JPH10151176A - Infusion container for instillation - Google Patents

Infusion container for instillation

Info

Publication number
JPH10151176A
JPH10151176A JP8327752A JP32775296A JPH10151176A JP H10151176 A JPH10151176 A JP H10151176A JP 8327752 A JP8327752 A JP 8327752A JP 32775296 A JP32775296 A JP 32775296A JP H10151176 A JPH10151176 A JP H10151176A
Authority
JP
Japan
Prior art keywords
holder
vial
container
container body
projection
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.)
Granted
Application number
JP8327752A
Other languages
Japanese (ja)
Other versions
JP3128756B2 (en
Inventor
Ikuo Araki
郁雄 荒木
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.)
ARAKI KOGYO KK
Original Assignee
ARAKI KOGYO KK
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 ARAKI KOGYO KK filed Critical ARAKI KOGYO KK
Priority to JP08327752A priority Critical patent/JP3128756B2/en
Publication of JPH10151176A publication Critical patent/JPH10151176A/en
Application granted granted Critical
Publication of JP3128756B2 publication Critical patent/JP3128756B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/32Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents for packaging two or more different materials which must be maintained separate prior to use in admixture
    • B65D81/3205Separate rigid or semi-rigid containers joined to each other at their external surfaces
    • B65D81/3211Separate rigid or semi-rigid containers joined to each other at their external surfaces coaxially and provided with means facilitating admixture

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Medical Preparation Storing Or Oral Administration Devices (AREA)
  • Package Specialized In Special Use (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide an infusion container for communicating a drug container and a dissolving fluid container to each other in a single operation. SOLUTION: The upper part of a container body 1 with a liquid delivery means 4 containing a dissolving fluid and an elastic plug 3 on a lower end for allowing a puncture with an infusion needle and an air supply needle, is provided with a first separation means 5 having the whole of both side areas inscribed to the inner surface of the container body 1 and thermally fused thereto, and formed to be broken upon exposure to external pressure or the like. Furthermore, the container body 1 with a dissolved fluid chamber of large capacity is laid under the first separation means, together with a holder 9 connected to the upper part of the container body 1 and formed to have an opening at a lower end and an intermediate separation part 1e made of an upper movable holder 9a and a lower fixed holder 9b, and an inverted vial 10 housed in the holder 9, jointed to the upper movable holder 9a as part of the holder 9 and formed to be capable of removing the second separation means 11 fitted to a mouth 10a on the vertical motion of the upper movable holder 9a for communication to the container body 1.

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、点滴注射用輸液
容器に係る技術分野に属する。
TECHNICAL FIELD [0001] The present invention belongs to the technical field of an infusion container for infusion.

【0002】[0002]

【従来の技術】 従来この種点滴注射用輸液容器とし
て、内部に溶解液または希釈液が収納され、最上端に閉
鎖膜を有する液体通路部を有する可撓性容器と、該可撓
性容器に連結されたカプセルと、口部が刺通可能な栓で
密封されており、前記カプセル内に保持される薬剤容器
と、前記可撓性容器の内部と薬剤容器の内部とを連通す
る連通手段とからなり、前記連通手段が、中間にハブを
有し両端に刃先を有する中空の穿刺針と、該穿刺針の一
方の刃によって薬剤容器の栓が刺通された後、穿刺針の
他方の刃によって可撓性容器の閉鎖膜が刺通されるよう
に連通順序を制御する制動手段とによって構成されたも
のが知られている。(例えば、特開平2−1277号公
報参照) このような従来技術にあっては、可撓性容器の内部と薬
剤容器の内部とを連通させる手段が、中空の穿刺針によ
るため、両者間を交流する液の入出量が小量で、薬剤の
溶解速度が遅く多くの時間を要するとともに、構造が複
雑でコストが嵩み不経済である。
2. Description of the Related Art Conventionally, as an infusion container for infusion of this kind, a flexible container having a liquid passage portion containing a dissolving solution or a diluent therein and having a closed film at the uppermost end, A connected capsule, a medicine container whose mouth is sealed with a pierceable stopper, and held in the capsule; and a communication means for communicating between the inside of the flexible container and the inside of the medicine container. The communicating means comprises a hollow puncture needle having a hub in the middle and having a cutting edge at both ends, and after the stopper of the drug container is pierced by one of the puncture needles, the other blade of the puncture needle And a braking means for controlling the order of communication so that the closing membrane of the flexible container is pierced by the device. (See, for example, Japanese Patent Application Laid-Open No. 2-1277.) In such a conventional technique, since the means for communicating the inside of the flexible container with the inside of the medicine container is a hollow puncture needle, The amount of liquid flowing in and out is small, the dissolution rate of the drug is slow, and much time is required, and the structure is complicated, the cost is increased, and it is uneconomical.

