JPH02218329A - Endoscope - Google Patents

Endoscope

Info

Publication number
JPH02218329A
JPH02218329A JP63244850A JP24485088A JPH02218329A JP H02218329 A JPH02218329 A JP H02218329A JP 63244850 A JP63244850 A JP 63244850A JP 24485088 A JP24485088 A JP 24485088A JP H02218329 A JPH02218329 A JP H02218329A
Authority
JP
Japan
Prior art keywords
reinforcing member
endoscope
section
reinforcing
pipe
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP63244850A
Other languages
Japanese (ja)
Other versions
JPH0677565B2 (en
Inventor
Yoshio Tashiro
田代 芳夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olympus Corp
Original Assignee
Olympus Optical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Olympus Optical Co Ltd filed Critical Olympus Optical Co Ltd
Priority to JP63244850A priority Critical patent/JPH0677565B2/en
Publication of JPH02218329A publication Critical patent/JPH02218329A/en
Publication of JPH0677565B2 publication Critical patent/JPH0677565B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Instruments For Viewing The Inside Of Hollow Bodies (AREA)
  • Endoscopes (AREA)

Abstract

PURPOSE:To provide an endoscope which possesses the superior operation performance by fitting a reinforcing member which is freely bendable over the whole length of the operation part of an insertion part and reinforcing the hardness of the operation part. CONSTITUTION:The flexible pipe 9 in an insertion part 3 consists of a spiral pipe 13 as core member for preventing collapse which is formed by winding an elastic thin strip 12 made of metal into spiral form to form a tubular form, and a screen pipe 14 which is formed by braiding a thin wire made of metal or resin into a tubular form is fitted onto the outer periphery of the spiral pipe 13. A tape-shaped reinforcing member 18 which is formed by an elastic material over the nearly whole length is fitted onto the operation part 17 of the flexible pipe 9. The outer periphery of the reinforcing member 18 is formed into tapered form which becomes thinner on the top edge side, and the softness on the top edge side is gradually increased. Therefore, when the insertion part 3 of an endoscope 1 is inserted into an uterus 19, the flexible pipe 9 is prevented from curving by the reinforcing action of the reinforcing member 18, and bending and slackening are prevented, and easy operation is permitted.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は長尺な軟性挿入部を有する内視鏡に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to an endoscope having a long flexible insertion section.

[従来の技術] 従来、長尺な軟性挿入部を有する内視鏡はその先端側に
湾曲部を構成してこれを手元操作部からの遠隔操作によ
って湾曲し得るように構成されている。そして、この挿
入部は先端から手元操作部近傍までほぼ等しい外径で形
成されている。また、この挿入部の長さはその使用対象
とするほとんどの臓器に使用する場合、その挿入部の全
長が体腔内に挿入されることがない充分な長さに作られ
ている。
[Prior Art] Conventionally, an endoscope having a long flexible insertion section has a bending section on its distal end side, which can be bent by remote control from a hand control section. The insertion section is formed with an approximately equal outer diameter from the tip to the vicinity of the hand operation section. Further, the length of the insertion portion is made to be long enough to prevent the entire length of the insertion portion from being inserted into a body cavity when used in most organs for which the insertion portion is intended.

このように体腔内に挿入されることがない部分を充分に
とる長さに作られている理由はその内視鏡の使用状況に
おいて必要だからである。すなわち、通常の内視鏡の使
用方法では術者は片手で操作部を保持し、もう一方の手
で挿入部を把持して挿入を補助する。このため、挿入部
が体腔内に最も深く挿入されたときにも、把持できるだ
けの長さ分が挿入されずに外に残るようにその挿入部の
長さが決められている。また、他の理由として内視鏡を
操作する術者と患者との距離が接近しすぎると操作しに
くいから一定の距離をあけるためにも挿入部を長くして
いる。
The reason why the endoscope is made long enough to have a sufficient length that is not inserted into the body cavity is because it is necessary in the usage situation of the endoscope. That is, in a normal method of using an endoscope, the operator holds the operating section with one hand and grasps the insertion section with the other hand to assist in insertion. For this reason, the length of the insertion portion is determined so that even when the insertion portion is inserted to the deepest point into the body cavity, a length sufficient for grasping remains outside without being inserted. Another reason is that if the operator operating the endoscope and the patient are too close together, it will be difficult to operate the endoscope, so the insertion section is made long to maintain a certain distance.

