JP2002210022A - Medical equipment - Google Patents
Medical equipmentInfo
- Publication number
- JP2002210022A JP2002210022A JP2001011059A JP2001011059A JP2002210022A JP 2002210022 A JP2002210022 A JP 2002210022A JP 2001011059 A JP2001011059 A JP 2001011059A JP 2001011059 A JP2001011059 A JP 2001011059A JP 2002210022 A JP2002210022 A JP 2002210022A
- Authority
- JP
- Japan
- Prior art keywords
- tube
- groove
- medical device
- tubes
- connection
- 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
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/50—General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
- B29C66/51—Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
- B29C66/52—Joining tubular articles, bars or profiled elements
- B29C66/522—Joining tubular articles
- B29C66/5229—Joining tubular articles involving the use of a socket
- B29C66/52291—Joining tubular articles involving the use of a socket said socket comprising a stop
- B29C66/52292—Joining tubular articles involving the use of a socket said socket comprising a stop said stop being internal
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C57/00—Shaping of tube ends, e.g. flanging, belling or closing; Apparatus therefor, e.g. collapsible mandrels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C57/00—Shaping of tube ends, e.g. flanging, belling or closing; Apparatus therefor, e.g. collapsible mandrels
- B29C57/12—Rim rolling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/56—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using mechanical means or mechanical connections, e.g. form-fits
- B29C65/562—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using mechanical means or mechanical connections, e.g. form-fits using extra joining elements, i.e. which are not integral with the parts to be joined
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/56—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using mechanical means or mechanical connections, e.g. form-fits
- B29C65/565—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using mechanical means or mechanical connections, e.g. form-fits involving interference fits, e.g. force-fits or press-fits
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/05—Particular design of joint configurations
- B29C66/10—Particular design of joint configurations particular design of the joint cross-sections
- B29C66/12—Joint cross-sections combining only two joint-segments; Tongue and groove joints; Tenon and mortise joints; Stepped joint cross-sections
- B29C66/122—Joint cross-sections combining only two joint-segments, i.e. one of the parts to be joined comprising only two joint-segments in the joint cross-section
- B29C66/1222—Joint cross-sections combining only two joint-segments, i.e. one of the parts to be joined comprising only two joint-segments in the joint cross-section comprising at least a lapped joint-segment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/05—Particular design of joint configurations
- B29C66/10—Particular design of joint configurations particular design of the joint cross-sections
- B29C66/12—Joint cross-sections combining only two joint-segments; Tongue and groove joints; Tenon and mortise joints; Stepped joint cross-sections
- B29C66/122—Joint cross-sections combining only two joint-segments, i.e. one of the parts to be joined comprising only two joint-segments in the joint cross-section
- B29C66/1224—Joint cross-sections combining only two joint-segments, i.e. one of the parts to be joined comprising only two joint-segments in the joint cross-section comprising at least a butt joint-segment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/50—General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
- B29C66/51—Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
- B29C66/52—Joining tubular articles, bars or profiled elements
- B29C66/522—Joining tubular articles
- B29C66/5221—Joining tubular articles for forming coaxial connections, i.e. the tubular articles to be joined forming a zero angle relative to each other
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- External Artificial Organs (AREA)
- Media Introduction/Drainage Providing Device (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はチューブを構成部品
として有する医療用具であって、特にこれらのチューブ
と医療用具を構成する接続管の接続形態の発明に関す
る。本発明の医療用具とは血液回路、輸血・輸液セッ
ト、輸液バッグ、血液バッグ等の医療用具を含む。さら
に詳述すれば本発明はメインチューブの途中に分岐部
(例えばY字管、T字管)等の接続管を設けてこれに分
岐ラインチューブ(メインチューブへの薬液注入用、メ
インチューブへの圧力モニター用)を接続した医療用
具、または前記分岐部に栓体を挿入して、メインチュー
ブ内へ薬液の注入、メインチューブ内からの液体のサン
プリング、メインチューブ内の圧力モニター等を行うた
めの処理部(例えば混注部、採液部、圧力モニター部)
を形成した医療用具、例えば体液処理用回路、輸液、採
血、輸血セット、これらの各セット及び回路と接続して
一緒にまたは単独で使用される輸液、採血、輸血バッグ
等の前記チューブと接続管を有する医療用具に関するも
のである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a medical device having a tube as a component, and more particularly to an invention of a connection form between these tubes and a connecting tube constituting the medical device. The medical device of the present invention includes medical devices such as a blood circuit, a blood transfusion / infusion set, an infusion bag, and a blood bag. More specifically, in the present invention, a connection pipe such as a branch portion (for example, a Y-shaped pipe or a T-shaped pipe) is provided in the middle of the main tube, and a branch line tube (for injecting a chemical solution into the main tube, A medical device to which a pressure monitor is connected) or a plug inserted into the branch portion to inject a drug solution into the main tube, sample a liquid from the main tube, monitor the pressure in the main tube, and the like. Processing unit (for example, co-injection unit, liquid sampling unit, pressure monitor unit)
Medical devices formed with, for example, body fluid processing circuits, transfusions, blood collection, blood transfusion sets, and the tubes and connection tubes such as transfusions, blood collections, blood transfusion bags, etc. used together or alone with these sets and circuits The present invention relates to a medical device having:
【0002】[0002]
【従来技術及び発明が解決しようとする課題】以下、体
液処理用回路を構成する合成樹脂製のメインチューブの
途中に、分岐ラインチューブや混注部等の処理部を溶着
した体液処理用回路の一例について詳述する。人工腎
臓、人工肺臓、血漿分離装置そのほかの体液処理装置に
は人体とこれら装置を連結するための体液処理用回路が
セットされることはよく知られている。図4は人工腎臓
に連結される動脈側血液回路の前記混注部付近の一例を
示す断面図である。従来こうした混注部103を組み立
てるにあたっては、チューブ本体101を適所で切断し
た後、各チューブ本体101の先端部に溶剤105を塗
布するとともに、これを接続管107に指で押し込み、
次いで接続管107の開口部106を密封するようにゴ
ム栓108を挿入し、かつこのゴム栓108の上部にカ
バー109をかぶせるようにしているものである。2. Description of the Related Art Hereinafter, an example of a body fluid processing circuit in which a processing section such as a branch line tube or a co-injection section is welded in the middle of a synthetic resin main tube constituting a body fluid processing circuit. Will be described in detail. It is well known that an artificial kidney, an artificial lung, a plasma separation device, and other body fluid processing devices are provided with a body fluid processing circuit for connecting the human body to these devices. FIG. 4 is a cross-sectional view showing an example of the vicinity of the co-injection part of the arterial blood circuit connected to the artificial kidney. Conventionally, when assembling the co-injection unit 103, the tube body 101 is cut in place, and then the solvent 105 is applied to the tip of each tube body 101, and the solvent 105 is pushed into the connection pipe 107 with a finger.
