BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is an overall construction view of an electrosurgical treatment equipment showing one embodiment according to the present invention;
FIG. 2 is an exterior view of the FIG. 1 electrosurgical treatment equipment at its tip;
FIG. 3 is a sectional view of the FIG. 1 electrosurgical treatment equipment at the tip of the FIG. 1 electrosurgical treatment equipment;
FIG. 4 is a sectional view in the state an electrosurgical knife is retracted in a flexible sheath, in a position as viewed 90-degree different from that in FIG. 3;
FIG. 5 is a structural explanatory view of the tip of the flexible sheath in the state the electrosurgical knife is projected;
FIG. 6 is a sectional view of the FIG. 1 electrosurgical treatment equipment, taken in a direction of a main stem and along the slit groove thereof;
FIG. 7 is a sectional view taken on line X-X in FIG. 6;
FIG. 8 is an exterior view of an electrosurgical treatment equipment showing one embodiment of the invention, in the state passed through an treatment equipment-passage channel for an endoscope;
FIG. 9 is a plan view showing the state marks are put on a diseased mucous membrane;
FIG. 10 is a sectional view of a tissue showing the state that local injection is being made to the diseased point of the mucous membrane;
FIG. 11 is a sectional view of the tissue showing the state that incision is being performed by use of the electrosurgical treatment equipment;
FIG. 12 is a plan view including the diseased point of the mucous membrane showing the state that incision with the electrosurgical treatment equipment is completed;
FIG. 13 is a sectional view of the tissue showing the state that exfoliation is made of the mucous membrane;
FIG. 14 is a sectional view showing a second embodiment of the invention, taken in a direction along the slit groove of the main stem in an incisive position;
FIG. 15 is a sectional view showing the second embodiment of the invention, taken in the direction along the slit groove of the main stem in an exfoliative position;
FIG. 16 is a structural explanatory view showing a third embodiment of the invention, illustrating a coupling of between a terminal pin and a swing arm; and
FIG. 17 is an explanatory view showing the third embodiment, illustrating a connection state of a terminal pin, a conductor wire and a wiring cable.
DETAILED DESCRIPTION OF THE INVENTION
Based on the drawings, explanation will now be made on embodiments according to the present invention. The embodiments explain on the mechanism adapted to incise and exfoliate a diseased mucous membrane. Note that the electrosurgical treatment equipment in the invention is naturally to be applied to other types of procedures. FIG. 1 shows an overall construction of an electrosurgical treatment equipment, FIG. 2 an exterior view of a tip thereof, and FIG. 3 a sectional view taken on line X-X in FIG. 2.
In FIG. 1, reference numeral 1 designates an electrosurgical treatment equipment. The electrosurgical treatment equipment 1 has a flexible sheath 2 made up by an elongate insulation tube. The flexible sheath 2 has a base that is connected with a connection pipe 3 while the connection pipe 3 is coupled with a handle section 4 at the end thereof. The handle section 4 is structured with a main stem 5 that is coupled to the connection pipe 3 and a slider 6 that is fit axially movably over the main stem 5 and to be handled by operator's fingers.
At the tip of the flexible sheath 2, an electrosurgical knife 10 is arranged formed of an electrode member in a circular rod form having a semispherical tip, as shown in FIG. 2. As shown in FIG. 3, the electrosurgical knife 10 is coupled with a flexible cord 11. The flexible cord 11 is formed by a conductive wire 11a covered with an insulation coat 11b. The flexible cord 11 extends through the interior of the flexible sheath 2 and connection pipe 3, the base of which is coupled to the slider 6 of the handle section 4. Accordingly, by moving the slider 6 forward over the main stem 5 as shown in the solid lines in FIG. 1, the electrosurgical knife 10 is positioned projecting at the tip of the flexible sheath 2 as shown in FIG. 3. In this position, the electrosurgical knife 10 is operative, i.e. in an incisive position. In case the slider 6 is moved rearward from the incisive position into a position shown with the virtual lines in the figure, the electrosurgical knife 10 is completely retracted in the flexible sheath 2 as shown in FIG. 4. In this position, exfoliation is possible to perform on a mucous membrane under the supply of a radio-frequency current to RF current conductors 14, referred later.
