JP4013248B2 - Mixed injection tool - Google Patents

Mixed injection tool Download PDF

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Publication number
JP4013248B2
JP4013248B2 JP2002153511A JP2002153511A JP4013248B2 JP 4013248 B2 JP4013248 B2 JP 4013248B2 JP 2002153511 A JP2002153511 A JP 2002153511A JP 2002153511 A JP2002153511 A JP 2002153511A JP 4013248 B2 JP4013248 B2 JP 4013248B2
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Japan
Prior art keywords
mixed injection
syringe
rubber plug
injection device
mixed
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Expired - Fee Related
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JP2002153511A
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Japanese (ja)
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JP2003339876A (en
Inventor
信雄 高木
徳寛 比恵島
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Nipro Corp
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Nipro Corp
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Description

【0001】
【発明が属する技術分野】
本発明は、シリンジ内の薬液を輸液セットや輸血セットの混注口より導入する混注操作を行う際に、該操作を安全かつ衛生的に行うために用いられる混注具に関する。
【0002】
【従来の技術】
輸液や輸血を行う場合に、予めセットされた液に、他の薬液を混注する操作が一般に行われる。この混注操作は、通常、輸液セットや輸血セットに予め設けられた混注口より行われる。一般的な混注口は、液が収容された容器の開口部に、ゴム栓が液密に装着されてなるものである。一般的な混注操作は、混注したい薬液を収容したシリンジの先に注射針を接続し、該針でゴム栓を穿刺することにより、シリンジ内部と輸液セットや輸血セットの内部を連通させ、次いでシリンジ内の薬液を注入することにより行われる。
混注する薬液が無菌状態のものでない場合、混注は除菌フィルターを介して行われることがある。該除菌フィルターは、混注操作時にシリンジの先端に接続され、さらに該フィルターを介して注射針を接続して使用される。
【0003】
しかしながら、このような従来の混注操作においては、混注操作を行う医療従事者が注射針の誤穿刺を起こすおそれがあるだけでなく、混注操作中、シリンジが不安定であるため操作自体が困難であった。また、混注操作終了後、シリンジを混注口から取り外すと、ゴム栓に残された穿刺孔から内部の液が外部へ漏れ出したり、外部の菌が内部へ侵入したりするおそれがあり、輸液または輸血処置中、シリンジを混注口に接続したままの状態で保持しておかなければならなかった。
【0004】
【発明が解決しようとする課題】
上記事情に鑑み、本発明は注射針を使用せずに、混注操作中の液漏れや菌混入のおそれがなく、シリンジの取り外しが可能となる混注具を提供することを目的とする。
【0005】
【課題を解決するための手段】
本発明者らは、上記課題を解決するために種々鋭意検討した結果、除菌フィルターと逆止弁を内部に有し、先端に鋭利な刃先を有する混注具をシリンジ先端に接続して混注口への穿刺を行うことにより、上記課題を解決しうるのみならず、さらに複数回の混注操作が可能となる混注具を提供できることを見出した。
【0006】