Next, a rubber plug 108 is inserted so as to seal the opening 106 of the connection pipe 107, and a cover 109 is placed over the rubber plug 108.
【0003】このように溶剤を使用してチューブと接続
管を接続する手段は、溶剤の塗布量の調整が難しくかな
りの熟練が要求される。即ち、溶剤の塗布量が多すぎる
と、接合部分から溶剤がチューブ内面方向にはみ出し、
これが固まって図4に示すような塊状部分110が形成
される。こうした塊状部分110が形成されると、チュ
ーブ本体内部を流れる血液の摩擦抵抗が増大し、通常の
平滑な管路では層流として流れている血液の流れに乱流
が生じることになる。この結果血液成分の破壊やそのた
めに誘発される血液凝固の原因ともなる。[0003] The means for connecting the tube and the connecting pipe using a solvent as described above makes it difficult to adjust the amount of the solvent applied, and requires considerable skill. That is, if the coating amount of the solvent is too large, the solvent protrudes from the joint portion toward the inner surface of the tube,
This solidifies to form a lump 110 as shown in FIG. When such a lump 110 is formed, the frictional resistance of blood flowing inside the tube main body increases, and turbulence occurs in the flow of blood flowing as a laminar flow in a normal smooth conduit. This results in the destruction of blood components and the resulting blood coagulation.
【0004】また逆に溶剤の量が少なすぎると、チュー
ブ本体101と接続管107との接着が不充分となるば
かりか、これらの間に間隙が生じてそこから血液が漏出
する可能性がある。さらに、このような溶剤を塗布して
接続する方法は菌による汚染の危険性や溶剤が血液中に
溶解して人体に入り込み人体に悪影響を及ぼす心配もあ
る。またチューブ本体101の切断面の歪のため、チュ
ーブ本体101と接続管107の不適合および溶剤の密
着根が生じ、凹凸が形成されて血液凝固等の原因とな
る。そこで本発明者は、以上の課題を解決するために鋭
意検討を重ねた結果、次の発明に到達した。On the other hand, if the amount of the solvent is too small, not only the adhesion between the tube body 101 and the connecting tube 107 will be insufficient, but also a gap may be formed between them and blood may leak therefrom. . Furthermore, such a method of applying and connecting a solvent involves a risk of contamination by bacteria and a risk that the solvent may dissolve in blood and enter the human body, thus adversely affecting the human body. In addition, due to the distortion of the cut surface of the tube main body 101, incompatibility between the tube main body 101 and the connection pipe 107 and the root of the solvent adhere to each other, and unevenness is formed, which causes blood coagulation and the like. The inventor of the present invention has made intensive studies in order to solve the above-mentioned problems, and as a result, has arrived at the following invention.
【0005】[0005]
【課題を解決するための手段】[1]本発明は、チュー
ブ11と、溝部25を形成した接続管21を接続した医
療用具であって、前記チューブ11の先端に、外筒状の
折り返し部14を形成し、該折り返し部14の外周を接
続管21の前記溝部25に装着した医療用具1を提供す
る。 [2]本発明は、チューブ11と、溝部25を形成した
接続管21を接続した医療用具であって、前記チューブ
11の先端に、外筒状の折り返し部14を形成し、該折
り返し部14の外周を接続管21の前記溝部25に装着
し、前記チューブ11の前方部と前記折り返し部14の
間の空間に、かしめリング31を圧入した医療用具1A
を提供する。 [3]本発明は、チューブ11と、溝部25を形成した
接続管21を接続した医療用具であって、前記補強部材
付きチューブ11の先端に、外筒状の折り返し部14を
形成し、該折り返し部14の外周を接続管21の前記溝
部25に装着し、前記チューブ11の先端と前記折り返
し部14の間の空間に、アンダーカット36を有する外
筒34を突設したかしめリング31Aを圧入した医療用
具1Bを提供する。 [4]本発明は、チューブ11と、アンダーカット26
を有する溝部25を形成した接続管21Aを接続した医
療用具であって、前記チューブ11の先端に、外筒状の
折り返し部14を形成し、該折り返し部14の外周を接
続管21Aの前記溝部25に装着し、前記チューブ11
の前方部と前記折り返し部14と前記溝部25の間の空
間に、かしめリング31Bを圧入した医療用具1Cを提
供する。 [5]本発明は、チューブ11A、11Bと、アンダー
カット26を有する溝部25を形成した接続管21Aを
接続した医療用具であって、前記チューブ11A、11
Bの先端に、鍔状の折り返し部15、16を形成し、該
折り返し部15、16を接続管21Aの前記溝部25に
装着し、前記チューブ11A、11Bの前方部と前記折
り返し部15、16と前記溝部25の間の空間に、かし
めリング31を圧入した医療用具1Dを提供する。 [6]本発明は、チューブ11A、11Bと、溝部25
を形成した接続管21を接続した医療用具であって、前
記チューブ11A、11Bの先端に、鍔状の折り返し部
15、16を形成し、該折り返し部15、16を接続管
21の前記溝部25に装着し、前記チューブ11A、1
1Bの前方部と前記折り返し部15、16と前記溝部2
5の間の空間に、アンダーカット36を有する外筒34
を突設したかしめリング31Aを圧入した医療用具1E
を提供する。 [7]本発明は、[1]から[6]に記載の医療用具1
Aから1Eにおいて、前記かしめリング31Aの外筒3
4の内周または前記接続管21Aの溝部25のいずれか
にアンダーカット26、36を形成して、チューブ1
1、11A、11Bと接続管21、21Aを接続する代
わりに、前記かしめリング31、31A、31Bと前記
接続管21、21Aのそれぞれ対向する壁面に突起と溝
を形成し、これらを係合ないし嵌合させて接続するかま
たは前記それぞれ対向する突起と溝をネジ状に形成し、
これらを螺合してチューブ11、11A、11Bと接続
管21、21Aを接続した医療用具1、1A、1B、1
C、1D、1Eを提供する。Means for Solving the Problems [1] The present invention relates to a medical device in which a tube 11 is connected to a connection tube 21 having a groove 25 formed therein. 14 is provided, and the medical device 1 in which the outer periphery of the folded portion 14 is attached to the groove 25 of the connection tube 21 is provided. [2] The present invention relates to a medical device in which the tube 11 is connected to the connection tube 21 having the groove 25 formed therein. The tube 11 has an outer cylindrical folded portion 14 formed at the tip thereof. Is attached to the groove 25 of the connecting pipe 21 and the medical device 1A in which the caulking ring 31 is press-fitted into the space between the front part of the tube 11 and the folded part 14.
