Other products from "MICROVISION, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10818255011323 Style 277 5431 Concave Silicone Tire 7.0mm, 2.5mm groove HQX Implant, Orbital, Extra-Ocular 2 NA
2 10818255011521 Style 112 5460 Meridional Implant 12.0mm HQX Implant, Orbital, Extra-Ocular 2 NA
3 10818255011460 Style 42 5450 Silicone Strip 1.25mm x 4.0mm x 125mm HQX Implant, Orbital, Extra-Ocular 2 NA
4 10818255011453 Style 40 5449 Circling Band 0.75mm x 2.0mm x 125mm HQX Implant, Orbital, Extra-Ocular 2 NA
5 10818255011446 Style 48 5448 Silicone Strip 0.75mm x 3.5mm x 125mm HQX Implant, Orbital, Extra-Ocular 2 NA
6 10818255011439 Style 70 5447 Silicone Sleeve 1.0mm x 2.1mm x 30mm HQX Implant, Orbital, Extra-Ocular 2 NA
7 10818255011422 Style 270 5446 Silicone Sleeve 0.76mm x 1.65mm x 30mm HQX Implant, Orbital, Extra-Ocular 2 NA
8 10818255011415 Style 240 5445 Circling Band 0.60mm x 2.5mm x 125mm HQX Implant, Orbital, Extra-Ocular 2 NA
9 10818255011392 Style 287 5441 Convex Silicone Tire 7.0mm, 2.5mm groove HQX Implant, Orbital, Extra-Ocular 2 NA
10 10818255011385 Style 286 5440 Convex Silicone Tire 6.0mm, 2.5mm groove HQX Implant, Orbital, Extra-Ocular 2 NA
11 10818255011378 Style 276 5438 Asymmetrical Silicone Tire 7.0mm, 2.5mm groove HQX Implant, Orbital, Extra-Ocular 2 NA
12 10818255011330 Style 279 5432 Concave Silicone Tire 9.0mm, 2.5mm groove HQX Implant, Orbital, Extra-Ocular 2 NA
13 10818255011231 Style 507 5408 Oval Silicone Sponge 5.5mm x 7.5mm x 80mm HQX Implant, Orbital, Extra-Ocular 2 NA
14 10818255011224 Style 506 5407 Oval Silicone Sponge 3.0mm x 5.0mm x 100mm HQX Implant, Orbital, Extra-Ocular 2 NA
15 10818255011217 Style 505 5405 Round Silicone Sponge 5.0mm x 80mm HQX Implant, Orbital, Extra-Ocular 2 NA
16 10818255011200 Style 504 5404 Round Silicone Sponge 4.0mm x 80mm HQX Implant, Orbital, Extra-Ocular 2 NA
17 10818255011194 Style 503 5403 Round Silicone Sponge 3.0mm x 80mm HQX Implant, Orbital, Extra-Ocular 2 NA
18 10818255011163 NA 5316 Chandelier Fiber Probe with Adjustable Ring, 25Ga. with 19Ga. Needle Type Connector FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
19 10818255011095 NA 5259 Fiber Optic Illuminator, 25Ga. (Compatible with Bausch + Lomb Stellaris PC System) FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
20 10818255011088 N/A 5257 Dual Bore Subretinal BSS Injection Needle, 23Ga. with 0.1mm/41Ga. tip HMX Cannula, Ophthalmic 1 N/A
21 10818255011057 N/A 5248 Disposable Viscous Fluid Injection Cannula, 23Ga. with 10mm thin-wall polyimide tip HMX Cannula, Ophthalmic 1 N/A
22 10818255011040 NA 5247 Fiber Optic Illuminator, 23Ga. (Compatible with Bausch + Lomb Stellaris PC System) FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
23 10818255011033 N/A 5244 Disposable One-Step Trocar System, 25Ga. (3 Trocar Knives with Pre-Loaded Self-S Disposable One-Step Trocar System, 25Ga. (3 Trocar Knives with Pre-Loaded Self-Sealing Trocar Cannula & 1 Infusion Line) NGY Cannula, Trocar, Ophthalmic 1 N/A
24 10818255011026 N/A 5243 Disposable Two-Step Trocar System, 23Ga. (3 Trocar Cannula Inserters with Pre-Lo Disposable Two-Step Trocar System, 23Ga. (3 Trocar Cannula Inserters with Pre-Loaded Self-Sealing Trocar Cannula & 1 Infusion Line) NGY Cannula, Trocar, Ophthalmic 1 N/A
25 10818255010234 N/A 5067-6 Disposable Polypropylene Iris Retractors HOC Clip, Iris Retractor N/A
26 10818255010975 N/A 5229 Disposable One-Step Trocar System, 23Ga. (3 Trocar Knives with Pre-Loaded Self-S Disposable One-Step Trocar System, 23Ga. (3 Trocar Knives with Pre-Loaded Self-Sealing Trocar Cannula and 1 Infusion Line) NGY Cannula, Trocar, Ophthalmic 1 N/A
27 10818255010968 NA 5228 Chandelier Illuminator, 0.5mm Fiber with Ocutome Connector FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
28 10818255010883 N/A 5203 Disposable Dual Bore PFC Cannula, 23Ga. HMX Cannula, Ophthalmic 1 N/A
29 10818255010852 N/A 5197 Disposable Backflush Instrument - Passive Aspiration KYG Device, Irrigation, Ocular Surgery 1 N/A
30 10818255010845 N/A 5196 Disposable Backflush Instrument - Active Aspiration KYG Device, Irrigation, Ocular Surgery 1 N/A
31 10818255010791 N/A 5188 Fixation Plate and Marker for 23Ga. Vitrectomy NGY Cannula, Trocar, Ophthalmic 1 N/A