すなわち、本発明は、内部に連通路を有してなる本体と、該連通路を遮断するように設けられた除菌フィルターおよび逆止弁を有してなり、該本体は一端にシリンジ接続部を有し、他端にゴム栓穿刺部を有し、該シリンジ接続部には前記連通路と連通する液流入口が設けられてなり、該ゴム栓穿刺部には前記連通路と連通する液流出口が設けられてなる混注具である。
【0007】
【作用】
本発明の混注具は、先端に鋭利な刃先を有しているためシリンジに注射針を接続する必要がないだけでなく、該混注具のみを予め混注口に穿刺しておくことも可能であるため、医療従事者の誤穿刺のおそれが大幅に低減される。
また、該混注具は、本体内部の連通路に除菌フィルターと逆止弁とを有しているため、混注薬液注入後にシリンジを取り外しても、液漏れや菌の侵入がおこるおそれがない。
さらに、該混注具は複数回の使用が可能であるため、薬液の追加注入や、他の薬液の混注操作などを行うことも可能である。
【0008】
【発明の実施の形態】
以下に、本発明の混注具を添付図面に示す好適な実施例に基づいて詳細に説明するが、本発明はこれらの説明に限定されるものではない。
図1は本発明の混注具の一実施例を示す断面図であり、図2は本発明の混注具の他の実施例を示す断面図である。また、図3は図2に示す混注具の使用例の説明図である。図1および図2に示されるように、本発明の混注具1は本体2、除菌フィルター3および逆止弁4を有してなる。
【0009】
本発明の混注具1の本体2は、一端にシリンジの先端を直接接続しうるシリンジ接続部21を有し、多端に輸液セットや輸血セットなどの混注口のゴム栓に穿刺することが可能なゴム栓穿刺部22を有している。
該シリンジ接続部21は、混注しようとする薬液を収容したシリンジ先端が挿入されたときに、シリンジと混注具1とが容易に外れることがないように、シリンジ先端と嵌合しうる形状および大きさの内腔を有する。したがって、該内腔は、本体内部に向かってその内径が徐々に減少しうるテーパー状であることが好ましい。また、ロック機構付きのシリンジを接続して使用する場合においては、該シリンジ接続部21はロック付きメスルアー形状とするなど、シリンジ先端との係合手段を設けてもよい。
また、ゴム栓穿刺部22は、混注具1を輸液セットや輸血セットなどの混注口のゴム栓に穿刺しうる鋭利な刃先と、ゴム栓を貫通するために十分な長さの全長を有してなる。該刃先の形状は、ゴム栓を穿刺しうるものであれば特に限定されないが、穿刺抵抗がより低いものであることが好ましく、注射針の先端形状と同じものが好ましく用いられる。該ゴム栓穿刺部22は、混注する薬液の導入を速やかに行いうる内径を有し、ゴム栓への穿刺抵抗を低減させうる外径を有し、ゴム栓への穿刺時に折れたり捲れたりするおそれのない厚みを有する必要がある。そこで、ゴム栓穿刺部22のこれらの寸法は、薬液の種類や量、ゴム栓の材質により、適宜変更されうる。
【0010】
本発明の混注具1がゴム栓に穿刺されたときに、ゴム栓の内側と外側とを連通しうるように、本体2の内部には連通路23が設けられている。前記シリンジ接続部21には液流入口211が設けられ、前記ゴム栓穿刺部22には液流出口221が設けられており、該連通路23は該液流入口211及び液流出口221を両端とするように本体2に設けられている。したがって、本発明の混注具1の使用時、シリンジ内の薬液は、液流入口211より連通路23内に流入し、ゴム栓部分を通過して液流出口221から流出することにより、混注操作が行われる。
【0011】
前記液流入口211は、シリンジ接続部21に接続されたシリンジ先端より、シリンジ内の薬液が注入されたとき、該薬液を漏らすことなく連通路23内に導入させるものである。したがって、該液流入口211はシリンジ接続部21の内腔と連通していることが好ましく、該内腔の本体内部側の端に設けられることが、薬液が漏れるおそれが少なくより好ましい。
前記液流出口221は、混注具1がゴム栓に穿刺された状態の時に、連通路23内に導入された薬液をゴム栓の向こう側に導入させるものである。すなわち、該液流出口221はゴム栓穿刺部22のうち、ゴム栓を貫通してゴム栓の向こう側に突出した部分に設けられる。したがって、該液流出口221はゴム栓穿刺部22の先端部に設けられることが好ましい。該液流出口221の具体例としては、図1に示されるように、ゴム栓穿刺部22先端に設けられた、先端に向かって開口する孔である。また液流出口221の他の具体例としては、図2に示されるように、ゴム栓穿刺部22先端の側面に設けられた孔である。
【0012】
なお、混注具1が上述したようにシリンジ内の薬液を混注しうる位置に確実に配置されるように、本体2のゴム栓穿刺部22の基端側にフランジ部24が設けられていることが好ましい。この構造によれば、混注具1は、該フランジ部24が混注口に当接するまで穿刺されることで、液流出口221がゴム栓を貫通してゴム栓の向こう側に配置されるため、混注操作に適切な挿入位置を、混注具1を穿刺しながら確認する必要がない。
