JPS6257555A - Medical bag - Google Patents
Medical bagInfo
- Publication number
- JPS6257555A JPS6257555A JP60196012A JP19601285A JPS6257555A JP S6257555 A JPS6257555 A JP S6257555A JP 60196012 A JP60196012 A JP 60196012A JP 19601285 A JP19601285 A JP 19601285A JP S6257555 A JPS6257555 A JP S6257555A
- Authority
- JP
- Japan
- Prior art keywords
- density
- medical bag
- copolymer
- ethylene
- transparency
- 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
Links
- 229920001577 copolymer Polymers 0.000 claims description 14
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 description 12
- -1 polyethylene Polymers 0.000 description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000001954 sterilising effect Effects 0.000 description 5
- 238000004659 sterilization and disinfection Methods 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920001684 low density polyethylene Polymers 0.000 description 3
- 239000004702 low-density polyethylene Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 230000037303 wrinkles Effects 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001802 infusion Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000008155 medical solution Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 101100023124 Schizosaccharomyces pombe (strain 972 / ATCC 24843) mfr2 gene Proteins 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
Ll二二且J上1
本発明は衛生性、柔軟性、透明性、耐熱性などにすぐれ
た血液、薬液などを入れる医療用袋に関する。さらにく
わしくは、密度が0.935 g / c m’以下で
あるエチレンと1−オレフィンとの共重合体からなる医
療用袋に関するものであり、衛生性、柔軟性、透明性、
#熱性などにすぐれた血液、薬液などを入れる医療用袋
を提供することを目的とするものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a medical bag for containing blood, medical solutions, etc., which is excellent in hygiene, flexibility, transparency, and heat resistance. More specifically, it relates to a medical bag made of a copolymer of ethylene and 1-olefin that has a density of 0.935 g/cm' or less, and has excellent hygiene, flexibility, transparency,
#The purpose is to provide a medical bag that can hold blood, medical solutions, etc. that have excellent heat resistance.
良釆二ュ遺
現在、医療用容器として、ガラス、ポリエチレン、ポリ
プロピレンなどからなる硬質の容器と可茄剤を含むポリ
塩化ビニルからなる軟質の袋が知られている。しかし、
前者は内容液を滴下するさいに通気針または通気孔つき
の輸液セットを用いて空気を導入せねばならない。さら
に、内容液の汚染などを生じる。一方、後者は、柔軟性
に富み、外圧によって自然滴下するために空気孔の導入
が不要である。しかし、ポリ塩化ビニルに含まれる可塑
剤、残留上ツマ−の毒性などの問題がある。At present, hard containers made of glass, polyethylene, polypropylene, etc., and soft bags made of polyvinyl chloride containing a softening agent are known as medical containers. but,
In the former case, air must be introduced using a ventilation needle or an infusion set with a ventilation hole when dropping the contents. Furthermore, contamination of the liquid content may occur. On the other hand, the latter is highly flexible and drips naturally due to external pressure, so there is no need to introduce air holes. However, there are problems such as the plasticizer contained in polyvinyl chloride and the toxicity of residual additives.
これらの問題点を解決するために柔軟素材を中間層に用
い、内外層にポリエチレン、ポリプロピレンなどを用い
た積層体の医療用袋が提案されてともない、外層面にシ
ワが発生するために商品価値を低下させる。In order to solve these problems, a laminated medical bag using a flexible material for the middle layer and polyethylene, polypropylene, etc. for the inner and outer layers was proposed. decrease.
口が ・ しようと る1点
以上のことから、本発明はこれらの欠点(問題点)がな
く、すなわち衛生性が良好であるのみならず、柔軟性お
よび透明性が著しくすぐれ、かつ1耐熱性についても良
好な医療用袋を得ることでちる。The present invention does not have these drawbacks (problems), namely, it not only has good hygiene, but also has extremely good flexibility and transparency, and has excellent heat resistance. You can also get a good medical bag.
rO′ 占 ・ るため ゛よび本発明に
したがえば、これらの問題点は密度が0.935 g
/ c m’以下であるエチレンと1−オレフィンとの
共重合体からなる医療用袋、
によって解決することができる。以下、本発明を具体的
に説明する。According to the present invention, these problems are solved when the density is 0.935 g.
