M425672 五、新型說明： 【新型所屬之技術領域】 本新型是有關一種醫療器材，且特別是有關一種壓迫 _ 裝置。 【先前技術】 由於血管穿刺手術會將一根細小的導管由接近皮膚的 血管穿刺置入，因此對於血管穿刺手術後的病人來說，穿 • 刺的部位會在血管與皮膚表面分別產生内、外傷口。常見 的穿刺部位例如股動脈穿刺、股靜脈穿刺和鎖骨下靜脈穿 刺。醫護人員藉由穿刺手術可以為病人進行抽血、輸血、 輸液以及血管造影等醫療行為。 ^ 一般來說，對於血管穿刺手術後的病人，醫護人員通 常會以施加壓力的方式來按壓穿刺後皮下的内傷口以達 到加速止血的目的。習知用來止血的醫療器材通常是以旋 紐下壓、氣囊下壓或重物下壓等方式對外傷口的皮膚表面 #施加壓力，使得内傷口可較快地止企。然而，目前的止血 器材並不易控制施加壓力的大小與位置，且在施壓時，無 法對外傷口同時施覆相關的止血藥物。因此，醫護人員還 ㈤額外使用其他醫療用品(例如：沾有藥水的紗布與透氣膠 帶）來治療外傷口。 练上所述，若希望減少血管穿刺後的出血量與縮短止 血夺間S«蒦人員最好同時對血管的内傷口施壓以及對外 傷口施覆藥物。也就是說，除了使用習知的壓迫器材對内 傷口施壓外，尚需配合其他醫療用品施覆在外傷口上。因 此， 外傷 醫護人員f花費較多 σ進行止血。 的時間與人力來對穿刺後的内、 【新型内容】 本新型之一技術態樣為一種壓迫裝置。 體、=體本：實施方式，-種丄包含基座本 第-二=::其卜基座本趙具有相對之 體包含貫穿第-表面與第二 有凸=二:性體設置於第二表面上對應穿孔。握把具 相a穿孔“及收體設置於第二表面上，位於彈性 彈性靜侧。在使用時’凸出部藉由穿孔穿出第二表面接觸 本新型之另一技術態樣為一種壓迫裝，置。 _根據本新型一實施方式，一種壓迫裝置包含基座本 體、彈性體、握把、凸出部與吸收體。《中，基座本體具 有相對之第一表面與第二表面。基座本體包含貫穿第一表 面與第二表面之穿孔。彈性體設置於第二表面上對應穿 孔。握把具有一空腔貫穿握把並對齊穿孔。握把設置於第 一表面上。凸出部位於空腔中且至少部分凸出握把。凸出 部輕合穿孔。吸收體設置於第二表面上，位於彈性體之一 侧。當凸出部下壓時會迫使彈性體變形。 在本新型上述實施方式中，使用者先將吸附藥液的吸 收體接觸傷口’此時彈性體亦會接觸傷口附近的皮膚。接 著’將握把上的凸出部藉由穿孔穿出第二表面來壓迫彈性 體’使得彈性體凸出變形並施壓於皮膚内的血管，達到止 M4-25672 血效果。同時，吸附藥液的吸收體對傷口進行治療。此外， 凸出部凸出第二表面的長度可依使用者實際需求來決定。 當凸出4凸出第二表面的長度越多，則表示彈性體凸出的 幅度越大，因此對皮膚内的血管也會施加較大的壓力。這 樣的設計不僅同時利用彈性體與吸收體分別對傷口進行壓 迫止血與敷藥治療’還可讓使用者自行調整施加於血管的 壓力’減少止血所花費的時間與人力。 I 【實施方式】 以下將以圖式揭露本新型之複數個實施方式，為明確 說明起見，許多實務上的細節將在以下敘述中一併說明。 然而’應瞭解到’這些實務上的細節不應用以限制本新型。。 也就是說’在本新型部分實施方式中，這些實務上的細節 是非必要的。此外’為簡化圖式起見’一些習知慣用的結 構與元件在圖式中將以簡單示意的方式繪示之。 … 第1A圖繪示根據本新型第一實施方式之壓迫裝置丨 _ 的侧視圖。第1B圖繪示第1A圖之壓迫裝置1〇〇使用時的 侧視圖。同時參閱第1A圖與第1B圖，壓追裝置1〇〇包含 基座本體120、彈性體130、握把；π〇與吸收體14〇 ^ 本體120具有相對之第一表面121與第二表面丨23。^座 本體120包含貫穿第一表面121與第二表面123之穿孔 122。彈性體130設置於第二表面123上對應穿孔122。吸 收體140設置於第二表面123上，位於彈性體1 %之一側。 握把110具有凸出部112耦合穿孔122。凸出部112 藉由穿過穿孔122穿出第二表面123接觸彈性體13〇。當 M425672 握把110下壓時，會迫使彈性體130變形。在本實施方式 中，凸出部112與穿孔122具有對應的螺紋114,使得凸出 部112可藉由螺紋114從基座本體120之第二表面123旋 轉凸出。凸出部112外壁上之螺紋114為外螺紋，穿孔122 内壁上之螺紋114為内螺紋。當使用者操作握把110相對 於基座本體120旋轉時，透過螺紋114的設計，可以使得 握把110相對於基座本體120上下移動，並可在握把110 到達預定位置時，藉由凸出部112與穿孔122上之螺紋114 的相互耦合而定位凸出部112。 ® 在進行血管穿刺手術時，醫護人員會將一根細小的導 管針由接近皮膚150的穿刺置入血管160中，因此對於血 管穿刺手術後（此時導管針已經取出）的病人來說，穿刺的 部位會在血管160與皮膚150表面分別產生内傷口 162以 及外傷口 152。即，内傷口 162意指穿刺手術後皮膚150 内部的血管160之傷口，外傷口 152意指穿刺手術後皮膚 150表面的傷口。 本壓迫裝置100可用以壓迫止血内傷口 162並對外傷 • 口 152施覆藥物。具體而言，使用者先將吸附或塗佈藥物 的吸收體140施覆於外傷口 152上，此時彈性體130亦會 接觸内傷口 162外部的皮膚150表面。接著，使用者旋轉 握把110讓凸出部112連帶於穿孔122中轉動。因此，凸 出部112會藉由穿孔122中相對應的螺紋114從基座本體 120之第二表面123逐漸旋轉凸出。接著，凸出部112會 因壓迫彈性體130而使彈性體130凸出變形（如第1B圖所 示），使得彈性體130對其下方的内傷口 162施加壓力。當 凸出部112凸出第二表面123的長度越多，則彈性體130 572 凸出，幅度越大，對内傷口 162施加的壓力也會越大。 這樣的設計可讓使用者同時利用彈性體13〇與吸收體 140刀別對内傷σ 162壓迫止血與外傷口 152敷藥治療， 2利用螺紋m調整凸出部112凸出的第二表面123、的 又’避免壓迫感太大而產生不適。再者，使用者除了可 用，紋114無段式微調凸出部112凸出穿孔122的位置 外丄還可螺紋114來固定凸出部112於穿孔122中， 不而持’對凸出部112施予向下的力量來壓迫彈性體13〇。 本實施方式中凸出部112的長度大於基座本體120 的旱度’且凸出部112的截面積小或等於穿孔122的截面 f。握把110與凸出部112為一體成型。然而，在其他實 =式中，握把110與凸出部112可以為分開的兩個體。 方面，設計者可以在凸出部112與穿孔122之間設置 :他固疋結構(例如卡榫或插銷）來取代螺紋114，使得凸出 / 112於穿孔122巾的位置仍可被調整與固定。彈性體⑽ ^以為橡膠墊。吸收體刚可以為紗布、止血棉或海錦塊， 吸140可具有止血、治療或消毒用的藥物 液、樂膏、藥片或藥布）。 第1C圖繪示根據本新型第二實施方式之壓迫裝置剛 =視圖。如圖所示，凸出部112與穿孔122可以不具有 圖中之螺紋114。如此一來，當使用者將握把11〇下 則凸出部m會直接地凸出第二表面123 受壓迫而快速地凸出變形。也就是說，使用者雖 :無法藉由螺紋114固定或微調凸出部112的位置，但口 下的力量於握把11〇’凸出部ιΐ2將可更快速地達 使用者期望的位置，依照實際需求而定。 M425672 第2圖繪示根據本新型第三實施方式之壓迫裝置100 的侧視圖。彈性體130至少部分與第二表面123分離。具 體而言，彈性體130具有第一側132與第二側134。其中， 彈性體130之第一側132設置於基座本體120之第二表面 123上，第二側134與第二表面123分開。當凸出部112 凸出第二表面123時，雖然彈性體130之第二側134未固 定於第二表面123上，但彈性體130仍會受凸出部112壓 迫而具有凸出的外型，對彈性體130下方的内傷口 162(如 第1A圖所示）施加壓力，達到止血的目的。 * 然而，上述實施方式中的吸收體140在使用時，其中 一面接觸皮膚150，另一面則設置於基座本體120之第二 表面123上，因此當吸收體140上的藥液不足時，使用者 需移開壓迫裝置100來對吸收體140補充藥液而造成使用 上的不便。在以下實施方式中，將具體說明解決上述問題 的技術内容。 第3圖繪示根據本新型第四實施方式之壓迫裝置100 的侧視圖。基座本體120除了具有穿孔122外，還具有貫 ® 穿第一表面121與第二表面123的進料孔124。其中，進 料孔124的位置與吸收體140的位置相對應。在使用此壓 迫裝置100時，使用者可方便地從第一表面121的進料孔 124填充用來止血或消毒的藥液，讓吸收體140逐漸地吸 附由第二表面123之進料孔124流下來的藥液來對外傷口 152(見第1A圖）進行治療。另外，配合使用時可凸出的彈 性體130對内傷口 162(見第1A圖）施壓，而加快止血的速 度0 第4圖繪示根據本新型第五實施方式之壓迫裝置100 M425672 的侧視圖。壓迫裝置100更包含彈簧116 ’其套裝在凸出 部112上並設置於第一表面121與握把110之間。此壓迫 裝置100之凸出部112與穿孔122不具有螺紋114。當使用 者未透過凸出部112向下施力於彈性體130時’彈簧116 能將凸出部112定位到未施力時的位置。也就是說，此壓 迫裝置100在皮膚15〇(見第1A圖）表面操作時，僅需對握 把110施予向下的力量’即可讓凸出部112凸出於第二表 面123，使彈性體13〇變形而壓迫内傷口 162(見第1A圖） 以止血。若壓力太大造成使用者不適時，只要放鬆握把110 即可透過彈簧116復歸之彈力讓凸出部112彈回第二表面 123或穿孔122中，彈性體130便會恢復平坦的形狀。 第5A圖繪示根據本新型第六實施方式之壓迫裝置200 的侧視圖。第5B圖繪示第5A圖之壓迫裝置200使用時的 侧視圖。同時參閱第5A圖與第5B圖，壓迫裝置200具有 基座本體120、彈性體130、握把220、凸出部212與吸收 體140。握把220設置於基座本體120之第一表面121上。 握把220具有空腔222貫穿握把220並對齊穿孔122。凸 出部212位於空腔222中且至少部分凸出握把220。此外， 凸出部212耦合穿孔122。當凸出部212下壓時，凸出部 212迫使彈性體130變形。在本實施例中，壓迫裝置2〇〇 還具有按壓部210位於握把220外，並實體連接凸出部212 相對於彈性體130之一端。凸出部212的長度大於基座本 體120的厚度與握把220的高度之和，且凸出部212的截 面積小於或等於穿孔122的截面積。 具體而言，餘220係固定於基座本體12〇上，凸出 部212可以於穿孔122與空腔222内自由移動。在本實施 方式中，當使用者將按聲 壓部2H)T方之凸出部21 = 10㊣下壞時’實體連接於按 接著，凸出部2丨2會壓@同時向下凸出基座本體U0。 出變形來對其下方的内傷。㈣13^ ’使得彈性體⑼凸 第5C圖繪示根據本新^2(見第1A圖）施加壓力。 的側視圖。如圖所示，屢七實施方式之壓迫I置2〇〇 ⑵具有相對應的螺纹;;f震置200之凸出部扣與穿孔 接於凸出部2!2上方的㈣^使用者可減地轉動實體連 二位置。此外，裝置_之基座本二具有=L2 4讓使用者方便地填充藥液於吸收體⑽。在其他實施例 中，彈性體130可以部分與基座本體120之第二表面123 分離(如第2圖所示）’依照設計者實際需求而定。 第6圖繪示根據本新型第八實施方式之壓迫裝置2〇〇 的侧視圖。壓迫裝置200更包含彈簧214，其套接於凸出 部212並設置於按壓部21〇與握把220之間。當使用者未 透過按壓部210向下施力於彈性體13〇時，彈簧214能將 凸出部212定位到未施力時的位置。也就是說，此壓迫裝 置200在皮膚150(見第ία圖）表面操作時，僅需對按壓部 210施予向下的力量，即可讓凸出部212凸出於第二表面 123’使彈性體130變形而壓迫内傷口 162(見第1A圖）以止 血。若壓力太大造成使用者不適時，只要放鬆按壓部210 即可透過彈簧214復歸之彈力讓凸出部212彈回第二表面 123或穿孔122中，彈性體130便會恢復平坦的形狀。 本新型上述實施方式與已知先前技術相較，具有以下 優點： (1)此壓迫裝置可讓使用者同時利用彈性體與吸收體 M425672 分別對内傷口進行壓迫止血與外傷口敷藥治療，減少止血 過程中花費的時間與人力。 (2)此壓迫裝置具有可調整的凸出部。當凸出部伸出第 二表面的長度越多，則彈性體凸出的幅度越大，而對内傷 口施加的壓力也會越大。因此，使用者可藉由凸出部與握 把分別調整對内傷口施加的壓力大小與施加壓力的位置。 〜雖然本新型已以實施方式揭露如上，然其並非用以限 定本新型’任何熟習此技藝纟，在不脫離本新型之精神和 範圍内，當可作各種之更動與潤飾，因此本新型之保護範 圍當視後附之申請專利範圍所界定者為準。 【圖式簡單說明】 第1A圖繪示根據本新型第一實施方式之壓迫裝置的 侧視圖。 第1B⑽示第1A圖之壓迫裝置使用時的侧視圖。 第1C圖繪示根據本新型第二實施方式之壓迫裝置的 侧視圖。M425672 V. New description: [New technical field] The present invention relates to a medical device, and in particular to a compression device. [Prior Art] Since a vascular puncture procedure involves a small catheter inserted from a blood vessel close to the skin, the patient who wears the thorn after the vascular puncture is generated inside the blood vessel and the skin surface, External wound. Common puncture sites such as femoral artery puncture, femoral vein puncture, and subclavian vein puncture. Medical personnel can perform blood tests such as blood draw, blood transfusion, infusion, and angiography by puncture. ^ In general, for patients after vascular puncture, the medical staff usually presses the inner wound under the puncture to apply pressure to achieve accelerated blood stasis. Conventional medical devices used for hemostasis usually apply pressure to the skin surface of the wound by means of a squeezing pressure, a balloon depression or a weight depression, so that the internal wound can be stopped