また、該混注具1には、いったんシリンジ内の薬液を混注しうる位置に確実に配置された後、容易にゴム栓から脱落しないように、該混注具1を保持するロック手段が設けられていてもよい。該ロック手段としては、例えば図1および図2に示されるように、ゴム栓穿刺部22の鋭利な先端側に向かって径が減少する、テーパー状の突出部25があげられる。該ロック手段が設けられることにより、混注具1はシリンジが接続された状態での混注操作時に誤って混注口から脱落することを防止するだけでなく、混注操作終了後にシリンジが取り外される際に、誤って混注具1が混注口から脱落することも防止できる。
【0013】
前記混注具1の本体2を構成する材料としては、ポリエチレン、ポリプロピレン、ポリ塩化ビニル、ポリカーボネート、ABS樹脂などの熱可塑性樹脂が用いられる。また、該本体2は、公知の熱可塑性樹脂を用いうる成形方法により成形しうるが、好ましくは射出成形により成形される。該本体2は、一部品であってもよいが、後述するように二部品であることが構成上好ましい。本体2が二部品である場合、それぞれの部品は成形後、超音波溶着や熱溶着などによって接合され、一体化される。
【0014】
前記本体2の連通路23には、除菌フィルター3が設けられる。該除菌フィルター3は、無菌状態でない薬液を混注する場合に薬液中の菌の混入を防止したり、混注操作終了後、シリンジを取り除いた後の混注口からの菌の進入を防止したりするものである。該除菌フィルター3としては、酢酸セルロースや再生セルロース、セルロースエステル、ポリアミド、ポリスルホン、ポリエーテルスルホン等の合成樹脂から形成されたものが用いられる。該フィルター3の孔径は好ましくは0.45μm以下であり、より好ましくは0.2μm以下である。
該除菌フィルター3は、液流入口211と液流出口221との間で、連通路23を遮断するように設けられる。本体2が図1または図2に示されるように二部品からなる場合、該フィルターは二つの部品の接合時に、該部品間に狭持されることが成形が容易で好ましい。
【0015】
前記本体2の連通路23には、さらに逆止弁4が設けられる。該逆止弁4は、混注操作終了後、シリンジを取り除いた後の混注口からの内部の液体の漏出を防止するためのものである。該逆止弁4としては、ダックビルタイプ、アンブレラタイプ、もしくはチューブタイプのものが好ましく用いられる。
該逆止弁4は、連通路22に設けられるものであるが、その位置は前記除菌フィルター3の液流入口211側であっても、液流出口221側であってもよい。また、ゴム栓穿刺部22が図2に示すように、側面に液流出口221を有する形状である場合、該逆止弁4は該液流出口221に設けられていても差し支えないが、その場合の該逆止弁4の形状は、チューブタイプであることが好ましい。
【0016】
本発明の混注具1は、逆止弁4を設けたことにより、シリンジを接続してから混注口に穿刺する使用方法の他に、混注具1のみを予め輸液セットや輸血セットなどの混注口に穿刺した後、シリンジを接続して混注操作を行う使用方法も用いられる。これにより、シリンジを接続した不安定な状態での穿刺による誤穿刺の可能性を低減させ、より安全に混注操作を行うことができる。
【0017】
次に図3を用いて、本発明の混注具1の使用方法について説明する。なお、ここでは、前述した使用方法のうち、前者のシリンジを接続してから混注口に穿刺する使用方法についてのみ説明するが、後者の混注具のみを予め穿刺する使用方法についても、シリンジ接続の順序が異なるだけで、その作用および効果については同じである。
まず、混注具1のシリンジ接続部21と混注薬液を収容したシリンジ51の先端とを嵌合し、混注具1を注射器5に接続させる(図3(a))。次いで、注射器5が接続された混注具1のゴム栓穿刺部22を、混注口6のゴム栓61に穿刺し、混注具1のフランジ部24がゴム栓61表面に当接するまで押し込む(図3(b))。この状態で、混注具1のゴム栓穿刺部22はゴム栓61を貫通してゴム栓61の向こう側に突出しており、液流出口221もゴム栓61の向こう側に位置している。またロック手段である突出部25がゴム栓61から混注具1の脱落を防止している。ここで、注射器のプランジャ52を押すことによってシリンジ内の薬液が液流入口211から連通路23内に流入し、混注口6の内部に位置する液流出口221流出し、輸液セットや輸血セット内部の液体と混合される(図3(c))。混注操作が終了すれば、混注具1を混注口6に穿刺した状態のまま、注射器5のみを取り外す。さらに別に薬液を混注する場合は、薬液を収容した注射器5のシリンジ51先端を混注具1のシリンジ接続部21に接続し、同様の操作を繰り返す。該混注具1は、最終的に輸液処理または輸血処理終了後、輸液セットや輸血セットと共に廃棄するため、廃棄処理に伴う誤穿刺や感染のおそれは全くない。