しかしながら、術者は使用中宮に挿入部を把持している
とは限らない″。たとえば処置具を操作する場合等には
挿入部を把持していた手を離すことも多い。このような
場合にはそれまで操作部を把持していた手による操作部
を通じて操作部に力を伝え、その挿入部の挿入やねじり
の操作を行なうことになり、この際、特に、挿入部の外
径の細い内視鏡では外部から支えられることのない体腔
外に露出した部分が容易に折れ曲がったり、弛んだりし
てしまい、操作部の動きに追従しにくいという不具合が
あった。
However, the surgeon does not always hold the insertion tube while using it.For example, when operating a treatment instrument, the operator often releases his/her hand from gripping the insertion tube. In this case, force is transmitted to the operating section through the operating section by the hand that was previously grasping the operating section, and the insertion tube is inserted or twisted. The endoscope has a problem in that the part exposed outside the body cavity that is not supported from the outside easily bends or loosens, making it difficult to follow the movement of the operating section.

そこで、この操作上の不具合を解決する手段として体腔
内に挿入されることがない挿入部の手元側部分の硬さを
特に硬くして追従性を良好にするいくつかの手段が提供
されている。特開昭61−68026号公報や特B8昭
61−162929号公報に示されるものはその挿入部
の可撓管を構成する部材の硬度を調整して硬さを変え、
また、特開昭61−162929号公報のものでは各部
材の厚さを変えて可撓管を太くする方式がとられている
Therefore, as a means to solve this operational problem, several methods have been proposed to improve the followability by making the proximal portion of the insertion section, which is not inserted into the body cavity, particularly hard. . What is shown in Japanese Patent Application Laid-open No. 61-68026 and Japanese Patent Application Publication No. B8-162929 adjusts the hardness of the member constituting the flexible tube of the insertion part to change the hardness,
Furthermore, in the method disclosed in Japanese Patent Application Laid-Open No. 61-162929, a method is adopted in which the thickness of each member is changed to make the flexible tube thicker.

[発明が解決しようとする課題] しかしながら、上記特開昭61−68026号公報や特
開昭61−162929号公報に示される方式はその挿
入部の可撓管を構成する部材の硬度を調整して硬さを変
えるものであるから、−般的に希望する硬さに調節する
ことが難しく、その原材料となる樹脂の硬度のばらつき
で可撓管の性状が大きく影響を受けやすい。また、樹脂
の硬度には限度があるため、その硬さの調節の範囲は狭
く、希望通りの硬さが得られるとは限らなかった。また
、特開昭61−162929号公報のもののように可撓
管の手元側部分のみを太くすると、その可撓管の途中か
らその内部構成を変えなければならず、当然ながらその
構造が複雑になる。
[Problems to be Solved by the Invention] However, the methods shown in the above-mentioned Japanese Patent Laid-Open No. 61-68026 and Japanese Patent Laid-Open No. 61-162929 do not adjust the hardness of the members constituting the flexible tube of the insertion portion. Since the hardness is changed by changing the hardness, it is generally difficult to adjust the hardness to the desired hardness, and the properties of the flexible tube are likely to be greatly affected by variations in the hardness of the resin used as the raw material. Furthermore, since there is a limit to the hardness of the resin, the range of adjustment of the hardness is narrow, and it is not always possible to obtain the desired hardness. Furthermore, if only the proximal portion of the flexible tube is made thicker, as in the case of JP-A No. 61-162929, the internal configuration must be changed from the middle of the flexible tube, which naturally complicates the structure. Become.

さらに、上記各従来のものはいずれもその挿入部の可撓
管の製造工程が複雑になり、特殊な製造設備が必要であ
った。このためにもコストアップの原因になっていた。
Furthermore, in each of the above conventional devices, the manufacturing process of the flexible tube of the insertion portion is complicated, and special manufacturing equipment is required. This also caused an increase in costs.

