JP2001017553A - Puncture member and syringe with puncture member - Google Patents

Puncture member and syringe with puncture member

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Publication number
JP2001017553A
JP2001017553A JP11193578A JP19357899A JP2001017553A JP 2001017553 A JP2001017553 A JP 2001017553A JP 11193578 A JP11193578 A JP 11193578A JP 19357899 A JP19357899 A JP 19357899A JP 2001017553 A JP2001017553 A JP 2001017553A
Authority
JP
Japan
Prior art keywords
injection
puncture member
cap
puncture
base
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP11193578A
Other languages
Japanese (ja)
Inventor
Takayuki Abe
隆行 阿部
Seiichi Ono
誠一 小野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SB Kawasumi Laboratories Inc
Original Assignee
Kawasumi Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kawasumi Laboratories Inc filed Critical Kawasumi Laboratories Inc
Priority to JP11193578A priority Critical patent/JP2001017553A/en
Publication of JP2001017553A publication Critical patent/JP2001017553A/en
Pending legal-status Critical Current

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  • Infusion, Injection, And Reservoir Apparatuses (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a puncture member and a syringe with a puncture member that allow the use of both medical instrument and pharmaceutical container in which a non-slit mixed injection member and a mouth and a slit mixed injection member and a mouth are used jointly in the same facility. SOLUTION: A puncture member 1 in which an injection portion 3 is provided projectingly below a base 2, a pressing portion 6 is formed in the upper portion of the injection portion 13, a projection 7 is formed in the periphery of the pressing portion 6, a needle base 9 is formed at the tip of the injection portion 3 through a breaking opening 15, and a metal needle 4 is mounted in the needle base 9.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は例えば輸液セット、
採血セット、輸血セット、体外循環回路等の医療器具の
途中に配置される混注部材、薬剤(輸液、生理食塩水溶
液、血液保存液等)を封入した医薬容器に装着される口
部及び医薬容器に接続されたチューブの途中に配置され
る混注部材に穿刺する穿刺部材の改良に関する。
TECHNICAL FIELD The present invention relates to an infusion set, for example,
A blood injection set, a blood transfusion set, a co-injection member placed in the middle of a medical device such as an extracorporeal circulation circuit, a mouth attached to a medicine container enclosing a drug (infusion solution, physiological saline solution, blood preservation solution, etc.) and a medicine container The present invention relates to an improvement in a puncture member that punctures a co-injection member arranged in the middle of a connected tube.

【0002】[0002]

【発明が解決しようとする課題】薬液の混注及び採血を
行う時、シリンジに装着した先端が鋭利な金属針で、そ
れぞれの前記医療器具及び医薬容器に配置されるスリッ
トのない混注部材や口部に穿刺が行われる。先端が鋭利
な金属針を用いているので、作業中に針の先端に触れる
危険がある為、先端を非鋭利に形成した穿刺部材(以下
「注入部付穿刺部材」と略記する)が考案され、これに
対応する混注部材として栓体天面にスリットを入れ刺通
抵抗を低くして刺し易くした混注部材(以下「スリット
付混注部材」と略記する)がある。出願人は特願平10
−373886号で「注入部付穿刺部材」を提案した
が、従来からの先端が鋭利な金属針を用いた穿刺部材が
まだ主流となっている。従って従来のスリットなしの混
注部材(シリコーンゴム等の弾性体を本体の天面に突設
した栓体に装着し、天面の中央部が開口したキャップを
前記筒体に嵌着したもの)が大半を占めている。従って
施設では従来の混注部材を配置した規格の医療器具及び
医薬容器とスリット付混注部材を配置した規格の医療器
具及び医薬容器が併用されており、先端が鋭利な金属針
を装着した穿刺部材又は先端を非鋭利に形成した穿刺部
材のどちらか一方でしか選択できない。そこで、本発明
者は以上の課題を解決するために鋭意検討を重ねた結
果、次の発明に到達した。
When performing co-injection and blood collection of a drug solution, a sharp-tipped metal needle attached to a syringe, a co-injection member or a mouth portion without a slit arranged in each of the medical instruments and medical containers. Puncture is performed. Since a metal tip having a sharp tip is used, there is a danger of touching the tip of the needle during the operation. Therefore, a puncturing member having a non-sharp tip (hereinafter abbreviated as “puncturing member with an injection portion”) has been devised. As a co-injection member corresponding to this, there is a co-infusion member (hereinafter abbreviated as “slit co-injection member”) in which a slit is formed in the top surface of the plug body to reduce piercing resistance to facilitate piercing. Applicant is Japanese Patent Application Hei 10
No. 373886 proposes a "puncture member with an injection portion", but a conventional puncture member using a metal needle having a sharp tip is still mainstream. Therefore, a conventional co-injection member without a slit (a member in which an elastic body such as silicone rubber is attached to a plug protruding from the top surface of the main body and a cap whose central portion of the top surface is opened is fitted to the cylinder). Make up the majority. Therefore, in the facility, a standard medical instrument and a medical container with a conventional co-injection member and a standard medical instrument and a medical container with a co-injection member with a slit are used in combination, and a puncture member or a puncture member equipped with a sharp metal needle is used. Only one of the puncturing members having a non-sharp tip can be selected. The inventor of the present invention has made intensive studies in order to solve the above-mentioned problems, and as a result, has arrived at the next invention.