【0018】
【発明の効果】
本発明の混注具は、先端に鋭利な刃先を有し、除菌フィルターおよび逆止弁を備えているため、従来の混注操作のように、シリンジに注射針を接続する操作が不要である。また、混注操作後は鋭利な刃先を有する混注具が混注口に残され、シリンジのみ取り外されるため、該混注具は混注口を含む輸液セットあるいは輸血セットと共に廃棄されるため、廃棄処理に伴う誤穿刺および感染のおそれが全くない。
また、該混注具はシリンジを接続する前に混注口に穿刺することが可能であり、医療従事者の誤穿刺のおそれが低減される。なお、混注操作後に混注具からシリンジを取り外しても、液漏れや菌の侵入がおこらず、再度該混注具にシリンジを接続して混注操作を行うことも可能である。また、従来の混注操作のように、混注終了後もシリンジを混注口に保持させておく必要がなく、より容易に混注操作を行うことができる。
【図面の簡単な説明】
【図1】 本発明の混注具の一実施例を示す断面図である。
【図2】 本発明の混注具の他の実施例を示す断面図である。
【図3】 図2に示す混注具の使用例の説明図である。
【符号の説明】
1 混注具
2 本体
21 シリンジ接続部
211 液流入口
22 ゴム栓穿刺部
221 液流出口
23 連通路
3 除菌フィルター
4 逆止弁
[0001]
[Technical field to which the invention belongs]
The present invention relates to a mixed injection device used for performing a mixed injection operation for introducing a drug solution in a syringe from a mixed injection port of a transfusion set or a transfusion set safely and hygienically.
[0002]
[Prior art]
When transfusion or blood transfusion is performed, an operation of mixing another drug solution with a preset solution is generally performed. This mixed injection operation is usually performed from a mixed injection port provided in advance in the infusion set or blood transfusion set. A common co-injection port is formed by attaching a rubber stopper in a liquid-tight manner to an opening of a container in which a liquid is stored. In general mixed injection operation, a syringe needle is connected to the tip of a syringe containing a drug solution to be mixed, and a rubber stopper is punctured with the needle, thereby communicating the inside of the syringe with the inside of the infusion set or blood transfusion set. This is done by injecting the chemical solution inside.
If the chemical solution to be mixed is not aseptic, the mixed injection may be performed through a sterilization filter. The sterilization filter is connected to the tip of a syringe during a mixed injection operation, and is further used by connecting an injection needle through the filter.
