TWM368453U - Improved syringe base structure for artificial blood vessel - Google Patents

Improved syringe base structure for artificial blood vessel Download PDF

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TWM368453U
TWM368453U TW98207431U TW98207431U TWM368453U TW M368453 U TWM368453 U TW M368453U TW 98207431 U TW98207431 U TW 98207431U TW 98207431 U TW98207431 U TW 98207431U TW M368453 U TWM368453 U TW M368453U
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Taiwan
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injection
blood vessel
artificial blood
catheter
metal wire
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TW98207431U
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Chinese (zh)
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bo-ren Ke
Qing-Yang Wu
yong-heng Liu
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bo-ren Ke
Qing-Yang Wu
yong-heng Liu
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Priority to TW98207431U priority Critical patent/TWM368453U/en
Publication of TWM368453U publication Critical patent/TWM368453U/en

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M368453 五、新型說明: 【新型所屬之技術領域】 ,.纟創作係-種有關於人工血管注射座之技術4貝域,尤指一種 改良式人工血管注射座結構。 【先前技術】 對於需要接受化學治療的癌症病患,亦或需要長期使用靜脈 -營養補充的病患而言’有—良好的靜脈注射途徑相當重要,因為 φ化學治療藥劑以及靜脈營養製劑對血管内皮都有很強的刺激性, 長期使用會造成靜脈炎(pheblmis)甚至是靜脈检塞(venous thrombosis) ’ 一旦出現這些情況,會使得病患在接受治療的過 程中需要接受反覆的靜脈穿刺(ven〇_puncture)來建立靜脈注射 的官道來維持治療的進行,這不僅使得病患在接受病痛折磨的同 時也要接受治療所帶來的苦痛,因此植人式人U管注射座 (P〇rt A)在當今醫學中扮演-個十分重要的角色。 • 習用的植入式人工灰管注射座(Port A catheter)為臨床上 作為長期置放的-種人工赢管通路。其材質是由鈦金屬及石夕化合 ‘物所組成’有較高的生物相合性,因此可以完全的植人於體内並 長期置放。習用的植入式人工企管注射座係有-個注射座 (Portal)和一條含鎖扣的導管(Cathete。,整個系統完全植入 於皮下’導管末端置於右心房内,注射座通常置於胸腔壁上,有 -個自Μ合的隔膜’使用時可利用專用的彎針穿刺過皮膚及隔 M368453 膜到達注射座。與外置導管系統不同,植入式人工血管注射座並 不需要每天照護。 習用的植入式人工血管的置放,一般係選用鎖骨下靜脈 (subclavian vein)、内頸靜脈(internal jugular vein)、 或頭靜脈(cephalic vein)進行穿刺。一般手術方式為由外科醫 師在手術房内執行,先於皮膚表面注射局部麻醉後,將大約1〇 元硬幣大小的注射座置放於胸前的皮膚下方,而血管注射座相連 的矽質導管,則置入身體大血管内,如此一來,往後當患者需要 靜脈注射化學治療時,不用擔心沒有合適的血管可以打針,所注 射的藥物因直接送到身體的大血管内,更可避免因藥物造成注射 的血管硬化以及皮膚潰爛的風險。 5月參閱第七圖至第九圖所示,然而,現今使用的植入式人工 血管注射座(6 0 )仍未臻理想,其中導管(6 2 )斷裂 (catheter)仍是臨床上常會遇到的併發症,一旦出現這些併發 症,會讓病患再次接受手術座導管移除或是調整。這不僅是增加 病患痛苦’同時也讓治療的連續性打了折扣。目前市面上可獲得 的植入式人工血管注射座(6 〇)係由三個構件所組成,分別是 注射座體(port) ( 6 1 )、導管(catheter) ( 6 2 )與連接帽 (cap) ’該注射座體(port) (61)形成一注射腔。 在組成時,係將導管(6 2)套到注射座體(6丄)的連接處, 在連接帽卡在連接處的卡榫上,因此連接處是植入式人工血管注 射座(6 0)組成上較脆弱的地方,容易在這裡出現導管(6 M368453 2 )斷裂。另外市面上亦有出產連接處一體成型的植入式人工血 管注射座。然而此款植入式人工血管注射座僅具可供注射的—注 射頂面(6 1 2),注射孔位於注射座體(6 2 )的正上方植 入時,導致金屬導線(wire) ( 7 〇 )必需轉9 〇度角才可進入導 管(6 2) ’造成不易植入(如第八圖所示)問題,再者習用的 金屬導線(7 0)必須對準注射鞘的一端開口穿入,置入動作相 ' 當不便,因此習用植入式人工血管注射座(Θ 0 )在病患血管管 ®徑較小或是血管角度較大的情況下會存在不容易植入等多種問 題,由此可見,目前的植入式人工血管注射座(6 〇),仍存在 諸多問題,實有改良之必要。 【新型内容】 欲解決之技術問題點:現今使用的植入式人工血管注射座仍 未臻理想,其中導管斷裂(catheter)仍是臨床上常會遇到的併 發症,一旦出現這些併發症,會讓病患再次接受手術座導管移除 # 或是調整。這不僅是增加病患痛苦,同時也讓治療的連續性打了 、折扣。目前市面上可獲得的植入式人工血管注射座係由三個構件 «所組成,分別是注射座(p0rt)、導管(catheter)與連接帽 (cap)。在組成時,係將導管套到注射座的連接處,在連接帽卡 在連接處的卡榫上,因此連接處是植入式人工血管注射座組成上 較脆弱的地方,容易在這裡出現導管斷裂。目前市面上只有巴德 公司出產連接處一體成型的植入式人工血管注射座。然而此款植 入式注射座僅具可供注射的一注射頂面,注射孔位於注射座的正 上方,植入時,導致金屬導線(wire)必需轉9 〇度角才可進入導 5 M368453 管,造成不易植入問題,再者習用的金屬導線必須對準注射鞘的 一端開口穿入,置入動作相當不便,因此習用植入式人工血管注 射座在病患血管管徑較小或是血管角度較大的情況下會存在不容 易植入等多種問題,由此可見,目前的植入式人工血管注射座, 仍存在諸多問題。 解決問通的技術特點:提供一種改良式人工血管注射座結 構,係包括:一注射座體與一導管。其中,該注射座體係包括一 注射腔、-強化《主射頂面與一強化注射侧面;料管係連通於該 /主射座體的一侧,該強化注射侧面係對應該導管設於該注射座體 的另側,該導管係與該注射座體為一體成型的結構。 其中,該人工血管注射座結構更包括一金屬導線,該金屬導 線外係包覆一包膜。 其中’該金屬導線更包括—長度,該長度約為5 〇公分^ 八中該人工企管注射座結構更包括一注射鞘,該注射鞘具 有一側開口,藉以便利該金屬導線套入該注射鞘内。 其中該金屬導線具有—弧形端,該弧形端係概呈微彎曲 狀。 其中胃強化^射頂面與該強化注射側面係為一體成型的结 構。 對照先前技術之功效: -、^創作巾的注射㈣除了同樣具有―強化注射頂面,更包括 一強化注射側面,該強化注射側㈣指在該注射座體的側面 ]了個主射孔,且該強化注射側面係位於連接導管側 」η藉以有效便利金屬導線(Wire)入導管的路徑,有 文解决習用植人式人卫血管注射座在病患血管管徑較小或是 M368453 血营角度較大的情況下不容易植入等問題。 