faster. However, current hemostasis devices do not easily control the magnitude and location of the applied pressure, and when applied, it is not possible to simultaneously apply the relevant hemostatic drug to the external wound. Therefore, the medical staff also (5) additionally use other medical supplies (for example: gauze with a syrup and a breathable tape) to treat the external wound. In practice, if you want to reduce the amount of bleeding after vascular puncture and shorten the stoppage of blood, it is best to apply pressure to the internal wounds of the blood vessels and to apply drugs to the external wounds. That is to say, in addition to the use of conventional compression equipment to apply pressure to the inner wound, it is necessary to apply other medical supplies to the outer wound. Therefore, the trauma medical staff f spends more σ to stop bleeding. Time and manpower to the inside of the puncture, [new content] One of the technical aspects of the present invention is a compression device. Body, = body: implementation, - the species contains the base of the first - two =:: its base pedestal Zhao has a relative body containing the first surface and the second convex = two: the body is set at Corresponding perforations on the two surfaces. The handle has a perforation "and the receiving body is disposed on the second surface and is located on the elastic elastic side. In use, the protrusion protrudes out of the second surface by the perforation to contact the other technical aspect of the present invention as an oppression. According to an embodiment of the present invention, a compression device includes a base body, an elastic body, a grip, a protrusion, and an absorber. In the middle, the base body has opposite first and second surfaces. The base body includes a through hole penetrating the first surface and the second surface. The elastic body is disposed on the second surface corresponding to the through hole. The grip has a cavity penetrating the grip and aligning the perforations. The grip is disposed on the first surface. The protrusion is located at least partially protruding from the cavity. The protrusion is lightly perforated. The absorber is disposed on the second surface on one side of the elastic body. When the protrusion is pressed down, the elastic body is forced to deform. In the above embodiment, the user first contacts the absorbent body of the adsorbing liquid to the wound. At this time, the elastic body also contacts the skin near the wound. Then, the protrusion on the grip is pressed through the second surface to perforate the protrusion. bomb The sexual body' causes the elastic body to be deformed and pressed against the blood vessels in the skin to achieve the blood effect of M4-25672. At the same time, the absorbent body of the adsorbing liquid absorbs the wound. In addition, the convex portion protrudes from the second surface. The length can be determined according to the actual needs of the user. The more the length of the convex surface 4 protrudes from the second surface, the larger the amplitude of the elastic body protrusion, and therefore the greater the pressure on the blood vessels in the skin. The design not only uses the elastic body and the absorbent body to