JPH02255148A - Double chamber container - Google Patents

Double chamber container

Info

Publication number
JPH02255148A
JPH02255148A JP1077391A JP7739189A JPH02255148A JP H02255148 A JPH02255148 A JP H02255148A JP 1077391 A JP1077391 A JP 1077391A JP 7739189 A JP7739189 A JP 7739189A JP H02255148 A JPH02255148 A JP H02255148A
Authority
JP
Japan
Prior art keywords
chamber
container
irradiated
electron beam
liquid
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
JP1077391A
Other languages
Japanese (ja)
Other versions
JP2796727B2 (en
Inventor
Shinobu Nakajima
忍 中島
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.)
NIPPON SEIYAKU KK
Original Assignee
NIPPON SEIYAKU 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 NIPPON SEIYAKU KK filed Critical NIPPON SEIYAKU KK
Priority to JP1077391A priority Critical patent/JP2796727B2/en
Publication of JPH02255148A publication Critical patent/JPH02255148A/en
Application granted granted Critical
Publication of JP2796727B2 publication Critical patent/JP2796727B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Medical Preparation Storing Or Oral Administration Devices (AREA)

Abstract

PURPOSE:To facilitate the mixing of components and preparations at the time of use by forming a double chamber container of radiation crosslinkable plastic, irradiating at least a part of a partition part to form a part irradiated with an electron beam and adhering this part by heating or press welding the same by clamping. CONSTITUTION:Two sheets of, for example, low-density polyethylene 1 which is the material crosslinkable by irradiation of radiations are superposed and the circumference thereof exclusive of liquid introducing ports 3 and 3' is sealed by thermal welding and thereafter, the central part of this container is irradiated with the electron beam to cause the crosslinking reaction of the polyethylene and to form the part 4 irradiated with the electron beam. The center of this part 4 irradiated with the electron beam is adhered by heating to provide the partition part 5. The double chamber container for transfusion is thus produced. A saccharoelectrolysis liquid is introduced from the introducing port 3 into the chamber A if this container and an amino acid liquid is introduced from the introducing port 3' into the chamber B. After the ports 3 apd 3' are sealed, the container is heated to execute a sterilization treatment. The partition part 5 is peeled when either of the chamber A or the chamber is pushed by hand. The chamber A and the chamber B are then communicated with each other and the liquids in both the chambers are easily mixed with each other.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は主として医療用そこ使用される輸液用の容器又
は経管栄養剤用の容器、特に輸液及び/又は栄養剤を保
存するに当ってその品質変化を防ぐため、各成分又は製
剤によって2種以上(こ分割して保存し、用時に容易に
混合しうるようにした複室容器に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to containers for infusions or tube feedings used primarily in medical applications, particularly for storing infusions and/or nutrients. In order to prevent quality changes, it relates to a multi-chamber container in which each component or preparation is divided into two or more types and stored so that they can be easily mixed at the time of use.

〔従来の技術〕[Conventional technology]

従来栄養輸液やその他の液状の栄養剤は、糖、脂肪、ア
ミノ酸、電解質及びビタミンからなる群から選択した成
分の少なくとも211Iを配合して製剤化されている。
Conventionally, nutritional infusions and other liquid nutritional supplements are formulated by incorporating at least 211I, an ingredient selected from the group consisting of sugars, fats, amino acids, electrolytes, and vitamins.

しかしながら、上記成分の選択昏こよっては、例えばぶ
どう糖とアミノ酸を配合して一剤にするといわゆるメイ
ラード反応を生じ着色する欠点を有する。又脂肪を乳化
した液を電解質及び/又はアミノ酸等と配合して一剤に
すると、乳化した油が凝集して分離する欠点を有する。
However, depending on the selection of the above-mentioned ingredients, for example, when glucose and amino acids are combined into a single agent, a so-called Maillard reaction occurs, resulting in coloring. Furthermore, when a fat emulsified liquid is mixed with an electrolyte and/or an amino acid to form a single agent, it has the disadvantage that the emulsified oil coagulates and separates.

このため、−剤もしくは一部として製造もしくは保存し
得ない成分又は製剤は、別々の容器に入れて保存し、供
給され、使用時にこれらの成分もしくは製剤を混合して
使用している。
For this reason, components or preparations that cannot be manufactured or stored as a component or a part thereof are stored and supplied in separate containers, and these components or preparations are mixed at the time of use.