一、本創作透過於該注射鞘具有一側開口的設計,可以方便直接 套入該金屬導線(wire),毋須像習用一樣要找到注射鞘的 一端開口,而且還要準確對準其一端開口,才能穿置該金屬 導線進入該注射鞘内。 三、本創作透過該導管係與該注射座體為一體成型的結構設計, 可以有效強化該人工血管注射座的結構強度,有效改善習用 導管套到注射座的連接處較脆弱的問題。 有關本創作所採用之技術、手段及其功效,茲舉較佳實施例 並配合圖式詳細說明如后,相信本創作上述之目的、構造及其特 徵,當可由之得一深入而具體的瞭解。 【實施方式】 明參閱第一圖至第六圖所示,本創作係提供一種改良式人工 血官注射座結構,係包括:一注射座體(1〇)與一導管 0)。其中,該注射座體(10)係包括一注射腔(11)、一 強化注射頂面(1 2 )與一強化注射側面(i 3);該導管(2 〇)係連通於該注射座體(i 〇)的一側,該強化注射側面(工 3)係對應該導管(2 〇)設於該注射座體(i 〇)的另側,該 導^ (20)係與該注射座體(1 〇)為一體成型的結構。 其中,該人工血管注射座結構更包括一金屬導線(3〇), 該金屬導線(3 0)外係包覆一包膜。 中’該金屬導線(30)的長度約5〇公分。 其中,該人工血管注射座結構更包括一注射鞘(4 〇 ),該 射鞘(4 0)具有一側開口( 4 1 ),藉以便利該金屬導線 M368453 (3 〇)套入該注射鞘(4 〇)内。 其中,該金屬導線(30)具有一狐形端(curved tip) (3 1 ),該孤形端(curved tip) ( 3 i )係概呈微臂曲狀, 使用上更為實用’毋須像習用金屬導線J形端U-tip)這麼彎。 其中,該強化注射頂面(1 2)與該強化注射側面3) 係為一體成型的結構。 另外本創作所提供之該改良式人工金管注射座結構的使用 方法係分述如下: 一、本創作係與習用植入式人工血管一樣以頭靜脈 (cephalic vein)作為植入導管(2 〇 )的首選,若是血管很 J可以將胸大肌(Pect〇ral is major)翻起尋找穿通靜脈 (perforator vein) ° 二、依血管管徑大小選定適當的導管(2〇)大小及長度 1.適當的血管大小時:處理方式可包括下列步驟: 將金管遠端結紮後,剪開金管; 將導管(20)植人’並以移動式χ光機確定導管(2〇)位 置;若導管(2 0)位置不佳或是導管(2 〇)的途經曲折不好 置放; cl.自連接處的對側的外殼新開的注射點以專用i針打人並將針 頭往前送到植入式人工血管注射座前端; c 2.可以先注射顯影劑來蜂定正確路徑; c3.再以金屬導線(wire) (3〇)自專用直針穿入,經導管(2 0)尖端穿出並在移動式X光機下建立導管(2〇)預計置放的 正確路徑; c4.將導管(2 0 )推至預計置放的位置; M368453 c5.抽出金屬導線(wire) ( 3 〇 )及專用直針。 2· i官管經小或是金管的角度大:係包括兩方法,其中, 方法一 ’係包括下列步驟: 在術中發現血官很小’可先以金屬導線(3 〇)先進行正蜂路 徑; b.套上改良型的注射鞘(puncture汕⑸讣)(4 〇 ); C.順著金屬導線(wire) ( 3 Q )將注射鞘(puncture sheath) (4 Ο)穿入; d. 移除擴張器(dilator)以及金屬導線(wire) ( 3 〇 ),留鞘 (sheath)維持皮下通道; e. 送入導管(2 〇 )並在移動式X光機下確定導管(2 〇 )位 置; f·植入注射座體(1 〇 ); g.完成注射座體(1 〇)置放。 方法二’係包括下列步驟: a. 將導管(2 0 )塞入血管中, b. 自連接處的對側的外殼新開的注射點以專用直針打入並將針頭 往刖送到植入式人工灰管注射座前端; c. 可以先注射顯影劑確定正確之路徑; d. 再以金屬導線(3 〇 )自專用直針穿入,經導管(2 〇 )尖端 穿出並在闕《錢下建立㈣(2Q)料置放的正球路 徑; e. 將導管(2 0 )順著金屬導線(wire) ( 3 〇 )推至預計置放的 位置; f. 抽出金屬導線(wire) ( 3 0 )及專用直針; 9 M368453 g.完成注射座體(10)置放。 總結而言,首先,本創作中的注射座體除了同樣具有一強化 注射頂面,更包括一強化注射側面,該強化注射侧面係指在該注 射座體的側面更多開了-個注射孔’且該強化注射側面係位於連 接導管側的另側,藉以有效便利金屬導線(wire)A導管的路徑, 有效解決習用植人式人工血管注射座在病患血管管徑較小或是企 管角度較大的情況下不料植人等問題。其次,本創作透過於該 注射鞘具有-側開口的設計,可时便直接套人該金屬導線 (wire),毋須像習用—樣要找到注射賴的—端開口,而且還要準 確對準其-端開口,才能穿置該金屬導線進入該注射勒内。再 者’本創作透過料管係與該注射座體為—體成型的結構設計, 可以有效強化該人卫血管注射座的結構強度,錢改善習用導管 套到注射座的連接處較脆弱的問題。 前文係針對摘作之可行實_為本㈣之技_徵進行具 體說明;惟,熟悉此項技術之人士#可在不脫離本創作之精神虚 原則下對本創作進行變更與修改,而該等變更與修改,皆應涵蓋 於如下申請專利範圍所界定之範疇中。 【圖式簡單說明】 第一圖:係本創作可行實施例之側視示意圖。 第二圖:係本創作可行實施例之剖視示意圖。 第三圖:係本創作可行實施例之金屬導線路徑剖視示意圖。 第四圖:係本創作另一可行實施例之剖視示意圖。 第五圖:係本創作可行實施例之注射稍剖視示意圖。 第五A圖:係本創作可行實施例之注射鞘側開口示意圖。 M368453 第六圖:係本創作可行實施例之金屬導線示意圖。 第七圖.係習用人工血管注射座之剖視示意圖。 剖視示意 第八圖.係習用人工血管注射座之金屬導線路徑 圖。 第九圖:係習用人工血管注射座之金屬導線示意圖 •【主要元件符號說明】 .•習用部份· (6 0)人工金管注射座 (611)注射腔 (6 2)導管 *本創作部份. (1 0)注射座體 (1 2)強化注射頂面 (2 0 )導管 (3 1 )弧形端 (4 1 )側開口 (6 1 )注射座體 (6 1 2)注射頂面 (7 0)金屬導線 (1 1)注射腔 (1 3)強化注射侧面 (3 0)金屬導線 (4 0)注射鞘 11M368453 V. New description: [New technical field], 纟 纟 - - - - - - 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工[Prior Art] For cancer patients who need chemotherapy, or patients who need long-term use of intravenous-nutrition supplements, it is important to have a good intravenous route because φ chemotherapeutic agents and intravenous nutrient preparations are important for blood vessels. The endothelium is highly irritating, and long-term use can cause phlebitis or even venous thrombosis. Once these conditions occur, the patient will need to undergo repeated venipuncture during the treatment ( Ven〇_puncture) to establish the official route of intravenous injection to maintain the treatment, which not only makes the patient suffer from the pain of treatment, but also suffers from the treatment. Therefore, the implanted U-tube injection seat (P 〇rt A) plays a very important role in today's