【0003】[0003]

【課題を解決する為の手段】[1]本発明は、基部2
(2a)の下方に注入部3(3a)が突設され、前記注
入部3(3a)の上部に押圧部6(6a)が形成され、
該押圧部6(6a)の外周に凸部7(7a)を形成し、
前記注入部3(3a)の先端に折り口15(15a)を
介して針基9(9a)が形成され、該針基9(9a)に
金属針4(4a)を装着した穿刺部材1(1A)を提供
する。 [2]本発明は、前記基部2(2a)の外周に翼部5、
5a(5b、5c)を設け且つ該翼部5、5a(5b、
5c)の上端部に鍔部8(8a)を形成し、前記翼部
5、5bの側部に溝10(10a)を設けた[1]に記
載の穿刺部材1(1A)を提供する。 [3]本発明は、前記溝10(10a)と嵌合する突部
14(14a)を形成したキャップ13を装着した
[2]に記載の穿刺部材1(1A)を提供する。 [4]本発明は、[1]ないし[3]に記載の穿刺部材
1(1A)の基部2(2a)を挿入部12に挿着または
[1]ないし[3]に記載の穿刺部材1(1A)の基部
2(2a)をシリンジ11の下部に一体成形した穿刺部
材付シリンジを提供する。
Means for Solving the Problems [1] The present invention relates to a base 2
An injection part 3 (3a) protrudes below (2a), and a pressing part 6 (6a) is formed above the injection part 3 (3a).
A convex portion 7 (7a) is formed on the outer periphery of the pressing portion 6 (6a),
A needle base 9 (9a) is formed at the tip of the injection part 3 (3a) through a folding opening 15 (15a), and the puncture member 1 (9) having a metal needle 4 (4a) attached to the needle base 9 (9a). 1A) is provided. [2] The present invention provides a wing 5 on the outer periphery of the base 2 (2a).
5a (5b, 5c) and the wings 5, 5a (5b,
The puncture member 1 (1A) according to [1], wherein a flange 8 (8a) is formed at the upper end of 5c) and a groove 10 (10a) is provided on the side of the wings 5, 5b. [3] The present invention provides the puncture member 1 (1A) according to [2], in which a cap 13 having a protrusion 14 (14a) fitted with the groove 10 (10a) is mounted. [4] In the present invention, the base 2 (2a) of the puncture member 1 (1A) according to [1] to [3] is inserted into the insertion portion 12 or the puncture member 1 according to [1] to [3]. Provided is a syringe with a puncture member in which the base 2 (2a) of (1A) is integrally formed at the lower part of the syringe 11.

【0004】[0004]

【発明の実施の形態】以下穿刺部材及び混注部材につい
て薬剤の混注を行なう場合の一例について説明する。図
1は本発明の穿刺部材1とシリンジ11を接続した概略
図である。穿刺部材1は、シリンジ11に形成された挿
入部12に嵌合する基部2と、後述する混注部材2Aに
挿入する注入部3と、金属針4を装着した針基9と、前
記注入部3と金属針4を覆うキャップ13から構成さ
れ、前記注入部3と金属針4は該注入部3の先端に折り
口15を介して形成される。前記基部2の外周に、翼部
5と翼部5aがそれぞれ対となり90度間隔に設けられ
ている。前記翼部5は翼部5aより長く形成されている
ので指先の掛かり具合が良く、前記翼部5を指先で回動
させることによりシリンジ11との脱着がし易くなる。
翼部5は翼部5aより長く形成されているので、注入部
付穿刺部材が後述する混注部材2Aに挿入、嵌合、回
動、固定した時、翼部5は本体20の長さ方向に対して
垂直方向を示し、目視により締付けている状態を確認す
ることができる。前記翼部5、5aの下端部には、板状
の押圧部6が形成され、該押圧部6の外周には少なくと
も2ヶ所の凸部7が形成されている。前記翼部5、5a
の上端部には必要により鍔部8が形成される。これによ
りシリンジ11と穿刺部材1が抜けない様に、ルアーロ
ックタイプのシリンジ(図示せず)とも嵌合できる。注
入部3の先端には、折り口15を介して針基9が形成さ
れ、該針基9に金属針4が装着されている。前記折り口
15は溝状で薄肉に形成され、押圧すると360度のど
の方向からも折ることができ、前記注入部3と金属針4
を装着した針基9を切り離すことができる。前記折り口
15の強度は後述する図5の様に金属針4を装着した穿
刺部材1を混注部材2Bに穿刺した時、前記折り口15
から折れること無く且つ後述する図2の様に折り口15
より押圧して折る時に折れる適切な強度を備えている。
前記キャップ13は大径の基部の内面に前記溝10と嵌
合する突部14が形成され、該突部14を前記溝10に
嵌合することにより、注入部3と金属針4を覆うように
装着することができる。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, an example in which a medicine is co-injected into a puncture member and a co-infusion member will be described. FIG. 1 is a schematic view in which a puncture member 1 of the present invention and a syringe 11 are connected. The puncture member 1 includes a base portion 2 fitted into an insertion portion 12 formed in a syringe 11, an injection portion 3 inserted into a co-injection member 2A described later, a needle base 9 on which a metal needle 4 is mounted, and an injection portion 3. And the cap 13 that covers the metal needle 4. The injection part 3 and the metal needle 4 are formed at the tip of the injection part 3 through a folding hole 15. A pair of wings 5 and wings 5a are provided on the outer periphery of the base 2 at 90-degree intervals. The wings 5 are formed longer than the wings 5a, so that the fingertips can be easily hooked. By rotating the wings 5 with the fingertips, the wings 5 can be easily attached to and detached from the syringe 11.
Since the wing portion 5 is formed longer than the wing portion 5a, the wing portion 5 moves in the longitudinal direction of the main body 20 when the puncturing member with the injection portion is inserted, fitted, rotated, and fixed to the co-injection member 2A described later. On the other hand, the vertical direction is shown, and the tightening state can be visually confirmed. At the lower ends of the wing portions 5, 5a, a plate-shaped pressing portion 6 is formed, and at least two convex portions 7 are formed on the outer periphery of the pressing portion 6. The wings 5, 5a
A collar portion 8 is formed at the upper end of the as required. As a result, a luer lock type syringe (not shown) can be fitted so that the syringe 11 and the puncture member 1 do not come off. A needle base 9 is formed at the tip of the injection part 3 through a folding opening 15, and the metal needle 4 is mounted on the needle base 9. The folding opening 15 is formed in a groove shape and is thin, and can be folded from any direction of 360 degrees when pressed.
Can be cut off. When the puncture member 1 with the metal needle 4 attached thereto is punctured into the co-injection member 2B as shown in FIG.
From the fold 15 as shown in FIG.
It has the appropriate strength to break when it is pressed and folded.
The cap 13 has a protrusion 14 formed on the inner surface of the large-diameter base portion so as to fit into the groove 10. By fitting the protrusion 14 into the groove 10, the injection part 3 and the metal needle 4 are covered. Can be attached to