本発明は上記課題にむ目してなされたもので、その目的
とするところは挿入部側の構造を特に変えなくともよい
とともに簡単な構成により挿入部の手元側部分を操作し
やすい硬さに設定できる操作性のよい内視鏡を提供する
ことにある。
The present invention has been made in view of the above-mentioned problems, and its purpose is to eliminate the need to particularly change the structure of the insertion part side, and to make the proximal part of the insertion part hard enough to easily operate with a simple structure. The object of the present invention is to provide an endoscope that can be set and has good operability.

[課題を解決するための手段および作用]上記課題を解
決するために本発明は操作部に連結した軟性の挿入部の
基端側の部分を体腔内に挿入しないで把持操作を行なう
操作用部分とした内視鏡において、上記挿入部の操作用
部分のほぼ全長にわたり曲がり自在な補強部材を被嵌し
たものである。補強部材は挿入部の操作用部分の硬さを
補強し、また、握り易くして操作性を向上する。
[Means and effects for solving the problems] In order to solve the above problems, the present invention provides an operation portion that performs a grasping operation without inserting the proximal end portion of a flexible insertion portion connected to an operation portion into a body cavity. In this endoscope, a bendable reinforcing member is fitted over substantially the entire length of the operating portion of the insertion portion. The reinforcing member reinforces the hardness of the operating portion of the insertion portion, and also makes it easier to grip and improves operability.

[実施例] 第1図ないし第3図は本発明の第1の実施例を示すもの
である。この実施例では細径内視鏡の一例として子宮用
の内視vL1を示す。この内視鏡1は操作部2と長尺な
挿入部3とからなり、操作部2にはライトガイドケーブ
ル4が連結されている°。さらに、操作部2には接眼部
5と後述する湾曲操作を行なう操作レバー6とが設けら
れている。
[Embodiment] FIGS. 1 to 3 show a first embodiment of the present invention. In this embodiment, an endoscope vL1 for uterus is shown as an example of a small-diameter endoscope. This endoscope 1 consists of an operating section 2 and an elongated insertion section 3, and a light guide cable 4 is connected to the operating section 2. Further, the operating section 2 is provided with an eyepiece section 5 and an operating lever 6 for performing a bending operation, which will be described later.

また、上記挿入部3はその基端側に可撓管9を配置し、
この可撓管9の先端に湾曲管1oを介して先端部11が
連結して構成されている。湾曲管10は上記操作レバー
6による操作によって遠隔的に湾曲操作されるようにな
っている。
Further, the insertion section 3 has a flexible tube 9 disposed on its proximal end side,
A distal end portion 11 is connected to the distal end of the flexible tube 9 via a curved tube 1o. The bending tube 10 is remotely operated to bend by operating the operating lever 6.

上記挿入部3の可撓管9は第3図で示すように構成され
ている。この可撓管9は金属製の弾性薄帯12をら旋状
に巻いて管状に形成したら旋管13を潰れ防止用の芯材
としてなり、このら旋管13の外周には金属あるいは樹
脂などからなる細線を管状に編成した網管14が被嵌さ
れている。
The flexible tube 9 of the insertion section 3 is constructed as shown in FIG. This flexible tube 9 is formed into a tubular shape by spirally winding a metal elastic ribbon 12, and a spiral tube 13 is used as a core material to prevent crushing. A mesh pipe 14 made of thin wires knitted into a tubular shape is fitted.

この網管14の外周には柔軟性のある合成樹脂等からな
る外皮15が被覆されている。そして、このように構成
された可撓管9の基端(つまり、操作部2側端)はその
操作部2の本体における接続用口金16に取付は固定さ
れている。つまり、ら旋管13と網管14との重合部外
周に上記口金16を被嵌するとともに、これらをはんだ
や接着剤により固着する。さらに、外皮15の基端側部
分は上記口金16の外周に被嵌して接着剤等で固着しで
ある。
The outer periphery of the net pipe 14 is covered with an outer skin 15 made of flexible synthetic resin or the like. The proximal end (that is, the end on the operating section 2 side) of the flexible tube 9 configured as described above is fixedly attached to the connection base 16 on the main body of the operating section 2. That is, the base 16 is fitted onto the outer periphery of the overlapping portion of the spiral pipe 13 and the mesh pipe 14, and these are fixed with solder or adhesive. Further, the base end portion of the outer skin 15 is fitted onto the outer periphery of the cap 16 and fixed with an adhesive or the like.

