Other products from "FCI S A S FCI 20 22"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 13700773724939 S3.3020 OCULID GOLD 2,0g NCB Weights, Eyelid, Implantable 2 OCULID GOLD 2,0g
2 13700773727732 S3.60104 EXTERNAL OCULID DARK BROWN® - 1,0 g MML Weights, Eyelid, External 2 EXTERNAL OCULID DARK BROWN® - 1,0 g
3 13700773727800 S3.60141 EXTERNAL OCULID PINK® - 1,4 g MML Weights, Eyelid, External 2 EXTERNAL OCULID PINK® - 1,4 g
4 13700773727794 S3.60140 EXTERNAL OCULID LIGHT® - 1,4 g MML Weights, Eyelid, External 2 EXTERNAL OCULID LIGHT® - 1,4 g
5 13700773727862 S3.60162 EXTERNAL OCULID TAN® - 1,6 g MML Weights, Eyelid, External 2 EXTERNAL OCULID TAN® - 1,6 g
6 13700773727688 S3.60084 EXTERNAL OCULID DARK BROWN® - 0,8 g MML Weights, Eyelid, External 2 EXTERNAL OCULID DARK BROWN® - 0,8 g
7 13760087126249 S1.1470 A hand-held manual ophthalmic surgical instrument with small blades designed to A hand-held manual ophthalmic surgical instrument with small blades designed to grasp and manipulate ophthalmic implants (excluding sutures) during implantation/explantation; it is not intended for use on tissues. Its design may be tweezers-like, or it may be probe-like with a proximal handle, a thin cannula-like shaft, and small grasping blades that protrude from the distal end of the shaft. This is a reusable device intended to be sterilized prior to use. HNR Forceps, Ophthalmic 1 RITLENG ENDONASAL FORCEPS
8 13760087123828 S1.4122 A collection of various ophthalmic surgical instruments and the necessary materi A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not comprised exclusively of dedicated implantation tools and it does not contain any pharmaceuticals. This is a single-use device. OKS Lacrimal Stents And Intubation Sets U OPHTACATH® 2 mm Kit Bilateral Kit
9 13700773727930 S3.60184 EXTERNAL OCULID DARK BROWN® - 1,8 g MML Weights, Eyelid, External 2 EXTERNAL OCULID DARK BROWN® - 1,8
10 13700773727275 S3.4006 OCULID GOLD SLIM 0,6g NCB Weights, Eyelid, Implantable 2 OCULID GOLD SLIM 0,6g
11 13700773724694 S3.6016 OCULID PLATINUM SLIM® 1,6 g NCB Weights, Eyelid, Implantable 2 OCULID PLATINUM SLIM® 1,6 g
12 13700773724588 S3.4006 OCULID GOLD SLIM 0,6g NCB Weights, Eyelid, Implantable 2 OCULID GOLD SLIM 0,6g
13 13700773723390 S9.1314.23 FCI directional LASER PROBE 23G NIDEK HQB Photocoagulator And Accessories 2 FCI directional LASER PROBE 23G NIDEK
14 13700773723512 S9.1325.23 FCI directional LASER PROBE / EXTENDABLE 23G DORC HQB Photocoagulator And Accessories 2 FCI directional LASER PROBE / EXTENDABLE 23G DORC
15 13700773721327 S9.6015.23 DISPOSABLE VERTICAL SCISSORS, 23G HNR Forceps, Ophthalmic 1 DISPOSABLE VERTICAL SCISSORS, 23G
16 13700773721280 S9.6013.23 DISPOSABLE END-GRASPING FORCEPS, 23G HNR Forceps, Ophthalmic 1 DISPOSABLE END-GRASPING FORCEPS, 23G
17 13700773721259 S9.6011.25 DISPOSABLE SERRATED FORCEPS 25G HNR Forceps, Ophthalmic 1 DISPOSABLE SERRATED FORCEPS 25G
18 13700773721235 S9.6017.25 DISPOSABLE TANO FORCEPS 25G HNR Forceps, Ophthalmic 1 DISPOSABLE TANO FORCEPS 25G
19 13700773720771 S9.1404.27 STRAIGHT ILLUM LASER PROBE,27G NIDEK & 19G NEEDLE HQB Photocoagulator And Accessories 2 STRAIGHT ILLUM LASER PROBE,27G NIDEK & 19G NEEDLE
20 13700773720719 S9.1403.25 STRAIGHT ILLUM LASER PROBE,25G QUANTEL & 19G NEEDLE HQB Photocoagulator And Accessories 2 STRAIGHT ILLUM LASER PROBE,25G QUANTEL & 19G NEEDLE
21 13700773720641 S9.1401.23 STRAIGHT ILLUM LASER PROBE,23G IRIDEX/B&L & 19G NEEDLE HQB Photocoagulator And Accessories 2 STRAIGHT ILLUM LASER PROBE,23G IRIDEX/B&L & 19G NEEDLE
22 13700773720610 S9.1403.20 STRAIGHT ILLUM LASER PROBE,20G QUANTEL & 19G NEEDLE HQB Photocoagulator And Accessories 2 STRAIGHT ILLUM LASER PROBE,20G QUANTEL & 19G NEEDLE
23 13700773720498 S9.1301.23 90° ADJUSTABLE LASER PROBE, 23G IRIDEX/B&L HQB Photocoagulator And Accessories 2 90° ADJUSTABLE LASER PROBE, 23G IRIDEX/B&L
24 13700773720405 S9.1212.23 FLEX CURVED LASER PROBE, 23G ALCON/COHERENT/ZEISS/ELLEX/OS4 HQB Photocoagulator And Accessories 2 FLEX CURVED LASER PROBE, 23G ALCON/COHERENT/ZEISS/ELLEX/OS4