/ cm' or less, a medical bag made of a copolymer of ethylene and 1-olefin can solve the problem. The present invention will be explained in detail below.
(A)エチレンと 1−オレフィンとの共重合体本発明
において用いられるエチレンと 1−オレフィンとの共
重合体(以下「エチレン系共重合体」と云う)は、その
密度は0.935 g / c tn’以下であり、
0.930 g / c m”以下のものが好ましく、
特に0.925 g / c m’以下のものが好適で
ある。このエチレン系共重合体の製造に用いられる 1
−オレフィンとは、通常炭素数が多くとも12個のα−
オレフィンであり、代表例としてプロピレン、ブテン−
1、ヘキセン−1、4−メチルペンテン−1およびオク
テン−1があげられる。この共重合体において、コモ/
マーとして共重合された1−オレフィンは、コモノマー
の共重合割合が高くなるにともない、密度が低下する。(A) Copolymer of ethylene and 1-olefin The copolymer of ethylene and 1-olefin used in the present invention (hereinafter referred to as "ethylene copolymer") has a density of 0.935 g / c tn' or less,
0.930 g/cm" or less is preferable,
Particularly suitable is one having a weight of 0.925 g/cm' or less. 1 used in the production of this ethylene copolymer
-Olefins usually have at most 12 carbon atoms.
It is an olefin, typical examples of which are propylene and butene.
1, hexene-1, 4-methylpentene-1 and octene-1. In this copolymer, como/
The density of the 1-olefin copolymerized as a monomer decreases as the copolymerization ratio of the comonomer increases.
すなわち、 】−オレフィンが生じる短鎖分岐の増加に
ともない、密度が低下するばかりでなく、柔軟性に富み
、かつ透明性がすぐれてくるのは、低密度ポリエチレン
の長鎖分岐の増加とともに密度が低下する点では同じで
あるが、低密度ポリエチレンでは、密度の低下とともに
融点も低下するのに対し、該エチレンと 1−オレフィ
ンとの共重合体では、融点が約120°C近傍でサチレ
ートとし、従来の密度と融点との関係よりはずれている
。この特性を生かすことによって柔軟性に富み、透明性
および耐熱性にすぐれる中間層の材質として応用するこ
とにより、柔軟性があるのみならず、耐熱性にも良好で
あることを見出し、本発明に至った。前記の“短鎖分岐
パとは、主鎖と比較して充分短く、炭素数が15未満の
分岐をさす、該共重合体の密度が0.915 g /
c m”以下(とりわけ、0.910 g / c m
″以下のものは、透明性がすぐれているばかりでなく、
特に柔軟性にも富むために好都合である。That is, the density not only decreases with an increase in the short chain branching of low-density polyethylene as the short chain branching increases, but it also becomes more flexible and transparent. However, in low-density polyethylene, the melting point also decreases as the density decreases, whereas in the case of the copolymer of ethylene and 1-olefin, the melting point is saturated at around 120°C, This deviates from the conventional relationship between density and melting point. By making use of this characteristic, it has been found that by applying it as an intermediate layer material that has excellent flexibility, transparency and heat resistance, it is not only flexible but also has good heat resistance, and the present invention. reached. The above-mentioned "short chain branched chain" refers to a branch that is sufficiently short compared to the main chain and has less than 15 carbon atoms, and the density of the copolymer is 0.915 g /
cm” or less (especially 0.910 g/cm
``The following are not only highly transparent, but also
It is especially advantageous because it is highly flexible.
該エチレンと 1−オレフィンとの共重合体のメルトフ
ローインデックス(JIS K7210にしたが、l
′い・条件4で測定・以下r MFRJと云
う)は成形性、強度などの点から通常0.1〜20 g
/ 10分であり、 0.1−15g/10分のもの
が望ましく、殊に0.1〜10 g 710分のものが
好適である。The melt flow index of the copolymer of ethylene and 1-olefin (JIS K7210, but l
Measured under condition 4, hereafter referred to as MFRJ) is usually 0.1 to 20 g from the viewpoint of formability, strength, etc.
/10 minutes, preferably 0.1-15 g/10 minutes, particularly preferably 0.1-10 g/710 minutes.