respectively pressurize the wound to stop bleeding and applicator treatment, but also allows the user to adjust the pressure applied to the blood vessel to reduce the time and labor required for hemostasis. I [Embodiment] The various embodiments of the present invention are disclosed in the drawings. For the sake of clarity, many practical details are set forth in the following description. However, it should be understood that the details of the practice are not applied to limit the present invention. In other words, in the implementation of this new part, these practical details are not necessary. In addition, 'for the sake of simplifying the schema', some conventionally used knots. The components and the components will be shown in a schematic manner in the drawings. Fig. 1A is a side view of the pressing device 丨_ according to the first embodiment of the present invention. Fig. 1B is a view showing the pressing device 1 of Fig. 1A. A side view of the 〇〇 when used. Referring to FIGS. 1A and 1B, the press-fighting device 1 〇〇 includes a base body 120, an elastic body 130, and a grip; π 〇 is opposite to the absorber 14 本体 ^ body 120 The first surface 121 and the second surface 丨23. The base 120 includes a through hole 122 extending through the first surface 121 and the second surface 123. The elastic body 130 is disposed on the second surface 123 corresponding to the through hole 122. The absorber 140 is disposed at The two surfaces 123 are located on one side of the elastic body. The grip 110 has a projection 112 coupled to the through hole 122. The projection 112 contacts the elastic body 13 by passing through the second surface 123 through the through hole 122. When the M425672 grip 110 is depressed, the elastomer 130 is forced to deform. In the present embodiment, the projection 112 has a corresponding thread 114 with the perforation 122 such that the projection 112 can be rotated from the second surface 123 of the base body 120 by the thread 114. The thread 114 on the outer wall of the projection 112 is externally threaded, and the thread 114 on the inner wall of the perforation 122 is internally threaded. When the user operates the grip 110 to rotate relative to the base body 120, the design of the thread 114 can cause the grip 110 to move up and down relative to the base body 120, and can be protruded when the grip 110 reaches a predetermined position. The portion 112 is coupled to the threads 114 on the perforations 122 to position the projections 112. ® During a vascular puncture, the medical staff places a small catheter needle into the blood vessel 160 from a puncture close to the skin 150. Therefore, for a patient after a vascular puncture (when the catheter needle has been removed), the puncture The site will produce an inner wound 162 and an outer wound 152 on the surface of the blood vessel 160 and the skin 150, respectively. That is, the inner wound 162 means the wound of the blood vessel 160 inside the skin 150 after the puncture operation, and the outer wound 152 means the wound on the surface of the skin 150 after the puncture operation. The compression device 100 can be used to compress the hemostasis wound 162 and apply a drug to the wound 152. Specifically, the user first applies the