TWI695716B - Diversion bracket for eyeball drainage - Google Patents
Diversion bracket for eyeball drainage Download PDFInfo
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- TWI695716B TWI695716B TW108110396A TW108110396A TWI695716B TW I695716 B TWI695716 B TW I695716B TW 108110396 A TW108110396 A TW 108110396A TW 108110396 A TW108110396 A TW 108110396A TW I695716 B TWI695716 B TW I695716B
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- 210000005252 bulbus oculi Anatomy 0.000 title claims abstract description 23
- 239000011521 glass Substances 0.000 claims abstract description 23
- 239000007788 liquid Substances 0.000 claims description 37
- 239000005313 bioactive glass Substances 0.000 claims description 24
- 210000001508 eye Anatomy 0.000 claims description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 230000035515 penetration Effects 0.000 claims 2
- 239000005312 bioglass Substances 0.000 description 21
- 210000002159 anterior chamber Anatomy 0.000 description 10
- 230000004410 intraocular pressure Effects 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 102000008186 Collagen Human genes 0.000 description 4
- 108010035532 Collagen Proteins 0.000 description 4
- 230000001746 atrial effect Effects 0.000 description 4
- 229920001436 collagen Polymers 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 210000001742 aqueous humor Anatomy 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 210000004872 soft tissue Anatomy 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007943 implant Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 230000017423 tissue regeneration Effects 0.000 description 2
- 208000010412 Glaucoma Diseases 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
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- Prostheses (AREA)
Abstract
一種眼球排水之分流支架,由生物活化玻璃層組成支架本體,支架本體具有嵌入結構及導液管,嵌入結構及導液管呈一體成形,將支架本體嵌入眼球內側壁,可達到疏導房液的功效,且隨著時間流逝,支架本體會逐漸為人體所吸收。 A shunting bracket for drainage of the eyeball is composed of a biologically activated glass layer. The bracket body has an embedded structure and a catheter. The embedded structure and the catheter are integrally formed. The bracket body is embedded in the inner wall of the eyeball, which can reach Efficacy, and with the passage of time, the stent body will be gradually absorbed by the human body.
Description
本發明為一種分流支架,尤指一種眼球排水之分流支架,藉由將支架本體設置於眼球內壁側邊,將眼球內的房水排出,以達到降低眼壓之目的。 The invention is a shunting bracket, especially a shunting bracket for draining the eyeball. By setting the bracket body on the side of the inner wall of the eyeball, the aqueous humor in the eyeball is discharged to achieve the purpose of reducing intraocular pressure.
習用的應用於治療青光眼的分流支架係使用金屬、矽膠或塑膠所製成,雖然分流支架體積小,但異物感重,會使傷口產生結痂,造成眼睛不舒服;另外,若要取出分流支架仍須再動一次手術,而每一次的手術都有其風險性,因此發明人憑藉在本業數十年累積的經驗,積極尋找替代性材料及改良結構,經過長期無數次試驗及改善,終於找到了替代性的材料與改良結構。 The conventional shunt support used for the treatment of glaucoma is made of metal, silicone or plastic. Although the shunt support is small in size, the foreign body feels heavy, which will cause the wound to scab and cause discomfort to the eyes. In addition, if you want to remove the shunt support It is still necessary to perform another operation, and each operation has its risks. Therefore, with decades of experience in the industry, the inventor actively sought alternative materials and improved structures. After long-term countless trials and improvements, I finally found Alternative materials and improved structure.
本發明揭露一種眼球排水之分流支架,包括一支架本體,由生物活化玻璃纖維編織混合膠原蛋白(Collagen)而成之管體,該支架本體具有至少一嵌入結構及一導液管,該導液管的內壁呈中空,該嵌入結構及該導液管呈一體成形,上述根據不同的纖維編織可以控制前房內部的房液流速以達降低眼壓的功效。 The invention discloses a shunting bracket for drainage of eyeballs, comprising a bracket body, a tube body made of biologically activated glass fiber woven mixed collagen (Collagen), the bracket body having at least one embedded structure and a liquid guiding tube, the liquid guiding The inner wall of the tube is hollow, the embedded structure and the catheter are integrally formed, and the above-mentioned weaving according to different fibers can control the flow rate of the atrial fluid in the anterior chamber to reduce the intraocular pressure.
