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An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT (20 mm)
In Commercial Distribution
- 03760087123074 ()
- Outer Diameter: 20 Millimeter
S6.5320U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT (18 mm)
In Commercial Distribution
- 03760087123067 ()
- Outer Diameter: 18 Millimeter
S6.5318U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT (16 mm)
In Commercial Distribution
- 03760087123050 ()
- Outer Diameter: 16 Millimeter
S6.5316U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 22 mm
In Commercial Distribution
- 03760087122992 ()
- Outer Diameter: 22 Millimeter
S6.5122U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 21 mm
In Commercial Distribution
- 03760087122985 ()
- Outer Diameter: 21 Millimeter
S6.5121U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 20 mm
In Commercial Distribution
- 03760087122978 ()
- Outer Diameter: 20 Millimeter
S6.5120U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 19 mm
In Commercial Distribution
- 03760087122961 ()
- Outer Diameter: 19 Millimeter
S6.5119U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 18 mm
In Commercial Distribution
- 03760087122954 ()
- Outer Diameter: 18 Millimeter
S6.5118U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 17 mm
In Commercial Distribution
- 03760087122947 ()
- Outer Diameter: 17 Millimeter
S6.5117U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 16 mm
In Commercial Distribution
- 03760087122930 ()
- Outer Diameter: 16 Millimeter
S6.5116U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 14 mm
In Commercial Distribution
- 03760087122923 ()
- Outer Diameter: 14 Millimeter
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
BIOCERAMIC ORBITAL IMPLANT Ø 12 mm
In Commercial Distribution
- 03760087122916 ()
- Outer Diameter: 12 Millimeter
S6.5112U
- Orbital sphere implant
An ophthalmic device, typically constructed from moulded plastic, that is intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following eye surgery. This is a single-use device.
FCI S A S FCI 20 22
PERFORATED CONFORMER LARGE SIZE
In Commercial Distribution
- 03760087122756 ()
- Length: 28.3 Millimeter
- Width: 24.4 Millimeter
S6.2232U
- Ophthalmic conformer
An ophthalmic device, typically constructed from moulded plastic, that is intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following eye surgery. This is a single-use device.
FCI S A S FCI 20 22
PERFORATED CONFORMER MEDIUM SIZE
In Commercial Distribution
- 03760087122749 ()
- Length: 25.2 Millimeter
- Width: 22 Millimeter
S6.2231U
- Ophthalmic conformer
An ophthalmic device, typically constructed from moulded plastic, that is intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following eye surgery. This is a single-use device.
FCI S A S FCI 20 22
PERFORATED CONFORMER SMALL SIZE
In Commercial Distribution
- 03760087122732 ()
- Length: 22.8 Millimeter
- Width: 29.3 Millimeter
S6.2230U
- Ophthalmic conformer
An ophthalmic device, typically constructed from moulded plastic, that is intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following eye surgery. This is a single-use device.
FCI S A S FCI 20 22
S6.2001
In Commercial Distribution
- 13760087122586 ()
- 03760087122589 ()
- Ophthalmic conformer
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 22 MM
In Commercial Distribution
- 03760087122527 ()
- Outer Diameter: 22 Millimeter
S6.1022U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 20 MM
In Commercial Distribution
- 03760087122510 ()
- Outer Diameter: 20 Millimeter
S6.1020U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 19 MM
In Commercial Distribution
- 03760087122503 ()
- Outer Diameter: 19 Millimeter
S6.1019U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 18 MM
In Commercial Distribution
- 03760087122497 ()
- Outer Diameter: 18 Millimeter
S6.1018U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 17 MM
In Commercial Distribution
- 03760087122480 ()
- Outer Diameter: 17 Millimeter
S6.1017U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 16 MM
In Commercial Distribution
- 03760087122473 ()
- Outer Diameter: 16 Millimeter
S6.1016U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 15 MM
In Commercial Distribution
- 03760087122466 ()
- Outer Diameter: 15 Millimeter
S6.1015U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 14 MM
In Commercial Distribution
- 03760087122459 ()
- Outer Diameter: 14 Millimeter
S6.1014U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 13 MM
In Commercial Distribution
- 03760087122442 ()
- Outer Diameter: 13 Millimeter
S6.1013U
- Orbital sphere implant
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
FCI S A S FCI 20 22
ENUCLEATION EVISCERATION IMPLANT Ø 12 MM
In Commercial Distribution
- 03760087122435 ()
- Outer Diameter: 12 Millimeter
S6.1012U
- Orbital sphere implant
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.