(B)フィルムの製造、医療用袋の製造本発明の医療用
袋を製造するにあたり、まず以上のエチレンと 1−オ
レフィンとの共重合体を一般のポリエチレン、ポリプロ
ピレンなどの分野において実施されているフィルムの製
造方法と同様にインフレーション法、Tダイ法など採用
することによって得ることができるが、透明性の点から
は水冷式インフレーション法および急冷Tダイ法が好ま
しい。得られるフィルムは通常チューブ状、シート状で
あり、ヒートシールにより適宜所定の形状、寸法に製袋
し注出入口を取付けることによって本発明の医療用袋を
製造することができる。(B) Production of film, production of medical bag In producing the medical bag of the present invention, first, the above-mentioned copolymer of ethylene and 1-olefin is prepared in the field of general polyethylene, polypropylene, etc. It can be obtained by employing an inflation method, a T-die method, etc. in the same manner as the film manufacturing method, but from the viewpoint of transparency, a water-cooled inflation method and a quenching T-die method are preferable. The obtained film is usually in the form of a tube or sheet, and the medical bag of the present invention can be manufactured by heat-sealing the bag into a suitably predetermined shape and size and attaching a pouring port.
得られるフィルムの厚みは好ましくは0.15〜0.6
mmであり、0.15mm未満では、質量感が損なわ
れる、一方、 0.8mmを越えると、柔軟性が不足気
味である。The thickness of the obtained film is preferably 0.15 to 0.6
If it is less than 0.15 mm, the feeling of mass will be impaired, while if it exceeds 0.8 mm, the flexibility will be insufficient.
このようにして得られた医療用袋は必要ならば、内容液
の充填前に袋の内外面を所定温度の蒸留水、消毒水など
で洗浄され、乾燥後に内容液を充填するとよい。次いで
、滅菌処理が施されるが、この方法としては高圧蒸気に
よる方法があげられ、滅菌の条件としては特に限定され
る訳ではないが通常115℃の温度では30分間、 1
21℃の温度では20分間などである。滅菌後、40°
C以上の温度において10分間程度の熱処理をすること
によって該医療用袋の透明性が向上する。If necessary, the medical bag thus obtained is preferably washed with distilled water, sterilized water, etc. at a predetermined temperature on the inner and outer surfaces of the bag before being filled with the liquid content, dried, and then filled with the liquid content. Next, sterilization is performed, and this method includes a method using high-pressure steam, and the sterilization conditions are not particularly limited, but usually at a temperature of 115 ° C. for 30 minutes.
For example, 20 minutes at a temperature of 21°C. After sterilization, 40°
The transparency of the medical bag is improved by heat treatment for about 10 minutes at a temperature of C or higher.
・ よび
以下、実施例によって本発明をさらにくわしく説明する
。- The present invention will be explained in more detail below with reference to Examples.
なお、実施例および比較例において、密度はJIS
K?112(7) D法ニシタがイ、23℃+0.1℃
の温度において測定した。さらに、融点はDSC−法に
したがい、昇温速度が1分間当り10℃で昇温させ、ピ
ークの温度を求めた。また、柔軟性はASTMD−88
2に準拠し、引張弾性率を測定し、自然排出法は肉眼で
観察することによって評価した。さらに、透明性は内容
液充填した後、 115°Cの温度で30分間高圧蒸気
滅菌処理をし、40℃において40分間熱処理したさい
に肉眼で観察した。また、透明性は生理食塩水を充填し
、滅菌後の透視性を肉眼で観察すること、およびAST
M D−1003法に準拠して測定することによって求
めたヘーズ(Haze)によって評価した。さらに、衛
生性は日本薬局方輸液用プラスチック容器試験法に基づ
いて試験した結果を評価した。また、外観は得られた医
療用袋を肉眼で観察した。以上のうち、耐熱性および外
観は、それぞれ、シワ、変形および破袋の状態を観察し
た。なお、耐熱性、柔軟性の自然排出性、透明性の肉眼
による観察、衛生性、外観および総合判定は下記の四ラ
ンクで示した。In addition, in the examples and comparative examples, the density is JIS
K? 112 (7) D method Nishitagai, 23℃ + 0.1℃
Measured at a temperature of Furthermore, the melting point was determined according to the DSC method by increasing the temperature at a rate of 10° C. per minute and determining the peak temperature. In addition, the flexibility is ASTM D-88
2, the tensile modulus was measured, and the natural drainage method was evaluated by observing with the naked eye. Furthermore, transparency was visually observed after filling with the contents, autoclaving at 115°C for 30 minutes, and heat-treating at 40°C for 40 minutes. Transparency is determined by filling with physiological saline and observing the transparency with the naked eye after sterilization, and by AST.