32 10818255010746 NA 5179 Fiber Optic Illuminator, 23Ga. - B & L FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
33 10818255010739 NA 5178 Wide Angle Fiber Optic Illuminator, 23Ga. - ALN FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
34 10818255010722 NA 5177 Fiber Optic Illuminator, 23Ga. - ALN FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
35 10818255010715 N/A 5173 Reusable Two-Step Trocar System with Closure Plugs, 23Ga. NGY Cannula, Trocar, Ophthalmic 1 N/A
36 10818255010708 NA 5172 Associate High Speed Posterior Vitrectomy Probe, 23Ga., 30psi HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered 2 NA
37 10818255010685 NA 5169 Wide Angle Fiber Optic Illuminator, 23Ga. FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
38 10818255010661 N/A 5164 Charles Flute Cannula, 23Ga. HMX Cannula, Ophthalmic N/A
39 10818255010654 NA 5163 Fiber Optic Illuminator, 23Ga. FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
40 10818255010647 N/A 5162 Retinal Cannula with Silicone Brush Tip, 23Ga. HMX Cannula, Ophthalmic N/A
41 10818255010630 N/A 5161 Retinal Cannula with Silicone Top, 23Ga. HMX Cannula, Ophthalmic N/A
42 10818255010623 N/A 5160 Retinal Cannula with Silicone Brush Tip, 25Ga. HMX Cannula, Ophthalmic N/A
43 10818255010609 NA 5157 Associate Posterior Vitrectomy Probe, 25Ga, 2500CPM, 30psi HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered 2 NA
44 10818255010593 N/A 5156 Charles Flute Cannula, 25Ga. HMX Cannula, Ophthalmic N/A
45 10818255010562 N/A 5152 Retinal Cannula with Silicone Tip, 25Ga. HMX Cannula, Ophthalmic 1 N/A
46 10818255010548 N/A 5150 Disposable One-Step Trocar System, 25Ga. (4 insert handles with preloaded trocar Disposable One-Step Trocar System, 25Ga. (4 insert handles with preloaded trocars & 1 infusion line) NGY Cannula, Trocar, Ophthalmic 1 N/A
47 10818255010531 N/A 5147 Replacement Reservoir for Backflush Instrument - Passive Aspiration KYG Device, Irrigation, Ocular Surgery 1 N/A
48 10818255010487 NA 5140 Posterior Vitrectomy Probe, 25Ga. for use with 25psi systems HKP Instrument, Vitreous Aspiration And Cutting, Battery-Powered 2 NA
49 10818255010470 NA 5138 Fiber Optic Illuminator, 25Ga. - B & L FFS Image, Illumination, Fiberoptic, For Endoscope 2 NA
50 10818255010456 N/A 5127 Reusable Flexible Iris Retractors HOC Clip, Iris Retractor N/A
Other products with the same Product Code "HQX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 03760087127355 SPONGE 7.0 x 3.25 TYPE 907 S5.6585U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
2 03760087122428 ePTFE BAND 2.1 X 5.5 mm S5.4821U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
3 03760087122152 4 X 3 mm ePTFE SPONGE (CHAUVAUD) S5.6670U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
4 03760087122145 9 mm ePTFE STRIP (DESIGNED BY O. LEQUOY) S5.6660U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
5 03760087122138 ePTFE SPONGE 5 mm S5.6650U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
6 03760087122121 ePTFE HALF SPONGE 2.5 X 7.5 mm S5.6645U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
7 03760087122114 ePTFE SPONGE 4 mm S5.6640U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
8 03760087122091 ePTFE SPONGE 3.0 X 5.0 mm S5.6635U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
9 03760087122084 ePTFE SPONGE 3 mm S5.6630U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
10 03760087122077 ePTFE SPONGE 2 X 5 mm S5.6625U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
11 03760087122060 HALF-SPONGE 2.75 x 7.5 TYPE 511 S5.6575U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
12 03760087122053 SPONGE 3 x 5 TYPE 506 S5.6535U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
13 03760087122008 GROOVED SPONGE 7.5 x 3.5 TYPE 509 G S5.6570U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
14 03760087121988 GROOVED SPONGE Ø 5 mm TYPE 505 G S5.6520U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
15 03760087121971 S5.6475 A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. HALF-SPONGE 2.75 X 7.5 TYPE 511 FCI S A S FCI 20 22
16 03760087121957 HALF-SPONGE 2.5 x 5 TYPE 510 S5.6550U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
17 03760087121902 GROOVED SPONGE 5.5 x 7.5 TYPE 507 G S5.6560U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