本發明揭露一種眼球排水之分流支架,包括一支架本體,由至少一生物活化玻璃層組成,該支架本體具有一嵌入結構及一導液管,該 嵌入結構及該導液管呈一體成形;該嵌入結構外壁設有至少一固定結構;及該導液管的內壁呈中空,該導液管連接至該嵌入結構。 The invention discloses a shunting bracket for draining eyeballs, comprising a bracket body composed of at least one biologically activated glass layer, the bracket body having an embedded structure and a liquid guide tube, the The embedded structure and the catheter are integrally formed; the outer wall of the embedded structure is provided with at least one fixed structure; and the inner wall of the catheter is hollow, and the catheter is connected to the embedded structure.
藉由上述結構,本發明所製成的該支架本體嵌入眼球側邊內壁後,能導流出房水,進而達到降低眼壓的功效;另外,該支架本體係使用可被生物體吸收的該生物活化玻璃層(Bioactive glass),該支架本體對於生物體親和性佳,裝配時沒有異物感,且術後待時間久了之後,該支架本體的該生物活化玻璃層會被人體吸收,形成內原性管狀軟組織修復。 With the above structure, the stent body made by the present invention can be drained out of the aqueous humor after being embedded in the inner wall of the side of the eyeball, thereby achieving the effect of reducing intraocular pressure; in addition, the stent system uses the Bioactive glass layer (Bioactive glass), the stent body has a good affinity for organisms, there is no foreign body sensation during assembly, and after a long period of time after the operation, the bioactive glass layer of the stent body will be absorbed by the body to form an internal Repair of original tubular soft tissue.
另外,該支架本體亦可為具有複數結構而成,外層為該生物活化玻璃層,內層為一生物玻璃層,該生物玻璃層可為高密度矽含量之生物活化玻璃(Bioactive glass),或者為生物惰性玻璃(Bioinert glass);根據內層不同的材質可以控制該支架本體的強度及該支架本體被生物體吸收至體內的時間。 In addition, the holder body may also have a plurality of structures, the outer layer is the bioactive glass layer, the inner layer is a bioglass layer, the bioglass layer may be a high-density silicon content bioactive glass, or It is a bioinert glass; different materials according to the inner layer can control the strength of the stent body and the time the stent body is absorbed into the body by the living body.
10‧‧‧支架本體 10‧‧‧Bracket body
111‧‧‧生物活化玻璃層 111‧‧‧Biologically activated glass layer
112‧‧‧生物玻璃層 112‧‧‧biological glass layer
12‧‧‧嵌入結構 12‧‧‧Embedded structure
121‧‧‧槽道 121‧‧‧Slot
1212‧‧‧第二槽道 1212‧‧‧Second channel
122‧‧‧固定結構 122‧‧‧Fixed structure
123‧‧‧尖端 123‧‧‧tip
124‧‧‧彎弧缺口 124‧‧‧Curved arc notch
13‧‧‧凹部 13‧‧‧recess
14‧‧‧導液部 14‧‧‧Drainage Department
141‧‧‧導液管 141‧‧‧Catheter
16‧‧‧抵頂緣 16‧‧‧ reached the top edge
20‧‧‧植入器 20‧‧‧Implant
31‧‧‧前房 31‧‧‧Front room
圖1為本發明使用生物活化玻璃纖維編織混合膠原蛋白的支架本體立體示意圖 FIG. 1 is a perspective view of a scaffold body using bio-activated glass fiber braided mixed collagen according to the present invention
圖2為本發明第二實施例的支架本體正面立體示意圖 2 is a front perspective view of a bracket body according to a second embodiment of the invention
圖3為本發明第二實施例的支架本體底面立體示意圖 3 is a perspective schematic view of the bottom surface of the bracket body of the second embodiment of the invention
圖4為本發明第二實施例具有生物活化玻璃層的剖面示意圖 4 is a schematic cross-sectional view of a second embodiment of the present invention having a bioactive glass layer
