JPH039741Y2 - - Google Patents
Info
- Publication number
- JPH039741Y2 JPH039741Y2 JP1986038752U JP3875286U JPH039741Y2 JP H039741 Y2 JPH039741 Y2 JP H039741Y2 JP 1986038752 U JP1986038752 U JP 1986038752U JP 3875286 U JP3875286 U JP 3875286U JP H039741 Y2 JPH039741 Y2 JP H039741Y2
- Authority
- JP
- Japan
- Prior art keywords
- compartment
- bag
- sterilization
- film
- diaphragm
- 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.)
- Expired
Links
- 230000001954 sterilising effect Effects 0.000 claims description 29
- 238000004659 sterilization and disinfection Methods 0.000 claims description 29
- 238000004806 packaging method and process Methods 0.000 claims description 18
- 238000004378 air conditioning Methods 0.000 claims description 7
- 241000894006 Bacteria Species 0.000 claims description 5
- 239000004745 nonwoven fabric Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 description 9
- 230000002093 peripheral effect Effects 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
Landscapes
- Apparatus For Disinfection Or Sterilisation (AREA)
Description
[産業上の利用分野]
本考案は医療用滅菌袋に関する。さらに詳しく
は、滅菌済みの医療用具を細菌に触れさせずに運
搬、保管するために用いられる滅菌袋に関する。
[従来の技術]
従来の医療用滅菌袋を第10a〜10d図に基
づき説明する。
この医療用滅菌袋は、内袋30と外袋40を用
いるもので、内袋30は非通気性フイルムで作ら
れ、その一部に通気部分31が設けられていり
る。また外袋40は非通気性フイルムのみで作ら
れ、ガスバリヤー性が付与されている。
医療用具aの封入は、まず内袋30にそれを入
れたのち、上縁部32を熱融着などでシールする
(第7b図)。ついで内袋30ごと滅菌して、外袋
40に入れる(第7c図)。このとき併せて脱ガ
ス剤などの空気調整剤bを入れる。さいごに外袋
40の上縁部41をシールする(第7b図)。
以上のように、従来の滅菌袋は二重に包装され
ている。
[考案が解決しようとする問題点]
従来の二重包装タイプの滅菌袋のばあい、包装
材を2個必要とするので、製作コストが高くな
り、医療用具を封入する手間も多くかかるという
問題がある。
本考案はかかる事情に鑑み、製作コストが低
く、封入の手間も少ない滅菌袋を提共することを
目的とする。
[問題点を解決するための手段]
本考案の医療用滅菌袋は、非通気性フイルムで
密閉された包装袋と、該包装袋の内部を滅菌済み
医療用具を入れるための第1画室とこれに隣り合
う空気調整剤を入れるための第2画室とに分ける
隔膜とからなり、前記隔膜の少なくとも一部が通
気性および細菌不透過性を有するフイルムで構成
されている。
[作用]
滅菌袋の第1画室に医療用具を挿入したのち、
第1画室側の開口部のみシールして滅菌処理を行
なう。そして滅菌処理後、さらに第2画室内に空
気調整剤を挿入して第2画室側の開口部をシール
する。その状態で搬送、保管されたばあい、第1
区画室の空気は通気性を有する隔膜を通つて第2
区画室の方に拡散するので、第1画室内の空気が
調整される。
[実施例]
つぎに本考案の実施例を説明する。
第1図は本考案の一実施例にかかわる滅菌袋の
部分破断斜視図、第2図は第1図に示される滅菌
袋の外観図、第3図は第2図における()−
()線断面図、第4図は第2図における()−
()線断面図、第5図は他の構成例を示す断面
図、第6図はシール前の滅菌袋の縦断面図、第7
〜8図は隔膜2の他の構成例を示す斜視図、第9
a〜9b図は医療器具の封入作業の説明図であ
る。
第1〜4図において、1は包装袋、2は隔膜で
ある。包装袋1は袋状に周囲を密閉される入れ物
で、非通気性のフイルムで作られる。ここで用い
られる非通気性フイルムとしては、アルミあるい
はポリエステルとポリエチレンあるいはポリプロ
ピレンなどのラミネートフイルムが好適である。
なおここでいうフイルムには、いわゆるフイルム
のほかにシートも含まれる。
包装袋1の表面側フイルム1aと裏面側フイル
ム1bとの間には隔膜2がはさまれており、第1
画室3とこれと隣り合う第2画室4とに分けられ
ている。隔膜2は少なくともその一部が通気性お
よび細菌不透過性を有するフイルム(以下単に通
気性フイルムという)で作られるが、かかるフイ
ルム材料としては、不織布、布、紙などが用いら
れる。紙のばあいはフイルタペーパが好ましい。
該隔膜2は縦寸法も横寸法も包装袋1のそれと同
じであるか、好ましくはそれよりも若干小さく作
られており(包装袋と同じ寸法の場合若干ガス不
透過性が劣る)、表面側フイルム1aと裏面側フ
イルム1bとの間にはさまれ熱融着などの手段に
より接合される。そのようにして接合された四周
のシール部5には、第3〜4図に示されるよう
に、表面側フイルム1aと裏面側フイルム1bと
が2層に接合された外周シール部6と、それらの
間に隔膜2がはさまれて3層になつている内周シ
ール部7とが形成される。外周シール部6は通気
性の隔膜2を外気から遮断しているので、包装袋
1の気密性を保証する。また内周シール部7は隔
膜2を包装袋1の内部に固定する機能を奏する。
なお前記包装袋1は前記のごとく、2枚の表面側
フイルム1aと裏面側フイルム1bとをたがいに
貼着してもよいが、第5図に示されるように1枚
のフイルム材を折り畳み部8で折り重ね、そのう
えで熱融着などによりシール部5を形成してもよ
い。
前記隔膜2は、全体を通気性を有するフイルム
