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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Urinary Diversion Stent
BOSTON SCIENTIFIC CORPORATION
M0061603350
In Commercial Distribution

  • 08714729821151 ()

  • 8 F Stent Diameter
  • 2.7 mm Stent Diameter
  • 80 cm Effective Length


  • Polymeric ureteral stent
Urinary Diversion Stent
BOSTON SCIENTIFIC CORPORATION
M0061603300
In Commercial Distribution

  • 08714729821144 ()

  • 80 cm Effective Length
  • 7 F Stent Diameter
  • 2.3 mm Stent Diameter


  • Polymeric ureteral stent
Urinary Diversion Stent
BOSTON SCIENTIFIC CORPORATION
M0061603250
In Commercial Distribution

  • 08714729821137 ()

  • 6 F Stent Diameter
  • 2.0 mm Stent Diameter
  • 80 cm Effective Length


  • Polymeric ureteral stent
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).
FCI S A S FCI 20 22
S1.1495
In Commercial Distribution

  • 33760087127271 ()
  • 03760087127270 ()
  • 13760087127277 ()


  • Lacrimal tube
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).
FCI S A S FCI 20 22
S1.1455
In Commercial Distribution

  • 33760087127264 ()
  • 03760087127263 ()
  • 13760087127260 ()


  • Lacrimal tube
FCI NUNCHAKU 105
FCI S A S FCI 20 22
S1.1371
In Commercial Distribution

  • 13760087123743 ()
  • 03760087123746 ()


  • Lacrimal tube
FCI NUNCHAKU 90
FCI S A S FCI 20 22
S1.1361
In Commercial Distribution

  • 13760087123736 ()
  • 03760087123739 ()


  • 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
MASTERKA ® 40 (DESIGNER B. FAYET, M.D.)
In Commercial Distribution

  • 03760087123661 ()

  • Length: 40 Millimeter
  • Outer Diameter: 0.90 Millimeter
S1.1610

  • 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
AUTOSTABLE BICANALICULUS INTUBATION SET II (30 MM) WITH DILATOR
FCI S A S FCI 20 22
S1.1391
In Commercial Distribution

  • 13760087120339 ()
  • 03760087120332 ()


  • Lacrimal tube
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