medicine. • The conventional implanted artificial ash tube (Port A catheter) is clinically used as a long-term placement of artificial win-tube access. Its material is composed of titanium metal and Shixia compound, which has high biocompatibility, so it can be completely implanted in the body and placed for a long time. The conventional implanted manual tube injection seat has a portal (Portal) and a catheter with a lock (Cathete. The entire system is completely implanted under the skin. The end of the catheter is placed in the right atrium, and the injection seat is usually placed. On the chest wall, there is a self-coupling diaphragm that can be used to puncture the skin with a special curved needle and to separate the M368453 membrane from the injection seat. Unlike the external catheter system, the implantable artificial blood vessel injection seat does not need daily The placement of conventional implantable artificial blood vessels is generally performed by subclavian vein, internal jugular vein, or cephalic vein. The general surgical procedure is performed by a surgeon. Performed in the operating room, before the local anesthesia is injected on the surface of the skin, the injection seat of about 1 硬币 coin size is placed under the skin on the chest, and the sputum catheter connected to the vascular injection seat is placed in the large blood vessels of the body. Inside, as a result, when the patient needs intravenous chemotherapy, there is no need to worry that there is no suitable blood vessel for injection, and the injected medicine is sent directly to the body. In the large blood vessels, the risk of hardening of the injected blood vessels and skin ulceration caused by the drug can be avoided. May 7th to 9th, however, the implantable artificial blood vessel injection seat (60) still used today is still Unexpected, in which the catheter (62) break is still a clinically common complication, and once these complications occur, the patient will be removed or adjusted again. This is not only an increase. The pain of the patient also compromises the continuity of the treatment. The implantable artificial blood vessel injection seat (6 〇) currently available on the market consists of three components, the injection port (6). 1), a catheter (6 2 ) and a cap (the cap) (61) form an injection chamber. In the composition, the catheter (62) is placed over the injection seat ( 6丄) The connection is made on the cassette where the connection cap is stuck at the connection, so the connection is the vulnerable part of the implantable artificial blood vessel injection seat (60), and the catheter is easy to appear here (6 M368453 2 ) Breaking. There is also a joint at the market. Molded implantable vascular injection seat. However, this implantable artificial blood vessel injection seat is only available for injection-injection top surface (6 1 2), and the injection hole is located directly above the injection seat (6 2 ). When entering, the metal wire (7 〇) must be turned 9 degrees to enter the catheter (6 2) 'caused to be difficult to implant (as shown in Figure 8), and the conventional metal wire (7) 0) It is necessary to align the opening of one end of the injection sheath and insert the action phase. When it is inconvenient, the conventional implantable artificial blood vessel injection seat (Θ 0 ) has a small diameter or a large blood vessel angle in the patient. In the case, there are many problems such as not easy to implant, and thus it can be seen that the current implantable artificial blood vessel injection seat (6 〇) still has many problems, and it is