圖4A為本發明第二實施例具有生物活化玻璃層及生物玻璃層的剖面示意圖 4A is a schematic cross-sectional view of a second embodiment of the present invention having a bioactive glass layer and a bioglass layer
圖5為本發明第三實施例的支架本體正面立體示意圖 5 is a front perspective view of a third embodiment of the bracket body of the present invention
圖6為本發明第三實施例具有生物活化玻璃層的剖面示意圖 6 is a schematic cross-sectional view of a third embodiment of the present invention having a bioactive glass layer
圖6A為本發明第三實施例具有生物活化玻璃層及生物玻璃層的剖面示意圖 6A is a schematic cross-sectional view of a third embodiment of the present invention having a bioactive glass layer and a bioglass layer
圖7為本發明第四實施例的支架本體立體示意圖 7 is a three-dimensional schematic view of the bracket body of the fourth embodiment of the present invention
圖7A為本發明第四實施例的支架本體具有生物活化玻璃層及生物玻璃層的剖面示意圖 7A is a schematic cross-sectional view of a stent body having a bioactive glass layer and a bioglass layer according to a fourth embodiment of the invention
圖8為本發明第五實施例的支架本體立體示意圖 8 is a schematic perspective view of a fifth embodiment of the stent body of the present invention
圖8A為本發明第五實施例的支架本體側視圖 FIG. 8A is a side view of a bracket body according to a fifth embodiment of the invention
圖9為本發明使用植入器將第一實施例的支架本體穿過前房並嵌入眼睛內壁側邊的示意圖 9 is a schematic diagram of the present invention using an implanter to insert the stent body of the first embodiment through the anterior chamber and embedded into the side of the inner wall of the eye
圖10為本發明第二實施例的支架本體將房液導流的示意圖 10 is a schematic diagram of the stent body of the second embodiment of the present invention to guide the flow of atrial fluid
圖11為圖10圈選部分放大示意圖 Figure 11 is an enlarged schematic view of the circled part of Figure 10
圖12為第三實施例的支架本體嵌設於眼睛內壁側面的示意圖 12 is a schematic view of the third embodiment of the bracket body embedded in the side of the inner wall of the eye
參閱圖1,為一種眼球排水之分流支架,包括一支架本體10,該支架本體10由生物活化玻璃纖維編織混合膠原蛋白而成之管體,該支架本體10具有至少一嵌入結構12及一導液管141,該導液管141的內壁呈中空,該嵌入結構12及該導液管141呈一體成形,根據不同的纖維編織可以控制前房內部的房液流速以達降低眼壓的功效;另外,從圖中可看出該支架本體10不具有方向性,其兩端均可以作為該嵌入結構12。
Referring to FIG. 1, it is a shunting stent for draining eyeballs, including a
參閱圖2~圖4,揭露本發明第二種實施例,為一種眼球排
水之分流支架,由至少一生物活化玻璃層111組成一支架本體10,該支架本體10具有一嵌入結構12及一導液管141,該嵌入結構12延伸一導液部14,該嵌入結構12與該導液部14使該支架本體10呈L形,該導液部14設有一個貫通該導液部14之該導液管141;該嵌入結構12底部具有一槽道121並與該導液管141相通且呈L形,該嵌入結構12的自由端呈一尖端123,該尖端123底部連通該槽道121且凹設一彎弧缺口124,該嵌入結構12外壁側邊設有複數呈倒勾狀之固定結構122;該導液管141的內壁呈中空,管口為橢圓形,然而該導液管141的管口形狀不限於橢圓形,亦可為圓形、六邊形或多邊形,該導液管141外壁面呈光滑平面,該導液管141沿著內軸的長度小於0.25mm,且內徑小於0.2mm。藉由上述結構,該支架本體10可在數週內溶解於生物體內,形成內原性管狀軟組織修復。
Referring to FIGS. 2 to 4, a second embodiment of the present invention is disclosed, which is an eyeball row
The water-shunting support is composed of at least one
圖4A揭露第二種實施例的該支架本體10具有雙層結構的示意圖,該生物活化玻璃層111位於該支架本體10的外層,該生物活化玻璃層111的內層設置一生物玻璃層112,若該生物玻璃層112為高密度矽含量之生物活化玻璃(Bioactive glass)則需要數個月的時間才會溶解於生物體內,該生物玻璃層112亦可為生物惰性玻璃(Bioinert glass)。若該生物玻璃層112為生物惰性玻璃,則該生物玻璃層112不會溶解,會一直存在生物體內。
FIG. 4A discloses a schematic diagram of the
圖5、圖6揭露第三種實施例示意圖,為一種眼球排水之分流支架,包括由至少一生物活化玻璃層111組成的一支架本體10,該支架本體10具有一嵌入結構12及一導液管141,該嵌入結構12延