さらに、上記挿入部3の可撓管9の基端側部分において
体腔内に挿入しない範囲の部分は術者が把持して挿入部
3の操作を行なう操作用部分17としである。そして、
この可撓管9の操作用部分17にはこのほぼ全長にわた
り弾性のある材料、たとえばゴムなどで形成したチュー
ブ状の補強部材18を被嵌してなり、この補強部材18
を術者が把持して挿入部3を操作できるようにしである
Furthermore, the portion of the proximal end portion of the flexible tube 9 of the insertion section 3 that is not inserted into the body cavity serves as an operation section 17 that is grasped by the operator to operate the insertion section 3. and,
A tubular reinforcing member 18 made of an elastic material such as rubber is fitted over almost the entire length of the operating portion 17 of the flexible tube 9.
The insertion section 3 is designed so that the operator can grasp it and operate the insertion section 3.

このため、この補強部材18の長さノはかなり長く、た
とえばこの種、子宮用の内視鏡1の場合では7〜10C
Mである。なお、この内視鏡1の挿入部3の外径は2.
5〜5.5mmである。また、上記補強部材18の長さ
は一般的な患者の体位および姿勢を考慮すると、挿入部
3の外径の30倍以上である10〜20crxが最も適
している。
Therefore, the length of this reinforcing member 18 is quite long, for example, in the case of this type of endoscope 1 for uterus, the length is 7 to 10C.
It is M. Note that the outer diameter of the insertion section 3 of this endoscope 1 is 2.
It is 5 to 5.5 mm. Further, considering the general body position and posture of a patient, the most suitable length of the reinforcing member 18 is 10 to 20 crx, which is 30 times or more the outer diameter of the insertion section 3.

また、第3図で示すようにこのチューブ状の補強部材1
8は外周を、先端側を細くしたテーパ状に形成してなり
、比較的先端側がその柔軟性が次第に高まるようになっ
ている。また、この補強部材1tはその基端が端部に埋
め込んだ接続金具17aにより操作部2の本体側に対し
て着脱自在に装着できるようになっている。
Moreover, as shown in FIG. 3, this tubular reinforcing member 1
8 has an outer periphery formed in a tapered shape with a tapered end, and its flexibility gradually increases relatively toward the end. Further, the base end of this reinforcing member 1t can be detachably attached to the main body side of the operating section 2 by means of a connecting fitting 17a embedded in the end portion.

次に、上記内視鏡1の使用方法を説明する。第2図で示
すように、この内視鏡1の挿入部3を子宮19内に挿入
するする場合、術者は一方の手で操作部2を把持すると
ともに他方の手でチューブ状の補強部材18を握りなが
ら、その挿入部3を子宮19内に押し進める。このとき
補強部材18の補強作用で可撓管9がいたずらに湾曲せ
ず、折れたり弛んだりしないから、操作しやすい。また
、処置具を使用するような場合のようにその補強部材1
8から手を離すような場合においても、その体腔外にあ
る可撓管9の部分が折れたり弛んだりしないから、操作
部2の動きを先端側に確実に伝え、挿入部3の追従性を
向上することができる。
Next, how to use the endoscope 1 will be explained. As shown in FIG. 2, when inserting the insertion section 3 of the endoscope 1 into the uterus 19, the operator grasps the operating section 2 with one hand and inserts the tube-shaped reinforcing member with the other hand. 18, push the insertion section 3 into the uterus 19. At this time, the reinforcing action of the reinforcing member 18 prevents the flexible tube 9 from unnecessarily bending, bending, or loosening, making it easy to operate. In addition, when using a treatment instrument, its reinforcing member 1
Even if you take your hand off the body cavity 8, the portion of the flexible tube 9 outside the body cavity will not break or loosen. can be improved.

