JP2818520B2 - Treatment of bloody waste liquid - Google Patents
Treatment of bloody waste liquidInfo
- Publication number
- JP2818520B2 JP2818520B2 JP4135370A JP13537092A JP2818520B2 JP 2818520 B2 JP2818520 B2 JP 2818520B2 JP 4135370 A JP4135370 A JP 4135370A JP 13537092 A JP13537092 A JP 13537092A JP 2818520 B2 JP2818520 B2 JP 2818520B2
- Authority
- JP
- Japan
- Prior art keywords
- waste liquid
- bloody
- superabsorbent polymer
- blood
- protein
- 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 - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/88—Draining devices having means for processing the drained fluid, e.g. an absorber
- A61M1/882—Draining devices provided with means for releasing antimicrobial or gelation agents in the drained fluid
Landscapes
- Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Engineering & Computer Science (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Accommodation For Nursing Or Treatment Tables (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、血液を含んだ水系廃液
(血性廃液)の処理方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating aqueous waste liquid containing blood (bloody waste liquid).
【0002】[0002]
【従来の技術】手術中や手術後に患者から発生した体液
を含む廃液は、内部が負圧とされた収集容器に吸引収集
された後、汚物処理に供される。そして、廃液が取り出
された後の収集容器は洗浄、滅菌されて再使用されてい
る。しかし、収集容器はガラス製品であるため、破損し
やすく、また重い(通常、容量5〜8l)ので、取扱い
上、細心の注意を必要としていた。更に、汚物処理する
際、廃液の飛沫が取扱い者にかかる場合があり、危険で
ある。感染症患者から出た体液を含む廃液は、通常滅菌
処理が行われるが、行われない場合もあり、このような
廃液の飛沫がかかると感染の危険にさらされるからであ
る。2. Description of the Related Art Waste fluid containing body fluid generated from a patient during or after surgery is collected by suction in a collection container having a negative pressure, and then subjected to waste disposal. The collection container after the waste liquid is taken out is washed, sterilized, and reused. However, since the collection container is a glass product, it is easily broken, and is heavy (normally, a volume of 5 to 8 liters). Further, when disposing of filth, there is a case where the splash of the waste liquid is applied to a handler, which is dangerous. Waste fluids containing body fluids from infectious disease patients are usually sterilized, but may not be sterilized, and if such waste fluids are splashed, they are at risk of infection.
【0003】そこで、このような取扱い上の欠点を無く
するために、使い捨ての合成樹脂製の収集容器を用いた
廃液処理方法が特開昭51-48589号公報において提案され
ている。しかしながら、使い捨ての収集容器を使用する
場合においても、収集後の容器を処理施設へ搬送する段
階で容器が破損し、容器内廃液が溢れでたり、また容器
ごと廃棄焼却する際に廃液が飛散、流出するなどの問題
があり、衛生上問題があるばかりか、最終的に処理する
者にとっても危険である。[0003] To eliminate such drawbacks in handling, a waste liquid treatment method using a disposable synthetic resin collection container is proposed in Japanese Patent Application Laid-Open No. 51-48589. However, even when disposable collection containers are used, the containers are damaged at the stage of transporting the collected containers to the treatment facility, and the waste liquid in the containers overflows, and the waste liquid scatters when the entire container is incinerated and incinerated, There is a problem such as spillage, which is not only a hygienic problem, but also dangerous for those who ultimately dispose of it.
【0004】このような問題を解決するために、凝固剤
として高吸水性ポリマーを廃液中に投入し、廃液をゲル
化する方法が特開平2-157083号公報において提案されて
いる。高吸水性ポリマーが廃液中の水分を吸収してゲル
化するので、容器等が破損しても内容物が飛散、流出す
ることがない。[0004] In order to solve such a problem, Japanese Patent Application Laid-Open No. 2-157083 proposes a method in which a superabsorbent polymer is introduced into a waste liquid as a coagulant to gel the waste liquid. Since the superabsorbent polymer absorbs water in the waste liquid and gels, the contents do not scatter or flow out even if the container or the like is damaged.
【0005】[0005]
【発明が解決しようとする課題】しかし、手術中に発生
する廃液中には、水分の他に、血液並びに体液中のNa
イオン等の金属イオン及び糖類が含まれる場合が多い。
このように血液を含んだ廃液(以下、「血性廃液」とい
う)は、血液中のタンパク分が高吸水性ポリマーによっ
てはゲル化しないため、血性廃液全体が流動性がなくな
るまで長時間を要する。例えば、血液濃度が50%以上
の血性廃液では、凝固に2時間も要する。また、体液に
含まれる金属イオンや糖類等も高吸水性ポリマーの吸水
を妨害し、凝固遅延の一因となる。However, wastewater generated during surgery contains not only water but also Na in blood and body fluids.
Metal ions such as ions and saccharides are often included.
The waste fluid containing blood (hereinafter referred to as “blood waste fluid”) requires a long time until the entire blood waste fluid loses fluidity because the protein component in the blood does not gel by the superabsorbent polymer. For example, a bloody effluent having a blood concentration of 50% or more requires two hours for coagulation. In addition, metal ions, saccharides, and the like contained in body fluids also interfere with water absorption of the superabsorbent polymer, and contribute to coagulation delay.
【0006】廃液凝固の遅延は、血性廃液が凝固するま
で収集容器を保管しなければならないことを意味し、迅
速な廃棄処理ができず、安全面においても問題がある。
本発明は、このような事情に鑑みてなされたものであ
り、その目的とするところは、水分の他に、血液を含む
血性廃液であっても、短時間で凝固させることができる
血性廃液の処理方法を提供することにある。[0006] The delay of waste liquid coagulation means that the collection container must be stored until the bloody waste liquid coagulates, so that it is not possible to dispose of it promptly and there is a problem in safety.
The present invention has been made in view of such circumstances, and it is an object of the present invention to provide a bloody waste liquid that can be coagulated in a short time, in addition to water, even a bloody waste liquid containing blood. It is to provide a processing method.
【0007】[0007]
【課題を解決するための手段】本発明の廃液処理方法
は、血性廃液を合成樹脂製の収集容器に吸引して収集し
た後、血性廃液を収集容器ごと廃棄する血性廃液の処理
方法において、前記収集容器中の血性廃液に、高吸水性
ポリマー及びタンパク架橋剤を投入して、前記血性廃液
を凝固させることを特徴とする。According to the present invention, there is provided a method for treating bloody waste liquid, wherein the bloody wastewater is sucked into a collecting container made of synthetic resin and collected, and then the bloody wastewater is discarded together with the collecting container. A superabsorbent polymer and a protein crosslinking agent are added to the bloody waste liquid in the collection container to coagulate the bloody wastewater.
【0008】[0008]
【作用】本発明の処理方法において、高吸水性ポリマー
は血性廃液中の水分を吸水してゲル化し、高吸水性ポリ
マーに吸水されない血液タンパクはタンパク架橋剤の作
用により不溶化して沈澱する。よって、血性廃液であっ
ても、血液を含まない廃液と同様に短時間で凝固させて
処理することが可能となる。In the treatment method of the present invention, the superabsorbent polymer gels by absorbing the water in the bloody waste liquid, and blood proteins that are not absorbed by the superabsorbent polymer are insolubilized and precipitated by the action of the protein crosslinking agent. Therefore, even if it is a bloody waste liquid, it becomes possible to coagulate and process it in a short time in the same manner as a waste liquid containing no blood.
【0009】[0009]
【実施例】本発明の血性廃液の処理方法は、凝固剤であ
る高吸水性ポリマーとともに凝固促進剤としてタンパク
架橋剤を用いて、血性廃液を凝固して、処理する方法で
ある。高吸水性ポリマーとしては、ポリアクリル酸ソー
ダ、デンプンとポリアクリル酸ソーダとのグラフト共重
合物、酢酸ビニルとアクリル酸メチルとの共重合物のケ
ン化物、酢酸ビニルと無水マレイン酸共重合物のケン化
物、イソブチレンと無水マレイン酸共重合物のケン化物
等が用いられる。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The method for treating bloody waste liquid of the present invention is a method of coagulating and treating bloody waste liquid using a protein crosslinking agent as a coagulation accelerator together with a superabsorbent polymer as a coagulant. Examples of superabsorbent polymers include sodium polyacrylate, a graft copolymer of starch and sodium polyacrylate, a saponified product of a copolymer of vinyl acetate and methyl acrylate, and a copolymer of vinyl acetate and maleic anhydride. A saponified product, a saponified product of isobutylene and a maleic anhydride copolymer, and the like are used.
【0010】タンパク架橋剤は、血液タンパク中に遊離
しているアミノ基又はカルボキシル基と反応して不溶化
させるもので、具体的には、グルタルアルデヒド、グリ
オキサール、アセトアルデヒド等のアルデヒド系架橋剤
が用いられる。アルデヒド系架橋剤のうち、グルタルア
ルデヒドが特に好ましく用いられる。グルタルアルデヒ
ドは殺菌効果も有するので、保菌者から収集される血性
廃液に対して、衛生上の点からも好ましい。アルデヒド
系架橋剤は、粉末等の固体状又は液体状のものがあり、
いずれの形態で用いることもできる。固体状のアルデヒ
ド系架橋剤は水溶液として用いてもよい。[0010] The protein cross-linking agent reacts with the amino group or carboxyl group released in the blood protein to make it insoluble, and specifically, an aldehyde cross-linking agent such as glutaraldehyde, glyoxal or acetaldehyde is used. . Among the aldehyde-based crosslinking agents, glutaraldehyde is particularly preferably used. Since glutaraldehyde also has a bactericidal effect, it is preferable from a sanitary point to bloody waste liquid collected from a carrier. Aldehyde-based cross-linking agents may be solid or liquid, such as powder,
Any form can be used. The solid aldehyde-based crosslinking agent may be used as an aqueous solution.
【0011】上記タンパク架橋剤及び高吸水性ポリマー
の収集容器への投入方法は、タンパク架橋剤の形態及び
収集容器の種類等により適宜選択できる。例えば、先に
タンパク架橋剤を投下した後、高吸水性ポリマーを投
下;タンパク架橋剤と高吸水性ポリマーとを同時に投
下;高吸水性ポリマーを投下した後、タンパク架橋剤を
投下;又は粉粒状のタンパク架橋剤であれば高吸水性ポ
リマーと混合して、この混合物を投下する方法等が挙げ
られる。The method of putting the above-mentioned protein crosslinking agent and superabsorbent polymer into the collection container can be appropriately selected depending on the form of the protein crosslinking agent, the type of the collection container, and the like. For example, after the protein cross-linking agent is dropped first, the superabsorbent polymer is dropped; the protein cross-linking agent and the superabsorbent polymer are simultaneously dropped; after the superabsorbent polymer is dropped, the protein cross-linking agent is dropped; For example, a method of mixing a protein cross-linking agent with a superabsorbent polymer and dropping the mixture may be used.
【0012】図1に、本発明の処理方法を実施する収集
容器の一実施例を示す。図1において、1は血性廃液を
貯留するための容器本体であり、容器本体1の蓋部2に
は、該容器本体1内に廃液を注入するための注入管3及
び容器本体1内を負圧にするために吸引ポンプ(図示せ
ず)等に接続される吸引管4が設けられている。蓋部2
の中央部には上方突出状に凝固剤収納部5が設けられて
いて、この凝固剤収納部5の中心上方部にはプッシュバ
ーをガイドするためのガイド筒6が凝固剤収納部5のほ
ぼ中央にまで突設され、凝固剤収納部5の底部には収納
された凝固剤を容器本体1内に投下するための投下口7
が開口されている。該投下口7は、前記ガイド筒6に挿
入されたプッシュバー8の先端にロッドと一体的に形成
され且つロッドの径よりも大きい外径を有する栓部9に
より閉塞されている。図中、10は容器本体1内に所定
量の血性廃液が注入されると、吸引を停止する機能を有
するフィルターである。FIG. 1 shows an embodiment of a collection container for carrying out the processing method of the present invention. In FIG. 1, reference numeral 1 denotes a container body for storing a bloody waste liquid, and a lid 2 of the container body 1 has an injection pipe 3 for injecting the waste liquid into the container body 1 and a negative space inside the container body 1. A suction pipe 4 connected to a suction pump (not shown) or the like is provided to increase the pressure. Lid 2
A coagulant storage section 5 is provided in a central part of the coagulant storage section 5 so as to protrude upward, and a guide cylinder 6 for guiding a push bar is provided substantially above the center of the coagulant storage section 5. A dropout port 7 projecting to the center and provided at the bottom of the coagulant storage section 5 for dropping the stored coagulant into the container body 1.
Is open. The outlet 7 is closed by a stopper 9 formed integrally with the rod at the tip of a push bar 8 inserted into the guide cylinder 6 and having an outer diameter larger than the diameter of the rod. In the figure, reference numeral 10 denotes a filter having a function of stopping suction when a predetermined amount of bloody waste liquid is injected into the container body 1.
【0013】以上のような構成を有する収集容器の凝固
剤収納部5に高吸水性ポリマーとタンパク架橋剤粉末と
の均一混合物を収納しておく。容器本体1内に所定量の
血性廃液を注入した後、プッシュバー8を押し下げて、
凝固剤収納部5の投下口7を閉塞していた栓部9をはず
す。栓部9が下方に移動したことにより、投下口7に間
隙が生じ、この間隙を通じて高吸水性ポリマー及びタン
パク架橋剤が容器本体1内に落下する。血性廃液中の血
液タンパク成分はタンパク架橋剤によって不溶化され、
血性廃液中の水分は高吸水性ポリマーに吸水されて、血
性廃液全体がゲル化する。全体がゲル化するまでの時間
は、従来、血性廃液の凝固を遅延させていた原因である
血液タンパクがタンパク架橋剤により容易に不溶化され
てゲル化するため、高吸水性ポリマーのみを投下した場
合よりも大幅に短縮される。A uniform mixture of the superabsorbent polymer and the protein crosslinking agent powder is stored in the coagulant storage section 5 of the collection container having the above-described configuration. After injecting a predetermined amount of bloody waste liquid into the container body 1, the push bar 8 is pushed down,
The plug 9 that has closed the dropout port 7 of the coagulant storage unit 5 is removed. When the stopper 9 moves downward, a gap is formed in the outlet 7, and the superabsorbent polymer and the protein crosslinking agent fall into the container body 1 through the gap. Blood protein components in the bloody waste fluid are insolubilized by a protein crosslinking agent,
The water in the bloody waste liquid is absorbed by the superabsorbent polymer, and the whole bloody waste liquid gels. Conventionally, the time until the whole gelled is because blood protein, which was the cause of delaying coagulation of bloody waste liquid, was easily insolubilized by the protein crosslinking agent and gelled, so that only the superabsorbent polymer was dropped. Is significantly reduced.
【0014】タンパク架橋剤を併用したことによる凝固
促進効果を、具体的実施例に基づいて説明する。血液濃
度が50%の血性廃液2lに50%のグルタルアルデヒ
ド水溶液を100cc加えたところ、血性廃液中の血液
タンパクが沈澱した。次いで、血液タンパクが沈澱した
血性廃液中に、高吸水性ポリマーを120g添加したと
ころ、2分後には、血性廃液全体が凝固した。The coagulation promoting effect of the combined use of a protein crosslinking agent will be described based on specific examples. When 100 cc of a 50% aqueous glutaraldehyde solution was added to 2 liters of a bloody waste liquid having a blood concentration of 50%, blood proteins in the bloody waste liquid precipitated. Next, 120 g of the superabsorbent polymer was added to the bloody waste liquid in which the blood protein was precipitated, and after 2 minutes, the whole bloody waste liquid solidified.