【0003】又、上端に吊架手段を、下端に点滴針及び
通気針が刺通可能な弾性栓体を備え、かつ、可撓性樹脂
フィルム材料よりなる容器本体を、弱ヒートシールなど
により形成された易剥離性を有する隔壁手段にて複数室
に区劃分室し、使用時に容器本体を外部から押圧する
か、又は容器本体を構成する樹脂フィルムを引き離し方
向に引っ張ることにより、隔壁手段を容易に剥離して両
室を連通させ、薬剤を溶解させるようにした点滴注射用
輸液容器は知られている。(例えば、特公平6−265
63号公報,特開平1−240469号公報,特開平2
−4671号公報,特開平4−364850号公報,特
開平4−364851号公報,特開平6−14975号
公報参照) このような従来の点滴注射用輸液容器にあっては、容器
本体を易剥離性をもつ隔壁手段にて、例えば薬剤室,溶
解液室など複数室に分室している。この分室を構成する
隔壁手段は、樹脂フィルム同志のヒートシール温度を変
化させることにより、他のヒートシール部より弱い易剥
離性のヒートシール部によって構成されている。一般に
樹脂フィルムには厚さのバラツキがあり、又多層化する
場合は、各層それぞれに厚みのバラツキがあることか
ら、このバラツキから生じる弱ヒートシール状態の溶着
温度条件は樹脂フィルムのロット毎に変化し、たとえ同
ロットでも、これらの厚みのバラツキは巻きとられた樹
脂フィルム材料の部分部分に生じている。又ある一定の
押圧力で易剥離性を有する隔壁手段を剥離連通させるに
は、隔壁手段、詳しくは弱ヒートシール部を構成するめ
たの溶着圧力及び温度管理が非常に煩雑となり、薬剤及
び溶解液に対する長期安定保存を保証する容器の加工手
段としては、きわめて不安定である。このように、隔壁
手段、つまり弱ヒートシール部を形成することは非常に
デリケートであり、弱ヒートシール部の接着が強い場合
には、使用時の押圧ないしは引き離し作動によって容易
に剥離せず、又接着が弱い場合には、不本意に剥離さ
れ、輸液容器が使用不能となる事故の発生に連なること
がある。
Further, a container body made of a flexible resin film material is provided by a weak heat seal or the like, having a suspending means at an upper end, an elastic stopper at a lower end through which a drip needle and a ventilation needle can be pierced. The partitioning means is divided into a plurality of chambers by the partitioning means having easy peelability, and the partitioning means is easily formed by pressing the container body from outside at the time of use or pulling the resin film constituting the container body in the separating direction. There is known an infusion container for intravenous drip injection, which is peeled off to allow communication between the two chambers to dissolve the drug. (For example, Japanese Patent Publication No. 6-265
No. 63, JP-A-1-240469, JP-A-2-24069
-4671, JP-A-4-364850, JP-A-4-364851, and JP-A-6-14975. In such a conventional infusion container for drip injection, the container body is easily peeled off. The chamber is divided into a plurality of chambers such as a medicine chamber and a solution chamber by a partitioning means having a property. The partition means constituting this compartment is constituted by a heat-sealing portion which is weaker than other heat-sealing portions by changing the heat-sealing temperature of the resin films. In general, resin films have thickness variations, and when multiple layers are used, the thickness of each layer varies.Therefore, the welding temperature conditions in the weak heat sealing state resulting from these variations vary from resin film lot to lot. However, even in the same lot, these thickness variations occur in the portion of the wound resin film material. Also, in order to allow the partitioning means having easy peelability to communicate with a certain pressing force, the partitioning means, in particular, the welding pressure and temperature management of the weak heat seal portion become very complicated, and the medicine and the solution It is extremely unstable as a means of processing containers that guarantees long-term stable storage of the container. As described above, the formation of the partition means, that is, the weak heat seal portion, is very delicate, and when the weak heat seal portion has strong adhesion, it is not easily peeled off by a pressing or separating operation during use, and If the adhesion is weak, it may be unintentionally peeled off, which may lead to an accident that the infusion container becomes unusable.

【0004】本発明の目的は、ワンタッチ操作で薬剤容
器と溶解液容器の連通がなされるとともに、両室間の液
の交流量が多く、迅速な薬剤の溶解が行われ、点滴注射
効率の向上が図れる輸液容器を提供することにある。
An object of the present invention is to provide one-touch operation for communication between a drug container and a dissolving solution container, a large exchange of liquid between the two chambers, rapid dissolution of the drug, and an improvement in infusion efficiency. It is to provide an infusion container which can achieve the above.

【0005】[0005]

【課題を解決するための手段】 上記目的は、内部に溶
解液が収容され、下端に点滴注射針及び通気針が刺通可
能な弾性栓体を備えた吐液手段を付設せる可撓性樹脂材
料よりなる容器本体の上部に、容器本体を構成する可撓
性樹脂材料の内面に接する両側板面全域が熱溶着され、
かつ外部圧力などで破壊される第1の隔離手段を付設
し、この第1の隔離手段の下方に大容量の溶解液室を形
成した容器本体と、容器本体の上部に連結され下端に開
口部を設けるとともに、中途離間部が圧縮変形可能な液
密構造で連結された上部可動ホルダーと下部固定ホルダ
ーにより構成せるバイアルより長尺なホルダーと、ホル
ダー内に収容され、このホルダーを構成する上部可動ホ
ルダーに連結されるとともに、この上部可動ホルダーの
上下動作用によりびん口に付設した第2の隔離手段を除
去し、容器本体と連通しうるようにした倒立姿勢のバイ
アルとにより構成したことにより達成される。上記目的
は、請求項1において、第2の隔離手段を、下部固定ホ
ルダーの内面に形成した突起上面に、びん口に施栓せる
ゴム中栓の周縁が仮支持されるとともに、上部ホルダー
の下降下限時にゴム中栓の周縁が突起の下面に対応し、
上部可動ホルダーの上昇復帰時にゴム中栓の周縁が突起
の下面に係合してびん口から抜脱除去され、バイアルと
容器本体とが連通しうるよう構成したことにより達成さ
れる。上記目的は、請求項1において、第2の隔離手段
を、下部固定ホルダーの内面に形成した突起上面に、び
ん口に被嵌したキャップの周縁が仮支持されるととも
に、上部可動ホルダーの下降下限時にキャップの周縁が
突起の下面に対応し、上部可動ホルダーの上昇復帰時に
キャップの周縁が突起の下面に係合してびん口から抜脱
除去され、バイアルと容器本体とが連通しうるよう構成
したことにより達成される。上記目的は、請求項1にお
いて、第2の隔離手段を、下部固定ホルダーの内面に形
成した突起上面に、びん口周縁が仮支持されるととも
に、びん口に施栓したゴム中栓をバイアル内に突き上げ
押込む押込み体を下部固定ホルダーの下底部に設け、ゴ
ム中栓の押込みによりバイアルと容器本体とが連通しう
るよに構成したことにより達成される。上記目的は、請
求項1〜請求項4の何れかにおいて、吐液手段を構成す
る弾性栓体より上位に、異物類を除去する濾過手段を設
けたことにより達成される。
The object of the present invention is to provide a flexible resin in which a dissolving solution is accommodated inside and a discharge means having an elastic stopper at the lower end through which a drip injection needle and a ventilation needle can be pierced. On the upper part of the container body made of the material, the entire area of both side plate surfaces in contact with the inner surface of the flexible resin material constituting the container body is heat-welded,
A first isolating means which is destroyed by external pressure or the like, and a container body having a large-volume solution chamber formed below the first isolating means; And a holder longer than the vial composed of an upper movable holder and a lower fixed holder whose middle part is connected with a liquid-tight structure that can be compressed and deformed, and an upper movable part that is housed in the holder and constitutes this holder Achieved by the fact that the upper movable holder is connected to the holder, and the upper isolation holder is removed from the second isolation means attached to the bottle opening, so that the upper movable holder can communicate with the container body. Is done. The object of the present invention is to provide a method as set forth in claim 1, wherein the second isolating means is temporarily supported on the upper surface of a projection formed on the inner surface of the lower fixing holder, while the peripheral edge of the rubber inner plug which can be plugged into the bottle opening is lowered. Sometimes the periphery of the rubber plug corresponds to the underside of the projection,
This is achieved by the configuration in which the peripheral edge of the rubber inner plug engages with the lower surface of the projection and is removed from the bottle opening when the upper movable holder returns to the ascending position, so that the vial and the container body can communicate with each other. The object of the present invention is to provide a method as set forth in claim 1, wherein the second isolating means is provided on the upper surface of the projection formed on the inner surface of the lower fixed holder, the periphery of the cap fitted to the bottle opening is temporarily supported, and the lower limit of lowering of the upper movable holder is reduced. Occasionally, the peripheral edge of the cap corresponds to the lower surface of the protrusion, and when the upper movable holder rises and returns, the peripheral edge of the cap engages with the lower surface of the protrusion and is removed from the bottle opening so that the vial and the container body can communicate with each other. It is achieved by doing. The object of the present invention is to provide a method as set forth in claim 1, wherein the second isolating means is provided with a rubber stopper inserted into the vial, the periphery of the bottle opening being temporarily supported on the projection upper surface formed on the inner surface of the lower fixing holder. This is achieved by providing a pushing body for pushing up and pushing down on the lower bottom portion of the lower fixed holder so that the vial and the container body can communicate with each other by pushing in the rubber stopper. The above object is achieved by providing, in any one of claims 1 to 4, a filtering means for removing foreign substances above the elastic plug constituting the liquid discharging means.