Evaluation was made by haze determined by measurement according to MD-1003 method. Furthermore, hygiene was evaluated based on the results of a test based on the Japanese Pharmacopoeia Test Method for Plastic Containers for Infusions. In addition, the appearance of the obtained medical bag was visually observed. Among the above, heat resistance and appearance were determined by observing wrinkles, deformation, and bag breakage, respectively. Heat resistance, flexibility (natural drainage), visual observation (transparency), hygiene, appearance, and overall evaluation were given in the following four ranks.
■:非常に良好
O:良好
Δ:やや不良
×:不良
実施例 1〜3、比較例 1.2
実施例および比較例において、ポリマーとして 密度が
0.915 g / c m’である高圧法で製造した
低密度ポリエチレン(MFR2,Og/10分、以下r
PE(1) J と云う〕、密度が0.814 g /
c m’ テあるエチ1/ンとブテン−1との共重合
体(MFRl、1g/10分、短鎖分岐のアルキル基の
平均の炭素数 約2 、1000個の炭素に対する短鎖
分岐の平均の数 約23、以下rPE(2) Jと云う
)、密度が0、HEi g / c m’であるエチレ
ンとブテン−1との共重合体(MFR1,5g/10分
、短鎖分岐のアルキル基の平均の炭素数 約2 、10
00個の炭素に対する短鎖分岐の平均の数 約35、以
下rPE(3) Jと云う〕、密度が0.905 g
/ c m”であるエチレンとヘキセン−1との共重合
体(MFR1,5g/10分、短鎖分岐のアルキル基の
平均の炭素数的4 、1000個の炭素に対する短鎖分
岐の平均の数的29、以下rPE(4) Jと云う〕お
よび密度が0J50 g / e m’であるエチレン
−ブテン−1共重合体(MFR1,5g/10分、短鎖
分岐のアルキル基の平均の炭素数 約2 、1000個
の炭素に対する短鎖分岐の平均の数 約4、以下rPE
(5) J と云う〕を使った。■: Very good O: Good Δ: Slightly poor ×: Bad Examples 1 to 3, Comparative Examples 1.2 In the Examples and Comparative Examples, the polymer had a density of 0.915 g/cm' using a high pressure method. Manufactured low density polyethylene (MFR2, Og/10 min, hereinafter r
PE(1) J], the density is 0.814 g/
c m' Copolymer of 1/ethyene and 1-butene (MFRl, 1 g/10 min, average number of carbon atoms in short chain branched alkyl group approximately 2, average number of short chain branches per 1000 carbons) about 23, hereinafter referred to as rPE(2)J), a copolymer of ethylene and butene-1 with a density of 0, HEi g/cm' (MFR 1.5 g/10 min, short chain branched alkyl Average number of carbon atoms in group: about 2, 10
The average number of short chain branches per 00 carbons is approximately 35, hereinafter referred to as rPE(3)J], and the density is 0.905 g.
Copolymer of ethylene and hexene-1 (MFR 1,5 g/10 min, average carbon number of short chain branched alkyl group 4, average number of short chain branches per 1000 carbons) 29, hereinafter referred to as rPE(4)J] and an ethylene-butene-1 copolymer with a density of 0J50 g/e m' (MFR 1.5 g/10 min, average carbon number of short chain branched alkyl groups) 2, the average number of short chain branches for 1000 carbons is about 4, hereafter rPE
(5) J) was used.
以上のポリマーをインフレーション法によって厚みが2
5ミクロンであり、折中が1401のフィルムを製造し
た。The above polymer was made to a thickness of 2 by the inflation method.
A film was produced that was 5 microns and had a 1401 fold.
このようにして得られた各フィルムから医療用袋(内容
積 500m文)を製造した。このようにして得られた
医療用袋の各種特性の測定を行なった。それらの結果を
第1表に示す。Medical bags (inner volume: 500 m) were manufactured from each of the films thus obtained. Various characteristics of the medical bag thus obtained were measured. The results are shown in Table 1.