I will provide a. [3] The present invention is a medical device in which the tube 11 is connected to the connection tube 21 having the groove 25 formed therein. The outer periphery of the folded portion 14 is attached to the groove 25 of the connection pipe 21, and a caulking ring 31 </ b> A in which an outer cylinder 34 having an undercut 36 is protruded is inserted into a space between the tip of the tube 11 and the folded portion 14. The provided medical device 1B is provided. [4] The present invention provides a tube 11 and an undercut 26
A medical device to which a connection tube 21A having a groove 25 having a groove is formed, wherein an outer cylindrical folded portion 14 is formed at the tip of the tube 11, and an outer periphery of the folded portion 14 is formed in the groove of the connection tube 21A. 25 and the tube 11
And a medical device 1C in which a caulking ring 31B is press-fitted in a space between the folded portion 14 and the groove 25. [5] The present invention relates to a medical device in which tubes 11A and 11B are connected to a connecting tube 21A having a groove 25 having an undercut 26.
B, flange-shaped folded portions 15 and 16 are formed at the front end, and the folded portions 15 and 16 are mounted in the groove 25 of the connection pipe 21A, and the front portions of the tubes 11A and 11B and the folded portions 15 and 16 are formed. The medical device 1D in which the caulking ring 31 is press-fitted is provided in a space between the groove and the groove 25. [6] The present invention provides tubes 11A and 11B and a groove 25
A medical device to which a connecting tube 21 formed with a flange is connected, wherein flanges 15 and 16 are formed at the tips of the tubes 11A and 11B, and the folded portions 15 and 16 are connected to the grooves 25 of the connecting tube 21. To the tubes 11A, 1
1B, the folded portions 15, 16 and the groove 2
Outer cylinder 34 having an undercut 36 in the space between
Tool 1E press-fitted with caulking ring 31A
I will provide a. [7] The present invention provides the medical device 1 according to any one of [1] to [6].
A to 1E, the outer cylinder 3 of the caulking ring 31A
4 and the undercuts 26 and 36 are formed in the groove 25 of the connection pipe 21A.
Instead of connecting the connection pipes 21 and 21A to the connection pipes 1 and 11A and 11B, projections and grooves are formed on opposing wall surfaces of the caulking rings 31, 31A and 31B and the connection pipes 21 and 21A, and these are not engaged or disengaged. Fitted and connected or the respective opposed projections and grooves are formed in a screw shape,
These are screwed together to connect the medical devices 1, 1A, 1B, 1A with the tubes 11, 11A, 11B connected to the connecting tubes 21, 21A.
C, 1D and 1E are provided.
【0006】[0006]
【発明の実施の形態】本発明の医療用具1、1A、1
B、1C、1D、1Eは、以下に示すように、チューブ
11、11Aと、溝部25を形成した接続管21、21
Aを接続(装着)することにより構成される。本発明で
チューブ11、11A(以下チューブ11等)と接続管
21、21A(以下接続管21等)を「接続(装着)」
するとは、チューブ11等と接続管21等の双方の構成
材料、接続形態に応じて、A機械加工、B接着剤、Cイ
ンサート成形等を採用することができる。例えばa溶剤
接着(例えばポリ塩化ビニル同士の接続に使用される)
を除く、b高周波溶着(例えばポリ塩化ビニル同士、エ
チレンー酢酸ビニル共重合体同士の接続に使用され
る)、c熱溶着(例えばポリエチレン、ポリプロピレン
同士の接続に使用される)、d超音波溶着(例えばポリ
エチレン、ポリプロピレン同士の接続に使用される)、
e紫外線硬化剤による接着(紫外線硬化剤をチューブ1
1等と接続管21等の間に塗布し、紫外線を照射させて
硬化させる手段)、fかしめ嵌合(チューブ11等と接
続管21等の間にかしめリング31、31A、31B
(以下かしめリング31等)を圧入する手段、チューブ
31等と接続管21等の外周に太径チューブまたは収縮
チューブを被覆する手段等を含む。またかしめリング3
1等または接続管21等にアンダーカット26、36
(凸部とも云う)(以下アンダーカット36等)を形成
して接続管21等またはかしめリング31等を固定して
も良いし、かしめリング31等と接続管21等にそれぞ
れ対向する突起と溝を形成し、これらを係合ないし嵌合
させて固定しても良い。また前記それぞれ対向する突起
と溝をネジ状に形成し、螺合して固定するようにしても
良い。)、g係合(チューブ11等と接続管21等の双
方にお互いに係合する凹凸を形成し、これらを係合する
手段、または必要により前記凹と凸の間にゲルを入れる
ことができる)、hレーザービーム、i密着型接着(例
えばポリエチレン、ポリプロピレン同士の接続に使用さ
れる)等またはこれらの各接続手段の組み合わせも含
む。A機械加工とは、前記b高周波溶着、c熱溶着、d
超音波溶着、fかしめ嵌合、g係合、hレーザービーム
である。前記B接着剤とは、前記e紫外線硬化剤による
接着、i密着型接着である。前記Cインサート成形とは
チューブ11等を金型内に配置し、その外周を接続管2
1等の構成部材により被覆する手段である。チューブ1
1等と接続管21等の双方の構成材料がポリ塩化ビニル
系(塩素化ポリエチレンも含む)(接続層の一部がこれ
らの材料であっても良い)の場合は、前記b高周波溶
着、e紫外線硬化剤による接着、fかしめ嵌合、g係合
等またはこれらの各接続手段の組み合わせを採用するこ
とができる。またチューブ11等と接続管21等の双方
の構成材料が、前記ポリ塩化ビニル系以外の例えばポリ
オレフィン系(ポリエチレン系、ポリプロピレン系また
はこれらと共重合可能なモノマーを含む共重合体等)
(接続層の一部がこれらの材料であっても良い)の場合
は、c熱溶着、d超音波溶着、e紫外線硬化剤による接
着、fかしめ嵌合、g係合、i密着型接着またはこれら
の各接続手段の組み合わせを採用することができる。BEST MODE FOR CARRYING OUT THE INVENTION The medical device 1, 1A, 1
B, 1C, 1D, and 1E are tubes 11 and 11A and connecting tubes 21 and 21 each having a groove 25 as shown below.