【0006】[0006]

【発明の実施の形態】 図面について本発明実施の形態
を説明する。図1は本発明輸液容器の第1実施例を示す
一部切欠正面図、図2はバイアルの未連通姿勢を示す一
部切欠拡大正面図、図3はバイアルの連通姿勢を示す一
部切欠拡大正面図、図4は第1の隔離手段の一例を示す
斜視図、図5は第1の隔離手段の区劃状態の縦断側面
図、図6は輸液容器の第2実施例を示す一部切欠正面
図、図7はバイアルの未連通姿勢を示す一部切欠拡大正
面図、図8はバイアルの連通姿勢を示す一部切欠拡大正
面図、図9は輸液容器の第3実施例を示す一部切欠正面
図、図10はバイアルの未連通姿勢を示す一部切欠拡大
正面図、図11はバイアルの連通姿勢を示す一部切欠拡
大正面図である。
Embodiments of the present invention will be described with reference to the drawings. FIG. 1 is a partially cutaway front view showing a first embodiment of the infusion container of the present invention, FIG. 2 is a partially cutaway enlarged front view showing a non-communicating posture of a vial, and FIG. 3 is a partially cutout enlarged view showing a vial communicating posture. FIG. 4 is a perspective view showing an example of the first isolating means, FIG. 5 is a longitudinal sectional side view of the partitioned state of the first isolating means, and FIG. 6 is a partially cutaway view showing a second embodiment of the infusion container. Front view, FIG. 7 is a partially cut-away enlarged front view showing a vial unconnected position, FIG. 8 is a partially cut-out enlarged front view showing a vial connected position, and FIG. 9 is a partial view showing a third embodiment of an infusion container. FIG. 10 is a partially cutaway enlarged front view showing a non-communicating posture of the vial, and FIG. 11 is a partially cutout enlarged front view showing a vial communicating posture.

【0007】図1〜図5について本発明第1実施例の詳
細を説明する。Aは点滴注射用の輸液容器本体であっ
て、該輸液容器本体Aは、溶解液が収容される容器本体
1と、これの上部に連結されるバイアルが収容される薬
剤容体2とによって構成されている。
The first embodiment of the present invention will be described in detail with reference to FIGS. A is an infusion container main body for drip injection. The infusion container main body A is composed of a container main body 1 in which a solution is stored and a medicine container 2 in which a vial connected to an upper portion thereof is stored. ing.

【0008】容器本体1は、可撓性をもつ2枚の単層又
は複合樹脂フィルム1aをヒートシール1bしたものに
よって構成され、この容器本体1の下端に、点滴注射針
(図示略)及び通気針(図示略)が刺通可能なゴム栓3
を下端開口部に液密的に施栓した円筒構造の吐液体4が
液密的に熱溶着1cされている。
The container body 1 is formed by heat-sealing two flexible single-layer or composite resin films 1a. A drip injection needle (not shown) and a vent are provided at the lower end of the container body 1. Rubber stopper 3 through which needle (not shown) can be inserted
Is liquid-tightly heat-sealed 1c.

【0009】容器本体1の上方内部の全巾領域を、この
容器本体1を構成する樹脂フィルム1aの内面に接する
両面全域が熱溶着5aされ、かつ外部からの押圧力,衝
打力などで破壊され、第1の隔離手段を構成する連通部
材5によって隔離するとともに、この連通部材5の上方
には小容量の空室6が、又連通部材5の下側には薬剤量
に適応した溶解液を封入する溶解液室7を形成したもの
である。
The entire width region inside the upper portion of the container body 1 is thermally welded 5a to both surfaces in contact with the inner surface of the resin film 1a constituting the container body 1, and is broken by external pressing force, impact force, or the like. In addition, the isolation member is isolated by a communication member 5 constituting a first isolation means, and a small-capacity empty chamber 6 is provided above the communication member 5, and a dissolving solution adapted to the amount of drug is provided below the communication member 5. Is formed in a dissolving solution chamber 7 for enclosing.

【0010】吐液体4の上端部には、前記連通部材5の
破壊連通時に生ずる破片などの異物類を除去するフィル
ター部材8を設ける。このフィルター部材8にはバクテ
リアなどの濾過による滅菌又は減菌の機能を付与するこ
とができる。
At the upper end of the discharge liquid 4, a filter member 8 is provided for removing foreign matter such as debris generated when the communication member 5 breaks and communicates. The filter member 8 can be provided with a sterilizing or sterilizing function by filtering bacteria or the like.