このような別々の容器のものを使用時に混合して一部製
剤とするには、一つの容器に移送して混合する必要があ
るので混合前は各成分もしくは各製剤を収容する複数の
容器、混合用の容器例えば瓶もしくはバッグ等多数の容
器や器具を必要とするばかりでなく、移送及び混合操作
を無菌的に実施するための極度に慎重な取り扱が要求さ
れる。
In order to mix these separate containers at the time of use to make a partial preparation, it is necessary to transfer them to one container and mix them. Therefore, before mixing, multiple containers containing each component or each preparation, Not only do they require a large number of containers and equipment, such as bottles or bags, for mixing, but they also require extremely careful handling to ensure that the transfer and mixing operations are carried out aseptically.

この欠点を解決するための手段として、プラスチック製
の袋状容器を2室に仕切り、一部連通部を残し【上記仕
切部を融着して液密にし、上記連通部をクランプ等で圧
迫し、各室内の成分もしくは製剤が混合しないようにす
る(例えば特開昭51−132692号)が、或いは、
連通部にボール又は一端閉鎖チューブを挿入し1両室を
不連続状態に保つようにする(特開昭57−52455
号)ことが提案され、使用時に上記連通部を開放して両
室内の成分又は製剤を混合できるようにすることが提案
されている。
As a means to solve this drawback, we divided a plastic bag-like container into two chambers, leaving a part of the communication area. , prevent the components or preparations in each chamber from mixing (for example, JP-A-51-132692), or
A ball or a tube with one end closed is inserted into the communication part to keep one and both chambers in a discontinuous state (Japanese Patent Application Laid-Open No. 57-52455
It has been proposed that the communication section be opened during use so that the components or preparations in both chambers can be mixed.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

これらの従来の複室容器は各室を分離し、又連通させる
ためには、液密性切部形成のための融着操作以外に連通
部を残し、この部分の不使用時の連通防止のためには、
前述した如き特殊なりランプ等の用具もしくは部品を設
ける必要がある。
In these conventional multi-chamber containers, in order to separate and communicate each chamber, in addition to fusing to form a liquid-tight cut, a communicating part is left and the communication is prevented when this part is not in use. In order to
It is necessary to provide equipment or parts such as special lamps as described above.

又、複室容器を形成するための材料としては、日本薬局
方では輸液用プラスチック容器用としてポリ塩化ビニル
、ポリプロピレン及びポリエチレンが認められているが
、これらの材料から複室容器を製造して室間の連通防止
のため前述したクランプ等の手段を設けて滅菌処理を行
ったとき、上述した利料は飾1熱性が悪いためクランプ
等の連通防止手段を設けた部分か融着してしまい、使用
時即ち各室に含まれている成分もしくは製剤を混合せん
とするとき、連通部が開かず混合不能となって、使用不
可能になる゛ことがある欠点を有していた。
In addition, as materials for forming multi-chamber containers, the Japanese Pharmacopoeia allows polyvinyl chloride, polypropylene, and polyethylene for plastic containers for infusions; When sterilization is performed with the above-mentioned means such as a clamp provided to prevent communication between the parts, the above-mentioned material has poor heat resistance, so the part where the means to prevent communication such as a clamp is installed is fused. During use, that is, when trying to mix the components or preparations contained in each chamber, the communication part does not open, making it impossible to mix, which has the disadvantage of making it unusable.

従って本発明の目的は液密仕切部によって複数室に分割
された複室容器舎こおいて、日本薬局方で認められてい
る安価なプラスチック材料を使用し、充分な滅菌を行っ
ても各室間の連通部の融着を生ぜしめす、使用時には容
易に連通でき各室内の成分又は製剤を混合できるように
した輸液又は栄養剤の複室容器を提供すること(こある
。
Therefore, the object of the present invention is to construct a multi-chambered container house divided into multiple chambers by liquid-tight partitions, use inexpensive plastic materials approved by the Japanese Pharmacopoeia, and even after sufficient sterilization, each chamber will not be damaged. To provide a multi-chamber container for an infusion solution or a nutrient, which allows easy communication during use and allows mixing of components or preparations in each chamber by creating a fusion at a communicating part between the two chambers.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は液密仕切部によって複数室)こ分割されたプラ
スチック製複室容器において、上記プラスチックが放射
線架橋可能なプラスチックであり、上記仕切部の少なく
とも一部が放射線照射され、放射線照射部が加熱接着さ
れているか又は、クランプで圧着されている複室容器で
ある。
The present invention provides a multi-chambered plastic container divided into multiple compartments by a liquid-tight partition, wherein the plastic is a radiation-crosslinkable plastic, at least a part of the partition is irradiated with radiation, and the radiation irradiated part is heated. A multi-chamber container that is glued or crimped with a clamp.