伸一導液部14,該嵌入結構12與該導液部14使該支架本體呈I形,該導液部14設有一個貫通該嵌入結構12之該導液管141;該嵌入結構12外壁設有至少一呈倒勾狀之固定結構122,又該嵌入結構12另外貫設至少一第二槽道1212,該第二槽道1212的兩端貫通該嵌入結構12及該導液部14並環佈該導液管141外周圍且其軸向與該導液管141平行,該嵌入結構12與該導液部14相接處係環設一凹部13,使之於該導液部14側邊形成一抵頂緣16。另外,從圖中可看出該導液管141的管口為圓形,然而該導液管141的管口形狀不限於圓形,亦可為橢圓形、六邊形或多邊形。
FIGS. 5 and 6 show a schematic diagram of a third embodiment, which is a shunt support for eye drainage including a
圖6A揭露第三種實施例的該支架本體10具有多層結構的示意圖,該生物活化玻璃層111位於該支架本體10的外層,該生物活化玻璃層111的內層設置一生物玻璃層112,該生物玻璃層112為高密度矽含量之生物活化玻璃(Bioactive glass),或者該生物玻璃層112亦可為生物惰性玻璃(Bioinert glass)。若該生物玻璃層112為高密度矽含量之生物活化玻璃,則需要數個月的時間才會溶解於生物體內;若該生物玻璃層112為為生物惰性玻璃,則該生物玻璃層112不會溶解,會一直存在生物體內。
FIG. 6A discloses a schematic view of the third embodiment of the
圖7、圖7A揭露第四種實施例的一支架本體10,該支架本體10由至少一生物活化玻璃層111及一生物玻璃層112透過熱熔而成,該生物活化玻璃層111位於該生物玻璃層112的外層,該生物玻璃層112為高密度矽含量之生物活化玻璃(Bioactive glass),或者該生物玻璃層112亦可為生物惰性玻璃(Bioinert glass)。若該生物玻璃層112
為高密度矽含量之生物活化玻璃,則需要數個月的時間才會溶解於生物體內;若該生物玻璃層112為為生物惰性玻璃,則該生物玻璃層112不會溶解,會一直存在生物體內。該支架本體10具有一嵌入結構12及一導液管141,該嵌入結構12及該導液管141呈一體成形;該嵌入結構12外壁設有複數固定結構122,該等固定結構122呈圓形的球狀;及該導液管141的內壁呈中空,該導液管141連接至該嵌入結構12。
7 and 7A disclose a fourth embodiment of a
圖8、圖8A為本發明第五實施例示意圖,由至少一生物活化玻璃層111組成一支架本體10,該支架本體10具有一嵌入結構12及一導液管141,該嵌入結構12及該導液管141呈一體成形;該嵌入結構12外壁設有複數固定結構122,該等固定結構122呈倒勾狀;及該導液管141的內壁呈中空且兩側壁面均鏤空,該導液管141連接至該嵌入結構12。由於該支架本體10使用具生物親和性的該生物活化玻璃層111作為材料,因此可使該支架本體10可在數週內溶解於生物體內。
FIG. 8 and FIG. 8A are schematic diagrams of a fifth embodiment of the present invention. At least one
藉由上述結構,可將該支架本體10嵌入眼球內壁面,使房水經由該導液管141導出,達到降低眼壓功效,該支架本體10係由可被生物體吸收的玻璃材料所製成,因此該支架本體10具有親和生物性的特性,於植入眼睛內壁面後能降低異物感受,且該支架本體10隨著時間會慢慢被生物體吸收,形成內原性管狀軟組織修復,不需要再次動手術將該支架本體10從眼睛內側壁取出。
With the above structure, the
參閱圖9~圖12,為該支架本體10具體實施例示意圖。
9 to 12 are schematic diagrams of specific embodiments of the
參閱圖9~圖11並搭配圖2~4A,先將該支架本體10裝設於一植入器20上,透過該植入器20穿過眼球的一前房31,該尖端123能使該支架本體10更容易進入眼球的內壁,當該支架本體10嵌設於眼球的內壁側邊後,接著將該植入器20稍微轉向調整角度,使該嵌入結構12能盡量以水平貼附於眼球的內側壁面。
Referring to FIGS. 9 to 11 together with FIGS. 2 to 4A, first mount the
其中第二實施例的該支架本體10之該嵌入結構12嵌設於眼球的內側壁面,而該導液管141則是與該前房31連通,使該前房31內部的房液,能經由該導液管141,導流排出該前房31可降低眼壓。
The embedding
圖12並搭配圖5~圖6A,第三實施例的該支架本體10之該嵌入結構12嵌設於眼球的內側壁面,該導液管141則是與該前房31連通,使該前房31內部的房液,能經由該導液管141或該第二槽道1212導流排出該前房31可降低眼壓。
12 and FIG. 5 to FIG. 6A, the embedding
10‧‧‧支架本體 10‧‧‧Bracket body
111‧‧‧生物活化玻璃層 111‧‧‧Biologically activated glass layer
12‧‧‧嵌入結構 12‧‧‧Embedded structure
122‧‧‧固定結構 122‧‧‧Fixed structure
123‧‧‧尖端 123‧‧‧tip
124‧‧‧彎弧缺口 124‧‧‧Curved arc notch
14‧‧‧導液部 14‧‧‧Drainage Department
141‧‧‧導液管 141‧‧‧Catheter
Claims (6)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW108110396A TWI695716B (en) | 2019-03-26 | 2019-03-26 | Diversion bracket for eyeball drainage |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW108110396A TWI695716B (en) | 2019-03-26 | 2019-03-26 | Diversion bracket for eyeball drainage |
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| Publication Number | Publication Date |
|---|---|
| TWI695716B true TWI695716B (en) | 2020-06-11 |
| TW202034869A TW202034869A (en) | 2020-10-01 |
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| Application Number | Title | Priority Date | Filing Date |