【0011】図4〜図5について前記連通部材5の構成
の一例を説明する。この連通部材5は、工具類を使用せ
ずに手で比較的容易に破壊できる樹脂材料などで構成す
るとともに、破壊時の破片などによって容器本体1の樹
脂フィルム1aが破損しないものを選択する必要があ
る。このため破壊部分を中央部に集約するために、連通
部材5の断面形状をM字形,N字形、あるいは将棋の駒
形状とするなど、樹脂フィルム1aに熱溶着される両面
に比較的広巾の板部5bが存在し、この板部5b間に屈
折された易破壊性部分5cを設けたボックス形状とする
ことが望ましい。又連通部材5の両端部には、熱溶着5
aを確立するために、両端がナイフエッジ形状となる傾
斜面5dを形成せしめたものである。尚、この連通部材
5の形状構造は、図示以外のものでも易破壊性が得られ
ることから、図示実施例に特定されることはない。
An example of the structure of the communication member 5 will be described with reference to FIGS. The communication member 5 must be made of a resin material that can be relatively easily broken by hand without using tools, and a material that does not damage the resin film 1a of the container body 1 due to debris at the time of breaking must be selected. There is. For this reason, in order to consolidate the destruction part in the center, the cross-sectional shape of the communication member 5 is M-shaped, N-shaped, or a piece of shogi piece. It is desirable to have a box shape in which the portion 5b is present and the bent easily destructible portion 5c is provided between the plate portions 5b. Further, a heat welding 5 is provided at both ends of the communication member 5.
In order to establish a, an inclined surface 5d having both ends in a knife edge shape is formed. The shape and structure of the communication member 5 are not limited to the illustrated embodiment, since the shape and structure of the communication member 5 can be easily broken even if they are not shown.

【0012】容器本体1の上辺に連設された前記薬剤容
体2には、中途離間部が樹脂フィルム1aのヒートシー
ル1b部によって連結され、かつ円筒キャップ構造の上
部可動ホルダー9aと、下部固定ホルダー9bによって
構成したホルダー9を収容する。上部可動ホルダー9a
の外周と下部固定ホルダー9bの外周は夫々樹脂フィル
ム1aに熱溶着1dされている。又上部可動ホルダー9
aと下部固定ホルダー9bの上半部の内径は、これの内
部に収容されるバイアル10と略同径とし、下部固定ホ
ルダー9bの下半部に、バイアル10のびん口10a径
よりやや径大で下端が開口されたバイアル介入筒部9c
を形成する。又バイアル10のびん口10aには、抜脱
可能で外径がびん口10aよりやや径大で、前記バイア
ル介入筒部9cより少し径小な鍔11aを一体形成した
ゴム中栓11が施栓されている。9dは上部可動ホルダ
ー9aの内面に形成したリング構造の凸条で、この凸条
10dはバイアル10に形成せる凹溝10bに係合して
いる。図中12は吊架リング,1eは樹脂フィルム1a
によって形成された圧縮変形可能部である。
The medicine container 2 connected to the upper side of the container body 1 is connected to the medicine container 2 by a heat seal 1b of the resin film 1a, and has an upper movable holder 9a having a cylindrical cap structure and a lower fixed holder. 9b is accommodated. Upper movable holder 9a
And the outer periphery of the lower fixed holder 9b are thermally welded 1d to the resin film 1a, respectively. Upper movable holder 9
a and the inner diameter of the upper half of the lower fixing holder 9b are substantially the same as the diameter of the vial 10 accommodated therein, and the lower half of the lower fixing holder 9b is slightly larger than the diameter of the vial 10a of the vial 10. Vial intervention cylinder 9c with open lower end
To form In addition, the vial 10a of the vial 10 is capped with a rubber stopper 11 that is integrally formed with a flange 11a that is removable and has a slightly larger outer diameter than the vial 10a and a diameter slightly smaller than the vial intervention cylinder 9c. ing. Reference numeral 9d denotes a ring-shaped ridge formed on the inner surface of the upper movable holder 9a. The ridge 10d is engaged with a concave groove 10b formed in the vial 10. In the figure, 12 is a suspension ring, 1e is a resin film 1a.
Is a compressively deformable portion formed by

【0013】ホルダー9を構成するバイアル介入筒部9
cの中間部内面に、ゴム中栓11の鍔11a外周下面周
縁が係合し、バイアル10を仮支持する及びゴム中栓1
1をびん口10aから抜脱する作用をもつ突起13を設
け、更にバイアル介入筒部9cの下端開口部周縁に、抜
脱されたゴム中栓11が容器本体1内に介入するのを防
止するフランジ9eが設けられている。
The vial intervention cylinder 9 constituting the holder 9
c, the inner peripheral surface of the flange 11a of the rubber plug 11 is engaged with the inner surface of the intermediate portion to temporarily support the vial 10 and the rubber plug 1
A projection 13 having an action of withdrawing the vial 1 from the bottle opening 10a is provided, and furthermore, the removed rubber plug 11 is prevented from intervening in the container body 1 around the lower end opening of the vial intervention cylinder 9c. A flange 9e is provided.

【0014】ホルダー9を構成する上部可動ホルダー9
aの下端と、下部固定ホルダー9bの上面との圧縮間隔
長、詳しくは、圧縮変形可能部1eの長さは、バイアル
介入筒部9cに設けた突起13とフランジ9eとの距離
より若干大きく形成するとともに、突起13とフランジ
9e間の距離をゴム中栓11の鍔11aの肉厚より大き
く形成し、ゴム中栓11が遊動し溶解液が容易に流通し
うるようにしたものである。
Upper movable holder 9 constituting holder 9
The length of the compression interval between the lower end of a and the upper surface of the lower fixed holder 9b, more specifically, the length of the compressively deformable portion 1e, is slightly larger than the distance between the projection 13 provided on the vial intervention cylinder 9c and the flange 9e. At the same time, the distance between the projection 13 and the flange 9e is formed larger than the thickness of the flange 11a of the rubber plug 11, so that the rubber plug 11 moves and the solution can easily flow.

