disposablesyringe made of high polymer polypropylene which has good biocompatibility. itis divided into three parts and two parts.  the  three parts  structure  is composed of plunger, gasket, barrel,injection needle and outer packing. the two is plunger, barrel, injectionneedle and outer packing. medical needles and syringes should  be sterilized through ethylene oxide. asepticand non heat source. syringes are packed in a plastic bag or paper packaging,the packaging must indicate the name of the product, standards, specifications,batch number, production date, whether with a needle, whether sterilized byethylene oxide sterilization, valid date of  sterilization, matters needingattention, manufacturer and its information. qualified products require hightransparency, clear and accurate marking line and  not easy to  fall off  and better sliding performance. the end ofthe cylinder should be designed with an anti shedding structure to prevent  theoperation  from being  too strong to exit the barrel.  the plungershould be designed to have a self destruct structure so that it can be easilytreated  after one time using. asmentioned above, in order to meet the requirements  of production, the production of disposablesyringes must conform to the iso7886 standard and the process needs to be inthe 100 thousand level purification workshop. higher requirements for theproduction environment and the configuration of the machines. needs theguidance from experienced professionals and should use the equipment which aretested a lot in the market. the schematic diagram of the product is shown asfollows:

disposablesyringe made of high polymer polypropylene which has good biocompatibility. itis divided into three parts and two parts.  the  three parts  structure  is composed of plunger, gasket, barrel,injection needle and outer packing. the two is plunger, barrel, injectionneedle and outer packing. medical needles and syringes should  be sterilized through ethylene oxide. asepticand non heat source. syringes are packed in a plastic bag or paper packaging,the packaging must indicate the name of the product, standards, specifications,batch number, production date, whether with a needle, whether sterilized byethylene oxide sterilization, valid date of  sterilization, matters needingattention, manufacturer and its information. qualified products require hightransparency, clear and accurate marking line and  not easy to  fall off  and better sliding performance. the end ofthe cylinder should be designed with an anti shedding structure to prevent  theoperation  from being  too strong to exit the barrel.  the plungershould be designed to have a self destruct structure so that it can be easilytreated  after one time using. asmentioned above, in order to meet the requirements  of production, the production of disposablesyringes must conform to the iso7886 standard and the process needs to be inthe 100 thousand level purification workshop. higher requirements for theproduction environment and the configuration of the machines. needs theguidance from experienced professionals and should use the equipment which aretested a lot in the market. the schematic diagram of the product is shown asfollows: