Other products from "MIRA, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10850510007566 CR4080 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Baby Hammerhead
2 10850510007559 CR4075 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Hammerhead
3 10850510007528 CR4030 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Curved Glaucoma
4 10850510007467 CR4000 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Console
5 10850510007511 CR4025 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Mini Curved Cataract
6 10850510007580 CR4090 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Abramson Retinoblastoma
7 10850510007535 CR4040 GEH Unit, Cryosurgical, Accessories 2 MIRA Cryosurgical Probe, Straight Vitreous
8 10850510007443 519G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
9 10850510007436 517 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
10 10850510007429 516G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
11 10850510007412 511 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
12 10850510007405 510 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
13 10850510007399 509G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
14 10850510007382 509 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
15 10850510007375 508G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
16 10850510007368 508 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
17 10850510007351 507T HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
18 10850510007344 507G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
19 10850510007337 507 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
20 10850510007320 506G HQX Implant, Orbital, Extra-Ocular MIRA IMEX Scleral Buckling Component
21 10850510007313 506 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
22 10850510007306 505T HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
23 10850510007290 505G HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
24 10850510007283 505 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
25 10850510007276 504 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
26 10850510007269 503 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
27 10850510007252 5025 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
28 10850510007245 502 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
29 10850510007238 501 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
30 10850510007221 287 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
31 10850510007214 286 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
32 10850510007207 279 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
33 10850510007191 278 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
34 10850510007184 277 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
35 10850510007177 276 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
36 10850510007160 270 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
37 10850510007153 250 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
38 10850510007146 240 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
39 10850510007139 225 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
40 10850510007122 220 HQX Implant, Orbital, Extra-Ocular MIRA IMEX Scleral Buckling Component
41 10850510007115 219 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
42 10850510007108 106 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
43 10850510007092 75R HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
44 10850510007085 72 HQX Implant, Orbital, Extra-Ocular MIRA IMEX Scleral Buckling Component
45 10850510007078 70 HQX Implant, Orbital, Extra-Ocular MIRA IMEX Scleral Buckling Component
46 10850510007054 42 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
47 10850510007047 41 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
48 10850510007030 40 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
49 10850510007023 32 HQX Implant, Orbital, Extra-Ocular MIRA IMEX Scleral Buckling Component
50 10850510007016 20 HQX Implant, Orbital, Extra-Ocular 2 MIRA IMEX Scleral Buckling Component
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.