で作つてもよいが、第7〜8図に示されるように
一部だけ通気性を有するフイルム2aで作つても
よい。そのばあいの通気部の形状は円形状、帯状
のほか種々の形状を採用しうる。なお隔膜2の他
の部分2bは非通気性のフイルムあるいは通常の
フイルムで構成することができる。
本実施例の滅菌袋は、第1画室3に医療用具a
が入れられ、第2画室4に空気調整剤bが入れら
れる。なおここで第1画室3、第2画室4とは便
宜上付した名称で、いずれの画室が第1画室3に
なつても第2画室4になつてもよい。
前記医療用具aや空気調整剤bを第1画室3お
よび第2画室4に封入するときは、第9図に示さ
れるように、滅菌袋の三方をシールし、その一方
たとえば上縁をシールしないで開けておき、封入
ののちシールされる。その手順を第9a〜9d図
に基づき説明する。まず第1画室3に医療用具a
を入れ(第9a図)、その上縁の片面(5a)の
みをシールする(第9b図)。つぎに滅菌袋ごと
滅菌処理を行う。ここでの滅菌作業としては、
EOG滅菌(エチレンオキサイドガス滅菌、以下
同じ)放射線滅菌、高圧蒸気滅菌などが採用され
る。つぎに第2画室4に空気調整剤bを入れ(第
9c図)、上縁の他方(5b)を前記片面(5a)
とともにシールする(第9d図)。以上の工程に
よつて医療用具aの滅菌と封入が完了する。
前記工程において、第2画室4に封入される空
気調整剤bとしては、種々のものが用いられる
が、EOG滅菌をしたばあいは、吸湿剤や脱ガス
剤(たとえば活性炭など)、脱酸素剤などが用い
られる。また放射線滅菌をしたばあいは、脱酸素
剤や脱臭剤などが用いられる。さらに高圧蒸気滅
菌をしたばあいは脱酸素剤や吸湿剤などが用いら
れる。なお以上にあげた空気調整剤bはいずれも
代表的なものであり、これらのほかにも必要に応
じて種々のものを用いることができる。
以上のごとく封入を完了した滅菌袋は、外気と
遮断されているので、滅菌済みの医療用具aに細
菌が付着することはない。しかも内部にあつて
は、通気性を有する隔膜2を介して医療用具aと
空気調整剤bが併存するので、滅菌後の空気処理
が継続的に行われる。
つぎに種々の空気調整剤bによつて果される利
点を以下の第1〜3表に示す。
[Industrial Application Field] The present invention relates to a medical sterilization bag. More specifically, the present invention relates to a sterilization bag used for transporting and storing sterilized medical tools without exposing them to bacteria. [Prior Art] A conventional medical sterilization bag will be explained based on FIGS. 10a to 10d. This medical sterilization bag uses an inner bag 30 and an outer bag 40. The inner bag 30 is made of a non-breathable film, and a ventilation portion 31 is provided in a part thereof. Further, the outer bag 40 is made only of non-breathable film and is provided with gas barrier properties. To enclose the medical device a, first put it into the inner bag 30, and then seal the upper edge 32 by heat sealing or the like (FIG. 7b). Then, the inner bag 30 is sterilized and placed in the outer bag 40 (Fig. 7c). At this time, an air conditioner b such as a degassing agent is also added. Finally, the upper edge 41 of the outer bag 40 is sealed (Fig. 7b). As mentioned above, conventional sterilization bags are double wrapped. [Problems that the invention aims to solve] In the case of conventional double-wrapped sterilization bags, two packaging materials are required, which increases production costs and requires a lot of effort to enclose medical devices. There is. In view of these circumstances, the present invention aims to provide a sterile bag that is low in production cost and requires little effort to seal. [Means for Solving the Problems] The medical sterilization bag of the present invention includes a packaging bag sealed with a non-breathable film, a first compartment for storing sterilized medical tools inside the packaging bag, and a first compartment for storing sterilized medical tools. and a second compartment for containing an adjacent air conditioning agent, and at least a part of the diaphragm is made of a film that is breathable and impermeable to bacteria. [Operation] After inserting the medical device into the first compartment of the sterile bag,