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| TW108110396A TWI695716B (en) | 2019-03-26 | 2019-03-26 | Diversion bracket for eyeball drainage |
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| TW (1) | TWI695716B (en) |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6736791B1 (en) * | 2000-04-14 | 2004-05-18 | Glaukos Corporation | Glaucoma treatment device |
| CN101001589A (en) * | 2004-06-01 | 2007-07-18 | 贝克顿迪肯森公司 | Ocular implant and methods for making and using same |
| WO2009012406A1 (en) * | 2007-07-17 | 2009-01-22 | Transcend Medical, Inc. | Ocular implant with hydrogel expansion capabilities reference to priority document |
| US8506515B2 (en) * | 2006-11-10 | 2013-08-13 | Glaukos Corporation | Uveoscleral shunt and methods for implanting same |
| US9757276B2 (en) * | 2011-11-11 | 2017-09-12 | Opr Group Ltd. | Ocular implant with intraocular fluid pressure regulation |
| US20170333190A1 (en) * | 2016-04-19 | 2017-11-23 | Warsaw Orthopedic, Inc. | Implantable composite containing carbonated hydroxyapatite |
| TW201902435A (en) * | 2017-06-13 | 2019-01-16 | 美商英福卡斯公司 | Systems, methods, and apparatus for treatment of glaucoma |
-
2019
- 2019-03-26 TW TW108110396A patent/TWI695716B/en active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6736791B1 (en) * | 2000-04-14 | 2004-05-18 | Glaukos Corporation | Glaucoma treatment device |
| CN101001589A (en) * | 2004-06-01 | 2007-07-18 | 贝克顿迪肯森公司 | Ocular implant and methods for making and using same |
| US8506515B2 (en) * | 2006-11-10 | 2013-08-13 | Glaukos Corporation | Uveoscleral shunt and methods for implanting same |
| WO2009012406A1 (en) * | 2007-07-17 | 2009-01-22 | Transcend Medical, Inc. | Ocular implant with hydrogel expansion capabilities reference to priority document |
| US9757276B2 (en) * | 2011-11-11 | 2017-09-12 | Opr Group Ltd. | Ocular implant with intraocular fluid pressure regulation |
| US20170333190A1 (en) * | 2016-04-19 | 2017-11-23 | Warsaw Orthopedic, Inc. | Implantable composite containing carbonated hydroxyapatite |
| TW201902435A (en) * | 2017-06-13 | 2019-01-16 | 美商英福卡斯公司 | Systems, methods, and apparatus for treatment of glaucoma |
Non-Patent Citations (3)
| Title |
|---|
| Ejaz Ansari, "An Update on Implants for Minimally Invasive Glaucoma Surgery (MIGS)", Ophthalmology and Therapy, Volume 6, Issue 2, December 2017, pages 233-241. |
| Francesco Baino et al,, "Special Applications of Bioactive Glasses in Otology and Ophthalmology", Biocompatible Glasses. Advanced Structured Materials, Volume 53, 2016, pages 227-248. |
| Francesco Baino et al,, "Special Applications of Bioactive Glasses in Otology and Ophthalmology", Biocompatible Glasses. Advanced Structured Materials, Volume 53, 2016, pages 227-248. Ejaz Ansari, "An Update on Implants for Minimally Invasive Glaucoma Surgery (MIGS)", Ophthalmology and Therapy, Volume 6, Issue 2, December 2017, pages 233-241. * |
Also Published As
| Publication number | Publication date |
|---|---|
| TW202034869A (en) | 2020-10-01 |
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