【0005】次に穿刺部材1の使用方法の一例について
説明する。使用する輸液セット、採血セット、輸血セッ
ト、体外循環回路等の医療器具の途中に配置される混注
部材、薬剤(輸液、生理食塩水溶液、血液保存液等)を
封入した医薬容器に装着される口部及び医薬容器に接続
されたチューブの途中に配置される混注部材の形状が、
スリットの入ってない従来の口部及び混注部材か又はス
リット付混注部材及び口部かをまず見極める。そして従
来のスリットの入ってない口部及び混注部材ならば金属
針4を装着した穿刺部材1を用いて後述する図5のよう
に使用する。スリット付混注部材及び口部の場合、後述
する図2の様に金属針4を装着した針基9を折り口15
より折って切り離し、注入部3のみを装着した穿刺部材
1として後述する図3のように使用する。
Next, an example of a method of using the puncture member 1 will be described. Infusion set to be used, blood collection set, blood transfusion set, co-infusion member placed in the middle of medical equipment such as extracorporeal circulation circuit, mouth to be attached to a medicine container enclosing drugs (infusion, physiological saline solution, blood preservation solution, etc.) Part and the shape of the co-injection member arranged in the middle of the tube connected to the medicine container,
First, it is determined whether the conventional mouth portion and the co-injection member have no slit or the co-infusion member and the spout portion with the slit. In the case of a conventional mouth portion without a slit and a co-injection member, the puncture member 1 to which the metal needle 4 is attached is used as shown in FIG. In the case of a mixed injection member with a slit and a mouth, the needle base 9 on which the metal needle 4 is mounted as shown in FIG.
The puncture member 1 is further folded and separated, and is used as shown in FIG.

【0006】図2は穿刺部材1に装着したキャップ13
を用いて折り口15から金属針4を装着した針基9を折
った時の概略図である。前記穿刺部材1に装着したキャ
ップ13を外して、折り口15が挿入口16から露出す
るまで抜いて、金属針4の先端部をキャップ13の細径
部の内壁に押し当てると同時に針基9が挿入口16の上
端内周に当り、押圧力が折り口15に伝わり、金属針4
を装着した針基9が切り離され、キャップ13の中に金
属針4が針基9と共に収納される。
FIG. 2 shows a cap 13 attached to the puncture member 1.
FIG. 5 is a schematic view when the needle base 9 on which the metal needle 4 is mounted is folded from the folding opening 15 using the arrow. The cap 13 attached to the puncture member 1 is removed, and the cap 13 is pulled out until the folding opening 15 is exposed from the insertion opening 16. The distal end of the metal needle 4 is pressed against the inner wall of the small diameter portion of the cap 13 and the needle base 9 is simultaneously opened. Hits the inner circumference of the upper end of the insertion slot 16, and the pressing force is transmitted to the folding slot 15, and the metal needle 4
Is detached, and the metal needle 4 is stored in the cap 13 together with the needle base 9.

