Syringe assembly

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.

What is claimed is:  
     
         1 . A syringe assembly comprising: 
 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 said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least about 13.5 mm (0.53 inch), said chamber having a distal end defined by a distal wall through which said passageway passes;    a stopper in fluid-tight engagement inside said barrel;    a elongated rigid plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said barrel, a flange at a proximal end of said plunger rod said flange being shaped and positioned to limit the distal motion of said plunger rod in said barrel by contacting said proximal end of said barrel;    a tip cap releasably connected to said tip for sealing said passageway; and injectable liquid in said chamber.    
     
     
         2 . The syringe assembly of  claim 1  wherein the injectable liquid is selected from the group consisting of saline flush solution and heparin lock flush solution.  
     
     
         3 . The syringe assembly of  claim 1  wherein said stopper and said plunger rod are dimensioned so that when said plunger rod flange contacts said proximal end of said barrel there is a space between at least a portion of the distal end of said stopper and said distal wall of said barrel.  
     
     
         4 . The syringe assembly of  claim 1  wherein said plunger rod flange is smaller than said proximal end of barrel at said open proximal end when measured in a direction perpendicular to said longitudinal axis so that said flange does not extend radially beyond said barrel.  
     
     
         5 . The syringe assembly of  claim 1  further including volume measuring indicia on said barrel.  
     
     
         6 . The syringe assembly of  claim 5  wherein said volume measuring indicia indicates the stopper position for a chamber volume of about 3 ml.  
     
     
         7 . The syringe assembly of  claim 1  wherein the length of said stopper and said plunger rod measured from the distal side of said flange to the distal end of said stopper is about 51 mm (2.0 inches) or less.  
     
     
         8 . The syringe assembly of  claim 1  wherein said syringe assembly is contained in a package which provides a tamper evident barrier surrounding the syringe assembly.  
     
     
         9 . The syringe assembly of  claim 1  wherein said syringe assembly is contained in a package which provides a sterile barrier surrounding the syringe assembly.  
     
     
         10 . The syringe assembly of  claim 1  wherein said stopper is made of material selected from the group of natural rubber, synthetic rubber, thermoplastic elastomers and combinations thereof.  
     
     
         11 . The syringe assembly of  claim 1  wherein said tip cap is formed of material selected from the group of thermoplastic material and elastomeric material.  
     
     
         12 . A syringe assembly comprising: 
 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 said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least about 14 mm (0.55 inch), said chamber having a distal end defined by a distal wall through which said passageway passes, the length of said chamber being no more than about 57 mm (2.25 inches);    a stopper in fluid-tight engagement inside said barrel;    an elongated rigid plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said barrel; and    injectable liquid in said chamber.    
     
     
         13 . The syringe assembly of  claim 12  wherein the length of said chamber is no more than about 44.5 mm (1.75 inches).  
     
     
         14 . The syringe assembly of  claim 12  further including a tip cap releasably connected to said tip for sealing said passageway.  
     
     
         15 . The syringe assembly of  claim 12  wherein said chamber contains no more than 3.3 ml of injectable liquid.  
     
     
         16 . The syringe assembly of  claim 12  wherein the injectable liquid is selected from the group consisting of saline flush solution and heparin lock flush solution.  
     
     
         17 . The syringe assembly of  claim 12  further including volume measuring indicia on said barrel.  
     
     
         18 . The syringe assembly of  claim 17  wherein said volume measuring indicia indicates the stopper position for a chamber volume of about 3 ml.  
     
     
         19 . The syringe assembly of  claim 12  wherein said syringe assembly is contained in a package which provides a tamper evident barrier surrounding the syringe assembly.  
     
     
         20 . The syringe assembly of  claim 12  wherein said syringe assembly is contained in a package which provides a sterile barrier surrounding the syringe assembly.  
     
     
         21 . The syringe assembly of  claim 12  wherein said stopper is made of material selected from the group of natural rubber, synthetic rubber, thermoplastic elastomers and combinations thereof.  
     
     
         22 . The syringe assembly of  claim 14  wherein said tip cap is formed of material selected from the group of thermoplastic material and elastomeric material.  
     
     
         23 . A syringe assembly comprising: 
 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 said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least about 13.5 mm (0.53 inch), said chamber having a distal end defined by a distal wall through which said passageway passes, the length of said being no more than about 57 mm (2.25 inches);    a stopper in fluid-tight engagement inside said barrel;    an elongated rigid plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said barrel, a flange at a proximal end of said plunger rod, said flange being shaped and positioned to limit the proximal motion of said plunger rod by contacting said proximal end of said barrel;    a tip cap releasably connected to said tip for sealing said passageway; and    injectable liquid in said chamber.    
     
     
         24 . The syringe assembly of  claim 23  wherein the length of said chamber is no more than 44.5 mm (1.75 inches).  
     
     
         25 . The syringe assembly of  claim 23  wherein said chamber contains no more than 3.3 ml of injectable liquid.  
     
     
         26 . The syringe assembly of  claim 23  wherein the injectable liquid is selcted from the group consisting of saline flush solution and heparin lock flush solution.  
     
     
         27 . The syringe assembly of  claim 23  wherein said syringe assembly is contained in a package which provides a tamper evident barrier surrounding the syringe assembly.  
     
     
         28 . The syringe assembly of  claim 23  wherein said syringe assembly is contained in a package which provides a sterile barrier surrounding the syringe assembly.  
     
     
         29 . A catheter flush kit comprising: 
 a first syringe assembly and a second syringe assembly, each of said syringe assemblies including 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 said distal end having a tip passageway therethrough in fluid communication with said chamber, said chamber having an inside diameter of at least about 13.5 mm (0.53 inch), said chamber having a distal end defined by a distal wall through which said passageway passes; a stopper in fluid-tight engagement inside said barrel; a elongated rigid plunger rod defining a longitudinal axis and extending proximally from said stopper through said open proximal end of said barrel, a flange at a proximal end of said plunger rod; and a tip cap releasably connected to said tip for sealing said passageway;    said first syringe assembly having no more than about 3.3 ml of a first injectable liquid in said chamber;    said second syringe assembly having no more than about 10 ml of a second injectable liquid in said chamber; and    said injectable liquids being selected from the group consisting of saline flush solution and heparin lock solution.    
     
     
         30 . The kit of  claim 29  wherein 
 said syringe assemblies are contained in a package which provides a tamper evident barrier surrounding said syringe assemblies.  
 
     
     
         31 . The kit of  claim 29  wherein said plunger rod flange in at least one of said syringe assembles is shaped and positioned to limit the distal motion of said plunger rod in said barrel by contacting said proximal end of said barrel.