【0015】一方、血液濃度が50%の血性廃液2l
に、高吸水性ポリマーのみを120g添加したところ、
血性廃液全体が凝固するまで、105分要した。これら
の結果から、タンパク架橋剤を高吸水性ポリマーと併用
すれば、血性廃液の凝固時間を短縮できることがわか
る。本発明の処理方法は、Naイオンを含有する生理食
塩水など、イオンを含む血性廃液に対しても凝固促進効
果がある。例えば、生理食塩水と次亜塩素酸水溶液との
混合液2000cc(混合液中におけるNaCl濃度は
0.9%で、次亜塩素酸の濃度は0.5%である)を凝
固させるのに、120gの高吸水性ポリマーのみを添加
した場合には凝固まで17分要したにも拘らず、50%
のグルタルアルデヒド水溶液100ccと120gの高
吸水性ポリマーとを併用すると9分で凝固した。混合液
にグルタルアルデヒド水溶液を添加すると白濁したこと
から、グルタルアルデヒドは混合液中のイオンと作用し
あって、高吸水性ポリマーの水分吸収を補助していると
解される。なお、生理食塩水のみに対しても、高吸水性
ポリマーのみを添加する場合よりもグルタルアルデヒド
水溶液と併用した方が速く凝固した。On the other hand, 2 l of bloody waste liquid having a blood concentration of 50%
When only 120 g of superabsorbent polymer was added to
It took 105 minutes for the whole bloody waste liquid to solidify. These results show that the coagulation time of the bloody waste liquid can be reduced by using the protein crosslinking agent in combination with the superabsorbent polymer. The treatment method of the present invention also has a coagulation promoting effect on bloody waste fluid containing ions such as physiological saline containing Na ions. For example, to coagulate 2000 cc of a mixture of physiological saline and an aqueous solution of hypochlorous acid (the concentration of NaCl in the mixture is 0.9% and the concentration of hypochlorous acid is 0.5%), When only 120 g of the superabsorbent polymer was added, it took 50 minutes despite the fact that it took 17 minutes to solidify.
When 100 cc of a glutaraldehyde aqueous solution was used in combination with 120 g of a superabsorbent polymer, solidification occurred in 9 minutes. When the aqueous solution of glutaraldehyde was added to the mixed solution, the mixture became cloudy, and it is understood that the glutaraldehyde interacted with ions in the mixed solution and assisted the water absorption of the superabsorbent polymer. It should be noted that even with physiological saline alone, coagulation was faster when used in combination with an aqueous glutaraldehyde solution than when only the superabsorbent polymer was added.
【0016】[0016]
【発明の効果】本発明の処理方法によれば、高吸水性ポ
リマーによる凝固の遅延の原因となる血性廃液中の血液
は、タンパク架橋剤によって不溶化されるので、高吸水
性ポリマーのみの添加ではゲル化に長時間要するような
血液濃度が高い血性廃液であっても、短時間で迅速に凝
固することができる。従って、手術中又は手術後に発生
した血性廃液を、凝固させるために保管等する必要もな
く、安全且つ迅速に廃棄処分できる。According to the treatment method of the present invention, the blood in the bloody waste liquid which causes a delay in coagulation due to the superabsorbent polymer is insolubilized by the protein crosslinking agent. Even a bloody waste liquid having a high blood concentration that requires a long time for gelation can be quickly and quickly coagulated. Therefore, the bloody waste liquid generated during or after the operation does not need to be stored for coagulation, and can be safely and promptly disposed of.
【図1】本発明の処理方法を実施する処理装置の一実施
例を示す図である。FIG. 1 is a diagram illustrating an embodiment of a processing apparatus that performs a processing method of the present invention.