A is connected (attached). In the present invention, the tubes 11, 11A (hereinafter, tube 11 and the like) and the connection tubes 21, 21A (hereinafter, connection tube 21 and the like) are "connected (mounted)".
Then, A machining, B adhesive, C insert molding, or the like can be adopted depending on the constituent materials and connection forms of both the tube 11 and the like and the connection pipe 21 and the like. For example, a solvent bonding (for example, used for connection between polyvinyl chlorides)
B, high frequency welding (for example, used for connection between polyvinyl chloride and ethylene-vinyl acetate copolymer), c heat welding (for example, used for connection between polyethylene and polypropylene), d ultrasonic welding ( For example, used for connection between polyethylene and polypropylene)
e Adhesion with UV curing agent
A means for applying between the first and the like and the connecting pipe 21 and irradiating and curing the ultraviolet rays, and f-fitting (the swaging rings 31, 31A and 31B between the tube 11 and the connecting pipe 21 and the like)
(Hereinafter, means for press-fitting a caulking ring 31 and the like, means for covering the outer circumference of the tube 31 and the connecting pipe 21 with a large-diameter tube or a shrinking tube, and the like are included. In addition, caulking ring 3
Undercuts 26, 36 on 1st grade or connecting pipe 21 etc.
The connection pipe 21 or the caulking ring 31 or the like may be fixed by forming a protrusion (hereinafter also referred to as an undercut 36), or the projection and the groove facing the caulking ring 31 or the connection pipe 21 or the like. May be formed and fixed by engaging or fitting them. Further, the projection and the groove facing each other may be formed in a screw shape, and screwed and fixed. ), G-engagement (both of the tube 11 etc. and the connecting tube 21 etc. are formed with irregularities which engage each other, and means for engaging these, or gel can be inserted between the concave and convex if necessary. ), H laser beam, i-contact type adhesion (for example, used for connection between polyethylene and polypropylene) and the like, or a combination of these respective connection means. A machining refers to b high frequency welding, c heat welding, d
These are ultrasonic welding, f-fitting, g-engagement, and h-laser beam. The B adhesive is adhesion by the e ultraviolet curing agent and i-contact adhesion. In the C insert molding, the tube 11 and the like are arranged in a mold, and the outer periphery thereof is connected to the connecting pipe 2.
This is a means for coating with a component such as 1. Tube 1
In the case where the constituent materials of both 1 and the like and the connecting pipe 21 and the like are polyvinyl chloride (including chlorinated polyethylene) (a part of the connecting layer may be made of these materials), the above-mentioned b high frequency welding, e Adhesion with an ultraviolet curing agent, f-fitting, g-engagement, or the like, or a combination of these connection means can be employed. In addition, the constituent materials of both the tube 11 and the like and the connecting tube 21 and the like are other than the above-mentioned polyvinyl chloride-based materials such as polyolefin-based materials (polyethylene-based, polypropylene-based or copolymers containing a monomer copolymerizable therewith).
In the case of (a part of the connection layer may be made of these materials), c heat welding, d ultrasonic welding, adhesion with e ultraviolet curing agent, f crimping fitting, g engagement, i close adhesion bonding or A combination of these connection means can be adopted.
【0007】本発明のチューブ11等に使用する構成材
料がポリ塩化ビニルの場合は、「チューブ11等」の構
成材料は、可塑剤の配合量の多い(30質量%を超え8
0質量%以下)軟質(または可とう性ともいう)のポリ
塩化ビニルが使用される。またポリ塩化ビニル以外の材
料、例えばポリオレフィン材料を使用する場合、単一物
質の場合(例えばポリエチレン)はその材料の物性(密
度)を選択して、例えばチューブ11等に軟らかい(ま
たは可とう性ともいう)低密度ポリエチレン(密度;
0.910以下)を使用することができる。また二以上
の物質の場合(例えばエチレンと酢酸ビニルの共重合
体、エチレンとメチルアクリレートとのランダム共重合
体)は、その材料の結晶化度(重合度)を選択して、例
えばチューブ11等に低結晶化度(低重合度)の軟らか
い(または可とう性ともいう)エチレンと酢酸ビニル
(メチルアクリレート)の共重合体を使用することがで
きる。通常エチレン単体では結晶性が高く、規則的に結
晶化したものは、硬度も硬い。ところがエチレンと共重
合するモノマー(酢酸ビニル、メチルアクリレート)を
添加し、添加量(重合度)を増やすほど、エチレンの結
晶の成長が阻害されるので、重合体全体の硬度は軟らか
くなる。またチューブ11等に低結晶化度(低重合度)
の軟らかい(または可とう性ともいう)エチレンと酢酸
ビニル(メチルアクリレート)の共重合体を使用するこ
とができる。When the constituent material used for the tube 11 or the like of the present invention is polyvinyl chloride, the constituent material of the “tube 11 or the like” contains a large amount of the plasticizer (more than 30% by mass and 8%).
(Less than 0% by mass) soft (or also flexible) polyvinyl chloride is used. When a material other than polyvinyl chloride, for example, a polyolefin material is used, in the case of a single substance (for example, polyethylene), the physical property (density) of the material is selected and, for example, the material such as the tube 11 or the like is soft (or flexible). Low density polyethylene (density;
0.910 or less). In the case of two or more substances (for example, a copolymer of ethylene and vinyl acetate, and a random copolymer of ethylene and methyl acrylate), the degree of crystallization (degree of polymerization) of the material is selected and, for example, the tube 11 or the like is selected. A soft (or flexible) copolymer of ethylene and vinyl acetate (methyl acrylate) having low crystallinity (low polymerization degree) can be used. Normally, ethylene alone has high crystallinity, and the one crystallized regularly has a high hardness. However, as a monomer (vinyl acetate, methyl acrylate) copolymerizable with ethylene is added and the amount of addition (degree of polymerization) is increased, the growth of ethylene crystals is inhibited, so that the hardness of the entire polymer is softened. Low crystallinity (low polymerization degree) in tube 11 etc.
A soft (or flexible) copolymer of ethylene and vinyl acetate (methyl acrylate) can be used.