necessary to improve. [New content] The technical problem to be solved: The implantable artificial blood vessel injection seat used today is still not ideal. The catheter is still a clinically common complication. Once these complications occur, Have the patient receive the surgical seat removal again # or adjust. This not only increases the suffering of patients, but also makes the treatment continuity and discount. The implantable prosthetic injection site currently available on the market consists of three components, namely, the injection seat (p0rt), the catheter (catheter) and the cap. In the composition, the catheter is placed at the junction of the injection seat, and the connection cap is stuck on the connection of the connection, so the connection is a relatively fragile place of the implantable artificial blood vessel injection seat, and the catheter is easy to appear here. fracture. At present, only the implanted artificial blood vessel injection seat, which is integrally formed by the connection of the company, is produced on the market. However, this implantable injection seat has only one injection top surface for injection, and the injection hole is located directly above the injection seat. When implanted, the metal wire must be turned 9 degrees to enter the guide 5 M368453 The tube causes the implantation problem to be difficult. In addition, the conventional metal wire must be inserted into one end of the injection sheath, and the insertion action is rather inconvenient. Therefore, the implantable artificial blood vessel injection seat has a small diameter in the patient's blood vessel or When the blood vessel angle is large, there are various problems such as not easy to implant, and thus, there are still many problems in the current implantable artificial blood vessel injection seat. Solving the technical characteristics of the communication: providing an improved artificial blood vessel injection seat structure, comprising: an injection seat and a catheter. Wherein, the injection seat system comprises an injection chamber, an intensified "main shot top surface and a enhanced injection side; the material tube is connected to one side of the / main shot body, and the enhanced injection side is corresponding to the injection tube. On the other side of the seat body, the duct body is integrally formed with the injection seat body. Wherein, the artificial blood vessel injection seat structure further comprises a metal wire, and the metal wire is coated with a coating film. Wherein the metal wire further comprises a length, the length is about 5 〇 cm 八. The artificial tubular injection seat structure further comprises an injection sheath having a side opening for facilitating insertion of the metal wire into the injection sheath Inside. Wherein the metal wire has a curved end, and the curved end is slightly curved. The stomach-enhanced top surface and the reinforced injection side are integrally formed. In contrast to the efficacy of the prior art: -, ^ injection of the creation of the towel (four) in addition to the same - "intensified injection top surface, but also includes a reinforced injection side, the reinforced injection side (four) refers to the main perforation on the side of the injection seat, And the side of the reinforced injection is located on the side of the connecting catheter" η to effectively facilitate the path of the metal wire (Wire) into the catheter, and there is a solution to the use of implanted human vascular injection seat in the vessel diameter of the patient or M368453 blood camp It is not easy to implant and other problems when the angle is large. 