absorbent or drug-coated absorbent body 140 to the outer wound 152, at which time the elastomer 130 also contacts the surface of the skin 150 outside the inner wound 162. Next, the user rotates the grip 110 to cause the projection 112 to rotate in the perforation 122. Therefore, the projection 112 is gradually rotated from the second surface 123 of the base body 120 by the corresponding thread 114 in the through hole 122. Next, the projection 112 causes the elastic body 130 to be convexly deformed by pressing the elastic body 130 (as shown in Fig. 1B), so that the elastic body 130 applies pressure to the inner wound 162 below it. When the length of the projection 112 protruding from the second surface 123 is increased, the elastic body 130 572 is projected, and the greater the amplitude, the greater the pressure applied to the inner wound 162. Such a design allows the user to simultaneously use the elastic body 13 〇 and the absorbent body 140 to compress the hemostasis σ 162 to apply the hemostasis and the outer wound 152. 2 adjust the second surface 123 protruding from the protruding portion 112 by using the thread m. And 'to avoid too much pressure and discomfort. Moreover, in addition to the user, the pattern 114 has a stepless fine adjustment protrusion 112 protruding from the position of the through hole 122, and the thread 114 can also be used to fix the protrusion 112 in the through hole 122 without holding the pair of protrusions 112. Apply downward force to oppress the elastomer 13〇. In the present embodiment, the length of the projection 112 is greater than the dryness of the base body 120 and the cross-sectional area of the projection 112 is small or equal to the cross-section f of the perforation 122. The grip 110 is integrally formed with the projection 112. However, in other real forms, the grip 110 and the projection 112 may be separate bodies. In one aspect, the designer can provide between the projection 112 and the perforation 122: a solid structure (such as a latch or a latch) instead of the thread 114, so that the position of the projection / 112 in the perforation 122 can still be adjusted and fixed. . Elastomer (10) ^ Think rubber pad. The absorbent body may be gauze, hemostatic cotton or kelp, and the suction 140 may have a drug solution, a therapeutic cream or a medicated cloth for hemostasis, treatment or disinfection). FIG. 1C is a view showing the pressing device according to the second embodiment of the present invention. As shown, the projections 112 and perforations 122 may not have the threads 114 in the Figures. In this way, when the user lowers the grip 11 , the projection m directly protrudes from the second surface 123 to be pressed and rapidly deformed. That is to say, although the user cannot fix or finely adjust the position of the projection 112 by the thread 114, the force under the mouth on the grip 11〇' the projection ι2 can reach the position desired by the user more quickly. According to actual needs. M425672 FIG. 2 is a side view of the compression device 100 according to the third embodiment of the present invention. The elastomer 130 is at least partially separated from the second surface 123. In particular, the elastomer 130 has a first side 132 and a second side 