【0008】次に本発明の医療用具のチューブと接続管
の接続形態の実施例について説明する。図1は本発明の
医療用具を構成する折り返し部付チューブの先端加工例
を示す概略図である。図1のようにチューブ11、11
A、11Bの先端に折り返し部14、15、16を形成
し、溝部25を形成した接続管21に接続することがで
きる。例えば(図1a)のように前記チューブ11の先
端を加熱金型(図示せず)等に当接して加熱軟化させな
がら、外筒状の折り返し部14を形成することができ
る。例えば(図1b、図1c)のように前記チューブ1
1A、11Bの先端を加熱金型等に当接して加熱軟化さ
せながら、鍔状の折り返し部15、16を形成すること
ができる。図1bの折り返し部15は、単一の鍔に形成
されているのに対して図1cの折り返し部16は、二重
の鍔に形成されている。Next, an embodiment of a connection form between the tube and the connection pipe of the medical device of the present invention will be described. FIG. 1 is a schematic view showing an example of processing the distal end of a tube with a folded portion constituting the medical device of the present invention. As shown in FIG.
The folded portions 14, 15, 16 are formed at the tips of A, 11B, and can be connected to the connection pipe 21 in which the groove 25 is formed. For example, as shown in FIG. 1A, the outer cylindrical folded portion 14 can be formed while the distal end of the tube 11 is in contact with a heating mold (not shown) or the like to be heated and softened. For example, as shown in FIG. 1B and FIG.
The flanges 15 and 16 can be formed while the tips of 1A and 11B are in contact with a heating mold or the like to soften by heating. 1b is formed in a single flange, whereas the folded portion 16 in FIG. 1c is formed in a double flange.
【0009】例えば(図2a)の医療用具1のように前
記チューブ11の前記折り返し部14の外周を接続管2
1の前記溝部25に装着することができる。本実施例で
は、チューブ11と接続管21の双方の構成材料が前記
ポリ塩化ビニル系の場合、b高周波溶着、e紫外線硬化
剤による接着とすることができる。またチューブ11と
接続管21の双方の構成材料が前記ポリオレフィン系の
場合、c熱溶着、d超音波溶着、e紫外線硬化剤による
接着とすることができる。For example, as in the medical device 1 shown in FIG. 2A, the outer periphery of the folded portion 14 of the tube 11 is connected to the connecting tube 2.
1 can be mounted in the groove 25. In this embodiment, when the constituent materials of both the tube 11 and the connection tube 21 are the above-mentioned polyvinyl chloride, it is possible to perform b-high frequency welding and e-adhesion with an ultraviolet curing agent. When the constituent materials of both the tube 11 and the connection tube 21 are the polyolefin-based materials, it is possible to use c heat welding, d ultrasonic welding, and e adhesion using an ultraviolet curing agent.
【0010】また(図2b)の医療用具1Aのように前
記チューブ11の前記折り返し部14の外周を接続管2
1の前記溝部25に装着し、前記チューブ11の前方部
と前記折り返し部14の間の空間に、かしめリング31
(胴部32の端部に鍔部33を形成している)を圧入す
ることにより、前記折り返し部14をかしめリング31
の胴部32と接続管21の間に挟持して、チューブ11
と接続管21を装着することができる。本実施例では、
チューブ11と接続管21の双方の構成材料が前記ポリ
塩化ビニル系の場合、b高周波溶着、e紫外線硬化剤に
よる接着を併用することができる。またチューブ11と
接続管21の双方の構成材料が前記ポリオレフィン系の
場合、c熱溶着、d超音波溶着、e紫外線硬化剤による
接着を併用することができる。As shown in FIG. 2B, the outer periphery of the folded portion 14 of the tube 11 is connected to the connecting tube 2A.
1 in the groove 25, and a caulking ring 31 is provided in a space between the front portion of the tube 11 and the folded portion 14.
(The flange portion 33 is formed at the end of the body portion 32) to press the folded portion 14 to the caulking ring 31.
Of the tube 11
And the connection pipe 21 can be mounted. In this embodiment,
When the constituent material of both the tube 11 and the connection tube 21 is the above-mentioned polyvinyl chloride-based material, b high frequency welding and e adhesion with an ultraviolet curing agent can be used together. When the constituent material of both the tube 11 and the connection tube 21 is the polyolefin-based material, c-heat welding, d-ultrasonic welding, and e-adhesion with an ultraviolet curing agent can be used in combination.
【0011】また図3のようにチューブ11、11A、
11Bの前記折り返し部14、15、16を、かしめリ
ング31A(胴部32の端部に鍔部33を形成してい
る、さらに鍔部33に外筒34を形成している)を使用
して、前記溝部25を形成した接続管21、21Aに接
続するに際し、かしめリング31Aの外筒34の内周ま
たは接続管21、21Aの溝部25のいずれかにアンダ
ーカット(または凸部、突起ともいう)26、36を形
成して、チューブ11、11A、11Bと接続管21、
21Aを接続することができる。例えば(図3a)の医
療用具1Bのように、前記チューブ11の前記折り返し
部14の外周を接続管21の前記溝部25に装着し、前
記チューブ11の前方と前記折り返し部14の間の空間
に、アンダーカット36を形成した外筒34を有するか
しめリング31Aの胴部32を圧入し、前記外筒34と
胴部32の間に、前記折り返し部14と前記接続管21
の前方を挟持して、チューブ11と接続管21を装着す
ることができる。接続管21の外周はアンダーカット3
6により強固に固定される。本実施例では、チューブ1
1と接続管21の双方の構成材料が前記ポリ塩化ビニル
系の場合、b高周波溶着、e紫外線硬化剤による接着を
併用することができる。またチューブ11と接続管21
の双方の構成材料が前記ポリオレフィン系の場合、c熱
溶着、d超音波溶着、e紫外線硬化剤による接着を併用
することができる。As shown in FIG. 3, the tubes 11, 11A,
The folded portions 14, 15, 16 of 11 </ b> B are formed by using a caulking ring 31 </ b> A (a flange 33 is formed at the end of the body 32, and an outer cylinder 34 is formed at the flange 33). When connecting to the connecting pipes 21 and 21A in which the grooves 25 are formed, an undercut (or a protrusion or a protrusion) is formed on either the inner circumference of the outer cylinder 34 of the caulking ring 31A or the grooves 25 of the connecting pipes 21 and 21A. ) 26, 36 are formed, and the tubes 11, 11A, 11B and the connecting tube 21,
21A can be connected. For example, as in the case of the medical device 1B (FIG. 3A), the outer periphery of the folded portion 14 of the tube 11 is mounted on the groove 25 of the connection tube 21, and is inserted into the space between the front of the tube 11 and the folded portion 14. , A body portion 32 of a caulking ring 31A having an outer cylinder 34 having an undercut 36 is press-fitted, and between the outer cylinder 34 and the body portion 32, the folded portion 14 and the connection pipe 21 are inserted.