At the tip of the flexible sheath 2, provided are an introduction ring 12 and an insulation tip 13 as shown in FIG. 3. The insulation tip 13 is a pipe-like member formed of an electric insulation material having heat resistance and rigidity, e.g. ceramic. The introduction ring 12 is not necessarily formed of an electric insulation material but requires heat resistance. The introduction ring 12 and the insulation tip 13 are received in the tip of the flexible sheath 2 and fixed therein through the means of an adhesive or the like.
The introduction ring 12 has an introducing surface 12a formed slant at a predetermined angle relative to the outer periphery thereof while the insulation tip 13 has a reception passage 13a that receives the electrosurgical knife 10 therein. Accordingly, the electrosurgical knife 10 is axially aligned by being guided by the introduction ring 12 at its introducing surface 12a so that it can project to the outside through the reception passage 13a of the insulation tip 13. The electrosurgical knife 10 is received in a play-fit manner in the reception passage 13a of the insulation tip 13. As shown in FIGS. 3 and 4, a plurality of vanes 10a are formed in an outer peripheral surface of the electrosurgical knife 10 so that the electrosurgical knife 10 can be positioned stable without positional deviations at its axis when passed in the insulation tip 13. The vanes 10a are each formed with a stopper wall 10b at the base thereof in order to restrict the projection amount of the electrosurgical knife 10 out of the flexible sheath 2, so that those at the stopper walls 10b can abut against the base-end face of the insulation tip 13. Accordingly, this constitutes a greatest-projection regulating section that regulates the greatest projection of the electrosurgical knife 10 out of the flexible sheath 2. Here, the electrosurgical knife 10, when projected greatest at the tip of the flexible sheath 2, has a projection that is restricted in amount equal to or greater than a thickness of the mucous layer LU and equal to or smaller than the total thickness of the mucous layer LU and submucous layer LM. Accordingly, the electrosurgical knife 10 is not to reach a muscular layer LB even if it is projected greatest in the state the flexible sheath 2 is put at its tip surface in contact with the mucous layer LU.
As apparent in FIG. 2, the flexible sheath 2 is arranged with electrode members at the tip thereof, in both left and right positions, i.e. in positions having a 180-degree angular relationship. Those electrode members constitute RF current conductors 14 that are to be connected to an RF power source. The RF current conductors 14 are provided exposed in the outer peripheral surface of the flexible sheath 2, each of which has a width comparatively small and an axial length slightly greater than the fit length of the insulation tip 13.
The RF current conductors 14 are respectively connected with wires 15a, as shown in FIG. 4. The wires 15a extend along the inner surface of the flexible sheath 2 and united into one as a wire cable 15, thus extending from the flexible sheath 2 to an interior of the main stem 5 of the handle section 4 through the connection pipe 3.
The handle section 4 is removably connected with a cable 8 of from the RF power source 7 so that RF power can be fed to the electrosurgical knife 10 and RF current conductors 14. Meanwhile, the subject is placed in contact with not-shown opposite pole plates, which causes cauterization at the contact between the electrosurgical knife 10 and RF current conductors 14 and the body-cavity wall. The slider 6 has a terminal pin 9, allowing the cable 8 to be connected to the terminal pin 9.
FIGS. 6 and 7 show a structure of the handle section 4. As apparent from the figures, a slit groove 5a is formed in a manner penetrating in a left-right direction, in the main stem 5 over which the slider 6 is fit. The flexible cord 11, connected to the electrosurgical knife 10, extends to the slit groove 5a of the main stem 5 through the connection pipe 3. The slider 6 is removably attached with a coupling block 20. The coupling block 20 is coupled with an electrode member 21 formed of a conductive material and for pulling the flexible cord 11 in and out. Thus, the flexible cord 11 is coupled to the electrode member 21 while the conductor wire 11a of the flexible cord 11 is electrically connected with the electrode member 21.
The connection pin 9 has a rod portion 9a that is fit in an attachment hole 6a provided in the slider 6. The rod portion 9a is extended with an electric connection 9b on the side opposite to the connection pin 9. The electric connection 9b is received with a tip of the electrode member 21 that is coupled to the coupling block 20 removably attached in the slider 6. This places the conductor wire 11a of the flexible cord 11 in electrical connection with the connection pin 9, to supply RF current to the electrosurgical knife 10. Incidentally, the slider 6 and the coupling block 20 are formed of an electrically insulating material, e.g. synthetic resin.