1. The creation of the injection sheath has a side opening design, which can be easily inserted directly into the metal wire. It is not necessary to find an opening of the injection sheath as in the prior art, and it is also accurately aligned with one end opening. The metal wire can be placed into the injection sheath. Third, the creation of the catheter system and the injection seat body structure can effectively strengthen the structural strength of the artificial blood vessel injection seat, and effectively improve the problem that the connection between the conventional catheter sleeve and the injection seat is relatively weak. The techniques, means and functions of the present invention will be described in detail with reference to the preferred embodiments and the detailed description of the drawings, and it is believed that the above-mentioned objects, structures and features of the present invention can be obtained from an in-depth and specific understanding. . [Embodiment] Referring to the first to sixth figures, the present invention provides an improved artificial blood test injection seat structure comprising: an injection seat (1 inch) and a catheter 0). Wherein, the injection body (10) comprises an injection cavity (11), a fortified injection top surface (12) and a reinforced injection side surface (i3); the catheter (2 〇) is connected to the injection seat body On the side of (i 〇), the reinforced injection side (3) is disposed on the other side of the injection seat (i 〇), and the guide (20) is attached to the injection seat (1 〇) is a one-piece structure. Wherein, the artificial blood vessel injection seat structure further comprises a metal wire (3〇), and the metal wire (30) is coated with a coating film. The length of the metal wire (30) is about 5 cm. Wherein, the artificial blood vessel injection seat structure further comprises an injection sheath (4 〇), the sheath (40) has a side opening (4 1 ), thereby facilitating the metal wire M368453 (3 〇) to fit into the injection sheath ( 4 〇). Wherein, the metal wire (30) has a curved tip (3 1 ), and the curved tip (3 i ) is a micro-arm curved shape, which is more practical in use. The conventional metal wire J-shaped end U-tip) is so curved. Wherein, the reinforced injection top surface (12) and the reinforced injection side surface 3) are integrally formed. In addition, the method of using the improved artificial gold tube injection seat structure provided by the present invention is as follows: 1. This creation department uses the same cephalic vein as the implantation catheter (2 〇) like the conventional implanted artificial blood vessel. The first choice, if the blood vessels are very J, the Pect〇ral is major can be turned up to find the perforator vein. 2. Select the appropriate catheter (2〇) size and length according to the size of the vessel diameter. Vessel size: The treatment may include the following steps: After ligation of the distal end of the gold tube, the gold tube is cut; the catheter (20) is implanted' and the position of the catheter (2〇) is determined by a mobile calender; 0) Poor position or duct (2 〇) is not well placed; cl. From the opposite side of the joint, the newly opened injection point is hit by a special i-pin and the needle is forwarded to the implantable The front end of the artificial blood vessel injection seat; c 2. The developer can be injected first to determine the correct path; c3. Then the metal wire (3〇) is inserted through the special straight needle, and the tip of the catheter (20) is pierced and Establish a catheter (2〇) under the mobile X-ray machine. Correct path;. C4 catheter (20) to push the projected placement position;. M368453 c5 drawn metal wire (wire) (3 billion) and special straight needle. 