特に、細径の挿入部3で可撓性が高いものにおいて、こ
の作用効果を格段に奏する。また、上記補強部材18は
先端側に向かって次第に細くたわみ易くなっているため
、使用中いろいろな方向に可撓管9が曲げられても、常
に、スムーズな曲率の変化で曲がり、可撓管9が急激に
曲がったり折れたりしない。しかも、補強部材18はそ
の先端付近で最も柔らかいから、この先端付近で挿入部
3が座屈することがなく、すぐれた折止め効果を奏する
Particularly, in the case of the insertion portion 3 having a small diameter and high flexibility, this effect is particularly achieved. In addition, since the reinforcing member 18 becomes thinner and more flexible toward the distal end, even if the flexible tube 9 is bent in various directions during use, the reinforcing member 18 will always bend with a smooth change in curvature. 9 will not bend or break sharply. In addition, since the reinforcing member 18 is the softest near its tip, the insertion portion 3 does not buckle near this tip, providing an excellent breakage prevention effect.

また、通常の患者の体位ではその子宮19の高さは術者
が保持する操作部2の高さより低い位置にあるため、挿
入部3の可撓管9に被嵌された補強部材18は第2図で
示すように曲がった状態で使用される。その子宮19の
体腔内の検査に伴って挿入部3に進退動を加える必要が
あるが、この操作は上記操作力の伝達作用によって操作
部2の前後動を先端側に確実に伝えることによってスム
ーズに行なうことができる。
In addition, in a normal patient position, the height of the uterus 19 is lower than the height of the operating section 2 held by the operator, so the reinforcing member 18 fitted into the flexible tube 9 of the insertion section 3 is It is used in a bent state as shown in Figure 2. It is necessary to move the insertion section 3 forward and backward in order to inspect the body cavity of the uterus 19, but this operation is smooth because the forward and backward movement of the operating section 2 is reliably transmitted to the distal end side by the transmission of the operating force described above. can be done.

また、上記補強部材18の外径は挿入部3の外径よりも
太いため、これを術者は握り易くなり、上述したように
挿入部3の外径が小さいものでも操作し易い。挿入部3
の外径を太くする、この補強部材18は体腔内に入らず
、体外に位置するから、太いことによる挿入性の低下や
患者の苦痛を招くことがない。
Further, since the outer diameter of the reinforcing member 18 is larger than the outer diameter of the insertion section 3, it is easier for the operator to grasp it, and as described above, even if the outer diameter of the insertion section 3 is small, it is easy to operate. Insertion part 3
The reinforcing member 18, which increases the outer diameter of the reinforcing member 18, does not enter the body cavity but is located outside the body, so that the thicker part does not reduce insertability or cause pain to the patient.

また、この補強部材18はその材料の硬度や、肉厚を変
えた複数種のものを用意しておき、これを使用状況に応
じて選択使用すれば、最適な状態で使用できる。
Moreover, the reinforcing member 18 can be used in an optimal state by preparing a plurality of types of reinforcing members with different material hardnesses and wall thicknesses, and selecting and using them according to usage conditions.

そして、この構成では内視鏡1の挿入部3の構成とは別
の補強部材18で挿入部3における操作用部分17の硬
さを変えるため、その挿入部3側の構造を簡略化できる
。しかも、補強部材18の構成も簡単である。したがっ
て、これらの製造方法が容易で大幅なコ、ストダウンを
図ることができる。
In this configuration, the stiffness of the operating portion 17 in the insertion section 3 is changed by a reinforcing member 18 that is different from the configuration of the insertion section 3 of the endoscope 1, so that the structure on the insertion section 3 side can be simplified. Moreover, the structure of the reinforcing member 18 is also simple. Therefore, these manufacturing methods are easy and can significantly reduce cost.