134. The first side 132 of the elastic body 130 is disposed on the second surface 123 of the base body 120, and the second side 134 is separated from the second surface 123. When the protruding portion 112 protrudes from the second surface 123, although the second side 134 of the elastic body 130 is not fixed to the second surface 123, the elastic body 130 is still pressed by the protruding portion 112 to have a convex appearance. Pressure is applied to the inner wound 162 (shown in Figure 1A) below the elastomer 130 to achieve hemostasis. * However, when the absorbent body 140 in the above embodiment is in use, one side contacts the skin 150 and the other side is disposed on the second surface 123 of the base body 120, so when the liquid medicine on the absorber 140 is insufficient, the use The pressing device 100 needs to be removed to replenish the absorbent body 140 to cause inconvenience in use. In the following embodiments, the technical contents for solving the above problems will be specifically explained. FIG. 3 is a side view of the compression device 100 according to the fourth embodiment of the present invention. In addition to having perforations 122, the base body 120 has a feed aperture 124 that passes through the first surface 121 and the second surface 123. Here, the position of the feed hole 124 corresponds to the position of the absorber 140. When the pressing device 100 is used, the user can conveniently fill the liquid medicine for hemostasis or disinfection from the feeding hole 124 of the first surface 121, and the absorbent body 140 gradually adsorbs the feeding hole 124 of the second surface 123. The effluent is used to treat the wound 152 (see Figure 1A). In addition, the elastic body 130 which can be protruded during use is pressed against the inner wound 162 (see FIG. 1A) to accelerate the speed of hemostasis. FIG. 4 is a side view of the compression device 100 M425672 according to the fifth embodiment of the present invention. view. The compression device 100 further includes a spring 116' that fits over the projection 112 and is disposed between the first surface 121 and the grip 110. The projection 112 and the perforation 122 of the compression device 100 do not have threads 114. When the user does not apply downward force to the elastic body 130 through the projection 112, the spring 116 can position the projection 112 to a position where the force is not applied. That is, when the compression device 100 is operated on the surface of the skin 15 (see FIG. 1A), only the downward force of the grip 110 is required to make the projection 112 protrude from the second surface 123. The elastomer 13 is deformed to compress the inner wound 162 (see Figure 1A) to stop bleeding. If the pressure is too large and the user is uncomfortable, the elastic body 130 can be restored to a flat shape by simply releasing the grip 110 to cause the projection 112 to spring back into the second surface 123 or the perforation 122 by the elastic force of the spring 116. FIG. 5A is a side view of the compression device 200 according to the sixth embodiment of the present invention. Fig. 5B is a side view showing the use of the pressing device 200 of Fig. 5A. Referring also to Figures 5A and 5B, the