Meanwhile, the wire cables 14 of from the RF current conductors 14 are connected to the a wiring pattern 22 formed on the surface of the slit groove 5a. The wiring pattern 22 is covered with an insulation coat. A contact 23 is provided in a position where the electrode member 21 lies when the slider 6 is moved to the position shown by the virtual lines in FIG. 1, i.e. moved to the exfoliative position. The contact 23 is in electrical connected with the wiring pattern 22. Accordingly, when the slider is moved to the exfoliative position, the electrode member 21 is placed in connection with the contact 23, to supply power to the RF current conductors 14.
Furthermore, the electrosurgical treatment equipment 1 has a fluid supply/drain passage. The fluid supply/drain passage is structured with an interior path of the flexible sheath 2. A fluid connector 30 is formed on the connection pipe 3 coupled with the flexible sheath 2, to connect with a syringe, tube or the like. Meanwhile, a plurality of passages 31 are formed between adjacent ones of the vanes 10a, 10a of the electrosurgical knife 10, at the tip of the flexible sheath 2 (see FIG. 5). Accordingly, by connecting a liquid pressure-feed section to the fluid connector 30, a tissue-expander liquid, such as physiological saline or hyaluronic acid, is supplemented to a point to swell. Meanwhile, by connecting a vacuum section, aspiration is made available from the body interior.
The electrosurgical treatment equipment 1 thus constructed is to be inserted in a body cavity through an treatment equipment-passage channel C provided in an endoscope insertion tube S having an observation portion W, as shown in FIG. 8. When there is a diseased mucous membrane in a body cavity wall, say, of the esophagus, stomach, duodenum or large intestine, it is used to exfoliate and remove the diseased mucous membrane. Therefore, explanation is made on an example of the procedure to remove a diseased mucous membrane. The procedure is conducted when a diseased point is confirmed existing in a mucous membrane as a result of examination with an endoscope S.
At first, marking is made on a mucous membrane where there exists a diseased region D to remove, in a manner to surround the diseased region D. The marking is limited in area that can remove the diseased region can be removed completely with less damage to the healthy mucous membrane to a possible extent. Marking can be made, for example, by putting cauterization spots B at required points in a peripheral region A of the diseased mucous membrane D. The electrosurgical treatment equipment 1 can be used in forming such cauterization spots B. Namely, the endoscope insertion tube S at its tip is put facing to the diseased mucous membrane D at its outer edge with a predetermined spacing. In this state, the electrosurgical treatment equipment 1 is inserted in the treatment equipment-passage channel C and placed at its tip in contact with a surface of the mucous membrane. At this time, the electrosurgical knife 10 is in a state retracted to a position closer to the base end in the rigid cylinder 2, as shown in FIG. 4. Here, the flexible sheath 2 of the electrosurgical treatment equipment 1 has a tip made as an annular end wall having a dimension totalized over the thickness of the flexible tube 2 and the thickness of the insulation tip 12. The annular end wall is to contact with a mucous membrane surface at a broad area.
In this state, the handle section 4 of the electrosurgical treatment equipment 1 is operated to move the slider 6 forward to the solid-lined position in FIG. 1. Due to this, the electrosurgical knife 10 projects out of the flexible sheath 2. In this state, in case an RF current is applied to the electrosurgical knife 10, the mucous membrane is cauterized at a point the electrosurgical knife 10 is in contact therewith, thus effecting a marking. Here, in making such a marking, the electrosurgical knife 10 is not required to penetrate through a mucous layer LU. It is satisfactory to cause a cauterization in the mucous membrane surface to an extent that recognition is possible from an image obtained through the observation portion W. Because the electrosurgical knife 10 is always in electrical connection to the connection pin 9 through the conductor wire 11a of the flexible cord 11 and the electrode member 21, current supply is available even in a state the electrosurgical knife 10 is projected slightly out of the flexible sheath 2 provided that the cable 8 of from the RF power source 7 is connected to the connection pin 9 of the slider 6. Here, because the greatest projection of the electrosurgical knife 10 out of the flexible sheath 2 is given smaller than the total thickness of the mucous layer LU and submucous layer LM, even in case the slider 6 is moved fully in its stroke, the electrosurgical knife 10 is not to reach a contact point with a muscular layer LB. Thus, there is no fear to invade the muscular layer LB. Note that, marking can be by use of other types of treatment equipments. Meanwhile, provided that the mucous-membrane region to remove is to be recognized through the observation portion W, there is no need to employ the technique of cauterization as in the foregoing.
