Abstract: A syringe assembly comprises a syringe barrel having an elongated body defining a chamber for retaining fluid, an open proximal end, a distal end and a frusto-conically shaped tip extending from the distal end and having a passageway therethrough in fluid communication with the chamber. The chamber has an inside diameter of at least 13.5 mm. A stopper is in fluid-tight engagement inside the barrel. An elongated plunger rod extends proximally from the stopper through the open proximal end of the barrel. A flange is positioned at the proximal end of the plunger rod. The flange is shaped and positioned to limit the distal motion of the plunger rod in the barrel by contacting the proximal end of the barrel. A tip cap is releasably connected to the tip for sealing the passageway and the chamber contains injectable liquid.

Abstract: A syringe and detachable needle assembly having binary attachment features include an elongate syringe barrel having a longitudinal axis, an open proximal end and an open distal end including a collar. The collar includes the cylindrically shaped sidewall having an inside surface and an outside surface. A needle assembly includes the hub having a body portion including a proximal end, a distal end and a conduit therethrough. A cannula having a distal end, a proximal end and a lumen therethrough is attached to the distal end of the hub so that the lumen is in fluid communication with the chamber. A lug is provided on one of the collar and the hub and a ramp and a rest surface is provided on the other of the collar and the hub. The ramp is oriented at an acute angle with respect to longitudinal axis for guiding the lug during needle assembly attachment, to the rest surface forcing the hub to contact the barrel to form a seal the hub and the barrel.

Abstract: A luer connector assembly is provided for enhancing the frictional engagement between medical devices such as syringes and needle assemblies. The assembly needle includes a female luer fitting having a passageway and a relatively soft, resilient member bounding the passageway. The passageway is also bounded by the body of the fitting, which is harder than the soft, resilient member. A male luer fitting inserted into the passageway engages both the soft, resilient member and the body of the female luer fitting. A method of manufacturing such a connector assembly is further provided. A first material is injected into a mold to form the body of a female luer fitting, the fitting including a passageway and a recess extending into the body. A second material is then injected such that it extends into the recess and bounds the passageway. The second material, when cool, is softer than the first material.

Abstract: An adapter for a multiple capacity needle immobilizing device having a body portion and entry holes for allowing the distal ends of sharp needles to enter the body includes a base having a top portion and a bottom portion. The bottom portion having apertures positioned to align with the entry holes of the immobilizing device. A non-circular funnel projects upwardly from each of the entry holes to a funnel opening in the top portion of the adapter. The funnel opening is larger when measured perpendicularly to a line extending through the apertures of the adapter than when measured along this line. Structure is provided for connecting the adapter to the needle immobilizing device.

Abstract: A syringe assembly having passive disabling structure includes a barrel and a plunger rod assembly. The plunger rod assembly includes a plunger rod and a stopper connected by an indexing locking element. The number of strokes of the syringe plunger before the stopper is locked into the barrel rendering the syringe assembly unusable is determined by the number of detents on the plunger rod and stopper which engage the locking mechanism. Upon completion of the final delivery stroke, any attempt to withdraw the plunger rod from the barrel will cause the locking element to engage the barrel and trap the stopper in the barrel preventing further use of the syringe.

Abstract: A syringe assembly having passive disabling structure includes a barrel and a plunger rod assembly. The plunger rod assembly includes a plunger rod and a stopper connected by an indexing locking element. The number of strokes of the syringe plunger before the stopper is locked into the barrel rendering the syringe assembly unusable is determined by the number of detents on the plunger rod and stopper which engage the locking mechanism. Upon completion of the final delivery stroke, any attempt to withdraw the plunger rod from the barrel will cause the locking element to engage the barrel and trap the stopper in the barrel preventing further use of the syringe.

Abstract: An I.V. flush syringe assembly includes a barrel having an inside surface defining a chamber for retaining fluid, an open proximal end and a distal end including a distal wall with an elongate tip extending distally therefrom having a passageway therethrough in fluid communication with the chamber. A plunger having an elongate body portion and a stopper slidably positioned in fluid-tight engagement with the inside surface of the barrel is provided. Anti-reflux structure in said barrel is provided for controlling stopper deflection when fluid has been delivered from the chamber and the stopper is in contact with structure on the distal wall.

Abstract: A sharps disposable container (10) comprises a base (12) having a bottom wall (23) and a sidewall extending upwardly therefrom defining a receptacle. A top having an aperture (42) therethrough is connected to an upper portion (16) of the sidewall. A closure (48) is hingedly connected to the top and capable of moving from an open position which allows access to the aperture and a closed position wherein the closure releasably engages the top. A gripping tab (54) is hingedly connected to the closure and projects upwardly from the closure when the closure is in the closed position and releasably engages the top. The closure can be permanently locked to the top by pivoting the gripping tab in a downwardly position and moving the closure to the closed position.