[0003]
However, in such a conventional mixed injection operation, not only a medical worker who performs the mixed injection operation may cause erroneous injection of the injection needle, but also the operation itself is difficult because the syringe is unstable during the mixed injection operation. there were. In addition, if the syringe is removed from the co-infusion port after the co-infusion operation has been completed, the internal liquid may leak out from the puncture hole left in the rubber stopper, or external bacteria may enter the inside. During the transfusion procedure, the syringe had to be kept connected to the mixed injection port.
[0004]
[Problems to be solved by the invention]
In view of the above circumstances, an object of the present invention is to provide a co-injection device that allows removal of a syringe without using a syringe needle and without the risk of liquid leakage or mixed bacteria during the co-infusion operation.
[0005]
[Means for Solving the Problems]
As a result of various earnest studies to solve the above problems, the present inventors have connected a mixture injection tool having a sterilization filter and a check valve inside, and having a sharp cutting edge at the tip to the syringe tip, and a mixture injection port It has been found that not only can the above-mentioned problems be solved by performing puncture on the eye, but also a co-infusion device that allows multiple co-infusion operations can be provided.
[0006]
That is, the present invention includes a main body having a communication path therein, a sterilization filter and a check valve provided so as to block the communication path, and the main body has a syringe connection portion at one end. The syringe connecting portion is provided with a liquid inlet that communicates with the communication passage, and the rubber plug puncture portion is a fluid that communicates with the communication passage. This is a mixed injection device provided with an outlet.
[0007]
[Action]
Since the mixed injection device of the present invention has a sharp cutting edge at the tip, it is not necessary to connect an injection needle to the syringe, and it is also possible to puncture only the mixed injection device into the mixed injection port in advance. Therefore, the risk of erroneous puncture by medical staff is greatly reduced.
Further, since the mixed injection device has a sterilization filter and a check valve in the communication path inside the main body, even if the syringe is removed after the injection of the mixed injection chemical solution, there is no possibility of liquid leakage or invasion of bacteria.
Furthermore, since the mixed injection device can be used a plurality of times, it is possible to perform additional injection of a chemical solution, mixed injection operation of other chemical solutions, and the like.
[0008]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, the mixed injection device of the present invention will be described in detail based on preferred embodiments shown in the accompanying drawings, but the present invention is not limited to these descriptions.
FIG. 1 is a cross-sectional view showing an embodiment of the co-infusion device of the present invention, and FIG. 2 is a cross-sectional view showing another embodiment of the co-infusion device of the present invention. Moreover, FIG. 3 is explanatory drawing of the usage example of the mixed injection tool shown in FIG. As shown in FIGS. 1 and 2, the co-infusion device 1 of the present invention includes a main body 2, a sterilization filter 3, and a check valve 4.
[0009]
The main body 2 of the mixed injection device 1 of the present invention has a syringe connecting portion 21 that can be directly connected to the tip of a syringe at one end, and can puncture a rubber stopper of a mixed injection port such as an infusion set or a blood transfusion set at multiple ends. A rubber plug puncture portion 22 is provided.
The syringe connector 21 has a shape and a size that can be fitted to the syringe tip so that the syringe and the mixed injection device 1 are not easily detached when the syringe tip containing the drug solution to be mixed is inserted. It has a lumen. Therefore, it is preferable that the lumen has a tapered shape whose inner diameter can be gradually reduced toward the inside of the main body. Further, when a syringe with a lock mechanism is connected and used, the syringe connection portion 21 may be provided with a means for engaging with the syringe tip, such as a locker-shaped female luer shape.