2· i official tube small or gold tube angle: the system includes two methods, wherein the method 1 'includes the following steps: In the operation, the blood is found to be very small 'can be first with a metal wire (3 〇) first Path; b. Put on a modified injection sheath (puncture汕(5)讣) (4 〇); C. Insert a puncture sheath (4 Ο) along the metal wire (3 Q ); d Remove the dilator and wire (3 〇), sheath to maintain the subcutaneous access; e. Feed the catheter (2 〇) and determine the catheter under the mobile X-ray machine (2 〇 Position; f. Implanted injection seat (1 〇); g. Complete injection seat (1 〇) placement. The second method consists of the following steps: a. Inserting the catheter (20) into the blood vessel, b. Inserting the newly opened injection point from the opposite side of the joint with a special straight needle and sending the needle to the implant Artificial ash tube injection seat front; c. It is possible to inject the developer first to determine the correct path; d. Then insert the metal wire (3 〇) from the special straight needle, and pass through the tip of the catheter (2 〇) and 阙Under the money, establish the (4) (2Q) material to place the positive path; e. Push the conduit (20) along the metal wire (3 〇) to the position where it is expected to be placed; f. Pull out the metal wire (3 0 ) and special straight needle; 9 M368453 g. Complete the injection seat (10). In summary, first of all, the injection seat in the present creation has a reinforced injection top surface as well as a reinforced injection side, and the reinforced injection side means that more injection holes are opened on the side of the injection body. 'And the side of the reinforced injection is located on the other side of the connecting catheter side, thereby effectively facilitating the path of the wire A catheter, effectively solving the small diameter of the patient's blood vessel or the angle of the tube. In the larger case, it is not a problem to implant people. Secondly, the creation of the injection sheath has a side-opening design, so that the metal wire can be directly placed on the wire, and it is not necessary to find the end opening of the injection, as well as accurately aiming at it. - The end is open to allow the metal wire to enter the injection. Furthermore, the design of the body through the material tube system and the injection seat body can effectively strengthen the structural strength of the human vascular injection seat, and the problem of improving the connection between the conventional catheter sheath and the injection seat is relatively fragile. . The preceding paragraphs are specific to the technical essays of the above-mentioned (4); however, those who are familiar with the technology can change and modify the creation without departing from the spirit of this creation. Changes and modifications are to be covered in the scope defined by the scope of the patent application below. [Simple description of the drawings] The first figure is a side view of a feasible embodiment of the present invention. Second Figure: A schematic cross-sectional view of a possible embodiment of the present invention. Fig. 3 is a cross-sectional view showing the path of the metal wire of the presently feasible embodiment. Fourth Figure: A schematic cross-sectional view of another possible embodiment of the present invention. Fig. 5 is a schematic