本発明による複室容器を・製造するに当って使用しうる
プラスチック材料としては、放射線照射すること(こよ
って架橋することができる材料であり、しかも非照射部
分は加熱圧着に、よって融着されることができる材料で
あれば任意の材料を使用できる、例えばポリエチレン、
ポリ塩化ビニル、エチレン−酢酸ビニル共重合体、ポリ
塩化ビニリデン、ポリエチレンテレフタレートがあり、
これらのシート又はフィルムを使用できる。
The plastic material that can be used in manufacturing the multi-chamber container according to the present invention is a material that can be cross-linked by irradiation with radiation, and the non-irradiated parts can be fused by heat compression bonding. Any material that can be used can be used, such as polyethylene,
There are polyvinyl chloride, ethylene-vinyl acetate copolymer, polyvinylidene chloride, and polyethylene terephthalate.
These sheets or films can be used.

これらの材料を用いて本発明の複室容器を製造するに当
っては、前記材料からなるシート又はフィルムを重ね、
周囲部分は公知の方法で加熱圧着することによって融着
させる。又本発明暑こよれは前記容器の所望室数に応じ
て複数(二分割するため、直線状又は曲線状に融着させ
て液密仕切部を設けるのであるが、将来この複室容器中
の各成分又は製剤を混合使用するとき、各室間に連通を
生ぜしぬんとする部分、即ち連通部に相当する部分には
、使用したプラスチック材料に適した放射線を予め照射
させて、その月料に架橋反応を生せしめておく、そして
上述した如く融着(こより液密仕切部を構成すると、放
射線非照射部は融着するか、照射部は融着しない。従っ
てこの部分はクランプ等公知の手段で圧迫して連通防止
する。゛なお上記放射線非照射部を融着させたとき、放
射線照射部は融着はしないが、外力(こよって剥離可能
な程度の接着を生ずることがあり、この場合にはクラン
プ等で保持する必要はない。
When manufacturing the multi-chamber container of the present invention using these materials, sheets or films made of the above materials are stacked,
The surrounding portions are fused by heat and pressure bonding using a known method. In addition, in order to prevent the heat draft of the present invention, a liquid-tight partition is provided by fusion in a straight line or a curved line in order to divide the container into two parts depending on the desired number of chambers. When using a mixture of each component or preparation, the parts where communication is to be created between the chambers, that is, the parts corresponding to the communication parts, are irradiated in advance with radiation appropriate for the plastic material used, and the monthly charge is When a liquid-tight partition is formed by causing a cross-linking reaction, as described above, the non-irradiated area will be fused, or the irradiated area will not be fused. Pressure with means to prevent communication. ゛When the non-irradiated areas are fused together, the irradiated areas will not be fused, but external force (this may cause adhesion to the extent that it can be peeled off). In such cases, there is no need to hold it with a clamp or the like.

上記放射線非照射部を融着させ、照射部を融着でな(接
着させてお(ためには例えばポリエチレン、エチレン−
酢酸ビニル共重合体及びポリエチレンテレフタレートの
場合には熱融着により行い、ポリ塩化ビニル及びポリ塩
化ビニリデンの場合には高周波融着により行う。
The non-irradiated area is fused and the irradiated area is fused (adhered) (for example, polyethylene, ethylene, etc.).
In the case of vinyl acetate copolymer and polyethylene terephthalate, heat fusion is performed, and in the case of polyvinyl chloride and polyvinylidene chloride, high frequency fusion is performed.