【0015】[0015]

【取扱いの説明】 患者に点滴注射する場合には、卓上
に容器本体1を適宜に載置し、この状態で第1の隔離手
段の隔離解除を行なう。即ち、容器本体1に付設されて
いる連通部材5上に手の掌を当て押圧すると、連通部材
5の易破壊性部分5cが破壊され、空室6と溶解液室7
が連通状態となる。次に第2の隔離手段の隔離を解除す
る。即ち、例えば、下部固定ホルダー9bを左手で把持
し、右手で上部可動ホルダー9aに下降動作を加える
と、バイアル10のびん口10aに施栓したゴム中栓1
1が突起13を乗り越えると同時に、ゴム中栓11の下
面がバイアル介入筒部9cのフランジ9eに当接するま
でバイアル10は下降する。この状態で上部可動ホルダ
ー9aを上昇させると、突起13にゴム中栓11の鍔1
1a部周縁が係止し、ゴム中栓11の上昇復帰は阻止さ
れ、バイアル10が上昇復帰上限、即ち元の位置に復帰
する位置でゴム中栓11は、図3で示すように完全に抜
脱せしめられ、バイアル10の内部と容器本体1の溶解
液室7の内部とは連通状態となる。容器本体1に形成し
た溶解液室7内の溶解液がバイアル10内に流入し、薬
剤は溶解液によって溶解され、得られた薬剤液を常法に
より点滴注射する。このとき、連通部材5の破壊及びゴ
ム中栓11の摺動下降,びん口10aよりの抜脱作用な
どにより生じた破片などの異物類は、フィルター部材8
によって完全に除去され、有効薬剤成分のみが人体など
に点滴注射される。
[Explanation of Handling] When injecting a drip into a patient, the container main body 1 is appropriately placed on a table, and the isolation of the first isolation means is released in this state. That is, when the palm of the hand is pressed against the communication member 5 attached to the container body 1 and pressed, the easily breakable portion 5c of the communication member 5 is destroyed, and the empty chamber 6 and the solution chamber 7 are separated.
Becomes a communication state. Next, the isolation of the second isolation means is released. That is, for example, when the lower fixed holder 9b is gripped by the left hand and the lowering operation is applied to the upper movable holder 9a by the right hand, the rubber plug 1 plugged into the vial 10a of the vial 10 is moved.
At the same time as 1 gets over the projection 13, the vial 10 descends until the lower surface of the rubber plug 11 comes into contact with the flange 9 e of the vial intervention cylinder 9 c. When the upper movable holder 9a is raised in this state, the protrusion 13
The peripheral edge of the portion 1a is locked, the rubber stopper 11 is prevented from returning upward, and the rubber stopper 11 is completely pulled out at the upper return limit of the vial 10, that is, at the position where it returns to the original position, as shown in FIG. After being removed, the inside of the vial 10 and the inside of the solution chamber 7 of the container body 1 are in communication with each other. The solution in the solution chamber 7 formed in the container body 1 flows into the vial 10, the drug is dissolved by the solution, and the obtained drug solution is instilled by a conventional method. At this time, foreign matter such as debris generated by destruction of the communication member 5, sliding down of the rubber plug 11, and withdrawal action from the bottle opening 10a are removed by the filter member 8
, And only the active drug component is instilled into a human body or the like.

【0016】図6〜図8について、本発明第2実施例の
詳細を説明する。この第2実施例は、前述した第1実施
例に対してバイアルのびん口に施したキャップ構造部分
が異なるのみで、他の構成は同一であるので、同一構造
部分に同一の符号を付すことにより詳細な説明は省略す
る。
The details of the second embodiment of the present invention will be described with reference to FIGS. The second embodiment is different from the first embodiment only in the cap structure applied to the vial opening of the vial, and the other structures are the same. A more detailed description will be omitted.

【0017】ホルダー9を構成するバイアル介入筒部9
cの内壁面上部に突起21を設け、一方、バイアル10
のびん口10aにゴム中栓22を内設せるキャップ23
を施蓋するとともに、このキャップ23の天壁外周縁部
を前記突起21の上面に仮支持させたものである。図中
23aは通液孔,24はキャップ43の外周とバイアル
介入筒部9cの壁面との間に形成される通液路である。
図6〜図8で示した第2実施例では、突起21の上面に
キャップ23の天壁外周縁部が仮支持されるようにした
が、キャップ23の外側壁中途部に段面(図示略)を形
成し、この段面を突起21に仮支持させることにより、
バイアル10の下降及び上昇ストロークを小さくするこ
とができることから、突起21に対するキャップ23の
仮支持部位は、図示実施例のものに特定されるものでな
い。
The vial intervention cylinder 9 constituting the holder 9
c, a projection 21 is provided on the upper part of the inner wall surface.
Cap 23 for inserting rubber stopper 22 into bottle opening 10a
And the outer peripheral edge of the top wall of the cap 23 is temporarily supported on the upper surface of the projection 21. In the figure, reference numeral 23a denotes a liquid passage, and 24 denotes a liquid passage formed between the outer periphery of the cap 43 and the wall surface of the vial intervention cylinder 9c.
In the second embodiment shown in FIGS. 6 to 8, the outer peripheral edge of the top wall of the cap 23 is temporarily supported on the upper surface of the projection 21. ) Is formed, and this step surface is temporarily supported by the projections 21.
Since the lowering and raising strokes of the vial 10 can be reduced, the temporary support portion of the cap 23 with respect to the projection 21 is not limited to that of the illustrated embodiment.