【0007】図3は金属針4を切り離した後の穿刺部材
1の注入部3を混注部材2Aに穿刺し、押圧部6を栓体
23の天面に押圧した概略図で、図4は図3の穿刺部材
1を90度回動した時の概略図である。混注部材2Aは
管状の本体20の天面に突設された管状の筒体21にシ
リコーンゴム等の弾性を有し且つ少なくとも天面にスリ
ットを形成した栓体23を装着し、前記筒体21の外周
に形成した筒体突部25にキャップ22の内周に形成し
たキャップ凹部26を嵌合して、前記キャップ22を筒
体21に冠着することにより構成される。キャップ22
は天面の中央部が開口された筒状のキャップ22で前記
キャップ22の上部内周面には押圧部6の外周に設けら
れた凸部7と嵌合する凹部24が形成されている。前記
注入部3を混注部材2Aの栓体23の天面に形成された
スリットに挿入し押圧する。同時に押圧部6の外周に設
けられた凸部7と、キャップ22の上部内壁面に形成さ
れた凹部24を嵌合させ、さらに栓体23の天面を押圧
し、前記穿刺部材1を90度回動させる。前記穿刺部材
1を押圧することで、押圧部6と凸部7が栓体23を圧
縮し、さらに回動することにより凸部7がキャップ22
の上部内壁面と栓体23の天面の間にねじ込まれ、前記
穿刺部材1と前記混注部材2Aが強固に固定される。こ
れにより持続的な薬剤の注入の際、穿刺部材1が傾いた
り抜け落ちることがなくなり、栓体23からの液漏れも
なくなる。前記穿刺部材1を回動させる角度は40度か
ら140度であれば充分であるが、キャップ22の上部
内壁面には押圧部6の外周に設けられた凸部7が嵌合
し、回動した時外れなければ良く、好ましくは90度が
良い。
FIG. 3 is a schematic diagram in which the injection part 3 of the puncture member 1 after the metal needle 4 is cut off is punctured into the co-injection member 2A, and the pressing part 6 is pressed against the top surface of the stopper 23. FIG. 3 is a schematic diagram when the puncture member 1 is rotated 90 degrees. In the co-injection member 2A, a plug 23 having elasticity such as silicone rubber and having at least a slit formed on the top surface is attached to a tubular cylinder 21 protruding from the top surface of the tubular body 20. Is formed by fitting a cap concave portion 26 formed on the inner periphery of the cap 22 into a cylindrical projecting portion 25 formed on the outer periphery of the cap 22, and mounting the cap 22 on the cylindrical body 21. Cap 22
Is a cylindrical cap 22 having an opening at the center of the top surface. A concave portion 24 is formed in the upper inner peripheral surface of the cap 22 so as to fit with the convex portion 7 provided on the outer periphery of the pressing portion 6. The injection part 3 is inserted into a slit formed on the top surface of the plug 23 of the co-injection member 2A and pressed. At the same time, the convex portion 7 provided on the outer periphery of the pressing portion 6 and the concave portion 24 formed on the upper inner wall surface of the cap 22 are fitted together, and further, the top surface of the plug 23 is pressed, and the puncture member 1 is turned 90 degrees. Rotate. By pressing the puncture member 1, the pressing portion 6 and the convex portion 7 compress the plug 23, and by further rotating, the convex portion 7 becomes the cap 22.
The puncture member 1 and the co-injection member 2A are firmly fixed. This prevents the puncture member 1 from tilting or falling off during continuous drug injection, and prevents liquid leakage from the plug 23. It is sufficient that the puncture member 1 is rotated at an angle of 40 to 140 degrees, but the convex portion 7 provided on the outer periphery of the pressing portion 6 is fitted on the upper inner wall surface of the cap 22, and the cap 22 is rotated. It is good if it does not come off, and preferably 90 degrees.

【0008】図5は金属針4を装着した穿刺部材1を従
来の混注部材2Bに穿刺した時の概略図である。混注部
材2Bは管状の本体30の天面に突設された管状の筒体
31にシリコーンゴム等の弾性を有する栓体33を装着
し、前記筒体31の外周に形成した筒体突部35にキャ
ップ32の内周に形成したキャップ凹部36を嵌合し
て、前記キャップ32を筒体31に冠着する事により構
成される。スリットなしの混注部材2Bのキャップ天面
中央部が開口され栓体33が露出した面に、前記穿刺部
材1に装着されたキャップ13を外し金属針4を挿入し
て混注又は採血を行う。
FIG. 5 is a schematic diagram when the puncture member 1 on which the metal needle 4 is mounted is punctured into the conventional co-injection member 2B. In the co-injection member 2B, an elastic plug 33 such as silicone rubber is attached to a tubular cylinder 31 protruding from the top surface of the tubular main body 30, and a cylindrical projection 35 formed on the outer periphery of the cylinder 31 is formed. A cap concave portion 36 formed on the inner periphery of the cap 32 is fitted to the cap 32, and the cap 32 is mounted on the cylindrical body 31. The cap 13 attached to the puncture member 1 is removed and the metal needle 4 is inserted into the surface of the co-injection member 2B without a slit where the cap top surface is opened at the center of the cap and the plug 33 is exposed to perform co-infusion or blood collection.