Sterilization is performed by sealing only the opening on the first compartment side. After the sterilization process, an air conditioner is further inserted into the second compartment and the opening on the second compartment side is sealed. If transported or stored in that condition,
The air in the compartment passes through a breathable diaphragm into the second compartment.
As it diffuses towards the compartment, the air within the first compartment is conditioned. [Example] Next, an example of the present invention will be described. Fig. 1 is a partially cutaway perspective view of a sterilization bag according to an embodiment of the present invention, Fig. 2 is an external view of the sterilization bag shown in Fig. 1, and Fig. 3 is ()-- in Fig. 2.
() line cross-sectional view, Figure 4 is ()-- in Figure 2.
5 is a sectional view showing another configuration example, FIG. 6 is a longitudinal sectional view of the sterile bag before sealing, and 7
Figures 9 to 8 are perspective views showing other configuration examples of the diaphragm 2.
Figures a to 9b are explanatory diagrams of a medical device enclosing operation. In Figs. 1 to 4, 1 is a packaging bag and 2 is a diaphragm. The packaging bag 1 is a bag-like container whose periphery is sealed, and is made of a non-breathable film. The non-breathable film used here is preferably a laminate film of aluminum or polyester and polyethylene or polypropylene.
Note that the film referred to herein includes not only so-called films but also sheets. A diaphragm 2 is sandwiched between the front side film 1a and the back side film 1b of the packaging bag 1.
It is divided into a drawing room 3 and an adjacent second drawing room 4. The diaphragm 2 is made of a film that is at least partially breathable and impermeable to bacteria (hereinafter simply referred to as a breathable film), and nonwoven fabric, cloth, paper, etc. are used as the film material. In the case of paper, filter paper is preferred.
The diaphragm 2 has the same vertical and horizontal dimensions as the packaging bag 1, or is preferably made slightly smaller than that (if it has the same dimensions as the packaging bag, the gas impermeability is slightly inferior), and the surface side It is sandwiched between the film 1a and the back side film 1b and joined by means such as heat fusion. As shown in FIGS. 3 and 4, the four-circumference seal portion 5 joined in this manner includes an outer peripheral seal portion 6 in which the front side film 1a and the back side film 1b are joined in two layers, and A three-layer inner peripheral seal portion 7 is formed with the diaphragm 2 sandwiched therebetween. Since the outer peripheral seal part 6 blocks the air-permeable diaphragm 2 from the outside air, it guarantees the airtightness of the packaging bag 1. Further, the inner peripheral seal portion 7 functions to fix the diaphragm 2 inside the packaging bag 1.