cross-sectional view showing the injection of the presently feasible embodiment. Figure 5A is a schematic view of the side of the injection sheath of the presently feasible embodiment. M368453 Figure 6: Schematic diagram of the metal wires of the presently feasible embodiment. Figure 7 is a schematic cross-sectional view of a conventional artificial blood vessel injection seat. Fig. Illustrated Fig. 8 is a schematic diagram of the metal wire path of a conventional artificial blood vessel injection seat. Figure 9: Schematic diagram of the metal wire used in the artificial blood vessel injection seat • [Key component symbol description] • Conventional part · (6 0) Artificial gold tube injection seat (611) Injection cavity (6 2) Catheter * This part of the creation (1 0) injection seat (1 2) intensive injection top surface (20) catheter (3 1) curved end (4 1 ) side opening (6 1 ) injection seat (6 1 2) injection top surface ( 7 0) Metal wire (1 1) injection cavity (1 3) fortified injection side (30) metal wire (40) injection sheath 11

Claims (1)

M368453 六、 申請專利範圍: 1 .一種改良式人工血管注射座結構,係包括: 一注射座體,該注射座體係包括一注射腔、一強化注射頂面 與一強化注射側面;以及, 一導管,該導管係連通於該注射座體的一側,該強化注射側 面係對應該導管設於該注射座體的另側,該導管係與該注射座體 為一體成型的結構。 2 .如申請專利範圍第1項所述之改良式人工血管注射座結 構其中該人工也管注射座結構更包括一金屬導線,該金屬導 線外係包覆—包膜。 3如申請專利範圍第2項所述之改良式人工血管注射座結 構,其中,該金屬導線更包括一長度,該長度為5 〇公分。 4如申請專利範圍第2項所述之改良式人工血管注射座結 構,其中,該人工血管注射座結構更包括一注射鞘,該注射鞘具 有一側開α。 5 .如申請專利範圍第2項所述之改良式人工血管注射座結 構”中,該金屬導線具有一弧形端,該弧形端係概呈微彎曲 狀。 6如申請專利範圍第1項所述之改良式人工血管注射座結 構,其中,該強化注射頂面與該強化注射側面係為一體成型的結 構。 七、 圖式: 如次頁 12M368453 VI. Patent Application Range: 1. An improved artificial blood vessel injection seat structure, comprising: an injection seat system, the injection seat system comprising an injection cavity, a fortified injection top surface and a reinforced injection side; and a catheter The catheter is connected to one side of the injection body, and the reinforced injection side is disposed on the other side of the injection body, and the catheter is integrally formed with the injection body. 2. The improved artificial blood vessel injection seat structure according to claim 1, wherein the artificial injection tube base structure further comprises a metal wire, the metal wire is coated with a coating. 3. The improved artificial blood vessel injection seat structure of claim 2, wherein the metal wire further comprises a length of 5 〇 cm. 4. The improved artificial blood vessel injection seat structure of claim 2, wherein the artificial blood vessel injection seat structure further comprises an injection sheath having a side opening alpha. 5. The improved artificial blood vessel injection seat structure according to claim 2, wherein the metal wire has an arcuate end, and the curved end portion is slightly curved. 6 as claimed in claim 1 The improved artificial blood vessel injection seat structure, wherein the reinforced injection top surface and the reinforced injection side surface are integrally formed. VII. Schema:
TW98207431U 2009-05-01 2009-05-01 Improved syringe base structure for artificial blood vessel TWM368453U (en)

Priority Applications (1)

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TW98207431U TWM368453U (en) 2009-05-01 2009-05-01 Improved syringe base structure for artificial blood vessel

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Application Number Priority Date Filing Date Title
TW98207431U TWM368453U (en) 2009-05-01 2009-05-01 Improved syringe base structure for artificial blood vessel

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TWM368453U true TWM368453U (en) 2009-11-11

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