Then, tissue-expander liquid, such as hyaluronic acid, is locally injected to the diseased mucous membrane D, specifically to the submucous layer LM, as shown in FIG. 10. In order for this, the electrosurgical treatment equipment 1 is once withdrawn out of the treatment equipment-passage channel. In place therewith, a local-injection section, having an injection needle N at the tip of the flexible tube, is inserted in the treatment equipment-passage channel C. Here, the injection needle N is to be punctured to the submucous layer LM through the mucous layer LU, to inject a tissue-expander liquid. As a result, the submucous layer LM swells and rises. In this manner, the submucous layer LM is swelled in order to conduct the procedure smoothly and safely through fully isolating the mucous layer LU from the muscular layer LM.
After swelling the submucous layer LM, the local injection section is withdrawn out of the treatment equipment-passage channel C. The electrosurgical treatment equipment 1 is again inserted in the treatment equipment-passage channel C, to project the flexible sheath 2 by a predetermined amount. In this case, the cable 8 of from the RF power source 7 is kept connected to the connection pin 9. However, because the supply of power from the RF power source 7 is controlled by a switch section (not shown) separately provided, power is not necessarily immediately supplied in this state.
The slider 6 is moved forward from the virtual-lined position in FIG. 1 to the solid-lined position, by manual operation or so. Due to this, the electrosurgical knife 10 is projected from the tip of the insulation tip 13. However, once the vanes 10a at the stopper walls 10b come into abutment against the base-end face of the insulation tip 13, the electrosurgical knife 10 no longer projects out of the flexible sheath 2 furthermore. In this state, while supplying a current from the RF power source 7 to the electrosurgical knife 10 through the conductor wire 11a of the flexible cord 11, the electrosurgical treatment equipment 1 is operated in a manner to push the entire thereof out of the treatment equipment-passage channel C. Due to this, the mucous layer LU is cut by the electrosurgical knife 10 wherein the flexible sheath 2 at its tip face, specifically the flexible sheath 2 and insulation tip 13 at its tip face, is pushed upon the body cavity wall. The supply of power from the RF power source 7 is controlled by means of a switch section (not shown) provided separately. As a result, starting a cauterization by means of the electrosurgical knife 10, the electrosurgical knife 10 is lead down to the submucous layer LM through the membrane layer LU, thus incising the diseased mucous membrane D.
In this state, by moving the endoscope insertion tube S or bending its bend portion under the observation through the viewing window W, incision is proceeded with a movement along the cauterization spots B. Because the electrosurgical knife 10 is restricted in its projection amount and the submucous layer LM is swelled by local injection, the mucous layer LU can be positively incised unless the mucous membrane at its surface is deformed extremely by the tip of the flexible sheath 2. Moreover, the mucous layer LU can be incised without giving any damage to the muscular layer LB. Here, because the electrosurgical knife 10 is restricted in its projection amount out of the flexible sheath 2, the muscular layer LB is not invaded when the slider 6 is placed in an incisive position advanced fully in stroke, thus assuring safe operation without incurring such a situation as perforation or bleeding.
Incision is made throughout the periphery of the marked region as shown in FIG. 12, with a result that the mucous layer LU is incised at around the periphery of the diseased mucous membrane D, thus resulting in a state the submucous layer LM is exposed. Incidentally, the diseased mucous membrane D in its entirety was incised at one time in FIG. 12. Where such a diseased mucous membrane D is significantly broad, incision may be in a part followed by exfoliation, referred later, so that the procedure can be repeated a plurality of number of times.
The mucous layer LM cannot be removed by merely incising the diseased mucous membrane D at the entire periphery thereof. Namely, because the mucous layer LU and the muscular layer LB are connected through a fibrous submucous layer LM, there is a need to exfoliate the mucous layer LU by cutting the fibrous tissue. It is not desirable to exfoliate such a mucous membrane by use of an electrosurgical knife 10 in an elongate rod form and restricted in projection amount, in respect of efficiency, safety in handling and so on. Therefore, in place of the electrosurgical knife 10, exfoliation procedure is performed by means of the RF current conductors 14 provided in the flexible sheath 2 at the tip outer periphery thereof.