As described above, the packaging bag 1 may have two front side films 1a and a back side film 1b attached to each other, but as shown in FIG. 8, and then the seal portion 5 may be formed by heat fusion or the like. The diaphragm 2 may be made entirely of a film having air permeability, or may be made of a film 2a having only a part thereof as shown in FIGS. 7 and 8. In this case, the shape of the ventilation portion may be circular, band-like, or various other shapes. The other portion 2b of the diaphragm 2 may be made of a non-breathable film or a normal film. The sterilization bag of this example has medical tools a in the first compartment 3.
is introduced into the second compartment 4, and the air conditioner b is introduced into the second compartment 4. Note that the first compartment 3 and the second compartment 4 are names added for convenience, and either compartment may become the first compartment 3 or the second compartment 4. When enclosing the medical device a and the air conditioner b into the first compartment 3 and the second compartment 4, as shown in FIG. 9, the sterilization bag is sealed on three sides, while, for example, the upper edge is not sealed. It is opened and sealed after being enclosed. The procedure will be explained based on FIGS. 9a to 9d. First, medical equipment a is placed in the first room 3.
(Fig. 9a) and seal only one side (5a) of its upper edge (Fig. 9b). Next, the sterilized bag is sterilized. The sterilization work here is as follows:
EOG sterilization (ethylene oxide gas sterilization, the same applies hereinafter), radiation sterilization, high pressure steam sterilization, etc. are used. Next, put the air conditioner b into the second compartment 4 (Fig. 9c), and apply the other side (5b) of the upper edge to the one side (5a).
(Figure 9d). Through the above steps, sterilization and packaging of the medical device a are completed. In the above process, various types of air conditioning agent b can be used to fill the second compartment 4, but in the case of EOG sterilization, a moisture absorbent, a degassing agent (for example, activated carbon, etc.), or an oxygen absorbing agent can be used. etc. are used. When radiation sterilization is performed, oxygen absorbers and deodorizers are used. Furthermore, when high-pressure steam sterilization is performed, oxygen scavengers and moisture absorbers are used. Note that the air conditioning agents b listed above are all typical ones, and in addition to these, various other agents can be used as necessary. Since the sterilized bag that has been filled as described above is isolated from the outside air, bacteria will not adhere to the sterilized medical device a. Furthermore, since the medical device a and the air conditioning agent b coexist inside the device via the breathable diaphragm 2, air treatment after sterilization is continuously performed. Next, the advantages achieved by various air conditioning agents b are shown in Tables 1 to 3 below.
【表】【table】
【表】【table】
【表】
なお本考案の滅菌袋に封入しうる医療用具aと
しては、たとえば血液透析器、血液回路、注射
筒、カテーテルなどがある。
以上に本考案の一実施例を説明したが、本考案
の他の実施例としては、円筒状の包装袋のほぼ中
間位に隔膜を取りつけて、画室を2個設け、包装
袋の両端をそれぞれシールするようにしたものな
どがある。
[考案の効果]
本考案の滅菌袋は、包装袋を1個しか必要とし
ないので、二重包装を必要とする従来例に比べ、
製作コストが低くなり、医療用具などの封入の手
間も少なくなる。[Table] Examples of medical devices a that can be enclosed in the sterile bag of the present invention include hemodialyzers, blood circuits, syringes, catheters, and the like. One embodiment of the present invention has been described above, but as another embodiment of the present invention, a diaphragm is attached to a cylindrical packaging bag at approximately the midpoint, two compartments are provided, and both ends of the packaging bag are separated from each other. There are some that are designed to be sealed. [Effects of the invention] The sterilization bag of the invention requires only one packaging bag, so compared to the conventional example that requires double packaging,
Manufacturing costs are lower, and the time and effort required to encapsulate medical tools and the like is also reduced.
第1図は本考案の一実施例にかかわる滅菌袋の
部分破断斜視図、第2図は第1図に示された滅菌
袋の外観図、第3図は第2図における()−
()線断面図、第4図は第2図における()−
()線断面図、第5図は他の構成例を示す断面
図、第6図はシール前の滅菌袋の縦断面図、第7
〜8図は隔膜2の他の構成例を示す斜視図、第9
a〜9d図は医療器具の封入作業の説明図、第1
0a〜10d図は従来の滅菌袋の説明図である。
図面の主要符号、1……包装袋、2……隔膜、
3……第1画室、4……第2画室、5……シール
部、6……外周シール部、7……内周シール部、
a……医療用具、b……空気調整剤。
Fig. 1 is a partially cutaway perspective view of a sterilization bag according to an embodiment of the present invention, Fig. 2 is an external view of the sterilization bag shown in Fig. 1, and Fig. 3 is ()-- in Fig. 2.