Abstract: A syringe assembly having passive disabling structure includes a barrel and a plunger rod assembly. The plunger rod assembly includes a plunger rod and a stopper connected by an indexing locking element. The number of strokes of the syringe plunger before the stopper is locked into the barrel rendering the syringe assembly unusable is determined by the number of detents on the plunger rod and stopper which engage the locking mechanism. Upon completion of the final delivery stroke, any attempt to withdraw the plunger rod from the barrel will cause the locking element to engage the barrel and trap the stopper in the barrel preventing further use of the syringe.

Abstract: A syringe assembly having passive disabling structure includes a barrel and a plunger rod assembly. The plunger rod assembly includes a plunger rod and a stopper connected by an indexing locking element. The number of strokes of the syringe plunger before the stopper is locked into the barrel rendering the syringe assembly unusable is determined by the number of detents on the plunger rod and stopper which engage the locking mechanism. Upon completion of the final delivery stroke, any attempt to withdraw the plunger rod from the barrel will cause the locking element to engage the barrel and trap the stopper in the barrel preventing further use of the syringe.

Abstract: A single use syringe assembly includes a barrel having a chamber for retaining fluid, an open proximal end and a distal end including an elongate tip extending distally therefrom having a passageway therethrough in fluid communication with the chamber. A needle cannula having a lumen therethrough is connected to the elongate tip so that the lumen is in fluid communication with the passageway. An elongate needle shield having a longitudinal opening therein is hingedly connected to the barrel. A needle shield is capable of pivoting from an open position or a closed needle protecting position. The plunger including an elongate body portion and a stopper is slidably positioned in fluid-tight engagement with the inside surface of the barrel. Structure is provided for locking the plunger in the barrel by applying distally directed force to the plunger after fluid has been delivered from the chamber.

Abstract: An I.V. flush syringe assembly includes a barrel having an inside surface defining a chamber for retaining fluid, an open proximal end and a distal end including a distal wall with an elongate tip extending distally therefrom having a passageway therethrough in fluid communication with the chamber. A plunger having an elongate body portion and a stopper slidably positioned in fluid-tight engagement with the inside surface of the barrel is provided. Anti-reflux structure for controlling stopper deflection when fluid has been delivered from the chamber and the stopper is in contact with the distal wall is provided.

Abstract: A syringe assembly having passive disabling structure includes a barrel and a plunger rod assembly. The plunger rod assembly includes a plunger rod and a stopper connected by an indexing locking element. The number of strokes of the syringe plunger before the stopper is locked into the barrel rendering the syringe assembly unusable is determined by the number of detents on the plunger rod and stopper which engage the locking mechanism. Upon completion of the final delivery stroke, any attempt to withdraw the plunger rod from the barrel will cause the locking element to engage the barrel and trap the stopper in the barrel preventing further use of the syringe.

Abstract: A needle shield assembly and method of manufacturing a needle shield are provided. The needle shield assembly includes a needle hub having a needle cannula extending therefrom. A needle shield base is pivotably coupled to the needle hub. A locking assembly including a needle engagement member is coupled to the needle shield base. One or both of the needle shield base and the locking assembly include a cavity for receiving the needle cannula. The needle shield is manufactured by providing a needle shield base and a separate locking assembly including a needle engagement member, and connecting the locking assembly to the distal end portion of the needle shield base.

Abstract: A medical device for use with a fluid transfer device having a frusto-conically-shaped tip includes a hub having an open proximal end with a frusto-conically-shaped cavity therein, a distal end and a passageway therethrough. The cavity is part of the passageway. A release element in the passageway of the hub is positioned to block fluid-tight engagement of the frusto-conically-shaped tip with the cavity of the hub. Structure is provided to release at least part of the release element, upon application of a proximally directed force on the hub, to allow the abrupt fluid-tight engagement of the tip and the cavity in the hub.

Abstract: The present invention is directed to a medical transport carrier, as well as a medical waste disposal container. The medical transport carrier includes a carrier tray and a medical waste disposal container. The carrier tray includes a supply area adapted for containing medical supplies. The medical waste disposal container is interengagably and removably mated with the carrier tray and is located at a location remote from the supply area. The present invention is also directed to a medical waste disposal container adapted for engaging with a carrier tray having a supply area for containing medical supplies. The medical waste disposal container is interengagably and removably matable with the carrier tray and is adapted for containing medical waste at a location remote from the supply area of the carrier tray.

Abstract: A medical device having a releasable retaining includes needle cannula connected to a hub having an open proximal end with a frusto-conically shaped cavity therein. The cavity is part of a passageway through the hub which is in fluid communication with the lumen of the needle cannula. A retaining element is releasably connected to the hub. The hub includes an aperture and at least one protuberance projecting into the aperture for engaging the frusto-conically shaped tip of a fluid delivery device. The protuberance is shaped to offer less resistance to hub movement in a direction of engagement than in a direction of disengagement with the tip. The retaining element is connected to the hub so that when the hub is engaged to the tip, the force required to disengage the retaining element from the tip is greater than the force required to disengage the retaining element from the hub.