In order for this, the slider 6 constituting the handle section 4 is operated in a manner being slid rearward over the main stem 5. This pulls the flexible cord 11, coupled to the slider 6, toward the base end. The electrosurgical knife 10 is retracted in the flexible sheath 11. When the slider 6 is moved to the stroke end, i.e. to the virtual-lined position in FIG. 1, the electrode member 21, connected to the coupling block 20 and electrically connected to the terminal pin 9, is placed in abutment against the contact 23, thus resulting in a state that power is to be supplied to the RF current conductors 14 through the wiring pattern 22 and wiring cable 15. At this time, power is desirably shut down from being supplied to the electrosurgical knife 10. By separately providing a switch section, the supply of power to the electrosurgical knife 10 can be shut down when power is being supplied to the RF current conductors 14. By observing the tip of the flexible sheath 11 through the observation portion W of the endoscope S, confirmation is made on the position of RF current conductors 14. The RF current conductors 14 are desirably regulated nearly parallel with the mucous layer LU. Where there is a need for directional regulation as a result of observation through the observation portion W, directional adjustment is made in a manner twisting the flexible sheath 2.
In this state, the flexible sheath 2 is moved in the exposed portion of the submucous layer LM caused due to the incision by means of the electrosurgical knife 10, as shown in FIG. 13. While supplying an RF current from the RF power source 7, the flexible sheath 2 is moved horizontally or swung, thereby cutting the submucous layer LM in a manner cauterizing it through the action of the RF current. The movement can be easily done by incurvating the tip of the endoscope insertion tube S or so. As a result, the mucous membrane can be exfoliated with swiftness and efficiency. Here, because the RF current conductors 14 are adjusted nearly parallel with the mucous layer LU, exfoliation can be effected with smoothness and swiftness. Moreover, because the RF current conductors 14 are nearly parallel also with the muscular layer LB, there is no fear that the RF current conductors 14 be put in contact with the muscular layer LB in the procedure.
Here, even in the exfoliative position, the electrosurgical knife 10 is in connection to the RF power source 7. However, because the electrosurgical knife 10 is retracted in the electrically-insulating flexible sheath 2 and positively isolated from the body cavity wall, there is no possibility that current flow from the electrosurgical knife 10 to the opposite pole plate. The incised mucous layer LU can be exfoliated by the operation of the RF current conductors 14 only.
Incidentally, where a procedure is performed based on an RF current of from the RF power source 7 during incision or exfoliation, there is a possibility to cause bleeding at the procedure site, etc. In such a case, the bleeding point can be irrigated rapidly by supplying a cleaning liquid under pressure into the flexible sheath 2 through the connection port 3a of the connection pipe 3. The cleaning liquid can be supplied through the reception passage 13a of the insulation tip 13 where the electrosurgical knife 10 is retracted in the flexible sheath 2, or through the plurality of passages 31 given between the vanes 10a, 10a of the electrosurgical knife 10. Meanwhile, a tissue-expander liquid is necessarily supplied when exfoliating a mucous membrane. There is a possible case that a swelled region shrinks due to the outflow in the course of procedure or the imbibition in the body despite a tissue-expander liquid is already poured locally. In order to avoid this, mucous-membrane incision or exfoliation can be made while supplying a tissue-expander liquid in order to keep the mucous submucous layer LM in a swelled state.
As described so far, two types of procedures, i.e. mucous membrane incision and exfoliation, can be performed by use of one single electrosurgical treatment equipment 1. Moreover, incision is by use of the electrosurgical knife 10 made by a thin rod-like electrode whereas exfoliation is by means of the RF current conductors 14 provided a pair in side surfaces of the flexible sheath 2 and having a predetermined width and length. By making the electrosurgical knife 10 and RF current conductors 14 in a structure suited for the purpose, a diseased mucous membrane D can be removed smoothly by continuous procedure without requiring a troublesome handling, e.g. exchanging the treatment equipment at the treatment equipment-passage channel C. Moreover, the diseased mucous membrane D can be removed completely while reducing the damage to the health tissue to the minimum. Furthermore, because the electrosurgical knife 10 is regulated in projection amount out of the flexible sheath 2, procedure can be done with safety but less in invasion thus assuring safe operation without incurring such a situation as perforation or bleeding in the procedure.
