed of a resilient material structured and arranged to return to a curved state along the length of the flexible body according to a second curvature different from the first curvature of the needle. The internal channel is structured and arranged to receive the needle when the flexible body is deformed to conform the internal channel to the first curvature and frictionally bind against the needle when the flexible body is released back to the second curvature. An associated method of use is also provided.

Abstract: Provided is a system and method for an anti-foaming needle assembly for avoiding foam generation when extracting a liquid from a vessel having a chamber with a bottom and opposite thereto an opening sealed with a penetrable and re-sealable stopper providing an inner surface above the chamber.

Abstract: Provided is a system and method for an ergonomic needle protector. More specifically, provided is an ergonomic needle protector for a needle having a first curvature. The ergonomic needle protector has a flexible body having a first end and a second end, and an internal channel extending from the first end towards the second end. The flexible body is formed of a resilient material structured and arranged to return to a curved state along the length of the flexible body according to a second curvature different from the first curvature of the needle. The internal channel structured and arranged to receive the needle when the flexible body is deformed to conform the internal channel to the first curvature and frictionally bind against the needle when the flexible body is released back to the second curvature. An associated method of use is also provided.

Abstract: Provided is a system and method for a removable syringe micro pump. More specifically, the removable syringe micro pump includes a pump housing having a first end and opposite thereto an attaching end, and at least one sidewall there between, the housing having a base proximate to the first end and, the attaching end having an attacher structured and arranged to temporarily engage a syringe. At least one wave spring is nested within the housing and attached proximate to the base, the wave spring having a compressed first position wherein the wave spring is compressed under tension such that the initial height of the wave spring is disposed within the pump housing, the wave spring having a second extended position wherein, the release of tension extends the spring normally away from the pump housing. The wave spring has a diameter pre-selected to pass within a barrel of the engaged syringe.