() line cross-sectional view, Figure 4 is ()-- in Figure 2.
5 is a sectional view showing another configuration example, FIG. 6 is a longitudinal sectional view of the sterile bag before sealing, and 7
Figures 9 to 8 are perspective views showing other configuration examples of the diaphragm 2.
Figures a to 9d are explanatory diagrams of the medical device enclosing work, the first
Figures 0a to 10d are explanatory diagrams of conventional sterilization bags. Main symbols in the drawing: 1...Packaging bag, 2...Diaphragm,
3...First compartment, 4...Second compartment, 5...Seal part, 6...Outer seal part, 7...Inner seal part,
a...Medical equipment, b...Air conditioning agent.
Claims (1)
包装袋の内部を滅菌済み医療用具を入れるため
の第1画室とこれに隣り合う空気調整剤を入れ
るための第2画室とに分ける隔膜とからなり、
前記隔膜の少なくとも一部が通気性および細菌
不透過性を有するフイルムで構成されてなる医
療用滅菌袋。 2 前記通気性および細菌不透過性を有するフイ
ルムが、不織布またはフイルタペーパ製である
実用新案登録請求の範囲第1項記載の医療用滅
菌袋。[Scope of Claim for Utility Model Registration] 1. A packaging bag sealed with an air-impermeable film, and the inside of the packaging bag includes a first compartment for storing sterilized medical tools and an adjacent compartment for storing an air conditioning agent. It consists of a diaphragm that separates the second compartment and
A medical sterilization bag, wherein at least a portion of the diaphragm is made of a film that is breathable and impermeable to bacteria. 2. The medical sterilization bag according to claim 1, wherein the breathable and bacteria-impermeable film is made of nonwoven fabric or filter paper.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1986038752U JPH039741Y2 (en) | 1986-03-17 | 1986-03-17 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1986038752U JPH039741Y2 (en) | 1986-03-17 | 1986-03-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62152739U JPS62152739U (en) | 1987-09-28 |
JPH039741Y2 true JPH039741Y2 (en) | 1991-03-11 |
Family
ID=30851289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1986038752U Expired JPH039741Y2 (en) | 1986-03-17 | 1986-03-17 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH039741Y2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0527936Y2 (en) * | 1989-01-10 | 1993-07-16 | ||
SE9602352D0 (en) * | 1996-06-14 | 1996-06-14 | Astra Ab | Catheter package |
JP3999369B2 (en) * | 1998-09-08 | 2007-10-31 | 岡田紙業株式会社 | Sterilization bag |
US20110226762A1 (en) * | 2008-06-09 | 2011-09-22 | Beton Dickinson France S.A.S. | Sterile packing and sterilization method using this packing |
JP6027037B2 (en) * | 2014-02-04 | 2016-11-16 | ベクトン・ディキンソン・フランス・エス.エー.エス. | Aseptic package and sterilization method using the package |
JP6185631B2 (en) * | 2016-08-05 | 2017-08-23 | ベクトン・ディキンソン・フランス・エス.エー.エス. | Aseptic package and sterilization method using the package |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56132956A (en) * | 1980-03-24 | 1981-10-17 | Dainippon Printing Co Ltd | Bag for disinfecting |
JPS5714340A (en) * | 1980-07-01 | 1982-01-25 | Terumo Corp | Method of keeping medical appliance from getting moldy |
-
1986
- 1986-03-17 JP JP1986038752U patent/JPH039741Y2/ja not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56132956A (en) * | 1980-03-24 | 1981-10-17 | Dainippon Printing Co Ltd | Bag for disinfecting |
JPS5714340A (en) * | 1980-07-01 | 1982-01-25 | Terumo Corp | Method of keeping medical appliance from getting moldy |
Also Published As
Publication number | Publication date |
---|---|
JPS62152739U (en) | 1987-09-28 |
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