【0009】図6は前記穿刺部材1のその他の実施例を
示す穿刺部材1Aで、該穿刺部材1Aとシリンジ11を
接続した概略図である。基部2aの外周に、翼部5b、
5cがそれぞれ対となり90度間隔で四箇所に設けら
れ、前記翼部5b、5cの下端部には、間隔をあけて、
板状の略ひし形状の押圧部6aを形成し、且つ前記押圧
部6aの外周には凸部7aが設けられ、前記翼部5b、
5cの上端部には鍔部8aが形成されている。穿刺部材
1Aは前記穿刺部材1と同様、注入部3aの先端には折
り口15aを介して針基9aが形成され、該針基9aに
金属針4aが装着されている。前記折り口15aは溝状
で薄肉に形成され、押圧されると360度のどの方向か
らも折ることができ、前記注入部3aと金属針4aを装
着した針基9aを切り離すことができる。図示してない
が穿刺部材1Aも前記図1のキャップ13の突部14を
前記溝10aに嵌合することにより、注入部3aと金属
針4aを覆うように装着することができる。
FIG. 6 is a schematic view of a puncture member 1A showing another embodiment of the puncture member 1, in which the puncture member 1A and the syringe 11 are connected. On the outer periphery of the base 2a, wings 5b,
5c are provided as a pair at four positions at 90-degree intervals, and at the lower ends of the wings 5b and 5c,
A flat rhombus-shaped pressing portion 6a is formed, and a convex portion 7a is provided on the outer periphery of the pressing portion 6a.
A flange 8a is formed at the upper end of 5c. The puncture member 1A has a needle base 9a formed at the tip of the injection portion 3a through a folding opening 15a, and a metal needle 4a is attached to the needle base 9a, similarly to the puncture member 1. The folding opening 15a is formed in a thin groove shape and can be folded from any direction of 360 degrees when pressed, so that the injection portion 3a and the needle base 9a on which the metal needle 4a is mounted can be cut off. Although not shown, the puncture member 1A can also be mounted so as to cover the injection portion 3a and the metal needle 4a by fitting the protrusion 14 of the cap 13 of FIG. 1 into the groove 10a.

【0010】使用する際は前記穿刺部材1と同様に混注
部材、薬剤を封入した医薬容器に装着される口部及び医
薬容器に接続されたチューブの途中に配置される混注部
材の栓体にスリットの入ってない従来の口部及び混注部
材か又はスリット付混注部材及び口部かを見極め、従来
の口部及び混注部材では前記図5のように金属針4aを
装着したままの穿刺部材1Aで従来の混注部材2B及び
口部の栓体に穿刺して混注又は採血を行う。スリット付
混注部材の場合前記図2のように穿刺部材1Aに装着し
たキャップを利用し折り口15aで折り、金属針4aを
切り離し前記図3、図4のように注入部3aをスリット
付混注部材(図示せず)のスリットに挿入、押圧し、押
圧部6aと凸部7aが栓体を圧縮し、回動することによ
り凸部7aがキャップの上部内壁面と栓体の天面の間に
ねじ込まれ、前記穿刺部材1Aとスリット付混注部材が
強固に固定され混注又は採血が行われる。
When used, a co-injection member, a mouth portion to be attached to a medicine container enclosing a medicine, and a plug in the co-infusion member disposed in the middle of a tube connected to the medicine container as in the case of the puncture member 1. The conventional mouth and co-injection member without slits or the co-infusion member with slit and the spout are discriminated. With the conventional mouth and co-infusion member, the puncture member 1A with the metal needle 4a attached as shown in FIG. A conventional co-infusion member 2B and a plug at the mouth are punctured to perform co-infusion or blood collection. In the case of a co-injection member with a slit, as shown in FIG. 2, a cap attached to the puncture member 1A is used to fold it at the folding opening 15a, the metal needle 4a is cut off, and the infusion unit 3a is inserted into the co-infusion member with a slit as in FIGS. (Not shown) is inserted and pressed, and the pressing portion 6a and the convex portion 7a compress the plug, and the convex portion 7a is rotated between the upper inner wall surface of the cap and the top surface of the plug. The puncture member 1A and the co-injection member with slit are firmly fixed, and co-infusion or blood collection is performed.

【0011】穿刺部材1(1A)は図示したものに限ら
ず、翼部5、5a(5b、5c)は指先で回動させるこ
とでシリンジとの脱着を容易にする形状であればどのよ
うな形状でも採用することができる。特に翼部5、5a
(5b、5c)の数は2枚から6枚に形成するのが良
い。
The puncturing member 1 (1A) is not limited to the one shown in the drawing, and the wings 5, 5a (5b, 5c) may have any shape as long as they can be easily attached to and detached from a syringe by being rotated with a fingertip. Shapes can also be employed. Especially wings 5, 5a
The number of (5b, 5c) is preferably formed from two to six.