, The tube 11 and the connection tube 21 can be mounted. The outer circumference of the connection pipe 21 is undercut 3
6 firmly fixed. In this embodiment, the tube 1
When the constituent material of both 1 and the connection pipe 21 is the polyvinyl chloride-based material, b high frequency welding and e adhesion with an ultraviolet curing agent can be used together. Also, the tube 11 and the connecting pipe 21
When both of the constituent materials are the above-mentioned polyolefin-based materials, c-heat welding, d-ultrasonic welding, and e-adhesion with an ultraviolet curing agent can be used in combination.
【0012】また(図3b)の医療用具1Cのように接
続管21Aの前記溝部25にアンダーカット26を形成
し、チューブ11の前記折り返し部14の外周を接続管
21Aの前記溝部25に装着し、前記チューブ11の前
方部と前記折り返し部14と前記溝25の間の空間に、
かしめリング31B(胴部32の一端部に鍔部33を形
成し、他方の端部に溝部35を形成している)を圧入
し、前記折り返し部14を接続管21Aとかしめリング
31Bで挟持して、接続管21Aと前記チューブ11を
装着することができる。かしめリング31Bの胴部32
の外周はアンダーカット36により強固に固定される。
本実施例では、チューブ11と接続管21Aの双方の構
成材料が前記ポリ塩化ビニル系の場合、b高周波溶着、
e紫外線硬化剤による接着を併用することができる。ま
たチューブ11と接続管21Aの双方の構成材料が前記
ポリオレフィン系の場合、c熱溶着、d超音波溶着、e
紫外線硬化剤による接着を併用することができる。An undercut 26 is formed in the groove 25 of the connecting tube 21A as in the medical device 1C shown in FIG. 3B, and the outer periphery of the folded portion 14 of the tube 11 is attached to the groove 25 of the connecting tube 21A. In the space between the front part of the tube 11, the folded part 14, and the groove 25,
A caulking ring 31B (having a flange portion 33 at one end of the body portion 32 and a groove portion 35 at the other end) is press-fitted, and the folded portion 14 is sandwiched between the connecting tube 21A and the caulking ring 31B. Thus, the connection pipe 21A and the tube 11 can be mounted. Body 32 of caulking ring 31B
Is firmly fixed by an undercut 36.
In the present embodiment, when the constituent materials of both the tube 11 and the connection tube 21A are the above-mentioned polyvinyl chloride type, b high frequency welding,
e Adhesion with an ultraviolet curing agent can be used in combination. Further, when the constituent materials of both the tube 11 and the connecting tube 21A are the polyolefin-based materials, c heat welding, d ultrasonic welding, e
Adhesion with an ultraviolet curing agent can be used together.
【0013】また(図3c)の医療用具1Dのように接
続管21Aの前記溝部25にアンダーカット26を形成
し、前記チューブ11A、11Bの前記鍔状の折り返し
部15、16を、前記溝部25に装着し、前記チューブ
11A、11Bの前方部と前記折り返し部15、16と
前記溝部25の間の空間に、かしめリング31を圧入
し、かしめリング31と接続管21Aの間に、前記折り
返し部15、16を挟持して、チューブ11A、11B
と接続管21Aを装着することができる。かしめリング
31の胴部32の外周はアンダーカット26により強固
に固定される。本実施例では、チューブ11A、11B
と接続管21Aの双方の構成材料が前記ポリ塩化ビニル
系の場合、b高周波溶着、e紫外線硬化剤による接着を
併用することができる。またチューブ11A、11Bと
接続管21Aの双方の構成材料が前記ポリオレフィン系
の場合、c熱溶着、d超音波溶着、e紫外線硬化剤によ
る接着を併用することができる。An undercut 26 is formed in the groove 25 of the connecting tube 21A as in the medical device 1D shown in FIG. 3C, and the flange-shaped folded portions 15, 16 of the tubes 11A, 11B are connected to the groove 25. The swaging ring 31 is pressed into the space between the front portions of the tubes 11A, 11B and the folded portions 15, 16 and the groove 25, and the swaged portion is inserted between the swaged ring 31 and the connection pipe 21A. Tubes 11A, 11B
And the connection pipe 21A. The outer periphery of the body 32 of the caulking ring 31 is firmly fixed by the undercut 26. In this embodiment, the tubes 11A, 11B
When both the constituent materials of the connection pipe 21A and the connection pipe 21A are the above-mentioned polyvinyl chloride-based materials, b high frequency welding and e adhesion with an ultraviolet curing agent can be used together. When the constituent materials of both the tubes 11A and 11B and the connection tube 21A are the polyolefin-based materials, c heat welding, d ultrasonic welding, and e bonding with an ultraviolet curing agent can be used in combination.
【0014】また(図3d)の医療用具1Eのように、
前記チューブ11A、11Bの前記鍔状の折り返し部1
5、16を接続管21の前記溝部25に装着し、前記チ
ューブ11A、11Bの前方部と前記折り返し部15、
16と前記溝部25の間の空間に、アンダーカット36
を形成した外筒34を有するかしめリング31A(胴部
32の端部に鍔部33形成し、さらに鍔部33に外筒3
4形成している)を圧入し、かしめリング31Aと接続
管21の間に、前記折り返し部15、16を挟持してチ
ューブ11A、11Bを接続管21を装着することがで
きる。接続管21の外周は外筒34のアンダーカット3
6により強固に固定される。本実施例では、チューブ1
1A、11Bと接続管21の双方の構成材料が前記ポリ
塩化ビニル系の場合、b高周波溶着、e紫外線硬化剤に
よる接着を併用することができる。またチューブ11
A、11Bと接続管21の双方の構成材料が前記ポリオ
レフィン系の場合、c熱溶着、d超音波溶着、e紫外線
硬化剤による接着を併用することができる。Also, as in the medical device 1E (FIG. 3d),
The collar-shaped folded portion 1 of the tubes 11A and 11B
5 and 16 are attached to the groove 25 of the connection pipe 21, and the front parts of the tubes 11 A and 11 B and the folded part 15,
In the space between the groove 16 and the groove 25, an undercut 36
Ring 31A having an outer cylinder 34 formed with a flange (a flange 33 is formed at the end of the body 32, and the outer cylinder 3 is further formed on the flange 33).