compression device 200 has a base body 120, an elastomer 130, a grip 220, a projection 212, and an absorbent body 140. The grip 220 is disposed on the first surface 121 of the base body 120. The grip 220 has a cavity 222 that extends through the grip 220 and aligns with the perforations 122. The projection 212 is located in the cavity 222 and at least partially protrudes from the grip 220. In addition, the projection 212 couples the perforations 122. When the projection 212 is depressed, the projection 212 forces the elastic body 130 to deform. In the present embodiment, the pressing device 2A further has a pressing portion 210 located outside the grip 220 and physically connecting the projection portion 212 with respect to one end of the elastic body 130. The length of the projection 212 is greater than the sum of the thickness of the base body 120 and the height of the grip 220, and the cross-sectional area of the projection 212 is less than or equal to the cross-sectional area of the perforation 122. Specifically, the remaining 220 is fixed to the base body 12, and the projection 212 is freely movable within the through hole 122 and the cavity 222. In the present embodiment, when the user presses the convex portion 21 = 10 of the sound pressure portion 2H) T = 10 is bad, the physical connection is made to press, then the projection 2 2 is pressed @ and simultaneously protrudes downward. Base body U0. Deformed to the internal injury to the underside. (4) 13^' makes the elastic body (9) convex. Figure 5C shows the application of pressure according to this new ^2 (see Figure 1A). Side view. As shown in the figure, the compression I of the repeated seven embodiment is set to 2 (2) has a corresponding thread; the projection of the protrusion of the shock 200 and the perforation are connected to the upper part of the protrusion 2! 2 (4) Reduce the ground and rotate the entity to the second position. In addition, the base of the device has a =L2 4 for the user to conveniently fill the solution with the absorbent (10). In other embodiments, the elastomer 130 may be partially separated from the second surface 123 of the base body 120 (as shown in Figure 2), depending on the actual needs of the designer. Fig. 6 is a side view showing the pressing device 2A according to the eighth embodiment of the present invention. The pressing device 200 further includes a spring 214 that is sleeved between the protruding portion 212 and disposed between the pressing portion 21A and the grip 220. When the user does not apply downward force to the elastic body 13 through the pressing portion 210, the spring 214 can position the projection 212 to a position where the force is not applied. That is to say, when the pressing device 200 is operated on the surface of the skin 150 (see FIG. 355), it is only necessary to apply a downward force to the pressing portion 210, so that the protruding portion 212 protrudes from the second surface 123'. The elastomer 130 deforms to compress the inner wound 162 (see Figure 1A) to stop bleeding. If the pressure is too large and the user is uncomfortable, the elastic body 130 can be restored to a flat shape by loosening the pressing portion 210 to cause the protruding portion 212 to spring back into