FCI S A S FCI 20 22
ePTFE BAND 2.1 X 5.5 mm
In Commercial Distribution
- 03760087122428 ()
- Length: 120 Millimeter
- Width: 5.5 Millimeter
- Height: 2.1 Millimeter
S5.4821U
- Scleral buckling device, non-bioabsorbable
A sterile ophthalmic lens intended to be placed on the cornea of a patient to improve visualization of the fundus and retinal structures by surgical staff using an ophthalmic microscope during vitreoretinal surgery. Also known as a vitrectomy sutureless lens (VSL), it is made of various transparent materials [e.g., polymethylmethacrylate (PMMA), glass, quartz]. This is a single-use device.
FCI S A S FCI 20 22
S5.8000
In Commercial Distribution
- 53760087122348 ()
- 03760087122343 ()
- Vitrectomy contact lens, single-use
A sterile ophthalmic lens intended to be placed on the cornea of a patient to improve visualization of the fundus and retinal structures by surgical staff using an ophthalmic microscope during vitreoretinal surgery. Also known as a vitrectomy sutureless lens (VSL), it is made of various transparent materials [e.g., polymethylmethacrylate (PMMA), glass, quartz]. This is a single-use device.
FCI S A S FCI 20 22
DISPOSABLE PRISMATIC 30° LENS
In Commercial Distribution
- 53760087122201 ()
- 03760087122206 ()
- Angle: 30 degree
S5.7030U
- Vitrectomy contact lens, single-use
A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not dedicated to a specific intraocular procedure (e.g., device implantation). It does not contain any pharmaceuticals. This is a single-use device.
FCI S A S FCI 20 22
SELF-BLOCKING VITRECTOMY INFUSION AND CANNULA SET
In Commercial Distribution
- 53760087122195 ()
- 03760087122190 ()
S5.7020U
- Ophthalmic surgical procedure kit, non-medicated, single-use
A sterile ophthalmic lens intended to be placed on the cornea of a patient to improve visualization of the fundus and retinal structures by surgical staff using an ophthalmic microscope during vitreoretinal surgery. Also known as a vitrectomy sutureless lens (VSL), it is made of various transparent materials [e.g., polymethylmethacrylate (PMMA), glass, quartz]. This is a single-use device.
FCI S A S FCI 20 22
DISPOSABLE VITRECTOMY LENS
In Commercial Distribution
- 53760087122188 ()
- 03760087122183 ()
- Angle: 30 degree
S5.7010U
- Vitrectomy contact lens, single-use
A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not dedicated to a specific intraocular procedure (e.g., device implantation). It does not contain any pharmaceuticals. This is a single-use device.
FCI S A S FCI 20 22
DISPOSABLE VITRECTOMY SET
In Commercial Distribution
- 53760087122171 ()
- 03760087122176 ()
S5.7000U
- Ophthalmic surgical procedure kit, non-medicated, single-use
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.
