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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 DUCOURNAU BAND 2.5 X 7.0 mm
In Commercial Distribution
- 03760087121674 ()
- Length: 120 Millimeter
- Width: 7 Millimeter
- Height: 2.5 Millimeter
S5.4811U
- 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 DUCOURNAU BAND 2.5 X 5.5 mm
In Commercial Distribution
- 03760087121650 ()
- Length: 120 Millimeter
- Width: 5.5 Millimeter
- Height: 2.44 Millimeter
S5.4801U
- 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
FIXATION SLEEVE FOR S5.1025U TYPE 72
In Commercial Distribution
- 53760087121556 ()
- 03760087121551 ()
- Length: 30 Millimeter
- Outer Diameter: 2.41 Millimeter
- Lumen/Inner Diameter: 1.57 Millimeter
S5.3025U
- 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
FIXATION SLEEVE FOR S5.1015U TYPE 71
In Commercial Distribution
- 53760087121549 ()
- 03760087121544 ()
- Length: 30 Millimeter
- Outer Diameter: 2.16 Millimeter
- Lumen/Inner Diameter: 1.02 Millimeter
S5.3515U
- 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
FIXATION SLEEVE FOR S5.2005U TYPE 270
In Commercial Distribution
- 53760087121532 ()
- 03760087121537 ()
- Length: 30 Millimeter
- Outer Diameter: 1.65 Millimeter
- Lumen/Inner Diameter: 0.76 Millimeter
S5.3510U
- 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
FIXATION SLEEVE FOR S5.1005U TYPE 70
In Commercial Distribution
- 53760087121525 ()
- 03760087121520 ()
- Length: 30 Millimeter
- Outer Diameter: 2.16 Millimeter
- Lumen/Inner Diameter: 1.02 Millimeter
S5.3005U
- 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
ASYMMETRICAL TIRE 12 TYPE 280
In Commercial Distribution
- 53760087121471 ()
- 03760087121476 ()
- Width: 10 Millimeter
- Outer Diameter: 30 Millimeter
- Lumen/Inner Diameter: 23.08 Millimeter
S5.2345U
- 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
TIRE 11 TYPE 279
In Commercial Distribution
- 53760087121457 ()
- 03760087121452 ()
- Width: 9 Millimeter
- Outer Diameter: 31.23 Millimeter
S5.2335U
- 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
BICONVEX TIRE 9 TYPE 287
In Commercial Distribution
- 53760087121426 ()
- 03760087121421 ()
- Width: 7 Millimeter
- Outer Diameter: 31.28 Millimeter
S5.2315U
- 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
ASYMMETRICAL TIRE 9 TYPE 276
In Commercial Distribution
- 53760087121396 ()
- 03760087121391 ()
- Width: 7 Millimeter
- Outer Diameter: 30.9 Millimeter
S5.2295U
- 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
STRIP (8 mm) TYPE 225
In Commercial Distribution
- 53760087121327 ()
- 03760087121322 ()
- Length: 100 Millimeter
- Width: 5 Millimeter
- Height: 3.8 Millimeter
S5.2255U
- 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
STRIP (7.5 mm) TYPE 220
In Commercial Distribution
- 53760087121303 ()
- 03760087121308 ()
- Length: 100 Millimeter
- Width: 6 Millimeter
- Height: 1.50 Millimeter
S5.2205U
- 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
STRIP (6 mm) TYPE 219
In Commercial Distribution
- 53760087121297 ()
- 03760087121292 ()
- Length: 100 Millimeter
- Width: 4.5 Millimeter
- Height: 1.25 Millimeter
S5.2105U
- 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
BAND (2.5 x 0.6 mm) TYPE 240
In Commercial Distribution
- 53760087121259 ()
- 03760087121254 ()
- Length: 120 Millimeter
- Width: 2.5 Millimeter
- Height: 0.6 Millimeter
S5.2005U
- 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
TIRE 12 TYPE 78 G
In Commercial Distribution
- 53760087121242 ()
- 03760087121247 ()
- Width: 10 Millimeter
- Outer Diameter: 29.6 Millimeter
S5.1305U
- 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
STRIP (9.2 mm) TYPE 32
In Commercial Distribution
- 53760087121235 ()
- 03760087121230 ()
- Length: 100 Millimeter
- Width: 5 Millimeter
- Height: 2.5 Millimeter
S5.1255U
- 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
STRIP (7.2 mm) TYPE 31
In Commercial Distribution
- 53760087121211 ()
- 03760087121216 ()
- Length: 100 Millimeter
- Width: 4.5 Millimeter
- Height: 2 Millimeter
S5.1205U
- 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
STRIP (5.7 mm) TYPE 20
In Commercial Distribution
- 53760087121198 ()
- 03760087121193 ()
- Length: 100 Millimeter
- Width: 4 Millimeter
- Height: 1.25 Millimeter
S5.1105U
- 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
BAND (4.0 x 1.25 mm) TYPE 42
In Commercial Distribution
- 53760087121181 ()
- 03760087121186 ()
- Length: 120 Millimeter
- Width: 4.0 Millimeter
- Height: 1.25 Millimeter
S5.1025U
- 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
BAND (3.5 x 0.75 mm) TYPE 41
In Commercial Distribution
- 53760087121174 ()