【0012】本発明で前記押圧部6(6a)とは前記混
注部材2A等に装着した栓体23の天面を押圧する部材
であり、前記注入部3(3a)とは前記栓体23のスリ
ットに挿入して、該注入部3(3a)の先端が前記混注
部材2A等の本体20の流路に突出する部材である。従
って本発明では押圧部6(6a)と注入部3(3a)の
形状は、図示したものに限定されず金属針4を外した穿
刺部材1(1A)を混注部材2A等に挿入した時、混注
部材2A等の本体20の流路に、前記穿刺部材1(1
A)の注入部3(3a)の先端が届き且つ押圧部6(6
a)が栓体23の天面を押圧でき、更に回動できる形状
であれば何でも良い。さらに詳述すれば前記図2と図6
の注入部3(3a)の長さは翼部5、5a(5b、5
c)の長さと同程度に形成されているが、前記に述べた
ように該注入部3(3a)の先端が本体20の流路に突
出てその他の部分がスリットの中に埋れば良い。さらに
前記押圧部6(6a)は栓体23の天面を押圧できれば
良い。従って注入部3(3a)の長さは翼部5、5a
(5b、5c)より長くても良いし短くても良い。また
押圧部6は翼部5、5aと一体に成形せず、注入部3の
外周に押圧部6aのように単独で形成することもでき
る。すなわち押圧部6は押圧部6aのように翼部5b、
5cと間隔をあけて形成しても良いし、押圧部6(6
a)のみを形成して翼部5、5a(5b、5c)は設け
なくても良い。また押圧部6、6aの外周形状を該押圧
部6、6aの外周形状に嵌合するキャップ22の上部内
壁面の形状と同じにすれば、押圧部6、6aの外周に設
けた前記凸部7、7aは必要なくなる。つまり、キャッ
プ上部内壁面の形状と押圧部の形状が同じで嵌合させる
と前記図3、図4のように押圧部の形状がキャップ上部
内壁面と栓体の天面の間にねじ込まれ先端丸型穿刺部材
とスリット付混注部材が強固に固定できれば押圧部の形
状は特に限定しない。但し押圧部の形状が真円の場合、
キャップ上部内壁面も同様に真円を形成するので回動さ
せても固定できない。また押圧部の形状がキャップ上部
内壁面と栓体の天面の間にねじ込まれた時、キャップ上
部内壁面が割れない形状にする。
In the present invention, the pressing portion 6 (6a) is a member for pressing the top surface of the plug 23 attached to the co-injection member 2A or the like, and the injection portion 3 (3a) is a member for pressing the plug 23. The injection portion 3 (3a) is a member that is inserted into the slit and protrudes into the flow path of the main body 20 such as the co-infusion member 2A. Therefore, in the present invention, the shapes of the pressing portion 6 (6a) and the injection portion 3 (3a) are not limited to those shown in the figure, and when the puncture member 1 (1A) from which the metal needle 4 has been removed is inserted into the co-injection member 2A or the like, The puncture member 1 (1) is inserted into the flow path of the main body 20 such as the co-injection member 2A.
A), the tip of the injection part 3 (3a) reaches and the pressing part 6 (6
Any shape may be used as long as a) can press the top surface of the plug 23 and can further rotate. More specifically, FIG. 2 and FIG.
The length of the injection portion 3 (3a) of the wing portion 5, 5a (5b, 5b)
c) It is formed to the same length as the length, but it is sufficient that the tip of the injection part 3 (3a) protrudes into the flow path of the main body 20 and the other part is buried in the slit as described above. Further, it is sufficient that the pressing portion 6 (6a) can press the top surface of the plug 23. Therefore, the length of the injection part 3 (3a) is
It may be longer or shorter than (5b, 5c). Further, the pressing portion 6 may not be formed integrally with the wing portions 5 and 5a, but may be formed alone on the outer periphery of the injection portion 3 like the pressing portion 6a. That is, the pressing portion 6 has the wing portion 5b like the pressing portion 6a,
5c may be formed at an interval from the pressing portion 6 (6
It is not necessary to form only a) and to provide the wings 5, 5a (5b, 5c). If the outer peripheral shape of the pressing portions 6 and 6a is made the same as the shape of the upper inner wall surface of the cap 22 fitted to the outer peripheral shape of the pressing portions 6 and 6a, the convex portion provided on the outer periphery of the pressing portions 6 and 6a 7, 7a becomes unnecessary. That is, when the shape of the inner wall surface of the cap and the shape of the pressing portion are the same and fitted together, the shape of the pressing portion is screwed between the inner wall surface of the cap and the top surface of the plug as shown in FIGS. The shape of the pressing portion is not particularly limited as long as the round puncture member and the slit co-infusion member can be firmly fixed. However, if the shape of the pressing part is a perfect circle,
Since the inner wall surface of the cap also forms a perfect circle, it cannot be fixed by rotating. Also, when the shape of the pressing portion is screwed between the inner wall surface of the cap and the top surface of the plug, the inner wall surface of the cap is made not to be broken.

【0013】穿刺部材1(1A)に装着されるキャップ
13の形状や装着方法は前記で述べた溝10とキャップ
突部14との嵌合による装着に限らず、穿刺部材1(1
A)にキャップの着脱が容易にできれば特に限定はしな
い。
The shape and the mounting method of the cap 13 mounted on the puncturing member 1 (1A) are not limited to the mounting by fitting the groove 10 and the cap projection 14 described above.
There is no particular limitation as long as the cap can be easily attached and detached in A).