使用しうる放射線には例えば電子線又はγ線があり、通
常その強度はポリエチレンに対して1〜100MRad
、ポリ塩化ビニル及びポリ塩化ビニリチンに対しては0
,1〜50MRad、エチレンー酢酸ビニル共重合体に
対しては1〜30MRad 、ポリエチレンテレフタレ
ートGこ対しては1〜30MRadで充分である。
Radiation that can be used includes, for example, electron beams or gamma rays, the intensity of which is usually between 1 and 100 MRad for polyethylene.
, 0 for polyvinyl chloride and polyvinyritine chloride
, 1 to 50 MRad, 1 to 30 MRad for ethylene-vinyl acetate copolymer, and 1 to 30 MRad for polyethylene terephthalate G.

〔作 用〕[For production]

本発明の複室容器は、液密性切部形成Gこ際し、その少
なくとも一部を予め放射線で照射しであるため、この部
分は融着しておらす、剥離可能な程度の接着とすること
ができ、或いは接着しない場合にはクランプ等で保持す
ることによって各室間の連通を防止できる。また放射線
照射によりその部分は架橋されているため、各室に成分
又は製剤を封入した後滅菌処理、即ち高温処理をしても
、その部分の融着を生ずることがない。このため各室の
成分又は製剤を混合しようとするときには、一つの室を
手で押圧するだけで又はクランプを除くだけで放射線照
射部の接着が剥離して画室を連通させ、混合することが
できる。
In the multi-chamber container of the present invention, at least a portion of the liquid-tight cut portion is irradiated with radiation in advance to form the cut portion G, so that this portion is fused and has a peelable level of adhesion. Alternatively, if not bonded, communication between the chambers can be prevented by holding with a clamp or the like. In addition, since those parts are crosslinked by radiation irradiation, even if components or preparations are sealed in each chamber and then sterilized, that is, subjected to high temperature treatment, the parts will not fuse together. Therefore, when trying to mix components or preparations in each chamber, simply pressing one chamber by hand or removing the clamp will release the adhesive in the radiation irradiated area, allowing the chambers to communicate and mixing. .

〔実施例〕〔Example〕

以下に実施例を挙げ図面を参照して本発明を説明する。 The present invention will be described below with reference to Examples and drawings.

第1図及び第2図は各実施例の平面図である。1 and 2 are plan views of each embodiment.

実施例 1 第1図に示すように縦30cm、横18cm、厚さ20
0μmの低密度ポリエチレンシート1の2枚を重ね、そ
の周囲部2を幅1(1mで通常の加熱融着装置を用いて
約120℃で液導入口3及び3′を除いて熱融着させて
封止した。次に図示する如くこの容器の中央部(こ縦幅
3 Cm %横幅18いで電子線照射(吸収線量20 
MRad )を行ってポリエチレンを架橋反応させ、電
子線照射部4を形成させた。次裔ここの電子線照射部4
の中央に図示する伸く幅1儂で180°Cの温度で加熱
接着して仕切部5を設けて、A室とB室に分けた輸液用
複室容器を作った。
Example 1 As shown in Figure 1, the length is 30 cm, the width is 18 cm, and the thickness is 20 cm.
Two low-density polyethylene sheets 1 of 0 μm are stacked, and the peripheral part 2 is heat-sealed to a width of 1 m (1 m) at about 120° C., except for the liquid inlet ports 3 and 3'. Next, as shown in the figure, the central part of this container (vertical width: 3 cm, width: 18 cm) was irradiated with an electron beam (absorbed dose: 20 cm).
MRad) was performed to cause a crosslinking reaction of the polyethylene to form the electron beam irradiation part 4. Next descendant here electron beam irradiation section 4
A partition 5 was provided in the center of the container by heating and bonding at a temperature of 180° C. with a width of 1 degree as shown in the figure, thereby creating a multi-chamber container for infusion divided into chambers A and B.

この容器のA室に糖加重解室液を導入口3より入れ、B
室(こアミノ酸液を導入口3′より入れ、導入口3及び
3′を封止した。次いでこの輸液を入れた容器を115
℃で30分加熱し、滅菌処理をし、冷却した。画室の液
は混合されずに保存できた。
Pour the sugar-weighted decomposition solution into chamber A of this container from inlet 3, and
(This amino acid solution was put into the infusion chamber from the inlet 3', and the inlets 3 and 3' were sealed.Then, the container containing this infusion solution was placed in the 115
The mixture was heated at ℃ for 30 minutes, sterilized, and cooled. The fluid in the compartment could be stored without being mixed.