18 03760087121896 SPONGE 5.5 x 7.5 TYPE 507 S5.6557U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
19 03760087121872 GROOVED SPONGE 3 x 5 TYPE 506 G S5.6540U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
20 03760087121827 SPONGE Ø 5 mm TYPE 505 S5.6505U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
21 03760087121810 SPONGE Ø 4 mm TYPE 504 S5.6504U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
22 03760087121803 SPONGE Ø 3 mm TYPE 503 S5.6503U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
23 03760087121674 ePTFE DUCOURNAU BAND 2.5 X 7.0 mm S5.4811U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
24 03760087121650 ePTFE DUCOURNAU BAND 2.5 X 5.5 mm S5.4801U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
25 03760087121551 FIXATION SLEEVE FOR S5.1025U TYPE 72 S5.3025U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
26 03760087121544 FIXATION SLEEVE FOR S5.1015U TYPE 71 S5.3515U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
27 03760087121537 FIXATION SLEEVE FOR S5.2005U TYPE 270 S5.3510U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
28 03760087121520 FIXATION SLEEVE FOR S5.1005U TYPE 70 S5.3005U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
29 03760087121476 ASYMMETRICAL TIRE 12 TYPE 280 S5.2345U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
30 03760087121452 TIRE 11 TYPE 279 S5.2335U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
31 03760087121438 BICONVEX TIRE 12 TYPE 289 S5.2325U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
32 03760087121421 BICONVEX TIRE 9 TYPE 287 S5.2315U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
33 03760087121391 ASYMMETRICAL TIRE 9 TYPE 276 S5.2295U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
34 03760087121322 STRIP (8 mm) TYPE 225 S5.2255U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
35 03760087121308 STRIP (7.5 mm) TYPE 220 S5.2205U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
36 03760087121292 STRIP (6 mm) TYPE 219 S5.2105U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
37 03760087121254 BAND (2.5 x 0.6 mm) TYPE 240 S5.2005U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
38 03760087121247 TIRE 12 TYPE 78 G S5.1305U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
39 03760087121230 STRIP (9.2 mm) TYPE 32 S5.1255U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
40 03760087121216 STRIP (7.2 mm) TYPE 31 S5.1205U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
41 03760087121193 STRIP (5.7 mm) TYPE 20 S5.1105U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
42 03760087121186 BAND (4.0 x 1.25 mm) TYPE 42 S5.1025U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
43 03760087121179 BAND (3.5 x 0.75 mm) TYPE 41 S5.1015U A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
44 03760087121162 BAND (2.0 x 0.75 mm) TYPE 40 S5.1005 A sterile, non-bioabsorbable device intended to be implanted for intrascleral an A sterile, non-bioabsorbable device intended to be implanted for intrascleral and episcleral buckling for the surgical treatment of retinal detachment. It is typically a moulded solid silicone or silicone sponge device available in a variety of shapes and sizes that is used to compress the retina long-term (up to months) to support its reattachment following the operative treatment of severe retinal detachment. This device, also known as a scleral buckling component, will occupy the intraocular space to provide compression against the retina so that it can reattach. It is typically removed after a period of time depending upon the clinical findings. Scleral buckling device, non-bioabsorbable FCI S A S FCI 20 22
45 00300090297015 Gelfilm® Sterile Ophthalmic Film Ophthalmic film 6's (12.5 sq cm) Anti-adhesion dressing, bioabsorbable Gelfilm PHARMACIA & UPJOHN COMPANY LLC
46 20850510007457 175 Scleral Marker For Proton Beam Irradiation MIRA Gragoudas Ring MIRA, INC.
47 10871321001208 S 1981-7.5 Oval Sponge Oval Sponge LABTICIAN OPHTHALMICS, INC
48 10850510007443 519G MIRA IMEX Scleral Buckling Component MIRA, INC.
49 10850510007436 517 MIRA IMEX Scleral Buckling Component MIRA, INC.
50 10850510007429 516G MIRA IMEX Scleral Buckling Component MIRA, INC.