【0014】製品規格の都合上、例えば一つの輸液セッ
ト、採血セット、輸血セット、体外循環回路等の医療器
具及び医薬容器に、従来のスリットなしの混注部材及び
口部とスリット付混注部材及び口部を2個以上併用して
使用する可能性は少ないが、近接してスリットなしの混
注部材及び口部とスリット付混注部材及び口部を使用す
る場合は十分に想定される。よって穿刺部材1(1A)
は一本で、金属針4(4a)を装着した穿刺部材1(1
A)として使用できるし金属針4(4a)を折り口15
(15a)から折って、注入部のみを装着した穿刺部材
1(1A)としても使用することができる。
For the sake of product specifications, for example, conventional medical devices such as a transfusion set, a blood collection set, a blood transfusion set, an extracorporeal circulation circuit and a medical container, and a conventional mixed injection member without a slit and a mouth portion and a mixed injection member with a slit and a mouth. Although it is unlikely that two or more parts are used together, a mixed injection member without a slit and a mouth and a mixed injection member with a slit and a mouth which are close to each other are sufficiently assumed. Therefore, puncturing member 1 (1A)
Is a puncture member 1 (1) to which a metal needle 4 (4a) is attached.
A) The metal needle 4 (4a) can be used as
It can be used as the puncture member 1 (1A) which is folded from (15a) and has only the injection section.

【0015】スリット付混注部材を装着した前記医療器
具及び医薬容器の混注部材及び口部には本来注入部付穿
刺部材を用いて薬剤の注入や採血を行うが、前記スリッ
ト以外の栓体表面に金属針を装着した穿刺部材を穿刺す
ることで、緊急の場合の対応も可能となる。
[0015] Injection and blood collection of a drug are originally performed by using a puncture member with an injection part in the co-infusion member and the mouth of the medical device and the medical container equipped with the co-infusion member with a slit. By puncturing the puncture member with the metal needle attached, it is possible to cope with an emergency.

【0016】なおこれらの穿刺部材1(1A)はスリッ
ト付混注部材を装着する医療器具及び医薬容器と共に包
材に同封せず別途提供する場合もある。
The puncture member 1 (1A) may be provided separately without being enclosed in a packaging material together with a medical device and a medical container equipped with a co-injection member with a slit.

【0017】本発明の前記穿刺部材1(1A)は基部2
(2a)をシリンジ11の挿入部12に装着又は基部2
(2a)をシリンジ11の下部に一体成形して一つの部
材、すなわち穿刺部材付シリンジ(図示せず)として使
用することができる。
The puncture member 1 (1A) of the present invention comprises a base 2
(2a) is attached to the insertion portion 12 of the syringe 11 or the base 2
(2a) can be integrally molded with the lower part of the syringe 11 and used as one member, ie, a syringe with a puncture member (not shown).

【0018】[0018]

【発明の作用効果】輸液セット、採血セット、輸血セッ
ト、体外循環回路等の医療器具の途中に配置される混注
部材及び薬剤を封入した医薬容器に装着される口部の形
状が、従来のスリットのない混注部材及び口部とスリッ
ト付混注部材及び口部を配置した規格の医療器具及び医
薬容器が同一施設内で併用されていても、本発明の穿刺
部材1(1A)では、従来のスリットなしの混注部材及
び口部では金属針4(4a)を装着した穿刺部材1(1
A)として使用し、スリット付混注部材及び口部の場合
は金属針4(4a)を装着した針基9(9a)を折り口
15(15a)より切り離した注入部付穿刺部材として
使用することができるので臨機応変に対処できる。
The effect of the present invention is that a conventional slit is used for a co-injection member disposed in the middle of a medical device such as an infusion set, a blood collection set, a blood transfusion set, an extracorporeal circulation circuit, and a medicine container enclosing a medicine. Even if a standard medical device and a medical container having a mixed injection member and a mouth and a mixed injection member with a slit and a mouth are used together in the same facility, the puncture member 1 (1A) of the present invention has a conventional slit. No co-infusion member and puncture member 1 (1
A) to be used as a co-injection member with a slit and, in the case of a mouth portion, a needle member 9 (9a) equipped with a metal needle 4 (4a) as a puncture member with an injection portion separated from a folding opening 15 (15a). Can be dealt with flexibly.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の穿刺部材1とシリンジ11を接続した
概略図
FIG. 1 is a schematic diagram in which a puncture member 1 and a syringe 11 of the present invention are connected.

【図2】折り口15から折り、金属針4を装着した針基
9から切り離した穿刺部材1の概略図
FIG. 2 is a schematic view of the puncture member 1 folded from a folding opening 15 and separated from a needle base 9 on which a metal needle 4 is mounted.

【図3】金属針4を装着した針基9から切り離した穿刺
部材1を混注部材2Aに穿刺し押圧部を栓体に押圧した
概略図
FIG. 3 is a schematic diagram in which a puncture member 1 separated from a needle base 9 on which a metal needle 4 is mounted is punctured into a co-injection member 2A and a pressing portion is pressed against a stopper.

【図4】図3の穿刺部材1を90度回転した時の概略図4 is a schematic diagram when the puncture member 1 of FIG. 3 is rotated by 90 degrees.