The rubber plug puncture portion 22 has a sharp cutting edge that can pierce the mixed injection device 1 into a rubber plug of a mixed injection port such as an infusion set or a blood transfusion set, and a full length that is sufficient to penetrate the rubber plug. It becomes. The shape of the blade edge is not particularly limited as long as it can puncture a rubber stopper, but it is preferably one having lower puncture resistance, and the same shape as the tip shape of the injection needle is preferably used. The rubber plug puncture portion 22 has an inner diameter that allows quick introduction of a medicinal solution to be mixed, has an outer diameter that can reduce puncture resistance to the rubber plug, and breaks or droops when puncturing the rubber plug. It must have a thickness that is not feared. Therefore, these dimensions of the rubber plug puncture portion 22 can be appropriately changed depending on the type and amount of the chemical solution and the material of the rubber plug.
[0010]
A communication passage 23 is provided inside the main body 2 so that the inner side and the outer side of the rubber plug can communicate with each other when the co-infusion device 1 of the present invention is punctured into the rubber plug. The syringe connection part 21 is provided with a liquid inlet 211, the rubber stopper puncture part 22 is provided with a liquid outlet 221, and the communication path 23 connects the liquid inlet 211 and the liquid outlet 221 at both ends. The main body 2 is provided as follows. Therefore, when the mixed injection device 1 of the present invention is used, the chemical solution in the syringe flows into the communication path 23 from the liquid inlet 211, passes through the rubber plug portion, and flows out from the liquid outlet 221. Is done.
[0011]
The liquid inflow port 211 is to introduce the chemical solution into the communication path 23 without leaking when the chemical solution in the syringe is injected from the syringe tip connected to the syringe connector 21. Therefore, it is preferable that the liquid inflow port 211 communicates with the lumen of the syringe connection portion 21 and it is more preferable that the liquid inlet 211 is provided at an end of the lumen on the inner side of the main body because there is no possibility of leakage of the chemical liquid.
The liquid outlet 221 is for introducing the chemical introduced into the communication passage 23 to the other side of the rubber plug when the co-injection device 1 is punctured by the rubber plug. That is, the liquid outlet 221 is provided in a portion of the rubber plug puncture portion 22 that protrudes beyond the rubber plug through the rubber plug. Therefore, the liquid outlet 221 is preferably provided at the tip of the rubber plug puncture portion 22. As a specific example of the liquid outlet 221, as shown in FIG. 1, a hole provided toward the tip of the rubber plug puncture portion 22 is provided. Another specific example of the liquid outlet 221 is a hole provided on the side surface of the distal end of the rubber plug puncture portion 22 as shown in FIG.
[0012]
In addition, the flange part 24 is provided in the base end side of the rubber plug puncture part 22 of the main body 2 so that the mixed injection tool 1 may be reliably arrange | positioned in the position which can mix and mix the chemical | medical solution in a syringe as mentioned above. Is preferred. According to this structure, since the co-infusion device 1 is punctured until the flange portion 24 comes into contact with the co-infusion port, the liquid outlet 221 passes through the rubber plug and is disposed on the other side of the rubber plug. There is no need to confirm an appropriate insertion position for the mixed injection operation while puncturing the mixed injection device 1.
The mixed injection device 1 is provided with a locking means for holding the mixed injection device 1 so as not to easily fall off from the rubber stopper after the chemical solution in the syringe is once securely disposed at a position where it can be mixed and injected. May be. As the locking means, for example, as shown in FIGS. 1 and 2, there is a tapered protruding portion 25 whose diameter decreases toward the sharp distal end side of the rubber plug puncture portion 22. By providing the locking means, the mixed injection device 1 not only prevents accidental dropping from the mixed injection port during the mixed injection operation with the syringe connected, but also when the syringe is removed after completion of the mixed injection operation. It is also possible to prevent the mixed injection device 1 from being accidentally dropped from the mixed injection port.
[0013]
A thermoplastic resin such as polyethylene, polypropylene, polyvinyl chloride, polycarbonate, or ABS resin is used as the material constituting the main body 2 of the mixed injection device 1. The main body 2 can be molded by a molding method using a known thermoplastic resin, but is preferably molded by injection molding. The main body 2 may be a single component, but preferably has two components as will be described later. When the main body 2 has two parts, each part is joined and integrated by ultrasonic welding or heat welding after molding.
