Other products from "D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNATIONAL) B.V."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08717872031798 9110.IAD01 HQC,HQE,HQF Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Laser, Ophthalmic 2 EVA NEXUS™ Irrigation and Aux. Aspiration Tubing
2 08717872032412 1279.HF27 1279.HF27 NGY Cannula, Trocar, Ophthalmic 1 27G High Flow infusion line
3 08717872031903 7227.DORC HQF Laser, Ophthalmic 2 Directional Laser Probe with DORC connector.(27 gauge / 0.4 mm)
4 08717872031897 7227.ALC HQF Laser, Ophthalmic 2 Directional Laser Probe with Alcon / Lumenis connector.(27 gauge / 0.4 mm)
5 08717872033365 8430.22AF1 HQC Unit, Phacofragmentation 2 2.2 mm Disposable phaco set with 30° angled flared needle Note: Incision size 2.
6 08717872033419 8445.22AF1 HQC Unit, Phacofragmentation 2 2.2 mm Disposable phaco set with 45° angled flared needle Note: Incision size 2.
7 08717872034355 9545.18SF1 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered 2 EVA NEXUSTM Custom Phaco Pack 1.8mm 45 (Straight)
8 08717872034416 9000.ANTU1 HQC Unit, Phacofragmentation 2 EVA NEXUS™, Phaco emulsification system
9 08717872034379 9545.22AF1 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered 2 EVA NEXUSTM Custom Phaco Pack 2.2mm 45 (Angled)
10 08717872034300 9530.18SF1 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered 2 EVA NEXUSTM Custom Phaco Pack 1.8mm 30 (Straight)
11 08717872031569 3445.18SF1 3445.18SF1 HQC Unit, Phacofragmentation 2 MICS 1.8 mm Reusable phaco set with 45° straight flared needle
12 08717872031477 8430.24SF1 8430.24SF1 HQC Unit, Phacofragmentation 2 2.4 mm Disposable phaco set with 30° straight flared needle
13 08717872031439 8430.18SF1 8430.18SF1 HQC Unit, Phacofragmentation 2 MICS 1.8 mm Disposable phaco set with 30° straight flared needle
14 08717872031224 3269.SBS4S 3269.SBS4S 27G Ultra Short Shielded TotalView Endoillumination Probe, including scleral depressor HQC Unit, Phacofragmentation 27G Ultra Short Shielded TotalView Endoillumination Probe, including scleral dep
15 08717872030753 8310.23G12 8310.23G12 HQF,HQE,HQC Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Phacofragmentation EVA TDC Vitrectomy Pack VGPC Input 23G
16 08717872030739 8300.27G12 8300.27G12 HQF,HQE,HQC Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Phacofragmentation EVA Vitrectomy Pack VGPC Input 27G
17 08717872027463 7625.DORC 7625.DORC HQB Photocoagulator And Accessories Illuminated Curved Laser probe, 25 gauge / 0,5mm with DORC® connector
18 08717872022093 8527.202 8527.202 HQF,HQE,HQC Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Phacofragmentation Custom TDC Vitrectomy Pack VGP 27G
19 08717872021942 3269.MBD27 3269.MBD27 MPA Endoilluminator Disposable Eckardt Twinlight Chandelier. (27 gauge / 0.4mm)
20 08717872021010 8310.23G02 8310.23G02 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered EVA TDC Vitrectomy Pack VGPC Input 23G
21 08717872020228 3008.IRD25 3008.IRD25 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered Disposable infusion sleeve for 2.5 mm phaco needle Including test chamber
22 08717872020211 3008.IRD22 3008.IRD22 HQE,HQC Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Phacofragmentation Disposable infusion sleeve for 2.2 mm phaco needle Including test chamber
23 08717872019710 8005.F4 8005.F4 HQF,HQE,HQC Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Laser, Ophthalmic,Instrument, Vitreous Aspiration And Cutting, Ac-Powered,Unit, Phacofragmentation 2 Safety filter for Leica Microscopes, Passive
24 08717872019116 8110.VGP01 8110.VGP01 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered Disposable EVA VGPC Input Set
25 08717872019086 8267.VIT25 8267.VIT25 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered Disposable High Speed Cutter 25G/8000CPM
26 08717872019079 8267.VIT27 8267.VIT27 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered Disposable High Speed Cutter 27G/8000CPM
27 08717872019055 8300.27G02 8300.27G02 HQC,HQE Unit, Phacofragmentation,Instrument, Vitreous Aspiration And Cutting, Ac-Powered EVA Vitrectomy Pack VGPC Input 27G
28 08717872018881 1272.VFI04 1272.VFI04 HMX Cannula, Ophthalmic 1 Disposable VFI cannula, with 6mm thin wall polyimide tip. (27 gauge / 0.4 mm)
29 08717872018850 3008.IR18 3008.IR18 HQC Unit, Phacofragmentation Irrigation sleeve for 1.8 mm phaco needle.