【図5】金属針4を装着した穿刺部材1を従来のスリッ
トのない混注部材2Bに穿刺した時の概略図
FIG. 5 is a schematic diagram when a puncture member 1 equipped with a metal needle 4 is punctured into a conventional slitless co-injection member 2B.

【図6】穿刺部材1のその他の実施例を示す穿刺部材1
Aで、シリンジ11と接続した概略図
FIG. 6 shows a puncture member 1 showing another embodiment of the puncture member 1.
Schematic diagram connected to the syringe 11 at A

【符号の説明】[Explanation of symbols]

1、1A 穿刺部材 2A、2B 混注部材 2、2a 基部 3、3a 注入部 4、4a 金属針 5、5a、5b、5c 翼部 6、6a 押圧部 7、7a 凸部 8、8a 鍔部 9、9a 針基 10、10a 溝 11 シリンジ 12 挿入部 13 キャップ 14 突部 15、15a 折り口 16 挿入口 20、30 本体 21、31 筒体 22、32 キャップ 23、33 栓体 24 凹部 25、35 筒体突部 26、36 キャップ凹部 1, 1A Puncture member 2A, 2B Mixed injection member 2, 2a Base 3, 3a Injection part 4, 4a Metal needle 5, 5a, 5b, 5c Wing part 6, 6a Pressing part 7, 7a Convex part 8, 8a Flange part 9, 9a Needle base 10, 10a Groove 11 Syringe 12 Insertion section 13 Cap 14 Projection 15, 15a Folding opening 16 Insertion opening 20, 30 Main body 21, 31 Cylindrical body 22, 32 Cap 23, 33 Plug body 24 Concave part 25, 35 Cylindrical body Projections 26, 36 Cap recess

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】基部2(2a)の下方に注入部3(3a)
が突設され、前記注入部3(3a)の上部に押圧部6
(6a)が形成され、該押圧部6(6a)の外周に凸部
7(7a)を形成し、前記注入部3(3a)の先端に折
り口15(15a)を介して針基9(9a)が形成さ
れ、該針基9(9a)に金属針4(4a)を装着したこ
とを特徴とする穿刺部材1(1A)。
An injection section 3 (3a) is provided below a base 2 (2a).
And a pressing portion 6 is provided above the injection portion 3 (3a).
(6a) is formed, a convex portion 7 (7a) is formed on the outer periphery of the pressing portion 6 (6a), and the needle base 9 (7) is formed at the tip of the injection portion 3 (3a) through a folding hole 15 (15a). 9A) is formed, and a metal needle 4 (4a) is attached to the needle base 9 (9a).
【請求項2】前記基部2(2a)の外周に翼部5、5a
(5b、5c)を設け且つ該翼部5、5a(5b、5
c)の上端部に鍔部8(8a)を形成し、前記翼部5、
5bの側部に溝10(10a)を設けたことを特徴とす
る請求項1に記載の穿刺部材1(1A)。
2. Wings 5 and 5a are provided on the outer periphery of the base 2 (2a).
(5b, 5c) and the wings 5, 5a (5b, 5c).
c) a flange 8 (8a) is formed at the upper end of the wing 5,
The puncture member 1 (1A) according to claim 1, wherein a groove 10 (10a) is provided on a side portion of 5b.
【請求項3】前記溝10(10a)と嵌合する突部14
(14a)を形成したキャップ13を装着したことを特
徴とする請求項2に記載の穿刺部材1(1A)。
3. A projection 14 fitted in the groove 10 (10a).
The puncture member 1 (1A) according to claim 2, wherein a cap 13 formed with (14a) is mounted.
【請求項4】請求項1ないし請求項3に記載の穿刺部材
1(1A)の基部2(2a)を挿入部12に挿着または
請求項1ないし請求項3に記載の穿刺部材1(1A)の
基部2(2a)をシリンジ11の下部に一体成形したこ
とを特徴とする穿刺部材付シリンジ。
4. The puncture member 1 (1A) according to claim 1, wherein the base 2 (2a) of the puncture member 1 (1A) according to claim 1 is inserted into the insertion portion 12. 3. The syringe with a puncture member, wherein the base 2 (2a) of (1) is formed integrally with the lower part of the syringe 11.
JP11193578A 1999-07-07 1999-07-07 Puncture member and syringe with puncture member Pending JP2001017553A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11193578A JP2001017553A (en) 1999-07-07 1999-07-07 Puncture member and syringe with puncture member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11193578A JP2001017553A (en) 1999-07-07 1999-07-07 Puncture member and syringe with puncture member

Publications (1)

Publication Number Publication Date
JP2001017553A true JP2001017553A (en) 2001-01-23

Family

ID=16310341

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11193578A Pending JP2001017553A (en) 1999-07-07 1999-07-07 Puncture member and syringe with puncture member

Country Status (1)

Country Link
JP (1) JP2001017553A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007503859A (en) * 2003-08-29 2007-03-01 プリモジェクス ゲーエムベーハー Device for injecting injectable preparations

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007503859A (en) * 2003-08-29 2007-03-01 プリモジェクス ゲーエムベーハー Device for injecting injectable preparations
JP4674209B2 (en) * 2003-08-29 2011-04-20 プリモジェクス ゲーエムベーハー Device for injecting injectable preparations

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