次にA室及びB室の両液を混合せんとするとき、A室又
はB室の何れかを手で押圧すると、上記電子線照射加熱
接着仕切部5が剥□離し、A室とB室ば連通して画室、
内の液は容易に混合することかできた。
Next, when trying to mix both the liquids in chambers A and B, if either chamber A or chamber B is pressed by hand, the electron beam irradiation heating adhesive partition 5 will peel off, and chambers A and B will be separated. It is connected to the art room,
The liquids inside could be mixed easily.

実施例 2 第2図に示すように縦30cIrL1横18σ、厚さ2
00μmの軟質ポリ塩化ビニルシート1の2枚を重ね、
その周囲部2を幅1−で高周波加熱装置を用いて約12
5℃で液導入口3及び3′を除いて融着させて封止した
。次に図示する如くこの容器の中央右側で周囲部2に接
して縦幅2α、横幅4c!ILで電子線照射(吸収線量
1o MRad)を行って架橋反応させて電子線照射部
4を形成させた。次にこの電子線照射部4及びその延長
部6を幅約1cIrLで高周波加熱(約135°C) 
L、上記延長部6を融着させて仕切りかつ照射部4内の
加熱仕切部5を接着させてA室とB室に分けて輸液用複
室容器を作った。
Example 2 As shown in Fig. 2, length 30cIrL1 width 18σ, thickness 2
00 μm soft polyvinyl chloride sheets 1 are stacked together,
The peripheral part 2 is heated to a width of about 12 mm using a high frequency heating device.
The liquid inlets 3 and 3' were fused and sealed at 5°C. Next, as shown in the figure, the container has a vertical width of 2α and a width of 4c on the right side of the center, in contact with the surrounding area 2! Electron beam irradiation (absorbed dose 10 MRad) was performed using IL to cause a crosslinking reaction and form the electron beam irradiated portion 4. Next, this electron beam irradiation part 4 and its extension part 6 are subjected to high frequency heating (approximately 135°C) with a width of approximately 1 cIrL.
L. The extension part 6 was fused to form a partition and the heating partition part 5 in the irradiation part 4 was adhered to create a multi-chamber container for infusion divided into a chamber A and a chamber B.

この容器のA室に糖加電解質液を導入口3より入れ、B
室にアミノ酸液を導入口3′より入れ、導入口3及び3
′を封止した。次にこの輸液を入れた容器を121℃で
30分間加熱滅菌処理をし、冷却した。画室の液は混合
されずに保存できた。
Pour the sugar electrolyte solution into chamber A of this container from inlet 3, and
Pour the amino acid solution into the chamber from the inlet 3', and
' was sealed. Next, the container containing this infusion solution was heat sterilized at 121° C. for 30 minutes and cooled. The fluid in the compartment could be stored without being mixed.

次にA室及びB室の両液を混合せんとするとき、A室又
はB室の何れかを手、で抑圧すると電子線照射部4内の
接着仕切部5が剥離し、A室とB室は連通して両室内の
液は容易(こ混合することができた。
Next, when trying to mix the liquids in chambers A and B, if either chamber A or chamber B is pressed down by hand, the adhesive partition 5 in the electron beam irradiation section 4 will peel off, and the liquids in chamber A and B will be separated. The chambers were in communication and the liquid in both chambers could be mixed easily.

実施例 3 実施例2において、電子線照射部4を縦幅及び横幅共に
2cmとし、その延長部6のみを高周液加熱して融着さ
せて仕切部を作り、上記電子線照射部4は高周波加熱を
行わなかった。その代りにこの電子線照射部4をクラン
プに【抑圧してA室とB室の連通を防止させて仕切り複
室容器を作った。
Example 3 In Example 2, the electron beam irradiation section 4 was made to have both a vertical width and a width of 2 cm, and only its extension section 6 was heated with high frequency fluid and fused to form a partition section, and the electron beam irradiation section 4 was High frequency heating was not performed. Instead, this electron beam irradiation unit 4 was suppressed with a clamp to prevent communication between chambers A and B, thereby creating a partitioned multi-chamber container.