【0018】[0018]

【取扱いの説明】 患者に点滴注射する場合には、卓上
に容器本体1を適宜に載置し、この状態で第1の隔離手
段の隔離解除を行なう。即ち、容器本体1に付設されて
いる連通部材5上に手の掌を当て押圧すると、連通部材
5の易破壊性部分5cが破壊され、空室6と溶解液室7
が連通状態となる。次に第2の隔離手段の隔離を解除す
る。即ち、例えば、下部固定ホルダー9bを左手で把持
し、右手で上部可動ホルダー9aに下降動作を加える
と、バイアル10のびん口10aに施蓋したキャップ2
3の周縁が突起21を乗り越えると同時に、キャップ2
3の下面がバイアル介入筒部9cのフランジ9eに当接
するまでバイアル10は下降する。この状態で上部可動
ホルダー9aを上昇させると、突起21にキャップ23
の裾端縁面が係止し、キャップ23の上昇復帰は阻止さ
れ、バイアル10が上昇復帰上限、即ち元の位置に復帰
する位置でゴム中栓22及びキャップ23が図8で示す
ように完全に抜脱せしめられ、バイアル10の内部と容
器本体1の溶解液室7の内部とは連通状態となる。容器
本体1に形成した溶解液室7内の溶解液がバイアル10
内に流入し、薬剤は溶解液によって溶解され、得られた
薬剤液を常法により点滴注射する。このとき、連通部材
5の破壊及びキャップ23の摺動下降,びん口10aよ
りの抜脱作用などにより生じた破片などの異物類は、フ
ィルター部材8によって完全に除去され、有効薬剤成分
のみが人体などに点滴注射される。
[Explanation of Handling] When injecting a drip into a patient, the container main body 1 is appropriately placed on a table, and the isolation of the first isolation means is released in this state. That is, when the palm of the hand is pressed against the communication member 5 attached to the container body 1 and pressed, the easily breakable portion 5c of the communication member 5 is destroyed, and the empty chamber 6 and the solution chamber 7 are separated.
Becomes a communication state. Next, the isolation of the second isolation means is released. That is, for example, when the lower fixed holder 9b is grasped with the left hand and the lower movable holder 9a is lowered with the right hand, the cap 2 covering the vial 10a of the vial 10 is moved.
At the same time as the peripheral edge of 3
The vial 10 descends until the lower surface of 3 contacts the flange 9e of the vial intervention cylinder 9c. When the upper movable holder 9a is raised in this state, the cap 23
And the cap 23 is prevented from rising and returning, and the rubber stopper 22 and the cap 23 are completely closed as shown in FIG. Then, the inside of the vial 10 and the inside of the solution chamber 7 of the container body 1 are in communication with each other. The solution in the solution chamber 7 formed in the container body 1 is filled with the vial 10
Then, the drug is dissolved by the dissolving solution, and the obtained drug solution is instilled by an ordinary method. At this time, foreign matter such as debris generated by destruction of the communication member 5, sliding down of the cap 23, and withdrawal from the bottle opening 10a is completely removed by the filter member 8, and only the effective drug component is removed from the human body. Intravenous injection is given.

【0019】次に、図9〜図11について、本発明第3
実施例の詳細を説明する。この第3実施例は、前述した
第1,第2実施例とは異なり、ゴム中栓又はキャップを
抜脱外脱させずに、バイアルの下降動作のみでバイアル
のゴム中栓をバイアル内に押込むように構成した点、即
ち第2の隔離手段の構成が異なるのみで、他の構成は前
述の各実施例と同一であることから、同一構造部分につ
いては同一の符号を付すことにより詳細な説明は省略す
る。
Next, referring to FIG. 9 to FIG.
The details of the embodiment will be described. In the third embodiment, unlike the first and second embodiments, the rubber stopper of the vial is pushed into the vial only by the lowering operation of the vial without removing and removing the rubber stopper or the cap. Since the other configuration is the same as that of each of the above-described embodiments, except that the configuration is different, that is, only the configuration of the second isolating means is different, detailed description is given by assigning the same reference numerals to the same structural portions. Omitted.

【0020】ホルダー9を構成するバイアル介入筒部9
cの内壁面上部にバイアル10のびん口10a周縁が仮
支持される突起31を設け、一方、バイアル10のびん
口10aに押込み可能に構成したゴム中栓32を施栓す
るとともに、びん口10aの口径より径小の円筒構造の
押込み体33を前記バイアル介入筒部9cの底壁に立設
したものである。図中9f,9gは押込み体33の内外
に形成した通液孔である。
The vial intervention cylinder 9 constituting the holder 9
In the upper portion of the inner wall surface of the vial 10, a projection 31 is provided for temporarily supporting the periphery of the vial 10a of the vial 10. On the other hand, a rubber inner plug 32 which can be pushed into the vial 10a of the vial 10 is plugged, and the vial 10a is closed. A pusher 33 having a cylindrical structure smaller in diameter than the caliber is erected on the bottom wall of the vial intervention cylinder 9c. In the drawing, 9 f and 9 g are liquid passage holes formed inside and outside the pushing body 33.

【0021】[0021]

【取扱いの説明】 患者に点滴注射する場合には、卓上
に容器本体1を適宜に載置し、この状態で第1の隔離手
段の隔離解除を行なう。即ち、容器本体1に付設されて
いる連通部材5上に手の掌を当て押圧すると、連通部材
5の易破壊性部分5cが破壊され、空室6と溶解液室7
が連通状態となる。次に第2の隔離手段の隔離を解除す
る。即ち、例えば、下部固定ホルダー9bを左手で把持
し、右手で上部可動ホルダー9aに下降動作を加える
と、バイアル10のびん口10a周縁が突起31を乗り
越えると同時に、ゴム中栓32の下面中央が押込み体3
3に押しつけられ、この作用でゴム中栓32はバイアル
10の内に押し込まれるとともに、びん口10aの下面
がバイアル介入筒部9cのフランジ9eに当接するまで
バイアル10は下降する。この状態でバイアル10の内
部と容器本体1の溶解液室7の内部とは連通状態とな
る。容器本体1に形成した溶解液室7内の溶解液がバイ
アル10内に流入し、薬剤は溶解液によって溶解され、
得られた薬剤液を常法により点滴注射する。このとき、
連通部材5の破壊及びゴム中栓32の押込み作用などに
より生じた破片などの異物類は、フィルター部材8によ
って完全に除去され、有効薬剤成分のみが人体などに点
滴注射される。
[Explanation of Handling] When injecting a drip into a patient, the container main body 1 is appropriately placed on a table, and the isolation of the first isolation means is released in this state. That is, when the palm of the hand is pressed against the communication member 5 attached to the container body 1 and pressed, the easily breakable portion 5c of the communication member 5 is destroyed, and the empty chamber 6 and the solution chamber 7 are separated.
Becomes a communication state. Next, the isolation of the second isolation means is released. That is, for example, when the lower fixed holder 9b is grasped with the left hand and the lower movable holder 9a is lowered with the right hand, the peripheral edge of the vial 10a of the vial 10 goes over the projection 31 and the center of the lower surface of the rubber plug 32 is Push body 3
3, the rubber inner plug 32 is pushed into the vial 10 by this action, and the vial 10 descends until the lower surface of the bottle opening 10a contacts the flange 9e of the vial intervention cylinder 9c. In this state, the inside of the vial 10 and the inside of the solution chamber 7 of the container body 1 are in communication. The solution in the solution chamber 7 formed in the container body 1 flows into the vial 10, and the drug is dissolved by the solution,
The obtained drug solution is instilled by a conventional method. At this time,
Foreign matter such as debris generated by the destruction of the communication member 5 and the pushing action of the rubber plug 32 is completely removed by the filter member 8, and only the effective drug component is injected by instillation into a human body or the like.