- 03760087121179 ()
- 33760087121170 ()
- Length: 120 Millimeter
- Width: 3.5 Millimeter
- Height: 0.75 Millimeter
S5.1010
- 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
BAND (2.0 x 0.75 mm) TYPE 40
In Commercial Distribution
- 03760087121162 ()
- 53760087121167 ()
- Length: 120 Millimeter
- Width: 2 Millimeter
- Height: 0.75 Millimeter
S5.1005
- Scleral buckling device, non-bioabsorbable
An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the eyelid to restore upper eyelid muscle (musculus orbicularis oculi) function. This device is used for the treatment of lagophthalmos, a condition that frequently results from facial paralysis caused by Bell's palsy, trauma, a stroke, or as an indirect consequence of the surgical removal of certain types of tumour in close proximity to the facial nerve. This device uses gravity to gently close the upper eyelid when blinking or when the eyelid muscle is relaxed, and is made of a heavy material [e.g., gold (Au), platinum (Pt)].
FCI S A S FCI 20 22
PTOSE-UP 2 mm WIDTH J.M. RUBAN M.D.
In Commercial Distribution
- 03760087120806 ()
- Length: 150 Millimeter
S3.3021u
- Eyelid weight, implantable
An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the eyelid to restore upper eyelid muscle (musculus orbicularis oculi) function. This device is used for the treatment of lagophthalmos, a condition that frequently results from facial paralysis caused by Bell's palsy, trauma, a stroke, or as an indirect consequence of the surgical removal of certain types of tumour in close proximity to the facial nerve. This device uses gravity to gently close the upper eyelid when blinking or when the eyelid muscle is relaxed, and is made of a heavy material [e.g., gold (Au), platinum (Pt)].
FCI S A S FCI 20 22
PTOSE-UP 3 mm WIDTH J.M. RUBAN, M.D.
In Commercial Distribution
- 03760087120721 ()
- Length: 150 Millimeter
S3.3001u
- Eyelid weight, implantable
An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the eyelid to restore upper eyelid muscle (musculus orbicularis oculi) function. This device is used for the treatment of lagophthalmos, a condition that frequently results from facial paralysis caused by Bell's palsy, trauma, a stroke, or as an indirect consequence of the surgical removal of certain types of tumour in close proximity to the facial nerve. This device uses gravity to gently close the upper eyelid when blinking or when the eyelid muscle is relaxed, and is made of a heavy material [e.g., gold (Au), platinum (Pt)].
FCI S A S FCI 20 22
PTOSIS SLING SET LLOUQUET & GUERIN, M. D.
In Commercial Distribution
- 33760087120715 ()
- 03760087120714 ()
- Length: 280 Millimeter
S3.1000u
- Eyelid weight, implantable
A sterile device inserted into a punctal opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
SNUG PLUG
In Commercial Distribution
- 23760087120701 ()
- 03760087120707 ()
- Outer Diameter: 0.55 Millimeter
S2.4002u
- Lacrimal punctum plug
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (MICRO, 0.6)
In Commercial Distribution
- 23760087120688 ()
- 03760087120684 ()
- Outer Diameter: 0.45 Millimeter
S2.3652u
- Lacrimal punctum plug
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (SLIM PETIT, 0.5-SL)
In Commercial Distribution
- 23760087120671 ()
- 03760087120677 ()
- Outer Diameter: 0.43 Millimeter
S2.3642u
- Lacrimal punctum plug
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (SLIM MINI, 0.4-SL)
In Commercial Distribution
- 23760087120664 ()
- 03760087120660 ()
- Outer Diameter: 0.43 Millimeter
S2.3632u
- Lacrimal punctum plug
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (LARGE, US 0.1)
In Commercial Distribution
- 23760087120657 ()
- 03760087120653 ()
- Outer Diameter: 1 Millimeter
S2.3522u
- Lacrimal punctum plug
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (SMALL, US 0.8)
In Commercial Distribution
- 23760087120640 ()
- 03760087120646 ()
- Outer Diameter: 0.7 Millimeter
S2.3422u
- Lacrimal punctum plug
A sterile device inserted into a punctal opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (MEDIUM, US 0.9)
In Commercial Distribution
- 23760087120633 ()
- 03760087120639 ()
- Outer Diameter: 0.8 Millimeter
S2.3122u
- Lacrimal punctum plug
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
PVP MONO-CRAWFORD WIDE COLLARETTE B. FAYET, MD
In Commercial Distribution
- 33760087120623 ()
- 03760087120622 ()
- Length: 320 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1953u
- Lacrimal tube
A sterile device inserted into a punctal opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
PRE-LOADED PVP MINI PERFORATED PLUG J.A. BERNARD, M.D.