[0014]
A sterilization filter 3 is provided in the communication passage 23 of the main body 2. The sterilization filter 3 prevents the entry of bacteria in the chemical solution when a non-sterile chemical solution is mixed, or prevents the entry of the bacteria from the mixed injection port after removing the syringe after completion of the mixed injection operation. Is. As the sterilization filter 3, a filter formed from a synthetic resin such as cellulose acetate, regenerated cellulose, cellulose ester, polyamide, polysulfone, or polyethersulfone is used. The pore diameter of the filter 3 is preferably 0.45 μm or less, more preferably 0.2 μm or less.
The sterilizing filter 3 is provided so as to block the communication path 23 between the liquid inlet 211 and the liquid outlet 221. When the main body 2 is composed of two parts as shown in FIG. 1 or FIG. 2, it is preferable that the filter is sandwiched between the two parts at the time of joining the two parts because of easy molding.
[0015]
A check valve 4 is further provided in the communication passage 23 of the main body 2. The check valve 4 is for preventing leakage of the liquid inside the mixed injection port after removing the syringe after completion of the mixed injection operation. As the check valve 4, a duckbill type, umbrella type or tube type is preferably used.
The check valve 4 is provided in the communication passage 22, but the position thereof may be on the liquid inlet 211 side or the liquid outlet 221 side of the sterilization filter 3. Further, when the rubber plug puncture portion 22 has a liquid outlet 221 on the side as shown in FIG. 2, the check valve 4 may be provided at the liquid outlet 221, In this case, the shape of the check valve 4 is preferably a tube type.
[0016]
The mixed injection device 1 of the present invention is provided with the check valve 4 so that, in addition to the usage method of puncturing the mixed injection port after connecting the syringe, only the mixed injection device 1 is previously mixed injection port such as an infusion set or a blood transfusion set. A method of using a syringe by connecting a syringe and performing a mixed injection operation after puncture is also used. Thereby, the possibility of erroneous puncturing due to puncturing in an unstable state with the syringe connected can be reduced, and the mixed injection operation can be performed more safely.
[0017]
Next, the usage method of the mixed injection device 1 of this invention is demonstrated using FIG. Here, among the above-described usage methods, only the usage method for puncturing the mixed injection port after connecting the former syringe will be described, but the usage method for puncturing only the latter mixed injection device in advance is also used for syringe connection. Only the order is different, and the actions and effects are the same.
First, the syringe connection part 21 of the mixed injection device 1 and the tip of the syringe 51 containing the mixed injection drug solution are fitted, and the mixed injection device 1 is connected to the syringe 5 (FIG. 3A). Next, the rubber plug puncture portion 22 of the mixed injection device 1 to which the syringe 5 is connected is inserted into the rubber plug 61 of the mixed injection port 6 and pushed in until the flange portion 24 of the mixed injection device 1 comes into contact with the surface of the rubber plug 61 (FIG. 3). (B)). In this state, the rubber plug puncture portion 22 of the co-injection device 1 penetrates the rubber plug 61 and protrudes beyond the rubber plug 61, and the liquid outlet 221 is also positioned beyond the rubber plug 61. Further, the protruding portion 25 serving as a locking means prevents the mixed injection device 1 from dropping from the rubber stopper 61. Here, by pushing the plunger 52 of the syringe, the drug solution in the syringe flows into the communication path 23 from the liquid inlet 211 and flows out of the liquid outlet 221 located inside the mixed injection port 6, and the inside of the infusion set or blood transfusion set (Fig. 3 (c)). When the mixed injection operation is completed, only the syringe 5 is removed while the mixed injection device 1 is punctured into the mixed injection port 6. Further, when separately injecting a chemical solution, the tip of the syringe 51 of the syringe 5 containing the chemical solution is connected to the syringe connecting portion 21 of the mixed injection device 1 and the same operation is repeated. Since the co-infusion device 1 is finally discarded together with the infusion set or the transfusion set after the end of the infusion processing or the transfusion processing, there is no possibility of erroneous puncture or infection associated with the disposal processing.