the second surface 123 or the through hole 122 by the elastic force of the spring 214. Compared with the prior art, the above-mentioned embodiments of the present invention have the following advantages: (1) The pressing device allows the user to simultaneously use the elastic body and the absorbent body M425672 to respectively pressurize the inner wound and the external wound dressing treatment, thereby reducing The time and manpower spent in the hemostasis process. (2) The pressing device has an adjustable projection. The greater the length of the projection extending beyond the second surface, the greater the extent to which the elastomer projects, and the greater the pressure applied to the internal wound. Therefore, the user can adjust the magnitude of the pressure applied to the inner wound and the position where the pressure is applied, respectively, by the projection and the grip. </ RTI> Although the present invention has been disclosed in the above embodiments, it is not intended to limit the present invention. Any of the various modifications and refinements can be made without departing from the spirit and scope of the present invention. The scope of protection is subject to the definition of the scope of the patent application attached. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1A is a side view showing a pressing device according to a first embodiment of the present invention. Fig. 1B(10) shows a side view of the pressing device of Fig. 1A in use. Fig. 1C is a side view showing the pressing device according to the second embodiment of the present invention.
第2圖綠示根據本新型第三實施方式之壓迫置側 視圖。 第3圖繪示根據本新型第四實施方式之壓迫裝置的侧 視圖。 、第4圖、’、曰不根據本新型第五實施方式之壓迫裝置的側 第5A圖緣示根據本新型第六實施方式之壓迫裝置的 4則視圖。 12 M425672 第5B圖繪示第5A圖之壓迫裝置使用時的側視圖。 第5C圖繪示根據本新型第七實施方式之壓迫裝置的 側視圖。 第6圖繪示根據本新型第八實施方式之壓迫裝置的侧 視圖。Fig. 2 is a green view showing the compression side view according to the third embodiment of the present invention. Figure 3 is a side elevational view of the compression device in accordance with a fourth embodiment of the present invention. 4, ′′, ′′, a side view of the pressing device according to the fifth embodiment of the present invention, and a view of the pressing device according to the sixth embodiment of the present invention. 12 M425672 Figure 5B shows a side view of the compression device of Figure 5A in use. Fig. 5C is a side view showing the pressing device according to the seventh embodiment of the present invention. Figure 6 is a side elevational view of the compression device in accordance with an eighth embodiment of the present invention.
【主要元件符號說明】 100 ： 壓迫裝置 110 ： 握把 112 ： 凸出部 114 ： 螺紋 116 ： 彈簧 120 ： 基座本體 121 ： 第一表面 122 ： 穿孔 123 ： 第二表面 124 ： 進料孔 130 ： 彈性體 132 ： 第一側 134 ： 第二側 140 ： 吸收體 150 ： 皮膚 152 ： 外傷口 160 : 血管 162 ： 内傷口 200 ： 壓迫裝置 210 ： 按壓部 212 ： 凸出部 214 ： 彈簧 220 ： 握把 222 ： 空腔 13[Main component symbol description] 100 : Compression device 110 : Grip 112 : Projection 114 : Thread 116 : Spring 120 : Base body 121 : First surface 122 : Perforation 123 : Second surface 124 : Feed hole 130 : Elastomer 132: first side 134: second side 140: absorbent body 150: skin 152: outer wound 160: blood vessel 162: inner wound 200: compression device 210: pressing portion 212: projection 214: spring 220: grip 222 : cavity 13