In Commercial Distribution
- 23760087120572 ()
- 03760087120578 ()
- Outer Diameter: 0.7 Millimeter
S1.3522u
- Lacrimal punctum plug
A sterile device inserted into a punctal opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
PRE-LOADED PVP PERFORATED PLUG J.A. BERNARD, M.D.
In Commercial Distribution
- 23760087120565 ()
- 03760087120561 ()
- Outer Diameter: 0.9 Millimeter
S1.3512u
- Lacrimal punctum plug
A sterile, hand-held, manual, ophthalmic surgical instrument used for enlarging the lacrimal canal (the lacrimal duct) during an ophthalmic procedure. This is a single-use device.
FCI S A S FCI 20 22
DISPOSABLE PUNCTUM DILATOR AND PLUG INSERTER
In Commercial Distribution
- 33760087120555 ()
- 03760087120554 ()
- Length: 133 Millimeter
S1.3090U
- Lacrimal dilator, single-use
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
PVP MONO-CRAWFORD MEDIUM COLLARETTE B. FAYET, MD
In Commercial Distribution
- 33760087120517 ()
- 03760087120516 ()
- Length: 320 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1943u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
MONO-CRAWFORD WIDE COLLARETTE B. FAYET, MD
In Commercial Distribution
- 33760087120500 ()
- 03760087120509 ()
- Outer Diameter: 0.64 Millimeter
S1.1913u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
MONO-CRAWFORD MEDIUM COLLARETTE B. FAYET, MD
In Commercial Distribution
- 33760087120494 ()
- 03760087120493 ()
- Outer Diameter: 0.64 Millimeter
S1.1903u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
PVP SELF-THREADING MONOKA FAYET, BERNARD, RITLENG
In Commercial Distribution
- 33760087120487 ()
- 03760087120486 ()
- Outer Diameter: 0.64 Millimeter
S1.1820u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
SELF-THREADING MONOKA MEDIUM COLLARETTE FAYET, BERNARD, RITLENG
In Commercial Distribution
- 33760087120470 ()
- 03760087120479 ()
- Outer Diameter: 0.64 Millimeter
S1.1810u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
SELF-THREADING MONOKA WIDE COLLARETTE FAYET, BERNARD, RITLENG
In Commercial Distribution
- 33760087120463 ()
- 03760087120462 ()
- Outer Diameter: 0.64 Millimeter
S1.1800u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
MEDIUM COLLARETTE MONOKA ® BY FAYET & BERNARD ®
In Commercial Distribution
- 33760087120456 ()
- 03760087120455 ()
- Length: 270 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1710
- Lacrimal tube
FCI directional LASER PROBE 23G QUANTEL
FCI S A S FCI 20 22
S9.1313.23
In Commercial Distribution
- 23700773723373 ()
- 03700773723379 ()
- Ophthalmic laser system beam guide
SIZER FOR LACRIJET
FCI S A S FCI 20 22
S1.1288
In Commercial Distribution
- 03700773723287 ()
- Surgical depth gauge, single-use
A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device.
FCI S A S FCI 20 22
S1.1550
In Commercial Distribution
- 13700773723277 ()
- 03700773723270 ()
- Lacrimal intubation set
A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device.
FCI S A S FCI 20 22
S1.1545
In Commercial Distribution
- 13700773723260 ()
- 03700773723263 ()
- Lacrimal intubation set
A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device.
FCI S A S FCI 20 22
S1.1515
In Commercial Distribution
- 13700773723246 ()
- 03700773723249 ()
- Lacrimal intubation set
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
PVP MONO-CRAWFORD WIDE COLLARETTE B. FAYET, MD
In Commercial Distribution
- 03700773722181 ()
- Length: 320 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1951u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
PVP MONO-CRAWFORD MEDIUM COLLARETTE B. FAYET, MD
In Commercial Distribution
- 03700773722150 ()
- Length: 320 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1941u
- Lacrimal tube
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
MONO-CRAWFORD WIDE COLLARETTE B. FAYET, MD
In Commercial Distribution
- 03700773722143 ()
- Length: 320 Millimeter
- Outer Diameter: 0.64 Millimeter
S1.1911u
- Lacrimal tube