第4図は本発明の第2の実施例を示すものである。この
実施例はその補強部材18の構造が異なり、弾性材料か
らなるチューブ本体21の内面部にら旋状の金属製部材
からなる芯材22を埋め、込んだものである。この実施
例での芯材22は容易に塑性変形可能な金属材料(例え
ば軟鋼線)からなる素線を手元側から先端側に向けて徐
々にピッチが粗くなるように配設したものである。した
がって、芯材22自体の可撓性も先端側程高まり、挿入
部3に対する折止め効果が向上する。
FIG. 4 shows a second embodiment of the invention. In this embodiment, the structure of the reinforcing member 18 is different, and a core material 22 made of a spiral metal member is embedded in the inner surface of a tube body 21 made of an elastic material. The core material 22 in this embodiment is made of wires made of a metal material (for example, mild steel wire) that can be easily plastically deformed and arranged so that the pitch gradually becomes coarser from the proximal side to the distal end side. Therefore, the flexibility of the core material 22 itself increases toward the distal end, and the effect of securing the insertion portion 3 is improved.

しかして、この実施例によれば、その補強部材18を任
意の角度に湾曲してその状態に保持して使用できる。つ
まり、補強部材18で挿入部3における操作用部分17
の形状を必要な曲げ形状に保持させて使用できる。その
他の構成、および作用効果は上記実施例と同様である。
According to this embodiment, the reinforcing member 18 can be bent at any angle and held in that state. In other words, the reinforcing member 18 is used for the operation portion 17 of the insertion portion 3
It can be used by keeping the shape in the required bent shape. Other configurations and effects are the same as those of the above embodiment.

なお、上記芯材22の素線の形状としては丸の場合に限
らず、第5図(A)で示すように矩形状のものや、第5
図(B)で示すように潰し線材を使用するものでもよい
。また、次の表1は挿入部の全長とその挿入部の外径、
および補強部材を被嵌する操作用部分の長さ(補強用部
材の長さgにほぼ相当する)の関係を各種内視鏡ごとに
示したものである。
Note that the shape of the wire of the core material 22 is not limited to a round shape, but may also be a rectangular shape as shown in FIG.
As shown in Figure (B), a crushed wire rod may be used. In addition, the following Table 1 shows the total length of the insertion section, the outer diameter of the insertion section,
and the length of the operating portion into which the reinforcing member is fitted (which approximately corresponds to the length g of the reinforcing member) is shown for each type of endoscope.

表  1 [発明の効果] 以上説明したように本発明は操作部に連結した軟性の挿
入部の基端側の部分を体腔内に挿入しないで把持操作を
行なう操作用部分とした内視鏡において、上記挿入部の
操作用部分のほぼ全長に弾性のある補強部材を被嵌し、
この補強部材を把持して挿入部を操作できるようにした
ものであるから、その挿入部側の構造を特に変えなくと
もよく、また、簡単な構成により挿入部の手元側部分を
操作しやすい硬さに設定できて内視鏡の操作性を向上で
きるなど種々の格別な効果を奏することができる。
Table 1 [Effects of the Invention] As explained above, the present invention provides an endoscope in which the proximal portion of the flexible insertion portion connected to the operation portion is used as the operation portion for performing grasping operations without inserting into the body cavity. , an elastic reinforcing member is fitted over almost the entire length of the operating portion of the insertion portion;
Since the insertion tube can be operated by grasping this reinforcing member, there is no need to change the structure of the insertion tube side, and the simple structure makes it easy to operate the proximal side of the insertion tube. It is possible to achieve various special effects such as being able to set the endoscope to the desired position and improving the operability of the endoscope.