A室及びB室に実施例2と同様にしてそれぞれ糖加電解
質液及びアミノ酸液を入れて、実施例2と同様に加熱滅
菌処理をした。
A sugar electrolyte solution and an amino acid solution were placed in chambers A and B in the same manner as in Example 2, respectively, and heat sterilization was performed in the same manner as in Example 2.

画室の液は混合されずに保存できた。次にA室とB室の
両液を混合せんとするとき、上記電子線照射部4を抑圧
封止したクランプを取り外すと電子線照射部4は開き、
両液は容易に混合された。
The fluid in the compartment could be stored without being mixed. Next, when the liquids in chambers A and B are to be mixed, the clamp that suppresses and seals the electron beam irradiation section 4 is removed, and the electron beam irradiation section 4 opens.
Both solutions were easily mixed.

(発明の効果〕 本発明の複室容器は、液密仕切部の少なくとも一部を予
め放射線で照射したため、この部分は、加熱滅菌等の高
温処理をしても単に接着するか、クランプで押圧するこ
とによって液密に保持でき、使用時には容易に剥離もし
くは開くことができて画室を連通ずることができる。
(Effects of the Invention) In the multi-chamber container of the present invention, at least a part of the liquid-tight partition is irradiated with radiation in advance, so even after high-temperature treatment such as heat sterilization, this part is simply glued or pressed with a clamp. By doing so, it can be kept liquid-tight, and when in use, it can be easily peeled off or opened to allow communication between the compartments.

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

第1図及び第2図は本発明の複室容器の実施例の平面図
である。 1・・・シート、2・・・周囲部、3,3′・・・液導
入口、4・・・電子線照射部、5・・・仕切部、6・・
・延長仕切部。
1 and 2 are plan views of an embodiment of the multi-chamber container of the present invention. DESCRIPTION OF SYMBOLS 1... Sheet, 2... Surrounding part, 3, 3'... Liquid inlet, 4... Electron beam irradiation part, 5... Partition part, 6...
・Extension partition.

Claims (1)

【特許請求の範囲】[Claims] 1、液密仕切部によつて複数室に分割されたプラスチッ
ク製複室容器において、上記プラスチックが放射線架橋
可能なプラスチックであり、上記仕切部の少なくとも一
部が放射線照射され、放射線照射部が加熱接着されてい
るか又はクランプで圧着されている複室容器。
1. In a plastic multi-chamber container divided into a plurality of chambers by a liquid-tight partition, the plastic is a radiation crosslinkable plastic, at least a part of the partition is irradiated with radiation, and the radiation irradiated part is heated. Multi-chamber containers that are glued or crimped together.
JP1077391A 1989-03-28 1989-03-28 Double chamber container Expired - Fee Related JP2796727B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1077391A JP2796727B2 (en) 1989-03-28 1989-03-28 Double chamber container

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1077391A JP2796727B2 (en) 1989-03-28 1989-03-28 Double chamber container

Publications (2)

Publication Number Publication Date
JPH02255148A true JPH02255148A (en) 1990-10-15
JP2796727B2 JP2796727B2 (en) 1998-09-10

Family

ID=13632595

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1077391A Expired - Fee Related JP2796727B2 (en) 1989-03-28 1989-03-28 Double chamber container

Country Status (1)

Country Link
JP (1) JP2796727B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0531153A (en) * 1991-07-26 1993-02-09 Kawasumi Lab Inc Infusion container
JP2009062094A (en) * 1996-05-13 2009-03-26 B Braun Medical Inc Flexible, multi-compartment drug container and method of making and using same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57123149U (en) * 1981-01-24 1982-07-31
JPS6319149A (en) * 1986-07-10 1988-01-26 株式会社新素材総合研究所 Medical container and its production

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57123149U (en) * 1981-01-24 1982-07-31
JPS6319149A (en) * 1986-07-10 1988-01-26 株式会社新素材総合研究所 Medical container and its production

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0531153A (en) * 1991-07-26 1993-02-09 Kawasumi Lab Inc Infusion container
JP2009062094A (en) * 1996-05-13 2009-03-26 B Braun Medical Inc Flexible, multi-compartment drug container and method of making and using same

Also Published As

Publication number Publication date
JP2796727B2 (en) 1998-09-10

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