4) is press-fitted, the tubes 11A, 11B can be attached to the connecting tubes 21 with the folded portions 15, 16 sandwiched between the caulking ring 31A and the connecting tubes 21. The outer circumference of the connection pipe 21 is an undercut 3 of the outer cylinder 34.
6 firmly fixed. In this embodiment, the tube 1
When the constituent materials of both 1A and 11B and the connecting pipe 21 are the above-mentioned polyvinyl chloride type, b high frequency welding and e adhesion with an ultraviolet curing agent can be used together. Tube 11
When the constituent materials of both A and 11B and the connection pipe 21 are the polyolefin-based materials, it is possible to use together c heat welding, d ultrasonic welding, and e-adhesion with an ultraviolet curing agent.
【0015】また、本発明では前記のように「かしめリ
ング31Aの外筒34の内周または前記接続管21Aの
溝部25のいずれかにアンダーカット(または凸部、突
起ともいう)26、36を形成して、チューブ11、1
1A、11Bと接続管21、21Aを接続する」代わり
に、前記かしめリング31、31Aと前記接続管21、
21Aのそれぞれ対向する壁面(かしめリング31で
は、胴部32と外筒34、接続管31では前記胴部32
と外筒34に接する溝部25と外周)に突起と溝を形成
し、これらを係合ないし嵌合させて接続しても良い。ま
たは前記それぞれ対向する突起と溝をネジ状に形成し、
これらを螺合してチューブ11、11A、11Bと接続
管21、21Aを接続するようにしても良い。Further, in the present invention, as described above, the undercuts (also referred to as protrusions or protrusions) 26, 36 are formed on either the inner periphery of the outer cylinder 34 of the caulking ring 31A or the groove 25 of the connection pipe 21A. Forming the tubes 11, 1
1A, 11B and connecting pipes 21, 21A ”instead of the caulking rings 31, 31A and the connecting pipe 21,
The opposing wall surfaces of 21A (the caulking ring 31, the body 32 and the outer cylinder 34, and the connecting pipe 31 the body 32
And the groove 25 in contact with the outer cylinder 34 and the outer periphery), a projection and a groove may be formed, and these may be engaged or fitted to be connected. Or the protrusions and grooves facing each other are formed in a screw shape,
These may be screwed together to connect the tubes 11, 11A, 11B to the connecting tubes 21, 21A.
【0016】[0016]
【発明の作用効果】以上説明したように、本発明はチュ
ーブと接続管を溶剤を使用することなく、確実に接続す
ることができる。このため従来のように溶剤の塗布量の
調整等に煩わされることがない。すなわち溶剤の塗布量
の過多により、溶剤のチューブ内面へのはみ出しによる
液体(血液)の摩擦抵抗の増大や液体(血液)の流れが
乱流に変化することにより誘発される血液成分の破壊や
血液凝固等の課題を解消することができる。また溶剤の
塗布量が少なすぎるとことにより、チューブと接続管の
接着が不良による、これらの間の間隙からの血液の漏出
等の課題を解消することができる。さらに、溶剤塗布に
よる菌による汚染の危険性や溶剤が血液中に溶解して人
体に入り込み人体に悪影響を及ぼす懸念も解消すること
ができる。As described above, according to the present invention, the tube and the connecting pipe can be securely connected without using a solvent. For this reason, there is no need to bother with adjusting the amount of solvent to be applied as in the related art. That is, due to the excessive amount of the solvent applied, the frictional resistance of the liquid (blood) increases due to the solvent protruding into the inner surface of the tube, and the destruction of blood components and blood induced by the change of the flow of the liquid (blood) into turbulent flow. Problems such as solidification can be solved. Further, when the amount of the applied solvent is too small, problems such as leakage of blood from a gap between the tube and the connection tube due to poor adhesion between the tube and the connection tube can be solved. Furthermore, the danger of bacterial contamination due to the application of the solvent and the concern that the solvent dissolves in the blood and enters the human body to adversely affect the human body can be eliminated.
【図1】本発明の医療用具を構成する折り返し部付チュ
ーブの先端加工例を示す概略図FIG. 1 is a schematic view showing an example of processing a distal end of a tube with a folded portion constituting a medical device of the present invention.
【図2】本発明の医療用具を構成する折り返し部付チュ
ーブと接続管の接続形態の一例を示す概略図FIG. 2 is a schematic view showing an example of a connection form between a tube with a folded portion and a connection tube which constitute the medical device of the present invention.
【図3】本発明の医療用具を構成する折り返し部付チュ
ーブと接続管の接続形態の一例を示す概略図FIG. 3 is a schematic view showing an example of a connection form between a tube with a folded portion and a connection tube which constitute the medical device of the present invention.
【図4】従来の医療用具を構成するチューブと接続管の
接続形態の一例を示す概略図FIG. 4 is a schematic view showing an example of a connection form between a tube and a connection tube constituting a conventional medical device.
1、1A、1B、1C、1D、1E 医療用具 11、11A、11B 折り返し部付チューブ(チュー
ブ) 14 折り返し部(外筒) 15 折り返し部(鍔) 16 折り返し部(二重鍔) 21、21A 接続管 25 溝部 26 アンダーカット(凸部、突起) 31、31A、31B かしめリング 32 胴部 33 鍔部 34 外筒 35 溝部 36 アンダーカット(凸部、突起)1, 1A, 1B, 1C, 1D, 1E Medical tool 11, 11A, 11B Tube with folded part (tube) 14 Folded part (outer cylinder) 15 Folded part (flange) 16 Folded part (double flange) 21, 21A Connection Tube 25 Groove 26 Undercut (projection, projection) 31, 31A, 31B Caulking ring 32 Body 33 Flange 34 Outer cylinder 35 Groove 36 Undercut (convex, projection)
Claims (7)
管21を接続した医療用具であって、 前記チューブ11の先端に、外筒状の折り返し部14を
形成し、該折り返し部14の外周を接続管21の前記溝
部25に装着した、ことを特徴とする医療用具1。1. A medical device comprising a tube 11 and a connecting tube 21 having a groove 25 formed therein. The tube 11 has an outer cylindrical folded portion 14 formed at the tip thereof, and an outer periphery of the folded portion 14. Is mounted in the groove 25 of the connection pipe 21.