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

第1図は本発明の第1の実施例の内視鏡の側面図、第2
図は同じくその内視鏡の使用状態の説明図、第3図は同
じくその内視鏡の要部の断面図、第4図は本発明の第2
の実施例の内視鏡の要部の断面図である。 1・・・内視鏡、2・・・操作部、3・・・挿入部、9
・・・可撓管、17・・・操作用部分、18・・・補強
部材。 1、事件の表示 特願昭63−244850号 発明の名称 補正をする者 事件との関係  特許出願人 (037)  オリンパス光学工業株式会社4、代理人 東京都千代田区霞が関3丁目7番2号 7、補正の内容 (1)第2頁第20行目の「手による操作部を通じて操
作部に」を「手により操作部を通じて挿入部に」に補正
する。 (2)第7頁第6行目から第12行目の「このため、こ
の補強部材〜最も適している。」を「たとえば、子宮用
の内視vL1の場合では、挿入部3の外径は2.5〜5
.5mmで、体腔内に挿入される部分の長さは7〜10
cmである。そして、補強部材18の長さは一般的な患
者の体位および姿勢を考慮すると、挿入部3の外径の3
0倍以上である10〜20cmが最も適している。」に
補正する。 手 続 補 正 書 (方式) 事件の表示 特願昭63−244850号 発明の名称 内     視     鏡 補正をする者 事件との関係  特許出願人
FIG. 1 is a side view of an endoscope according to the first embodiment of the present invention, and FIG.
The figure is also an explanatory diagram of the use state of the endoscope, FIG. 3 is a sectional view of the main parts of the endoscope, and FIG.
FIG. 3 is a cross-sectional view of main parts of the endoscope according to the embodiment. 1... Endoscope, 2... Operation section, 3... Insertion section, 9
. . . Flexible tube, 17. Operation portion, 18. Reinforcement member. 1. Indication of the case Patent Application No. 63-244850 Person amending the name of the invention Relationship with the case Patent applicant (037) Olympus Optical Industry Co., Ltd. 4 Agent 3-7-2-7 Kasumigaseki, Chiyoda-ku, Tokyo , Contents of correction (1) In the 20th line of page 2, "to the operating section through the operating section by hand" is corrected to "to the insertion section via the operating section by hand." (2) From page 7, line 6 to line 12, “For this reason, this reinforcing member is the most suitable.” is 2.5-5
.. The length of the part inserted into the body cavity is 7 to 10 mm.
cm. Considering the general body position and posture of the patient, the length of the reinforcing member 18 is set to 3
The most suitable distance is 10 to 20 cm, which is 0 times or more. ”. Procedural amendment (method) Indication of the case Patent application No. 1983-244850 In the title of the invention Person making the amendment Relationship with the case Patent applicant

Claims (1)

【特許請求の範囲】[Claims] 操作部に連結した軟性の挿入部の基端側の部分を体腔内
に挿入しないで把持操作を行なう操作用部分とした内視
鏡において、上記挿入部の操作用部分のほぼ全長にわた
り曲げ自在な補強部材を被嵌したことを特徴とする内視
鏡。
In an endoscope in which the proximal portion of the flexible insertion section connected to the operation section is used as an operation section for grasping without being inserted into a body cavity, the operation section of the insertion section is bendable over almost the entire length. An endoscope characterized by being fitted with a reinforcing member.
JP63244850A 1988-09-29 1988-09-29 Endoscope Expired - Fee Related JPH0677565B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63244850A JPH0677565B2 (en) 1988-09-29 1988-09-29 Endoscope

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63244850A JPH0677565B2 (en) 1988-09-29 1988-09-29 Endoscope

Publications (2)

Publication Number Publication Date
JPH02218329A true JPH02218329A (en) 1990-08-31
JPH0677565B2 JPH0677565B2 (en) 1994-10-05

Family

ID=17124905

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63244850A Expired - Fee Related JPH0677565B2 (en) 1988-09-29 1988-09-29 Endoscope

Country Status (1)

Country Link
JP (1) JPH0677565B2 (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5143029U (en) * 1974-09-27 1976-03-30
JPS6264330A (en) * 1985-09-17 1987-03-23 オリンパス光学工業株式会社 Endoscope
JPS62113124A (en) * 1985-11-12 1987-05-25 Asahi Optical Co Ltd Breakage preventer for flexible tube of endoscope
JPS63122419A (en) * 1986-11-11 1988-05-26 富士写真光機株式会社 Hysteroscope
JPS63140902U (en) * 1987-03-10 1988-09-16

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5143029U (en) * 1974-09-27 1976-03-30
JPS6264330A (en) * 1985-09-17 1987-03-23 オリンパス光学工業株式会社 Endoscope
JPS62113124A (en) * 1985-11-12 1987-05-25 Asahi Optical Co Ltd Breakage preventer for flexible tube of endoscope
JPS63122419A (en) * 1986-11-11 1988-05-26 富士写真光機株式会社 Hysteroscope
JPS63140902U (en) * 1987-03-10 1988-09-16

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