FCI S A S FCI 20 22
4 X 3 mm ePTFE SPONGE (CHAUVAUD)
In Commercial Distribution
- 03760087122152 ()
- Length: 120 Millimeter
- Width: 4 Millimeter
- Height: 3 Millimeter
S5.6670U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
9 mm ePTFE STRIP (DESIGNED BY O. LEQUOY)
In Commercial Distribution
- 03760087122145 ()
- Length: 90 Millimeter
- Width: 7 Millimeter
- Height: 2.22 Millimeter
S5.6660U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE SPONGE 5 mm
In Commercial Distribution
- 03760087122138 ()
- Length: 90 Millimeter
- Outer Diameter: 5 Millimeter
S5.6650U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE HALF SPONGE 2.5 X 7.5 mm
In Commercial Distribution
- 03760087122121 ()
- Length: 120 Millimeter
- Width: 7.5 Millimeter
- Height: 2.5 Millimeter
S5.6645U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE SPONGE 4 mm
In Commercial Distribution
- 03760087122114 ()
- Length: 90 Millimeter
- Outer Diameter: 4 Millimeter
S5.6640U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE SPONGE 3.0 X 5.0 mm
In Commercial Distribution
- 03760087122091 ()
- Length: 90 Millimeter
- Width: 5 Millimeter
- Height: 3 Millimeter
S5.6635U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE SPONGE 3 mm
In Commercial Distribution
- 03760087122084 ()
- Length: 90 Millimeter
- Outer Diameter: 3 Millimeter
S5.6630U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
ePTFE SPONGE 2 X 5 mm
In Commercial Distribution
- 03760087122077 ()
- Length: 90 Millimeter
- Width: 5 Millimeter
- Height: 2 Millimeter
S5.6625U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
HALF-SPONGE 2.75 x 7.5 TYPE 511
In Commercial Distribution
- 53760087122065 ()
- 03760087122060 ()
- Length: 100 Millimeter
- Width: 7.5 Millimeter
- Height: 2.75 Millimeter
S5.6575U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
SPONGE 3 x 5 TYPE 506
In Commercial Distribution
- 53760087122058 ()
- 03760087122053 ()
- Length: 100 Millimeter
- Width: 5 Millimeter
- Height: 3 Millimeter
S5.6535U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
GROOVED SPONGE 7.5 x 3.5 TYPE 509 G
In Commercial Distribution
- 53760087122003 ()
- 03760087122008 ()
- Length: 100 Millimeter
- Width: 7.4 Millimeter
- Height: 3.5 Millimeter
S5.6570U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
GROOVED SPONGE Ø 5 mm TYPE 505 G
In Commercial Distribution
- 53760087121983 ()
- 03760087121988 ()
- Length: 100 Millimeter
- Outer Diameter: 5 Millimeter
S5.6520U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
S5.6475
In Commercial Distribution
- 33760087121972 ()
- 03760087121971 ()
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
HALF-SPONGE 2.5 x 5 TYPE 510
In Commercial Distribution
- 53760087121952 ()
- 03760087121957 ()
- Length: 100 Millimeter
- Height: 2.5 Millimeter
- Outer Diameter: 5 Millimeter
S5.6550U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
GROOVED SPONGE 5.5 x 7.5 TYPE 507 G
In Commercial Distribution
- 53760087121907 ()
- 03760087121902 ()
- Length: 100 Millimeter
- Width: 7.5 Millimeter
- Height: 5.5 Millimeter
S5.6560U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
SPONGE 5.5 x 7.5 TYPE 507
In Commercial Distribution
- 53760087121891 ()
- 03760087121896 ()
- Length: 100 Millimeter
- Width: 7.5 Millimeter
- Height: 5.5 Millimeter
S5.6557U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
GROOVED SPONGE 3 x 5 TYPE 506 G
In Commercial Distribution
- 53760087121877 ()
- 03760087121872 ()
- Length: 100 Millimeter
- Width: 5 Millimeter
- Height: 3 Millimeter
S5.6540U
- Scleral buckling device, non-bioabsorbable
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.
FCI S A S FCI 20 22
SPONGE Ø 5 mm TYPE 505
In Commercial Distribution
- 53760087121822 ()
- 03760087121827 ()
- Length: 100 Millimeter
- Outer Diameter: 5 Millimeter
S5.6505U
- Scleral buckling device, non-bioabsorbable