1 容器本体 5 凝固剤収納部 7 投下口 Reference Signs List 1 container body 5 coagulant storage part 7 dropper
フロントページの続き (72)発明者 東 美恵 大阪府堺市浜寺船尾町東4丁36番地 大 研医器株式会社 総合研究所内 (72)発明者 増田 行雄 大阪府大阪市福島区福島1丁目1番50号 大阪大学医学部附属病院 中央手術部 内 (72)発明者 中谷 博 大阪府大阪市福島区福島1丁目1番50号 大阪大学医学部附属病院 中央手術部 内 (72)発明者 池端 信孝 大阪府大阪市福島区福島1丁目1番50号 大阪大学医学部附属病院 中央手術部 内 (72)発明者 中田 精三 大阪府大阪市福島区福島1丁目1番50号 大阪大学医学部附属病院 中央手術部 内 (72)発明者 池田 卓也 大阪府大阪市福島区福島1丁目1番50号 大阪大学医学部附属病院 中央手術部 内 (56)参考文献 特開 平2−157083(JP,A) 特開 平4−264183(JP,A) (58)調査した分野(Int.Cl.6,DB名) C02F 1/00 A61B 19/00 A61G 12/00Continued on the front page (72) Inventor Mie Higashi 4-36, Hamadera-Funaomachi, Sakai-shi, Osaka Dai-ken Medical Device Co., Ltd. (72) Inventor Yukio Masuda 1-150 Fukushima, Fukushima-ku, Osaka-shi, Osaka No. Osaka University Hospital Hospital Central Surgery Department (72) Inventor Hiroshi Nakatani 1-1-1 Fukushima, Fukushima-ku, Osaka City, Osaka Prefecture Osaka University Hospital Hospital Central Surgery Department (72) Inventor Nobutaka Ikehata Osaka-shi, Osaka Osaka University University Hospital, Central Surgery Department (72) Inventor Seizo Nakata 1-1-1 Fukushima, Fukushima-ku, Osaka City, Osaka City Osaka University Hospital, Central Surgery Department (72) ) Inventor Takuya Ikeda 1--50 Fukushima, Fukushima-ku, Osaka-shi, Osaka, Japan Central Hospital, Osaka University Hospital (56) References JP-A-2-157083 (JP, A) JP-A-4-264183 ( JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) C02F 1/00 A61B 19/00 A61G 12/00
Claims (2)
して収集した後、血性廃液を収集容器ごと廃棄する血性
廃液の処理方法において、 前記収集容器中の血性廃液に、高吸水性ポリマー及びタ
ンパク架橋剤を投入して、前記血性廃液を凝固させるこ
とを特徴とする血性廃液の処理方法。1. A method for treating a bloody waste liquid, wherein the bloody waste liquid is sucked into a collecting container made of synthetic resin and collected, and then the bloody waste liquid is discarded together with the collecting container. And treating the bloody waste liquid by coagulating the bloody waste liquid by adding a protein crosslinking agent.
ヒドを用いたことを特徴とする血性廃液の処理方法。2. A method for treating bloody waste liquid, wherein glutaraldehyde is used as a protein crosslinking agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4135370A JP2818520B2 (en) | 1992-05-27 | 1992-05-27 | Treatment of bloody waste liquid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4135370A JP2818520B2 (en) | 1992-05-27 | 1992-05-27 | Treatment of bloody waste liquid |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05329471A JPH05329471A (en) | 1993-12-14 |
JP2818520B2 true JP2818520B2 (en) | 1998-10-30 |
Family
ID=15150139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP4135370A Expired - Lifetime JP2818520B2 (en) | 1992-05-27 | 1992-05-27 | Treatment of bloody waste liquid |
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JP (1) | JP2818520B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2609810B2 (en) * | 1994-05-13 | 1997-05-14 | 大研医器株式会社 | Waste liquid collector |
JP2005003637A (en) * | 2003-06-16 | 2005-01-06 | Yokogawa Electric Corp | Method for treating waste liquid in cartridge, and the cartridge for diagnosis using the same |
CH699120A1 (en) | 2008-07-15 | 2010-01-15 | Medela Holding Ag | Fluid collection. |
CN108853616A (en) * | 2018-06-25 | 2018-11-23 | 河南驼人贝斯特医疗器械有限公司 | The negative pressure drainage device that achievable waste liquid solidifies at any time |
-
1992
- 1992-05-27 JP JP4135370A patent/JP2818520B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
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JPH05329471A (en) | 1993-12-14 |
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