Prefilled medical injection device

Abstract

A prefilled medical injection device with production specific elements is provided as a single use disposable injection device that is optimally suited for mass production through the Blow Fill Seal manufacturing process. The device utilizes a valve and a needle assembly fused to an insert. The valve and the needle assembly are positioned within the insert forming a conduit. The needle assembly is covered with a needle cap that is detachably coupled to protecting the needle assembly from contamination and a user from accidental needle stick. The insert is engaged to the bellows during the BFS manufacturing process and hermetically sealed by a paris on layer that covers exterior portion of the insert and the needle cap. The parison layer is formed and trimmed creating exterior features that facilitate the use of the prefilled medical injection.

We claim: 
     
         1 . An integrated injection device with pre-packaged medication, comprising:
 a compressible, hermetically-sealed medication compartment at least partially filled with the pre-packaged medication;   a needle;   a pressure-actuated valve in selectable fluid communication between the compartment and the needle wherein, upon compression of the compartment, the pre-packaged medication is caused to flow from the compartment, through the valve, and then through the needle, and wherein the valve resists a backflow of any fluid from the needle back into the compartment;   a body that retains and aligns the compartment, the valve and the needle, thereby ensuring that they are in selectable fluid communication; and   a web package at least partially encapsulating the injection device, wherein upon opening the web package, at least a tip of the needle is exposed.   
     
     
         2 . The integrated injection device of  claim 1 , wherein the body is asymmetrically balanced. 
     
     
         3 . The integrated injection device of  claim 1 , wherein the body comprises an insert fluid channel to account for variation in diameter between the valve and the needle. 
     
     
         4 . The integrated injection device of  claim 1 , wherein the web package is frangible, and upon breaking the web package, at least a tip of the needle is exposed. 
     
     
         5 . The integrated injection device of  claim 1 , wherein the device is manufactured using a blow-fill-seal manufacturing process. 
     
     
         6 . The integrated injection device of  claim 1 , wherein the compartment comprises a translucent low-density polyethylene. 
     
     
         7 . The integrated injection device of  claim 1 , wherein the compartment is at least partially filled with an inert gas in addition to the medication, and the inert gas facilitates removal of the medication from the compartment upon compression of the compartment. 
     
     
         8 . The integrated injection device of  claim 1 , wherein the needle comprises either an integrated or Luer-lok threaded needle. 
     
     
         9 . The integrated injection device of  claim 1 , wherein the medication is inserted either into a patient or into an intravenous fluid bag. 
     
     
         10 . A process for forming an integrated injection device with pre-packaged medication, comprising the steps of:
 forming a hot, tubular-shaped prison into a mold having at least a first compartment;   at least partially filling the at least first compartment with a dose of the medication; and   positioning a premade insert assembly within the mold in order to engage the at least first compartment.   
     
     
         11 . The process of  claim 10 , thereby providing an integrated injection device with pre-packaged medication having:
 a compressible, hermetically-sealed medication compartment at least partially filled with the pre-packaged medication;   a needle;   a pressure-actuated valve in selectable fluid communication between the compartment and the needle wherein, upon compression of the compartment, the pre-packaged medication is caused to flow from the compartment, through the valve, and then through the needle, and wherein the valve resists a backflow of any fluid from the needle back into the compartment; and   a body that retains and aligns the compartment, the valve and the needle, thereby ensuring that they are in selectable fluid communication.   
     
     
         12 . The process of  claim 11 , wherein the device also includes a web package at least partially encapsulating the injection device, wherein upon opening the web package, at least a tip of the needle is exposed. 
     
     
         13 . The process of  claim 10 , further comprising the step, after the positioning step, of hermetically sealing a coupling between the insert assembly and the at least first compartment. 
     
     
         14 . The process of  claim 10 , further comprising the step of shaping the mold to conform to an exterior of the insert assembly. 
     
     
         15 . The process of  claim 10 , wherein the premade insert assembly comprises at least a valve and a needle. 
     
     
         10 . process of  claim 10 , wherein each of the steps occurs continuously, substantially without human intervention, in a sterile, enclosed area inside a machine. 
     
     
         17 . The process of  claim 10 , wherein following the introduction of the premade insert assembly into the mold, a frangible web at least partially encapsulates the injection device. 
     
     
         18 . The process of  claim 10 , wherein an electronic fill system is utilized to deliver a precise dose of the medication into the at least first compartment.