FIGS. 14 and 15 shows a second embodiment according to the invention. In this embodiment, a slider 41 constituting a handle section 40 is arranged with a terminal pin 42 for connection to an RF power source wherein the terminal pin 42 is to be connected, by switchover, to an electrosurgical knife 10 and RF current conductors 14. For this reason, the slider 41 is coupled therein with a clamp member 43 formed of an electrical insulation material wherein the clamp member 43 is coupled with a flexible cord 11 at its end. The flexible cord 11 has a conductor wire 11a electrically connected to a contact 44 provided in the clamp member 43. Furthermore, the slider 41 is also provided with a slide electrode 45 to be electrically connected to the terminal pin 42. The slide electrode 45 is to be slid axially of the main stem 5 by means of a not-shown knob. The slide electrode 45, if slid to any position, is to be in electrical conduction to the terminal pin 42. Furthermore, the wiring cable 15 of from the RF current conductors 14 is connected to a contact member 46 provided fixedly on a predetermined position of the main stem 5. The contact member 46 has a contact 46a.
With the above structure, the electrosurgical treatment equipment 1 is put in an operative position, i.e. in a position the slider 41 is positioned forward, as shown in FIG. 14, to project the electrosurgical knife 10 out of the tip of the flexible sheath 2. By placing the slide electrode in a forward position, the contact 44 electrically connected with the conductor wire 11a of the flexible cord 11 is brought in a state connected with the slide electrode 45 and terminal pin 42. Accordingly, incision is made possible to perform by feeding a current to the electrosurgical knife 10.
The slider 41, if slid rearward, takes the position shown in FIG. 15, thus placing the electrosurgical tool 1 in an exfoliative position. Namely, because the clamp member 43 coupled to the slider 41 moves, the flexible cord 11 coupled to the clamp member 43 is pulled out to retract the electrosurgical knife 10 coupled to the tip of the flexible cord 11 in the flexible sheath 2. In this state, in case the slide electrode 45 is moved backward, the slide electrode 45 is placed out of conduction from the contact 44 that is closer to the flexible cord 11, thus being placed into electrical connection with the contact 46a of the contact member 46 connected to the wiring cable 46 and hence conducted to the RF current conductors 14. As a result, exfoliation can be performed on the mucous membrane continuously from incision, without exchanging the treatment equipment in the treatment equipment-passage channel C. Moreover, during exfoliation of the mucous membrane, no RF current flows through the electrosurgical knife 1.
Here, in the second embodiment, by manually operating the slide electrode 45, the terminal pin 42 arranged on the slider was switched over to between the conductor line 11a of the flexible cord 11 leading to the electrosurgical knife 10 and to the wiring cable 15 leading to the RF current conductors 14. Alternatively, switchover is available in conjunction with the movement of the slider 41. As shown in FIG. 16, a swing arm 51 is coupled onto the terminal pin 50 arranged on the slider, to rotate about the axis 50a of the terminal pin 50. As shown in FIG. 17, the swing arm 51 is fit with a contact 52. The slider is fit with a clamp member 53 coupled to the flexible cord 11. The clamp member 53 has a contact 54 connected with the conductor wire 11a of the flexible cord 11. Meanwhile, a contact member 55 connected to the wiring cable 15 is fixed on the main stem 5 in a position closer to the base end. The contact member 55 is fit with a contact 55a.
Here, the main stem 5 is formed with a cam surface 56 in a position frontward of the arrangement of the contact member 55. When the slider is moved rearward, the cam surface 56 causes the swing arm 51 to rotate about the terminal pin 50 in conjunction with the operation thereof.
With this structure, when the slider is in a forward state, electric connection is available with the conductor wire 11a of the flexible cord 11 connected to the electrosurgical knife 10, as shown by the solid lines in FIG. 17. Meanwhile, when the slider is moved rearward along the arrow “b” in FIG. 17 into a position shown by the virtual line in the figure, the swing arm 51 having the contact 52 is guided on the cam surface 56 and rotated in a direction of the arrow “r” in conjunction with the operation thereof. As a result, the contact 52 is brought out of connection from the contact 54, thus automatically being changed into a state connected to the contact 55a that is connected to the wiring cable 15.
The two procedure sections, built in the flexible sheath at its tip, allow for two types of procedures, i.e. mucous-membrane incision and exfoliation. Those can perform the procedures continuously with smoothness and efficiency in the state being passed through the endoscopic treatment equipment-passage channel.
The entire disclosure of each and every foreign patent application from which the benefit of foreign priority has been claimed in the present application is incorporated herein by reference, as if fully set forth.
Patent Application
20080027429