【0022】[0022]

【発明の効果】 上述のように本発明の構成によれば、
次のような効果が得られる。 (a)第1及び第2の隔離手段が同時に解除されない限
り、薬剤と溶解液が交流することがないことから、薬剤
及び溶解液の長期保存効果が簡単な構成によって確実に
保証される。 (b)第1及び第2の隔離手段の隔離解除によって生じ
る破片などの異物類は、フィルター部材によって完全に
除去することができ、異物が体内に注射される不安は全
くない。
According to the configuration of the present invention as described above,
The following effects can be obtained. (A) As long as the first and second isolation means are not simultaneously released, the drug and the solution do not interact with each other, so that the long-term storage effect of the drug and the solution can be reliably ensured by a simple configuration. (B) Foreign matter such as debris generated by the release of the first and second isolation means can be completely removed by the filter member, and there is no fear that the foreign matter is injected into the body.

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

【図1】 本発明輸液容器の第1実施例を示す一部切欠
正面図である。
FIG. 1 is a partially cutaway front view showing a first embodiment of the infusion container of the present invention.

【図2】 バイアルの未連通姿勢を示す一部切欠拡大正
面図である。
FIG. 2 is a partially cutaway enlarged front view showing a non-communicating posture of a vial.

【図3】 バイアルの連通姿勢を示す一部切欠拡大正面
図である。
FIG. 3 is a partially cutaway enlarged front view showing a communicating posture of a vial.

【図4】 第1の隔離手段の一例を示す斜視図である。FIG. 4 is a perspective view illustrating an example of a first isolation unit.

【図5】 第1の隔離手段の区劃状態の縦断側面図であ
る。
FIG. 5 is a vertical sectional side view of a partitioning state of the first isolating means.

【図6】 輸液容器の第2実施例を示す一部切欠正面図
である。
FIG. 6 is a partially cutaway front view showing a second embodiment of the infusion container.

【図7】 バイアルの未連通姿勢を示す一部切欠拡大正
面図である。
FIG. 7 is a partially cutaway enlarged front view showing a non-communicating posture of the vial.

【図8】 バイアルの連通姿勢を示す一部切欠拡大正面
図である。
FIG. 8 is a partially cutaway enlarged front view showing a communicating posture of the vial.

【図9】 輸液容器の第3実施例を示す一部切欠正面図
である。
FIG. 9 is a partially cutaway front view showing a third embodiment of the infusion container.

【図10】 バイアルの未連通姿勢を示す一部切欠拡大
正面図である。
FIG. 10 is a partially cutaway enlarged front view showing a non-communicating posture of the vial.

【図11】 バイアルの連通姿勢を示す一部切欠拡大正
面図である。
FIG. 11 is a partially cutaway enlarged front view showing a communicating posture of the vial.

【符号の説明】[Explanation of symbols]

A 輸液容器本体 1 容器本体 1a 単層又は複合樹脂フィルム 1b ヒートシール 1c 熱溶着 1d 熱溶着 1e 圧縮変形可能部 2 薬剤容体 3 ゴム栓 4 吐液体 5 連通部材 5a 熱溶着 5b 板部 5c 易破壊性部分 5d 傾斜面 6 空室 6a びん口 7 溶解液室 7a 鍔 8 フィルター部材 9 ホルダー 9a 上部可動ホルダー 9b 下部固定ホルダー 9c バイアル介入筒部 9d リング構造の凸条 9e フランジ 9f 通液孔 9g 通液孔 10 バイアル 10a びん口 11 ゴム中栓 11a 鍔 12 吊架リング 13 突起 21 突起 22 ゴム中栓 23 キャップ 24 通液路 31 突起 32 ゴム中栓 33 押込み体 43 キャップ A Infusion container main body 1 Container main body 1a Single layer or composite resin film 1b Heat seal 1c Heat welding 1d Heat welding 1e Compressible deformable part 2 Drug container 3 Rubber stopper 4 Discharge liquid 5 Communication member 5a Heat welding 5b Plate part 5c Fragility Part 5d Inclined surface 6 Vacancy 6a Bottle mouth 7 Dissolution liquid chamber 7a Flange 8 Filter member 9 Holder 9a Upper movable holder 9b Lower fixed holder 9c Vial intervention cylinder 9d Ring-shaped protrusion 9e Flange 9f Liquid passage 9g Liquid passage DESCRIPTION OF SYMBOLS 10 Vial 10a Bottle opening 11 Rubber stopper 11a Flange 12 Suspension ring 13 Projection 21 Projection 22 Rubber stopper 23 Cap 24 Liquid passage 31 Projection 32 Rubber stopper 33 Push body 43 Cap

