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Lacrimal Stents And Intubation Sets

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Name
Company Name
Description
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JEDMED
JEDMED INSTRUMENT COMPANY
LACRIMAL INTUBATION SET CRAWFORD
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JEDMED
JEDMED INSTRUMENT COMPANY
LACRIMAL INTUB SET/ SUTURE CRAWFORD
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JEDMED
JEDMED INSTRUMENT COMPANY
PROBE HOLDER BELLAN SS
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Crawford
JEDMED INSTRUMENT COMPANY
Pigtail Probe Syst Crawford Bellan
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JEDMED
JEDMED INSTRUMENT COMPANY
TUBING STRIPPER
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JEDMED
JEDMED INSTRUMENT COMPANY
DIRECTOR GROOVED ANDERSON/ HWANG
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JEDMED
JEDMED INSTRUMENT COMPANY
TUBING REMOVER INTUBATION CRAWFORD
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JEDMED
JEDMED INSTRUMENT COMPANY
HOOK CRAWFORD
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Crawford
JEDMED INSTRUMENT COMPANY
Lacrimal Intubation Set Crawford
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Crawford
JEDMED INSTRUMENT COMPANY
Lacrimal Intubation Set With Suture Crawford
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Crawford
JEDMED INSTRUMENT COMPANY
Lacrimal Intubation Set Crawford II
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Crawford
JEDMED INSTRUMENT COMPANY
Lacrimal Intubation Set With Suture Crawford II
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Crawford
JEDMED INSTRUMENT COMPANY
Intubation Set Mono-Canalicular Crawford
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LacriCATH
QUEST MEDICAL INC
LacriCATH kit DCR508-BIT contains two lacrimal duct catheters (5 mm), one AQL 1015 inflation device, and two LIS052 STENTube intubation devices.
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LacriCATH
QUEST MEDICAL INC
LacriCATH kit DCR508-UNIT contains one lacrimal duct catheter 5mm, one AQL 1015 inflation device, and one LIS052 STENTube intubation device.
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LacriCATH
QUEST MEDICAL INC
LacriCATH kit DCP315-BIT contains two lacrimal duct catheters (3 mm), one AQL1015 inflation device, and one K12-01811 stopcock.
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LacriCATH
QUEST MEDICAL INC
LacriCATH DCP315-UNIT contains one lacrimal duct catheter (3mm), and one AQL 1015 Inflation device.
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LacriCATH
QUEST MEDICAL INC
LacriCATH Model DCP213-BIT contains two lacrimal duct catheters, one AQL1015 Inflation device, and one K12-01811 stopcock.
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LacriCATH
QUEST MEDICAL INC
LacriCATH DCP2mm Unilateral kit. Contains one Lacrimal Duct Catheter and one AQL1015 Inflation device.
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RITLENG PROBE
FCI S A S FCI 20 22
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.
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OPHTACATH® 3 mm Kit Bilateral Kit
FCI S A S FCI 20 22
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OPHTACATH® 3 mm Kit Unilateral Kit
FCI S A S FCI 20 22
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.
0
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OPHTACATH® 2 mm Kit Bilateral Kit
FCI S A S FCI 20 22
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.
0
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OPHTACATH® 2 mm Kit Unilateral Kit
FCI S A S FCI 20 22
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.
0
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STENTube Lacrimal Intubation Set
QUEST MEDICAL INC
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LacriCATH
QUEST MEDICAL INC
LacriCATH Lacrimal Duct Balloon Catheter 5 mm
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LacriCATH
QUEST MEDICAL INC
LacriCATH Lacrimal Duct Balloon Catheter, 3 mm.
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LacriCATH
QUEST MEDICAL INC
2.0 mm LacriCATH lacrimal duct catheter.
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STENTube
QUEST MEDICAL INC
STENTube intubation set
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Lacrimal Intubation Set, Crawford Type
QUEST MEDICAL INC
Lacrimal Intubation Set, Crawford Type
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LACRIFLOW CL
KANEKA CORPORATION
The Lacriflow CL is indicated in treatments of epiphora in patients 12 months and older, in cases of:- Canalicular pathologies (stenosis, obstruction, lacerations),- During Dacryocystorhinostomy (conventional or laser),- Congenital nasolacrimal duct obstruction.
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LACRIFLOW CL
KANEKA CORPORATION
The Lacriflow CL is indicated in treatments of epiphora in patients 12 months and older, in cases of:- Canalicular pathologies (stenosis, obstruction, lacerations),- During Dacryocystorhinostomy (conventional or laser),- Congenital nasolacrimal duct obstruction.
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LACRIFLOW
KANEKA CORPORATION
The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of:- Canalicular pathologies (stenosis, obstruction, lacerations),- During Dacryocystorhinostomy (conventional or laser),- Congenital nasolacrimal duct obstruction.
0
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LACRIFLOW
KANEKA CORPORATION
The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of:- Canalicular pathologies (stenosis, obstruction, lacerations),- During Dacryocystorhinostomy (conventional or laser),- Congenital nasolacrimal duct obstruction.
0
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RITLENG+ PVP
FCI S A S FCI 20 22
An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with 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 (e.g., Lester Jones type), it is implanted after surgery to dilate or maintain a surgically-created passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer materials (e.g., silicone).
0
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RITLENG+
FCI S A S FCI 20 22
An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with 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 (e.g., Lester Jones type), it is implanted after surgery to dilate or maintain a surgically-created passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer materials (e.g., silicone).
0
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LACRIJET® 40
FCI S A S FCI 20 22
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.
0
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LACRIJET® 35
FCI S A S FCI 20 22
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.
0
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LACRIJET® 30
FCI S A S FCI 20 22
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.
0
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FCI NUNCHAKU 105
FCI S A S FCI 20 22
FCI NUNCHAKU 105
0
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FCI NUNCHAKU 90
FCI S A S FCI 20 22
FCI NUNCHAKU 90
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
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Lacrimal tube
FCI S A S FCI 20 22
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].
0
-
Lacrimal tube
FCI S A S FCI 20 22
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].
0
-
Lacrimal tube
FCI S A S FCI 20 22
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].
0
-
Lacrimal tube
FCI S A S FCI 20 22
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].
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