管21を接続した医療用具であって、 前記チューブ11の先端に、外筒状の折り返し部14を
形成し、該折り返し部14の外周を接続管21の前記溝
部25に装着し、前記チューブ11の前方部と前記折り
返し部14の間の空間に、かしめリング31を圧入し
た、ことを特徴とする医療用具1A。2. A medical device comprising a tube 11 and a connecting tube 21 having a groove 25 formed therein, wherein the tube 11 has an outer cylindrical folded portion 14 formed at an end thereof, and an outer periphery of the folded portion 14. Is attached to the groove 25 of the connection pipe 21, and a caulking ring 31 is press-fitted into a space between a front part of the tube 11 and the folded part 14.
管21を接続した医療用具であって、 前記補強部材付きチューブ11の先端に、外筒状の折り
返し部14を形成し、該折り返し部14の外周を接続管
21の前記溝部25に装着し、前記チューブ11の先端
と前記折り返し部14の間の空間に、アンダーカット3
6を有する外筒34を突設したかしめリング31Aを圧
入した、ことを特徴とする医療用具1B。3. A medical device in which a tube 11 and a connecting tube 21 having a groove 25 formed therein are connected to each other, wherein an outer cylindrical folded portion 14 is formed at an end of the tube 11 with a reinforcing member, and the folded portion is formed. 14 is mounted in the groove 25 of the connection pipe 21, and an undercut 3 is formed in a space between the tip of the tube 11 and the folded part 14.
6. A medical tool 1B, characterized by press-fitting a swaging ring 31A provided with an outer cylinder 34 having a protrusion 6.
する溝部25を形成した接続管21Aを接続した医療用
具であって、 前記チューブ11の先端に、外筒状の折り返し部14を
形成し、該折り返し部14の外周を接続管21Aの前記
溝部25に装着し、前記チューブ11の前方部と前記折
り返し部14と前記溝部25の間の空間に、かしめリン
グ31Bを圧入した、ことを特徴とする医療用具1C。4. A medical device in which a tube 11 and a connecting tube 21A having a groove 25 having an undercut 26 are connected thereto, wherein an outer cylindrical folded portion 14 is formed at the tip of the tube 11. The outer periphery of the folded portion 14 is attached to the groove 25 of the connecting pipe 21A, and a caulking ring 31B is press-fitted into a space between the front portion of the tube 11 and the folded portion 14 and the groove 25. Medical tool 1C.
ト26を有する溝部25を形成した接続管21Aを接続
した医療用具であって、 前記チューブ11A、11Bの先端に、鍔状の折り返し
部15、16を形成し、 該折り返し部15、16を接続管21Aの前記溝部25
に装着し、 前記チューブ11A、11Bの前方部と前記折り返し部
15、16と前記溝部25の間の空間に、かしめリング
31を圧入した、ことを特徴とする医療用具1D。5. A medical device in which tubes 11A and 11B are connected to a connecting tube 21A having a groove 25 having an undercut 26. The tubes 11A and 11B have flange-shaped folded portions 15 and 16 at their ends. And forming the folded portions 15 and 16 into the groove portions 25 of the connection pipe 21A.
A medical device 1D, wherein a caulking ring 31 is press-fitted into a space between the front portions of the tubes 11A, 11B, the folded portions 15, 16 and the groove 25.
成した接続管21を接続した医療用具であって、 前記チューブ11A、11Bの先端に、鍔状の折り返し
部15、16を形成し、 該折り返し部15、16を接続管21の前記溝部25に
装着し、 前記チューブ11A、11Bの前方部と前記折り返し部
15、16と前記溝部25の間の空間に、アンダーカッ
ト36を有する外筒34を突設したかしめリング31A
を圧入した、ことを特徴とする医療用具1E。6. A medical device in which tubes 11A and 11B are connected to a connecting tube 21 having a groove 25, wherein flanges 15 and 16 are formed at the ends of the tubes 11A and 11B. An outer cylinder 34 having an undercut 36 in a space between the front portions of the tubes 11A and 11B and the folded portions 15 and 16 and the groove 25. Caulking ring 31A
A medical device 1E, wherein the medical device 1E is press-fitted.
Aから1Eにおいて、前記かしめリング31Aの外筒3
4の内周または前記接続管21Aの溝部25のいずれか
にアンダーカット26、36を形成して、チューブ1
1、11A、11Bと接続管21、21Aを接続する代
わりに、 前記かしめリング31、31A、31Bと前記接続管2
1、21Aのそれぞれ対向する壁面に突起と溝を形成
し、これらを係合ないし嵌合させて接続するかまたは前
記それぞれ対向する突起と溝をネジ状に形成し、これら
を螺合してチューブ11、11A、11Bと接続管2
1、21Aを接続した、ことを特徴とする医療用具1、
1A、1B、1C、1D、1E。7. The medical device 1 according to claim 1, wherein:
A to 1E, the outer cylinder 3 of the caulking ring 31A
4 and the undercuts 26 and 36 are formed either in the groove 25 of the connecting pipe 21A or in the tube 1A.
Instead of connecting the connection pipes 21 and 21A to the connection pipes 1, 11A and 11B, the caulking rings 31, 31A and 31B and the connection pipe 2
A projection and a groove are formed on the opposed wall surfaces of the first and the first 21A, and these are engaged or fitted to be connected to each other, or the opposed projection and the groove are formed in a screw shape, and these are screwed together to form a tube. 11, 11A, 11B and connecting pipe 2
1, 21A connected, medical device 1, characterized in that
1A, 1B, 1C, 1D, 1E.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001011059A JP2002210022A (en) | 2001-01-19 | 2001-01-19 | Medical equipment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001011059A JP2002210022A (en) | 2001-01-19 | 2001-01-19 | Medical equipment |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002210022A true JP2002210022A (en) | 2002-07-30 |
Family
ID=18878244
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001011059A Pending JP2002210022A (en) | 2001-01-19 | 2001-01-19 | Medical equipment |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002210022A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008017987A (en) * | 2006-07-12 | 2008-01-31 | Jms Co Ltd | Pipe connection structure and infusion set |
| JP2008206641A (en) * | 2007-02-26 | 2008-09-11 | Kawasumi Lab Inc | Blood collection instrument and channel opening / closing means |
-
2001
- 2001-01-19 JP JP2001011059A patent/JP2002210022A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008017987A (en) * | 2006-07-12 | 2008-01-31 | Jms Co Ltd | Pipe connection structure and infusion set |
| JP2008206641A (en) * | 2007-02-26 | 2008-09-11 | Kawasumi Lab Inc | Blood collection instrument and channel opening / closing means |
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