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 内部に溶解液が収容され、下端に点滴注
射針及び通気針が刺通可能な弾性栓体を備えた吐液手段
を付設せる可撓性樹脂材料よりなる容器本体の上部に、
容器本体を構成する可撓性樹脂材料の内面に接する両側
板面全域が熱溶着され、かつ外部圧力などで破壊される
第1の隔離手段を付設し、この第1の隔離手段の下方に
大容量の溶解液室を形成した容器本体と、 容器本体の上部に連結され下端に開口部を設けるととも
に、中途離間部が圧縮変形可能な液密構造で連結された
上部可動ホルダーと下部固定ホルダーにより構成せるバ
イアルより長尺なホルダーと、 ホルダー内に収容され、このホルダーを構成する上部可
動ホルダーに連結されるとともに、この上部可動ホルダ
ーの上下動作用によりびん口に付設した第2の隔離手段
を除去し、容器本体と連通しうるようにした倒立姿勢の
バイアルと、 により構成したことを特徴とする点滴注射用輸液容器。
1. An upper portion of a container body made of a flexible resin material, in which a dissolving solution is accommodated and a discharging means having an elastic stopper body through which a drip injection needle and a ventilation needle can be pierced is provided at a lower end. ,
A first isolating means which is entirely welded to the inner surfaces of the flexible resin material constituting the container body and which is thermally welded and is destroyed by external pressure or the like is provided, and a first isolating means is provided below the first isolating means. An upper movable holder and a lower fixed holder that are connected to the upper part of the container body and have an opening at the lower end, and the middle part is connected with a liquid-tight structure that can be compressed and deformed. A holder which is longer than the vial to be constituted, and which is accommodated in the holder, is connected to the upper movable holder which constitutes the holder, and is provided with a second isolating means attached to the bottle opening for vertically moving the upper movable holder. An infusion container for drip injection, comprising: an inverted vial that is removed and can communicate with the container body.
【請求項2】 請求項1において、第2の隔離手段を、
下部固定ホルダーの内面に形成した突起上面に、びん口
に施栓せるゴム中栓の周縁が仮支持されるとともに、上
部ホルダーの下降下限時にゴム中栓の周縁が突起の下面
に対応し、上部可動ホルダーの上昇復帰時にゴム中栓の
周縁が突起の下面に係合してびん口から抜脱除去され、
バイアルと容器本体とが連通しうるよう構成したことを
特徴とする点滴注射用輸液容器。
2. The method according to claim 1, wherein the second isolating means comprises:
The periphery of the rubber plug that can be plugged into the bottle mouth is temporarily supported on the upper surface of the projection formed on the inner surface of the lower fixed holder, and the lower edge of the upper holder corresponds to the lower edge of the rubber plug at the lower limit of the upper holder, allowing the upper part to move At the time of return of the holder, the peripheral edge of the rubber inner plug engages with the lower surface of the projection and is removed from the bottle opening and removed.
An infusion container for drip injection, characterized in that the vial and the container main body can communicate with each other.
【請求項3】 請求項1において、第2の隔離手段を、
下部固定ホルダーの内面に形成した突起上面に、びん口
に被嵌したキャップの周縁が仮支持されるとともに、上
部可動ホルダーの下降下限時にキャップの周縁が突起の
下面に対応し、上部可動ホルダーの上昇復帰時にキャッ
プの周縁が突起の下面に係合してびん口から抜脱除去さ
れ、バイアルと容器本体とが連通しうるよう構成したこ
とを特徴とする点滴注射用輸液容器。
3. The method according to claim 1, wherein the second isolating means comprises:
On the upper surface of the projection formed on the inner surface of the lower fixed holder, the periphery of the cap fitted to the bottle opening is temporarily supported, and at the lower limit of the lowering of the upper movable holder, the periphery of the cap corresponds to the lower surface of the projection, An infusion container for drip injection, wherein the peripheral edge of the cap is engaged with the lower surface of the projection to be pulled out and removed from the vial at the time of returning to elevation, so that the vial and the container body can communicate with each other.
【請求項4】 請求項1において、第2の隔離手段を、
下部固定ホルダーの内面に形成した突起上面に、びん口
周縁が仮支持されるとともに、びん口に施栓したゴム中
栓をバイアル内に突き上げ押込む押込み体を下部固定ホ
ルダーの下底部に設け、ゴム中栓の押込みによりバイア
ルと容器本体とが連通しうるよに構成したことを特徴と
する点滴注射用輸液容器。
4. The method according to claim 1, wherein the second isolating means comprises:
On the upper surface of the projection formed on the inner surface of the lower fixing holder, the periphery of the bottle opening is temporarily supported, and a pusher that pushes up and pushes the rubber inner plug plugged into the bottle opening into the vial is provided at the lower bottom of the lower fixing holder, An infusion container for drip injection, characterized in that the vial and the container body can communicate with each other by pushing the inner stopper.
【請求項5】 請求項1〜請求項4の何れかにおいて、
吐液手段を構成する弾性栓体より上位に、異物類を除去
する濾過手段を設けたことを特徴とする点滴注射用輸液
容器。
5. In any one of claims 1 to 4,
An infusion container for drip injection, characterized in that a filtering means for removing foreign substances is provided above the elastic stopper constituting the liquid discharging means.
JP08327752A 1996-11-22 1996-11-22 Infusion container for infusion Expired - Fee Related JP3128756B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP08327752A JP3128756B2 (en) 1996-11-22 1996-11-22 Infusion container for infusion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP08327752A JP3128756B2 (en) 1996-11-22 1996-11-22 Infusion container for infusion

Publications (2)

Publication Number Publication Date
JPH10151176A true JPH10151176A (en) 1998-06-09
JP3128756B2 JP3128756B2 (en) 2001-01-29

Family

ID=18202597

Family Applications (1)

Application Number Title Priority Date Filing Date
JP08327752A Expired - Fee Related JP3128756B2 (en) 1996-11-22 1996-11-22 Infusion container for infusion

Country Status (1)

Country Link
JP (1) JP3128756B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016045599A1 (en) * 2014-09-25 2016-03-31 胡绍勤 Precise filtering transfusion container
WO2017107599A1 (en) * 2015-12-22 2017-06-29 胡绍勤 Precision filter infusion set
WO2017113904A1 (en) * 2015-12-29 2017-07-06 胡绍勤 Precision filtering infusion container
WO2017113906A1 (en) * 2015-12-29 2017-07-06 胡绍勤 Infusion container

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016045599A1 (en) * 2014-09-25 2016-03-31 胡绍勤 Precise filtering transfusion container
WO2017107599A1 (en) * 2015-12-22 2017-06-29 胡绍勤 Precision filter infusion set
WO2017107600A1 (en) * 2015-12-22 2017-06-29 胡绍勤 Precise filtering infusion container
WO2017113904A1 (en) * 2015-12-29 2017-07-06 胡绍勤 Precision filtering infusion container
WO2017113906A1 (en) * 2015-12-29 2017-07-06 胡绍勤 Infusion container
WO2017113907A1 (en) * 2015-12-29 2017-07-06 胡绍勤 Infusion container

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