30 08717872018560 2286.PD04 2286.PD04 HNF Scissors, Ophthalmic 1 Disposable Microscissors: Hooked. (27 gauge / 0.4 mm)
31 08717872018270 3269.EXS06 3269.EXS06 MPA Endoilluminator Extendible Shielded Light Probe (23 gauge / 0.6 mm)
32 08717872018232 3008.K 3008.K HQC Unit, Phacofragmentation 2 Universal metal wrench for star phaco needles. Accessory to the DORC phaco handp
33 08717872018195 3269.EX06 3269.EX06 MPA Endoilluminator Extendible Light Probe (23 gauge / 0.6 mm)
34 08717872017822 1290.ECS06 1290.ECS06 HND Spatula, Ophthalmic 1 Extendible curved spatula. (23 gauge / 0.6 mm)
35 08717872017594 1250.VGPC 1250.VGPC HQC Unit, Phacofragmentation Vented Global Pressure Control Set to be used with Associate Cartridge
36 08717872017372 1272.ED205 1272.ED205 NGY Cannula, Trocar, Ophthalmic 1 Disposable One Step Cannula System (25 gauge/0.5 mm)
37 08717872017150 1292.E04 1292.E04 HND Spatula, Ophthalmic 1 Eckardt Membrane Pic, angled at 120 degrees. (27 gauge / 0.4 mm)
38 08717872017044 1286.ILM06 1286.ILM06 HNR Forceps, Ophthalmic 1 Microforceps: ILM.(23 gauge / 0.6 mm)
39 08717872017037 1286.ILM05 1286.ILM05 HNR Forceps, Ophthalmic 1 Microforceps: ILM.(25 gauge / 0.5 mm)
40 08717872016818 3005.F106 3005.F106 HQC Unit, Phacofragmentation Phaco fragmentation needles, 23G / 0.6 mm, incl. needle wrench.
41 08717872016535 2267.MIL06 2267.MIL06 HQC Unit, Phacofragmentation Disposable High-Speed cutter with Millennium Vitrectomy Enhancer connector.(23 g
42 08717872016009 3269.A27 3269.A27 MPA Endoilluminator Disposable Chandelier fiber (one fiber) incl. guidance needle. (27 gauge/0.4 mm)
43 08717872014654 92-50-5R 92-50-5R HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style 505, 5.0mm Round Sponge
44 08717872014647 92-50-55G 92-50-55G HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style 507G, 5.5mm x 7.5mm Grooved Sponge
45 08717872014586 92-50-3G 92-50-3G HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style 506G, 3.0mm x 5.0mm Grooved Sponge
46 08717872014531 92-35 92-35 HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style N/A, 2.5mm Oval Silicone Sleeve
47 08717872014289 92-06 92-06 HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style 219, 2.5mm Grooved Strip
48 08717872014241 92-02 92-02 HQX Implant, Orbital, Extra-Ocular Scleral Buckling Products: Style 240, 2.5mm Circling Band
49 08717872013435 6279.ASD2S 6279.ASD2S HQC Unit, Phacofragmentation Disposable I/A silicone replacement Tubing set for REF: 6279.ASD1 Cartridge, inc
50 08717872013428 6279.ASD2 6279.ASD2 HQC Unit, Phacofragmentation Disposable I/A replacement Tubing set for REF: 6279.ASD1 Cartridge, including co
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.