25 13700773720399 S9.1211.23 FLEX CURVED LASER PROBE, 23G IRIDEX/B&L HQB Photocoagulator And Accessories 2 FLEX CURVED LASER PROBE, 23G IRIDEX/B&L
26 13700773720320 S9.1204.23 CURVED LASER PROBE, 23G NIDEK HQB Photocoagulator And Accessories 2 CURVED LASER PROBE, 23G NIDEK
27 13700773720238 S9.1005.27 STRAIGHT LASER PROBE, 27G DORC HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 27G DORC
28 13700773720221 S9.1004.27 STRAIGHT LASER PROBE, 27G NIDEK HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 27G NIDEK
29 13700773720191 S9.1001.27 STRAIGHT LASER PROBE, 27G IRIDEX/B&L HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 27G IRIDEX/B&L
30 13700773720184 S9.1005.25 STRAIGHT LASER PROBE, 25G DORC HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 25G DORC
31 13700773720061 S9.1003.20 STRAIGHT LASER PROBE, 20G QUANTEL HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 20G QUANTEL
32 13700773720054 S9.1002.20 STRAIGHT LASER PROBE, 20G ALCON/COHERENT/ZEISS/ELLEX/OS4 HQB Photocoagulator And Accessories 2 STRAIGHT LASER PROBE, 20G ALCON/COHERENT/ZEISS/ELLEX/OS4
33 13700773707499 S9.6017.27 TANO FORCEPS 27 G HNR Forceps, Ophthalmic 1 TANO FORCEPS 27 G
34 13700773706973 S9.3013.27 Disposable Backflush Handpiece HMX Cannula, Ophthalmic 1 Disposable Backflush Handpiece
35 13700773706966 S9.3011.27 Disposable Backflush Handpiece HMX Cannula, Ophthalmic 1 Disposable Backflush Handpiece
36 13700773706959 S9.3010.27 Disposable Backflush Handpiece HMX Cannula, Ophthalmic 1 Disposable Backflush Handpiece
37 13700773703774 S9.1214.27 FLEX CURVED LASER PROBE COMPATIBLE WITH NIDEK THREAD 27 G HQB Photocoagulator And Accessories 2 FLEX CURVED LASER PROBE COMPATIBLE WITH NIDEK THREAD 27 G
38 13700773700292 S9.2301.25 CHANDELIER 25G HQF,HQB,MPA Laser, Ophthalmic,Photocoagulator And Accessories,Endoilluminator 2 CHANDELIER 25G
39 03760087126075 DOUBLE DILATOR A8.4050 A hand-held, manual, ophthalmic surgical instrument used for enlarging the lacri A hand-held, manual, ophthalmic surgical instrument used for enlarging the lacrimal canal (the lacrimal duct) during an ophthalmic procedure. This is a reusable device. HNW Dilator, Lachrymal 1 Lacrimal dilator, reusable
40 13700773724533 S3.3010 OCULID GOLD 1,0g NCB Weights, Eyelid, Implantable 2 OCULID GOLD 1,0g
41 13700773727718 S3.60102 EXTERNAL OCULID TAN® - 1,0 g MML Weights, Eyelid, External 2 EXTERNAL OCULID TAN® - 1,0 g
42 13700773727671 S3.60083 EXTERNAL OCULID MEDIUM BROWN® - 0,8 g MML Weights, Eyelid, External 2 EXTERNAL OCULID MEDIUM BROWN® - 0,8 g
43 13700773727640 S3.60080 EXTERNAL OCULID LIGHT® - 0,8 g MML Weights, Eyelid, External 2 EXTERNAL OCULID LIGHT® - 0,8 g
44 13760087126386 S6.3050 A hand-held manual ophthalmic instrument designed to hold and insert an orbital A hand-held manual ophthalmic instrument designed to hold and insert an orbital sphere implant into the orbital cavity (eye socket). It typically has a body made of high-grade stainless steel with a piston used to forward the implant, which is held and positioned by the size-adjustable head of the device. This is a reusable device. HNP Introducer, Sphere 1 SPHERE INTRODUCER
45 13760087126232 S1.1460 A hand-held, manual, slender rod-like ophthalmic surgical instrument made of fle A hand-held, manual, slender rod-like ophthalmic surgical instrument made of flexible metal, with a blunt bulbous tip, used for exploring the lacrimal canal (the lacrimal duct) during an ophthalmic procedure. This is a reusable device. OKS Lacrimal Stents And Intubation Sets U RITLENG PROBE
46 13700773727602 S3.60061 EXTERNAL OCULID PINK® - 0,6 g MML Weights, Eyelid, External 2 EXTERNAL OCULID PINK® - 0,6 g
47 13700773727596 S3.60060 EXTERNAL OCULID LIGHT® - 0,6 g MML Weights, Eyelid, External 2 EXTERNAL OCULID LIGHT® - 0,6 g
48 13700773727343 S3.6008 OCULID PLATINUM SLIM® 0,8 g NCB Weights, Eyelid, Implantable 2 OCULID PLATINUM SLIM® 0,8 g
49 13700773727251 S3.3016 OCULID GOLD 1,6g NCB Weights, Eyelid, Implantable 2 OCULID GOLD 1,6g
50 13700773727220 S3.3010 OCULID GOLD 1,0g NCB Weights, Eyelid, Implantable 2 OCULID GOLD 1,0g
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.