[0018]
【The invention's effect】
Since the mixed injection device of the present invention has a sharp cutting edge at the tip and includes a sterilization filter and a check valve, an operation for connecting an injection needle to a syringe is not required as in the conventional mixed injection operation. In addition, after the mixed injection operation, the mixed injection device having a sharp cutting edge is left in the mixed injection port, and only the syringe is removed, so that the mixed injection device is discarded together with the infusion set or the blood transfusion set including the mixed injection port. There is no risk of puncture and infection.
In addition, the mixed injection device can puncture the mixed injection port before connecting the syringe, thereby reducing the risk of erroneous puncturing by the medical staff. It should be noted that even if the syringe is removed from the mixed injection device after the mixed injection operation, liquid leakage or bacteria intrusion does not occur, and the mixed injection operation can be performed again by connecting the syringe to the mixed injection device. Further, unlike the conventional mixed injection operation, it is not necessary to hold the syringe in the mixed injection port even after the completion of the mixed injection, and the mixed injection operation can be performed more easily.
[Brief description of the drawings]
FIG. 1 is a cross-sectional view showing an embodiment of a mixed injection device of the present invention.
FIG. 2 is a cross-sectional view showing another embodiment of the co-infusion device of the present invention.
FIG. 3 is an explanatory view of an example of use of the mixed injection device shown in FIG. 2;
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Mixed injection tool 2 Main body 21 Syringe connection part 211 Liquid inflow port 22 Rubber plug puncture part 221 Liquid outflow port 23 Communication path 3 Bacteria elimination filter 4 Check valve

Claims (1)

内部に連通路を有してなる本体と、該連通路を遮断するように設けられた除菌フィルターおよび逆止弁を有してなり、該本体は一端にシリンジ接続部を有し、他端にゴム栓穿刺部を有し、該シリンジ接続部には前記連通路と連通する液流入口が設けられてなり、該ゴム栓穿刺部には前記連通路と連通する液流出口が設けられてなる混注具であって、前記ゴム栓穿刺部は、先端に鋭利な刃先を有し、側面に液流出口が設けられてなり、前記逆止弁は液流出口に設けられたチューブタイプの逆止弁であることを特徴とする混注具。 A main body having a communication path inside, a sterilization filter and a check valve provided so as to block the communication path, the main body having a syringe connection portion at one end, and the other end The syringe plug has a liquid inlet that communicates with the communication passage, and the rubber stopper puncture portion has a liquid outlet that communicates with the communication passage. The rubber plug puncture portion has a sharp cutting edge at the tip, a liquid outlet is provided on a side surface, and the check valve is a tube type reverse valve provided at the liquid outlet. A mixed injection device characterized by being a stop valve.
JP2002153511A 2002-05-28 2002-05-28 Mixed injection tool Expired - Fee Related JP4013248B2 (en)

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US9205248B2 (en) 2010-02-24 2015-12-08 Becton, Dickinson And Company Safety Drug delivery connectors
US8465461B2 (en) * 2010-07-27 2013-06-18 Becton, Dickinson And Company Blunt needle safety drug delivery system
KR101222881B1 (en) 2011-07-11 2013-01-17 김근배 Filter needle
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KR101833899B1 (en) 2016-02-18 2018-03-05 (주)선메딕스 Blood access apparatus with pressor sensor and drug filter
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JP3034694U (en) * 1996-08-13 1997-02-25 敏倉 許 IV injection device
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CN105451795B (en) * 2012-12-03 2020-04-17 佳迈特股份公司 Filter syringe

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