(以下余白)
以上の実施例および比較例の結果から、本発明の医療用
袋は、柔軟性が良好であるばかりでなく、透明性にもす
ぐれており、かつ耐熱性および衛生性が良好であること
は明らかである。(Left below) From the results of the above Examples and Comparative Examples, the medical bag of the present invention not only has good flexibility, but also excellent transparency, as well as good heat resistance and hygiene. It is clear that there is.
免且立力1
本発明の医療用袋は下記のごとき効果(特徴)を発揮す
る。Immunity 1 The medical bag of the present invention exhibits the following effects (features).
(1)耐熱性がすぐれているために滅菌のさいに袋にシ
ワ、変形などの発生がほとんどなく、外観的にも良好で
ある。(1) Due to its excellent heat resistance, the bag hardly wrinkles or deforms during sterilization and has a good appearance.
(2)柔軟性がすぐれているために内容液の排出などを
生じることがない。(2) Due to its excellent flexibility, the liquid content will not be discharged.
(3)透明性が良好であるから、内容液の状態の判断が
簡易である。(3) Good transparency makes it easy to judge the state of the liquid content.
(4)外a(シワ、変形など)がよく、破袋がほとんど
ない。(4) The outside is in good condition (wrinkles, deformation, etc.) and there is almost no tearing of the bag.
Claims (1)
−オレフィンとの共重合体からなる医療用袋。Ethylene with a density of 0.935g/cm^3 or less and 1
-Medical bags made of copolymers with olefins.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60196012A JPS6257555A (en) | 1985-09-06 | 1985-09-06 | Medical bag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60196012A JPS6257555A (en) | 1985-09-06 | 1985-09-06 | Medical bag |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6257555A true JPS6257555A (en) | 1987-03-13 |
Family
ID=16350758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60196012A Pending JPS6257555A (en) | 1985-09-06 | 1985-09-06 | Medical bag |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6257555A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4912448A (en) * | 1988-10-04 | 1990-03-27 | Mitsubishi Denki Kabushiki Kaisha | Coil device with coil and lead terminals |
| JPH02191458A (en) * | 1988-12-03 | 1990-07-27 | Showa Denko Kk | Medical bag |
| JP2016069073A (en) * | 2014-10-02 | 2016-05-09 | 大日本印刷株式会社 | Packaging material for outer packaging bag of infusion bag and outer packaging bag of infusion bag composed of the same, and method for manufacturing the same |
| JP2016069072A (en) * | 2014-10-02 | 2016-05-09 | 大日本印刷株式会社 | Infusion solution packaging material, infusion bag comprising the same, and method for producing the same |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59115349A (en) * | 1982-12-20 | 1984-07-03 | レクセン・プロダクツ・カンパニー | Thermally sterilizable polyolefin composition and product |
| JPS59203560A (en) * | 1983-05-02 | 1984-11-17 | 株式会社ニツシヨ− | Plastic container for injection |
| JPS61290954A (en) * | 1985-06-19 | 1986-12-20 | 磯野 啓之介 | Liquid container |
-
1985
- 1985-09-06 JP JP60196012A patent/JPS6257555A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59115349A (en) * | 1982-12-20 | 1984-07-03 | レクセン・プロダクツ・カンパニー | Thermally sterilizable polyolefin composition and product |
| JPS59203560A (en) * | 1983-05-02 | 1984-11-17 | 株式会社ニツシヨ− | Plastic container for injection |
| JPS61290954A (en) * | 1985-06-19 | 1986-12-20 | 磯野 啓之介 | Liquid container |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4912448A (en) * | 1988-10-04 | 1990-03-27 | Mitsubishi Denki Kabushiki Kaisha | Coil device with coil and lead terminals |
| JPH02191458A (en) * | 1988-12-03 | 1990-07-27 | Showa Denko Kk | Medical bag |
| JP2016069073A (en) * | 2014-10-02 | 2016-05-09 | 大日本印刷株式会社 | Packaging material for outer packaging bag of infusion bag and outer packaging bag of infusion bag composed of the same, and method for manufacturing the same |
| JP2016069072A (en) * | 2014-10-02 | 2016-05-09 | 大日本印刷株式会社 | Infusion solution packaging material, infusion bag comprising the same, and method for producing the same |
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